Jump to content
RemedySpot.com

RE: Re: [LDN] Realistic, why?for Aage

Rate this topic


Guest guest

Recommended Posts

Guest guest

I agree with you totally … one of the reasons

I hardly read any of the stuff from the LDN groups anymore is all this blame on

big Pharma… It’s BS they are a business they do have to make profit

and they do put a lot into getting drugs approved and they need to make profit

to do more and keep employees it’s part of life!! Once the time runs out

on patent there will be other companies making the big drugs and competition

makes it cheaper. Naltrexone too is made by a drug company in fact several so

if your mad at them maybe they should just stop making it! As for studies there

should be studies for everything under the sun and there are several studies going

on for several treatments some cheap and already used in other illnesses most

expensive and new. Enough pointing fingers get over it, it will be studied when

money is raised to begin trials! Maybe this cable tv program should ask for

donations for research into LDN and MS? If you have the ability use it!

From: Strecker

[mailto:rebeccastrecker@...]

Sent: Friday, March 05, 2004 3:24

PM

To:

low dose naltrexone

Subject: [low dose naltrexone] Re:

[LDN] Realistic, why?for Aage

Dear Aage

FYI:

You took what I said out of context. Here is the

dictionary definition

of realize:

re·al·ize

v. re·al·ized, re·al·iz·ing, re·al·iz·es

v. tr.

1.To comprehend

completely or correctly.

*********

So I do not think you are making things clearer by

saying that a

" realist " becomes " real lies " .

Those word games are cutsie, but you

negated the intent of my sentence. I said to

" be a realist, but not to give up hope " .

That said, I do hope you will get LDN on to your

TV show, and be sure

to give us all advance notice of the time and

channel so we can watch.

Try to control your anger at the pharm industry.

If you rant and rave

you will not attract the kind of people who can

help. I don't know

what type of TV show you have. I can tell you that

if I see a person

making wild accusations --even if they are true, I

tune out. One must

appear level-headed to gain respect. Of course,

this is my opinion

only, and I do wish you well--but we don't want to

have LDN come off

as another " snake oil " pitched by an

angry man.

Love,

> I heard someone say the words " be

realistic " .

> Think about

this: The word comes from " realise "

> Brake that up and you have: " real

lies " .

> We are being fed lies by the pharmacutical

companies every day.

> The reason there is no official cure for MS

is simple. There is no

money in

> the cure.

> There is only money in the problem. As long

as there is a problem,

they make

> profits.

> I have been exposing the fraud in the

pharmacutical industry on my

cyndicated

> TV show

> for 5 years, (among other things).

> We are being told there is no cure for MS.

Not so. My wife was in a

very bad

> shape. We went and got her Live Cell Therapy.

She totally rebuilt

the body.

> Ofcourse, Live Cell therapy works, and

therefore it is illegal to do

in this

> country. There is no profit in the cure. You

have to go to Germany

or elswhere

> out of the country to get it. The only thing

we were not able to do

was to bring

> back her eye sight. That is what we are

trying to do now. And I am

all ears -

> - - -. I do not cover anything on the air

that I can not prove.

> A Billionare told me one time: " True and

great success is only

achieved on

> the fringes of fear. " It is comfortable

to listen to a doctor

telling us that

> there is no cure, and take the pills everyone

else gets. There is

comfort in

> numbers, but look at the trackrecord of the

general treatment. It is

miserable. I

> have great respect for Dr. Sullivan, Victor,

and Dr. Bihari and others

> mentioned on this list. They are pioneers and

maverics of the

industry. They have

> stepped outside of the norm and are really

helping.

> I am gathering material on LDN and I will do

a TV show on MS and the

> treatment of it soon. Hopfully I can get

someone qualified on as a

live guest.

> Keep sharing and researching.

> Good luck to us all.

> Aage

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...