What a lovely weekend … my younger daughter, son-in-law and two lovely granddaughters came to visit us for a few days. We haven’t been able to do this since before Covid, and my Myeloma diagnosis. That’s 3 years plus, and it was absolute wonderful (and quite emotional).
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DAY 207🗣️🥱
Hottest day of the year so far 🥵 I’ve sent a request to my Consultant, via my support team, to request that he considers swapping Rivaroxaban for Apixaban. Apparently he’s on leave at the moment 🙄.
DAY 206🙂
DAY 205😴
DAY 204🗣️🙂
I am a bit tired of all this chemical stuff, and wish that there was a more sophisticated treatment … but I’m glad and grateful for what’s available right now. Today I was out with Mandy, and called in to have coffee with Max. Suddenly I was being complained to, for not keeping track of… Continue reading DAY 204🗣️🙂
DAY 203😴
DAY 202🗣️💊
After a week off … it’s back on the Lenalidomide again today 🫤🙂
DAY 201🗣️🙂
Really enjoying these warm sunny days – BUT tomorrow I must start taking Lenalidomide again (after a week’s holiday) 🙄