Mattie Miracle Walk 2023 was a $131,249 success!

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

May 20, 2022

Friday, May 20, 2022

Friday, May 20, 2022

Tonight's picture was taken in May of 2006. Mattie was four years old and that weekend we took him to Sesame Street Place. Ironically I did not know that the park had a big water feature to it. So while there, we bought both Peter and Mattie swim suits, and Mattie was eager to experience slides and things with Peter.  This was NOT my thing, so I gladly followed along and took photos. THANKFULLY. 


Quote of the day: We must accept finite disappointment, but never lose infinite hope.Martin Luther King, Jr.


I couldn't fall asleep last night. Typically each night I take migraine medication to help keep my chronic daily migraines at bay. Or at least make the daily pain manageable. However, with all I have going on, I honestly couldn't remember whether I took my meds last night or not. However, when it was close to 1am, and I was still up and couldn't fall asleep, I knew! I then took my meds and fell asleep soon thereafter.

When Mattie was diagnosed with cancer, my sleep patterns changed. I learned, while living in the hospital with Mattie, not to sleep. I was lucky back then if I got two to three hours of sleep a night. How I functioned for over a year like this, I have NO IDEA. However, once Mattie died the anxiety and panic further set in, making sleeping close to impossible. Without sleep, my migraine condition worsens. Which is why I am grateful for migraine meds that both help with headaches and also make me sleepy. In fact, Peter used to be a terrible sleeper prior to Mattie getting cancer. Now he sleeps beautifully, and I am the one with the pervasive issue.

I got up at 6am today so that I could get myself ready, make breakfast, straighten up downstairs, and then get my dad up, showered, and dressed. I was taking my mom to the salon today in Georgetown, and in order to get there by 10am, that required me to perform a miracle. Of course in the  midst of my usual chaos, Sunny began chemotherapy this morning. Within two hours of receiving his dosage, Sunny was a mess. He was highly anxious, glued to my side, panting uncontrollably and he seemed to have issues using his hind legs. I called the vet in a total panic and gave it to them. I made them write a note to their ER department in case I have to bring Sunny in this weekend. 

Fortunately I think some of Sunny's gastro-intestinal meds and nausea meds have kicked in. I hope this is a trend, but honestly I am frazzled with daily tasks, demands, and one crisis after the other. While driving my mom to Georgetown, I have to say I was having a meltdown. I am not a crier, but a screamer. There is so much on my plate on a daily basis, that something has to give. 

Any case, while my mom was having her hair done, I got to get my nails done. I have seen this manicurist since 2009, I was introduced to her when Mattie died. Going out every two weeks to get my nails done, was how I initially began re-integrating back into the world after I lost Mattie. Needless to say, after seeing someone for 13 years, we developed a rapport and friendship. So having two hours away from home, away from my dad's questions, constant demands, his bowel issues, and other problems, was very welcomed. Of course no good deed goes unpunished. Coming home from the salon, I picked my dad up at the memory care center. As soon as we walked into the house, he had an IBS attack and he was covered in poop. I had quite the clean up job to face and I assure you this isn't an isolated problem. It is a problem I face practically daily. 

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