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 11, 2008

Saturday, October 11, 2008

Saturday, October 11, 2008

We had a peaceful night of sleep on friday night. Though Mattie's sleep-wake cycle is very off. By 1am, Peter and I were thoroughly wiped out and literally told Mattie enough was enough and it was time to go to sleep. We all slept in late this morning and had a slow start to the day. Then we got ready and walked to Washington Harbor to meet Peter's family to go on a Potomac River boat ride. Originally the plan for today was to go canoeing, but Mattie told me he did not want to do that today because this frightened him. The irony is Mattie has gone canoeing many times prior to being sick, but I think he is very careful with his body these days, and in his assessment canoeing wasn't safe. So we changed plans and went on a different type of boat ride. Below you will see some pictures from our Potomac River adventure, which took us from Washington, DC to Old Town, Alexandria. We ate in Old Town and walked through a lovely park by the water.




Grandma, Mattie, Sydney, Aunt Lisa, and Will on the Matthew Hayes boat










Nat, Aunt Lisa, Mattie, Sydney, and Will at Old Town, Alexandria, VA











Monkey see, Monkey do! Mattie saw his cousins climbing a fence, and he wasn't going to be left behind. Mattie started to climb, but did not go any higher.








Right: Will, Sydney, and Mattie climbing a statue





Left: Nat, Mattie, Sydney, and Will






After having lunch in Old Town, we headed to the boat which took us back to Washington Harbor, in DC. Mattie thoroughly enjoyed being on the boat today. The water was calm and the weather was ideal. It was glorious to be out in the fresh air and to see the sights and sounds of DC. Once at the dock, we walked back home and the kids had a great time playing outside, with balls and remote control cars. It was at that point, where I had to go lie down, I am now losing my voice, and just need to rest. So Mattie went for a walk around Foggybottom with his family and they stopped at the Albert Einstein famous bronze statue in DC. See the picture below.




Will, Nat, Sydney, Mattie, and Grandma

On the electronic front, we want to thank Lorraine, Susan, Kim, and Karen for the wonderful e-cards and Jacky (thanks for the great bird video) and Allen for your e-mails. Mattie wants to thank his cat friend, Brian Boru for the wonderful VA postcard and spiderman PJs. A cat with great taste! Also Mattie and his cousins enjoyed the Dunkin Donut treats that our resident Jack Russell Terrier, JJ, brought down to our home. Thanks JJ!
Mattie has enjoyed the time with his Boston Family this weekend! We plan on doing something nice with Mattie on sunday as well, and then will of course need to get ready for another week in the hospital. It is funny being out and about and seeing people walking around with their children. I look at these folks and think, wow do you know how lucky you are? You have healthy children who can run, jump, attend school, and lead a normal everyday life. I feel this way on one hand, and but then on the other I look at Mattie, and despite having cancer and being under treatment, he appears to be so full of life, happiness, and energy. How on earth does he do it? I don't have an answer, but I sit in amazement. It is interesting, Dr. Synder and my neighbor, Kathleen, made the same comment to me this weekend. Both told me they know Mattie is 6 and of course acts like a 6 year old at times, but at other times they say he acts wise beyond his years. I have no doubt this year's experience will have an impact on Mattie, not only physically, but emotionally and psychologically.

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