Mattie Miracle 15th Anniversary Video

Mattie Miracle Cancer Foundation Promotional Video

Thank you for keeping Mattie's memory alive!

Dear Mattie Blog Readers,

It means a great deal to us that you take the time to write to us and to share your thoughts, feelings, and reflections on Mattie's battle and death. Your messages are very meaningful to us and help support us through very challenging times. To you we are 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 stop writing on September 9, 2010. However, at the moment, I feel like our journey with grief 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 us, and most importantly thank you for keeping Mattie's memory alive.


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



The Mattie Miracle Cancer Foundation celebrates its 7th anniversary!

The Mattie Miracle Cancer Foundation was created in the honor of Mattie.

We are a 501(c)(3) Public Charity. We are dedicated to increasing childhood cancer awareness, education, advocacy, research and psychosocial support services to children, their families and medical personnel. Children and their families will be supported throughout the cancer treatment journey, to ensure access to quality psychosocial and mental health care, and to enable children to cope with cancer so they can lead happy and productive lives. Please visit the website at: www.mattiemiracle.com and take some time to explore the site.

We have only gotten this far because of people like yourself, who have supported us through thick and thin. So thank you for your continued support and caring, and remember:

.... Let's Make the Miracle Happen and Stomp Out Childhood Cancer!

A Remembrance Video of Mattie

September 8, 2013

Sunday, September 8, 2013

Sunday, September 8, 2013 -- THE FOURTH ANNIVERSARY OF MATTIE'S DEATH

Tonight's picture was taken in September of 2008. This has to be one of my favorite photos of Mattie while he was battling cancer. You need to understand the context behind this photo. Mattie spent several hours digging out plastic dinosaur bones from a lump of clay. He had goggles on and had all sorts of tools in his hands. Once all the bones were dug out, Mattie assembled them together, like a 3-D puzzle. Creating the dinosaur you see lying in front of Mattie. I captured that moment in time.... Mattie with the dinosaur! Mattie was tired from the dig and yet at the same time proud of his accomplishment.


Quote of the day: They say time heals all wounds, but that presumes the source of the grief is finite. ~ Cassandra Clare



Today is the fourth anniversary of Mattie's death. Before I share what this day was like for us, I want to thank so many of you who made a contribution to the Foundation on behalf of Mattie's memory, I want to thank you for the emails, and the text messages. Your kindness and thoughtfulness are NOT forgotten and are greatly appreciated.

It was a day filled with many highs and lows for us. Some lows of which I can't discuss on this blog, but I assure you there are many stories that could easily fill a book. Stories not told on this blog, and yet stories that are very much part of the grieving process. As Peter profoundly said today, part of our grief is compounded by how people react and interact with us now. I am not doing his words justice, but they caught my attention and they resonated with me.


We needed a plan today. Without a plan, we would most definitely be in trouble on anniversary dates! The plan was to visit Mattie's tree at his school and then have lunch at Mattie's favorite restaurant. Earlier in the week I bought Legos. Peter drilled holes in each Lego piece for me, and I strung a chord through each piece and created ornaments for the tree. Since Mattie was IN LOVE with Legos, I thought this would be the perfect remembrance. This photo captures the tree in CONTEXT. You can see me standing next to it. The tree is much taller than me and sits right by the field Mattie had recess at during Kindergarten. In fact, where my car is parked is where I dropped off and picked Mattie up from school each day.  

