Tuesday, February 8, 2011 -- Mattie died 74 weeks ago today.
Tonight's picture was taken in July of 2003. Mattie managed to scoot himself between all my flower pots and land up at the back of our plant stand. He wanted an up close and personal view of my violets, so he could feel their soft and fuzzy leaves. As you can see he was very successful, and despite not walking at 15 months, he had an incredible way of moving around quickly!
Quote of the day: One often calms one's grief by recounting it. ~ Pierre Corneille
It seems ironic that Mattie died at Georgetown University Hospital 74 weeks ago today, and that tonight I returned to the hospital for a three hour long parent advisory board meeting. As I drove into the hospital parking lot, I had an immediate reaction. Naturally I have returned to the hospital numerous times since Mattie's death, but today, as I drove to find a parking space, I couldn't help but remember Mattie and I struggling together in this concrete labyrinth. I can still vividly remember driving to the hospital when Mattie was sick, and trying to unload him and some of our things in order to check into the hospital. Finding a parking spot was nearly impossible and then I recall the elevators in the parking structure weren't always working, and I would then have to push Mattie's wheelchair through the parking lot, up the ramps, and finally into the hospital. Those moments of panic about Mattie's health, the desperation of trying to find a parking space during each hospital visit, and the feelings of sheer exhaustion from caring for Mattie all came back to me tonight. So this is the state I entered a three hour of meeting.
Naturally because Peter and I lived at the hospital for over a year, we know many people there. In three hours, I ran into three people in the hallway that we knew. The first person I saw and chatted with was Sharon, Mattie's hospital chaplain. Sharon and I caught up with each other and the running commentary I heard from everyone tonight is they are all thinking of us. Later on in the hallway I then ran into Julia, one of Mattie's HEM/ONC nurses from the Lombardi Clinic. Julia was one of our favorite nurses in the clinic. She has a calm demeanor, which was needed by both Mattie and I. Unfortunately Mattie did not get assigned to Julia often. I was very touched to hear that Julia continues to read our blog, and loves looking at the nightly pictures of Mattie. After I saw Julia, I then ran into Dr. Abu-Ghosh. Dr. Abu-Ghosh is Brandon's (Mattie's big buddy) doctor and she was also Cody's doctor. Some of you may recall me talking about Cody. Cody was Mattie's age and died from Neuroblastoma about 7 months before Mattie. I still recall the video I saw of Dr. Abu-Ghosh holding Cody as a baby (since he battled cancer for years), and it can still brings tears to my eyes. Mainly because you could see the hope Dr. Abu-Ghosh and Cody's mom had in their eyes, as they were caring for Cody. In any case, Dr. Abu-Ghosh was surprised to see me, we gave each other a hug, and it seems to me in the hug many memories were exchanged between the two of us. Words weren't needed, since we lived through many anxious Mattie moments together in the PICU and the clinic.
Tonight's meeting was in a way bittersweet. The sweet portion is I am hearing and learning about the needs of parents caring for hospitalized children and through my position on the board, I am able to participate in some exciting projects. Projects that The Mattie Miracle Cancer Foundation maybe able to fund and oversee. I am working on two initiatives in particular and I hope to unfold my thinking at our Foundation Walk on May 22. However, there is also a bitter side to these meetings. Tonight, our pediatric advisory board met with the Neonatal Intensive Care Unit (NICU) advisory board. Since our groups do not know each other, we all went around and introduced ourselves. Every board member is intimately involved with the hospital because his/her child was treated there. So naturally I have this in common with these board members, however, what we do not share in common is that special club I write so often about. The grieving club. Each time I have to introduce myself in this type of setting, I find that I want to scream. I want to scream because others can't possibly understand my pain. Their children are alive, their children survived. Most of them do not know how hard it is to come back to the hospital and try to help, to try to run a foundation, and to try to keep Mattie's memory alive. After the meeting was over, the woman sitting next to me came over to talk to me. She wanted to tell me that she admired me and also couldn't understand how I look so together. She told me if she were me, she doesn't think she would be able to participate in tonight's meeting. While chatting with her, another mom came up to talk with both of us. This other mom lost her premature baby after a six month battle. This other mom sits on the NICU board and she basically said the same thing I did. She said that no one understands her, no one sees that before she enters the hospital, she debates for minutes whether she is up to going in. Her internal dialogue goes like this..... Am I up to helping someone else? Am I up to accepting that others don't understand and can be insensitive to me? I told her I appreciated her sharing her feelings with me, because we are definitely in the minority, but clearly feeling in a simple fashion.
In the midst of the meetings tonight, I learned that the fish tank Mattie loved on the fifth floor of the hospital has been removed. I can't tell you how upsetting that was for me to hear. I honestly don't know how we would have gotten Mattie out of his hospital room during the weekends without those fish. Mattie felt responsible for them, and would get up and out just to feed them. I am not sure why the loss of the fish tank seems so huge to me, but it does.
I am signing off for the evening because I feel extremely worn out from the day. As I repeat to myself often........ one day at a time, and maybe tomorrow will be different.
February 8, 2011
February 7, 2011
Monday, February 7, 2011
Monday, February 7, 2011
Tonight's picture was taken in July of 2003, in the Outer Banks of North Carolina. Fortunately that summer we stayed in a house right on the water, because that was the extent of us seeing the ocean that July. Mattie did not like the sand or the ocean for that matter in the beginning. He was far more interested in the garden hose on the deck. I love this photo because if I could give it a title, I would call it, Monkey see, Monkey do! Mattie was ALWAYS interested in whatever projects Peter was doing. Despite not walking independently, Mattie desperately tried to keep up. They were quite a twosome together!
Quote of the day: She was no longer wrestling with the grief, but could sit down with it as a lasting companion and make it a sharer in her thoughts. ~ George Eliot
I suppose George Eliot's quote is something to strive for. I want to thank so many of you for reaching out to me last night and today and sharing your thoughts about my weekend postings. My writings this weekend focused upon the challenges of cleaning out a closet filled with history and memories. Or perhaps in my case, the challenge was really to confront grief head on. I have been unable until now to really contend with the piles around me. As things came home from the hospital, and I dropped them all over the place, that is where they remained. Every living space in our home is occupied with Mattie's things, and it is hard to face the fact that I have to address this. For over a year, I wouldn't, couldn't, and refused to. But the thing is, seeing these piles is not making me feel any better. In many ways it makes me feel further trapped and isolated. So it is a catch 22. I am conflicted to live this way, and I am conflicted when I touch the piles, clean out, and reorganize. I wasn't sure I adequately conveyed in the blog the level of difficulty and pain this weekend brought, but clearly from the feedback I am getting, my words obviously struck a chord. So thank you for sharing your thoughts and support with me.
I began my day with a lovely picture of Mattie's tree. This picture was sent to me by Mattie's lower school head, Bob, aka "the magic man." Bob wrote, "As I leave my office in the evening or come in on the weekend, in the quiet of the campus I will often pause to look at Mattie’s tree. On a breezy day, of course, I can listen to it as well! This weekend I took a picture of it on my phone as I passed by. Despite some of the harsh weather that we have had, the beautiful cranes remain on its branches. And it still has its leaves!"
I agree with Bob. Isn't it fascinating that this tree doesn't lose its leaves? All the other trees around it are barren, but NOT Mattie's tree. It is a tiny but strong tree, which seems to be a very meaningful symbol of Mattie. The tree not only holds it leaves but it has a birdhouse on it, praying origami cranes, a butterfly wind chime, and its most recent addition, a butterfly Christmas tree ornament. As many of you know this tree was a gift to the school from Mattie's classmates and parents, and to us, it is a very important living symbol of Mattie's memory.
I had the wonderful opportunity to have lunch with Linda today. As many of my faithful readers know, Linda was Mattie's childlife specialist at Georgetown University Hospital. Linda was an integral part of Mattie's life and ours as well. She helped us survive many horrific days and also worked hard to make Mattie feel important, special, and normal. Linda is an amazing professional and I told her she is also part therapist. She assesses situations and people very well, and also is a beautiful patient and family advocate. Needless to say, Linda's professionalism, kindness, and compassion will remain with me always. We had a lovely lunch together and I chatted with her about ways the Mattie Miracle Cancer Foundation can help the childlife program at the hospital. One of our Foundation's goals is to address the psychosocial needs of children with cancer and their families. The term psychosocial may sound amorphous, but it actually describes very commonplace issues. In fact, every human being on this planet has a psychosocial issue and concern, and naturally when struck by cancer, such concerns, if left unaddressed, can escalate into full blown mental health issues.
The Diagnostic and Statistical Manual of Mental Disorders (DSM) is published by the American Psychiatric Association and provides a common language and standard criteria for the classification of mental disorders. It is used in the United States and in varying degrees around the world, by clinicians, researchers, psychiatric drug regulation agencies, health insurance companies, pharmaceutical companies, and policy makers. When diagnosing a client, mental health professionals consider the extent and type of psychosocial issues present in one's life. According to the DSM, "A psychosocial or environmental problem may be a negative life event, an environmental difficulty or deficiency, a familial or other interpersonal stressor, an inadequacy of social support of personal resources, or other problems relating to the context in which an individual's difficulties have developed. Psychosocial and Environmental Problems fall into nine categories, including:
1) Problems with primary support group
2) Problems related to the social environment
3) Educational problems
4) Occupational problems
5) Housing problems
6) Economic problems
7) Problems with access to health care services
8) Problems related to interaction with the legal system/crime
9) Other psychosocial and environmental problems
The point is when cancer hits a family, almost all nine categories of psychosocial issues arise. Cancer can impact your family relationships, so much so that sometimes it separates people rather than brings them closer together. Cancer can also severe friendships and leave you feeling very socially isolated. Naturally as with Mattie's case, he was unable to go to school, and missed the ability to attend first grade. We certainly had a housing problem, because we lived most of our life confined to a two by four of a hospital room. Keep in mind that meant that I slept in a chair and also shared a shower with other families! Economic problems are huge for families living with cancer. The cost of cancer care is enormous and a good percentage of families are left bankrupt from the battle. Access to health care services is also a problem, because depending upon the type of health insurance coverage you have, you quickly will see what types of services and medications your child will have access to. Plainly stated, CANCER affects individuals' ability to function in their daily activities of life. So from our Foundation's perspective cancer is a psychosocial concern and one of our mission's is to help children and their families manage the issues that arise from these categories listed above.
Linda and I chatted about specific needs she sees within the hospital, and her insights helped to stimulate my thinking. As our Foundation is growing, we are in the position to begin to make a difference in the lives of children and their families, and I want to make sure whatever we are involved in, that it will be helping families psychosocially and naturally would be something that captures Mattie's incredible spirit.
Peter and I received this wonderful sermon below from a colleague of Peter's. She attends The Old Presbyterian Meeting House in Alexandria, VA and the pastor at her church recently lost his son in an accident. I was so moved by this meaningful sermon, that I wanted to share it with you. I was impressed with his honesty, openneness, and his permission to be vulnerable with his congregation. Here is a man who has helped many people grieve over the years, and yet, he freely acknowledges that in all his year's of service, the death of his son has been earth shattering and unlike anything he could ever image. I can appreciate his questionning God's existence, and I understand when he is feeling uncertain about his faith, he looks to others in his life to help ground him. In a way he sees the face and hands of God in every kind action and support offered to him by those around him. I couldn't have stated it better myself. The whole message is very thought provoking and powerful and I hope you enjoy reading it as much as I did.
===========================================
The Problems and the Promises of Waiting by Dr. Robert R. Laha, Jr
Psalm 130; Romans 8:18‐27, 31‐39
I stand here before you today to tell you that what you have heard all of your life is true, there is nothing worse than the loss of one’s own child. I am well acquainted with death. I have experienced the death of countless numbers of people over the years‐ some old, some young, some well‐known, others less so‐ and I can tell you that each and every one of them was dearly loved by their families, their churches, and by me, their pastor. I have also experienced the death of most of my family members‐ grandparents, parents, aunts, uncles, and numerous cousins. I dug the graves of my mother and my father and laid them to rest with my own hands. But in terms of their affects on me, there is not a one of those deaths or burials that can compare to the death of my son, Rob. It feels as though something or someone has reached into my chest and torn my heart into pieces.
As so many of you have said to me, “It is not supposed to be this way. Children are not supposed to die before their parents.” But they do. They die and leave big holes in our lives that can never be filled. They die and leave us changed, never again to be the persons we were before. But worse than that, their dying changes the future‐ not just theirs but ours as well. Their dying leaves us to face a radically altered future, a future with nothing but their memories to guide and console us. The theologian, Nicholas Wolterstorff, says something very similar about the death of his son. His words give voice to the tragedy of a life lost too soon and the grieving that inevitably follows such a tragedy.
“I give of myself to the formation of this other person, from helplessness to independence…I take it on myself to stay with him so that he has a future, a future in which I can delight…But now he has slipped out my arms. He’s gone and that future has been destroyed…He’s only in my memory now, not in my life. Nothing new can happen between us. Everything is sealed tight, shut in the past. But I am still here. I have to go on. I have to start over. But this new start is different from the first. Then I wasn’t carrying this load, this thing that’s over.”
As you can imagine, it is hard for me to believe that Rob’s life is really over, hard to believe that I and other members of my family have to start over without him. For the first few days after his death, I found myself in denial. It’s just a bad dream, I thought to myself. I’ll wake up and see him walking into my house, or meet him at the Home Depot, or share a meal with him at some restaurant. But I soon woke up to the realization that it was true, he was dead and I would never see him again. And then I got angry‐ angry with Rob and angry with myself. I made myself sick playing the coulda, shoulda game, second guessing all we had ever done or failed to do. Only then, did I begin to grieve in a way that I had never grieved before. And only then, did I begin to question God in a way that I had never questioned God before. I am supposed to know something about grieving. As a pastoral theologian, I have taken and taught numerous courses on grieving to seminarians and church members. As a pastor, I have grieved with and for many people. Even so, I find myself ill prepared for the kind of grieving that now consumes me and my family. Like the Psalmist, I find myself crying out from the deep, dark, and deathly places of another world, a world that I have been forced to enter against my will. I cry out “Why, God? Why did you let this happen? Why didn’t you do something to help my son?” For years, I have prayed for you to heal his mind and body from the terrible of effects of war, drugs, and alcohol. I have prayed for you to help him chase away the demons of his past so that he might find his way in life. I have prayed that you might show him how to use the enormous talents you gave him to some good end. I have prayed for you give him a home and family of his own, things for which I know he longed. But you did not do any of these things, God, a fact that hurts and confuses me.
The poet, Ann Weems, speaks to my hurt and confusion in a heart‐wrenching psalm of lament written after the death of her son, Todd.
O God, I live in the land of the forgotten.
I stretch out my hand to you
and there is nothing.
I cry night and day,
and you do not take pity on me.
I pray to you,
but you turn away.
O God, why won’t you help me?
You show compassion for your enemies
and long for the faithless to return to you,
Yet I have worshiped you
since I was a child,
and have lived in covenant with you,
yet, like a fly,
I am brushed away
from your throne
as though I don’t belong
in your presence.
How long will I have to live
outside your holiness?
How long will I have to endure
the unholy hell
of the presence of death?
How long will I have to feel
the ever‐fresh wound
of the absence
of him whom I loved?
Undo it, O God!
Give him back!
O God, why did you create a life
that includes death?
Why did you create us
to love one another
and then take from us
the ones we love?
