Hi Martin,
I have MM and my wife has a blood cancer Polycythemia Vera. She has a forum which is extremely well supported and very supportive. This forum does not seem to be and people are left for weeks without anyone responding which seems very strange to me.
I was very lucky as I have been monitored by haematology for the the last 7 seven years. At first it was MGUS so I half knew it would become MM, no shock there when it was confirmed in October 2018 However treatment didn’t start until May this year. Unlike others I still have no idea of what “bone pain ” feels.
I don’t know if it is evening with you, for me it is 8.45 and I am off to do bloods for tomorrows consultant meeting.
Roger