I’ve just been told I’m going home tomorrow! I feel as well now as I did when I came in here, so I can only imagine that things will get better and better as time goes by. Years of drugs and chemo take their toll. This procedure will give me the best possible chance of having some long drug-free time.
I do feel tired, but that’s because my HGB hasn’t returned to normal yet, and there was that high dose melphalan a couple of weeks ago. I’m sure it takes time just to get over that assault.
When I get home, I’m starting a new life. I’m going to take good care of myself and make it as difficult as possible for the myeloma to come back.
Oh! I get this catheter out tomorrow! That alone is worth some celebration.