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 11, 2019

Wednesday, December 11, 2019

Wednesday, December 11, 2019

Tonight's picture was taken in December of 2008. Typically I feature a Mattie photo. This instead was a Mattie creation in the middle of our living room. Though we did not set up a big Christmas tree that year (because we were rarely home), Mattie decided to decorate in his own way. The Christmas Train was a Mattie tradition that went around every one of our family Christmas trees.  


Quote of the day: Sooner or later comes a crisis in our affairs, and how we meet it determines our future happiness and success. Since the beginning of time, every form of life has been called upon to meet such crisis.Robert Collier



Peter's morning started with this dot on the elevator of the Acute Rehab Facility. What is it? A penny! We took it as a Mattie sign. 

Peter got his mom into Spaulding Rehab Hospital. It is the number one rehab hospital in the Boston area and it is the official teaching hospital for Harvard Medical School’s Department of Physical Medicine. 


Check out this view from Barbara's hospital room! Very different from Mattie's views. I remember one room Mattie was in faced a brick wall! A dark and depressing two by four of a room. 
Peter sent me this x-ray! You can see the rods and screws inside of Barbara. Not to mention the pacemaker they inserted LAST Monday. A lot can happen in a week! I remember this so vividly with Mattie. In his case, a lot could happen within minutes! 
Barbara was visited by two friends today. But from what I understand, Barbara is freely walking and standing up and sitting down without issues. Honestly I think the neurosurgeon has to be a miracle worker. 

But at the end of the day, I credit Peter. He really pushed the hospital to get his mom scheduled for surgery. We felt the sooner she was stabilized and able to return to movement the better her recovery would be. 

Barbara's night view from her room, with the Zakim Bunker Hill Memorial Bridge in the background. 



No comments: