Heard from Springfield today - my new prescription will be available Tuesday afternoon (26th) when I go in for the next set of bloods. So we start on Wednesday.
If things go as usual, I'll have to wait while a pharmacist brings the stuff over from the main building and goes through all the pills, how I should take them, side effects, etc. That'll take nearly as long as a Zometa drip would, and will bring me into prolonged close (well, 2m) contact with someone from the main hospital building. And yet I can't have Zometa once a month because "it's all about minimising the time in the hospital" as someone from MyelomUK told me when I phoned them about this. Doesn't make a whole lot of sense to me.
28/04/24 Cement!
An early morning trip to London last Thursday morning, and straight into anaesthesia and the procedure. I gather it took a bit over two hou...
-
The first frost of the year on the flat roof at the back of the house this morning: Bright and sunny at the front, with the maple doing its ...
-
I got into the habit of blogging at night after my shower but now I always seem to have other things to do. If it isn't the Facebook gr...
-
A bit of a complicated day yesterday. Speaking of "normal life", my plan for the morning was to make a loaf of soda bread with the...
No comments:
Post a Comment