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Re: Autism/CFS/LDN

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Posted

In a message dated 1/7/2006 6:48:18 P.M. Pacific Standard Time,

susan.lucey@... writes:

What does LDN stand for?

Low Dose Naltrexone, it is a opiate receptor blocker and is thought to act

on the immune system

Joy

Research Assistant to Dr Enlander

_www.enlander.com_ (http://www.enlander.com/)

Posted

Joy, I want to ask you something but I am a little queasy

since is no longer with us, but it seems important to follow up

on. He sent me an email on 12/5 asking for my thoughts on his theory.

I think I saw where he sent the same to others. His treatment for his

theory was LDN plus he often talked about LDN, but since he did not

seem to be doing that well, it was hard for me to think that LDN was

worth looking into, but you bring it up that Dr E is, or has?, using

it for CFS. Below is just the opening of his email about his

thinking. I mean no disrepect toward in saying I didn't think

LDN was doing that much for him, but it must have been helpful for

him to keep saying it was the best treatment he saw so far. He was

way above my understanding. God bless you .

Bob,

I am writing up a paper on endogenous opioidergic dysfunction in the

pathogenesis of CFS.

Posted

Dear Bob

Joy asked me to answer your email regarding 's LDN thoughts. On his

last visit two days before he passed away, he talked to me about his thoughts

on Naltrexone. Naltrexone (50mg) is used in heroin addiction, I must

immediately state that was not a drug addict.

Low Dose Naltrexone (LDN) is used in 3mg - 4.5mg doses, less than 10% of

the opiate therapeutic dose. It was found by research workers to positively

affect the immune response, some thought it changed the cytokine production,

others considered it acted on a cellular response.

He was keen to explore the LDN effect after we had weaned him slowly off

some of his other medicine, in collaboration with his local doctor.

His vivacious thinking will be missed

Enlander MD

New York

=================================

In a message dated 1/7/2006 9:09:57 P.M. Pacific Standard Time,

blue74730@... writes:

Bob wrote: Joy, I want to ask you something but I am a little queasy

since is no longer with us, but it seems important to follow up

on. He sent me an email on 12/5 asking for my thoughts on his theory.

I think I saw where he sent the same to others. His treatment for his

theory was LDN plus he often talked about LDN, but since he did not

seem to be doing that well, it was hard for me to think that LDN was

worth looking into, but you bring it up that Dr E is, or has?, using

it for CFS. Below is just the opening of his email about his

thinking. I mean no disrepect toward in saying I didn't think

LDN was doing that much for him, but it must have been helpful for

him to keep saying it was the best treatment he saw so far. He was

way above my understanding. God bless you .

Bob,

I am writing up a paper on endogenous opioidergic dysfunction in the

pathogenesis of CFS.

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