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 11, 2022

Sunday, September 11, 2022

Sunday, September 11, 2022

Tonight's picture was taken in September of 2008. This was before any of Mattie's limb salvaging surgeries. So he was able to walk and do independent activities. As you can see by this point in Mattie's treatment (two months in), Mattie lost his hair. Despite all the new adjustments however, Mattie still loved creating, playing, and building. Those things remained consistent throughout his journey. Thankfully as activities were our diversions and provided moments of sanity through very long and arduous days. 




Quote of the day: Grief is like a long valley, a winding valley where any bend may reveal a totally new landscape…. there is something new to be chronicled every day. ~ CS Lewis


On the 21st anniversary of 9/11, I certainly remember and will never forget where I was on that horrific day. I was home in Washington, DC and Peter was at work in Virginia. I was pregnant with Mattie and had my first OB/GYN appointment that day. Needless to say, that never happened. Instead, I was glued to the television and worried about how Peter was going to get home. I was also worried that we would be a target somehow as we lived so close to all the monuments in the city. Peter said the drive home was eerie as people were escaping the city on car and foot, and yet he was driving back in. It was a day never to be forgotten, nor will I ever forget the lives of thousands taken that day and families that are forever changed. 

My goal was to get a lot done today! I started working on the Foundation's September newsletter, and I got side lined by having to create our annual candy and item drive wish list. I can't tell you how long that took and I wish Amazon made it easier for me to update lists from year to year without having to recreate them. In the  midst of working, I had my dad jumping up and down to go to the bathroom and NOW, we are totally without power. I have no idea why! All I do know is if we did not have a generator this would be very challenging to manage with my parents. 

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