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

November 1, 2018

Thursday, November 1, 2018

Thursday, November 1, 2018


Tonight's picture was taken in October of 2004. Mattie and I went to Target and together we picked out this costume. The costume had to be just right otherwise Mattie wouldn't wear it. Mattie had no problem with sweat suit material and when we spotted this pooh outfit, we knew it had to be the one. Mattie and I both loved Winnie the Pooh, and in my opinion Mattie made the cutest pooh.








Quote of the day: Anger is a short madness. Horace 


It is the day after Halloween and I can't tell you how many emails I received today about our candy drive. Every question possible..... what type of candy do you want, what size, can the candy have nuts, where should we drop off the candy, must the candy be sorted.................... get the picture?! What would drive the average person crazy, doesn't bother me at all. I like interfacing with people who contact me about the Foundation and I don't view it as a bother but instead a way to spread awareness about what we do. I must admit candy peaks the curiosity of people of all ages!

However, what I did not expect today was feedback from someone I know about my role in the Foundation. As of tomorrow, Mattie Miracle with be 9 years old. November 2nd is Mattie Miracle's birthday. The Foundation is older than Mattie was when he died. I have babied a Foundation longer than my own son. Needless to say, because the Foundation represents Mattie, I keep a close eye on everything the Foundation does.... whether it is visiting our hospitals, interacting with our child life specialists, assessing our snack/item carts, interfacing with donors, and of course working with our national researchers on our psychosocial standards agenda. What I deem as providing oversight, commitment, and love to everything we do, I found out today that others view me as controlling and a micro-manager. This is a new one to me because I have never received such feedback before on any of the jobs I have ever done, and I have worked with a lot of people in my lifetime doing various tasks. 

Naturally despite my anger over hearing this perspective, I did listen, because this is a friend. Mind you I can listen, absorb what is being said, and appreciate someone else's feelings, but that doesn't mean I agree with it. But, I am mature enough to hear it, yet I am not quite sure those who are willing to judge me would be as open to hearing my perspective or how I see it from my vantage point. 

At the end of the day, the conversation reminded me that there are two sets of people in the world..... those lucky enough to have children and those who lost their children and are childless. These two groups co-exist in the world but I am not quite sure we can ever fully understand the other. I feel quite certain of this because I interact with many Foundations in the childhood cancer space, and all Founders are heavily involved, dedicated, committed, and provide the direction for their organization. They do this because like Peter and me, they too have lost children to cancer. It is a loss that is so great that it is hard to comprehend or try to describe. Yet what keeps all of us going is the work we do in our child's memory. Therefore, receiving such hurtful feedback, which I deem wasn't merited, can be personally devastating to a bereaved parent. 

No comments: