Hi everyone,

I came across this site while googling some treatments for MS.

I'm 30, F diagnosed 3 years ago and have RRMS...I was on copaxone for a year. It was painful (duh!) and whne I skipped a few doses while on a brief holiday or not being able to get my meds in time, I found that when I started injecting again - I got optic neutiris and other symptoms. I stopped taking it last Aug and have had nothing noticiable happen.

However, my recent MRI shows more lesions (quite a few) and a bunch in my cervical Vertebrae area which has be very scared.

I hate medication. I also believe my condition was brought on or at least agitated by the Gardasil vaccine and I am not a fan of MERCK (rebif) or many other pharma companies because I have researched the side effects of many of their drugs (including the deaths etc from Copaxone and I have experienced the dreaded shortness of breat, heart palpataions after it a couple of times)

I do not want to go on genilya or the other tablets that require ekgs, checks on various parts of the body because I don't want to put much more into my body and create more issues.

I'm not a hippie, I'm not a kook...I just think that I've done my dash and don't want to disrupt another system besides my CNS which these drugs seem to entail doing.

I've read about LDN but as someone who is poly-cystic I am apprehensive to look into something that would make more cortisol in my body.

Is there anything anyone can tell me?