I posted before Christmas about my symptoms. After MRI and lumbar puncture I was diagnosed with MS last Friday. I am still in a bit of shock even though I half expected it since I thought my initial diagnosis of a stroke was wrong. However what has been on my mind all weekend is that when I asked was their any medication I could take the neurologist said NO. He said come back in 6 months and would send me details of an MS nurse I could call if I got anymore symptoms to by pass my GP. When I asked what sort of symptoms to expect he didn’t really answer. I have read on this website that their is medication for RRMS but not PPMS, he didn’t tell me anything abut what type. I now feel I should have asked a lot more questions. I was thinking of going to my GP and asking about medication and for a possible second opinion. Can anyone advice me on what I should ask my GP in terms of medication?