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 22, 2012

Saturday, December 22, 2012

Saturday, December 22, 2012

Tonight's picture was taken on December 5, 2002. Last night I decided to post the first photo in  a series that was taken on December 5th. Our goal that day to to take the "perfect" Christmas photo for our first family holiday card. We took MANY photos that afternoon. Peter was snapping away at the camera and I was jumping around in front of Mattie trying to get his attention. I clearly got it here, with his laughter. Again, a cute photo, but this was NOT what was featured on our 2002 card!


Quote of the day: How easy it was to lose everything you had always thought you'd have forever. ~ Cassandra Clare


This morning I came across this story about a mom in England who went to court because she did not want her seven year old son to be given radiation treatment for his brain cancer. The boy's doctors and his father however felt this was the only treatment which was going to give this boy a chance at survival. The boy's mother ran away with the boy, to avoid treatment, and ultimately she wanted to protect him from what she deemed would be scary, toxic, and scaring treatment to her son.
 
I imagine to anyone reading this story, the first reaction you have is that something is very wrong with this mother. How could she deny him standard and the most effective treatments available to combat cancer? Peter and I had to make challenging decisions for Mattie throughout his battle. However, the guiding factor was always life over death. Even life that meant disability, impairment, and being disfigured. These are not easy decisions for a parent to make and I unfortunately understand this mom's fears all too well. In fact, everything she is worried about is most likely going to happen maybe ten fold once her son is on treatment. As a mom we worry about the psychological and emotional health of our children, and the long term impact. Unfortunately medical personnel do not always look at these issues in the same light. I am not excusing this mom's behavior, but I do understand it. If you want to read more about this mom and the court's decision, please follow this link: "Neon Roberts: judge criticises mother over lost cancer treatment legal row"

 
When I woke up this morning and looked outside, this is what I saw. Living up in the hills is quite beautiful when the sun is shining and it is a clear day. I hear that it will be raining all next week, so I am trying not to think about the greyness headed our way. Yet life in the hills surrounds you with birds, beautiful terrain, less people, and my favorites... bunnies and deer! 

As we were returning home this evening, I glanced up the hill and low and behold I could see the "LA Cappuccino's." Naturally this is only my name for these beautiful blacktail deer. But their coats are such a rich and deep brown!

Near my parent's house is a patch of land and no matter what time of day it is, you can ALWAYS see a bunny grazing in the greens. It is a special sight!

No comments: