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

December 19, 2021

Sunday, December 19, 2021

Sunday, December 19, 2021

Tonight's picture was taken on December 24, 2008. Mattie was going to be released that day from the hospital to go home, so he could celebrate Christmas at home. I get why hospitals push people out during the holidays, but in all reality this wasn't the best decision for us. Going home was challenging, isolating, and impossible to manage without the support of our medical team. Right before being released, Mattie's best preschool friend, Zachary, came to visit. While they were playing, two marines walked into the room to bring holiday cheer and presents. They graciously allowed us to take photos together which Mattie enjoyed because even at a young age he had great respect for people in the military.


Quote of the day: Today's coronavirus update from Johns Hopkins

  • Number of people diagnosed with the virus: 50,832,991
  • Number of people who died from the virus: 806,438


This morning wasn't my finest moment. I need to constantly remind myself that my dad isn't who he once was and even though I have inordinate patience, I need to tap into an even deeper reserve. As I got him up this morning to get into the shower, he said he wanted to use the bathroom first. I got him to the toilet, but what I did not realize is that walking along with us was a trail of urine (of course my mistake was I took him depends off first because I thought we were walking directly to the shower). While on the toilet, he mentioned that he saw water on the floor, but I said that couldn't be, until I looked closer. Sure enough it wasn't water but urine. Which I was stepping in and walking through. Needless to say when juggling a lot, I at times crack. I started yelling. Not at my dad, but he took it like I was yelling at him. He doesn't like any loud voices or noise now and therefore the internal message I have to remind myself is that he can't control what he does and accidents like this will happen. Just deal with it and move on. I can't prevent them and I certainly don't want him to feel bad about what happens. Though the one beautiful thing about dementia is that in a few minutes my dad forgets what just transpired. So it is like working with a clean slate, which is the only blessing, and I really mean the ONLY one, as I think dementia is another horrible disease. 

We focused on placing furniture on the first floor today. I was determined to get rid of the warehouse look! I have to take photos during the daylight hours, but this is my mom's furniture in the living room. Fortunately my mom and I have a very similar color palate and similar taste. So our furniture talks to each other. But I had to be strategic when purchasing a house, as it had to have space for my things as well as hers. 
Our piano room. Or I should say the room that features Mattie's piano, which was given to Mattie for free by a former neighbor. I will never forget Susan, she felt Mattie needed to learn an instrument. Next to the piano is a Victrola. On top of this Victrola is a marquetry box which houses Mattie's ashes. The piano room and the room pictured below are new additions to our house. The former owners built them because the wife literally wanted her own private space in the house away from her husband and children during certain parts of the day. This new addition enables us to house all our furniture. 
We did not name this room, instead when the house was sold to us it was called the Oakton Room. So the name has stuck with us. I have now removed enough furniture in it so that I am not going to have an anxiety attack. Ironically Indie and Sunny absolutely love this space. Of course you have NO IDEA what our basement looks like. It is packed to the gills with boxes and furniture we removed from the first floor. I will slowly begin working on the basement post-Christmas. 

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