Spreading the word...

February 12, 2004

" Message: 25

Date: Wed, 11 Feb 2004 21:06:31 -0000

From: " cheystay " <c_chey@...>

Subject: Re: talking about LDN

Lynda, I, we, are banging our heads against that same wall.

I'm experienced in antibiotics, food, allergies and now more and

more LDN. But who listens? Nobody does, unless they are told by a

doctor. So few ppl are eiger to do their own studies and/or

experiment. And even if you do so, like my group and me, the doctors

just nod their heads and say; if it works for you... But actually do

something with the tons of experience of the patients self? No! I

frustrates me. That is the reason I never attend a support group,

its banging against a wall. Sometimes it looks like patients rather

complain then do something to help themselfs. "

Hi again Chey...I feel the same way about the ms support groups now. Just

too depressing listening to all those people that keep talking up the ABCR's

and then complaining that they don't really work. I try to spread the word

as much as I can on bulletin boards but what I usually do as well is suggest

that everyone that is taking it and having great results go back to the

board where you normally post and probably found out about the LDN and post

that you are having good results. Sometimes I just get the feeling that they

think it is just a loony couple of us posting about it over and over. I

won't give up though because I am sure that others have read my posts and

have at least been informed. It is everyone's right to be informed about it

I say. JoyceF

_________________________________________________________________

Plan your next US getaway to one of the super destinations here.

Recommended Posts