This Is MS Multiple Sclerosis Knowledge & Support Community

Hi John

What dose of simvastatin do you take and what effects has it had on your MS?

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I havent tried lipitor but I have to confess thats one treatment option I dont really know anything about. Is it meant to stabilise the MS or have people had symptom improvements as well? Also, is it available in the UK?

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Im just wondering how many people out there (well on this board at least lol) have tried aimspro and what their experiences were. Im trying not to get caught up with the miracle stories floating about but Ive come to a point where I feel that I have little choice other than to at least try aimspro. ...

I havent actually been to this messageboard for a while so was quite suprised to discover someone from here had sent me a PM. Didnt know what to make of it but then I realised that it was pretty much identical to what had been said here. Like Bromley I have no idea what the Witters agenda is but wha...

Hi Deb This is pretty interesting stuff! Its reasonably well known that people who come from different areas are more or less susceptable to MS, presumably because of differences in diet and different exposures to vit D from sunlight. Id never really thought much about the potential differences from...

Hi Becky That is another really weird coincidence although I dont really know what it means! I live in England, just outside London, and my first ever MS symptom was also numbness in my legs and that happened just after I flew to New York for a holiday with my family. I had never really associated t...

Hi Becky Im really glad your family are so supportive. It must be awful for you all that both you and your mum have to deal with this but like you say, in some ways it makes things slightly easier in that they already know what theyre dealing with. This genetic connection is a funny one though becau...

Hi Arron Thanks for the lovely warm welcome! :D I had already been thinking about posting about my experiences with LDN and other treatments. As I said before Im cautiously hopeful about my antibiotic regimen and will certainly post about this when Ive been on it a bit longer and will hopefully be a...

Hi Sheila Thanks for the reply. I’m sorry to hear of your daughter’s dx. I can remember how I felt when I was dx at 18 and like your daughter I tried to block it out and just get on with my life. If I’m honest then I’ve only really come to terms with it in the last couple of years but mainly because...

Hi, I’ve been lurking around the site for a while now and there’s some excellent information here. I’m 23 and was diagnosed with MS 5 years ago. After a bit of a rough patch about 18 months ago I think I have finally found my feet again (in a manner of speaking :D ) and got things under control. I’v...