Like Weems and so many others before me, I cannot make sense of what has happened. I cannot bring myself to say that God caused Rob’s death but neither can I say that God could not have done something to prevent it. This is what hurts and confuses me so. I grieve the fact that Rob is dead, that he did not have the time to realize his hopes and dreams. I grieve the fact that neither I, nor Sally, nor Jenny, nor Ben, nor Robyn, nor little Grace will ever again see his face or hear his voice. I grieve that none of us will ever again feel his arms around us, or ours around him. I grieve the deep, painful wounds that his death has brought to me and my family. And like C. S. Lewis, I believe that our wounds, and the wounds of all humanity, are
unanswered questions for which God must one day give an account. I have no satisfactory explanation for Rob’s untimely death. I do not know why God did not intervene and save my son. But then again, I do not know why God did not intervene and save his own son who also cried out from the darkness, “My God, my God, why have you forsaken me?” So, like the Psalmist, and like Jesus, I have to wait in the darkness for the answers, hoping that, sooner or later, I will see the light. Waiting is hard to do. I don’t like being kept in the dark. I don’t like the questions that hound me in the night. Waiting induces its own kind of suffering. But I am learning that what the scriptures say is true‐ suffering produces endurance, and endurance leads to a hope that doesn’t disappoint us.
In a sermon preached some 20 years after the death of his daughter, Laura Lue, the late John Claypool noted that there are times when the only thing God offers us “is the power to endure what cannot be changed, to allow the change to take place within us rather than in the outward circumstance we face.” For Claypool, and for me, the power to endure the death of one’s child and not fall into a deep and debilitating despair is perhaps one of the most relevant and miraculous things God can do for us. But how, you might ask, does this power manifest itself?
For me, the power to endure comes with knowing that I am not alone in my suffering, that even in the darkest valley with the shadow of death all around me, God is with me. In A Letter of Consolation, Henri Nouwen speaks to both the problems and the promises of waiting and, in doing so, he helps me to understand that death and darkness will not hem me in forever.
“If the God who loved us so much that he wanted to experience with us the total absurdity of death, then‐ yes, there must be hope; then there must be something more than death; then there must be a promise that is not fulfilled in our short existence in this world; then leaving behind the ones we love…cannot be just the destruction and cruel end of things; then indeed I have to wait for the third day.”
This, of course, is what the Apostle Paul is getting at when he says that our present sufferings are not worth comparing to the future glory that will be revealed to us. He knows that waiting is hard for us, that it makes us groan inwardly. But he also affirms that while we groan and wait for the redemption of our bodies, the Holy Spirit helps us in our weakness and intercedes for us with sighs too deep for words. The Spirit knows what we need. The Spirit also knows what God wills for us and all of creation. And the Spirit works to bring those things into harmony, doing for us what we cannot do for ourselves. Just so, we can endure this time of waiting because, as God has shown us in the work of both Jesus and the Holy Spirit, we know
that nothing, not even death, can separate us from the love of God. But the power to endure this dark and deathly time of waiting has manifested itself to me in another way that is every bit as remarkable as the first. It has come to me through other people‐ friends and family members, preachers and poets, known and unknown members of the faith community. It has come to me through people like you, people who dare to enter into my grief, people who dare to stand with me in my dark time of waiting. While I am weak, you
are strong. While I am blind, you see. While my faith falters, you stand firm in yours. While I am lost, you know the way home. And so I give thanks to God for many ways in which you ministered to me and my family.
Over these past few weeks, I have learned, as if for the first time, that nothing, not even death can separate me from the love of God. I have learned that, with your help and God’s, I can now wait with a new confidence that there will come a time when “God will wipe away every tear from our eyes, a time when death will be no more; a time when mourning and crying and pain will be no more, for the first things will have passed away…and the glory of God will be our light.” And I can wait with the confidence that such a time has already come for Rob; that for him a new morning has dawned, flooding his darkness with the glorious light of our loving God. Amen.
A sermon preached on
January 30, 2011 by
Dr. Robert R. Laha, Jr. at
The Old Presbyterian Meeting House
Alexandria, Virginia
after the death of his son, Rob.
In memoriam:
Robert R. Laha III
February 1, 1979‐December 19, 2010
Copyright 2011
=============================================
Tonight's picture was taken in July of 2003, in the Outer Banks of North Carolina. Fortunately that summer we stayed in a house right on the water, because that was the extent of us seeing the ocean that July. Mattie did not like the sand or the ocean for that matter in the beginning. He was far more interested in the garden hose on the deck. I love this photo because if I could give it a title, I would call it, Monkey see, Monkey do! Mattie was ALWAYS interested in whatever projects Peter was doing. Despite not walking independently, Mattie desperately tried to keep up. They were quite a twosome together!
Quote of the day: She was no longer wrestling with the grief, but could sit down with it as a lasting companion and make it a sharer in her thoughts. ~ George Eliot
I suppose George Eliot's quote is something to strive for. I want to thank so many of you for reaching out to me last night and today and sharing your thoughts about my weekend postings. My writings this weekend focused upon the challenges of cleaning out a closet filled with history and memories. Or perhaps in my case, the challenge was really to confront grief head on. I have been unable until now to really contend with the piles around me. As things came home from the hospital, and I dropped them all over the place, that is where they remained. Every living space in our home is occupied with Mattie's things, and it is hard to face the fact that I have to address this. For over a year, I wouldn't, couldn't, and refused to. But the thing is, seeing these piles is not making me feel any better. In many ways it makes me feel further trapped and isolated. So it is a catch 22. I am conflicted to live this way, and I am conflicted when I touch the piles, clean out, and reorganize. I wasn't sure I adequately conveyed in the blog the level of difficulty and pain this weekend brought, but clearly from the feedback I am getting, my words obviously struck a chord. So thank you for sharing your thoughts and support with me.
I began my day with a lovely picture of Mattie's tree. This picture was sent to me by Mattie's lower school head, Bob, aka "the magic man." Bob wrote, "As I leave my office in the evening or come in on the weekend, in the quiet of the campus I will often pause to look at Mattie’s tree. On a breezy day, of course, I can listen to it as well! This weekend I took a picture of it on my phone as I passed by. Despite some of the harsh weather that we have had, the beautiful cranes remain on its branches. And it still has its leaves!"
I agree with Bob. Isn't it fascinating that this tree doesn't lose its leaves? All the other trees around it are barren, but NOT Mattie's tree. It is a tiny but strong tree, which seems to be a very meaningful symbol of Mattie. The tree not only holds it leaves but it has a birdhouse on it, praying origami cranes, a butterfly wind chime, and its most recent addition, a butterfly Christmas tree ornament. As many of you know this tree was a gift to the school from Mattie's classmates and parents, and to us, it is a very important living symbol of Mattie's memory.
I had the wonderful opportunity to have lunch with Linda today. As many of my faithful readers know, Linda was Mattie's childlife specialist at Georgetown University Hospital. Linda was an integral part of Mattie's life and ours as well. She helped us survive many horrific days and also worked hard to make Mattie feel important, special, and normal. Linda is an amazing professional and I told her she is also part therapist. She assesses situations and people very well, and also is a beautiful patient and family advocate. Needless to say, Linda's professionalism, kindness, and compassion will remain with me always. We had a lovely lunch together and I chatted with her about ways the Mattie Miracle Cancer Foundation can help the childlife program at the hospital. One of our Foundation's goals is to address the psychosocial needs of children with cancer and their families. The term psychosocial may sound amorphous, but it actually describes very commonplace issues. In fact, every human being on this planet has a psychosocial issue and concern, and naturally when struck by cancer, such concerns, if left unaddressed, can escalate into full blown mental health issues.
The Diagnostic and Statistical Manual of Mental Disorders (DSM) is published by the American Psychiatric Association and provides a common language and standard criteria for the classification of mental disorders. It is used in the United States and in varying degrees around the world, by clinicians, researchers, psychiatric drug regulation agencies, health insurance companies, pharmaceutical companies, and policy makers. When diagnosing a client, mental health professionals consider the extent and type of psychosocial issues present in one's life. According to the DSM, "A psychosocial or environmental problem may be a negative life event, an environmental difficulty or deficiency, a familial or other interpersonal stressor, an inadequacy of social support of personal resources, or other problems relating to the context in which an individual's difficulties have developed. Psychosocial and Environmental Problems fall into nine categories, including:
1) Problems with primary support group
2) Problems related to the social environment
3) Educational problems
4) Occupational problems
5) Housing problems
6) Economic problems
7) Problems with access to health care services
8) Problems related to interaction with the legal system/crime
9) Other psychosocial and environmental problems
The point is when cancer hits a family, almost all nine categories of psychosocial issues arise. Cancer can impact your family relationships, so much so that sometimes it separates people rather than brings them closer together. Cancer can also severe friendships and leave you feeling very socially isolated. Naturally as with Mattie's case, he was unable to go to school, and missed the ability to attend first grade. We certainly had a housing problem, because we lived most of our life confined to a two by four of a hospital room. Keep in mind that meant that I slept in a chair and also shared a shower with other families! Economic problems are huge for families living with cancer. The cost of cancer care is enormous and a good percentage of families are left bankrupt from the battle. Access to health care services is also a problem, because depending upon the type of health insurance coverage you have, you quickly will see what types of services and medications your child will have access to. Plainly stated, CANCER affects individuals' ability to function in their daily activities of life. So from our Foundation's perspective cancer is a psychosocial concern and one of our mission's is to help children and their families manage the issues that arise from these categories listed above.
Linda and I chatted about specific needs she sees within the hospital, and her insights helped to stimulate my thinking. As our Foundation is growing, we are in the position to begin to make a difference in the lives of children and their families, and I want to make sure whatever we are involved in, that it will be helping families psychosocially and naturally would be something that captures Mattie's incredible spirit.
Peter and I received this wonderful sermon below from a colleague of Peter's. She attends The Old Presbyterian Meeting House in Alexandria, VA and the pastor at her church recently lost his son in an accident. I was so moved by this meaningful sermon, that I wanted to share it with you. I was impressed with his honesty, openneness, and his permission to be vulnerable with his congregation. Here is a man who has helped many people grieve over the years, and yet, he freely acknowledges that in all his year's of service, the death of his son has been earth shattering and unlike anything he could ever image. I can appreciate his questionning God's existence, and I understand when he is feeling uncertain about his faith, he looks to others in his life to help ground him. In a way he sees the face and hands of God in every kind action and support offered to him by those around him. I couldn't have stated it better myself. The whole message is very thought provoking and powerful and I hope you enjoy reading it as much as I did.
===========================================
The Problems and the Promises of Waiting by Dr. Robert R. Laha, Jr
Psalm 130; Romans 8:18‐27, 31‐39
I stand here before you today to tell you that what you have heard all of your life is true, there is nothing worse than the loss of one’s own child. I am well acquainted with death. I have experienced the death of countless numbers of people over the years‐ some old, some young, some well‐known, others less so‐ and I can tell you that each and every one of them was dearly loved by their families, their churches, and by me, their pastor. I have also experienced the death of most of my family members‐ grandparents, parents, aunts, uncles, and numerous cousins. I dug the graves of my mother and my father and laid them to rest with my own hands. But in terms of their affects on me, there is not a one of those deaths or burials that can compare to the death of my son, Rob. It feels as though something or someone has reached into my chest and torn my heart into pieces.
As so many of you have said to me, “It is not supposed to be this way. Children are not supposed to die before their parents.” But they do. They die and leave big holes in our lives that can never be filled. They die and leave us changed, never again to be the persons we were before. But worse than that, their dying changes the future‐ not just theirs but ours as well. Their dying leaves us to face a radically altered future, a future with nothing but their memories to guide and console us. The theologian, Nicholas Wolterstorff, says something very similar about the death of his son. His words give voice to the tragedy of a life lost too soon and the grieving that inevitably follows such a tragedy.
“I give of myself to the formation of this other person, from helplessness to independence…I take it on myself to stay with him so that he has a future, a future in which I can delight…But now he has slipped out my arms. He’s gone and that future has been destroyed…He’s only in my memory now, not in my life. Nothing new can happen between us. Everything is sealed tight, shut in the past. But I am still here. I have to go on. I have to start over. But this new start is different from the first. Then I wasn’t carrying this load, this thing that’s over.”
As you can imagine, it is hard for me to believe that Rob’s life is really over, hard to believe that I and other members of my family have to start over without him. For the first few days after his death, I found myself in denial. It’s just a bad dream, I thought to myself. I’ll wake up and see him walking into my house, or meet him at the Home Depot, or share a meal with him at some restaurant. But I soon woke up to the realization that it was true, he was dead and I would never see him again. And then I got angry‐ angry with Rob and angry with myself. I made myself sick playing the coulda, shoulda game, second guessing all we had ever done or failed to do. Only then, did I begin to grieve in a way that I had never grieved before. And only then, did I begin to question God in a way that I had never questioned God before. I am supposed to know something about grieving. As a pastoral theologian, I have taken and taught numerous courses on grieving to seminarians and church members. As a pastor, I have grieved with and for many people. Even so, I find myself ill prepared for the kind of grieving that now consumes me and my family. Like the Psalmist, I find myself crying out from the deep, dark, and deathly places of another world, a world that I have been forced to enter against my will. I cry out “Why, God? Why did you let this happen? Why didn’t you do something to help my son?” For years, I have prayed for you to heal his mind and body from the terrible of effects of war, drugs, and alcohol. I have prayed for you to help him chase away the demons of his past so that he might find his way in life. I have prayed that you might show him how to use the enormous talents you gave him to some good end. I have prayed for you give him a home and family of his own, things for which I know he longed. But you did not do any of these things, God, a fact that hurts and confuses me.
The poet, Ann Weems, speaks to my hurt and confusion in a heart‐wrenching psalm of lament written after the death of her son, Todd.
O God, I live in the land of the forgotten.
I stretch out my hand to you
and there is nothing.
I cry night and day,
and you do not take pity on me.
I pray to you,
but you turn away.
O God, why won’t you help me?
You show compassion for your enemies
and long for the faithless to return to you,
Yet I have worshiped you
since I was a child,
and have lived in covenant with you,
yet, like a fly,
I am brushed away
from your throne
as though I don’t belong
in your presence.
How long will I have to live
outside your holiness?
How long will I have to endure
the unholy hell
of the presence of death?
How long will I have to feel
the ever‐fresh wound
of the absence
of him whom I loved?
Undo it, O God!
Give him back!
O God, why did you create a life
that includes death?
Why did you create us
to love one another
and then take from us
the ones we love?
Like Weems and so many others before me, I cannot make sense of what has happened. I cannot bring myself to say that God caused Rob’s death but neither can I say that God could not have done something to prevent it. This is what hurts and confuses me so. I grieve the fact that Rob is dead, that he did not have the time to realize his hopes and dreams. I grieve the fact that neither I, nor Sally, nor Jenny, nor Ben, nor Robyn, nor little Grace will ever again see his face or hear his voice. I grieve that none of us will ever again feel his arms around us, or ours around him. I grieve the deep, painful wounds that his death has brought to me and my family. And like C. S. Lewis, I believe that our wounds, and the wounds of all humanity, are
unanswered questions for which God must one day give an account. I have no satisfactory explanation for Rob’s untimely death. I do not know why God did not intervene and save my son. But then again, I do not know why God did not intervene and save his own son who also cried out from the darkness, “My God, my God, why have you forsaken me?” So, like the Psalmist, and like Jesus, I have to wait in the darkness for the answers, hoping that, sooner or later, I will see the light. Waiting is hard to do. I don’t like being kept in the dark. I don’t like the questions that hound me in the night. Waiting induces its own kind of suffering. But I am learning that what the scriptures say is true‐ suffering produces endurance, and endurance leads to a hope that doesn’t disappoint us.
