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

August 7, 2019

Wednesday, August 7, 2019

Wednesday, August 7, 2019

Tonight's picture was taken in August of 2009. By this point we knew that Mattie's situation was terminal. He was having trouble breathing and needed to be constantly on oxygen (as you can see in this photo). Mattie's care team encouraged us to wait until the end of treatment in order for him to apply to the Make a Wish Foundation, for something special. NOT a good plan, as that day of remission never came! Instead, Peter and I went out (with my parent's help) and purchased this ride on vehicle. Mattie always wanted one and it truly made him happy to spend his last couple of weeks on this earth riding and driving. He was a natural driver. I did not know that at first, which was why I was sitting in the passenger seat sticking close just in case. Mattie called this vehicle, "Speedy Red." In fact, I recently learned through Facebook that one of our supporters has a daughter and her daughter (who I never met) wrote a short story about Speedy Red! 


Quote of the day: Expect nothing. Live frugally on surprise. Alice Walker


Out of the blue, I was contacted today by a former researcher at NIH. Peter and I don't work with her often, but we have had the opportunity to interact with her at conferences and at a brainstorming session regarding how to implement the Standards. In any case, to my surprise, she told me that she nominated me for the Ellen Stovall Award. The announcement for the award recipients went out today, and unfortunately I wasn't selected. But I am deeply honored to be nominated, especially given the caliber of the person nominating me. 

The award is given by the National Coalition of Cancer Survivorship (NCCS). NCCS’ mission is to advocate for quality cancer care for all people touched by cancer.  Founded by and for cancer survivors, NCCS created the widely accepted definition of survivorship and defines someone as a cancer survivor from the time of diagnosis and for the balance of life. In fact, NCCS considers caregivers as survivors too. 

The award is named after longtime NCCS CEO Ellen Stovall. Through years of perseverance and dedication, Ellen Stovall was instrumental in improving cancer care delivery for millions of Americans. Her warm personality and infectious drive to create change fueled a movement of collaboration throughout the cancer community to advance cancer care and cancer survivorship. After she died in 2016 due to cardiac complications from her cancer treatment, NCCS created the Stovall Award to honor her memory, carry on her legacy, and ensure the momentum she helped foster continues to benefit patients.

I have always thought of applying for the award, but never have. My gut feeling is that childhood cancer is not in the forefront of the hearts and minds of NCCS. The focus is adult cancer. With that said, I am honored that someone feels that the work we have done for the childhood cancer community is worthy of recognition.  

To learn more about the award and the nomination process, go to:
https://www.canceradvocacy.org/stovall-award/nominations/

No comments: