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 23, 2015

Wednesday, September 23, 2015

Wednesday, September 23, 2015
Tonight's picture was taken in August of 2008. Mattie was in the hospital coping with his first month of chemotherapy. Mattie hadn't lost his hair at that point, but Peter took him to the barber to get it cut very short, to start preparing us all for the transition. Right from the beginning Mattie used his creativity skills to cope with the crisis at hand. Mattie could build and design with just about any material!

Quote of the day: In youth one has tears without grief; in age, griefs without tears. ~ Joseph Roux

THREE more days left to vote in the WTOP Click-For-A-Cause contest! Voting is easy and takes ONLY SECONDS to do! Winning this contest would enable us to provide more support to children with cancer and their families!
Recently we attended childhood cancer events on Capitol Hill and on the National Mall, and several people we interacted with thought the ONLY thing Mattie Miracle did was advocacy and awareness. That is only one of the things Mattie Miracle does! We also proudly support children with cancer and their families by completely funding a child life specialist at MedStar Georgetown University Hospital (a professional assisting 3,500 children/families per year), providing a free snack cart to families caring for children who are in-patient (a cart which supports 1,500 families per year), and supporting a monthly pediatric nurse support group luncheon to assist these professionals who are on the front line of psychosocial care.
Help us bring awareness to childhood cancer... please vote and share this post with friends and family.

In March, Peter and I participated in an Institute of Medicine workshop in Washington, DC. At the workshop, we had the opportunity to hear Dr. Kira Bona (Pediatric Oncologist) discuss her research. For years I have heard that families can go practically bankrupt while financing their child's cancer treatment, yet I really did not have much data to support this claim. In the link below, Dr. Bona acknowledges that even at Dana Faber, which is one of the more well-resourced treatment centers in the Country, about a third of families are reporting food, housing or energy insecurity six months into treatment. This is truly significant, because in addition to a family in crisis over a cancer diagnosis and the havoc that ensues with treatment, many families are also worrying about money and their family's livelihood. 
Childhood Cancer Devastates Family Finances too

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