In a sermon preached some 20 years after the death of his daughter, Laura Lue, the late John Claypool noted that there are times when the only thing God offers us “is the power to endure what cannot be changed, to allow the change to take place within us rather than in the outward circumstance we face.” For Claypool, and for me, the power to endure the death of one’s child and not fall into a deep and debilitating despair is perhaps one of the most relevant and miraculous things God can do for us. But how, you might ask, does this power manifest itself?
For me, the power to endure comes with knowing that I am not alone in my suffering, that even in the darkest valley with the shadow of death all around me, God is with me. In A Letter of Consolation, Henri Nouwen speaks to both the problems and the promises of waiting and, in doing so, he helps me to understand that death and darkness will not hem me in forever.
“If the God who loved us so much that he wanted to experience with us the total absurdity of death, then‐ yes, there must be hope; then there must be something more than death; then there must be a promise that is not fulfilled in our short existence in this world; then leaving behind the ones we love…cannot be just the destruction and cruel end of things; then indeed I have to wait for the third day.”
This, of course, is what the Apostle Paul is getting at when he says that our present sufferings are not worth comparing to the future glory that will be revealed to us. He knows that waiting is hard for us, that it makes us groan inwardly. But he also affirms that while we groan and wait for the redemption of our bodies, the Holy Spirit helps us in our weakness and intercedes for us with sighs too deep for words. The Spirit knows what we need. The Spirit also knows what God wills for us and all of creation. And the Spirit works to bring those things into harmony, doing for us what we cannot do for ourselves. Just so, we can endure this time of waiting because, as God has shown us in the work of both Jesus and the Holy Spirit, we know
that nothing, not even death, can separate us from the love of God. But the power to endure this dark and deathly time of waiting has manifested itself to me in another way that is every bit as remarkable as the first. It has come to me through other people‐ friends and family members, preachers and poets, known and unknown members of the faith community. It has come to me through people like you, people who dare to enter into my grief, people who dare to stand with me in my dark time of waiting. While I am weak, you
are strong. While I am blind, you see. While my faith falters, you stand firm in yours. While I am lost, you know the way home. And so I give thanks to God for many ways in which you ministered to me and my family.
Over these past few weeks, I have learned, as if for the first time, that nothing, not even death can separate me from the love of God. I have learned that, with your help and God’s, I can now wait with a new confidence that there will come a time when “God will wipe away every tear from our eyes, a time when death will be no more; a time when mourning and crying and pain will be no more, for the first things will have passed away…and the glory of God will be our light.” And I can wait with the confidence that such a time has already come for Rob; that for him a new morning has dawned, flooding his darkness with the glorious light of our loving God. Amen.
A sermon preached on
January 30, 2011 by
Dr. Robert R. Laha, Jr. at
The Old Presbyterian Meeting House
Alexandria, Virginia
after the death of his son, Rob.
In memoriam:
Robert R. Laha III
February 1, 1979‐December 19, 2010
Copyright 2011
=============================================
February 6, 2011
Sunday, February 6, 2011
Sunday, February 6, 2011
Tonight's picture was taken on our deck in July of 2003. Mattie had just begun to enjoy being in water, and what he really loved was playing in it. Particularly he was fascinated by things that would float, sink, and so forth. He was our little scientist, full of investigation and curiosity.
Quote of the day: There are places in the heart that do not yet exist; suffering has to enter in for them to come to be. ~ Leon Bloy
Despite the fact that we had a hawk visit us yesterday and basically devour a pigeon on our balcony, the sparrows fortunately did return today. I asked Peter what the chances are of having a hawk visit us, when we live right in the middle of the city. Our goal is to feed sparrows and small birds, and it upsets me when this hawk stops by. Mattie and I have experienced this sighting one other time, in which a hawk came down from the sky and grabbed a sparrow right off the bird feeder. Needless to say, Mattie and I were stunned and we talked about this for years.
As you can see the feeder was very busy today! In the corner of the picture, you can also see Mattie's purple stained glass butterfly that remains on our window.
I spent the entire day at home, cleaning out our walk-in closet. I was at it for over six hours. I am happy to report that I can now walk into the closet, see actual shelf space, and a level of organization. I couldn't have done this without Peter, who was removing bags as quickly as I was generating them. In the midst of all of this, Peter would come up and give me a pep talk, and acknowledge the progress being made. This is not a project I would take on during the week alone. It is something that I need support on, encouragement, and at times we land up chatting.
Peter told me tonight, as he was throwing out things I gave him, that he in essence was saying "good-bye to our future." That may sound strange to our readers, because you most likely are saying.... aren't they cleaning up and throwing things out from their past? The answer is yes, but think about why you keep things. In our case, we held onto things because it was our hope to share them with Mattie in the future. A future that will never happen. In addition, Peter and I saved things because we were not sure if we would need them again. What we learned from cancer and Mattie's death is we really don't need THINGS anymore. The objects that once meant so much to us, no longer mean a thing.
Last night, Peter and I chatted about the cleaning up and reorganization process. We are not going through things and crying, we are going through it and are simply numb. Numb again, a feeling I am well acquainted with. Though this time I am numb and disgusted at the same time. Disgusted because we can't believe what happened to our lives. I told Peter that I feel in many ways that I have jumped through several developmental stages, and instead of being where I should be chronologically, I have aged dramatically and find myself dealing with death and dying issues. As I was going through the closet, I came across the cub scout uniform I bought Mattie. I literally bought him this outfit a month before he was diagnosed with cancer. He was looking forward to starting cub scouts in the fall of 2008, and having Peter as his den leader. In addition to that, I came across Mattie's baby shoes, his baptism outfit, and several more cards that he wrote to me. So naturally none of this was easy to see and go through. There was just so much in this closet, and as we were either throwing things away or making piles for Goodwill, I just felt unhappy. This is not how life was supposed to be. I had accumulated many books over the years while raising Mattie. One of them was "What to expect during the toddler years." I asked Peter if he thought we would find a chapter on pediatric cancer in this book. Of course not! Who expects their baby to develop cancer and die!? No one!
I am exhausted tonight physically and mentally, and though I could try to describe the chaos I am cleaning and sifting through or how hard this really is on a grieving parent, no words I feel will do this justice. Sometimes only a visual picture will do. Image if you spent the last two days cleaning out a closet in your child's room. The task alone is challenging, but then factor into the equation that your child died. Typically we clean out our children's closets because new things are going in. However, in this scenario nothing new related to your child is going in, ONLY out. In a way, what is happening to the closet is it is looking more like you and LESS like your child. It is an illustration of loss in a major way.
While I have been contending with the closet, Peter has been going through thousands and thousands of Lego brick pieces. Many of the Lego bricks we are donating, but I know this task has to be hard on Peter. Peter and Mattie connected over Legos. Through Legos they created, chatted, and learned together. Legos were our saving grace through Mattie's 15 month battle with cancer, and during that time we bought every Lego kit on the market. So needless to say, Peter estimates that we have over 80,000 lego bricks in our home! We are saving some of Mattie's special creations, and the rest we will have to make peace with and say good-bye to them. Though I feel we made a significant dent this weekend, there is still so much to do, and looking at it in total is overwhelming. So we take it bit by bit and one day at a time.
Tonight's picture was taken on our deck in July of 2003. Mattie had just begun to enjoy being in water, and what he really loved was playing in it. Particularly he was fascinated by things that would float, sink, and so forth. He was our little scientist, full of investigation and curiosity.
Quote of the day: There are places in the heart that do not yet exist; suffering has to enter in for them to come to be. ~ Leon Bloy
Despite the fact that we had a hawk visit us yesterday and basically devour a pigeon on our balcony, the sparrows fortunately did return today. I asked Peter what the chances are of having a hawk visit us, when we live right in the middle of the city. Our goal is to feed sparrows and small birds, and it upsets me when this hawk stops by. Mattie and I have experienced this sighting one other time, in which a hawk came down from the sky and grabbed a sparrow right off the bird feeder. Needless to say, Mattie and I were stunned and we talked about this for years.
As you can see the feeder was very busy today! In the corner of the picture, you can also see Mattie's purple stained glass butterfly that remains on our window.
I spent the entire day at home, cleaning out our walk-in closet. I was at it for over six hours. I am happy to report that I can now walk into the closet, see actual shelf space, and a level of organization. I couldn't have done this without Peter, who was removing bags as quickly as I was generating them. In the midst of all of this, Peter would come up and give me a pep talk, and acknowledge the progress being made. This is not a project I would take on during the week alone. It is something that I need support on, encouragement, and at times we land up chatting.
Peter told me tonight, as he was throwing out things I gave him, that he in essence was saying "good-bye to our future." That may sound strange to our readers, because you most likely are saying.... aren't they cleaning up and throwing things out from their past? The answer is yes, but think about why you keep things. In our case, we held onto things because it was our hope to share them with Mattie in the future. A future that will never happen. In addition, Peter and I saved things because we were not sure if we would need them again. What we learned from cancer and Mattie's death is we really don't need THINGS anymore. The objects that once meant so much to us, no longer mean a thing.
Last night, Peter and I chatted about the cleaning up and reorganization process. We are not going through things and crying, we are going through it and are simply numb. Numb again, a feeling I am well acquainted with. Though this time I am numb and disgusted at the same time. Disgusted because we can't believe what happened to our lives. I told Peter that I feel in many ways that I have jumped through several developmental stages, and instead of being where I should be chronologically, I have aged dramatically and find myself dealing with death and dying issues. As I was going through the closet, I came across the cub scout uniform I bought Mattie. I literally bought him this outfit a month before he was diagnosed with cancer. He was looking forward to starting cub scouts in the fall of 2008, and having Peter as his den leader. In addition to that, I came across Mattie's baby shoes, his baptism outfit, and several more cards that he wrote to me. So naturally none of this was easy to see and go through. There was just so much in this closet, and as we were either throwing things away or making piles for Goodwill, I just felt unhappy. This is not how life was supposed to be. I had accumulated many books over the years while raising Mattie. One of them was "What to expect during the toddler years." I asked Peter if he thought we would find a chapter on pediatric cancer in this book. Of course not! Who expects their baby to develop cancer and die!? No one!
I am exhausted tonight physically and mentally, and though I could try to describe the chaos I am cleaning and sifting through or how hard this really is on a grieving parent, no words I feel will do this justice. Sometimes only a visual picture will do. Image if you spent the last two days cleaning out a closet in your child's room. The task alone is challenging, but then factor into the equation that your child died. Typically we clean out our children's closets because new things are going in. However, in this scenario nothing new related to your child is going in, ONLY out. In a way, what is happening to the closet is it is looking more like you and LESS like your child. It is an illustration of loss in a major way.
While I have been contending with the closet, Peter has been going through thousands and thousands of Lego brick pieces. Many of the Lego bricks we are donating, but I know this task has to be hard on Peter. Peter and Mattie connected over Legos. Through Legos they created, chatted, and learned together. Legos were our saving grace through Mattie's 15 month battle with cancer, and during that time we bought every Lego kit on the market. So needless to say, Peter estimates that we have over 80,000 lego bricks in our home! We are saving some of Mattie's special creations, and the rest we will have to make peace with and say good-bye to them. Though I feel we made a significant dent this weekend, there is still so much to do, and looking at it in total is overwhelming. So we take it bit by bit and one day at a time.
February 5, 2011
Saturday, February 5, 2011
Saturday, February 5, 2011
Tonight's picture was taken in July of 2003. Mattie was 15 months old, and almost walking independently. I captured him maneuvering from the staircase to the chair. Grabbing at these objects for balance and support along the way. Teaching Mattie to walk was a very humbling process. What I learned was I couldn't do it for him. He had to decide when he was ready to walk on his own. This illustrated Mattie's personality and style because he was very strong willed and wanted things to go according to his timeline, not someone else's. As a new mom, I wanted to prevent Mattie from falling and hurting himself. However, I also had to learn the importance of Mattie's self-exploration and initiative. So Mattie may have been learning to walk, but I assure you the learning was always two ways.
Quote of the day: Grief and sadness knits two hearts in closer bonds than happiness ever can; and common sufferings are far stronger than common joys. ~ Alphonse de Lamartine
Tonight's quote is not only moving, but it is profoundly true. Grief can bond people together in absolutely extraordinary ways. I am not sure this statement would have meant anything to me before experiencing Mattie's cancer and death. I could elaborate on this here, but there are certain revelations that I have learned over the course of the last three years, that I would prefer to write about in a book. Capturing Mattie's life is important to me, and as I muster the courage and strength to take on a book, I also realize that there are some very powerful stories and connections that I have made through this ordeal that deserve exploration. My blog readers know so much about Mattie's story and "our" story, but in Mattie's book I want to tell you about his incredible life as well as uncover much, much more.
Peter and I had the wonderful opportunity to go out to lunch with Robbie today. As some of my blog readers know, Robbie was one of Mattie's favorite hospital childlife volunteers. Robbie understood Mattie and he also understands Peter and I. When we meet with Robbie, I find that I am easily myself, and I do not need to mince words or sugar coat things. Needless to say, we sat together for over three hours discussing the upcoming Foundation Walk. We truly appreciate Robbie's willingness to brainstorm ideas with us, and his willingness to take on tasks and responsibilities. Sometimes talking about the Walk is challenging for Peter and I, but Robbie helps balance our thoughts, shares his insights, and motivates us at the same time. I came to the luncheon with ideas, and when I left I felt as if Peter and I had covered a great deal of ground, and also had action items to pursue. I do my best thinking while I sleep and while I am busy. I woke up yesterday focused on creating a theme for this year's Foundation Walk. As the day moved on, I was focused upon other things, but by the end of the day, it just came to me. When I shared my thoughts with Peter and Robbie today, they both loved the idea, which I will announce shortly.
Despite the rain, Peter and I walked to lunch as well as walked home. We covered about three miles. I wasn't happy about the cold, but I was most definitely happy to be walking. Upon our return, I looked outside our balcony window, and as you can see we had a huge red tailed hawk sitting in our flower box. Peter was able to grab my camera and capture this sight (with Mattie's American flag in the background), but I was very upset to see that the hawk had caught a pigeon and basically de-feathered it on our balcony and had it in its claws. As Peter reminded me, this is how nature works. I suppose that was a reality lesson I did not need to see this afternoon.
I spent the rest of the day trying, with the emphasis on trying, to clean out the walk in closet in Mattie's room. This closet is an absolute disaster, and I haven't been able to walk into it since Mattie got sick. Needless to say, this is not a one day project, and I will be returning to it tomorrow. What a weekend! In the midst of cleaning out this closet, I found shoes of Mattie's from all sorts of stages in his development. I also found cards he drew for me (which I quickly piled together and saved), and I also came across cards from a long time friend of mine. Unfortunately this friend severed our friendship after Mattie died. She told me his death was too hard for her to handle, and therefore for her physical and mental health, she had to discontinue our relationship. This is definitely another book chapter, so therefore I am not elaborating on this here, but I do want to say that re-reading my friend's cards allowed me to further see that NOTHING is forever. Including friendships, especially ones you perceived as special and close, and motherhood. When I became a mother, I thought this was a role I would have for a lifetime. Cancer taught me about that faulty notion. So cleaning out the closet is not easy by any stretch of the imagination, and I knew it was going to be tough going into this project, but I did not expect to be reflecting on additional losses tonight. Many of the items I am throwing out or donating pertain to my former life. Specifically I am seeing my professional life (text books, workbooks, notes, notebooks) coming out of the closet, I am seeing toys of Mattie's coming out of the closet, and I am seeing reminders of my role as a mom coming out of the closet. There is a lot of history in this closet, and by giving these items away or throwing them out, it is to some extent saying good-bye to who I once was. I am a sentimentalist at heart, so asking someone like me to purge things is challenging on a good day, factor in my life's circumstances, and this task is not only daunting, but it is painful.
