Mattie Miracle Walk 2023 was a $131,249 success!

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 11, 2021

Saturday, December 11, 2021

Saturday, December 11, 2021

Tonight's picture was taken in December of 2007. Mattie was five years old and looked and acted like the picture of health. Never in my wildest imagination would I think that 7 months later he would be diagnosed with cancer. Each Christmas Mattie got a special sweater in order to take a holiday photo. Mattie was featured on the front of our family's card. Ironically I never captured all three of us on the card, only Mattie. Mattie loved decorating the tree and also loved his Christmas train. Which he assembled around the tree. It was a tradition.


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

  • Number of people diagnosed with the virus: 49,874,867
  • Number of people who died from the virus: 797,121



Peter and I have NOT bought a Christmas tree or decorated for Christmas since 2008, when Mattie was diagnosed with cancer. When Mattie died, so did most of the joy in our lives. A reality most don't want to hear about, but nonetheless the fact of the matter. 

With my parents moving in, I felt it was important to decorate, as I think it helps to orient my dad to the season and it brings some festivities to winter and the cold. In other words temperatures my parents are not used to. But here's the funny part..... we had a warm snap today, and it close to 70 degrees! 

This afternoon, we took my parents to a Clyde's restaurant in Ashburn, VA. Outside the restaurant were huge nutcrackers. Another guest of the restaurant offered to take our photo, and we did it! It is naturally hard to leave behind one's routine and restaurants one has gotten accustomed to, but we are trying to make new connections and traditions here for them. I have concluded that I will cook Monday through Friday, but Saturday and Sunday, we will go out. I feel this is the best way to manage food, as I want Peter to be a part of our meals and process, and though my parents are used to eating their main meal at lunch time, I am switching this up to dinner time. Otherwise if I kept their LA schedule, we would only eat one meal a day in the afternoon (outside the house), and I would never be eating and connecting with Peter. I am determined to find the right balance and fortunately Peter and I have been through so much already, that we are good working together under the worst of conditions and chaos.

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