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

August 24, 2015

Monday, August 24, 2015

Monday, August 24, 2015

Tonight's picture was taken in August of 2007. This is a follow up photo to the one I posted last night. We took Mattie to the La Brea Tar Pits and after exploring the Museum and Tar Pits, Mattie loved to walk around and climb on the prehistoric creatures they had outside. These creatures were designed for just these purposes, for kids to climb and interact with them, as well as appreciate their impressive size.


Quote of the day:  I have been impressed with the urgency of doing. Knowing is not enough; we must apply. Being willing is not enough; we must do. ~ Leonardo da Vinci

This spring, Peter and I were invited to serve on the Family Advisory Board for The Center for Pediatric Traumatic Stress: http://www.chop.edu/centers-programs/center-pediatric-traumatic-stress. The Center for Pediatric Traumatic Stress (CPTS) at The Children's Hospital of Philadelphia addresses medical trauma in the lives of children and families. Founded in 2002 as a multidisciplinary intervention development center within the National Child Traumatic Stress Network, CPTS has recently received additional funding by the Substance Abuse Mental Health Services Administration (SAMHSA) to further its work in preventing and treating medical traumatic stress in healthcare settings.

Peter and I are NO STRANGERS to Medical Traumatic Stress. This was something Mattie dealt with as a result of his treatment. In fact, Peter and I still contend with aspects of these issues, especially when walking through the hallways of Georgetown University Hospital or during scans and procedures for ourselves. 

Pediatric medical traumatic stress is a set of psychological and physiological responses children and their families have to:

  • Pain
  • Injury
  • Serious illness
  • Medical procedures
  • Invasive or frightening treatment experiences in medical settings


These responses may include symptoms of arousal, re-experiencing and avoidance. Symptoms can vary in intensity and are often related to the child's or family member's subjective experience.

Recently, the Center contacted Peter and asked him whether he would submit an article for their blog. Peter has a reputation in our psychosocial circle for being the social media guru. So it was no surprise to me that these professionals reached out to Peter. He can effectively write and he is technologically savvy, so I am happy Peter had the opportunity to promote and chat on the blog about the National Psychosocial Standards of Care that will be published this Fall in the journal of Pediatric Blood and Cancer! Mattie Miracle had the vision to establish such Standards back in 2012. Standards which we felt needed to be created to ensure that all children with cancer and their families would have access to a minimum level of psychological, social, and emotional care from the time of diagnosis, through survivorship or end of life and bereavement care. 

To see the blog posting hosted by Children's Hospital of Philadelphia, go to:

https://www.healthcaretoolbox.org/latest-news/22-e-emotional-support/383-psychosocial-care-for-children-with-cancer-and-their-families.html

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