Day +23

This is Bill's second day at home and he is trying to get used to the idea of being able to actually walk around and sleep in his own bed. He is still very shakey. The doctors say it will take a few weeks to get some strength back. Baby steps at a time. He goes back every Wed. to the clinic for blood work and to see the doctor. This will go on for several months. Dr. Selby said every visit is a mile stone from this point. His blood work will tell how he is progressing. I have learned to do his antibiotic IV which he gets every morning thru Aug. 7. I think this and all the medicines he is taking is what is so overwhelming. Jen and Nick came this weekend and with her being a nurse, she made sure I was doing the IV right. We're just taking a day at a time and hoping to gain strength each day and the donor cells to be working hard,