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 18, 2015

Wednesday, February 18, 2015

Wednesday, February 18, 2015



Tonight I attached a video instead of a photo of Mattie taken in February of 2009. It was taken during a physical therapy session on the inpatient floor of the hospital. This was what a typical session looked like with Mattie. In the lead of the session was Anna, Mattie's physical therapist. Behind Mattie were Jessie, one of Mattie's art therapists and Linda, Mattie's child life specialist. Mattie had a whole entourage when doing physical therapy. He really needed this moral support because movement for Mattie was painful and required a great expenditure of energy. So he truly needed people to encourage him, to egg him on, and to he needed an audience. Sometimes he needed people to even compete against. It just depended on his mood and the situation. Because Mattie practically lived at the hospital and we were always roaming around on the floor, all the staff who worked on the floor got used to seeing us pass by. Many would wave to Mattie. Though this video clip doesn't show it, I can assure you there were some therapy session where we were blasting ABBA's Dancing Queen on a boom box to motivate Mattie to move his body. When Dancing Queen was blaring every office door would open to see exactly what was going on in the hallway. As soon as people would see Mattie trying to do physical therapy with his merry band of followers people couldn't help but smile! 


Quote of the day: You have power over your mind - not outside events. Realize this, and you will find strength. ~ Marcus Aurelius


When I reflect on Marcus Aurelius' quote and one having "power over your mind," I can't help but think about parents who help care for their children who have cancer. Particularly I am thinking about moms, since I was a mom and today I communicated back and forth with two moms who are helping their daughters battle cancer. One mom I know very well, she is my friend and her daughter was diagnosed around the same time Mattie was diagnosed with cancer, and another I was just recently introduced to. In any case the mom I was recently introduced to contacted me because she needed some information and help. Information that I did not know but I knew that my friend Cathy could supply her with it given that I consider Cathy a guru in stem cell transplant issues. Needless to say I text messaged Cathy and within seconds she responded and literally within minutes one mom was connected to another mom. I have no doubt that Cathy was able to help this other mom, but you should know that my friend Cathy is knee deep in helping her own daughter with cancer. 

Cathy's daughter is a truly special young woman who is witty, humorous, and very introspective. She deeply cares about her family and the world around her and yet she was struck down with cancer at the age of 15 and has been in and out of hospitals ever since. She is 21 now, and hasn't had the opportunity to really live a normal life. The average 21 year old would be sulking in the corner and pitching a fit, but not Bridget. She finds a way to cope and courageously plot through her six year cancer journey. I do think having a committed and loving family by her side helps tremendously. Cathy is a steadfast mom who is focused, determined, diligent and can talk as intelligently as most medical doctors. She knows every treatment option available out there and is very familiar with the major medical institutions on the Eastern seaboard. I met Cathy and her husband George early on in Mattie's treatment phase, and I always remember that they were in awe of me for what we seemed to be enduring. But as I told Cathy today.... she is my hero, because I admire the incredible role she plays in her family's life. Despite all Cathy is balancing, she found the time to help another mom and child today with cancer. That to me leaves a lasting memory. Not surprising coming from the source, but it speaks to the way that childhood cancer unites us.  

This morning when I looked outside my window I was greeted with a "Hi" sign!!! Peter created this cutie last night in the snow. I am sure all our neighbors are enjoying this.... as I know they are enjoying watching the birds at our feeders! 














Today my good friend Mary Ann sent me a photo of the rose bushes near her home. I endearingly call these bushes.... "Margaret's" rose bushes. I like to track these bushes at all times of the year! Of course these bushes are not Margaret's. But my friend Margaret loved to grow roses. When Margaret died in June, Mary Ann was walking by these rose bushes and sent a photo of them to me in honor of Margaret. As soon as I saw the photo, I told Mary Ann that they reminded me of Margaret. So to this day, we both refer to these bushes as Margaret's rose bushes! 

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