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

November 2, 2019

Saturday, November 2, 2019

Saturday, November 2, 2019

Tonight's picture was taken in October of 2008. That day, I believe my students dropped off this large Halloween basket for Mattie. They wanted him to know they were thinking of him. It was a beautiful and thoughtful gesture. But as you can see, it wasn't a good day for Mattie. He felt sad and depressed, because he was very aware of his differences. In the beginning of his treatment, the hospital was considered foreign to us, and we were the outsiders. As time went on, I would say things flipped. The hospital became our home and the outside world no longer made sense to us. 


Quote of the day: Time cannot be packaged and ribboned and left under trees for Christmas morning. Time can’t be given. But it can be shared.Cecilia Ahern

Today was the first day of candy sorting for the Foundation. I was at it from 9:30am to 4pm. Non-stop, never sat down or ate anything. Candy is trickling in this year, unlike years past. We had many volunteers on hand today, but it was a challenge to keep them busy. But we managed and process through many, many bags of candy today
Pictured from left to right:
Vicki, Dr. Nita Seibel, Grace, Pat, Christine, and Jack

Dr. Seibel has served on the Mattie Miracle board for ten years and she was actually part of Mattie's treatment team. She worked at another institution in DC, but she consulted on Mattie's case numerous times. In fact, she was the one who counseled us to add certain chemotherapy medications to Mattie's treatment protocol early on. As she felt you only get one real good chance to attack this form of cancer, so you might as well address it head on. It was good advice. 

Later in the afternoon, we had a team of moms and daughters from The National Charity League of Alexandria helping us. With many hands, sorting candy goes VERY quickly. 







These children are my friend Margaret's grandchildren. Margaret was Mattie's preschool teacher and my dear friend. From left to right are Grayson, Charlotte, and Parker. To me, Charlotte is the spitting image of Margaret. When I see her, I can't help but think of my friend. 

Margaret's daughter, Ali, hosts our candy drive at her home. That sounds cute, but the candy drive is a huge production and I am so glad that in the process I get to spend time with the children and get to know them better. 

No comments: