A Remembrance Video of Mattie

Thank you for keeping Mattie's memory alive!

Dear Mattie Blog Readers,

It means a great deal to me that you take the time to write and to share your thoughts, feelings, and reflections on Mattie's battle and death. Your messages are very meaningful and help support me through very challenging times. I am forever grateful. As my readers know, I promised to write the blog for a year after Mattie's death, which would mean that I could technically have stopped writing on September 9, 2010. However, like my journey with grief there is so much that still needs to be processed and fortunately I have a willing support network still committed to reading. Therefore, the blog continues on. If I should find the need to stop writing, I assure you I will give you advanced notice. In the mean time, thank you for reading, thank you for having the courage to share this journey with me, and most importantly thank you for keeping Mattie's memory alive.


As Mattie would say, Ooga Booga (meaning, I LOVE YOU)! Vicki



September 9, 2023

Saturday, September 9, 2023

Saturday, September 9, 2023

Tonight's picture was taken in September of 2008. Mattie was in his second month of treatment. That day, his technology teacher from school came by and gave Mattie a laptop. I imagine all the children that year received one and therefore she wanted Mattie to be just like the other kids. Mary was an amazing and kind teacher. She visited Mattie on a regular basis and taught him technology skills while also trying to engage and play with him. Mattie responded very well to Mary and when they were together, I would try to go into the hallway for an hour to get a reprieve from the 2x4 of a hospital room. 


Quote of the day: Just as it is impossible to explain childbirth to a woman who has never given birth, it is impossible to explain child loss to a person who has never lost a child. ~ Lynda Cheldelin Fell


I went to the shopping mall with Peter this morning, so we could walk and talk. Ironically there doesn't seem to be anywhere in my own home where I can sit down, talk, and relax without being disturbed. Therefore, I am trying to find outlets now, to leave the house and connect with people. I got to hear about the trip Peter was on over the last two days. Peter had the opportunity to take part in a taping of a commercial for an adult cancer patient receiving oral chemotherapy. The process sounded fascinating but the part I wanted to highlight here was the simple fact that Peter, the patient, and her family were able to connect almost immediately. I attribute this gift to Mattie, as Mattie was our greatest teacher in life. I truly believe that experiencing Mattie's cancer enables us to speak a language that only those dealing with life threatening illnesses can understand.

There is something to be said about the lived experience. I remember when I was in graduate school or teaching counseling to students, my philosophy was that a therapist did not have to experience the exact same problem a client is coping with in order to be able to help the client. I am not sure I share this same philosophy now. As I could try to describe Mattie's journey and Mattie's loss from my perspective, but I am not sure it can be truly processed and understood without having a personal lens into the depths of this loss. 

It was another red letter day for Vicki. I took my parents out for lunch, as I do every Saturday. Between my dad's dementia and irritable bowel syndrome, I think some days I could lose my mind. I try to keep patient, but no meal is ever pleasant (whether home or out). Soon after eating his entree, I could see my dad's face. He was grimacing. I know that sign well, but he doesn't! So I got him up to go to the bathroom. Unfortunately I was too late. When I tell you there was urine and poop everywhere I am not kidding. I had to clean myself, him, the toilet, the bathroom floor, etc! Truly it can be nauseating and the disaster unfolds so quickly that I don't have time to get gloves on to manage all of this. Of course while this is happening, my dad has NO concept of what is going on around him and unless I direct his every move, he would be covered in poop. Truly it is a horrific scene and no amount of scrubbing of my hands will remove this smell. Thankfully for my dad, I travel with a big tote bag, that has a change of clothes, which was greatly needed today. All I can say is there is a special place for me!

My mom is on this kick that she wants to travel and get away from our usual routine. I hear what she is saying and if I could make this happen I would. But then I have a day like today, and it further reinforces why their days of traveling maybe non-existent. So many reasons why traveling would be complicated.... my dad's dementia decline, his irritable bowel syndrome, his level of daily exhaustion, my mom's issues with walking and balance, the fact that she tires easily and the list goes on and ON and ON!

September 8, 2023

Friday, September 8, 2023

Friday, September 8, 2023

On the 14th anniversary of Mattie's death, we remember him, today and always! This was the quintessential photo of Mattie. A friend brought Mattie a lump of clay, some tools, and googles to the hospital. Mattie spent hours digging through the clay for find plastic dinosaur bones. He then had to assemble the bones to create the skeleton of the dinosaur. It was a great activity for Mattie. He was focused, determined, and happy. Once the project was completed, he and the dinosaur posed for a photo. A day I will never forget, as sheets were all over the floor, clay was everywhere, and it looked like Mattie went on an official archeological dig! 


