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 5, 2019

Thursday, December 5, 2019

Thursday, December 5, 2019

Tonight's picture was taken in December of 2005. Mattie was three years old and we took him to Boston for Christmas. Regardless of the weather, Mattie was out and about in it. He did not get to see a lot of snow in Washington, DC, but he made up for it in Boston. 


Quote of the day: Losing your head in a crisis is a good way to become the crisis. ~ C.J. Redwine


Tonight's quote is spot on. I would say that with any life threatening medical issue, a crisis ensues. Especially for family members. In fact, it is hard to sometimes think rationally when placed in a very difficult situation, and you are worried that the person you love maybe dying or in pain. However, I would say that Peter and I now excel in crisis mode. We do because Mattie's 14 month ordeal with cancer, pushed us over the edge many days and nights, and forced us to keep it together, make smart decisions, take in information, but also to live one day at a time. In a crisis, living moment to moment is the best way to cope. In fact, when you are so mindful to the present moment, it is actually an amazing experience. You become solely focused of making the most out of the present. It is freeing to some extent, because you are not worried about what will happen at 5pm, or next week, or next year. Something we humans are programmed to do.... be forward looking.  

Though I remain in Washington, DC and Peter is in Boston with his mom, I am virtually there. Peter keeps me posted about everything and in the midst of the information he sends me, I do research into the issue or resource. Today's issue was trying to press the hospital to get Barbara on the surgery calendar. The operation rooms seem completely booked up this week and they view Barbara's case as stable. Rather hysterical, since she is immobilized and unable to move because movement could sever the spinal chord and cause paralysis. Peter was determined to put pressure on folks today and though I don't think Barbara will have surgery tomorrow, the hope is she will early next week. 

The big issue today is discomfort and the fact that Barbara's arm is swelling. It is swelling because of the IV in her arm. Infiltration occurs when I.V. fluid or medications leak into the surrounding tissue. Infiltration can be caused by improper placement or dislodgment of the catheter. So now she is scheduled for a procedure tomorrow morning to get the insertion of a PICC line.

A peripherally inserted central catheter (PICC), also called a PICC line, is a long, thin tube that's inserted through a vein in the arm and passed through to the larger veins near one's heart. A PICC line can help avoid the pain of frequent needle sticks and reduce the risk of irritation to the smaller veins in the arms.


Meanwhile, we are trying to focus on next steps and how things will proceed after surgery. With the given that we hope the surgery goes smoothly and effectively. Once Barbara is medically stable, the therapy team at the hospital will come visit her. She will be assessed by a physical therapist who will get Barbara up and moving and will evaluate how she is doing and basically what the next steps are in her care plan. A plan that could involve going to an acute rehab center (which is a more intensive option, as acute care will give her 3 hours of physical therapy a day for 1-7 weeks, with the goal of transitioning her back home) or a skilled nursing facility (which is in essence a nursing home, where access to physical therapy will not be as intense or frequent and her long terms goals may look different). Naturally either option is a possibility, it just depends on how well the surgery goes and Barbara's ability to move and manage pain. Given that she has been immobilized for a week is not good, because muscles can atrophy and this can impact her recovery timeline. 

Of course I did not mention Peter's dad in all of this. But managing his needs and where he should be living while Peter's mom in recovering is something else we are also juggling. Which reminds us once again, that when one person becomes ill, it affects an entire family system.

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