Tonight's picture was taken in July of 2003. Mattie was 15 months old, and almost walking independently. I captured him maneuvering from the staircase to the chair. Grabbing at these objects for balance and support along the way. Teaching Mattie to walk was a very humbling process. What I learned was I couldn't do it for him. He had to decide when he was ready to walk on his own. This illustrated Mattie's personality and style because he was very strong willed and wanted things to go according to his timeline, not someone else's. As a new mom, I wanted to prevent Mattie from falling and hurting himself. However, I also had to learn the importance of Mattie's self-exploration and initiative. So Mattie may have been learning to walk, but I assure you the learning was always two ways.
Quote of the day: Grief and sadness knits two hearts in closer bonds than happiness ever can; and common sufferings are far stronger than common joys. ~ Alphonse de Lamartine
Tonight's quote is not only moving, but it is profoundly true. Grief can bond people together in absolutely extraordinary ways. I am not sure this statement would have meant anything to me before experiencing Mattie's cancer and death. I could elaborate on this here, but there are certain revelations that I have learned over the course of the last three years, that I would prefer to write about in a book. Capturing Mattie's life is important to me, and as I muster the courage and strength to take on a book, I also realize that there are some very powerful stories and connections that I have made through this ordeal that deserve exploration. My blog readers know so much about Mattie's story and "our" story, but in Mattie's book I want to tell you about his incredible life as well as uncover much, much more.
Peter and I had the wonderful opportunity to go out to lunch with Robbie today. As some of my blog readers know, Robbie was one of Mattie's favorite hospital childlife volunteers. Robbie understood Mattie and he also understands Peter and I. When we meet with Robbie, I find that I am easily myself, and I do not need to mince words or sugar coat things. Needless to say, we sat together for over three hours discussing the upcoming Foundation Walk. We truly appreciate Robbie's willingness to brainstorm ideas with us, and his willingness to take on tasks and responsibilities. Sometimes talking about the Walk is challenging for Peter and I, but Robbie helps balance our thoughts, shares his insights, and motivates us at the same time. I came to the luncheon with ideas, and when I left I felt as if Peter and I had covered a great deal of ground, and also had action items to pursue. I do my best thinking while I sleep and while I am busy. I woke up yesterday focused on creating a theme for this year's Foundation Walk. As the day moved on, I was focused upon other things, but by the end of the day, it just came to me. When I shared my thoughts with Peter and Robbie today, they both loved the idea, which I will announce shortly.
Despite the rain, Peter and I walked to lunch as well as walked home. We covered about three miles. I wasn't happy about the cold, but I was most definitely happy to be walking. Upon our return, I looked outside our balcony window, and as you can see we had a huge red tailed hawk sitting in our flower box. Peter was able to grab my camera and capture this sight (with Mattie's American flag in the background), but I was very upset to see that the hawk had caught a pigeon and basically de-feathered it on our balcony and had it in its claws. As Peter reminded me, this is how nature works. I suppose that was a reality lesson I did not need to see this afternoon.
I spent the rest of the day trying, with the emphasis on trying, to clean out the walk in closet in Mattie's room. This closet is an absolute disaster, and I haven't been able to walk into it since Mattie got sick. Needless to say, this is not a one day project, and I will be returning to it tomorrow. What a weekend! In the midst of cleaning out this closet, I found shoes of Mattie's from all sorts of stages in his development. I also found cards he drew for me (which I quickly piled together and saved), and I also came across cards from a long time friend of mine. Unfortunately this friend severed our friendship after Mattie died. She told me his death was too hard for her to handle, and therefore for her physical and mental health, she had to discontinue our relationship. This is definitely another book chapter, so therefore I am not elaborating on this here, but I do want to say that re-reading my friend's cards allowed me to further see that NOTHING is forever. Including friendships, especially ones you perceived as special and close, and motherhood. When I became a mother, I thought this was a role I would have for a lifetime. Cancer taught me about that faulty notion. So cleaning out the closet is not easy by any stretch of the imagination, and I knew it was going to be tough going into this project, but I did not expect to be reflecting on additional losses tonight. Many of the items I am throwing out or donating pertain to my former life. Specifically I am seeing my professional life (text books, workbooks, notes, notebooks) coming out of the closet, I am seeing toys of Mattie's coming out of the closet, and I am seeing reminders of my role as a mom coming out of the closet. There is a lot of history in this closet, and by giving these items away or throwing them out, it is to some extent saying good-bye to who I once was. I am a sentimentalist at heart, so asking someone like me to purge things is challenging on a good day, factor in my life's circumstances, and this task is not only daunting, but it is painful.
February 4, 2011
Friday, February 2, 2011
Friday, February 2, 2011
Tonight's picture was taken in July of 2003, on the beach of Duck, North Carolina. When I look at this picture, it actually makes me laugh. I laugh because, if this was a cartoon, the bubble over Mattie's head would read...... "I have my eye on the water, and you better not be thinking of putting me down in it!" Mattie was partly fascinated by the water, but for the most part he was simply frightened. Which in reality I was okay with. If you believe a child is born with common sense, Mattie was. He had an understanding for things that could harm and hurt him, and you only had to tell him once not to touch or go near something. In that respect Mattie was easy. I never had to childproof anything, nor did I have to protect him from corners and other sharp things he could fall into. I was hyper vigiliant anyway, but in all reality, his instinct for his surroundings was always spot on.
Quote of the day: I measure every grief I meet with narrow, probing eyes - I wonder if it weighs like mine - or has an easier size. ~ Emily Dickinson
Today I joined Ann and her mother, Mary, on an adventure. The adventure was taking Mary to get her hair cut and styled. Transferring Mary from her wheelchair to Ann's car takes incredible effort and fortunately for Mary, Ann is an occupational therapist by training. Otherwise, I am not sure the average person could safely take Mary on. My role in the transfer process is totally non-existent and frankly I am surprised Ann hasn't hit me over the head yet. Because at times the whole scene of getting her mom into the car is so complicated it makes me laugh. Mary is usually right along side me laughing, and I suppose humor helps us all get through times of stress. Despite it being cold out, I know Mary enjoyed her trip out, conversing with us, and of course returning back home with her hair done.
While out, we had lunch together. Our lunch gathering grew by the time lunch was done, because our friend, Tina (the friend who hosted my birthday party at her house this summer), her daughter, and Bob joined us. Mary was quiet and eating, but I know she took it all in. At lunch we talked about many topics. However, after lunch I found myself quite upset, and I honestly did not know why. At least not initially. I went back with Mary to her assisted living facility, and sat with her for a while. Mary took a cat nap, and while she was napping, I tried reading the book I brought with me. It is a fiction book called, Handle with Care, which is about a child born with a disease called Osteogensis Imperfecta and the impact of this disease on the entire family. What I found however, was I couldn't read the book. Not because of the book itself. I enjoy books by this particular author, but I couldn't focus since something was bothering me. So I sat there and wondered what exactly it was. One of the topics discussed at lunch was summer trips and summer camp. Somehow just the notion of this was overwhelming. This is NOT part of my life. Summer trips mean nothing to me, and summer camp, which are two innocuous words, now pack a powerful punch. The punch or sting of not having a child.
In the midst of this conversation, the travel location of Hawaii came up. As we were talking about the different islands, I reflected on my last trip to Hawaii. It was like I was sucked out of the current conversation, and was transported back in time. My mind went to March of 2008, when I was in Oahu attending a counseling conference. March of 2008 seemed like an exciting time in my life professionally. I had been elected the president of a very large professional counseling association, something that I never thought I would achieve early on in my career. My leadership role officially began on July 1, 2008. So I literally had 22 days in office before my world crashed around me, and Mattie was diagnosed with cancer. Somehow I look back at this trip to Hawaii and I realize I was such a different person back then. Naturally when Mattie developed cancer, he came first and though I had the title of president, during my year in office I wasn't empowered in this role. All my other officers had to step up and fill my role. This is something that will always bother me, something that will always upset, and yet something that I had to let go of because Mattie was my priority. I don't regret that decision, I just regret that I had to even be put in such a position. Cancer had great ramifications on our professional development, and for me it has changed my whole future outlook on what I want to do.
When I got home later tonight, I was emailing my lifetime friend, Karen, back and forth. I was telling her I had a hard day, and naturally she asked why. When I told her about my reflections on Hawaii in particular she encouraged me to "hold onto the memories of the event as good ones. That July was bad, but Hawaii was good. You should be proud of that, and cancer shouldn't take that from you too." I told her it was sage advice, which she knows I am not good at following. But I wrote it down here, so perhaps I will try to absorb it.
The ramifications of cancer and Mattie's death are huge. It clouds everything and anything Peter and I do. The worst part of it however, is the disease leaves you such a changed person, and truly altered that it becomes very challenging to want to re-engage with the world again. At times I find when I do re-engage, I get hurt, which only further hones one's natural instinct to retreat and protect one's self. In these times, I say to myself..... one day at a time, and try to reset for tomorrow.
In the midst of all of this today, Tina was telling us that she is taking a group of girl scouts to the musical Wicked, which is coming to Washington, DC in June. I really enjoy most musicals, though I admit I like some more than others. Tina invited me to go with her and her group in June, and I am looking forward to hearing the music again. I used many of the songs from Wicked in Mattie's memorial video that we created for his celebration of life ceremony. Some of the songs from Wicked are haunting, and I when Mattie died, I found that I listened to the CD of Wicked often. I imagine this is one of the reasons Peter doesn't want to see the play again, the music is very linked to Mattie's memory.
I leave you tonight with a comment from Mary (Ann's mom). As I left Mary this evening, she was staring into my eyes and she told me that I have stunning eyes. I thanked her for the lovely compliment, but what I wanted to say was I have Mattie's eyes. When you stare into my eyes, you are staring into his eyes as well.
Tonight's picture was taken in July of 2003, on the beach of Duck, North Carolina. When I look at this picture, it actually makes me laugh. I laugh because, if this was a cartoon, the bubble over Mattie's head would read...... "I have my eye on the water, and you better not be thinking of putting me down in it!" Mattie was partly fascinated by the water, but for the most part he was simply frightened. Which in reality I was okay with. If you believe a child is born with common sense, Mattie was. He had an understanding for things that could harm and hurt him, and you only had to tell him once not to touch or go near something. In that respect Mattie was easy. I never had to childproof anything, nor did I have to protect him from corners and other sharp things he could fall into. I was hyper vigiliant anyway, but in all reality, his instinct for his surroundings was always spot on.
Quote of the day: I measure every grief I meet with narrow, probing eyes - I wonder if it weighs like mine - or has an easier size. ~ Emily Dickinson
Today I joined Ann and her mother, Mary, on an adventure. The adventure was taking Mary to get her hair cut and styled. Transferring Mary from her wheelchair to Ann's car takes incredible effort and fortunately for Mary, Ann is an occupational therapist by training. Otherwise, I am not sure the average person could safely take Mary on. My role in the transfer process is totally non-existent and frankly I am surprised Ann hasn't hit me over the head yet. Because at times the whole scene of getting her mom into the car is so complicated it makes me laugh. Mary is usually right along side me laughing, and I suppose humor helps us all get through times of stress. Despite it being cold out, I know Mary enjoyed her trip out, conversing with us, and of course returning back home with her hair done.
While out, we had lunch together. Our lunch gathering grew by the time lunch was done, because our friend, Tina (the friend who hosted my birthday party at her house this summer), her daughter, and Bob joined us. Mary was quiet and eating, but I know she took it all in. At lunch we talked about many topics. However, after lunch I found myself quite upset, and I honestly did not know why. At least not initially. I went back with Mary to her assisted living facility, and sat with her for a while. Mary took a cat nap, and while she was napping, I tried reading the book I brought with me. It is a fiction book called, Handle with Care, which is about a child born with a disease called Osteogensis Imperfecta and the impact of this disease on the entire family. What I found however, was I couldn't read the book. Not because of the book itself. I enjoy books by this particular author, but I couldn't focus since something was bothering me. So I sat there and wondered what exactly it was. One of the topics discussed at lunch was summer trips and summer camp. Somehow just the notion of this was overwhelming. This is NOT part of my life. Summer trips mean nothing to me, and summer camp, which are two innocuous words, now pack a powerful punch. The punch or sting of not having a child.
In the midst of this conversation, the travel location of Hawaii came up. As we were talking about the different islands, I reflected on my last trip to Hawaii. It was like I was sucked out of the current conversation, and was transported back in time. My mind went to March of 2008, when I was in Oahu attending a counseling conference. March of 2008 seemed like an exciting time in my life professionally. I had been elected the president of a very large professional counseling association, something that I never thought I would achieve early on in my career. My leadership role officially began on July 1, 2008. So I literally had 22 days in office before my world crashed around me, and Mattie was diagnosed with cancer. Somehow I look back at this trip to Hawaii and I realize I was such a different person back then. Naturally when Mattie developed cancer, he came first and though I had the title of president, during my year in office I wasn't empowered in this role. All my other officers had to step up and fill my role. This is something that will always bother me, something that will always upset, and yet something that I had to let go of because Mattie was my priority. I don't regret that decision, I just regret that I had to even be put in such a position. Cancer had great ramifications on our professional development, and for me it has changed my whole future outlook on what I want to do.
When I got home later tonight, I was emailing my lifetime friend, Karen, back and forth. I was telling her I had a hard day, and naturally she asked why. When I told her about my reflections on Hawaii in particular she encouraged me to "hold onto the memories of the event as good ones. That July was bad, but Hawaii was good. You should be proud of that, and cancer shouldn't take that from you too." I told her it was sage advice, which she knows I am not good at following. But I wrote it down here, so perhaps I will try to absorb it.
The ramifications of cancer and Mattie's death are huge. It clouds everything and anything Peter and I do. The worst part of it however, is the disease leaves you such a changed person, and truly altered that it becomes very challenging to want to re-engage with the world again. At times I find when I do re-engage, I get hurt, which only further hones one's natural instinct to retreat and protect one's self. In these times, I say to myself..... one day at a time, and try to reset for tomorrow.
In the midst of all of this today, Tina was telling us that she is taking a group of girl scouts to the musical Wicked, which is coming to Washington, DC in June. I really enjoy most musicals, though I admit I like some more than others. Tina invited me to go with her and her group in June, and I am looking forward to hearing the music again. I used many of the songs from Wicked in Mattie's memorial video that we created for his celebration of life ceremony. Some of the songs from Wicked are haunting, and I when Mattie died, I found that I listened to the CD of Wicked often. I imagine this is one of the reasons Peter doesn't want to see the play again, the music is very linked to Mattie's memory.
I leave you tonight with a comment from Mary (Ann's mom). As I left Mary this evening, she was staring into my eyes and she told me that I have stunning eyes. I thanked her for the lovely compliment, but what I wanted to say was I have Mattie's eyes. When you stare into my eyes, you are staring into his eyes as well.