Quote of the day: When the young bury the old, time heals the pain and sorrow. But when the process is reversed, the sorrow remains forever. ~ Joseph P. Kennedy


Despite the fact that our lives dramatically changed 14 years old today, I had to push myself through the day. As my parent's routine continued for them and it was business as usual. Unfortunately today was NOT an ordinary day for me or Peter. We will never forget September 8, 2009. This is the first anniversary of Mattie's death where Peter and I are in separate locations. Peter was on the Eastern Shore of Maryland working with a pharmaceutical company. It was an interesting assignment as he had the opportunity to be on a photo shoot (for a commercial) of a patient who is receiving oral chemotherapy. Not just anyone can understand the plight of a cancer patient and her family. So though it was hard to have Peter gone, I also knew that this was an opportunity that could be beneficial for both him and the current cancer patient. 

While going about my chores this morning, something freaked me out. The only explanation for what happened is I feel we were receiving a message from Mattie. This morning I made the bed. I do this SAME routine EVERYDAY. Later in the morning, I took the vacuum into the room the clean things up. When I entered the room, I felt a strange sensation. I then looked at the bed, and Peter side was turned down. You know like they do at a fancy hotel. It was neatly and perfectly done, so this wasn't something Indie may have done by running over the bed. I truly stopped in my tracks. I tried to find a logical explanation, but there is NONE. Nothing explains this in my mind, and I know I am not going crazy..... I made the bed hours before. 

Soon after Mattie died, I received other unexplained signs. The first one I ever received happened when I drove my car to Alexandria, VA and visited a friend. When I came back into the car, I found the passenger side seat COMPLETELY reclined. I used to do this to the seat when taking Mattie to the hospital, when his leg was in a cast from surgery. He would be sitting in the back seat, and I would rest his leg on the reclined front passenger seat. However, in this particular instance, the seat wasn't reclined when I left the car. The only way to recline the seat would be to push the buttons inside the car to adjust the seat. Needless to say, that day, I felt like I received a message from Mattie. He was with me in that car. 

