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

February 27, 2018

Tuesday, February 27, 2018

Tuesday, February 27, 2018 -- Mattie died 441 weeks ago today. 

Tonight's picture was taken in March of 2009. Mattie was home between treatments and you can see two things for sure. First, Mattie wasn't putting pressure on his right leg. He never did post-surgery, as Mattie was never able to walk independently again. But the second things was, look at Mattie's room. Mattie's room became a warehouse filled with toys and gifts he practically received everyday while in treatment. I was unable to keep track of things, so instead they went into piles. Also notice the aeromattress on the floor. When we were home, this was where I slept while Mattie was in his bed. Because Mattie was hooked up to all sorts of IVs, he couldn't be left alone at night, especially as he needed help using the bathroom. After Mattie died, it took me YEARS to clean out this room. Now of course we use it as our Mattie Miracle work space. 


Quote of the day: Strength is the capacity to break a Hershey bar into four pieces with your bare hands - and then eat just one of the pieces. ~ Judith Viorst



Next week, Mattie Miracle is hosting its annual volunteer dinner. How did this event get started? Well it really started as a planning meeting for our Walk & Family Festival. It was held at a friend's home and finger food was served. But food wasn't the main reason for coming. Since that time, this event has evolved out of a home, into a restaurant, and now to a hotel. I really think in the beginning of the Foundation's history, I needed a lot of help brainstorming the Walk, which is why the planning meeting was crucial. Back then, I wasn't long on ideas and I certainly did not have the energy to devote to a fundraiser. As the journey of grief was all encompassing. However, with time this changed, and I would say the bulk of the Walk is my responsibility. It's a rather daunting proposition, because without these funds we can't run many of our programs and initiatives. 

Though I plan, coordinate, and do a great deal of the heavy lifting for the Walk, I can't do it alone. Especially on the day of the Walk, this group of dedicated volunteers are miracle workers. My core group of volunteers are invited to our annual appreciation dinner because Peter and I know how lucky we are to have these friends. They have been with us long term and are generous with their time, skills, and resources. The event goes smoothly because of these individuals who run activities, fundraise, and help market the Walk. 

I feel like a juggler. One of the things I am planning is next Tuesday night's dinner. On top of that I am trying to finalize Walk sponsors, raffle donors, updating the Walk website, and now just learned today that I have another strategy session for the Psychosocial Standards to plan on March 10. Of which I have to coordinate all the logistics. It doesn't end there, because April is our Item Drive month. 

We invite our friends and supporters to HELP US stock the Mattie Miracle Carts with toiletries in memory of Mattie's upcoming 16th birthday. We ask that all of the items on our AMAZON WISH LIST arrive to us by Monday, April 16



We fund and operate a Snack and Item cart at both the MedStar Georgetown University Hospital in Washington, DC and at Children's Hospital at Sinai in Baltimore, MD. These carts provide nutritious snacks, drinks, candy, and toiletry items free of charge to families caring for children with cancer. The carts revolve around the pediatric units three times a week and support families who are providing around the clock care to their children. The carts are greeted with sheer gratitude and appreciation.

Check out our Amazon Wish List:

https://smile.amazon.com/gp/registry/wishlist/2UQOK4GY955ZL/ref=nav_wishlist_lists_1


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