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Hi everyone..

I do not post very often but I read everyone's posts.

I have been on LDN since August 20, 04. It had worked very good with me up until about a month ago or maybe a little bit longer ago. I started feeling very tired all the time. I was sleeping constantly. As time has gone by I am slowly going downhill. Right now it is at the point that I am getting very weak and especially walking around my small apt. It is getting really hard to hold my arms up. I cannot carry anything at all. If I do there is so much weakness that I could actually sit down on the floor and not get up.

My question is "Is it possible that the LDN is no longer working?" Did I become immune to it now?

I go for a MRI on Thursday but it was only for my brain. I will be having my friend (who also has MS) drive me to the neuro and I will have to use my wheelchair that has been in my storage cage for at least 10 years.

Any input would be so welcomed on this end.......

Bless you all.

Love and HugsCJFriends are angels who lift us to our feetwhen our wings have trouble remembering how to fly

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>

> Hi everyone..

> I do not post very

often but I read

everyone's posts.

> I have been on LDN

since August 20, 04. It

had worked very good

with me up

> until about a month ago

or maybe a little bit

longer ago. I started

feeling

> very tired all the

time. I was sleeping

constantly. As time has

gone by I

> am slowly going

downhill. Right now it

is at the point that I am

getting very

> weak and especially

walking around my small

apt. It is getting

really hard

> to hold my arms up. I

cannot carry anything at

all. If I do there is so

> much weakness that I

could actually sit down

on the floor and not get

up.

> My question is " Is it

possible that the LDN is

no longer working? " Did

I

> become immune to it

now?

> I go for a MRI on

Thursday but it was only

for my brain. I will be

having

> my friend (who also has

MS) drive me to the

neuro and I will have to

use my

> wheelchair that has

been in my storage cage

for at least 10 years.

> Any input would be so

welcomed on this

end.......

> Bless you all.

> Love and Hugs

> CJ

> Friends are angels who

lift us to our feet

> when our wings have

trouble remembering how

to fly

>

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

If you have developed

candida yeast overgrowth

LDN cannot battle that

and your sympoms will

return if you have

candida. Anyone who has

been having success that

long on LDN and it

suddenly stop working the

first 4 things to look at

are...possible candida,

has pharmacy changed how

they make LDN, are you

under undue stress, could

you have an infection,

like bladder, kidney, etc.

Find a homeopathic or

alternative medicine

doctor who will be

willing to check you for

candida. Most

traditional docs do not

believe candida yeast

overgrowth exists. The

autistic kid's who use

LDN, their moms can tell

you what candida tests

you need to have done.

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--- In low dose naltrexone , " Bren " <b63powell@...>

hey bren shelly here maybe u should try increasing d dosage, but u do

take your vit. we need a lot am currently on LDN but still use a

wheelchair however am thinkin bout increasing my dosage 2 4.5mg...dont

worry girl everything will work out

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CJ, I've never heard of anyone becoming immune to LDN. An

exacerbation can be caused by infection, injury, stress, a reaction

to weather, even while on LDN.

Do you take supplements--vitamins? minerals? If you write to me

directly, I will send you a list of Dr. Lawrence's recommendations.

He's an MS doctor in Wales who prescribes LDN and who has been

extremely helpful. His recommendations are also part of a " welcome

package " that Aletha sends out to new people. If you never received

it, just ask her here and she'll e-mail it to you.

>

> Hi everyone..

> I do not post very often but I read everyone's posts.

> I have been on LDN since August 20, 04. It had worked very good

with me up

> until about a month ago or maybe a little bit longer ago. I

started feeling

> very tired all the time. I was sleeping constantly. As time has

gone by I

> am slowly going downhill. Right now it is at the point that I am

getting very

> weak and especially walking around my small apt. It is getting

really hard

> to hold my arms up. I cannot carry anything at all. If I do

there is so

> much weakness that I could actually sit down on the floor and not

get up.

> My question is " Is it possible that the LDN is no longer

working? " Did I

> become immune to it now?

> I go for a MRI on Thursday but it was only for my brain. I will

be having

> my friend (who also has MS) drive me to the neuro and I will have

to use my

> wheelchair that has been in my storage cage for at least 10

years.

> Any input would be so welcomed on this end.......

> Bless you all.

> Love and Hugs

> CJ

> Friends are angels who lift us to our feet

> when our wings have trouble remembering how to fly

>

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Hi,

I have recently read that it is recommended that you occasionally take a couple of days off from ldn as your body will become accustomed to the medication and no longer provide positive results. Recommended at one-two days per week or every other week. Sorry, I did not save the source of this information to colloborate my statement.