I felt the same way today...... 14 years later. I felt as if something/someone was with me in the bedroom and the folded sheets and blankets were a sign!

~~~~~~~~~~~~~~~~

On this day, 14 years ago, Mattie died from osteosarcoma. It was a 14 month journey of high dose chemotherapy, limb salvaging surgeries, a sternotomy, experimental treatment, and cyberknife radiation. Mattie was my life's greatest teacher, and he showed us that CHILDHOOD CANCER IS NOT JUST ABOUT THE MEDICINE. 

Within three months of starting treatment, Mattie was diagnosed with clinical depression, anxiety, and medical traumatic stress. Issues he did NOT have before receiving chemotherapy. Mattie was prescribed psychotropic medications, but very little research had been done on the interactions of these meds with chemotherapy on children. So in essence each day of Mattie's cancer journey was traumatic, in which we were constantly making life and death decisions and in the process we faced grief and loss daily. All this sadness and trauma does go somewhere! It builds up in our minds and bodies. 

Those of us who lost a child to cancer, may look physically "normal" to the world, but that is just our façade. Instead, we have an internal fight each day to get up, to try to carry on our child's legacy, and to try to maintain our own physical health (which is ironically compromised from the incredible stresses and forever loss that we continually face), and to find the hope, love, and support needed to navigate life without our child. 

I will never forget the day Mattie's cancer diagnosis turned terminal (August 5, 2009). On that day, Mattie and I went to the hospital rose garden and he jumped into my lap and wanted to hear about the day he was born. A story Mattie loved hearing me tell, and usually wanted to hear it during challenging times. I always share my "Dearest Mattie" story on Facebook and the blog on this day. This was a story I wrote and had on display during Mattie's celebration of life. 

Mattie is forever missed, he has left a hole in our hearts and spirit. We are passionate about keeping his legacy alive at Mattie Miracle and taking the lessons learned from him to help other children facing their own cancer journey. 

Ooga Booga (in Mattie-ese, that means I love you!)

-----------------------------

My Dearest Mattie,

It is said that parents love their children right from the moment they are born. However, in your case, our love for you began as soon as we learned we were going to have a baby. In fact, right after seeing your sonogram picture, we felt like proud parents. We posted those pictures everywhere. We shared these pictures with practically anyone who would listen or showed interest, and each September when I taught prenatal development in my undergraduate human development class, out would come your sonogram pictures to illustrate my points. Even my students got a sneak peek at our baby, a baby who would have a profound and meaningful impact on not just his parents but also every community he touched. Daddy and I did not only love you, we FELL IN LOVE with you, and that love grew stronger with each day. Your energy, spirit, love for life, intellectual challenges, sense of humor, and loyalty to your friends and family were only some of the wonderful traits we always admired in you.

This video is a tribute to you and your wonderful, yet short life. It seems fitting as we celebrate you, and say good-bye to your physical presence that I share the story about how you entered the world. The story of your birth had to be one of your most favorite stories to hear, and I found during times when you were reflective, overly tired, or in need of hugs and tenderness, the request for this story arose. In fact, I remember on August 5th, the day we found out that your cancer metastasized everywhere, you and I were sitting in the hospital’s rose garden, and you requested the story. It was almost as if you knew this was going to be a bad day, so in essence we might as well brace ourselves, cuddle, and prepare for this together.

Here is the story I always shared with you. A story Daddy and I will never forget. On April 2, 2002, at 11pm, I decided to head to bed. I was anxiously awaiting your birth, and as your due date approached, I couldn’t help but wonder, when will “the baby” be coming? I was restless and uncomfortable, so while in bed, I began to watch television. I was having trouble concentrating on what I was hearing, mainly because you were kicking up a storm inside of me. At which point, the kicking became so intense, that I literally felt something pop. You clearly wanted OUT, and you were going to kick your way into the world on your terms. Naturally after feeling this pop, I looked down at my tummy, and when I jumped out of bed, I realized my water had broken. This only happens to 25% of moms, and in retrospect, I should have guessed that this was just the beginning of how different our lives were going to be together. I immediately called the doctor and told her what happened. She asked if I was in pain, which I wasn’t, and she instead told me to get a good night’s rest, because my baby was going to be born the following day. Well I can assure you after hearing this news, sleeping was the farthest thing from our minds.

So on April 3, 2002, Daddy and I headed to the hospital and we were admitted to the maternity unit at 8am. The labor process began, but it was a VERY slow process for me, and at times as you moved inside my tummy, Daddy could see your head pushing against my backbone. Needless to say Dr. Mike, the anesthesiologist, became my favorite doctor that day. The hours kept rolling by, and still there was NO sign of our baby! I was getting weaker, I developed an 102 fever, and by 11pm I really had no energy to give birth to you. In addition, to how I was feeling, your oxygen supply was getting cut off, and your chin was positioned in such a way that would make the birthing process almost impossible. So it was at that point that the doctor recommended an emergency c-section. Things began to happen very quickly around me. I was signing paperwork for surgery and Daddy was being transformed by putting on a bunny suit so he could enter the operating room.

