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 13, 2024

Monday, May 13, 2024

Monday, May 13, 2024

Tonight's picture was taken in May of 2009. Mattie had been working on this creation for weeks with his art therapists. Mattie made this clay vase in clinic, glazed it red (one of my favorite colors), and with his therapists designed tissue paper roses. This gift was presented to me for Mother's Day! To this day, I showcase this vase in our family room! It is a priceless piece to me. 

Quote of the day: It's amazing how someone can break your heart and you can still love them with all the little pieces. ~ Ella Harper


Some days are better for me than others. When I say better, I mean I feel like I can find a way through the day. Then there are other days like today, when I feel very anxious, very stressed out, and truly perplexed about my past, present, and future. I woke up at 5:30am, and typically when I wake up, my body is basically jolted awake. Since Peter has left, I start everyday off in a panic. I can feel my blood pressure rise, my head pounding, and this crazy fluttering in my ear. It is this fluttering which has caused my doctor to send me for an MRI in a week. 

The highlight of my day was I received a chocolate delivery from my cousin Cheryl. Though she and I have never met each other, she has become an incredible friend, support, and she is someone I trust. Given my life's circumstances, it probably makes sense to my readers that I do not give trust away very easily. 
The beauty of the chocolates inside. At the moment, four of these cuties have been devoured. Chocolate has always been my drug of choice!

Since Peter has left, I have gotten connected on-line to a woman in England. She is going through something quite similar as me. Though I met her in a support group (which I lasted in for only ONE session), we have remained connected ever since. Not just connected, we write to each other daily. What she and I are contending with on a daily basis is hard to describe unless you are living it. In some cases, sharing our stories, not only validates what we are experiencing, but we it eerie how we are thousands of miles apart and yet our thoughts and feelings are quite similar. Overall most people who are contending with what we do each day, are receiving intensive supports through counseling, medication, self help groups, and you name it. I of course do not have the time for any of this because of my caregiving demands. Nonetheless, despite how busy I am, it doesn't mean I am not acutely aware of the nightmare I am living. It is a nightmare that impacts every member of my household. 

If it is possible to die of a broken heart, I will be the medical world's case study. It is a taxing existence between being abandoned and managing the around the clock care of two people with dementia. As I say, I may not ever get over this, as there is just so much heartache one person can absorb. 

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