I don’t take drugs for my symptoms, but maybe I could but the side effects probably would affect my physio.
I notice a lot of people on here are married; this makes me feel a failure at 45!
As I need friendship; not just to go on about symptoms or drugs, that’s why I post. I notice female replies (as they can say what they want and be rude as they like).
Men get MS and it affects them in different ways! Just clarify that for people who do not understand.
To reply to some woman who answered earlier; first don’t take out your hubby on me; if I was not ill lately, I would go out as find staying in very difficult (find the isolation the hardest thing to deal with).
You no good at giving back; it all take on here!
To one message girl: I thought I said I was new to this area and knew nobody, so why you not reply?