I had never been in an operating room before in my life, but I really wasn’t concerned at that point about myself. I was solely focused upon you. I was wide-awake for the c-section, but unable to see the process, which as you know, was probably a good thing. Daddy on the other hand found the whole thing very exciting, and began to videotape and take pictures of the surgery. Literally a team of people surrounded me and I will never forget Dr. Mike, the anesthesiologist who sat by my side, and talked with me and did whatever he could to keep me pain free.

When you have a c-section, your arms are strapped to the operating table, so I couldn’t move, and directly over my head was what appeared to be a rope with a clamp that was holding open my abdominal cavity. Normally by this point I would have passed out, but when it came to you, I developed strength I never knew I had. As the doctor began cutting, and finally got to you, the first thing she said was, “what is this?” That is NOT what you typically hope to hear when having a c-section. The doctor let me know that I had a grapefruit sized tumor on my bladder, and my immediate thought was, did this affect the baby? The next thing I knew, I felt her tugging, and I heard the loudest cry ever. Now here is the part of the story that I know was always your FAVORITE! I would always try to replicate the sound I heard coming from you that day, a sound that will always remain in a parent’s ear. It was a very large WAAHHH! WAAHHH! At which point the doctor told us two things: first, that you were one of the most beautiful babies she had ever seen, and second, that you had quite a set of lungs on you! I concurred with both statements.

The doctor then brought you over to me, and she felt that I needed to be the first person to touch you. So despite my arms strapped to the table, my right hand miraculously reached out and grabbed your tiny, soft, and cute foot. It was a moment I will always cherish, a moment in which I will never forget, and a moment I am so happy you too enjoyed hearing about. Each time I retold the story I felt as if it further bonded us together, and I always enjoyed hearing your comments, thoughts, and reactions to your story.

Seeing you made Daddy very happy! Though he was worried about me, since after the c-section, I had to have bladder surgery to remove the tumor, we both agreed that Daddy should stay with you and accompany you to the nursery. It is there that Daddy got to see you cleaned up, he learned that you weighed 6 pounds and 13 ounces, and that you had high Apgar scores of 8 and 9. Within an instant, Daddy became one of your fiercest protectors, and he cared for you for five days straight while we were in the hospital together. In fact, Daddy is the first person who changed your diaper, and though those were five very challenging days in the hospital, they were days that helped us form our strong family ties. Ties that were imperative and that we relied on for seven years of your life!

Your presence is so greatly missed. Nothing seems the same, is the same, looks, feels, or tastes the same without you in our lives. May you always know that Mommy and Daddy love you, cherish you, and that feeling will remain with us forever and always. Good-bye my Mooshi Moo angel and goodbye Daddy’s best buddy. With love from Una Moon and Daddy!

September 7, 2023

Thursday, September 7, 2023

Thursday, September 7, 2023

Tonight's picture was taken on October 10, 2009, at Mattie's celebration of life event. Though Mattie died on September 8th of 2009, it took us about a month to pull ourselves together, along with plan an event to acknowledge the beautiful life of Mattie Brown. Thankfully we had a lot of help from our community. In this photo you see a red balloon release done by many of Mattie's friends and classmates. Remember they were only 7 years old, and it was hard for an adult to understand the fact that Mattie died. It was even harder for the children. Many of my graduate school students got together and put together memory making activities for the children, such as painting a stone and this balloon release. Each balloon had a message attached to it. I will never forget this image.  

Quote of the day: His death brings a new experience to my life — that of a wound that will not heal. ~ Ernst Jünger


Tomorrow marks the 14th anniversary of Mattie's death. It is a day that will be forever ingrained in me. Mattie's death was harrowing, as it was many hours of suffering, excruciating pain, an inability to breathe, and the hospital room looked like a war zone. They couldn't give Mattie enough IV pain meds, so much so that literally his bed was strewn with syringes. When I tell you it was horrific, I am not exaggerating. In the end, Mattie received a lethal dose of propofol, to end his suffering. This dose was immediately followed by the heart wrenching flat line sound on his monitor. The horrors were compounded one right after the other. I have not been to war or been on a battlefield. I don't like making comparisons, but I do view our life in the hospital that year as being our own private war and on September 8, 2009, we left the hospital at TWO, though we had entered its doors a week before as THREE.  

These butterfly gifts were birthday presents to me. I received them today as a belated present. Ironically this gift has an even greater impact on me today, than it would have in July. Mattie is my butterfly, and whenever I see one of these flutterbys in nature, I feel it is a visit and message meant just for me. 


September 6, 2023

Wednesday, September 6, 2023

Wednesday, September 6, 2023

Tonight's picture was taken in September of 2008. Mattie was in his second month of treatment and that day, Mattie was making creations from cardboard boxes. He literally was carrying all the boxes throughout the main floor of the hospital. By that point in time, all of Mattie's psychosocial staff knew he LOVED boxes. I have a feeling they saved every box that came into the clinic that year, and Mattie found a use for each and every one of them!