[low dose naltrexone] I need some answer's.

Hi everyone..

I do not post very often but I read everyone's posts.

I have been on LDN since August 20, 04. It had worked very good with me up until about a month ago or maybe a little bit longer ago. I started feeling very tired all the time. I was sleeping constantly. As time has gone by I am slowly going downhill. Right now it is at the point that I am getting very weak and especially walking around my small apt. It is getting really hard to hold my arms up. I cannot carry anything at all. If I do there is so much weakness that I could actually sit down on the floor and not get up.

My question is "Is it possible that the LDN is no longer working?" Did I become immune to it now?

I go for a MRI on Thursday but it was only for my brain. I will be having my friend (who also has MS) drive me to the neuro and I will have to use my wheelchair that has been in my storage cage for at least 10 years.

Any input would be so welcomed on this end.......

Bless you all.

Love and HugsCJFriends are angels who lift us to our feetwhen our wings have trouble remembering how to fly

Want to start your own business? Learn how on Small Business.

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OLD ANCIENT RETRACTED OBSOLETE WRONG news

Would a diabetic take a break from insulin?

Re: [low dose naltrexone] I need some answer's.

Hi,

I have recently read that it is recommended that you occasionally take a couple of days off from ldn as your body will become accustomed to the medication and no longer provide positive results. Recommended at one-two days per week or every other week. Sorry, I did not save the source of this information to colloborate my statement.

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>

> --- In

low dose naltrexone@gro

ups.com, " Bren "

<b63powell@>

> hey bren shelly here

maybe u should try

increasing d dosage, but

u do

> take your vit. we need

a lot am currently on LDN

but still use a

> wheelchair however am

thinkin bout increasing

my dosage 2 4.5mg...dont

> worry girl everything

will work out

>

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

,

You must mean someone

else. I started at 4.5mg

of LDN and have stayed

there now for over 3

years.

also known as Bren

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>

> Hi,

> I have recently read

that it is recommended

that you occasionally

take a couple of days off

from ldn as your body

will become accustomed to

the medication and no

longer provide positive

results. Recommended at

one-two days per week or

every other week. Sorry,

I did not save the source

of this information to

colloborate my statement.

>

>

==========

That thought is no

longer. It was decided

at one of the LDN

conferences that breaks

are not needed. That was

a doctor from England who

used to recommend that.

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Yes, Dr. Lawrence used to recommend mini breaks from LDN, but he determined later that it was not necessary.

Aletha

[low dose naltrexone] Re: I need some answer's.

>> Hi,> I have recently read that it is recommended that you occasionally take a couple of days off from ldn as your body will become accustomed to the medication and no longer provide positive results. Recommended at one-two days per week or every other week. Sorry, I did not save the source of this information to colloborate my statement.> > ==========That thought is no longer. It was decided at one of the LDN conferences that breaks are not needed. That was a doctor from England who used to recommend that.

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Sorry,

LarryCG I have not been on LDN to date.

Re: [low dose naltrexone] I need some answer's.

Hi,

I have recently read that it is recommended that you occasionally take a couple of days off from ldn as your body will become accustomed to the medication and no longer provide positive results. Recommended at one-two days per week or every other week. Sorry, I did not save the source of this information to colloborate my statement.

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I tried to clean the previous message up a bit, apologies if it

didn't turn out quite right. My heart felt feelings on the

unexpected health problems.

LDN was started about 2 years ago. The wheelchair has been in

storage for 10 years. When was the MS diagnosed? Why was the wheel

chair purchased? Why was the wheel chair stored for 10 years? This

post sounds like an important story. For me it has sparked many

questions.

>

> Hi everyone..

> I do not post very often but I read everyone's posts.

> I have been on LDN since August 20, 04. It had worked very good

with me up until about a month ago or maybe a little bit longer

ago. I started feeling very tired all the time. I was sleeping

constantly. As time has gone by I am slowly going downhill. Right

now it is at the point that I am getting very weak and especially

walking around my small apt. It is getting really hard to hold my

arms up. I cannot carry anything at all. If I do there is so much

weakness that I could actually sit down on the floor and not get up.

> My question is " Is it possible that the LDN is no longer

working? " Did I become immune to it now?

> I go for a MRI on Thursday but it was only for my brain. I will

be having my friend (who also has MS) drive me to the neuro and I

will have to use my wheelchair that has been in my storage cage for

at least 10 years. Any input would be so welcomed on this

end.......

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