Proud of my work -- 16 Years of Service

Thank you for keeping Mattie's memory alive!

Dear Mattie Blog Readers,

It means a great deal to me that you take the time to write and to share your thoughts, feelings, and reflections on Mattie's battle and death. Your messages are very meaningful and help support me through very challenging times. I am 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 have stopped writing on September 9, 2010. However, like my journey with grief there is so much that 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 me, and most importantly thank you for keeping Mattie's memory alive.


As Mattie would say, Ooga Booga (meaning, I LOVE YOU)! Vicki



A Remembrance Video of Mattie

September 26, 2019

Thursday, September 26, 2019

Thursday, September 26, 2019

Tonight's picture was taken on September 29, 2007. That weekend we took Mattie to the Swedish embassy, as they were having an open house with all sorts of kid activities. In front of the embassy, they placed this HUGE chair. Mattie climbed on top of it and I snapped this photo! Almost every day, Sunny and I walk passed this embassy. When we do, I always look up to their terraced area and remember this exact moment in time. 







Quote of the day: Every man's life ends the same way. It is only the details of how he lived and how he died that distinguish one man from another.Ernest Hemingway


I received an email from a fellow cancer advocate today. She runs her own childhood cancer non-profit. We had the opportunity to meet her on Sunday at Curefest on the National Mall. She was intrigued by our Psychosocial Standards of Care, wants to learn more as well as share them with her Foundation's readers. Which is absolutely fantastic, because we need the advocacy community to be passionate about the Standards and to bring them back to their treatment sites, encouraging their adoption.

At Curefest, we have a brochure available for advocates to introduce them to the Standards and why they are important. Though we highlight the Standards on our Foundation's website, we did not have this brochure available on line. Well that is until today! I am so glad she brought this to my attention, because in 2020, we will be in the position of designing materials that will help advocates understand the Standards as well as provide them with a call to action as to what they can do to help with the implementation process.  

While working on our website today, I came across this video we posted back in 2015. It is three minutes long and features one of our core research team members, Dr. Andrea Patenaude (Dana-Farber Cancer Institute). We attended this world conference with Andrea, and while there she was interviewed. The association shared this video with us and I am so glad we have it on the record. Andrea was an intelligent, sensitive, and compassion professional and woman.  It is hard to believe she is no longer with us, as she died from cancer in January of 2018. We miss her greatly. She will always be listed as a legacy member of our core team!

The Standards in Andrea's words.......................
https://vimeo.com/135103105









Mattie Miracle's website and the Standards of Care:

https://www.mattiemiracle.com/standards


The Standards Brochure:

https://docs.wixstatic.com/ugd/27074d_6586dbd3a20a4080a05cba3a3a442ac4.pdf

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