"Please fix me Doctor," he said during his 4 am blood draw to the night shift nurse. Those words broke my heart even more than it already is. This is something Caleb & I have become accustomed to over the past few weeks. I usually know after that I'm up to start my day. I'm worrying till the Doctor does their rounds to hear his numbers and even more anxious lately because of his pancreatitis. The numbers have been decreasing, which is what they want them to do. They said he's made progress over the past few days that at times it takes people weeks to accomplish. That shows me how strong my little boy is. But he still has a lot of progress to make with the pancreatitis and before his treatment can resume. Still this is so hard. Seeing my little boy in pain and I am helpless. I'd do anything for it to be me laying on that bed instead of him. 11AM Dr just came in to tell us his numbers and talk to Caleb. His numbers dropped almost back to normal. That wa
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.