Re: MS Society's lastest damning comments on LDN (diane)

[Guest guest]

---Diane

I totally agree with you! I sent off my nasty email to the MS society

and they replied with a form letter! This even pissed me off more!

They don't realize--- " This Means War! " .

Steve

In low dose naltrexone , " cowgirls542001 "

<dpainter@m...> wrote:

> You could well be right that they are getting pressured. Either

that

> or they are just sick of getting repeated emails from all of us

> telling them about how wonderful LDN is and they are simply trying

to

> get rid of all of us by posting this one stupid and misleading

> article. Well, guess what? Now they have really done it. At the

> very least I am going to email them every single day if I can about

> LDN and will be working on possibly even more effective ways of

> trying to force them to wake up and smell the LDN roses for the

sake

> of everyone who has this miserable disease.

>

> Diane

>

>

> > At first I was as mad as all of you about this. (Ok, still am.)

> Then

> > after thinking about it and reading all your excellent comments,

> the

> > though occured to me, Why did they publish this article, right

now?

> > It's not like there's really anything " new " here. Just a rehash

of

> > old junk science.

> >

> > I'm thinking that someone is starting to take notice of how

> > much " buzz " LDN is getting, and they're running a bit scared. If

> the

> > general population of people suffering with the " auto-immune "

> > diseases really started finding out how good LDN is for many of

us,

> > the drug companies stand to loose a lot. Hence possible pressure

on

> > the MS society to publish this absurd article.

> >

> > Cinders

> >

> > " You will observe with concern how long a useful truth may be

known

> > and exist, before it is generally received and practiced on. "

> > lin