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

August 15, 2020

Saturday, August 15, 2020

Saturday, August 15, 2020

Tonight's picture was taken in August of 2008. Next to Mattie was Anna. Anna was the chief of pediatric physical therapy. We were very fortunate to get someone so capable, bright, and compassionate. During Mattie's first week in the hospital, she got him acclimated to a wheelchair. Given that Mattie was going to have several surgeries as part of his treatment protocol, Anna wanted to normalize the chair for Mattie and also work on his upper body strength. Anna played a significant role in Mattie's cancer journey right from day one. Ironically I thought Mattie would be spending a month or two in a wheelchair post surgery. Unfortunately after his surgery in November of 2008, Mattie was wheelchair bound.  


Quote of the day: Today's coronavirus update from Johns Hopkins
  • number of people diagnosed with the virus: 5,356,244
  • number of people who died from the virus: 169,423

Another busy day here! I begin each day at 6:15am. My dad's caregivers arrive at 8am, and basically it is non-stop activity until 1pm. Today, my dad's occupational therapy came for an appointment. However, in between appointments, we received a large mail delivery. Big boxes were left near my parents gate. Which is over 500 feet from where you see them now (as this is near their front door). I had to carry the boxes back to their front door and then open every box and put items away. After which, each of the these boxes needed to be broken down in order to fit in the recycling bin. I have ABSOLUTELY no idea how my parents manage any box deliveries when I am not here. As the walk and carry are extensive. Also today was 100 degrees, so this made moving around boxes debilitating. 


I would say the day to day existence here is difficult at best. Though my dad is more stable than he was in June, he is still fragile and agitates easily. He also has irritable bowel syndrome and it is very difficult leaving the house for any period of time because the need to have a bowel movement can come suddenly. Most times this week, he did not make it to the bathroom in time and therefore needs to be seriously cleaned up. All of this makes him anxious and of course the whole thing is overwhelming for my mom to manage. I frankly do not know how they both make it day to day when I am not around, because as it is, I am working around the clock. So I know the current state of affairs is not manageable long-term. Which of course weighs on my mind as we do not live around the corner from each other. 

Meanwhile, Miss Indie is in Boston and making herself at home at Peter's parents house. 












Out on the deck, Sunny is resting after a full day of being on squirrel and bunny patrol! 


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