Mattie Miracle -- 16 Years of Service

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

April 14, 2025

Monday, April 14, 2025

Monday, April 14, 2025

Tonight's picture was taken in April of 2009. That afternoon, we took Mattie to the hospital garden. This was a place we escaped to on warmer weather days. I will never forget that space, because it provided us freedom from the hospital unit, the ability to see greenery, and to get fresh air. If you haven't experience the dry and cold air within a hospital, then you are lucky. After a while, it feels very sickening. What this photo captures is me with my all time pal. Mattie trusted me to make the right decisions about his care and it was very daunting knowing that I held the life of Mattie in my hands. There wasn't anything I wouldn't have done to help Mattie, but what cancer taught me is that wishes, prayers, and all the best intentions sometimes can't change the outcome. 


Quote of the day: The greater the difficulty, the more glory in surmounting it. Skillful pilots gain their reputation from storms and tempests. ~ Epictetus


Today did not go at all as I had planned. I thought my dad was going to go to his memory care center this morning. However, since he was discharged from the hospital on Saturday, his in-home care agency had to send the nurse to assess my dad and as well get a physical therapy evaluation. All of which HAD TO HAPPEN TODAY! I have to tell you, I do not like surprises. I would have preferred knowing this on Sunday, so I could have better prepared for today. My dad's in-home care agency was just lucky that I did not have anything else scheduled today, so that I could keep my dad home for the day with me. But since I care for my mom as well, I juggle her needs and doctor appointments too! 

Any case, in between juggling these appointments I also had a Mattie Miracle board meeting. I am fighting to get a breast MRI, and don't get me started about my second floor furnace. Which doesn't work! Truly by 2pm, I felt like I went ten rounds. Jumping from one task and need to the other. Of course, neither of my parents can interface with the health care professionals alone. I must be present, to answer questions, provide a summary of my dad's hospitalizations and current medications. 

It is 6:15pm, and I am so anxious and need to do something. Which means, tonight's blog will be shorter, because I am headed outside to the garden to do more painting of my deck. Until tomorrow. 

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