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

May 23, 2022

Monday, May 23, 2022

Monday, May 23, 2022

Tonight's picture was taken in May of 2007. Mattie was five years old and it was Mother's Day. We went to one of his favorite restaurants. Peter snapped a photo of us and as you can see Mattie was crossing his arms. It was meant to signify how much he loved me. A moment in time I will never forget. 








Quote of the day: One's best success comes after their greatest disappointments. ~ Henry Ward Beecher


Last evening, lightning struck down in our area and it somehow affected our electricity. At around 5:30pm, we lost power. Ironically all of our neighbors had power. Thankfully we have a generator, but of course, it can't power the entire house. We went through the night on the generator. This morning the power company came to help us, and it turns out we were getting power from the street to the house. So the problem was in the house itself. Given the luck or lack there of we have had with this house, Peter and I were prepared for a nightmare of a problem. Our electrician came over and thankfully it was a loose wire that had to be adjusted and secured. Amazing how one wire can impact an entire system. By noon, we were off the generator and back on the grid. 

This afternoon, I took my parents to see my eye doctor. Their internist asked that I take them for an eye exam, specifically because my dad has a cataract in both eyes. My parents handled the eye drops and dilation much better than me. My dad particularly liked the doctor because he is Italian. They had a good rapport, and we learned that the doctor's family and my dad's family are both from Calabria. Small world. I found this doctor about a year ago. This is after I gave my long term ophthalmologist his walking papers! This doctor is humorous, down to earth, not an alarmist, and doesn't quickly move to surgery. Especially with someone with my eye issue.... narrow angle glaucoma. 

After the eye appointment, I took my parents out for an early dinner. I am quite sure the average person wouldn't entertain taking my dad out to eat. First of all, he eats VERY VERY fast. This is definitely his dementia. No matter what you tell him, he can't seem to slow down, and instead eating with him feels like a race. The professionals at my dad's memory care center have even acknowledged this issue, as they feel he eats way too fast and is a candidate for choking. I am not sure whether they have ever seen the food get stuck in his throat, like we have, but it isn't pretty. In addition to this issue, we have the bathroom problem. My joke is my dad is like a goose. It goes in and it quickly comes back out. Managing his bathroom needs could be a full time job. A job that would make most people sick to their stomach. All I know is I feel like I am on autopilot, constantly moving from one task or chore to the next. 

Meanwhile, Sunny had his second chemotherapy dosage today. He seems to have handled it better than Friday's dosage! We are premedicating him with all sorts of pills for stomach upset and nausea and I just hope this chemo has an affect on Sunny's tumors. 

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