more tests to come

[Guest guest]

Hi everyone,

This may be off topic but I do use LDN and don;t feel any different. I have

recently been seeing a neurology /opthamologist and she seems to think since

I have uveitis that I don't really have MS. She claims that white matter on

the brain and the other symptoms mimic MS but aren't always MS. Has anyone

else had a dr. tell them this? Could it be possible we are being diagnosed

by a test alone and maybe it isn't what we are being treated for?

I am ready to just say no more spinal taps and I will keep on doing what I

am doing, but I would like my vision back. She mentioned lupus and Chron's

and I'm not sure if I would just be better off with the mild case of MS. I

won't even go thru the hassle I had with referrals and the barage of tests

to come.

Long

[Guest guest]

Roy Swank wrote a diet book on ms and says there is a flicker fusion

test and a red blood cell mobility test that are accurate in obtaining a

diagnosis. These tests are not well known but I am sure you could find

someone to do them for you. Also. make sure you are tested for lyme and

hughes syndrome. Also someone asked about the use of alpha lipoic acid. It

is 50 time more potent when taken with vitamin E. Carlton Fredericks was a

world renown nutritionist who prescribed it for neuropathy. The protocal is

as follows: 300mg with vitamin E four times daily for two weeks. Then

300mgxday thereafter.Kathy

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

From: " Long " <Clong38@...>

<low dose naltrexone >

Sent: Wednesday, March 24, 2004 2:45 AM

Subject: [low dose naltrexone] more tests to come

> Hi everyone,

>

> This may be off topic but I do use LDN and don;t feel any different. I

have

> recently been seeing a neurology /opthamologist and she seems to think

since

> I have uveitis that I don't really have MS. She claims that white matter

on

> the brain and the other symptoms mimic MS but aren't always MS. Has anyone

> else had a dr. tell them this? Could it be possible we are being diagnosed

> by a test alone and maybe it isn't what we are being treated for?

>

> I am ready to just say no more spinal taps and I will keep on doing what I

> am doing, but I would like my vision back. She mentioned lupus and Chron's

> and I'm not sure if I would just be better off with the mild case of MS. I

> won't even go thru the hassle I had with referrals and the barage of tests

> to come.

>

> Long

>

>

>

>

>

>