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LDN Effects

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Hi Everybody,

I've been on LDN for almost a week now - increasing slowly as my body

doesn't do well adjusting to anything new - even nutritional

supplements.

I started at 1.5 mg and have worked up to about 2.6 mg. using liquid.

The first night I slept so poorly, I could not function the next day

so I skipped the next night's dose but have taken it every night

since.

Some of the side effects I have been experiencing are dizziness,

stomach pains, gas, (tried taking with food but seemed to make no

difference), all over sweating. These seem to be settling down a bit

over the course of the week. Of course I am sleeping very poorly but

was expecting that. I do take 5 mg. melatonin at night.

I also have developed facial tics. Again these seem to be settling

down somewhat. I was increasing .5 mg nightly but was feeling so

absolutely awful the following day so now am increasing by about .2

nightly.

I'm wondering if anyone else has experienced similar effects. It is

only because of the glowing reports here that I persist, in the hopes

that it might be the answer for me too. I'm not taking LDN for MS as

many of you are but rather for ME/CFIDS/FMS (Chronic Fatique

Syndrome/Fibromyalgia).

Barb

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I am taking for CFS/FM with amazing improvement. My FM is basically

gone withi a week. I am on month 2 and continue to improve. It is a

slow process. I had severe sleep trobule which has stopped and now i

sleep BETTER. It took a month for that. I alternate my liquid dose

between 3.0 and 4.0 or 4.5 every night.

I did experience herx's, sort of like fevers, swollen glands, my

body started fighting infections. It was very strange. The low dose

naltrexone was the turning point in my battle with CFS. The only

other things i take are nattokinase, d-fraction, and

magnesium/glutathione/b12 injections which i had been taking wit no

results anyways.

Stick with it, take it at night with nothing else if possible, make

sure your dose is between 3.0-4.5 and take sleeping aids if needed

causeit did go away for me.

JL

> Hi Everybody,

>

> I've been on LDN for almost a week now - increasing slowly as my

body

> doesn't do well adjusting to anything new - even nutritional

> supplements.

>

> I started at 1.5 mg and have worked up to about 2.6 mg. using

liquid.

> The first night I slept so poorly, I could not function the next

day

> so I skipped the next night's dose but have taken it every night

> since.

>

> Some of the side effects I have been experiencing are dizziness,

> stomach pains, gas, (tried taking with food but seemed to make no

> difference), all over sweating. These seem to be settling down a

bit

> over the course of the week. Of course I am sleeping very poorly

but

> was expecting that. I do take 5 mg. melatonin at night.

>

> I also have developed facial tics. Again these seem to be settling

> down somewhat. I was increasing .5 mg nightly but was feeling so

> absolutely awful the following day so now am increasing by

about .2

> nightly.

>

> I'm wondering if anyone else has experienced similar effects. It

is

> only because of the glowing reports here that I persist, in the

hopes

> that it might be the answer for me too. I'm not taking LDN for MS

as

> many of you are but rather for ME/CFIDS/FMS (Chronic Fatique

> Syndrome/Fibromyalgia).

>

> Barb

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Some notes on water…Steam distilled

water carries a slight negative charge to it which helps to clear unwanted

materials from cells. Try to avoid anything out of a tap.

Chlorine, fluoride, etc… are all

poisons and you do not need to do that to yourself. Private well water tastes

better than city treated water, BUT carries bacteria and other not so wonderful

things. Reverse Osmosis is better because it is very clean. Distilled is

cleaner and as noted before is negatively charged to help with the evacuation

of unwanted debris in the cells.

As far as drinking, I don’t do tea,

coffee, pop, milk….just water and water alone. Great stuff. Minimum one

gallon per day for me. No one should drink less than 2 quarts daily.

Bruce Guilmette, Ph.D.

Survive Cancer Foundation, Inc.

http://www.survivecancer.net

From: low dose naltrexone [mailto:low dose naltrexone ] On Behalf Of kathy lintzenich

Sent: Friday, July 22, 2005 1:22

AM

low dose naltrexone

Subject: Re: [low dose naltrexone]

LDN Effects

I actually think it is a good sign that you are responding

in this manner. A healing opportunity has been created for your body and things

are getting all stirred up!!!!!!!!! I am betting you are very toxic- please

don't take that as rude. When I started massage school a nutritionist came in

and told us how much water we should drink. I raised my hand and said " but

I don't like water " she retorted back " it is because you are

toxic " After that I started drinking about 12 glasses of room temp water a

day and haven't had a soda in over a decade. Often when there is a worsening of

symptoms, it means it is really going to make a significant impact upon your

health. God Bless, Kathy P. S. I love water now! It is so

refreshing!!!!!!!!!!!

[low dose naltrexone] LDN Effects

Hi Everybody,

I've been on LDN for almost a week now -

increasing slowly as my body

doesn't do well adjusting to anything new - even

nutritional

supplements.

I started at 1.5 mg and have worked up to about

2.6 mg. using liquid.

The first night I slept so poorly, I could not function

the next day

so I skipped the next night's dose but have taken

it every night

since.

