This Is MS Multiple Sclerosis Knowledge & Support Community

My wife started the 300mg Biotene experiment 2 days ago. We started slow with 1 100mg capsule Saturday morning, another 100mg Sunday morning, both after breakfast. Sunday night she came down with a serious case of diahrea. We don't know if it something she ate over the weekend (we both ate the same ...

Any information on this drug? Is it available in the US?

http://www.gwpharm.com/Sativex.aspx

We live on the west coast, my wife has had the CCSVI procedure twice, once in WA the other at Synergy. Neither produced any noticeable improvements. Both were very professional and seemed to be well run.

I know of a case of husband comes down with MS first. Then wife develops MS several years after marriage and 6 kids. then 3 of the 6 kids are diagnosed with MS. The boy was diagnosed at about 30, the 2 girls were diagnosed in their 50's. No MS in either of the husband or wife's family, Figure that o...

No intention of going it alone, or juggling hand grenades. Just seeking some alternatives. The stuff I am taking offer me no relief nor seem to slow the progression. Just frustrated. Our medical science is sort of locked in a box of accepted practices, I am wondering if there is anything outside the...

Ok, try this source. I agree about the last one, FOX news has to be the least reliable "news"? network on any subject. So, went to google and found this http://www.nytimes.com/health/guides/disease/parkinsons-disease/levadopa-%28l-dopa%29.html I am a whole lot less of a scientist than you,...

This is the article that caught my eye.

Just got me wondering (hoping and praying) there might be a connection.

http://www.foxnews.com/health/2015/04/2 ... -symptoms/

Baclofen upsets my stomach. I have 3 drugs prescribed. Oxybutryn, 1 day, Tizanaden 6 divided day, Desmopresen as needed, usually just emergencys. I am not sure what would happen if I quit taking all of them, but as near as I can tell, they are doing nothing. By the way, I have primary progressive. N...

I have been reading articles about the use of L Dopa to relieve some of the spasticity caused by Parkinsons. My main MS related issue is the spasticity in my legs. Bad, getting worse. None of the "drugs' I have been prescribed help in any way. Has anyone tried L Dopa for spasticity relief?