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

April 19, 2023

Wednesday, April 19, 2023

Wednesday, April 19, 2023

Tonight's picture was taken in April of 2009. Given that Mattie was wearing clothes, and not pajamas, I know that this had to be a hospital admission day! Mattie refused to wear clothes once admitted to the hospital, and I did not fight his request. That evening, the fabulous musical duo of Jerry and Nancy came to visit us. They were playing a musical game with Mattie, in which he had to move his body to the music. For the most part, Mattie did not like the volunteers and did not let them even come in his room. But there were a handful of people Mattie did enjoy seeing despite how he was feeling. What I do know was singing along with Jerry and Nancy made all of us feel a little better. 


Quote of the day: In order to write about life first you must live it. ~ Ernest Hemingway


It is 6:45pm, and I feel like I went four rounds today. For no particular reason other than the simple daily tasks I perform. I got up early because I had to get both of my parents out the door by 9:15am. I can't tell you just how challenging that is to accomplish! My mom especially can't manage early mornings. My dad frankly doesn't know if it is morning or night! 

I haven't been providing nanny camera updates, but my dad is still up and down at night and spends practically 90 minutes or more sitting on the toilet. Watching my dad's daily decline is beyond depressing and as he slips further and further into his cognitive fog, I feel that in a way it takes yet an unrecorded mental toll on me. 

This morning, I went back to the pulmonologist's office. This time, it was for an appointment for my dad. He had to undergo a breathing test, which he did not like one bit. Ironically in 2005, my parents sold their house in Los Angeles and  relocated to Washington, DC to live closer to us. They lasted here three months and then returned back to Los Angeles. My dad at the time was having issues with the cold weather and was coughing non-stop. They told me the pulmonologist recommended that they go back to living on the West Coast for my dad's health. Since I wasn't part of this dialogue, I just accepted this pronouncement. 

Now that I am older and wiser, I realize that most physicians probably wouldn't tell a patient such a thing, particularly because physicians understand the value of having family nearby as their older patients age. So now looking back at what transpired in 2005, I am furthered bothered by my parent's decision. After all, this was the time they could have spent with Mattie, watching him grow up, and be a part of his and our lives. Certainly if they had remained living here with us in 2005, it would have made this transition now much easier. Because they would have potentially made new friends, got engaged in activities, and learned to drive and navigate around our area. Now it is too late, and instead, I have become everything from nurse, cook, housekeeper, coordinator of activities and appointments, and chauffer. 

The funny part about all of this is my dad got an excellent report from the pulmonologist. Certainly his lung functioning isn't great, but given his age and the fact that he is hunched over, this is no surprise. Nonetheless, the doctor wants me to schedule a CT of my dad's lungs so we have a baseline report, in case he should get ill or something arises. Now trying to get my dad flat on a table for a CT scan will be EXTREMELY stressful but yet another thing I will have to confront and manage. 

After my dad's appointment, my parents wanted to go out to lunch. Eating has become more of a chore than a pleasurable experience for me. My dad has two modes when eating.... one which entails needing constant support and supervision and the other is THIS! Completely asleep and disengaged with the world. Depressing I tell you!


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