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

March 10, 2020

Tuesday, March 10, 2020

Tuesday, March 10, 2020 -- Mattie died 545 weeks ago today. 

Tonight's picture was taken in March of 2009. We were all in the child life playroom at the Hospital, and celebrating the official ribbon cutting ceremony for the room. When Mattie was initially diagnosed in July of 2008, there was NO playroom at the hospital. Instead, the only space children had was in the hallways or their hospital rooms. I assure you it made life 10 times harder, as a hospital room is very confining, and having another space with activities made the time more bearable. Though the playroom was opened in the fall of 2008, the ribbon cutting took place in March. As you can see the Toys R Us mascot, Gilbert the giraffe, was on hand to celebrate the occasion and gave Mattie a high five. 


Quote of the day: Perhaps I know best why it is man alone who laughs; he alone suffers so deeply that he had to invent laughter. ~ Friedrich Nietzsche


Yesterday, March 9th, we experienced an amazing moon. The worm moon is the first full moon in the month of March. The moon in March has a lot of different nicknames: the Worm Moon, because the ground begins to thaw and earthworms reappear, soon followed by the return of robins.

Peter captured this wonderful Mattie Moon from our living room!
Sunny had his senior well visit today and before taking him, we took him to Roosevelt Island for a 3 mile walk. Along our journey we saw this momma dear with her baby. Peter and I were talking so I did not even see her, it was Sunny who stopped in his tracks and had a staring contest with the deer. 
The baby. Of course whenever I see a momma animal and her baby, I can't help but think of Mattie. As Mattie loved to tell him that these animal pairings were like him and me. 

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