It's not an FDA approved DMD but it sort of works that way, for me.

Thanx Sally. Is it a pill or shot? This isn't that chemo like thing is it? Im just having problems with my dmd and I see so many taking LDN I just wanted to know if it would be worth it to ask my neuro about it. Also see if it has a financial program to help pay for it like copaxone and them do.

I don't think it is too expensive and the good news is from what I have read it seems to be well tolerated by people with MS.

Things to consider is it likely wouldn't be appropriate for someone taking opioids for pain and I think I read that at higher doses there can be some liver issues but I'm guessing the Low Dose part of LDN means it isn't a high dose.

It's a capsule filled with pure naltrexone powder and a fast release filler. It must be compounded (Skips Pharmacy does it for me)

The Chemo med you're thinking of is Navatrone and it is a chemo drug. LDNaltrexone is not a chemo drug. There are no lasting or detrimental side effects to LDN...unless you are allergic, which is always a possibility.

My 4.5mg capsules cost me about 15.00 per month. Not all insurance will cover it, since it's used off label for MS, but some do. The cost is low though so it's pretty affordable.