something i got emailed from Dr Mercola's web page talks about adding some sort of super antioxidant(Alpha-Lipoic Acid) to the LDN to basicly turbo charge the effects

http://articles.mercola.com/sites/ar...e-Disease.aspx

there's a video clip too and Dr Mercolas comments to the article as well as 100 or so user type comments.

FluteMaker, I JUST came in here to post this!!

Not a member...couldn't read it..

just scan down the page - don't need to be a member -

Oops, duh.... Thanks..

i was reading it and it struck me much in the same way reading about the LDN did. its intriguing enough that i want to know more, maybe even try it to see for myself. the LDN has already gotten me the gift of having days where i feel normal. i still have bad days but i have more good days than bad.if this ALA can make that even better................

on a somewhat related note;
i did look into the colloidal silver too. i have a friend here in town who has been raving about it and the energy level it gives her. so she ordered her own 'generator' and makes her own.
she made me a batch a few weeks ago and i did give it a good fair try, but it seems to make my legs feel more tired than anything else('course my friend has been spms for 12 years and her legs are trashed already).i didnt notice any real boost in energy and in general i felt poor so ill be dropping that and i guess ill just stick with the coconut oil to deal with candida issues.

i did do the snapshot test for candida and it was there. when i got on the coconut oil and got it under control i did notice a further improvement ove the LDN alone

ALA is still in the trial stages, Kiddos. They don't have any idea of the proper dose and also how much is safe, long term. Taking a small amount probably won't hurt, but I would guard against taking too much.. JMO! Our own bodies usually make enough ALA for us, but who knows?

Some good news concerning LDN.

Had a neuro appointment two weeks ago and after going through all the usual motions, he asked if I was still taking the LDN. Well....duh......of course. He also asked if I thought it was helping at all.......YES. A couple times the prescription has gotten messed up and after a week without it, my legs were worse, believe it or not, and also my bladder "issues".

He said he feels after having had MS for such a long time (19 years diagnosed, probable 13 before), I should be in worse shape!!! As I've mentioned before, I just wish he would have agreed to let me try it before I became SPMS being none of the injectables were tolerable for me. He also mentioned the clinical trial now being started for LDN and appeared all happy and telling me something new. Why don't they ever listen to us????

If you haven't already, try it, you'll like it!! It's also much cheaper and less painful than those awful injections!!!

And so much safer, too!