Some of the side effects I have been experiencing

are dizziness,

stomach pains, gas, (tried taking with food but

seemed to make no

difference), all over sweating. These seem to be

settling down a bit

over the course of the week. Of course I am

sleeping very poorly but

was expecting that. I do take 5 mg. melatonin at

night.

I also have developed facial tics. Again these

seem to be settling

down somewhat. I was increasing .5 mg nightly but

was feeling so

absolutely awful the following day so now am

increasing by about .2

nightly.

I'm wondering if anyone else has experienced

similar effects. It is

only because of the glowing reports here that I

persist, in the hopes

that it might be the answer for me too. I'm not

taking LDN for MS as

many of you are but rather for ME/CFIDS/FMS

(Chronic Fatique

Syndrome/Fibromyalgia).

Barb

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I actually think it is a good sign that you are responding in this manner. A healing opportunity has been created for your body and things are getting all stirred up!!!!!!!!! I am betting you are very toxic- please don't take that as rude. When I started massage school a nutritionist came in and told us how much water we should drink. I raised my hand and said "but I don't like water" she retorted back "it is because you are toxic" After that I started drinking about 12 glasses of room temp water a day and haven't had a soda in over a decade. Often when there is a worsening of symptoms, it means it is really going to make a significant impact upon your health. God Bless, Kathy P. S. I love water now! It is so refreshing!!!!!!!!!!!

[low dose naltrexone] LDN Effects

Hi Everybody,I've been on LDN for almost a week now - increasing slowly as my body doesn't do well adjusting to anything new - even nutritional supplements.I started at 1.5 mg and have worked up to about 2.6 mg. using liquid. The first night I slept so poorly, I could not function the next day so I skipped the next night's dose but have taken it every night since.Some of the side effects I have been experiencing are dizziness, stomach pains, gas, (tried taking with food but seemed to make no difference), all over sweating. These seem to be settling down a bit over the course of the week. Of course I am sleeping very poorly but was expecting that. I do take 5 mg. melatonin at night.I also have developed facial tics. Again these seem to be settling down somewhat. I was increasing .5 mg nightly but was feeling so absolutely awful the following day so now am increasing by about .2 nightly.I'm wondering if anyone else has experienced similar effects. It is only because of the glowing reports here that I persist, in the hopes that it might be the answer for me too. I'm not taking LDN for MS as many of you are but rather for ME/CFIDS/FMS (Chronic Fatique Syndrome/Fibromyalgia).Barb

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Yes, but don't forget if you are drinking that much water to take a quarter spoon of sea salt so you are not depleting minerals. Kathy

[low dose naltrexone] LDN Effects

Hi Everybody,I've been on LDN for almost a week now - increasing slowly as my body doesn't do well adjusting to anything new - even nutritional supplements.I started at 1.5 mg and have worked up to about 2.6 mg. using liquid. The first night I slept so poorly, I could not function the next day so I skipped the next night's dose but have taken it every night since.Some of the side effects I have been experiencing are dizziness, stomach pains, gas, (tried taking with food but seemed to make no difference), all over sweating. These seem to be settling down a bit over the course of the week. Of course I am sleeping very poorly but was expecting that. I do take 5 mg. melatonin at night.I also have developed facial tics. Again these seem to be settling down somewhat. I was increasing .5 mg nightly but was feeling so absolutely awful the following day so now am increasing by about .2 nightly.I'm wondering if anyone else has experienced similar effects. It is only because of the glowing reports here that I persist, in the hopes that it might be the answer for me too. I'm not taking LDN for MS as many of you are but rather for ME/CFIDS/FMS (Chronic Fatique Syndrome/Fibromyalgia).Barb

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You are correct.

Bruce Guilmette, Ph.D.

Survive Cancer Foundation, Inc.

http://www.survivecancer.net

From:

low dose naltrexone [mailto:low dose naltrexone ] On Behalf Of kathy lintzenich

Sent: Saturday, July 23, 2005 2:26

AM

To:

low dose naltrexone

Subject: Re: [low dose naltrexone]

LDN Effects

Yes, but don't forget if you are drinking that much water to

take a quarter spoon of sea salt so you are not depleting minerals. Kathy

[low dose naltrexone] LDN Effects

Hi Everybody,

I've been on LDN for almost a week now -

increasing slowly as my body

doesn't do well adjusting to anything new - even

nutritional

supplements.

I started at 1.5 mg and have worked up to about

2.6 mg. using liquid.

The first night I slept so poorly, I could not

function the next day

so I skipped the next night's dose but have taken

it every night

since.

Some of the side effects I have been experiencing

are dizziness,

stomach pains, gas, (tried taking with food but

seemed to make no

difference), all over sweating. These seem to be

settling down a bit

over the course of the week. Of course I am

sleeping very poorly but

was expecting that. I do take 5 mg. melatonin at

night.

I also have developed facial tics. Again these

seem to be settling

down somewhat. I was increasing .5 mg nightly but

was feeling so

absolutely awful the following day so now am

increasing by about .2

nightly.

I'm wondering if anyone else has experienced

similar effects. It is

only because of the glowing reports here that I

persist, in the hopes

that it might be the answer for me too. I'm not

taking LDN for MS as

many of you are but rather for ME/CFIDS/FMS

(Chronic Fatique

Syndrome/Fibromyalgia).

Barb

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