why isnt there help on here for multiple sclerosis sufferer's like myself, there's lots of questions i'd like to ask MS sufferer's too, ____

[Faversham1970]

[Tiny1966]

You might go to Team Inspire website and sign up under the ms and scleroderma areas. Many people are on there and maybe you could find some answers.

[Hidden]

I don't have MS - or rather haven't yet been diagnosed with it but have been searching for answers to neuro symptoms. I do have RA and Hypothyroidism and probably have other mixed connective things going on. But nonetheless want to rule out MS also. So I joined the MS society forum and have been getting great responses. However its tiresome not being able to do this via HealthUnlocked because of course the format is different and I can't edit or delete in same way and don't see questions or posts in the context of other conditions either.

I think the answer lies with the MS Society - who could join HU if they chose to presumably? so they would be the best people for you to ask about this I believe. RArebird

[moimoi]

Hi

I have MS and Raynaud's but only look at this site for info on Raynaud's. If this disease is not in the family then it may be as a result of MS drugs. A discussion with your neuro would help on this but I am unsure how having a link would assist.