February 3, 2011
Thursday, February 3, 2011
Thursday, February 3, 2011
Tonight's picture was taken in July of 2003. This was Mattie's first trip to the Outer Banks of North Carolina, and the sand and ocean were down right overwhelming and intimidating to him. In fact, throughout that entire week's vacation, we may have ventured to the beach twice, and for very short periods of time. Mattie did not like the feel of the sand on his feet and the sound of the ocean waves crashing down on the shore scared him terribly. Needless to say, for a person who finds the beach therapeutic, I was very upset that Mattie did not share my love for this immediately. But we did not give up. Each summer thereafter, we kept bringing him back to the beach, and by the third summer, he loved it. Mattie began to see the building possibilities with sand and that could absorb him for hours!
Quote of the day: No greater grief than to remember days of gladness when sorrow is at hand. ~ Friedrich von Schiller
When I read this quote, I felt transported back to the last week of Mattie's life. We were at the hospital and fighting to make him comfortable, since his body was filling up with fluid and he was having a horrific time breathing. I recall those were days of gladness (because Mattie was still with us) but they were also clouded with a sense of sorrow, because we knew Mattie's death was imminent. I remember these days so well, and I concur they do produce and contribute to the grief Peter and I feel now.
February is turning out to be a very busy month for me. Perhaps focusing on different things right now will be good for me. The first and foremost thing on our mind is the Foundation's Walk on May 22, 2011. Peter and I are having our first planning meeting with our amazing volunteers in about two weeks. We have a core group of about 30 people who walk this journey with us each spring to plan this event. I am not sure where we would be without them?!
The other activity Peter and I are involved with this month is lobbying on Capitol Hill for pediatric cancer. Our Foundation is very grateful to Mercury, a high stakes public strategy firm, for working with us to develop an advocacy plan. I look forward to sharing more about this with you as it unfolds.
I mentioned this in the Fall, but I will be working with one of the kindergarten teachers at Mattie's school this semester to develop a three part series on Matisse and Picasso for the children. As many of my readers know, I have been an educator for many years, but of adults. Never of children, much less kindergarten aged children. I have been brainstorming several hands on activities for the children as they learn about the wonderful works and talents of two great artists. I appreciate Donna's invitation to come to her classroom, and her openness to share her students with me. One of the things you notice immediately in your life when your child dies, is that your opportunity to be around other children diminishes. When Mattie died, many aspects of my life died along with him, and in a way, I feel that Donna is trying to help me recapture this piece of myself. Needless to say, I went to the public library today and checked out several books on Matisse and Picasso, that I know will be helpful as I prepare for the sessions with the children.
It is funny how you can start out the day, and not really be prepared for how it will end up. This evening, as I drove back home and was parking in our complex's garage, I saw a neighbor of mine. I have known Kathleen for many years and she was very fond of Mattie. Kathleen is one of my older adult friends. When she learned that Mattie had cancer, she too was devastated. During our returns from the hospital, between treatments, she would always leave me something at my door, as a welcome home present. Many times she left me flowers because she knows how much I love gardening. She would leave me happy flowers like sunflowers or gerber daisies! She continues to reach out to me after Mattie died, but I wasn't in a reachable place for the most part, well maybe until today.
We started talking in the parking garage, and after I helped her inside the building, she asked me if I would like to visit with her in her home. Because Peter was working late tonight, I figured this was the perfect opportunity to connect. I spent several hours with her over tea and cookies. During that time, I learned all about her life. Her life story literally blew me away. It wasn't what I was expecting to hear, especially since she seems like such a happy, well-adjusted, and sensible lady. She has suffered many heartaches in her life, along with many losses. Her mother died when she was only 8 years old. When she learned of her mother's death, the nuns who were visiting her family basically told her "to make the most out of it!" I asked her what on earth that was supposed to mean? She said they were trying to tell her this was an opportunity for her to connect further with God. I get the message, but the delivery of this to an eight year old seems a little inappropriate. Because this is Kathleen's life, I am not going into details here on the blog, but suffice it to say, I can't remember the last time I listened so intently to a life story. I almost felt like I was a child again, listening to a story and was SO eager to hear all the details and the outcomes. I told Kathleen that her life story should be written down, and her response to me was no one would be interested in it. For some reason I got the feeling that no one ever told Kathleen that she was special, that she was a survivor in so many ways, and that despite her own pain, she carries on in a cheerful and spiritual manner. My visit with her made me pause tonight, because she wanted me to know that the hardship I am experiencing now is making me stronger than I know. She says this strength will be needed later on in life. I found that premonition actually daunting because when she said that I imagined that potentially I will experience something even worse than losing Mattie.
After our tea, I gave Kathleen a hug, and thanked her for sharing part of her life with me. She showed me family pictures, and a picture of her and her brothers when they were children. It is a very special feeling holding someone's memories in your hands, and as I looked at a picture of her mother, she recalled the dress her mother was wearing in the picture so vividly to me. The picture was black and white, but her description was most definitely in color. As I was leaving Kathleen told me that every time she sees my car, she thinks of Mattie, and almost looks to see if he is in the backseat. But of course he isn't, nonetheless, she wanted me to know that this doesn't prevent her from saying hi and talking internally to him.
Tonight's picture was taken in July of 2003. This was Mattie's first trip to the Outer Banks of North Carolina, and the sand and ocean were down right overwhelming and intimidating to him. In fact, throughout that entire week's vacation, we may have ventured to the beach twice, and for very short periods of time. Mattie did not like the feel of the sand on his feet and the sound of the ocean waves crashing down on the shore scared him terribly. Needless to say, for a person who finds the beach therapeutic, I was very upset that Mattie did not share my love for this immediately. But we did not give up. Each summer thereafter, we kept bringing him back to the beach, and by the third summer, he loved it. Mattie began to see the building possibilities with sand and that could absorb him for hours!
Quote of the day: No greater grief than to remember days of gladness when sorrow is at hand. ~ Friedrich von Schiller
When I read this quote, I felt transported back to the last week of Mattie's life. We were at the hospital and fighting to make him comfortable, since his body was filling up with fluid and he was having a horrific time breathing. I recall those were days of gladness (because Mattie was still with us) but they were also clouded with a sense of sorrow, because we knew Mattie's death was imminent. I remember these days so well, and I concur they do produce and contribute to the grief Peter and I feel now.
February is turning out to be a very busy month for me. Perhaps focusing on different things right now will be good for me. The first and foremost thing on our mind is the Foundation's Walk on May 22, 2011. Peter and I are having our first planning meeting with our amazing volunteers in about two weeks. We have a core group of about 30 people who walk this journey with us each spring to plan this event. I am not sure where we would be without them?!
The other activity Peter and I are involved with this month is lobbying on Capitol Hill for pediatric cancer. Our Foundation is very grateful to Mercury, a high stakes public strategy firm, for working with us to develop an advocacy plan. I look forward to sharing more about this with you as it unfolds.
I mentioned this in the Fall, but I will be working with one of the kindergarten teachers at Mattie's school this semester to develop a three part series on Matisse and Picasso for the children. As many of my readers know, I have been an educator for many years, but of adults. Never of children, much less kindergarten aged children. I have been brainstorming several hands on activities for the children as they learn about the wonderful works and talents of two great artists. I appreciate Donna's invitation to come to her classroom, and her openness to share her students with me. One of the things you notice immediately in your life when your child dies, is that your opportunity to be around other children diminishes. When Mattie died, many aspects of my life died along with him, and in a way, I feel that Donna is trying to help me recapture this piece of myself. Needless to say, I went to the public library today and checked out several books on Matisse and Picasso, that I know will be helpful as I prepare for the sessions with the children.
It is funny how you can start out the day, and not really be prepared for how it will end up. This evening, as I drove back home and was parking in our complex's garage, I saw a neighbor of mine. I have known Kathleen for many years and she was very fond of Mattie. Kathleen is one of my older adult friends. When she learned that Mattie had cancer, she too was devastated. During our returns from the hospital, between treatments, she would always leave me something at my door, as a welcome home present. Many times she left me flowers because she knows how much I love gardening. She would leave me happy flowers like sunflowers or gerber daisies! She continues to reach out to me after Mattie died, but I wasn't in a reachable place for the most part, well maybe until today.
We started talking in the parking garage, and after I helped her inside the building, she asked me if I would like to visit with her in her home. Because Peter was working late tonight, I figured this was the perfect opportunity to connect. I spent several hours with her over tea and cookies. During that time, I learned all about her life. Her life story literally blew me away. It wasn't what I was expecting to hear, especially since she seems like such a happy, well-adjusted, and sensible lady. She has suffered many heartaches in her life, along with many losses. Her mother died when she was only 8 years old. When she learned of her mother's death, the nuns who were visiting her family basically told her "to make the most out of it!" I asked her what on earth that was supposed to mean? She said they were trying to tell her this was an opportunity for her to connect further with God. I get the message, but the delivery of this to an eight year old seems a little inappropriate. Because this is Kathleen's life, I am not going into details here on the blog, but suffice it to say, I can't remember the last time I listened so intently to a life story. I almost felt like I was a child again, listening to a story and was SO eager to hear all the details and the outcomes. I told Kathleen that her life story should be written down, and her response to me was no one would be interested in it. For some reason I got the feeling that no one ever told Kathleen that she was special, that she was a survivor in so many ways, and that despite her own pain, she carries on in a cheerful and spiritual manner. My visit with her made me pause tonight, because she wanted me to know that the hardship I am experiencing now is making me stronger than I know. She says this strength will be needed later on in life. I found that premonition actually daunting because when she said that I imagined that potentially I will experience something even worse than losing Mattie.
After our tea, I gave Kathleen a hug, and thanked her for sharing part of her life with me. She showed me family pictures, and a picture of her and her brothers when they were children. It is a very special feeling holding someone's memories in your hands, and as I looked at a picture of her mother, she recalled the dress her mother was wearing in the picture so vividly to me. The picture was black and white, but her description was most definitely in color. As I was leaving Kathleen told me that every time she sees my car, she thinks of Mattie, and almost looks to see if he is in the backseat. But of course he isn't, nonetheless, she wanted me to know that this doesn't prevent her from saying hi and talking internally to him.
February 2, 2011
Wednesday, February 2, 2011
Wednesday, February 2, 2011
Tonight's picture was taken in July of 2003. I have posted other pictures from this time period the past two nights. I have come across a folder I haven't looked at in a while, so I am sharing some special moments with you from this folder. Though this picture may not seem that fascinating to you, to me it is a very special picture. It is special for two reasons. The first was because Mattie and I were walking hand in hand to see the lighthouse in Hatteras. Though Peter and I had been to the Outer Banks several times before Mattie was born, we were never able to walk up to the Hatteras Lighthouse because it was in the process of being moved to safer ground. Therefore, that was my first time venturing to see this structure. The second reason this picture is special was that you can see Mattie really trying to walk and doing a great job. He was studying his feet as he was walking. Mattie began walking independently at 16 months, so at 15 months here, he was basically almost there!
Quote of the day: Each substance of a grief hath twenty shadows. ~ William Shakespeare
I am beginning to see that Shakespeare really had a very deep understanding for the emotions of grief. He realized the complexities and the various dimensions associated with surviving the death of a loved one. His description of "twenty shadows" interests me, because the definition of a shadow is..... an area where direct light from a light source cannot reach due to obstruction by an object. So in this case, grief is ONE very large object, that not only obstructs light to one area inside a person, but TWENTY! Grief does this by casting almost a cloud or shadow of darkness within a person, and the struggle for the griever is to try to break through this confusion. A confusion which leaves you in an unrecognizable state, without any sort of guide posts or maps.
For some time I have viewed my perspective on cancer as different from others. But it wasn't until I emailed my friend and colleague, Nancy, today, did I actually verbalize it. It is a feeling that I am trying to work through, but it is very real and yet not very nice to admit to. As I say all the time, on July 23, 2008, I became a part of a club. The cancer club. Not a club anyone voluntarily joins, but just like any other club, it has its own culture, its own preferences, its own language, and it is VERY costly. However, when you lose someone to cancer, you then become a member of an even more exclusive cancer club. Not everyone is given the opportunity to join this club, because the first step toward initiation is death. So though I am a part of the first club, the cancer club, I find that I greatly identify with cancer death club. Or death in general. Where is this going? Well I believe that depending upon which club you are a part of, this influences how you take in and absorb information presented about cancer.
I find that I have a VERY, VERY difficult time listening to positive messages, sunny day scenarios, and other hopeful messages as it relates to cancer. In fact, I find it very difficult to listen to survivors. Naturally, I am happy when people can conquer cancer, and I understand the battle that entails, but for me it is simply bittersweet to hear these messages. Mainly because I am always left feeling..... well why not Mattie?! Why wasn't he spared? Cognitively I realize as a human being, I do not want to see others suffer and especially battle cancer. I want cures, I want the day where the word cancer doesn't even exist. However, the other side of me, the raw side, the Mattie mom side, simply looks at this whole picture and says, I can't hear your success story, your positive message, because my son never had a chance, and he will never be able to live like you. This in a conflict I have within myself, and it always flares up around the time when I am planning a Foundation event. Simply because I know on one hand I want to explain the reality of the situation and on the other hand I have to approach this with a degree of sensitivity since everyone doesn't view this topic with my lens and broken heart. So the moral of the story is that cancer is a disease, that affects the patient and his/her family, but the long term emotional consequences and impact varies greatly for each of us touched by the disease.
I wanted to alert my readers to the fact that Friday, February 4, is World Cancer Day. I received the below message from the LiveStrong organization. They designed a five question cancer quiz, which you may find interesting. It doesn't take long to complete, and you may find some of the responses fascinating.
----------------------------------------------------------------------
I’ve had a long, personal battle with cancer, but I was still shocked when I first learned the facts of cancer’s enormous impact around the world.
You’ll feel the same way when you take our five question World Cancer Day Quiz. It’s a great way to get the startling facts about this global epidemic.
The truth is, we can’t win the fight against cancer unless we know what we’re facing. That’s why on World Cancer Day—Friday, February 4—LIVESTRONG and our partners all over the world are working to raise awareness and shine a spotlight on the global challenge of cancer.
Take the quiz and share this link to help raise awareness for World Cancer Day:
http://Quiz.LIVESTRONG.org
Please do your part and help us move even closer to a world without cancer.
Thanks for taking action,
Doug Ulman
President and CEO, LIVESTRONG
-----------------------------------------------------------------
Tonight's picture was taken in July of 2003. I have posted other pictures from this time period the past two nights. I have come across a folder I haven't looked at in a while, so I am sharing some special moments with you from this folder. Though this picture may not seem that fascinating to you, to me it is a very special picture. It is special for two reasons. The first was because Mattie and I were walking hand in hand to see the lighthouse in Hatteras. Though Peter and I had been to the Outer Banks several times before Mattie was born, we were never able to walk up to the Hatteras Lighthouse because it was in the process of being moved to safer ground. Therefore, that was my first time venturing to see this structure. The second reason this picture is special was that you can see Mattie really trying to walk and doing a great job. He was studying his feet as he was walking. Mattie began walking independently at 16 months, so at 15 months here, he was basically almost there!
Quote of the day: Each substance of a grief hath twenty shadows. ~ William Shakespeare
I am beginning to see that Shakespeare really had a very deep understanding for the emotions of grief. He realized the complexities and the various dimensions associated with surviving the death of a loved one. His description of "twenty shadows" interests me, because the definition of a shadow is..... an area where direct light from a light source cannot reach due to obstruction by an object. So in this case, grief is ONE very large object, that not only obstructs light to one area inside a person, but TWENTY! Grief does this by casting almost a cloud or shadow of darkness within a person, and the struggle for the griever is to try to break through this confusion. A confusion which leaves you in an unrecognizable state, without any sort of guide posts or maps.
