Re: It will be studied when money is raised to begin trials!

[Guest guest]

Dear " I am a Canadian " ,

Thank you for stating the truth.

On the LDN website it stated that clinical trials for use of LDN for

Chrohn's were underway. If that is the only trial being conducted, it

should be funded. If it proves to be a success, LDN will be applied to

other disorders like MS. My disorder is so rare that it is not on the

radar screen. I am here to encourage research that may some day be

effective to treat the relative small group of people who have

erythema nodosum. Until then, I cheer for all medical research that

brings us closer to solving the autoimmune mystery.

Money talks. If anyone is able to find a medical school to do the

research and provide funding, I would bet they would listen. Do any of

the members have connections to medical schools? Until clinical trials

are run all we have in acecdotal talk.

With as many members as this group has, surely someone has the

connections to get the research underway. Please step forward!

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

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