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Re: You Know My Neuro Won't

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>

> My eyes can't see too well today so if this looks too big I am

sorry, you know, I went to the neuro on the 29th of November, and he

would not even discuss LDN with me, I don't know a damn thing about

it, don't understand it, and I had questions about it, kinda pi & & ed

me off. If you know what I mean. Anyways, just thought I would put

that in here, anyone had that happen to them, of course, I am in the

mist of a fibro flare and not MS, but dont see what that has anything

to do with the other...lol....not in my mind.

> Hugs to all,

> Tonya in Texas

>=============

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Tonya in Texas,

Forget using a Neurologist, try your PCP. Until recently there was little if anything official about LDN and MS (or any disease). My Neuro wouldn't even talk about it (now I think he has a couple of patients he prescribes it for). I got my PCP to write my first prescription (he said "well, it can't hurt you"). He implied that he was satisfied it wouldn't break me (put me in the poorhouse and gave me credit for some brains and he just assured himself it wouldn't hurt.

It is not on a Neurologists paradigm of how to treat MS so I'd skip that route.

Larry

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I am 100% with Larry on this one. 's Neurologist would not even look at the 60 stories I brought into her. We went elsewhere for his script and did fantastic on LDN. 3 years later I found out 's neurologist had 5 patients on LDN. has now been on LDN for 4 years. I wonder how many patients she has on LDN now?

My best

Aletha

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I get my LDN prescription through my neurologist.

Of course I had to suffer using Avonex, Copaxone and Novantrone for a

few years until he prescribed it for me.

Art

--

>

> I am 100% with Larry on this one. 's Neurologist would not even

look at the 60 stories I brought into her. We went elsewhere for his

script and did fantastic on LDN. 3 years later I found out

's

neurologist had 5 patients on LDN. has now been on LDN for 4

years. I wonder how many patients she has on LDN now?

>

> My best

> Aletha

>

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