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 30, 2022

Tuesday, August 30, 2022

Tuesday, August 30, 2022 -- Mattie died 674 weeks ago today. 

Tonight's picture was taken on August 5, 2009, the day after we learned Mattie's cancer diagnosis was terminal. That day Mattie was entertained in clinic, while Peter and I met with his doctor. I will never forget that meeting. Mainly because we think we are living in the 21st century with access to top notch medicine. But the sad reality is medicine is limited when it comes to cancer. It was almost impossible to rationalize that there was NOTHING else we could medically do for Mattie. In one day we went from finding a cure and trying to be hopeful for a future, to accepting that we had to make tough end of life care decisions, because Mattie was dying. Pictured next to Mattie was Roxanne. Roxanne was a traveling nurse from Florida. Typically I wasn't a fan of traveling nurses, but Roxanne seemed to have great insight and compassion immediately upon meeting her! Mattie took to her, as he really was a shrew judge of character. 


Quote of the day: At the end of the day, whether or not those people are comfortable with how you're living your life doesn't matter. What matters is whether you're comfortable with it. ~ Dr. Phil


I literally dragged myself out of bed today and pulled it together. Peter is leaving for Boston tomorrow for a week, and I will be balancing the daily routine alone. I try to manage all of it myself, as Peter is busy, but unfortunately I really can't do it all alone, so I am learning! For the past several weeks, Peter has been running all the chores and has taken on Sunny's cancer care and of course caring for Miss Indie. So he will be missed, but it is important he have this time with his parents and celebrate their 60th wedding anniversary. Normally this would be something I too would attend and Sunny and Indie would be in tow. Since November of 2021, I have done nothing but solid caregiving. 

Today, Peter drove my mom to Georgetown for a hair appointment. This is about a 40 minute drive with traffic. So that is 40 minutes there and 40 minutes back home. I was grateful he took this on, so that I only had to pick her up when she was done and come home and not make the trip twice. When Peter dropped my mom off, he called me immediately. He wanted me to know that she walked into the wrong salon and therefore I had to figure out how to rectify this as he was driving. Georgetown is a busy place and it is hard to find places to park and even lay by. Peter dropped her off about a half of a block away from the salon, but my mom walked the other way, away from the salon. This surprised Peter, as he isn't with my mom by day and wasn't aware of the extensive nature of support she needs. She needs as much support as my dad, perhaps in a different way, nonetheless, I can't leave either of them unattended. Thankfully my mom answered her phone and I got her turned around and to the right salon. My mom has been at this salon for months now, so it wasn't a question of it being a new experience. 

While my mom was at the salon, I helped my dad do his walking routine and brain exercises. Then I had about an hour to myself to get things done. I called the neurologist office because I still did not get my mom's results back from her transcranial ultrasound that she took on August 10. Fortunately the person on the phone was very helpful and immediately uploaded the results to the portal, so I got to read through them. I certainly don't understand everything, but I understand enough to know that there is a vascular issue that is either causing dementia or Parkinson's. I haven't discussed this with my mom yet as I am waiting for her to do a two hour neuropsych assessment in September. But I can't wait to get answers! I want it now, and it seems like I am waiting months to get something definitive. All I know is she is teetering around, unsteady on her feet, and has good and bad days. These symptoms have come on very quickly, and show no sign of improvement with physical therapy. 

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