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LDN lowdosenaltrexone - Enough already Oi!

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Idk, it seems that there has been a mass campaign on various chat groups

concerning LDN or Low dose naltrexone - a drug designed for and prescribed to

alcoholics.  I read about the drug and encourage all to perhaps avail themselves

of real information concerning this option as I fail to see why it would be a

good short or long term option for anyone who deals with celiacs.  Could it be

that there are individuals more involved with the pharma companies manufacturing

naltrexone and that this is a idea seeding event?  Very clever tactic, and it

works, but we are not all so gullible, so ease up already OK.

 

 

--- On Mon, 6/22/09, Eleni <jesusgirl34 wrote:

 

 

Eleni <jesusgirl34

Re: Rheumatoid arthritis + infections

 

Monday, June 22, 2009, 4:37 AM

 

 

 

 

 

 

 

 

 

Hi,

I haven't posted here ever...I'm always trying to gain knowledge and learn from

others experiences. I'm also on the

" LDN lowdosenaltrexone " . I always see many people posting about RA.

I'm on there bc of MS but I have read that LDN has helped many RA sufferers. LDN

is for cancer & many other autoimmune diseases incl. autism. Seems to be a

fascinating discovery. I've been on LDN for about a week so it is too soon to

tell you if I feel better. I need to give it some months to take charge. Sorry I

can't give you much more info for I am still learning & wouldn't want to mislead

you. You can also google " LDN and RA " to see what type of info you get or sign

up to that . I believe you'll learn lots for there's many there that

have lots of knowledge to help you & answer your questions. Make sure you

research LDN & if you decide to start on it maybe alot of your pain will be

alleviated. Just don't give up hope. Hang in there.

Oh and you'll get lots of info on the types of food diet you can do to benefit

your situation.

 

God Bless~

Eleni

 

Vegan-and-Gluten- Free@ .com, " hollyhedge_ 2004 " <bethbell@..

..> wrote:

>

> I posted here some time ago regarding RA and diet. I have had RA for 10 years,

have taken anti inflams, Panadol and Codeine in spite of being diagnosed with

severe RA have not moved on to methotrexate or the harder drugs. I was diagnosed

finally with gluten sensitivity late last year and have stuck to a g/f vegan

diet for this year. Am a long time vegetarian who has had too much dairy over

the years. My inflammation rate is normal but I still flare, quite severely but

they only last 24 hrs. I am still flaring quite frequently. Is this pattern

familiar to anyone. I dont quite understand what is happening.

> Also I have low grade infections which I believe are common to RA but would

like to boost my immune system to stop this happening. Any advice for me please.

> Sherene I read your post on RA with interest and wonder if I am not getting

enough nutrients. I have quite a small appetite, a lot of fatigue and while I am

g/f and vegan dont take in a lot of food.

> I dont think I would feel happy about taking fish oil from an ethical position

- I am not convinced fish oil is healthy anyway but it does cross my mind at

times, pain can be so wearying. Can you tell me what you would eat over a few

days please.

> Any help from here would be appreciated.

>

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

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I'm just learning about LDN. Actually it is not prescribed for alcoholics...

the higher dose is. The low dose is miniscule and has been on the market for

decades but it is not effective for alcoholics. I think the reason LDN is

getting better known now is that it has been shown in many cases to help all

kinds of auto immune diseases and because the Europeans are now conducting

serious clinical studies. My preference is to live drug free but if something

works, does not have negative side effects and improves the quality of my life -

which pretty much stinks now because of auto immune diseases, I'm willing to do

the research, read the studies and make an educated decision for myself. Then

I'm happy to share my experience, positive or negative with others. I

appreciate when others share their experiences with me. And that bloody LDN is

only about 10 dollars for a month's worth. I'm waiting for the results of more

studies before I take a decision.

 

Diana

 

 

 

 

-

DragonFly Simon<dragonfly777_68

To:

<\

om>

Monday, June 22, 2009 7:01 PM

LDN lowdosenaltrexone - Enough already Oi!

 

 

 

 

 

 

Idk, it seems that there has been a mass campaign on various chat groups

concerning LDN or Low dose naltrexone - a drug designed for and prescribed to

alcoholics. I read about the drug and encourage all to perhaps avail themselves

of real information concerning this option as I fail to see why it would be a

good short or long term option for anyone who deals with celiacs. Could it be

that there are individuals more involved with the pharma companies manufacturing

naltrexone and that this is a idea seeding event? Very clever tactic, and it

works, but we are not all so gullible, so ease up already OK.

 

 

--- On Mon, 6/22/09, Eleni

<jesusgirl34<jesusgirl34%40>> wrote:

 

Eleni <jesusgirl34<jesusgirl34%40>>

Re: Rheumatoid arthritis + infections

To:

<%40\

..com>

Monday, June 22, 2009, 4:37 AM

 

Hi,

I haven't posted here ever...I'm always trying to gain knowledge and learn

from others experiences. I'm also on the

" LDN lowdosenaltrexone " . I always see many people posting about

RA. I'm on there bc of MS but I have read that LDN has helped many RA sufferers.

LDN is for cancer & many other autoimmune diseases incl. autism. Seems to be a

fascinating discovery. I've been on LDN for about a week so it is too soon to

tell you if I feel better. I need to give it some months to take charge. Sorry I

can't give you much more info for I am still learning & wouldn't want to mislead

you. You can also google " LDN and RA " to see what type of info you get or sign

up to that . I believe you'll learn lots for there's many there that

have lots of knowledge to help you & answer your questions. Make sure you

research LDN & if you decide to start on it maybe alot of your pain will be

alleviated. Just don't give up hope. Hang in there.

Oh and you'll get lots of info on the types of food diet you can do to benefit

your situation.

 

God Bless~

Eleni

 

Vegan-and-Gluten- Free@ .com, " hollyhedge_ 2004 "

<bethbell@.. .> wrote:

>

> I posted here some time ago regarding RA and diet. I have had RA for 10

years, have taken anti inflams, Panadol and Codeine in spite of being diagnosed

with severe RA have not moved on to methotrexate or the harder drugs. I was

diagnosed finally with gluten sensitivity late last year and have stuck to a g/f

vegan diet for this year. Am a long time vegetarian who has had too much dairy

over the years. My inflammation rate is normal but I still flare, quite severely

but they only last 24 hrs. I am still flaring quite frequently. Is this pattern

familiar to anyone. I dont quite understand what is happening.

> Also I have low grade infections which I believe are common to RA but would

like to boost my immune system to stop this happening. Any advice for me please.

> Sherene I read your post on RA with interest and wonder if I am not getting

enough nutrients. I have quite a small appetite, a lot of fatigue and while I am

g/f and vegan dont take in a lot of food.

> I dont think I would feel happy about taking fish oil from an ethical

position - I am not convinced fish oil is healthy anyway but it does cross my

mind at times, pain can be so wearying. Can you tell me what you would eat over

a few days please.

> Any help from here would be appreciated.

>

 

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