This Is MS Multiple Sclerosis Knowledge & Support Community

I am suppose to pick an ABC or Ribif in 2 days. Diagnosed by MRI 2
weeks ago after bad optical Heuritis attack. Have been reading
everything on Vitmins, Nutrition, exercise, the main stream MS stuff
and came across LDN. Read as much as I could (still can't see well
in left eye).

All I have read so far about LDN sounds almost too good to be true.
Have any of you experienced or heard of LDN not working on MS at
least as good if not better than ABC or R?

Also interested in communicating with anyone in Ontario Canada (near
Toronto or Hamilton best)about Docs, treatment, sources of LDN etc.

I personally have never seen any negative responses to LDN in the few months I've been reading about it.

I myself have been on 3mg LDN capsules for 2 weeks now and feel better already. My pain has virtually gone, I am walking easier and sleeping all night without having to get up to use the toilet. I don't expect to be cured as it's not a cure but if it halts any more progression, then I'll be very very happy.

I obtained my LDN from USA.

Regards
Andy

Andy, it's really great to see you getting on so well. Please keep the site posted on your results, because you are one of the members for whom we have a very complete picture of your before and after status.

This will of course be very helpful to people like alan who are wondering whether to undertake LDN treatment or not.

Thank you for the info Wannabe. I've just been on there and had a look. I noticed there were only 3 people out of 42 people that reported no success with LDN and that you were one of them. I'm sorry to hear that.
I hadn't been on that website for ages and it was good to look through it again.
I wish you well for the future.

Regards
Andy