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

June 7, 2022

Tuesday, June 7, 2022

Tuesday, June 7, 2022 -- Mattie died 662 weeks ago today. 

Tonight's picture was taken in June of 2009. Mattie was in the outpatient clinic at the hospital and up to his antics. He and Jenny (one of his art therapists) were having a wheelchair race. You wouldn't believe some of the things we did to try to encourage Mattie to use his body and strengthen his muscles. Of course at that point we still thought we were fighting the disease and were hopeful for remission. 


Quote of the day: You have to be patient with Alzheimer’s. Once you understand that it’s a medical condition, you become a little more compassionate. You get less frustrated. ~ Kim Campbell


I absolutely appreciate the sentiments of tonight's quote! It is all very true. Yet there are some days I manage it better than others, as it is easy to get frustrated especially when I am tired. I can't be Florence Nightingale 100% of the time, and must accept that I am only human. 

This morning, my dad and I had an appointment with the foot doctor. Given my dad's history of diabetes, he has neuropathy in his feet and we have found it is a good idea for him to see a foot doctor every 9 weeks. When I first met this doctor, I thought he was socially awkward. But I have come to appreciate that he is just very scientific, but clearly knows his stuff. He tells me I am doing a great job at keeping my dad's feet clean, dry, and well maintained. I had a great foot doctor in the city, but since I moved in August of 2021, I needed to find someone closer for my dad. As moving my dad from one place to another is an act of God. 

Given that I have come to appreciate this new foot doctor, I made an appointment to see him today as my big toe nails hurt and have issues. Turns out even my feet experience trauma and he believes my nail issues are not an infection but from pressure and trauma on the toes. Seems fitting for me!

On an aside, I have noticed whenever I drive my dad in our neighborhood, his first question is.... do I know this person (walking along the road)? Typically I will respond, no! But today, I lost it. I asked him how on earth I could possibly know anyone when I never leave the house? Of course that comment was over his head, but this is an example of how I can get frustrated. I am a prisoner in my own home, tied to chores, cleaning, cooking, doctor appointments, managing bowel movements, and the list goes on. So meeting a neighbor is SO far from my reality, and yet my dad clearly has NO perception whatsoever of our daily existence. 

Later today, I spent some time at the computer downloading photos from the Foundation's walk from the internet. I then began creating some slides (which you see below) that will get featured in our Walk 2022 video. Making the video is a labor of love, and I am sure no one would miss it if I did not create it. But it is a matter of documentation, and slowly but surely I am doing it!















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