For some time I have viewed my perspective on cancer as different from others. But it wasn't until I emailed my friend and colleague, Nancy, today, did I actually verbalize it. It is a feeling that I am trying to work through, but it is very real and yet not very nice to admit to. As I say all the time, on July 23, 2008, I became a part of a club. The cancer club. Not a club anyone voluntarily joins, but just like any other club, it has its own culture, its own preferences, its own language, and it is VERY costly. However, when you lose someone to cancer, you then become a member of an even more exclusive cancer club. Not everyone is given the opportunity to join this club, because the first step toward initiation is death. So though I am a part of the first club, the cancer club, I find that I greatly identify with cancer death club. Or death in general. Where is this going? Well I believe that depending upon which club you are a part of, this influences how you take in and absorb information presented about cancer.
I find that I have a VERY, VERY difficult time listening to positive messages, sunny day scenarios, and other hopeful messages as it relates to cancer. In fact, I find it very difficult to listen to survivors. Naturally, I am happy when people can conquer cancer, and I understand the battle that entails, but for me it is simply bittersweet to hear these messages. Mainly because I am always left feeling..... well why not Mattie?! Why wasn't he spared? Cognitively I realize as a human being, I do not want to see others suffer and especially battle cancer. I want cures, I want the day where the word cancer doesn't even exist. However, the other side of me, the raw side, the Mattie mom side, simply looks at this whole picture and says, I can't hear your success story, your positive message, because my son never had a chance, and he will never be able to live like you. This in a conflict I have within myself, and it always flares up around the time when I am planning a Foundation event. Simply because I know on one hand I want to explain the reality of the situation and on the other hand I have to approach this with a degree of sensitivity since everyone doesn't view this topic with my lens and broken heart. So the moral of the story is that cancer is a disease, that affects the patient and his/her family, but the long term emotional consequences and impact varies greatly for each of us touched by the disease.
I wanted to alert my readers to the fact that Friday, February 4, is World Cancer Day. I received the below message from the LiveStrong organization. They designed a five question cancer quiz, which you may find interesting. It doesn't take long to complete, and you may find some of the responses fascinating.
----------------------------------------------------------------------
I’ve had a long, personal battle with cancer, but I was still shocked when I first learned the facts of cancer’s enormous impact around the world.
You’ll feel the same way when you take our five question World Cancer Day Quiz. It’s a great way to get the startling facts about this global epidemic.
The truth is, we can’t win the fight against cancer unless we know what we’re facing. That’s why on World Cancer Day—Friday, February 4—LIVESTRONG and our partners all over the world are working to raise awareness and shine a spotlight on the global challenge of cancer.
Take the quiz and share this link to help raise awareness for World Cancer Day:
http://Quiz.LIVESTRONG.org
Please do your part and help us move even closer to a world without cancer.
Thanks for taking action,
Doug Ulman
President and CEO, LIVESTRONG
-----------------------------------------------------------------
February 1, 2011
Tuesday, February 1, 2011
Tuesday, February 1, 2011 -- Mattie died 73 weeks ago today.
Tonight's picture coincides with last night's picture. Both were taken in July of 2003, during Mattie's first trip to the Outer Banks of North Carolina. In last night's picture you observed Peter and Mattie climbing the spiral staircase to the top of Corolla Light. Whereas tonight's picture shows them after they reached the top. As you can see Mattie looked upset. He was upset, because despite the heat and the stillness below, at the top of the lighthouse it was very windy, and he wasn't happy about that at all. The ironic part was Peter was smiling in the picture, but I remember him being extremely overheated from climbing up all those stairs with Mattie on his back.
Quote of the day: Grief drives men into habits of serious reflection, sharpens the understanding, and softens the heart. ~ John Adams
This Tuesday marks the 73rd week that Mattie has been gone from our lives. Somehow Tuesdays may just never be the same for me. Throughout the day, I was touched to receive several Mattie memory emails.
For example, my friend, Tanja, sent me a message, and in her message she stated, "I think it is not a coincidence that he was called Mattie Moon and that he loved the sun. Both of these natural elements are with us every day and everyone who got to know Mattie will always remember him when they see the sun and/or the moon." As Mattie's mom, I naturally feel this way when I see the sun and the moon, but it is a special feeling, knowing that I am NOT alone. That others too are thinking of my Mattie, when the sun shines brightly or when the moon sets the night sky aglow.
The other message that I received today was from a mom at Mattie's elementary school. Her daughter and Mattie were in the same kindergarten class together. This mom wanted me to know that her daughter thinks of Mattie often and remembers him as being "inclusive." In fact, the little girl stated that Mattie "never wanted another child to feel lonely or be by him or herself." She admired that trait in Mattie. I don't know about you, but hearing this feedback from Mattie's peer, actually made me stop and reflect. It made me pause because I agree with her, Mattie was definitely like that, but I am truly impressed by her ability to observe that, remember that, and to attach that special quality to Mattie. As parents we try to teach our children certain values, and to me being inclusive is important. Mattie and I had many teachable moments together on playgrounds over the years, and what today's email showed me, was all those moments of modeling appropriate behaviors paid off. Mattie integrated what he learned and incorporated it into his daily routine. It became a part of him. In any case, this memory from Mattie's classmate brought a smile to my face today, and a tear to Peter's!
On a lighter note, yet a meaningful one, I received an email today from my dad. He forwarded me Charles Schulz' philosophy on the important people in our lives. As you know, Mr. Schulz was the creator of the Peanuts comic strip. I think we all fall into the trap sometimes of striving for the medal, the certificate, the award, and recognition (which I am not implying is a bad thing per se), but at the end of the day, you do not need these things to be a good person, to do the right thing, to help someone in your life, and to make a difference. In fact, it is most likely the everyday things that you do, that are probably most memorable to those in your life.
========================================
The following is the philosophy of Charles Schulz, the creator of the 'Peanuts' comic strip.
You don't have to actually answer the questions. Just ponder on them.
Just read the e-mail straight through, and you'll get the point.
1. Name the five wealthiest people in the world.
2. Name the last five Heisman trophy winners.
3. Name the last five winners of the Miss America pageant.
4 Name ten people who have won the Nobel or Pulitzer Prize.
5. Name the last half dozen Academy Award winners for best actor and actress.
6. Name the last decade's worth of World Series winners.
The point is, none of us remembers the headliners of yesterday.
These are no second-rate achievers.
They are the best in their fields.
But the applause dies..
Awards tarnish.
Achievements are forgotten.
Accolades and certificates are buried with their owners.
Here's another quiz. See how you do on this one:
1. List a few teachers who aided your journey through school.
2. Name three friends who have helped you through a difficult time.
3. Name five people who have taught you something worthwhile.
4. Think of a few people who have made you feel appreciated and special!!
5. Think of five people you enjoy spending time with.
Easier?
The lesson: The people who make a difference in your life are not the ones with the most credentials..
the most money...or the most awards. They simply are the ones who care the most
=========================================
I would like to end tonight's posting with a message I received from my mom today. I had told her I came across a letter, this weekend while cleaning my desk, that she wrote to me when I was pregnant with Mattie. In essence these are her thoughts to my finding this letter. My Mom wrote, "You reminded me of the letter I wrote to you when you announced that you were pregnant. I wanted to be in Washington with you so much that 9/11 would not deter me and I convinced Daddy to take Amtrak. That in of itself was an experience traveling across the country on a train that had its share of mini-disasters that included a derailment, a suicide, a fire and a missed connection. But, I was determined to be as close to the new baby within you as I could the minute I found out. That impulse to be with Mattie never left me and accounted for my learning to be bi-coastal and loving it. I even flew shortly after 9/11 when the airports were empty and so were the planes. Most people had better sense than to tempt the fates. But where Mattie was concerned, my top priority was to be with him and I refused to let the terrorists get to me! When you reported that you were going through your desk and found the letter, it brought back fond memories of a beautiful time when Daddy and I were anxiously anticipating Mattie's arrival.The letter is a document that reveals how much I loved Mattie even before he was born and in retrospect, even though heartache ensued, it turned out to be a memorable everlasting love that I will cherish forever."
Tonight's picture coincides with last night's picture. Both were taken in July of 2003, during Mattie's first trip to the Outer Banks of North Carolina. In last night's picture you observed Peter and Mattie climbing the spiral staircase to the top of Corolla Light. Whereas tonight's picture shows them after they reached the top. As you can see Mattie looked upset. He was upset, because despite the heat and the stillness below, at the top of the lighthouse it was very windy, and he wasn't happy about that at all. The ironic part was Peter was smiling in the picture, but I remember him being extremely overheated from climbing up all those stairs with Mattie on his back.
Quote of the day: Grief drives men into habits of serious reflection, sharpens the understanding, and softens the heart. ~ John Adams
This Tuesday marks the 73rd week that Mattie has been gone from our lives. Somehow Tuesdays may just never be the same for me. Throughout the day, I was touched to receive several Mattie memory emails.
For example, my friend, Tanja, sent me a message, and in her message she stated, "I think it is not a coincidence that he was called Mattie Moon and that he loved the sun. Both of these natural elements are with us every day and everyone who got to know Mattie will always remember him when they see the sun and/or the moon." As Mattie's mom, I naturally feel this way when I see the sun and the moon, but it is a special feeling, knowing that I am NOT alone. That others too are thinking of my Mattie, when the sun shines brightly or when the moon sets the night sky aglow.
The other message that I received today was from a mom at Mattie's elementary school. Her daughter and Mattie were in the same kindergarten class together. This mom wanted me to know that her daughter thinks of Mattie often and remembers him as being "inclusive." In fact, the little girl stated that Mattie "never wanted another child to feel lonely or be by him or herself." She admired that trait in Mattie. I don't know about you, but hearing this feedback from Mattie's peer, actually made me stop and reflect. It made me pause because I agree with her, Mattie was definitely like that, but I am truly impressed by her ability to observe that, remember that, and to attach that special quality to Mattie. As parents we try to teach our children certain values, and to me being inclusive is important. Mattie and I had many teachable moments together on playgrounds over the years, and what today's email showed me, was all those moments of modeling appropriate behaviors paid off. Mattie integrated what he learned and incorporated it into his daily routine. It became a part of him. In any case, this memory from Mattie's classmate brought a smile to my face today, and a tear to Peter's!
On a lighter note, yet a meaningful one, I received an email today from my dad. He forwarded me Charles Schulz' philosophy on the important people in our lives. As you know, Mr. Schulz was the creator of the Peanuts comic strip. I think we all fall into the trap sometimes of striving for the medal, the certificate, the award, and recognition (which I am not implying is a bad thing per se), but at the end of the day, you do not need these things to be a good person, to do the right thing, to help someone in your life, and to make a difference. In fact, it is most likely the everyday things that you do, that are probably most memorable to those in your life.
========================================
The following is the philosophy of Charles Schulz, the creator of the 'Peanuts' comic strip.
You don't have to actually answer the questions. Just ponder on them.
Just read the e-mail straight through, and you'll get the point.
1. Name the five wealthiest people in the world.
2. Name the last five Heisman trophy winners.
3. Name the last five winners of the Miss America pageant.
4 Name ten people who have won the Nobel or Pulitzer Prize.
5. Name the last half dozen Academy Award winners for best actor and actress.
6. Name the last decade's worth of World Series winners.
The point is, none of us remembers the headliners of yesterday.
These are no second-rate achievers.
They are the best in their fields.
But the applause dies..
Awards tarnish.
Achievements are forgotten.
Accolades and certificates are buried with their owners.
Here's another quiz. See how you do on this one:
1. List a few teachers who aided your journey through school.
2. Name three friends who have helped you through a difficult time.
3. Name five people who have taught you something worthwhile.
4. Think of a few people who have made you feel appreciated and special!!
5. Think of five people you enjoy spending time with.
Easier?
The lesson: The people who make a difference in your life are not the ones with the most credentials..
the most money...or the most awards. They simply are the ones who care the most
=========================================
I would like to end tonight's posting with a message I received from my mom today. I had told her I came across a letter, this weekend while cleaning my desk, that she wrote to me when I was pregnant with Mattie. In essence these are her thoughts to my finding this letter. My Mom wrote, "You reminded me of the letter I wrote to you when you announced that you were pregnant. I wanted to be in Washington with you so much that 9/11 would not deter me and I convinced Daddy to take Amtrak. That in of itself was an experience traveling across the country on a train that had its share of mini-disasters that included a derailment, a suicide, a fire and a missed connection. But, I was determined to be as close to the new baby within you as I could the minute I found out. That impulse to be with Mattie never left me and accounted for my learning to be bi-coastal and loving it. I even flew shortly after 9/11 when the airports were empty and so were the planes. Most people had better sense than to tempt the fates. But where Mattie was concerned, my top priority was to be with him and I refused to let the terrorists get to me! When you reported that you were going through your desk and found the letter, it brought back fond memories of a beautiful time when Daddy and I were anxiously anticipating Mattie's arrival.The letter is a document that reveals how much I loved Mattie even before he was born and in retrospect, even though heartache ensued, it turned out to be a memorable everlasting love that I will cherish forever."
January 31, 2011
Monday, January 31, 2011
Monday, January 31, 2011
Tonight's picture was taken in July of 2003. Mattie was a year old, and that was his first trip to the Outer Banks of North Carolina. I have always been in love with lighthouses, and we took Mattie to Corolla Light that summer and naturally I wanted to climb to the top. Peter and Mattie went together, and I honestly do not know how I did not lose Peter that day from the heat. It was sweltering out, in the 90s with high humidity, and Mattie was too young to climb. So he rode in a carrier on Peter's back. As Peter still tells me, "THAT WAS ONE LONG CLIMB!" Needless to say we all made it to the top of the lighthouse, and Mattie loved the adventure and the climb.
Quote of the day: Given a choice between grief and nothing, I'd choose grief. ~ William Faulkner
Those closest to me have told me how impressed they are that I have made a start at trying to reorganize my home life. That may sound so simple to my readers, but it really isn't. My level of chaos began as soon as Mattie was diagnosed with cancer in July of 2008. At that point, mail began to pile up, toys coming from the hospital and being delivered to our home piled up, Mattie's clothes, medical supplies, and hundreds of his video tapes surrounded us. I guess what I should remind you is that I am not talking about one of two toys accumulated during a hospital visit, I am talking around 50 to 100 new items each time. Imagine 50 to 100 new items entering your home each week of your life for 15 months, and also imagine not having the time to address the accumulation because your priority was caring for a sick and dying child. You learn to live with clutter, you learn to overlook the chaos, because the sheer life and death situation before you is all encompassing, overwhelming, and requires every fiber of your being to manage. I try to remind myself, as I look at the chaos around me that there is an explanation for this, that this isn't me, but this is the result of a great life tragedy. This is a very real and tangible reaction to cancer! Cancer puts your life on hold and you basically stop living. Things are no longer important, all that is important are meeting the basic biological needs of your family, and all the other hierarchical needs (safety, love, belongingness, self-esteem, etc) are simply dispensable.
It is very hard to move from the world of cancer and death back to the living. Because living requires a different set of priorities, a different point of view, and most of all it requires interacting with others. I have always been an extroverted person, however, with Mattie's illness and certainly his death, I have become more introverted, and I need much more alone time. Sometimes when interacting with others I see just how different my life is and how I no longer fit in. Those moments of realization are challenging for me, because it only highlights Mattie's loss in my life.