 
If today wasn't hard enough, the sight of this tree was devastating! I am quite sure Mattie's tree died! This beautiful Red Oak should not look like this so soon in the season. In fact, I went back in my files to look at photos I took of the tree on September 8, 2012. Last year at this time the tree was ALL green. Now its leaves are brown, shriveled, and the tree looks bone dry. The tree is also missing its water gator bag, which it had around its base for years. I honestly can't tell you how heartbreaking it was to see this dead tree today. This is our only memorial to Mattie and to see it looking this way brought us great sadness. In fact, it practically sent Peter right over the edge. For quite some time, we couldn't even talk to each other today. It was that upsetting.   
Here is a close up of Mattie's tree filled with Lego pieces, butterflies, planes, hot wheel cars, and the list goes on!                  
My nickname for Mattie's tree has always been the "glimmering tree!" When the sun shines on it, it twinkles, and when the wind blows, the chimes that hang on it musically catch your attention!      
For Christmas of 2012, I hung a Mater ornament on Mattie's tree. Mattie loved the movie, Cars, and I was happy to see all the ornaments we placed on the tree are holding their own and keeping the tree company. If they could only breathe life into the tree!               
When we arrived home today, there was a note on my door that flowers were delivered for us. So I went downstairs and found this wonderful Mattie Miracle color themed arrangement and beautiful hand crafted poem waiting for me. My friend Carolyn and her children created this for us and after seeing the death of Mattie's tree, these flowers and sentiments were really cherished.  I would like to end tonight's posting with a message from my mom and then the posting I wrote from Mattie's last day on this earth (it gives you a feeling for Mattie's traumatic death and the agony of the decision to basically put him in a coma to allow him to die). My mom wrote, "We know how difficult it is to reflect on what happened on this day 4 years ago.  It is an unspeakable tragedy and the consequences of that fatal day will last a lifetime never giving you peace until your last dying breathe.  We too can never be the same and understand that this is a grief that goes on and on. We share your mourning for our beloved Mattie and our only hope is that he is free of the human bondage that took his life and that his spirit has been released, like the balloons at his memorial,  to float high above us with the sun, stars and  the moon, his symbol in life, so that they may shed their brilliant light upon him forevermore and be his companion through eternity!"



MATTIE'S BLOG -- SEPTEMBER 8, 2009

I am mentally wiped out from today. I received over 150 e-mails, but I am unable to stay awake long enough to actually read them! So I look forward to reading them tomorrow. Mattie's blog was hit over 5000 times today, so I appreciate you visiting electronically Thanks Norma (one of our great sedation nurses) for the chocolate cake today. It is inspiring me to write the blog.

Mattie had a VERY harrowing night. From 2am on, Mattie was having trouble breathing, and appeared to be in intense pain. It was the most intense five hours of our lives, and the sights and sounds we observed during this time were horrific, ones I don't wish on anyone else. I can still see Mattie's sweet face writhing in pain, gasping for breath, and making a horrible congested sound, which if I don't ever hear this again in my lifetime, that would be too soon! Dr. Shad called this chest congestion, the "Death Rattle." That is an accurate description because when you hear it, you know death is pending. In all reality I found these five hours frightening, because we just did not know how the death process would unfold.

We were blessed to have Sarah Marshall, one of Mattie's outstanding HEM/ONC nurses, working with us last night. I now have four angels in my life: Ann (my angel of Hope), Linda, (my angel of caring), Debbi (my sedation nurse angel), and Sarah Marshall (my angel of mercy). Sarah Marshall was assigned to work with Mattie only last night. Typically a HEM/ONC nurse is assigned three patients during a given shift. Sarah Marshall was proactive and did everything that was humanly possible to make sure that Mattie was relatively pain free, which WASN'T easy. Mattie was on IV dilaudid, dilaudid boluses by hand, a Versed continuous drip, as well as boluses of Versed. In addition, Mattie was receiving albuterol through an inhaler, which helped to keep his airways open.

Peter and I spoke to Mattie throughout the night. We weren't sure exactly what to say, but we told him we loved him, were proud of him, and in essence he could die and we would be fine. We wanted him to know we understood he was in control over how the night played out.

By 6:15am, Mattie was receiving very high dosages of pain medicine, however his pain wasn't subsiding, and frankly we were getting concerned with how we could manage his very over taxed heart and body. Dr. Shad prescribed propofol at that point to put Mattie in a twilight sleep. But propofol is known to slow down the heart rate, and this assisted in giving Mattie relief and helped to stop prolong the agony! Mattie died within one hour of the propofol infusion. While Mattie was in pain, I could see he would try to sit up and talk with Peter and I. At one point, he mentioned to us that "he was going to die." So we concurred with him and this provided some leeway to talk about our fears and hopes for him. We told him we loved him and that it was okay to let go. Periodically Mattie would sit up and try to open his eyes, and one time he looked at me and said someone else was in the room with us, by the door. Well no one earthly was in the room with us, but we knew Mattie's death was near. Here is the thing though, seeing him suffer in pain, and listening to this "death rattle" for hours on end, made the option of death much more peaceful and appealing. My heart was aching over the pain Mattie was in. Dr. Shad assures me that Mattie was always comfortable, and the "death rattle" is much harder for the caregiver to listen to for hours.

