Re: Re: Low-dose naltrexone (LDN) as a treatment for mult...

[Guest guest]

It doesn't sound as if there is much difference between the MS Society in the UK or US! I e-mailed the West Texas Chapter a couple of times about a year ago but never heard anything back!

Marcie

In a message dated 10/15/2004 11:13:36 AM Central Daylight Time, davidtaylor@... writes:

Re UK Ms Society

We live in the UK and whilst researching LDN for my wife I wrote 2 emails to

the UK MS society and they did not reply to either.

Have they publised what they belive - who knows.

Have they publised what they have to help MS poeple - if they had an

interest in helping I think they would have replied to at least one of my

emails.

My wife has been on LDN fo about 6 month with very good results.

[Guest guest]

I am not taking LDN but am a regular reader of the comments made on this site. I also have emailed my neuro

London Ontario Canada about LDN and the Goat Sirum as I read about a man not far from me who has taken the sirum with excellent results. I figured he must be receiving it thru the London Cinic in a trial which would be conducted in London.

I have not received an answer either from the neuro about either so I figure that there may be a liability by putting it in print, not that I'm being ignored. Hopfully my questions regarding both will be answered when I visit the clinic in November and can push for an opinion face to face

riginal Message -----

From: marciemjm@...

low dose naltrexone

Sent: Friday, October 15, 2004 12:50 PM

Subject: Re: [low dose naltrexone] Re: Low-dose naltrexone (LDN) as a treatment for mult...

It doesn't sound as if there is much difference between the MS Society in the UK or US! I e-mailed the West Texas Chapter a couple of times about a year ago but never heard anything back! Marcie In a message dated 10/15/2004 11:13:36 AM Central Daylight Time, davidtaylor@... writes:

Re UK Ms Society We live in the UK and whilst researching LDN for my wife I wrote 2 emails to the UK MS society and they did not reply to either. Have they publised what they belive - who knows. Have they publised what they have to help MS poeple - if they had an interest in helping I think they would have replied to at least one of my emails. My wife has been on LDN fo about 6 month with very good results.

[Guest guest]

Hello ldn-users,

the m.s. society in every country is the same. Also here in the Netherlands

the

big pharmaceuticals rule the society. The corruption etc. is everywhere.

You cannot count on the m.s. society, anywhere. A big breakthrough will

be Aimspro (in my opinion) and the big pharmaceuticals will be in big

trouble.

By the way: i still doing fine with the ldn. It's the best you can get.

The society, the neurologists and doctors never heard of it or disapprove

it.

It's all logical. The pharmaceutical industries rule everything (except us).

They decide what kind of medicines will be researched, approved and given

by the specialists. And they think just about one thing: how to make as much

as possible money. How doesn't matter.

Greetings, Simon

>From: marciemjm@...

>Reply-low dose naltrexone

>low dose naltrexone

>Subject: Re: [low dose naltrexone] Re: Low-dose naltrexone (LDN) as a

>treatment for mult...

>Date: Fri, 15 Oct 2004 12:50:36 EDT

>

>It doesn't sound as if there is much difference between the MS Society in

>the

>UK or US! I e-mailed the West Texas Chapter a couple of times about a year

>ago but never heard anything back!

>

>Marcie

>

>

>In a message dated 10/15/2004 11:13:36 AM Central Daylight Time,

>davidtaylor@... writes:

>

>

> > Re UK Ms Society

> >

> > We live in the UK and whilst researching LDN for my wife I wrote 2

>emails to

> > the UK MS society and they did not reply to either.

> >

> > Have they publised what they belive - who knows.

> >

> > Have they publised what they have to help MS poeple - if they had an

> > interest in helping I think they would have replied to at least one of

>my

> > emails.

> >

> > My wife has been on LDN fo about 6 month with very good results.

> >

> >

>

>

_________________________________________________________________

Ook een gouden buddy worden in Messenger? Go for gold!

http://mobile.msn.com/?lc=nl-nl

[Guest guest]

maybe he doesn't know and doesn't want to be sued.

ryoung wrote:

I

am not taking LDN but am a regular reader of the comments made on this

site. I also have emailed my neuroLondon

Ontario Canada about LDN and the Goat Sirum as I read about a man not far

from me who has taken the sirum with excellent results. I figured

he must be receiving it thru the London Cinic in a trial which would be

conducted in London. I

have not received an answer either from the neuro about either

so I figure that there may be a liability

by putting it in print, not that I'm being ignored. Hopfully my questions

regarding both will be answered when I visit the clinic in November and

can push for an opinion face to face riginal

Message -----

From:

marciemjm@...

low dose naltrexone

Sent: Friday, October 15, 2004 12:50

PM

Subject: Re: [low dose naltrexone] Re:

Low-dose naltrexone (LDN) as a treatment for mult...

It doesn't sound as if

there is much difference between the MS Society in the UK or US!

I e-mailed the West Texas Chapter a couple of times about a year ago but

never heard anything back!

Marcie

In a message dated 10/15/2004

11:13:36 AM Central Daylight Time, davidtaylor@...

writes:

Re

UK Ms Society

We live in the UK and whilst

researching LDN for my wife I wrote 2 emails to

the UK MS society and they

did not reply to either.

Have they publised what they

belive - who knows.

Have they publised what they

have to help MS poeple - if they had an

interest in helping I think

they would have replied to at least one of my

emails.

My wife has been on LDN fo

about 6 month with very good results.

[Guest guest]

Simon,

$$$$$$$$$$ Sad but oh so true $$$$$$$$$$$$$

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

From: simon cohen [mailto:simoncohen_2@...]

Sent: Friday, October 15, 2004 1:30 PM

low dose naltrexone

Subject: Re: [low dose naltrexone] Re: Low-dose naltrexone (LDN) as a

treatment for mult...

Hello ldn-users,

the m.s. society in every country is the same. Also here in the Netherlands

the big pharmaceuticals rule the society. The corruption etc. is everywhere.

You cannot count on the m.s. society, anywhere. A big breakthrough will be

Aimspro (in my opinion) and the big pharmaceuticals will be in big trouble.

By the way: i still doing fine with the ldn. It's the best you can get.

The society, the neurologists and doctors never heard of it or disapprove

it.

It's all logical. The pharmaceutical industries rule everything (except us).

They decide what kind of medicines will be researched, approved and given by

the specialists. And they think just about one thing: how to make as much as

possible money. How doesn't matter.

Greetings, Simon

>From: marciemjm@...

>Reply-low dose naltrexone

>low dose naltrexone

>Subject: Re: [low dose naltrexone] Re: Low-dose naltrexone (LDN) as a

>treatment for mult...

>Date: Fri, 15 Oct 2004 12:50:36 EDT

>

>It doesn't sound as if there is much difference between the MS Society

>in the UK or US! I e-mailed the West Texas Chapter a couple of times

>about a year ago but never heard anything back!

>

>Marcie

>

>

>In a message dated 10/15/2004 11:13:36 AM Central Daylight Time,

>davidtaylor@... writes:

>

>

> > Re UK Ms Society

> >

> > We live in the UK and whilst researching LDN for my wife I wrote 2

>emails to

> > the UK MS society and they did not reply to either.

> >

> > Have they publised what they belive - who knows.

> >

> > Have they publised what they have to help MS poeple - if they had an

> > interest in helping I think they would have replied to at least one

> > of

>my

> > emails.

> >

> > My wife has been on LDN fo about 6 month with very good results.

> >

> >

>

>

_________________________________________________________________

Ook een gouden buddy worden in Messenger? Go for gold!

http://mobile.msn.com/?lc=nl-nl