My doc not wanting to give me LDN

[Guest guest]

- yes I do realize that you all have decided for yourselves that LDN is the way to go, and I can always call Dr. Sullivan.

I was just hoping to possibly find out where ther is some info that Dr. Bihari had published himself regarding LDN and MS. I can sure find enough support for it out here, which was alot of what I took him. I have not found any published info by Dr. B regarding MS though, with the exception of the LDN site, which he does not run.

I wonder myself, now, why he hasn't proceeded to publish things on it? It sure seems that he should! He seems to have published quite alot on HIV and LDN.

And, Joyce - yes - I thought/hoped he was going to call Dr. Bihari, but apparently he didn't. I dont know how pushy to get, you know? I like him alot and don't want to make him mad I'm a coward maybe!! I don't know.

I am going to read a while more and very possibly call Dr. Sullivan.

I find it curious that my neuro would go ahead at this early point in time and give me the "real" MS drugs, should I say ok (which I will not). I want LDN, the question still is, do I get it now (not being dx yet, only have 1 small lesion and 1 flareup), or wait for another "possible" attack. Will I ever have one? I don't know, but I feel that the doc must feel fairly certain I have MS. Or he would not let me go on those drugs. That fact in itself, is just about enough to make me phone Dr. Sullivan.

I was just hoping someone knew why he hadn't published stuff himself regarding his findings on the LDN/MS.

Thanks!Kathy Kathy