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

December 6, 2024

Friday, December 6, 2024

Friday, December 6, 2024

Tonight's picture was taken in December of 2008. Mattie was home for Christmas, which one would have thought was a blessing. But actually being home was torture. Mattie was traumatized and managing his physical and emotional needs on our own was hard. As crazy as this may sound, the hospital became our second home, where we were surrounded by amazing nurses, art therapists, a child life specialist, and a physical therapist. These women made the impossible more manageable. 

That day, friends dropped off Christmas hats, head bands and these adorable Rudolph the Reindeer red noses. The Peter in this photo is the Peter I know and will always remember. He tried very hard to change the mood in our home, to lighten the sadness and fear, and I snapped a photo of that playful moment. A moment I will never forget, especially since Mattie was coping with depression, anxiety, and medical traumatic stress. It is very humbling as a parent being unable to "fix" a problem and make things better. Cancer illustrates to me that we truly are not in control of our lives and we can only do our best each day to cope and find a way forward. Which was what we tried to do for Mattie every step of the way.  


Quote of the day: You can fire your secretary, divorce your spouse, abandon your children. But they remain your co-authors forever. ~ Ellen Goodman


To all my faithful and loyal blog readers.... THANK YOU! After Mattie died in 2009, I continued to write this blog for two reasons.... one to keep me connected to Mattie (because time can be cruel on the memory, unless you actively work on it) and two to share his life with others. When Mattie was alive and I would write daily updates from the hospital and we had thousands of readers. After Mattie died, my focus wasn't necessarily on increasing readership. As the blog was my therapy, my therapeutic tool, and a special place where each day I can pause and remember a Mattie moment. I am so grateful that many of you continue to share my day with me. It is humbling!

Now more than ever, I am grateful for the support and deeply appreciative of all comments left on the blog. I read every one of them and your insights, reflections, and support mean more to me than you will ever know. Some days, these words get me through a difficult minute, hour, and day! 

After I dropped my dad off at his memory care center, I came home and spent HOURS sifting through December bills and then figuring out how and if I can pay them. It is a monthly stress that may do me in! In 2023, it was my first year paying bills without Peter. I was putting out fires then, and wasn't methodical in how bills were being paid. Now I am keeping monthly spreadsheets, to hopefully help me moving forward. Each month, I fear.... will I be able to maintain this house, pay bills, care for my parents, and not succumb to a nervous breakdown!? The verdict is still out. I can't discuss these issues with my parents because neither of them can process this kind of information any more, and it stresses them out hearing about these worries. So I hold the stress for all three of us.  


Normally I dread receiving mail, because chances are it is filled with bills. But today I received this symbolic pop up card from my friend and colleague, Jean. I have this beautiful cardinal on display in my kitchen! When I see a cardinal, I always think that this is a message from Mattie! 
Last week I ordered 10w replacement bulbs. I wasn't sure I could get Mattie's fiber optic tree to work again, but I dismantled the base, replaced the bulb and voila! Mattie received this Christmas tree from his child life specialist at the hospital in 2008. This adorable tree decorated his hospital room, and to me this little tree is a tribute to my amazing son. It lights up our hallway, in a similar way that Mattie lit up my life. 
This evening my neighbor surprised me with this cake! If you haven't figured it out already, my drug of choice is SUGAR! 



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