Quote of the day: I am a firm believer that helping others is the quick way to find true happiness, making someone's day a little bit brighter will in turn make your own day that much better. ~ Catherine Pulsifer


It was another busy day! While I was getting dressed this morning, I received a text message from my neighbors. They are in their late 70's. One of them is recovering from surgery and the other has just been diagnosed with COVID. They clearly needed help, as they couldn't get out to go grocery shopping. I asked my neighbor to make a list of all the items she needed and I would pick them up today and leave them by her doorstep. 

After dropping my dad off at his memory care center, I ran to my yearly skin check at my dermatologist's office. On my way home, I stopped off at the grocery store and picked up all the requested items. I added a bunch of sunflowers and a bag of mixed freshly baked cookies. To me, sugar and flowers always perk me up when I am not feeling well, and hoped this would be true for my neighbors. Though they wanted to pay me for shopping, I said no. It was our gift to them, in hopes they would have a speedy recovery. My neighbor said that I am "a gift" to her and thinks I am the sweetest. There is something to be said about tonight's quote. Maybe that is why I entered the helping profession, because I am a firm believer that in helping others, we deeply help ourselves and learn more about ourselves in the process. 

I help two 88 year old's everyday, but being able to help those in my community makes me feel good. It makes me feel like I serve a purpose and have meaning in my life. Once I dropped off the items at my neighbors, I then promised to take my mom out to lunch. So it was a day of constant running around and chores. When my parents first moved in, this kind of day would have gotten me down. After all, I couldn't get to my emails, I couldn't do Foundation work, or have a minute to myself. But being at this caregiving routine for almost two years now, I have learned that there is only one of me, and I can't do everything. I get things done when I can and I can't beat myself up if I can't get to everything. This is not in my nature, but it is the best I can do for now, so it has to suffice. 

September 5, 2023

Tuesday, September 5, 2023

Tuesday, September 5, 2023 -- Mattie died 727 weeks ago today.

Tonight's picture was taken in September of 2008. We took Mattie to New York to be evaluated by Memorial Sloan Kettering. What an experience! In any case, between hospital appointments, we took Mattie to various sites in hopes that it would be a positive diversion. This photo was taken in front of the Natural History Museum, but as you can see, Mattie was in no mood for fun and games. We did tour the Museum, and we tried our best, but our hearts and minds were too bogged down with the impact of Mattie's diagnosis. 


Quote of the day: In time, every post tends to be occupied by an employee who is incompetent to carry out its duties. ~ Laurence J. Peter


Today was a winner of a day! On top of so many other winners. I got my parents out the door by 10:15am, which I assure you is a feat. My dad had an 11am follow up visit to his primary care physician. This doctor is monitoring his diabetes. Some of you may recall that I did NOT like the aesthetics of this doctor's office when we first visited in the spring. Recap, my parent's doctor retired. This is the doctor I typically referred to as, "dopey." Dopey was replaced with this new doctor, who is at a different location. The "new" doctor has been practicing for decades and though I do not like his physical space, he turns out to be stellar. He answers text messages, phone calls, takes my opinion into account, and has really been trying to do the right thing for my parents. FINALLY! My dad had a good visit today and will be monitored every three months, unless something else pops up. 

After the appointment, while in the car, I called my dad's podiatrist. I wanted the podiatrist to send the appropriate Medicare forms to the primary care doctor, for my dad's new shoes. That went smoothly. I then decided to call my endocrinologist's office to schedule my Prolia injection. The specialty pharmacy sent me a confirmation text saying that the drug was delivered last week. When I called my doctor's office, the staff said.... NO the drug was delivered to the wrong address and isn't at the office. The staff implied that I provided the WRONG address to the pharmaceutical company. Not only the wrong address, but the doctor's address from 15 years old. ABSOLUTE nonsense as I only met this doctor two years ago. I do not know about her old office and have no idea about its address. Truly I was livid. Livid because I know the office won't help me manage this problem. 

In fact, I spoke to my doctor's nurse, WHO I CAN'T STAND. She is the one I told on the phone during our last conversation that she...... "needed to do your job." Mind you this nurse called me today, I did not ask to speak to her, after already having a frustrating conversation with the office staff. This nurse told me the exact same thing as the staff.... that I provided the wrong address and now the pharmaceutical company will not resend the drug without me paying an additional $1,000! While having this conversation, I was at lunch with my parents, and I was so furious. I think every diner in the restaurant overhead my conversation. In fact, one person came up to me after I was done and said, "sorry for overhearing, but GOOD FOR YOU!" 

But at the end of the day, I know the endocrinology office isn't going to lift a finger to help me with this issue. So I am now back to square one, which is very frustrating, as it has been a three month long process just to get this missing dose delivered. My patience is fleeting, and there is NO REGARD to what I am already juggling!

