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Nice to hear that others are doing well with LDN. I've also been on 4.5 mg. for 3+ years with zero disability and no relapses. Full disclosure - I also take copaxone. However, the compounding pharm ...

I've been taking LDN for 3+ years now...no progression, no MS symptoms. Unlike the approved MS drugs, LDN is cheap, safe and is proven to do no harm. Is it responsible for my long remission (I also ...

Nick, thank you for posting. I'm an infrequent poster, but avid reader on these forums. I've also spent a lot of time on DirectMS and truly appreciate the work that Ashton has done on behalf of MSer ...

Hello,

I'm a pretty infrequent poster, but avid reader on this forum. This revimmune treatment seems to be very promising to say the least. I was diagnosed in 2005 but had symptoms going back to ...

I'd tell her to stick with changing bedpans and taking blood pressure and leave the diagnosis to the doctors.

I was diagnosed positively with RRMS and had no banding. Just a couple spots on my MRI and some numbness in my leg. Diagnosing MS seems very suggestive in my opinion.

Glad you brought up this topic. The incident that led to my diagnosis 2 years ago in July followed a week of pretty intense running in the summer heat. I've had no relapses since, but running and/or ...

Hang in there Frank. Symptoms are known to be more pronounced when first starting LDN. Stick with it and hopefully you will level out in a week or so. I've been on LDN 4.5 mg. for a couple years no ...

PTWO, thanks for posting. It's little stories like yours that keep me injecting daily.

thinkingoutloud86, I sincerely hope we go for Peterson (we have bad luck with first round QBs!)

I do the same. Shouldn't effect how C works, as long as you inject in fat.

I've been on C for a couple years and think, while not perfect, it's better than the alternative immune-suppressing drugs. Also keep in mind that it takes at least 6 months before copaxone has any me ...

I've recently had a couple bouts of swollen glands with accompying dull pain - usually on one side of my neck/jaw. I did a quick google search and found that this is one possible side effect of GA. ...

Teva/Shared Solutions studies clearly show that copaxone doesn't even start making much of a difference until the 6-month mark. After that however, it appears that efficacy continues to increase the ...

Why was my message deleted anyway?

J