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

January 16, 2015

Friday, January 16, 2015

Friday, January 16, 2015

Tonight's picture was taken in December of 2006. Mattie and Peter were at Deerfield Beach in Florida building, not a sand castle, but one of their amazing structures. They could be at it for hours, designing moats, tunnels... you name it. Once the structure was actually built, then Mattie and I would comb the beach looking for debris to decorate it with. On some occasions, what they were designing was so intriguing that others kids would approach us and ask if they could join in! 




This morning Peter and I had the opportunity to meet with the Director of Quality of Life and Survivorship at the American Cancer Society. We met over tea and pastries. Which to me is the best way to meet. As of December, Mattie Miracle has been participating in a National lobbying agenda with over 100 childhood cancer organizations. Yesterday's conference call I as involved with tied into that work as did today's meeting. I always find a meeting that gets me to think slightly differently about things rather stimulating. It is hard as a parent who lost a child to cancer to think objectively all the time, but when I hear the guidance and advice from others who are invested in the process but who are not as emotionally attached to the subject matter, it helps.


Later in the day, I held a small birthday luncheon for my friend Ann. This is the seventh birthday I have celebrated with her. Though I have known Ann since 2005, we only began spending time together when Mattie developed cancer in 2008. All of the women, except for one at the table, had children who attended Mattie's preschool. It is one of the things that unites us all. In honor of the day, I made the flower arrangement for the table and to me there is something special about fresh flowers especially in January. 
pictured in the front row from left to right are Dawnee, Ann, and Ann Thomas
pictured in the back row from left to right are Mary, Catherine, and Vicki

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