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

May 31, 2014

Saturday, May 31, 2014

Saturday, May 31, 2014

Tonight's picture was taken on May 31 of 2009, in other words, five years old today. I remember this day as if it were yesterday. Mattie wanted to go out for a walk. However, he did not want to go out or be seen in his wheelchair. Instead, he decided to go in the radio flyer wagon that Linda (his child life specialist) gave him as a gift. So as you can see I pushed Mattie around my neighborhood in the red wagon. Clearly if you looked at his bald head, someone could tell he was sick, but that would mean someone would have to look inside the wagon. Mattie's wheelchair was a dead give away that something was wrong. There was no escape that way. After a while, that was tiring for Mattie.... the stares, looks, head turns, and side bar conversations were all hurtful and painful. Of course for Peter and me, the anger this generated was overwhelming and at times we wanted to scream at some of the people who passed us by. We never did, which is remarkable, because the natural instinct when your child is perceived to be made fun of or attacked is to protect him/her. 


Quote of the day: It is an absolute human certainty that no one can know his own beauty or perceive a sense of his own worth until it has been reflected back to him in the mirror of another loving, caring human being.  John Joseph Powell



On tonight's blog, I posted a few Foundation Walk photos that highlight some of the children's activities that we hosted. From my perspective if a child was bored at our Walk, this would greatly perplex me!!! 

This is Bob Weiman, Mattie's head of the St. Stephen's and St. Agnes Lower School. As my faithful readers know, I refer to him as the "Magic Man." Bob taught Mattie magic when he was hospitalized. Bob would visit Mattie on a regular basis at home and in the hospital. In fact, Bob even met Jocelyn a few times and shared magic tricks with her! Bob learned the skill and art of magic from his father, who he lost at a young age to cancer. Bob shares the gift of magic in his job as an educator to every fifth grade student at St. Stephen's and St. Agnes. Fifth graders then take these skills and share them in the community, at nursing homes, and hospitals. I have no doubt Bob's father would be proud of him. But as I tell Bob often, Bob shared a special gift with Mattie, because it was through magic, that Mattie found he possessed a skill that NO ONE else in the hospital had. He could entertain the nurses, doctors, and others in his room and in the hallways. Magic helped Mattie relate to others, especially at a time when he had trouble talking, using words, and feeling good about himself. Magic was magic for all of us. 

In 2009, Bob and Mattie performed several magic tricks together at the Mattie March, which is why, Bob and his fifth graders always have a magic show at each of our Foundation Walks! It is a tradition.



Bob draws a crowd and the crowd is always mesmerized. This is Emily and Abby, friends of Mattie's. They went to preschool with him and they are loyal Mattie Miracle supporters who come to EVERY ONE of our Walks! 






This is Lena! Lena is Bob's daughter! Do you see a resemblance? I know I do!











Here was what our crafts
table looked like at the walk. It is always a popular activity stop! This table was coordinated by our kid's activity coordinator, Debbie. Debbie has worked with us diligently for FIVE years now. Six, if we count the Mattie March which our caring community planned for us in 2009, when Mattie was still alive.



We had a Nail Art table, thanks to Molecule Salon, in Washington, DC! Molecule donates their services to us at every WALK! Pictured in orange is Celina, one of the owners of the Salon. Celina has styled my hair since I was in graduate school. She has known me when I was a student, then a professional and a mom. She is a Mattie Miracle supporter and over the years I have gotten to know her family as she has gotten to know mine. 


This is another one of the many activities Debbie planned for the little kids at the Walk. Water activities are always a popular stop! 
Check out the Hula Hooping! I love his smile! Not to mention that he makes it look easy. 




















This is Margaret, a high school student volunteer, who was helping to face paint at the Walk! Face painting is another popular stop!









Then for the adventuresome types we have a 26 foot rock climbing wall! You would be amazed who goes up on this! It may not look that high in the photo..... but it is huge!
















Wacky World, which is the name of this particular moon bounce, was a hit this year. It wasn't just your ordinary bounce. This thing had slides, twists, and other fun things inside of it. 







The fellow with the red t-shirt is Brian Will. Peter and I met Brian through one of the Georgetown University MBA classes we worked with several years ago. One of Peter's professors invited us to come into several of his classes to introduce his students to the Foundation. In addition, the Foundation served as the class community service project in which students had to analyze our Foundation and develop business strategies and models to help us develop and grow. It was in one of these classes, we met Brian. Brian has remained connected with us throughout this time and reached out to us several months ago with interest in volunteering at the Walk. Brian offered to conduct a kids Lacrosse Clinic at the Walk. Pictured with Brian is Amanda. Amanda is a Ewing's Sarcoma (a form of bone cancer) survivor and has come to our Foundation Walks before. Amanda loves sports and has an incredible 'can do' attitude. Amanda is a ray of sunshine and hope and I am so glad that Herman, our photographer, caught Amanda and her sister playing with Brian!

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