Mattie Miracle Walk 2023 was a $131,249 success!

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

September 7, 2014

Sunday, September 7, 2014

Sunday, September 7, 2014

Tonight's picture was taken in August of 2008. Mattie was pictured with JJ, our resident Jack Russell Terrier. Peter and I saw JJ tonight. JJ was just a puppy when Mattie got to know him and they practically grew up together. In a way it was as if Mattie had a dog without having the responsibility of maintaining a dog! Mattie got to walk and play with JJ whenever he wanted to and they were close buddies. When Mattie died, JJ was literally depressed. For months JJ would come down and visit me and would be looking for Mattie. In fact, JJ kept Mattie's sandals for the longest time right by his doggie bed and he refused to part with them. The funny part is JJ took these sandals from Mattie. He literally pulled them right off Mattie's feet and carried them home with him one day. He wanted a keepsake of Mattie's, and I was fine with it because the sandals were old and I wanted Mattie to actually transition to his new sandals (this sandal issue occurred before Mattie developed cancer, but JJ held onto the sandals for YEARS!). JJ became VERY attached to those sandals! They provided him some sort of comfort especially after Mattie's death. Who ever said that animals don't grieve, is VERY wrong!

Quote of the day: A tormented mind wants to forget, what a broken heart will always remember. Anthony Liccione

Peter and I worked at home today. I spent the morning designing a shadow box filled with Mattie's art work. This was art that I had taped up all over our kitchen. When we painted the kitchen in August, I took all the art down and decided to frame it. 




This is a close up of the shadow box. I had never used a shadow box before but I consulted with someone at AC Moore on Friday who was super helpful and he understood exactly what I was trying to do after I showed him some of the art pieces. What you see here is a combination of art from Mattie's preschool and kindergarten classes. Also note the star in the lower right hand corner. That was a star we created together while Mattie was battling cancer at the hospital. I will never forget that night we drew that star! It was May 30th and Mattie was HIGHLY agitated. He wanted to draw a star but he did not know how to and this notion sent him OVER the EDGE! I mean he went bonkers! You wouldn't think something so trivial could upset someone so, but Mattie snapped. I knew that what was troubling him had NOTHING to do with the star, but the issues were getting displaced onto the star because that seemed like a safe place to put them at the time. In any case, patiently I worked with him to generate this star. It was such a nightmare of a moment that once the star was completed I decided to always keep this star because I honestly did not know if either one of us were going to survive the anxiety, fear, anger, and hostility of that hour. We both got a gold star that night and as always we found a way through this difficult time together. So to me the star had to be a focal point of this art piece. 

Peter and I created this Mattie wall this weekend and we are proud of it! Our kitchen wall looked very different about two months ago! This is now a beautiful tribute to Mattie. Which is well timed on his fifth anniversary. I end tonight's blog with a reflection back in time to September 7th of 2009...... on the eve of Mattie's fifth anniversary of his death. 












Blog Posting from September 7, 2009:

Our day started out with a sad scene. Mattie's fish, the special gift my parents got Mattie yesterday, died! I knew this was an ominous sign today!

Mattie had a very difficult start to the day. His blood pressure has been dropping and is dangerously low, and he had a coughing fit, which left him gagging and unable to catch his breath. He was deathly scared and when Dr. Shad and Kathleen (Mattie's outstanding HEM/ONC nurse) saw him, they mobilized into action. In reality what happened next moved so fast, it was almost a blur. Mattie was in minutes being pumped up with pain medications and Versed (for anxiety). Now that I can reflect on the morning, I am so thankful we are in the hospital. Because Mattie couldn't possibly be cared for humanely at home based on the symptoms he is presenting. It is ironic that Mattie seemed to know this and had a better feeling for his condition and his decline than Peter and me. Once Mattie received all this medication, he asked if I could snuggle with him, which I happily did. However, Mattie is being kept in a comfortable state, so therefore he really isn't talking and spends a lot of time sleeping. The Mattie we knew is NO longer!

Dr. Shad came to the hospital early because she felt that the end was near for Mattie. She stayed at the hospital all day and we had a great deal of support from the HEM/ONC nurses (Kathleen, Tricia, and Miki). We were also surrounded by our THREE angels today: Ann (our angel of HOPE), Linda (child life specialist and our angel of caring), and Debbi (our sedation nurse angel). They all came to support us and Mattie. My parents sat with us as well and this whole scene of watching Mattie slowly dying is heart wrenching and at the same time surreal. How can my healthy, active, bright, and spunky son be dying? I see it happening, but it is SO hard to accept!

Eating wasn't easy for me today, but I had a lot of people around making sure that I actually did. Ann took me outside to eat something, and I needed that break, because sitting and watching death, and the death of Mattie almost takes your breath away.

Peter and I spent a great deal of time today monitoring Mattie and also talking with him. In fact, when everyone was visiting, we had solemn moments, but also moments of laughter. Laughter because Mattie was a very humorous fellow! Kathleen told me that the nurses love Mattie, but they also love us. That Mattie has left a legacy and his love will always live on within us. Mattie did not go to school this past year, but in a way he went through the hardest school of all. The school of cancer, which shows you the most vulnerable and raw sides of life. In fact, it has left me so raw, that I emotionally I am not the same person anymore.

Mattie's nurses all came in tonight at their shift change to kiss and say good-bye to Mattie! It was very touching. Kathleen told me that even though Mattie isn't awake, he can hear us, and that he worries about us and is holding on because he knows we do not know how to say good-bye to him. So tonight, Peter and I mustered the energy to talk with Mattie together. We told him we loved him, were proud of him, that he did a great job fighting the cancer, but now he is in control and can decide when he has had enough and wants to rest. That we will be okay, and that we will always, always love him. We told him that we couldn't have asked for a better son and that he was going to a place where he would be at peace, able to run and play, and meet up with family members and friends who love him but whom he has never met. My sign off tonight, as it always is to Mattie was, "Una Moon loves Mooshi Moo." Mattie coined the nickname, Una Moon for me, and he is my Mooshi Moo.

It is hard to say how long Mattie will be with us. It could be hours or days. But it is no longer weeks! His whole disease has been one crisis after another. His cancer required three major surgeries, 11 months of chemotherapy, and intensive physical therapy. However, there was NO break between treatment and recurrence. In addition, even death is not an easy process for Mattie. It has hit him hard and hasn't given us the chance to talk as a family. This year has left me shell shocked, questioning everything about life and the future, and the true purpose for our lives. Mattie is being kept comfortable, which is a blessing, because the sounds coming out of his body and lungs are frightening. I doubt we will sleep at all tonight! I am saddened that Mattie will be unable to go on a planned beach trip that the Lombardi Clinic arranged for us on September 13 through the Foundation, Believe in Tomorrow. It wasn't meant to be clearly. One thing I do know is I hate Osteosarcoma with every fiber of my being. I have seen Mattie suffer way too much this year, and this suffering will always remain a part of us.

No comments: