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

January 1, 2022

Saturday, January 1, 2022

Saturday, January 1, 2022

Tonight's picture was taken in December of 2008, our last Christmas with Mattie. It was a very hard holiday  being home, away from our support system in the hospital. Mattie was miserable, dealing with pain, and battling depression, anxiety, and medical trauma. It truly was beyond overwhelming for Peter and me. Much too hard to even describe, as we were living minute by minute on the edge. For just a short moment in time that day, we were able to play around with Mattie and get him to smile. But the good humor and lightness you see in this photo were short lived. 



Quote of the day: Today's coronavirus update from Johns Hopkins.

  • Number of people diagnosed with the virus: 54,859,966
  • Number of people who died from the virus: 825,816


After I got my dad up, washed, dressed, had breakfast and did his cognitive and physical exercises, I had him pose by the Christmas tree. I then sent this photo to his two caregivers in California. They worked with my parents for two years, and in a way become an important part of our family. 

Peter and I spent about five hours today dismantling Christmas all over the house. Including taking apart the Christmas tree. Now every ornament is safely away. I give myself credit because for over ten years our items were packed up and stored in our townhouse closets. This year we unearthed them and to my surprise nothing was broken. To me that is remarkable! 

But given that we haven't decorated since 2007, I had forgotten how horrible Christmas clean up is! There were pine needles everywhere and somehow putting stuff away was far more difficult that setting up and decorating. 

Since Peter will be traveling for the next two weeks, I knew we had to address this today because there is no way I would want to tackle this alone and balance my daily routine. I would say that my daily routine is challenging. Not so much because of any one task. The stressful part for me is that my parents do not have a network of friends here, they do not have a routine, and they know nothing that is around them. Therefore, it isn't like I can do something and they will have something else to occupy them. I am it and that alone is daunting. 

Given my dad's existence, he has little to no energy, therefore doing anything with him is limited. He would much prefer NOT moving all day long and sleeping, if we let him. Which we do not do! Even if my mom would want to go out and do something, she really can't. Because my parents have a togetherness philosophy, in which everything is done together. My dad doesn't like my mom leaving the house without him and he certainly doesn't want her driving. I could go on, but negotiating all of this is difficult and despite my best efforts so far, I haven't found much time to do any work much less anything for myself. 

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