My treatment with Daratumumab has been severe and and yet not working. This blog was supposed to be about the transplant. It is likely that these drugs, to get my myeloma under control, my not get me to the transplant. We should know more this Tuesday after another appointment with my oncologist.
We know that many reading this blog either care or just wonder how I am doing with my stem cell transplant. We know that perhaps you may like to call and check on my progress, but realize we may not be available to take your calls. So we have prepared this blog to give, it is hoped, a day-by-day posting of how I am doing. I will try to do the posting myself every day. It will give me a focus, a goal, and help me summon the energy to do something productive. On the days I can't post, Rose will be doing the posting. The month of August is full of tests, education classes, diagnostic studies, biopsies, and a minor preparatory surgery. The stem cell transplant itself will occur over three days, September 3-5. The infusion of my MILs (more on that below) will occur over two days, September 7 and 8. After that it will be months of monitoring, testing, and recovery. We expect to be living in hospital connected housing in Baltimore for 4 to 6 weeks starting around August 26. Then
Hello everyone. This is Rose blogging for the first time. Today we had a pleasant drive (I like sarcasm) downtown in a bunch of rain for Bob's Pet Scan . No it's not about the cat. Bob did not have any carbs for 24 hours and he was a bit cranky. He says not-- but I was there.We are currently at home and eating lots of carbs (pound cake). All went well at test.
Hahahaha
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