DAY 208😊🥳

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).

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 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 201🗣️🙂

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