I was diagnosed with MM in March this year after arriving at A&E with Pneumonia after a visit to a walk in centre for a cough.
I am just ending course 3 of VDT and have no date yet for SCT although I have an appointment with a consultant after course 5 so I may find out then.
Apparently my blood is responding well and my usual consultant is always amazed how well I am coping. But this is the easy bit isn’t it? Just taking the tablets/Velcade and injecting myself with the Clexane.
I’ll be 51 in the summer so still fairly “young” I guess.
The posts here have been interesting and useful.
I’m, quite a hardy person but the S&D might be the thing I fear most. Before MM I was rarely actually sick.
I’m certainly in the right place here to find out what it’s really like.