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

October 14, 2017

Saturday, October 14, 2017

Saturday, October 14, 2017

 Tonight's picture was taken in October of 2008. Mattie had already undergone his first limb salvaging surgery which was why he was in a wheelchair. I know that this photo was taken on a Friday. Why? Because Mattie was watching the chemistry club doing experiments on the hospital floor. Every Friday the club came and interacted with patients. They were fabulous and the chemistry club president took a liking to Mattie. On days Mattie wasn't able to come out into the hallway, Chris (the president) brought the experiments into Mattie's room. That particular day, Chris was making ice cream with nitrogen gas. This fascinated all of us. Mattie was surrounded by buddies... his two child life specialists (Whitney and Lesley) and his big buddy (and fellow childhood cancer friend), Brandon. Though that did not take Mattie pain or issues away, having this support made a huge difference to our quality of life. 

Quote of the day: We are shaped and fashioned by what we love. ~ Johann Wolfgang von Goethe
Peter and I were tired today after a long week. I have to remember that in addition to doing Mattie Miracle work, I was hit by a horrible migraine for a week. I am finally coming out of that. Despite the grayness and change of weather, Sunny needs to go out for a walk. So we headed to Roosevelt Island, a Mattie and now Sunny favorite. In the spring and summer, the Island is always packed with people and it is hard to find parking. But now that the weather is turning cooler, there is no parking competition. This is the one benefit of the weather changing. I also find that in the winter time, only Sunny and I are outside walking. There is no congestion on the sidewalks, and it is delightful. 


Meanwhile this afternoon, while I was sitting on the couch, I saw that the sun was coming out. It was such a glorious sight, I snapped a photo! I really rely on our room with view in the cooler weather months, and soon many of our outdoor plants will be brought in for the winter. Indie just LOVES all the plants coming in and we are entertained at watching her hide and jump around the plants. 
Posted by The Brown Family (DC) at 5:11 PM

1 comment:

Margy Jost said...

Vicki,
I love your room with the beautiful view and lots of light.. Even though the sun was peeking out then, I bet this room at least has natural light. We had a gray day in OC but all our window make it less gray. Light is very important to me!
I have to go to Roosevelt Island. Now I realize, you don't walk there since you mentioned parking. I had this vision of it being a place, you walked with Mattie & now you walk with Sunny. I am glad to know you go back frequently to this special place.
It sounds like Georgetown had some pretty good programs for patients when Mattie was in treatment. Posting about the different diversions, where Mattie participated always prompts me to take note. These kinds of activities buoy a child's spirits while they are hospitalized. They also encourage a child to look forward to something different & fun. I wonder how many Pediatric Oncology Units bring people from the outside to entertain their patients?

October 14, 2017 at 6:54 PM

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