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

February 25, 2025

Tuesday, February 25, 2025

Tuesday, February 25, 2025 -- Mattie died 783 weeks ago today. 

Tonight's picture was taken in February of 2004. Mattie was almost two years old. That day it snowed! Guess who wanted to go out and in it? Mattie loved being outside, it did not matter the weather! Mattie was fascinated by the snow and though I wasn't an outdoor kind of girl, I rose to the occasion with Mattie. Whatever interested Mattie, became my interests! To this day, I too prefer being outside. It is very freeing to be  surrounded by nature, and if I did not have Mattie, I am not sure I would have ever learned this important lesson. 



Quote of the day: No one ever told me how sorrow traumatizes your heart, making you think it will never beat exactly the same way again. No one ever told me how grief feels like a wet sock in my mouth. One I’m forced to breathe through, thinking that with each breath I’ll come up short and suffocate. ~ Sarah Noffke


This morning we had a visit from a nurse. She was coming to evaluate my mom for a needs assessment. We never met this nurse before but she prepared me that the visit was going to be around 90 minutes long. The nurse required a listing of my mom's medications and a list of her doctor's addresses and phone numbers. Believe it of not, my mom see about 10 different doctors on a regular basis. 

When the nurse arrived, she immediately reminded me of a friend of mine from graduate school. Turns out the nurse is Italian and therefore, all three of us started swapping stories. The nurse assessed everything, including my mom's memory. This is an issue I no long address with my mom. There are some things as a caregiver that you learn to pick your battles. I know what I know, and there is a fine line of knowing something versus trying to share the reality, which can cause frustration and embarrassment. My mom and dad, prior to dementia, were both sharp, intelligent, and gifted people. I remind myself often that they are still these things, but that their memories have been impacted. In any case, through today's assessment, my mom told the the nurse that it was April. She did not know her address, and was confused about other facts related to her medical history. 

We discussed physical issues my mom is facing and then she watched my mom walk and do other activities of daily living. What I do know is without my presence, there is no way either of my parents would be able to live independently. Which of course is a humbling reality for me..... as I face a future without my husband and my son. 

Any case, we survived the assessment. As soon as the nurse left, my dad's first question was.... what is for lunch?! Got to love him. Later on today, I decided to go to the basement. We have a TV there, which is not connected to the cable. I am sure there is probably a way to access the cable account remotely (maybe I have to download an app), who knows. But the TV has an Amazon Fire Stick. So I started playing around with it, and was able to connect to my Amazon account. Why did I want that to happen? Because I decided, I want to use the treadmill and elliptical machines in the basement. When we moved into the house we bought used machines. Since I rarely can leave the house and walk, nor do I really want to without Sunny, I decided to come up with Plan B. I am trying to do ONE thing for myself. Today was the first step to do something for my health and well-being. 

I was on the machines for 40 minutes and started watching a Hallmark movie. For me, Hallmark movies are my therapy. There is NO sadness and unhappy endings in a Hallmark movie. Which at this point is my speed and as much as I can emotionally handle. I am hoping that I can start a routine in the basement that will be beneficial for myself. Time will tell.

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