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

May 5, 2024

Sunday, May 5, 2024

Sunday, May 5, 2024

Tonight's picture was taken in May of 2007. That weekend we took Mattie to the Andrews Air Force Base Show. It was unforgettable. Mattie got to tour around many of the aircraft that were on display and then we got to see the Thunderbirds perform. The sound was thoroughly intense as they were flying through the air and it scared Mattie quite a bit. But overall, it was worth the trip and I am glad we did this adventure together. In fact, with Mattie there were many firsts for me, as the things he was interested in pushed me beyond my comfort zone. I credit Mattie for the person I am today....  for the courage, assertiveness, and tenacity that I developed while being his mom!


Quote of the day: The saddest thing in the world is loving someone who used to love you. ~ Unknown


After a full day of tasks, I took my parents out to brunch. We go out every Sunday to the same restaurant. Our server, text messaged me to let me know she was sick and wouldn't be there today. Typically that would cause me not to go the restaurant if Cheryl wasn't there, but I knew my parents were looking forward to going out, so I made the executive decision that we were going anyway. 

In the past, my dad could walk from the parking lot to the restaurant. He can't do this anymore. His energy level is quite low. So now, I pull the car up in front of the restaurant, I unload everyone and put my hazard lights on. I then take my parents into the restaurant and get them settled before parking the car. When I walked into the restaurant today, one of the managers greeted us. I told her that I knew Cheryl was sick and that she had to give us an attentive server. If not, it will be a bad experience for us and for the server. We worked with a delightful young woman today and she made it a very pleasant meal. Of course no meal is ever without trips the bathroom. It is a routine that I may never get used to or accept. But it is what it is when dealing with Alzheimer's combined with Irritable Bowel Syndrome. 

When we got home after brunch, I tackled changing the garden hose and trying to repair a closet door ball catch. I have just about had it with the old fashioned garden hoses. They are terribly heavy, they kink, they are hard to maneuver, and rolling them back up is a nightmare. So I literally absorbed the TV ad for the Copper Bullet Hose and ordered one. I tried it tonight and WOW, what a big difference. I liked it so much that I now ordered a second one. I will be doing a lot of gardening this summer and the work is hard enough, watering plants shouldn't add to the problem. 

As for the closet ball door catch, I naturally ordered the wrong one! So they have to be returned this week. I then pulled out YouTube and watched a video about how to remove a ball door catch from a door. I did it! I measured it and now ordered the correct part. We shall see when it comes in, whether I can actually install it correctly. 

The final thing I wanted to take on today was changing my gmail account password. I was alerted to suspicious activity on it. The problem with this is I am very leery about technology. It isn't my strong suit and just managing it brings about great anxiety. But I talked to myself and I said, if I can figure out finances, care give for two adults with dementia, fix things around the house that I have never done before, then why on earth can't I figure this out too. So I sat down, tried it, and accomplished that task. 

It has been eight months of self exploration. I have had to dig deep, develop confidence in myself to perform tasks that go beyond my knowledge, skills, and level of comfort. I take it one day and task at a time. 

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