September 4, 2023

Monday, September 4, 2023

Monday, September 4, 2023

Tonight's picture was taken in September of 2008. This was Mattie's second month on treatment and it was a rough evening. So Peter livened up the room by blowing up hospital gloves. Mattie then used the gloves like puppets and was trying to perform a show through his window for anyone who was in the hallway. Mattie's nurses were outstanding and they understood the psychosocial consequences of living with a life threatening illness and living around the clock in a pediatric intensive care unit. So rest assured, if they were anywhere near Mattie's window, they would have been reacting to Mattie's show! We were very lucky to have such an amazing team of women supporting us. 

Quote of the day: Everyone's got their poison, and mine is sugar. ~ Derrick Rose


This morning, after my usual routine, I tried to sit down with my dad and work on a puzzle of California. I realize a 500 piece puzzle is WAY TOO complicated for him, but the puzzle is for all of us. Therefore, we need a puzzle with many pieces. The task I had my dad work on with me was separating out the straight edge pieces from the other ones, so we could begin creating the border of the puzzle. 

No matter how many times I told my dad what we were looking for, I even showed him, and did a few sorts with him, he just couldn't get it. His memory is so bad that unless I kept saying... you are looking for straight edge pieces, every 30 seconds, he was lost. Needless to say, me, my mom, and Peter accomplished this much today. 

I took my parents back out to Maryland to see Dawn, one of our favorite servers. Going out to eat is our adventure for the day. It is something all three of us enjoy. We brought Dawn four cannoli's today in honor of Labor Day. 

Though we eat at this restaurant often, I never ordered the blueberry scones. All the bread products are made on-site, and their baker is excellent. Any case, Dawn brought several scones out for us on the house. YES sugar is my drug of choice and sugar can change my mood around, and quickly. Needless to say, this homemade scone was the highlight of day and I was thrilled traffic was light and moving. I try to look for the positives each day, otherwise, I most likely wouldn't be able to function. 


September 3, 2023

Sunday, September 3, 2023

Sunday, September 3, 2023

Tonight's picture was taken in September of 2008. That day, our neighbor gave Mattie this life sized stuffed animal. His name was "Dandy Dog." It was hand crafted for Mattie and the artist signed the bottom of the boot. Mattie couldn't get over that Dandy Dog was as tall as he was, you can see that Mattie was trying to demonstrate this in the photo. I will never forget all the amazing people around us who tried the best they could to support us, cheer Mattie up, and provide non-stop gifts and cards for over a year. It showed me the incredible spirit and compassion of a united community. 



Quote of the day: Sometimes things fall apart so that better things can fall together. ~ Marilyn Monroe


It was such an awful day that this evening, I left the house for 90 minutes and walked over 6 miles. The only peace I get is escaping the house, not listening to anyone, not absorbing people's stresses, anger, hostility, and other emotions. I truly believe that this is a test of my fortitude and sanity. 

There are many things happening in my house and when I took my parents out to brunch today, my mom kept peppering me. What I need now is support and understanding, and not more stress. Of course in the middle of trying to eat, my dad pooped in his pants and I had to change him in the restroom. But today's brunch was so upsetting, on top of my already upsetting existence, that I literally got up from the table and walked around the restaurant for ten minutes. It was the only thing I could do to keep my sanity. 

On my walk this evening, I saw this beautiful deer. To me this was a sign from Mattie. He is with me, he sees everything going on, and though he isn't physically with me, he stands with me always. This deer symbolized all of that to me..... a mother and son's undying love. 

September 2, 2023

Saturday, September 2, 2023

Saturday, September 2, 2023

Tonight's picture was taken in September of 2008. Mattie was in his second month of chemotherapy. That day we were admitted through the outpatient clinic. While waiting to get admitted to a bed on the inpatient floor, Mattie spent some time in the art therapy area of the clinic. By that time in his treatment process, his therapists knew he LOVED cardboard boxes. They saved many for him over that year. That particular day, Mattie was NOT in a happy place. He constructed a little house built for ONE, went into it, and stayed there for a bit. I don't think I need to say much else, as the picture speaks 1,000 words. 


Quote of the day: A poet warrior realizes both the brutality and the beauty in life, and apprehends that the suffering we tragically endure is partly what makes us human. What also makes us human is the ability to love, the ability to stand in nature’s presence, and to nurture this earthly paradise to tend to our family’s needs.  Kilroy J. Oldster


Every September, without fail, we visit Mattie's tree. Last year, 2022, this was a photo of Mattie's White Swamp Oak. Keep in mind that this is memorial tree #4. The other three had issues. This tree was dedicated to Mattie in 2010, by the families of the class of 2020 (Mattie's class, if he had graduated). 

Today, Peter and I went ALONE to visit the tree. We get little to no time with just the two of us. The past several times we took my parents to visit the tree, they were completely disinterested in the tree and didn't want to get out of the car. So today I made the executive decision to leave them at home, while my dad had his physical therapy session. My mom gave me a hard time about not being included, but frankly sometimes I have to be the adult on duty and say NO. I have given up every aspect of my life to manage my parent's care, therefore, if I want this time alone with Peter by Mattie's tree, that is exactly what I am going to do. 