I had lunch with my friend Christine today. Some of you may recall that Christine is Campbell's mom, and Campbell was one of Mattie's close friends in kindergarten. It at times seems absolutely surreal that my life once involved driving back and forth to school, caring for a child, organizing playdates, and being a mom. Being a mom was an identity I had for seven years, and sometimes now when I am by myself, I find that my mind plays tricks on me, and I wonder if my mom life was real, or is my current life real?! The rational part of me knows that both are unfortunately real, but the emotional side of me is simply confused and horrified at the same time. Christine and I caught up on our lives, we chatted about the holidays, and naturally the Foundation Walk. It is ironic that both of us talked about how rare pediatric cancer seemed to us while we were growing up. In fact, I can't even think of one child I knew or heard about growing up who had cancer. Yet now, Christine and I know so many. It is hard to believe with our advances in medical science that we are still in the dark ages with pediatric cancer. If you disagree with that notion, then I suggest you watch chemotherapy being infused into a child and see its ramifications. If that doesn't do it for you, then add major surgeries to the mix, and I have a feeling you will concur immediately with me.
Today, I had the opportunity to read an article in the January 25th edition of The Wall Street Journal, entitled, "When a friend grieves, how to get sympathy right" by Elizabeth Bernstein. My dad sent me this article, and between the Journal and Time magazine article I reviewed, I see that grief is a topic we struggle with as a society. In particular, we are uncertain how to help and react to someone's loss. The article lists SIX tips to guide us as we assist a friend. They are:
1) Reach out
2) Listen
3) Share a memory
4) Offer practical help
5) Ask before bringing a lot of food
6) Give something that will live on
For the most part the article was helpful because the author interviewed people who were grieving and asked them what specifically helped them through the process. The four things that resonated with me were: 1) avoid cliches when talking to someone who lost a loved one (such as: good things come from bad; what doesn't kill you makes you stronger; he's at peace now), 2) do not claim to know how the grieving person feels, you do not. Don't suggest that the mourner "move on," 3) certain religious condolences can be upsetting (such as he/she is in a better place), and 4) "if you are reaching out or offering help, don't expect a response. Explain that you are checking in but understand that the mourner may not be able to get back to you and so you will call again. Promise to be there in the coming weeks and months. And keep your promise."
The article also touches upon how we sometimes talk about our own grief as we reach out to friends who are grieving. We do this to try to help and let the other person know that we understand to a certain extent what they are going through. However, as the article so astutely says, this method of sympathy can be construed as equating the losses and what this can do is actually prevent conversation. Though I think the six tips are helpful, there are two key components for me that I would add to this list. The first one is that of acceptance. Not the acceptance of the loss but the acceptance of the mourner as a changed person. I can't imagine anyone surviving a traumatic grief and not being altered in some way. Expecting your friend to be the SAME person, or return to the same person he/she was before the death, is not only upsetting to the mourner, but it can also seem disrespectful. As if the person he/she is grieving for was not an important part of one's life. The second component is be a friend. When I say be a friend, I mean more than just "reaching out." I have found several things helpful from my closest friends, and that is emails and text messages throughout the day, but beyond that, it is the level of inclusiveness in their lives. The feeling that my presence matters, that I am an integral part of their world, and that I am included in their activities, holidays, and gatherings. This has been crucial for me, because without it, it would be very easy to get completely sucked up in the loss of Mattie and completely disengage from the world. Friends prevent this from happening, and in many cases are a key protective factor in surviving such a devastating loss.
Tonight's picture was taken in July of 2003. Mattie was a year old, and that was his first trip to the Outer Banks of North Carolina. I have always been in love with lighthouses, and we took Mattie to Corolla Light that summer and naturally I wanted to climb to the top. Peter and Mattie went together, and I honestly do not know how I did not lose Peter that day from the heat. It was sweltering out, in the 90s with high humidity, and Mattie was too young to climb. So he rode in a carrier on Peter's back. As Peter still tells me, "THAT WAS ONE LONG CLIMB!" Needless to say we all made it to the top of the lighthouse, and Mattie loved the adventure and the climb.
Quote of the day: Given a choice between grief and nothing, I'd choose grief. ~ William Faulkner
Those closest to me have told me how impressed they are that I have made a start at trying to reorganize my home life. That may sound so simple to my readers, but it really isn't. My level of chaos began as soon as Mattie was diagnosed with cancer in July of 2008. At that point, mail began to pile up, toys coming from the hospital and being delivered to our home piled up, Mattie's clothes, medical supplies, and hundreds of his video tapes surrounded us. I guess what I should remind you is that I am not talking about one of two toys accumulated during a hospital visit, I am talking around 50 to 100 new items each time. Imagine 50 to 100 new items entering your home each week of your life for 15 months, and also imagine not having the time to address the accumulation because your priority was caring for a sick and dying child. You learn to live with clutter, you learn to overlook the chaos, because the sheer life and death situation before you is all encompassing, overwhelming, and requires every fiber of your being to manage. I try to remind myself, as I look at the chaos around me that there is an explanation for this, that this isn't me, but this is the result of a great life tragedy. This is a very real and tangible reaction to cancer! Cancer puts your life on hold and you basically stop living. Things are no longer important, all that is important are meeting the basic biological needs of your family, and all the other hierarchical needs (safety, love, belongingness, self-esteem, etc) are simply dispensable.
It is very hard to move from the world of cancer and death back to the living. Because living requires a different set of priorities, a different point of view, and most of all it requires interacting with others. I have always been an extroverted person, however, with Mattie's illness and certainly his death, I have become more introverted, and I need much more alone time. Sometimes when interacting with others I see just how different my life is and how I no longer fit in. Those moments of realization are challenging for me, because it only highlights Mattie's loss in my life.
I had lunch with my friend Christine today. Some of you may recall that Christine is Campbell's mom, and Campbell was one of Mattie's close friends in kindergarten. It at times seems absolutely surreal that my life once involved driving back and forth to school, caring for a child, organizing playdates, and being a mom. Being a mom was an identity I had for seven years, and sometimes now when I am by myself, I find that my mind plays tricks on me, and I wonder if my mom life was real, or is my current life real?! The rational part of me knows that both are unfortunately real, but the emotional side of me is simply confused and horrified at the same time. Christine and I caught up on our lives, we chatted about the holidays, and naturally the Foundation Walk. It is ironic that both of us talked about how rare pediatric cancer seemed to us while we were growing up. In fact, I can't even think of one child I knew or heard about growing up who had cancer. Yet now, Christine and I know so many. It is hard to believe with our advances in medical science that we are still in the dark ages with pediatric cancer. If you disagree with that notion, then I suggest you watch chemotherapy being infused into a child and see its ramifications. If that doesn't do it for you, then add major surgeries to the mix, and I have a feeling you will concur immediately with me.
Today, I had the opportunity to read an article in the January 25th edition of The Wall Street Journal, entitled, "When a friend grieves, how to get sympathy right" by Elizabeth Bernstein. My dad sent me this article, and between the Journal and Time magazine article I reviewed, I see that grief is a topic we struggle with as a society. In particular, we are uncertain how to help and react to someone's loss. The article lists SIX tips to guide us as we assist a friend. They are:
1) Reach out
2) Listen
3) Share a memory
4) Offer practical help
5) Ask before bringing a lot of food
6) Give something that will live on
For the most part the article was helpful because the author interviewed people who were grieving and asked them what specifically helped them through the process. The four things that resonated with me were: 1) avoid cliches when talking to someone who lost a loved one (such as: good things come from bad; what doesn't kill you makes you stronger; he's at peace now), 2) do not claim to know how the grieving person feels, you do not. Don't suggest that the mourner "move on," 3) certain religious condolences can be upsetting (such as he/she is in a better place), and 4) "if you are reaching out or offering help, don't expect a response. Explain that you are checking in but understand that the mourner may not be able to get back to you and so you will call again. Promise to be there in the coming weeks and months. And keep your promise."
The article also touches upon how we sometimes talk about our own grief as we reach out to friends who are grieving. We do this to try to help and let the other person know that we understand to a certain extent what they are going through. However, as the article so astutely says, this method of sympathy can be construed as equating the losses and what this can do is actually prevent conversation. Though I think the six tips are helpful, there are two key components for me that I would add to this list. The first one is that of acceptance. Not the acceptance of the loss but the acceptance of the mourner as a changed person. I can't imagine anyone surviving a traumatic grief and not being altered in some way. Expecting your friend to be the SAME person, or return to the same person he/she was before the death, is not only upsetting to the mourner, but it can also seem disrespectful. As if the person he/she is grieving for was not an important part of one's life. The second component is be a friend. When I say be a friend, I mean more than just "reaching out." I have found several things helpful from my closest friends, and that is emails and text messages throughout the day, but beyond that, it is the level of inclusiveness in their lives. The feeling that my presence matters, that I am an integral part of their world, and that I am included in their activities, holidays, and gatherings. This has been crucial for me, because without it, it would be very easy to get completely sucked up in the loss of Mattie and completely disengage from the world. Friends prevent this from happening, and in many cases are a key protective factor in surviving such a devastating loss.
January 30, 2011
Sunday, January 30, 2011
Sunday, January 30, 2011
Tonight's picture was taken in March of 2003. Mattie was 11 months old, and that was his FIRST trip to Los Angeles. It was his first time flying ever, and he handled it very well. However, what you can't tell from this picture was the time of day. Mattie was very sensitive to the time change between the East and West coasts. I snapped this picture of Peter and Mattie at 4am. To Mattie it felt like 7am, and therefore it was time to wake up. I tried getting Mattie back to sleep that morning, but when Mattie was up, he was UP! So we began the first several days of our trip at 4am. Really NOT my hour, but with Mattie, I learned to do a lot of things I never thought I would do.
Quote of the day: While grief is fresh, every attempt to divert only irritates. You must wait till it be digested, and then amusement will dissipate the remains of it. ~ Samuel Johnson
Peter and I started the day talking about what we wanted to do today. I find that if I have NO plan on the weekends, this can be dangerous. So we chatted about going for a walk, having a late lunch out, and then tackling more cleaning. Today's cleaning adventure required muscle, so therefore, I had to have Peter's buy in into the process.
We returned to Roosevelt Island. Like yesterday, Peter walked the Island earlier in the morning, and then walked it with me in the early afternoon. During the winter months the Island is quiet, peaceful, and has very few visitors. Peter told me on his walk in the morning he saw a flock of robins. I had trouble believing this since it is winter and there is snow on the ground. I associate robins with the first sign of spring. However, to my amazement, as we were walking, I too got to see robins everywhere! In a way it was a beautiful reminder that spring will come, and all the wonderful trees and plants that are sleeping now, will return to life. Spring and particularly summer are my favorite times of year, and I am so happy Peter captured a picture of one of the robins today, because this bird signifies hope for a brighter tomorrow.
As we continued walking, in the distance I spotted something moving. A deer! As Peter tells me all the time, I have deerdar (or deer radar). That makes me laugh! But if there are deer around, I will spot them. This cutie turned its head to see us, and what I find absolutely amazing is how well camouflaged the deer are at this time of year. As the weather warms up, their fur coats seem to turn red in color. Today's temperature was in the 40s in Washington, DC and for some reason it just felt warmer. It was pleasant to be outside walking, and both of us enjoyed the peace, quiet, and openness of the Island. At times we just walked next to each other, quiet, and at other times we chatted. As we were leaving the Island we both reflected on how much Mattie loved visiting there with us, and all the things Mattie did on the Island. It was an amazing backyard to have where Mattie learned to climb rocks, feed ducks, play by the fountains, collect leaves, sticks, and rocks, skip stones on the water, and even sail his remote control boats. It is an Island rich with memories for us.
When Peter and I got home, the fun began. I am still cleaning out things in our bedroom, but today, I had Peter take apart our bed, so I could remove everything I have stored there for years. I cleaned and vacuumed under there, and bagged things to donate, as well as things to simply throw away. I have no idea why I feel compelled to save certain things, but today I wasn't in the saving sort of mood, I was in the remove it from our home quickly mood. While cleaning, I also came across a rug Peter's grandmother gave us from her home many years ago. I had it rolled up under our bed. So what I decided to do was literally have Peter pick up our current rug, throw it out, and replace it with his grandmother's rug. So there are big changes in our room, and it is my hope that this will inspire me to have the courage to take on other parts of our home.
Tonight marks day SIX, and the final day, I will be discussing the article, Good News About Grief: As the nation mourns those killed in Tucson, a new look at the science of loss shows we're more resilient than we thought. This article was featured in Time magazine (January 24, 2011, pp. 42-46) and was written by Ruth Davis Konigsberg.
Just like I have done the previous five nights, I will share with you Konigsberg's writing, and then give my commentary below. Here is the fifth myth presented in Konigsberg's Time magazine article.
==========================================
Myth No. 5 Counseling Helps
Grief counseling is now routinely offered in a range of settings, beginning with the places where most people die: hospitals, palliative-care units and, most of all, hospices, where a minimum of one year of counseling after a loved one's death is mandated by federal legislation passed in 1982. If family members don't encounter someone offering to help in one of those places, they surely will at one of the nearly 20,000 funeral homes across the U.S., where the industry-approved term for bereavement support is "aftercare services." There are also freestanding organizations across the country that offer a wide array of treatments. Some of these organizations are not for profit, but others are all for it: The Grief Recovery Institute in Sherman Oaks, Calif., has trademarked the term grief recovery and charges $995 for a three day workshop.
For a practice that has become so ubiquitous, it has been awfully hard to verify its effectiveness, no matter how well intentioned its advocates may be. When Robert Neimeyer, a psychology professor at the University of Memphis, and his colleague Joseph M. Currier analyzed the results of more than 60 controlled studies on grief interventions in 2008, they found no evidence that counseling helped most bereaved individuals any more than the simple passage of time. "Instead of finding that people who received counseling got better or stayed the same and that people who didn't receive counseling got worse or stayed the same, we found that everyone just got better," Currier says.
The only instance in which counseling showed a benefit was when it was targeted at people displaying marked difficulties adapting to loss. "Given the current research, we can not say that grief counseling is as effective with adults who are showing a normative response," says Currier, referring to the statistical norm for grief's length and intensity.
That doesn't mean that no one is ever helped by counseling but rather that counseling doesn't, on average, seem to hasten grief's departure. In retrospect, the practice was likely popularized before there was enough solid research on normal grief to base it upon. And while counseling may have enriched a few of its practitioners, its propagation was driven more by ideology than money. Grief counselors are, by and large, not a sinister bunch out to make a buck off other people's misery, but they do, in the interest of self-preservation, have a stake in convincing us that grief is long and hard and requires their help.
==========================================
Konigsberg mentioned that counseling was mandated in 1982, by federal legislation, to be offered for a year to those who are grieving. However, contrary to her first paragraph of myth 5, I honestly do not recall Peter and I being offered counseling at the hospital and most certainly not through the funeral home where Mattie was cremated. However, as Peter reminds me, we were in shock back in September of 2009, so it is quite possible we are not remembering accurately. If I was to seek grief counseling, my most likely place to turn to for help would have been the hospital. However, Mattie's hospital for the most part doesn't have a bereavement program in place for its families. So I really can't say whether this type of support would have helped me. I do know that I attended one support group meeting at the hospital, a month after Mattie died. I was the one who asked for the creation of the support group, and the staff were nice enough to try to accommodate this request. But for various reasons the group never met again after that first session, and frankly after that initial experience, I felt very dissatisfied, angered, and with a clear understanding that a group environment was not right for me at that time.
