Thanks for all the “Welcome” messages – you are a lovely bunch of people 😊
I’ve just had an appointment at Addenbrooke’s MS department. They are great people who actually told me to join you lovely guys, which I had done already!!
I have been given the option of going on Tecfidera. I am leaning towards trying it but was wondering what other people’s experience was on them?
I know there will be side effects, which I may or may not get, but how did everyone else get on with them?