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It’s a blood test day, and I’ve been slightly worried in case (like last time) my kidneys are playing up ……. BUT ……. I’ve just found out that EVERYTHING IS OK The Lenalidomide is affecting my fingers slightly, but exercises like this help I feel very very lucky

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).

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 .

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

After a week off … it’s back on the Lenalidomide again today

Really enjoying these warm sunny days – BUT tomorrow I must start taking Lenalidomide again (after a week’s holiday)