03/22/2025
It has been ONE year since Adam ended treatment! So thankful to report his one year scans show NO evidence of disease. He’s feeling really good and has very few side effects. His neuropathy is improving and we are hopeful that will eventually go away. We will now enter year two of scans and those will be spaced out to every four months. He’s loving college life, too! GBR 🌽❤️. And as rare as Ewing Sarcoma is, we met a new family in the beginning of their journey with ES. So many memories came flooding back for Adam today. It was really neat to watch these two young men interact knowing they each know exactly what each other are going thru. They have a bond of being a part of a club neither of them wanted to join. Their strength and resiliency is incredible 💛💪.
We are so thankful to continue to be surrounded by an incredible army of support and love this past year. I didn’t know what to expect when treatment ended and we were on our own. I can tell you it’s been scary to only see the doctor every three months…when we were used to three times a week. The week before scans is debilitating. The unknown is scary. Today I felt like I was having a heart attack because I was so nervous to hear the results. Scanxiety is real. And many times I wonder..how are we the lucky ones when I hear of so many cases of recurrence. Survivors guilt is real. I want to move on. But it hasn’t been easy. I am trying to accept that I shouldn’t just desire to move on. Instead I should work hard to accept the profound change this has had on us. I need to stop running but instead sit with these emotions and really feel. I was relying on “time heals all wounds” but life didn’t go back to “normal” as much as I hoped it would. It probably never will. Recovering from treatment has been an ongoing journey and the only way to heal is to feel. ❤️❤️🩹❤️❤️🩹❤️❤️🩹❤️