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Re: Notification of MS Societies about LDN

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It will be interesting to see how your

papers handle dealing with alternative therapies for MS. For cancer, they won’t

even return phone calls, for that matter take them in the first place. If it doesn’t’

come from the mainstream medical world, it will not be dealt with.

Bruce

Guilmette, Ph.D.

Survive

Cancer Foundation, Inc.

http://www.survivecancer.net

From: low dose naltrexone

[mailto:low dose naltrexone ]

On Behalf Of Tom

Sent: Friday, July 01, 2005 9:49

PM

low dose naltrexone

Subject: [low dose naltrexone]

Notification of MS Societies about LDN

To the

group from Tom in Edmonton:

What do

you think about forwarding opinions, news, etc. about LDN to your applicable

MS Societies? From what I have been able to gather, most societies do

not seem to even acknowledge its existence, but they publish everything the

big drug companies want them to.

Maybe a

flood of news about LDN, and feedback from actual patients on the crap drugs

the societies seem to be pushing might help raise their level of

consciousness.

In Canada, our

society won't even let me publish a letter saying that LDN helped me.

How about that for censorship!

Also,

what do you think about letters to the editor of your local newspapers

regarding how some information is being stifled by groups that are supposed

to be helping? And maybe the URL of remedyfind.com where of course they

will notice that LDN is the No.1 rated treatment for MS sufferers?

We

might even be able to coordinate our efforts to get better coverage.

If

these suggestions have already been made by others, I apologize, but I have

not had access to a computer for some time now and therefore am a little bit

out of touch.

Whatever,

I would appreciate your comments.

Tom in Edmonton

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I think the problem is..that many folks want others to do the work for

them. The only way to move forward is by being proactive and

participating. Recently, CNN had a program on MS..and they were

soliciting questions. I had posted the link, but I wonder how many

even bothered to write..certainly no one talked about the program on

CNN.

I run the LDNers group...with the express intention of having a

list of motivated individuals..willing to write the occasional letter

of support. There are about 25 of us..and motivated individuals should

consider applying for membership. This year I have deleted about 50

names from the LDNer list..because they only wanted to receive..and

not give anything in return...I continue to look for a few good men

and women..interested individuals should contact me after checking out

my group.

LDNers

A

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FWIW: I was unable to find the program on CNN TV. I did send in

several questions and comments and was hoping to get a report of the

program from you or someone else.

> I think the problem is..that many folks want others to do the work

for

> them. The only way to move forward is by being proactive and

> participating. Recently, CNN had a program on MS..and they were

> soliciting questions. I had posted the link, but I wonder how many

> even bothered to write..certainly no one talked about the program

on

> CNN.

>

> I run the LDNers group...with the express intention of having

a

> list of motivated individuals..willing to write the occasional

letter

> of support. There are about 25 of us..and motivated individuals

should

> consider applying for membership. This year I have deleted about 50

> names from the LDNer list..because they only wanted to receive..and

> not give anything in return...I continue to look for a few good men

> and women..interested individuals should contact me after checking

out

> my group.

> LDNers

>

>

> A

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