Post Transplant Day 2

Nothing new to report today. The blood counts have started to drop but are all still within the normal range. A longer post tomorrow!

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Here We Go Again...Stem Cell Transplant Take 2!

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Melphalan Day = T minus 1

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Before the update, thanks to everyone who reached out with messages and comments. I read each of them to Karl today and we felt very uplifted. We were especially comforted by the comments from people who have gone through the multiple myeloma fight with their loved ones. A few tears seeped out when I read the comments from Jane W, Deb D, and Rosalind Y. Hugs.  Now an update. Last night Karl was started on iv fluids that will continue for at least another 24 hours. Last night was in preparation for the Melphalan, today is to counteract the Melphalan, and tomorrow is more of the same plus to keep him hydrated in preparation for his stem cells. But that's for tomorrow.  Today the focus was Melphalan, a chemo drug used to kill his old bone marrow, where his cancer was living and growing. It has lots of harsh side effects including wrecking havoc with the digestive tract from the top to bottom. The top includes potential mouth sores which were counteracted with special mouth wash, ...
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