Some of you may recall that pretty soon after Mattie died, I moved into Ann's house to help her with her dad, who was also dying. Once Ann's dad died, I spent many days after that point sitting with Mary (Ann's mom). Hospice grief counselors would come to visit Mary and offer her support, and at the same time, when they heard my story, they wanted to reach out and help me too. Frankly one social worker couldn't grasp how I could have just lost my son, and yet here I was functioning in an assisted living facility helping someone else grieve. Her insistence that I needed counseling infuriated me, because she wasn't taking the time to listen to my story and make an accurate assessment. I am sure to an outsider, it seemed impossible to grasp how I could go through another death on top of the one I already lived through. But here is the thing, for over 15 months prior to Ann's dad getting ill, I was caring intensely for Mattie. I was up around the clock seven days of week. My body was programmed to be alert, on all the time, thinking, caring, and working in a medical environment. When Mattie died, I couldn't just shut that switch off. It made sense from a physical standpoint that I should be the one to help Ann and from an emotional standpoint I am happy she allowed me in to do this. It brought us even closer as friends, and it gave me a purpose at a time when my world was crashing all around me. So what this social worker couldn't understand was that helping Ann's dad and mom, was actually therapeutic, it forced me to engage with the world, and in essence as Ann's dad was dying, Mary and I had many opportunities to chat. Which is in essence the beginning of our friendship together, a friendship that continues today.
So what is my point? My point is that we all handle grief differently and need different things to heal. Counseling may not be one of the things we all need on our journey through grief. I might feel quite differently if I did not have others in my life I could connect and talk with, but for the most part I felt early on, why would I be going to a counselor? This person can't possibly change my situation! This person can't bring Mattie back, and this person can't certainly erase the months of trauma I witnessed Mattie endure. Unlike other reasons for seeking therapy, with grief, I am not looking to learn a new strategy, I am not looking to change my mindset on how I am thinking or viewing the situation (because the situation is just bad, and no amount of reframing is going to make it look better to me), and I was most certainly unwilling to invest the time in rehashing what I lived through with someone who doesn't know me. That would be draining beyond proportion to me, because unless you witnessed what I lived through, I couldn't possibly describe it accurately to you. I remember one day I met with Mattie's social worker, Denise, at the hospital. I said to Denise that maybe I should meet with her periodically to just chat. Denise listened to me and was open to doing this, but then she asked me.... "why are you doing this? Because you want to or because others are telling you that you should?" Denise was correct, I was doing it because I was receiving pressure from others. Pressure and evaluations from others which weren't helpful. Denise normalized things for me and helped me understand that others in my life were frustrated and they wanted me to feel better, and they think that counseling will fix things. However, as Denise and I both knew, counseling was not going to fix the situation. I appreciated Denise's honestly, and what you should know is Denise's specialty is grief counseling. So she is a perfect example of person not pushing her profession upon me.
Grief is a very personal, private, and all encompassing issue. It changes your view of yourself, the world, and everyone in it. Part of the healing process is finding the will and hope to continue living. NO ONE can do that for you, not even the best of therapists. Which is why I feel that a good chunk of grief work, has to be done independently. I am certainly not closed off to professional help, but I am aware of the fact that in therapy change comes from within, and I do not want someone I do not know sitting with me hearing my feelings and thoughts on one of my most intimate relationships, raising Mattie.
At the end of myth 5, Konigsberg says.... "Grief counselors are, by and large, not a sinister bunch - but they do, in the interest of self-preservation, have a stake in convincing us that grief is long and hard and requires their help." Reading this actually made me laugh. I am happy she doesn't consider mental health professionals (who wants to sit, listen, and help people at their lowest and most challenging points in their life) sinister! However, grief is long and hard, and most definitely I can see that there are times when professional help may be needed, but let's be honest. She is insinuating that grief counselors are convincing us as a society about the appropriate ways of grieving. I encourage you to step back, and think about this. Grief counselors are giving their opinions, sharing their insights from training and experience, and frankly how is this different than seeking the option of any other health specialist? Each specialist views a person from their own lens and training. You go to an eye doctor, because he/she understands eyes, and most likely this person will find an eye issue. You go to a cardiologist because he/she understands the working of the heart, and chances are this person will spot a heart issue. From my experience you go to these specialists to get their expert opinion, and most likely they will view your problem from their lens of knowledge. So why is it any different with a grief counselor? It isn't. In the end however, whether you are seeing a medical specialist or a mental health specialist, you as the PATIENT, must make the ultimate decision about your treatment. You are the one who is empowered, and you alone, know what is right for you. The same is true with grief. I can't think of a more imperative time in one's life where you must follow your own HEART and intuition about recovery than when you are surviving a profound loss.
Tonight's picture was taken in March of 2003. Mattie was 11 months old, and that was his FIRST trip to Los Angeles. It was his first time flying ever, and he handled it very well. However, what you can't tell from this picture was the time of day. Mattie was very sensitive to the time change between the East and West coasts. I snapped this picture of Peter and Mattie at 4am. To Mattie it felt like 7am, and therefore it was time to wake up. I tried getting Mattie back to sleep that morning, but when Mattie was up, he was UP! So we began the first several days of our trip at 4am. Really NOT my hour, but with Mattie, I learned to do a lot of things I never thought I would do.
Quote of the day: While grief is fresh, every attempt to divert only irritates. You must wait till it be digested, and then amusement will dissipate the remains of it. ~ Samuel Johnson
Peter and I started the day talking about what we wanted to do today. I find that if I have NO plan on the weekends, this can be dangerous. So we chatted about going for a walk, having a late lunch out, and then tackling more cleaning. Today's cleaning adventure required muscle, so therefore, I had to have Peter's buy in into the process.
We returned to Roosevelt Island. Like yesterday, Peter walked the Island earlier in the morning, and then walked it with me in the early afternoon. During the winter months the Island is quiet, peaceful, and has very few visitors. Peter told me on his walk in the morning he saw a flock of robins. I had trouble believing this since it is winter and there is snow on the ground. I associate robins with the first sign of spring. However, to my amazement, as we were walking, I too got to see robins everywhere! In a way it was a beautiful reminder that spring will come, and all the wonderful trees and plants that are sleeping now, will return to life. Spring and particularly summer are my favorite times of year, and I am so happy Peter captured a picture of one of the robins today, because this bird signifies hope for a brighter tomorrow.
As we continued walking, in the distance I spotted something moving. A deer! As Peter tells me all the time, I have deerdar (or deer radar). That makes me laugh! But if there are deer around, I will spot them. This cutie turned its head to see us, and what I find absolutely amazing is how well camouflaged the deer are at this time of year. As the weather warms up, their fur coats seem to turn red in color. Today's temperature was in the 40s in Washington, DC and for some reason it just felt warmer. It was pleasant to be outside walking, and both of us enjoyed the peace, quiet, and openness of the Island. At times we just walked next to each other, quiet, and at other times we chatted. As we were leaving the Island we both reflected on how much Mattie loved visiting there with us, and all the things Mattie did on the Island. It was an amazing backyard to have where Mattie learned to climb rocks, feed ducks, play by the fountains, collect leaves, sticks, and rocks, skip stones on the water, and even sail his remote control boats. It is an Island rich with memories for us.
When Peter and I got home, the fun began. I am still cleaning out things in our bedroom, but today, I had Peter take apart our bed, so I could remove everything I have stored there for years. I cleaned and vacuumed under there, and bagged things to donate, as well as things to simply throw away. I have no idea why I feel compelled to save certain things, but today I wasn't in the saving sort of mood, I was in the remove it from our home quickly mood. While cleaning, I also came across a rug Peter's grandmother gave us from her home many years ago. I had it rolled up under our bed. So what I decided to do was literally have Peter pick up our current rug, throw it out, and replace it with his grandmother's rug. So there are big changes in our room, and it is my hope that this will inspire me to have the courage to take on other parts of our home.
Tonight marks day SIX, and the final day, I will be discussing the article, Good News About Grief: As the nation mourns those killed in Tucson, a new look at the science of loss shows we're more resilient than we thought. This article was featured in Time magazine (January 24, 2011, pp. 42-46) and was written by Ruth Davis Konigsberg.
Just like I have done the previous five nights, I will share with you Konigsberg's writing, and then give my commentary below. Here is the fifth myth presented in Konigsberg's Time magazine article.
==========================================
Myth No. 5 Counseling Helps
Grief counseling is now routinely offered in a range of settings, beginning with the places where most people die: hospitals, palliative-care units and, most of all, hospices, where a minimum of one year of counseling after a loved one's death is mandated by federal legislation passed in 1982. If family members don't encounter someone offering to help in one of those places, they surely will at one of the nearly 20,000 funeral homes across the U.S., where the industry-approved term for bereavement support is "aftercare services." There are also freestanding organizations across the country that offer a wide array of treatments. Some of these organizations are not for profit, but others are all for it: The Grief Recovery Institute in Sherman Oaks, Calif., has trademarked the term grief recovery and charges $995 for a three day workshop.
For a practice that has become so ubiquitous, it has been awfully hard to verify its effectiveness, no matter how well intentioned its advocates may be. When Robert Neimeyer, a psychology professor at the University of Memphis, and his colleague Joseph M. Currier analyzed the results of more than 60 controlled studies on grief interventions in 2008, they found no evidence that counseling helped most bereaved individuals any more than the simple passage of time. "Instead of finding that people who received counseling got better or stayed the same and that people who didn't receive counseling got worse or stayed the same, we found that everyone just got better," Currier says.
The only instance in which counseling showed a benefit was when it was targeted at people displaying marked difficulties adapting to loss. "Given the current research, we can not say that grief counseling is as effective with adults who are showing a normative response," says Currier, referring to the statistical norm for grief's length and intensity.
That doesn't mean that no one is ever helped by counseling but rather that counseling doesn't, on average, seem to hasten grief's departure. In retrospect, the practice was likely popularized before there was enough solid research on normal grief to base it upon. And while counseling may have enriched a few of its practitioners, its propagation was driven more by ideology than money. Grief counselors are, by and large, not a sinister bunch out to make a buck off other people's misery, but they do, in the interest of self-preservation, have a stake in convincing us that grief is long and hard and requires their help.
==========================================
Konigsberg mentioned that counseling was mandated in 1982, by federal legislation, to be offered for a year to those who are grieving. However, contrary to her first paragraph of myth 5, I honestly do not recall Peter and I being offered counseling at the hospital and most certainly not through the funeral home where Mattie was cremated. However, as Peter reminds me, we were in shock back in September of 2009, so it is quite possible we are not remembering accurately. If I was to seek grief counseling, my most likely place to turn to for help would have been the hospital. However, Mattie's hospital for the most part doesn't have a bereavement program in place for its families. So I really can't say whether this type of support would have helped me. I do know that I attended one support group meeting at the hospital, a month after Mattie died. I was the one who asked for the creation of the support group, and the staff were nice enough to try to accommodate this request. But for various reasons the group never met again after that first session, and frankly after that initial experience, I felt very dissatisfied, angered, and with a clear understanding that a group environment was not right for me at that time.
Some of you may recall that pretty soon after Mattie died, I moved into Ann's house to help her with her dad, who was also dying. Once Ann's dad died, I spent many days after that point sitting with Mary (Ann's mom). Hospice grief counselors would come to visit Mary and offer her support, and at the same time, when they heard my story, they wanted to reach out and help me too. Frankly one social worker couldn't grasp how I could have just lost my son, and yet here I was functioning in an assisted living facility helping someone else grieve. Her insistence that I needed counseling infuriated me, because she wasn't taking the time to listen to my story and make an accurate assessment. I am sure to an outsider, it seemed impossible to grasp how I could go through another death on top of the one I already lived through. But here is the thing, for over 15 months prior to Ann's dad getting ill, I was caring intensely for Mattie. I was up around the clock seven days of week. My body was programmed to be alert, on all the time, thinking, caring, and working in a medical environment. When Mattie died, I couldn't just shut that switch off. It made sense from a physical standpoint that I should be the one to help Ann and from an emotional standpoint I am happy she allowed me in to do this. It brought us even closer as friends, and it gave me a purpose at a time when my world was crashing all around me. So what this social worker couldn't understand was that helping Ann's dad and mom, was actually therapeutic, it forced me to engage with the world, and in essence as Ann's dad was dying, Mary and I had many opportunities to chat. Which is in essence the beginning of our friendship together, a friendship that continues today.
So what is my point? My point is that we all handle grief differently and need different things to heal. Counseling may not be one of the things we all need on our journey through grief. I might feel quite differently if I did not have others in my life I could connect and talk with, but for the most part I felt early on, why would I be going to a counselor? This person can't possibly change my situation! This person can't bring Mattie back, and this person can't certainly erase the months of trauma I witnessed Mattie endure. Unlike other reasons for seeking therapy, with grief, I am not looking to learn a new strategy, I am not looking to change my mindset on how I am thinking or viewing the situation (because the situation is just bad, and no amount of reframing is going to make it look better to me), and I was most certainly unwilling to invest the time in rehashing what I lived through with someone who doesn't know me. That would be draining beyond proportion to me, because unless you witnessed what I lived through, I couldn't possibly describe it accurately to you. I remember one day I met with Mattie's social worker, Denise, at the hospital. I said to Denise that maybe I should meet with her periodically to just chat. Denise listened to me and was open to doing this, but then she asked me.... "why are you doing this? Because you want to or because others are telling you that you should?" Denise was correct, I was doing it because I was receiving pressure from others. Pressure and evaluations from others which weren't helpful. Denise normalized things for me and helped me understand that others in my life were frustrated and they wanted me to feel better, and they think that counseling will fix things. However, as Denise and I both knew, counseling was not going to fix the situation. I appreciated Denise's honestly, and what you should know is Denise's specialty is grief counseling. So she is a perfect example of person not pushing her profession upon me.
Grief is a very personal, private, and all encompassing issue. It changes your view of yourself, the world, and everyone in it. Part of the healing process is finding the will and hope to continue living. NO ONE can do that for you, not even the best of therapists. Which is why I feel that a good chunk of grief work, has to be done independently. I am certainly not closed off to professional help, but I am aware of the fact that in therapy change comes from within, and I do not want someone I do not know sitting with me hearing my feelings and thoughts on one of my most intimate relationships, raising Mattie.
At the end of myth 5, Konigsberg says.... "Grief counselors are, by and large, not a sinister bunch - but they do, in the interest of self-preservation, have a stake in convincing us that grief is long and hard and requires their help." Reading this actually made me laugh. I am happy she doesn't consider mental health professionals (who wants to sit, listen, and help people at their lowest and most challenging points in their life) sinister! However, grief is long and hard, and most definitely I can see that there are times when professional help may be needed, but let's be honest. She is insinuating that grief counselors are convincing us as a society about the appropriate ways of grieving. I encourage you to step back, and think about this. Grief counselors are giving their opinions, sharing their insights from training and experience, and frankly how is this different than seeking the option of any other health specialist? Each specialist views a person from their own lens and training. You go to an eye doctor, because he/she understands eyes, and most likely this person will find an eye issue. You go to a cardiologist because he/she understands the working of the heart, and chances are this person will spot a heart issue. From my experience you go to these specialists to get their expert opinion, and most likely they will view your problem from their lens of knowledge. So why is it any different with a grief counselor? It isn't. In the end however, whether you are seeing a medical specialist or a mental health specialist, you as the PATIENT, must make the ultimate decision about your treatment. You are the one who is empowered, and you alone, know what is right for you. The same is true with grief. I can't think of a more imperative time in one's life where you must follow your own HEART and intuition about recovery than when you are surviving a profound loss.
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