As Dr. Shad said to me today, "Mattie fought death." Mattie just did not want to die. Dr. Shad feels that this was because he did not want to leave Peter and I behind. After all the three of us thought we would be together for always. Careful when you assume things!!! Dr. Shad told me that she has been an oncologist for 25 years and in all her career she has only had to use propofol on one other child patient! She said Mattie was her second, and Mattie needed it because he was resisting death. I actually found her statement very empowering, because if Mattie was willing to be that congested for such a significant period of time then he really must love us dearly.

Once on propofol, Mattie's body started to relax, and I decided to lie down next to him on his bed, as we were awaiting death. I wasn't sure what death was going to look like, but slowly one by one his respiratory rate went to zero, his pulse oximeter went to zero, and his heart rate also went to zero. Hearing all these values flat line was another sound I won't forget any time soon. But by that point Mattie was in my arms. The nurses and doctors gave us about an hour alone with Mattie after he died, to say good-bye. This was a very touching and tearful hour. How do you say good-bye to your child? Both Peter and I know on some level that Mattie has died today, but on the other hand, we are having intense trouble believing this. As Debbi said today, Mattie's face looked like he was smiling and in peace. Thank God because the five hour ordeal was something I am trying to forget.

Sharon, the Lombardi Clinic chaplain, was with us starting at 4am. She helped say a prayer before and after Mattie's death. Sharon did a wonderful job, and though I have my own issues I am working out with God, I saw the need for prayer and to ask God to spare Mattie more pain and suffering.

After we had some private time with Mattie, he was visited by over 20 Georgetown Hospital employees. Jenny, Jessie, and Linda bought four stepping stone kits and we all worked around Mattie and did a stone for each foot and each hand. This is something I always wanted to do, and I am happy to have these cherished gifts that will always remind me of Mattie. I appreciate Tricia, Debbi, and Katie's help, because as Peter and I were pushing Mattie's hands and feet into the cement like substance, they were cleaning the substance off of Mattie. It was an amazing experience that occurred today, because in Mattie's postage stamp sized room, many employees came by to share their fond stories of Mattie with us. It was touching to see and hear how much Mattie has touched people's lives. My parents were so happy to be able to meet in person many of the people I have been writing about on the blog. In addition, Brandon, Mattie's big buddy, also visited. I could tell that Brandon was very upset to lose Mattie, and I told Brandon that Mattie loved him and considered him a good friend.

Once all the visits were over, Peter and I had the last chance to say good-bye to Mattie before preparing him to go to the hospital morgue. Lovely, no?! Saying good-bye to that beautiful face, those cute cheeks and hands was down right impossible. There are times the true reality hits me and I don't know how we will go on. Literally!

Tricia, Debbi, and Katie then gave Mattie a bath, and as unpleasant as this sounds, they had to place Mattie's body in a body bag and transport it to another floor in the hospital. I removed myself from the room, because I did not want to see the body bag. My precious son landing up in a body bag was a little hard to take. I sat outside with Dr. Shad and Linda, and Peter remained to help with the process. Mattie's "big brother" Jey came up to see us and also stayed to help transport Mattie to the morgue. He said no one else could do it, it was his responsibility today, because he loves Mattie and wants to give him a safe drive on is final destination within the hospital.

Saying good-bye to Georgetown today made me sad. I know we are always invited to C52, but it isn't the same. The nurses were clearly affected by Mattie's death and in many ways I was surrounded by this amazing community that we have gotten to know over 13 months of hospitalization. Jey also told us a funny story. Jey could picture Mattie up in heaven and arguing with God about his wings. Jey said Mattie would WIN about how large they would be!

We arrived at the hospital last Thursday with three of us, but today we only came home with two. How I miss the noise, sights, and directions given by Mattie, instead what I have floating around in my head are the sounds of hospital monitors. When we arrived home, I saw Speedy Red and almost lost it. In all reality being around Mattie's things bring about great sadness.

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