In comparison to last year's photo, look how much bigger the tree has grown!!! It is truly a mighty oak. 

As soon as I got to the tree, I saw that Mattie's plaque was missing. We looked high and low for it, and Peter found it buried in the mulch. I wrote to the school, because the stand for the plaque is missing and to me it is important to bring attention to the fact that this is NOT just any tree. But a tree that serves as a reminder of my beautiful 7 year old and his amazing life. 
I honestly couldn't get over the foliage on the tree. It was rich and healthy. You can see ornaments we hung from the past, such as orange awareness ribbons and butterflies. 
I placed this ornament on the tree in 2022, and it is one of my favorites! It is a statement I said to Mattie all the time.... I love you to the Moon and Back!
We added gold colored, sunflower themed, and donut ornaments to the tree. 
See the donuts? I know Mattie would have loved this, as he survived for a month on donuts during his first month of chemotherapy. 
See how big the tree is in comparison to me!
This afternoon, I took my parents out to lunch. We got to the same place in Maryland each Saturday, to visit with our favorite server, Dawn. My dad seems more exhausted than usual. He was periodically napping during lunch. While he was disengaged, so was my mom. She decided to ignore me for part of lunch. She took out her phone and wouldn't speak to me. 

Sometimes I feel like I could go insane. I am balancing and absorbing every emotion, every upset, all the anger, and so forth from every member of my household. I try to take it, to keep the peace, to empathize, to understand, and to keep my cool. But somedays it is very hard. I am not a bottom less pit, I too have feelings, have my own emotions, and need help. 
I was up and down multiple times at the restaurant taking my dad to the bathroom. It gets wearing! Sometimes I land up with intense hiccups, because I can't eat in peace. Any case, with the last bathroom trip, I left my dad in the restaurant lobby, by the front door. I went back to the table to pay the bill. While I was gone, Dawn (our server) handed my dad a sign. It was meant to be a joke. It says, "Free to ANY home!" Meaning whoever wants to take him home, can. Dawn snapped a photo and shared it with us. I would have hoped that my dad would know not to keep the sign up while we were gone! Forget it. He had it up for many minutes, and he had restaurant patrons coming up to him to ask him if he was okay or needed help! Honestly one day, I am going to get in trouble because people will think that I did this on purpose or I am not providing him quality care. If they only knew. Needless to say, no one offered to take him home. Instead, he got many chuckles from people walking passed him, and he thought that was funny. 

September 1, 2023

Friday, September 1, 2023

Friday, September 1, 2023

Tonight's picture was taken on September 1, 2009. I will never forget this day. Peter and I were struggling about Mattie's end of life care. We weren't sure whether Mattie should die at home or in the hospital. What happened? Mattie decided for us. He was in so much pain that he asked to return to the hospital. By that point, it was like our second home and he intuitively understood that he needed much more care than we could provide him at home. This photo was taken in the outpatient clinic, where Mattie was then admitted to the hospital. His art therapists gave him this remote controlled dinosaur and they were desperately trying to engage him and keep his mind off the horrific pain he was in. You can see that Mattie looked very sick and out of it. He was attached to a pain pump, but we got to the point that no amount of narcotics could relieve his suffering. This memory will remain with me always. 


Quote of the day: There is a fine line between challenging yourself and overwhelming yourself. ~ Brittany Burgunder


A childhood cancer diagnosis impacts the whole child and the whole family. September is childhood cancer awareness month and Mattie Miracle is proud to collaborate with the American Psychological Association's Caregiver Wellbeing Special Interest Group to shine a light on the importance of psychosocial care for children with cancer and their families. After years of research and collaboration between pediatric psychologists, oncologists, and more, 15 Standards were published that outline the kinds of psychosocial care that every child and family should receive after a childhood cancer diagnosis.

I am proud to say that there are now Psychosocial Standards of Care because of Mattie Miracle and ultimately because of Mattie Brown and his experience!


It was another winner of a day. I literally never stopped moving. After I got my dad washed and dressed, I brought him downstairs for breakfast. No breakfast is ever consumed in peace, because within minutes of eating (and he eats incredibly fast), he needs to jump up to the bathroom. After the bathroom, I got him in the car and took him to his memory care center. Keep in mind that I never returned to my breakfast (which remained sitting on the table) until about noon. At which point, I had to eat it quickly, because I needed to drive my mom to physical therapy. 

Back to dropping my dad off at his memory care center in the morning.... once that was complete, I went to mail my mom's things, filled the car up with gas, and then went to the grocery store to buy fresh fish. I am trying to do Fish Fridays at home. But fish is that kind of protein which I won't let sit around in the refrigerator. So that means schlepping to the store. Once I brought it home, I prepped the fish and other things for dinner, so that I wasn't scrambling later in the afternoon. 

