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 9, 2023

Friday, June 9, 2023

Friday, June 9, 2023

Tonight's picture was taken in June of 2004. Mattie was two years old and we were outside on our deck. Of course Mattie did not care what type of weather it was outside. He just loved being one with nature, exploring, and taking in his world. However, I do think rain and snow intrigued him, and Mattie definitely taught me to move passed my comfort zone.  

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


It is Friday at 8pm, and I am tired. But my day doesn't end here of course. Until my parents go to bed, I am on the go. My dad went to his memory care program this morning and I took my mom for her physical therapy appointment. After the appointment I took my mom home so she could rest for a while, and I caught up on laundry, dishes, and other chores. Physical therapy wiped my mom out and she napped for two hours. 

After I picked my dad up at the center, I then drove straight to the restaurant where we had a late lunch. Just like yesterday, my dad pooped in his pants while dining. I have concluded that his new medication is exacerbating his irritable bowel syndrome. For months now, I have told my dad's former doctor to assess him for diabetes. He did not listen, but agreed to shut me up and test him in June. Naturally this doctor retired, and when we met the doctor taking over his practice, I encouraged him to test my dad's blood. Sure enough, I was correct. His diabetes is back and on Tuesday he started this new medication. Since that point, I have had my hands full managing his toileting issues.

I text messaged his doctor this morning and alerted him of my observations. He wants me to give it a few more days and if my dad's body doesn't stabilize, we are pulling him from that medication. All I know is that my dad's gastrointestinal system is very fragile and any changes can cause massive havoc in our existence. 

I think coping with dementia is hard enough, but combining dementia with irritable bowel syndrome is enough to make any caregiver unstable. Unlike in the past when we could manage my dad's irritable bowel syndrome (IBS) with diet and other methods, now, NOTHING works. I have discussed this issue with several doctors and unfortunately there are NO good treatments for IBS. So here we are! My parents are lucky that I have a strong constitution and can manage these intense clean up jobs, but I am quite certain not every adult child would want to do this! 

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