10/13/2026
He may have lost his hair and most of his strength, but today, Carson wanted to practice for the homerun derby that Frostburg little league is hosting in his honor this weekend 🥹. If you ask Carson how he is, he will always respond with a little smile and say “I’m good,” even if he isn’t; he never complains about anything that he has to endure. Our last few days have been pretty uneventful, which is a great thing. Carson has had a week break since his last chemo infusion, so he is feeling pretty good right now. We are not taking any of these healthy moments for granted because we know that the next few months will bring so many unknowns. His bone marrow biopsy this Friday will determine next steps of his journey. We are praying so hard that he is in remission (or very close to it), so that he can move on to the first phase of immunotherapy, which is a 28-day continuous infusion; he will be admitted for the beginning, then come home with a backpack and IV pump that will run continuously through his port for 4 weeks. After a few rounds of the Blina, we will head to Pittsburgh to begin his bone marrow transplant process. I am so incredibly scared for that part of his journey because it is so risky and potentially life-threatening 💔. Carson is nervous, but ready to put this all behind him. He is truly so brave, though I wish he didn’t have to be 😢. This relapse journey is much scarier than the first time around. Please continue to pray that his bone marrow shows 0.000% leukemia cells on Friday. We also don’t have results from his spinal tap last Friday- I will keep you all updated. 🙏🧡🙏🎗️
I have had people ask me to post his updated wishlist, so here it is… and of course he added more sports cards; this is definitely a new hobby for him, but it gives him something to do & makes him so happy 🥹🧡🎗️
https://www.amazon.com/hz/wishlist/ls/1DB6VTUG4UOSN?ref_=wl_share