Once that was done, I folded the laundry and helped my mom with paperwork. Then I got her into the car and off we went to therapy. Once her session was over, my mom wanted to go out for frozen yogurt. I thought I would have time to manage this before picking up my dad. But we got stuck on the highway for an hour because of a car crash miles ahead of us. By the time we got off the highway, I decided to run home first to pick up the tote bag I use when I have my dad in tow (it has a change of clothes, depends, wipes, etc). I was going to chance it and take my dad for frozen yogurt without the bag, but then reality set in. So I went home first. When I saw Peter at home, I asked him to pick my dad up and take him home, because I just did not have the where with all to do it all today. Therefore, I was able to take my mom out for yogurt without my dad with us. 

My mom has now convinced herself that she wants to go away on vacation. Though I would love to do this, I continue to provide the reality check on our situation. My dad doesn't have the stamina to travel anymore. He also has no interest to do this either. If dealing with his dementia isn't hard enough, then his dementia combined with irritable bowel syndrome, is truly over the top. I literally can't figure out how I could take them anywhere, without assistance, and someone to stay with my dad while I toured my mom around to see friends. So without a plan, I am not moving forward with this request. 

My world maybe moving in twenty directions, but I will never forget September 8, 2009. The day our lives permanently changed forever. I can't believe that Mattie will be gone 14 years. Around the anniversary of Mattie's death, we always visit his memorial trees and decorate them. 

Since September is childhood cancer awareness month, and the awareness color is GOLD, I am happy I was able to find a few gold ornaments. But the theme here is really the SUN and Sunflowers. Mattie LOVED drawing and painting the sun and I love sunflowers. They remind me of Team Mattie, who gave me plenty of sunflowers between hospital admissions. Therefore, these ornaments resonated with me for the tree. 

Of course those of you who have been on this journey with me from the beginning, know that Mattie LOVED donuts! In fact, while on chemo, he went through a vanilla frosted donut phase! He practically ate them daily. Since Mattie refused food most days, we gave him whatever he wanted to eat in order to get calories into him! Therefore donuts on the memorial tree are very symbolic of Mattie, his journey, and his spirit to live life to the fullest. 




August 31, 2023

Thursday, August 31, 2023

Thursday, August 31, 2023

Tonight's picture was taken on August 7, 2008. It was Mattie's first week in the hospital. That day, Linda (Mattie's child life specialist) set up a painting project right outside Mattie's hospital room. Back then, the hospital did not have a playroom, so there was really no space for the children to congregate and play. When given the opportunity to paint something, Mattie decided to paint the sun and the earth. It is no surprise why the SUN became the symbol of Mattie Miracle. Mattie incorporated the sun in practically every drawing and painting he ever created. 

Quote of the day: To tie a knot at the end of your rope means that you have a rope as well as the ability to tie a knot. And while that’s not necessarily great news, imagine what things would be like without a rope or ability. ~ Craig D. Lounsbrough


Last night, my lifetime friend, Karen, asked me..... did you see the Blue Moon? When she said that, I immediately thought of my maternal grandmother who used the expression... "once in a blue moon" all the time! But as I have learned (thanks Karen!), a blue moon refers to the second FULL moon that appears in one calendar month. 

I went outside to look for the moon when I brought Sunny inside for the night. But I did not see it. Then I immediately thought while in my bedroom..... look outside at the front of the house. Sure enough my big Mattie Moon was there to greet me. Right through my bedroom blinds. It seemed like a very meaningful way to end the day, with Mattie and me thinking of each other. 

When I woke up this morning, I was greeted by this photo in a text message. The woman you see here is Amanda Thompson. She is one of the authors of the Psychosocial Standards of Care. She was doing a presentation in Scotland at the European Pediatric Psychology Meeting. Looks whose photo is on the screen? Mattie made it to Scotland!!!! As the anniversary of Mattie's death is upon us in a week, it is very meaningful to us to receive these reminders of his legacy work. 

It was another full day of running around. I took my parents to the podiatrist today, as my dad qualifies for a pair of shoes through Medicare. Medicare pays for shoes once a year for older patients with diabetes. The doctor literally measured my dad's feet and used an I-pad to take images that created a 3-D model of his feet. What I have learned is that his current shoes are TOO tight on him. Which is ironic since he got these shoes from his podiatrist in Los Angeles. I have no idea if that doctor measured my dad's feet or what, but today's podiatrist chastised me for selecting shoes that didn't fit my dad properly. Needless to say, I was in NO MOOD to be talked down to, so I pushed back. The podiatrist is edgy, so you can imagine together, we are quite a combination. This is not the first mistake my dad's podiatrist in Los Angeles made. Which is why I am glad I am now overseeing his care, and can proactively address issues like infections (which he had on his feet) and shoes. 

My dad stopped taking steroids on Sunday. The steroids helped him tremendously with his allergic reaction to antibiotics. But now we are dealing with the consequences of stopping them. He is lethargic, chronically exhausted, and seems stupefied. This reaction has happened in the past, it doesn't surprise me, but all I can say is WOW! 

It is now 6:30pm, and I am escaping the house to get fresh air and walk. As the weather starts turning colder, I am not sure what I am going to do. Because for me the wonderful part of walking is being surrounded by nature and away from the house.