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LDN- Focusing on Information dissemination,rather than testing

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I also have been ( & still am!) sympathetic to the reservations expressed by

Jan regarding calls for the testing of LDN:

Furthermore, surely there are other drugs which have been accepted/adopted

extensively for conditions other than their initial recognised purpose

without going through the unnecessary, horribly expensive & time consuming

rigmarole of further testing?! (-And I bet few of them are as free of side

effects or taken in such low, safe doses as LDN!)

This delaying may seem to be all very well for those for whom a major

consideration in drug production is the maximising of potential profits, but

for us steadily progressing patients, this unnecessary, time consuming, &

seemingly endless shillyshallying around can seem about as pertinent as

" Nero fiddling while Rome Burns " !

Might it not be more productive to put our energy into focussing people`s

minds on the already known, positive aspects of LDN usage, things like it`s

efficacy, safety, ease of use & cheapness, & also to draw attention to the

fact that it is already being utilized worldwide in a pragramatic, common

sense response to it`s obvious value?

Surely, as LDN continues to become more widely known & used, this knowledge

& awareness will itself develop a growing momentum of understanding that it

is the implementation of LDN`s wider usage that is now needed & appropiate?

If we are already confident of LDN`s value, why should we continue to act

as though we also are uncertain & need the reassurance of further

esting?! -This hardly seems an attitude likely to inspire confidence in

others!

-It seems to me that the dissemination of info on LDN through such vehicles

as Boyle Bradley`s recent book & radio interviews may very well be the

most effective & immediate way to foster the widespread recognition &

adoption of LDN as an important treatment for MS & many Autoimmune

Disorders.

Gerald

[low dose naltrexone] Re: Re - Just curious

>

>> Good point, Dave Tayler. I would like to urge everyone crying out

> for clinical trials o LDN to please stop!!! The drug has already had

> clinical triels and was approved, and the only way to get it off the

> market is to make it into an illegal drug and a controlled

> substance. Then it can be conhtrolled and made inaccessible.

>>

>> I talked to the wife of a renown neurologist in Texas who had been

> very infuential in the Ms Society at the national level. She told me

> she quit promoting the MS Society when a really high mucky muck told

> her (secretly) that no cure for any major disease would ever be found

> again, using polio as the example. When polio was 'cured', it took

> out part of the industry!!! Since then, I tell everyone to quit

> walking for MS, etc.

>>

>> If there was a clinical trial for LDN, it would cost millions, be

> made inaccesible, and then be 'approved' at a much higher cost to

> cover the cost of the trials. THINK, people. A month's supply of it

> now costs only about $20-30 a month. People with no insurance and on

> Medicare can afford that now. They will not be able to if it goes

> through clinbical trials. We don't need clinical trials now. The

> anecdotal is enough for D.O.s and other doctors to prescribe it

> without the trials. Neuros may not because it jeapordizes their

> profession. It would empty their offices.

>>

>> That is a GOOD thing!

>>

>> Jan

>>

> I must agree with the author of this post. It's legal and available.

> We know about it and use it. We recommend it to those we think would

> benefit. Why change things now?

>

> Artie

>

>

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