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

July 23, 2014

Wednesday, July 23, 2014

Wednesday, July 23, 2014

Tonight's picture was taken on July 23 of 2008, the day Mattie was diagnosed with cancer. This is a day Peter and I shall never forget and today marks the sixth anniversary of this event. But like all anniversaries, as time moves on, so do the people who shared this moment with us. Time may heal the wounds of everyone else around us, but it hasn't healed ours and as people forget it only exacerbates how we feel. 


Quote of the day: Oh, sometimes I think it is of no use to make friends. They only go out of your life after awhile and leave a hurt that is worse than the emptiness before they came.  L.M. Montgomery


On the anniversary of Mattie's diagnosis, it seems appropriate to reflect on the day that he was diagnosed. Two weeks before diagnosis, Mattie was enrolled in a tennis camp with his friend, Charlotte. In fact, I always credit this camp for identifying the issue before Mattie broke a bone, which is a very typical way kids with osteosarcoma are diagnosed. Mattie had never played tennis before, so it seemed very plausible that he injured himself in camp. Mattie complained of arm pain and he was having trouble lifting his arm. He couldn't lift his right arm over his head at all. While he was in the second week of camp, I had to attend a conference in San Diego. So I flew out to San Diego and Peter took off of work to spend those days with Mattie. It was during that time, Mattie and Peter designed two garden fountains for me for my birthday. Gifts that are precious and priceless to me and I still use them today! In fact while I am writing this book chapter this summer, I have the windows open to listen to Mattie's fountains!

While I was at the conference, I would call home daily. Peter would give me a report about Mattie's arm. I did not like what I was hearing and knew as soon as I got home, I was taking Mattie to the pediatrician. Which is literally what I did. I got home on a Saturday and on Monday, I took Mattie to be examined! Fortunately Mattie had a great pediatrician who took us seriously. Because the number one reason children's cancer metastasizes at the time of diagnosis is because it isn't detected early. Pediatricians are not used to screening for childhood cancers, and it is understandable because it is rare. After all, for example only 3% of children in the US are diagnosed with osteosarcoma, the kind of cancer Mattie had!  

Mattie's doctor sent us for an xray that day. Since Mattie never had an xray before or any kind of scanning, he was NOT afraid of the process at all. He hopped on up and complied. However, I was with the tech behind the glass partition and I could tell he wasn't happy with what he was seeing which perplexed me. He just kept taking xrays. But again, I thought nothing of it. He then escorted us to a holding room, which had other people in it, all adults. While in the room a phone rang. None of the other patients answered it, so I went over to get it. The person asked to talk to Mattie's mom, which of course was me. On the phone was the radiologist who proceeded to tell me that something was found on the xray and I had to go back to the pediatrician's office. But I did not like his tone on the phone, so I told him I wasn't leaving the room until he told me what he saw. It was at that point on the phone, in front of a group of strangers, that I heard Mattie had osteosarcoma. With Mattie watching me no less. 

When he told me Mattie had osteosarcoma, I had no idea what that meant, so I asked him for clarification. He told me it was a form of bone cancer and I asked him about treatments. Again, he was sketchy and told me to go see Mattie's doctor. I kept calm for Mattie's sake and somehow found my way back to the doctor's office with Mattie in tow. I then text messaged Peter to come to the hospital. Mattie's pediatrician seemed upbeat about the prognosis and treatment, while I felt my world was crashing in on me. Of course what she did not know at the time was this was only one of many primary bone tumors that Mattie had. With additional scanning, we learned that Mattie had a bone tumor in both arms, his right leg, and his left wrist, making Mattie's case HIGHLY unique and very rare.  

This may have occurred six years ago today, but for me, it may have happened yesterday! The details are very clear in my head. As I imagine anyone's cancer diagnosis day would be!

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