I can't believe it has been a full month since I blogged to let all of you know how Caleb is doing. He was doing great. Chugging along in Long Term Maintanence with awesome counts at each check. Had his monthly IV chemo, took his daily chemo pills at night & got his usual Spinal Tap with chemo at the end of March. He has been having a blast being able to go to school two days a week, play in his baseball games, hang out on his new swingset & celebrate Easter with Egg Hunts and brunch with family. .... Then we hit another bump in the road ... Caleb developed pancreatitis yet again :( Last Friday Caleb played in a baseball game & came home. He was super hungry but I had to hold him off from eating because he needed to not eat before his chemo pill. That ended up being the best thing for him - having him NOT eat because the pancreatitis was brewing. The week prior his labs showed his lipase level (pancreas enzymes) were at 10. That is normal range. After sleeping
This blog is dedicated to me, Caleb Blaise. I was diagnosed with Pre B cell Acute Lymphoblastic Leukemia on March 13, 2012, when I was 4 years old. On January 30, 2017, I found out that I relapsed. After a month of induction I was put in intermediate risk and need a Bone Marrow Transplant. This is my journey...Fight Strong.