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

August 25, 2018

Saturday, August 25, 2018

Saturday, August 25, 2018

Tonight's picture was taken on August 13, 2008. By this point, Mattie was a few weeks into treatment. That day, we received a visit from Scooby Doo. Mattie was thrilled as he was an enormous Scooby Doo fan. We had no idea we were going to get this surprise visit, but it perked Mattie up. Do you see the two Scooby Doo stuffed animals on the bed? Ironically years later (after Mattie died), we were introduced to the dad of the young man dressed as Scooby Doo. Apparently seeing this photo really touched this family and they wanted us to know. 


Quote of the day: Sometimes even to live is an act of courage.Seneca


Seneca's quote is quite poignant, especially when we are talking about the death of a child to cancer. Trying to move forward after a child dies is an absolute feat. In addition to this devastation is the sheer fact that people think you will return to normal. Especially after surviving the first year of grief. Unfortunately this is NOT the case, and I would have to say that with each successive year since the death the reality of the loss sets in further. All of which has consequences on one physically and emotionally. 

Yesterday I bumped into neighbors of mine whose mom died three years ago. This coming week is the third anniversary of her death. They mentioned to Peter and me that they were going out of town for the anniversary. I am sure to the average person, one is saying..... why? However, no explanation was needed for us, as we completely got it. 

Why do people leave or disengage from their lives on anniversaries? We do, NOT for ourselves, but because the world around us can't handle the reality that the death of a close family member is still painful. In fact, the world keeps revolving and carrying on, during these anniversary dates, and such busyness can be absolutely unsettling and surreal. So much so that a host of emotions can spring up from such insensitivity..... specifically sadness and anger come to mind. 

While talking to Peter last night, he mentioned how helpful it was in the beginning when we spoke and told our story at conferences and professional meetings. Back then, people WANTED to hear our story. I would have to say the MOST therapeutic thing a grieving parent can receive is a listening ear. Someone who understands that we have to tell our story over and over. I think by telling it and hearing it out loud, it engages us to come to terms with our reality. Otherwise, it just seems impossible to think that a once healthy child, could go through cancer treatment and then die. It makes no sense and frankly I am not sure it will ever make sense. But I appreciated Peter putting this into words and expressing the value of telling our story. 

However, as Peter was reflecting on the numerous conferences we presented at in 2008 and 2009, it made me pause. I paused because I said to him.... 'NO one wants to hear our story now.' Sure we continue to present on the work of the Foundation, but even the professional community is under some sort of delusion that we are all better now. That we have moved on and are stronger. Though it is important for first year grieving parents to tell their story, I would say that grieving parents throughout the continuum of grief need to be heard. I imagine professionals do not highlight people like Peter and me at their conferences because the truths that we would speak are overwhelming. Meaning the reality would be too scary to hear for parents who are new to grief, and certainly daunting for any professional to hear.  Daunting because providing support to a bereaved parent is not a short term endeavor. It can't be, because of the nature of the loss is not natural and unfortunately never goes away. Instead you carry it with you everyday and old wounds always get reopened at holidays, when the school year starts and ends, graduations, life events like religious ceremonies, college, vacations, marriage, and the list goes on.  



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