I had a few good perks right away , too. The first day, I could stand right up without holding on and my balance was much better. Before LDN, I couldn't close my eyes without falling over....after LDN, I could, without losing my balance.:)

I was already SPMS, so it didn't go back and wipe out the permanent nerve damage, already done, but I think, it sure did keep me from getting worse.

Like Martha would say.."It's A Good Thing" :D

Worth a try for anyone IMHO!!:hug:

Miracle for me, too. I have been on about a year with no side effects. I, also felt results immediatly. Started at 1.5 and now I take 3, nuero says that is high enough but I wouldn't mind trying more. I have more energy and less pain, what a relief it has been. My ins doesn't cover it but it is very inexpensive. I can get 5 months worth at a time from Skips so that saves on postage.

ive only been on it for a month or so but the first day after taking it the cold numb feeling in my feet was gone! if for that alone the LDN would be a bargan at twice the price

I just started taking 1.5 mg LDN this past week. Lucky for me, Skip's is fifteen minutes from my house. I was shocked at the price - $9.95 - what a deal! I am so encouraged by everyone's testimonials. I am thinking positive!

You're all making me jealous!!!


I tried to get the PA at my doctor's office to write me a Rx yesterday. She wouldnt do it...said she didnt want to step on my neuro's toes. (step on them! geeze, someone give me some LDN!!!)

I'm asking my neuro again when I see him later this month. If he thinks it's a placebo, then what would the harm be in writing me a Rx??

Im here and on LDn I post in the sticky thread above this thread on top

Pals would you like to take some LDn at my house ....hmmmmmmmm lol

it is unique, it took a couple days then I waited one or two more before I said something, there was a noticeable diff for me

step on those toes! stomp stomp stomp, then maybe he can feel something like neuropothy in his feet too.
im not sure where you're at but there is an LDN advocate who keeps a list of DRs willing to rx LDN. plus theres a list of DRs who will do a phone consultation and write you a script, and then fax it to reputable pharmacist like skips. people kept pointing out to me that LDN is an off lable script, its not FDA indicated for MS. guess what.... niether in the neurontin, or the immuran. and now they're both hugely popular drugs for MS