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 9, 2014

Tuesday, December 9, 2014

Tuesday, December 9, 2014 -- Mattie died 274 weeks ago today

Tonight's picture was taken in December of 2003. This was classic Farmer Brown at work. Mattie was in Los Angeles and helping me pick oranges and grapefruits from my parent's trees. Actually I am not sure what Mattie liked best, the picking part or the playing with fruit. Once the fruit was off the tree, Mattie loved holding the fruit, trying to stack it, sort it, and so forth! He could do that for hours. He would take it in and out of the basket and he wanted to do this outside in the cold. Despite it being Los Angeles, don't let that fool you..... LA can also get cold and at times you can need a coat and it was one of those times back then! From the photo, you can see how Mattie was eyeing the fruit intently!!!


Quote of the day: Problems that remain persistently insoluble should always be suspected as questions asked in the wrong way. ~ Alan Watts



Today I was invited to participate in a Round Table childhood cancer discussion held at the prestigious Cosmos Club in Washington, DC. The Round Table was hosted by the Alliance for Childhood Cancer and the Coalition Against Childhood Cancer (CAC2). The Alliance for Childhood Cancer represents more than 20 national patient advocacy groups and professional medical and scientific organizations and the CAC2 supports the advocacy efforts of childhood cancer organizations throughout the Country. Mattie Miracle is an organizational member of CAC2. I included links below to both organizations. 

The Alliance: 

CAC2:


The first Round Table discussion took place in September, today was a follow up discussion. These Round Tables are historic in a way because they are bringing together many childhood cancer organizations from around the Country to develop a unified childhood cancer advocacy platform. That may not sound tremendous or novel, but in a way it is!!!! Each childhood cancer organization has its own priorities, issues, and a particular cause and interest that it wants to lobby and advocate for on Capitol Hill. It makes sense if you think about it, because many of the leaders of these organizations have been directly impacted by childhood cancer. Therefore we are passionate about the issue and stand ready to make a difference. We come armed to correct a wrong for OUR child! Yet of course, from a legislator's standpoint these multiple messages are confusing and most likely muddy the waters. All the messages are compelling so whose message do you support?! The goal of the Round Table discussions is to pull us together to brainstorm the issues and develop a unified strategy and advocacy platform. 

Naturally this can be challenging because we all have varied interests and agendas and yet from what I saw today, there was a real concerted effort for people to be heard and having a professional consultant at the helm guiding the process definitely helps with the flow and strategy. Needless to say, I wasn't sure what this three hour meeting was going to look like, but I felt as if I learned a lot and that is always a wonderful way to leave a meeting. 

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