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New Here - Been Lurking/LDN for MS

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Hi Everyone!

I am new here, and thought I should introduce myself. I have been

lurking for a while now.

At this point, I'm listed as possible MS. Fortunately, so far, my

symptoms were extremely mild, and they found 1 very faint isolated

lesion on the c-spine which was non-enhanced at the time of the

MRI. I also had Optic Neuritis, and along with the other

symptoms/lesion, I suspect MS.

I see neuro in a month, but his suggestion initially, and I think I

tend to agree, was wait 3-6 months & do more MRI's, unless I get

further symptoms.

Meanwhile I'm gathering all of the LDN info possible to give him. I

gave him printouts from the LDN site, and I don't think that was

quite convincing. Now, I read here that I probably won't get the

script from him anyhow. I did find a doc in the next city over on

the acam.org page, and it says he's FP so that might be a

possibility.

I kind of wonder if anyone knows, if I did have a phone consultation

with Dr. Bahari, does he then get the records from my neuro? will

he do scripts from a phone conversation? is it $200 or something

like that? Any info on the phone consultations with him would be

appreciated.

I'm also wondering if you need an actual DX for MS to get the LDN?

I think I would be a great candidate to try it, being so new to it,

and I feel that the problems I had starting end of March were the

first MS symptoms I have ever had, and they all came along

together. The neuro says it's possible to be viral, but I doubt

it. I wonder how strong of a case you need to get the LDN?

Thanks & it's good to be here, every time I see a positive post on

the LDN, it becomes ammunition to take to the doc! :)

Kathy

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Hi Kathy

Welcome, it's nice hearing from you. I went to see Dr. Bihari but the day

of my appointment, he was taken to the hospital. So much for my

appointment. but I did leave important medical records with his secretary.

then I had a phone conversation with him the following week. His fee is

$450.00. But he gives you a form to send to your insurance company, to get

re-imbursed. I thought iventually that my PC doctor would prescribe it but I

wanted Dr. Bihari's guidance. Most doctors know nothing about LDN, so I

felt that I needed some questions answered first. So I thought that it was

best to get Dr. Bihari to prescribe it, then if I had probelms he could help

me with them.

Wishing you good luck.

Marie

----- Original Message -----

From: " Kathy Young " <schnebbles@...>

<low dose naltrexone >

Sent: Friday, July 04, 2003 11:17 AM

Subject: [low dose naltrexone] New Here - Been Lurking/LDN for MS

> Hi Everyone!

>

> I am new here, and thought I should introduce myself. I have been

> lurking for a while now.

>

> At this point, I'm listed as possible MS. Fortunately, so far, my

> symptoms were extremely mild, and they found 1 very faint isolated

> lesion on the c-spine which was non-enhanced at the time of the

> MRI. I also had Optic Neuritis, and along with the other

> symptoms/lesion, I suspect MS.

>

> I see neuro in a month, but his suggestion initially, and I think I

> tend to agree, was wait 3-6 months & do more MRI's, unless I get

> further symptoms.

>

> Meanwhile I'm gathering all of the LDN info possible to give him. I

> gave him printouts from the LDN site, and I don't think that was

> quite convincing. Now, I read here that I probably won't get the

> script from him anyhow. I did find a doc in the next city over on

> the acam.org page, and it says he's FP so that might be a

> possibility.

>

> I kind of wonder if anyone knows, if I did have a phone consultation

> with Dr. Bahari, does he then get the records from my neuro? will

> he do scripts from a phone conversation? is it $200 or something

> like that? Any info on the phone consultations with him would be

> appreciated.

>

> I'm also wondering if you need an actual DX for MS to get the LDN?

> I think I would be a great candidate to try it, being so new to it,

> and I feel that the problems I had starting end of March were the

> first MS symptoms I have ever had, and they all came along

> together. The neuro says it's possible to be viral, but I doubt

> it. I wonder how strong of a case you need to get the LDN?

>

> Thanks & it's good to be here, every time I see a positive post on

> the LDN, it becomes ammunition to take to the doc! :)

>

> Kathy

>

>

>

>

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