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

March 20, 2022

Sunday, March 20, 2022

Sunday, March 20, 2022

Tonight's picture was taken in March of 2009. I never really reflected on this but this clay piece Mattie was working on became a Mother's Day present for me. I am not sure why I never connected two and two together. But this piece was glazed a  beautiful bright red and then Mattie and his art therapists created tissue paper flowers, put them in the vase, and Mattie presented it to me on Mother's Day. To this day I still have this red vase. It sits in our family room and is a constant reminder of Mattie and the bond we will always share. 




Quote of the day: Be faithful in small things because it is in them that your strength lies. ~ Mother Teresa


When I got into my parents bedroom today, my mom looked more tired than usual. In fact most people tell me my mom looks sicker than my dad. It turns out my dad was up three times in the middle of the night having to use the bathroom. I made note of this because if this is what the diuretic will produce, this medication will have to stop. 

I got my dad up, washed, dressed, and downstairs for breakfast. I did his brain games with him and had him walk for five minutes. However, he is chronically exhausted and out of it. My parents wanted to go out for an early dinner, so Peter and I made this happen. 

This was my dad at dinner. Totally zoned out, not engaged with us or the world around him. It is a very sad sight. While eating our entrees, my mom stopped eating. I asked her what was going on and she proceeded to tell me that she hasn't been feeling well since last night. Why she waited to tell me at 4pm is beyond me, but then I had to mobilize and respond. It is my usual mode these days, I am constantly dealing with issues and crises. 

I called my mom's pulmonologist office and left a message for a call back from the after hours physician. I heard nothing back and after 45 minutes called Dopey, my parent's concierge doctor. Dopey responded and basically said he couldn't help. He told me to call back the pulmonology office until someone responded (as if I couldn't figure this out). Dopey lives up to his permanent dopey status. 

Thankfully the pulmonology office did call back. The doctor was wonderful and compassionate. He listened to all my concerns and he looked at her case notes. Since we just visited this week and completed a battery of tests, he was able to easily help us. He prescribed her antibiotics, steroids, and inhalers. But of course I live in the boonies, where the pharmacy closes at 6pm on a Sunday. Unlike my city pharmacy which was open 24 hours a day. In any case, I called CVS and spoke to the pharmacist. She was nice enough to process the four scripts and I told her I was on my way to pick them up before they closed their doors. 

Each day I hope for a smoother, calmer, and more manageable day. A day where I could do just 30 minutes of work for the Foundation! I haven't had a moment's peace yet and forget a minute for myself. 

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