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

May 26, 2020

Tuesday, May 26, 2020

 Tuesday, May 26, 2020 -- Mattie died 556 weeks ago today.

Tonight's picture was taken in May of 2005. Mattie was three years old and one of his favorite activities in the warmer weather months was using his sand box. I can't tell you how many items Mattie stored in that box. Toys, shovels, and vehicles. Now the sandbox sits outside our deck door. Kids in our complex use it and sure enough if you pop the lid, you will still see many of Mattie's things inside the box!


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

  • number of people who were diagnosed with the virus: 1,672,714
  • number of people who died from the virus: 98,636


Here is another story from this year's virtual walk, that I would like to share. I received an email from someone I do not know on the day of the event! She had never supported our Foundation before this year. But she learned about our event through her local neighborhood listserv. It turns out that her son has brain cancer, is in active treatment, and he is about five years old. 

Since the pandemic, this little boy and his family have remained home. They rescheduled even some of his treatments in fear of his susceptibility to the virus. Yet on May 17th, this little fellow, his siblings, and parents all got outside to walk together as a family. The mom wanted me to know that her son was eager to walk, seemed to have more energy than every before, and the virtual event gave the family something productive and fun to do altogether.

In fact, the mom said she experienced her own "MIRACLE" that day, when she saw her son outside, doing normal things, and watching the family bond over something other than illness and cancer. Hearing that our Walk provided her the opportunity to see this "miracle," made my day. As I remember exactly the feelings and sentiments she was expressing! The story remains with me now over a week later, and this mom and I agreed to keep in touch, with the hopes that when the pandemic is behind us, we can meet in person. 

Though our Walks are not typically geared to the cancer community (as I strongly believe in raising money from the non-cancer community to help those with cancer), I was deeply touched that this family living with childhood cancer would want to participate. I would never have guessed that our Walk could be a psychosocial intervention, but that was indeed what happened for this little guy and his family. 

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