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Re: LDN: Possibility of Pharma co. research - to Cinders/Group

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I understand your frustration in trying to get the docs to RX LDN

and support its use publicly. The good thing is, at worst, Dr.

Bihari will RX it if your local nueros won't. However, in time,

with the noise level increasing, LDN will be accepted as a safe and

hopefully very effective alternative that will get little

resistance. Docs in this country are just beginning to hear about

it, but my feelings are that LDN is starting to spread like

wildfire. Two big reasons docs are resistant now is that #1 many

have been burned in the past by patients wanting to try something a

little unconventional only to be sued for millions when things don't

go as expected. Because of the lawsuit happy " its not my fault "

society we live in docs are much more reluctant to take even what

seems to be a small risk. #2 to add to that, they are also

creatures of habit and even getting them to try a new and " better "

drug that has been approved for an illness or disease takes an army

of drug reps. since most do not like to change their habits or what

they have become comfortable with. It is interesting to note that

many of you sound just like a frustrated drug rep. who is convinced

there drug is the best but can't seem to get docs to RX it. Welcome

to my world! LOL.. I've been told hundreds of times by docs that

they won't change their habits, but over time they do if you believe

in what you have and present them with credible facts. We are at the

beginning of a long hard fight, but have faith, keep making noise.

Nothing worth doing is easy.

low dose naltrexone , " Cinders " <allentownusa@h...>

wrote:

> Koblitz -

>

> I want to wish you success with LDN. This treatment works better

for

> some than it does for others - but a lot of us have gotten good

> results and I sincerely hope you are one who reaps it's benefits.

> All of us fighting the MonSter should support each other in

whatever

> we do to make our lives more bearable. So - GOOD LUCK AND BEST

> WISHES!!! Please let us know how it goes with you.

>

> I have to admit, my reasons for wanting LDN to work for you are

> somewhat selfish. Since you are connected to the pharmacy

industry,

> you could turn out to be a very strong ally to those of us who

> support the use, and further study of LDN for MS and other

> conditions. You have the inside knowledge of how that industry

> works, as well as industry connections. Your perspective and

> knowledge is invaluable. Thanks for sharing, I have enjoyed

reading

> what you have to say and believe you are sincere in your beliefs

> that most of the people working in your industry do care very much

> about what they are doing. For me, my skepticism is more directed

to

> the corporate decision makers, board of directors and CEO's than

the

> other people in the industry. And I am skeptical of the motives of

> those groups in all industry, not just the pharmacy industry.

After

> all, America is a profit driven country and profit does not always

> follow good social conscience or morality.

>

> I would never be so arrogant to speak for anyone else on this

board,

> but I hope you do not take any of the comments against the ABCR's

or

> the drug companies personally. I have read hundreds and hundreds

of

> the posts here, and I believe that a lot of us are just very

> frustrated and angry because of the fight we have to go through to

> get LDN, and the resistance that the medical community at large

has

> for it's use. It is hard when you sincerely believe that something

> is working so well, and you see it being bashed and denied to

people

> you believe could benefit from it. And it would be different if

the

> treatments being offered were great (or even acceptable) - but the

> truth is, for many, they simply are not.

>

> Anyhow, I try to avoid OT conversations because I know it annoys

> some people, but I just had to put my two cents in, again - best

of

> luck, Cinders

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