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RE: T-cells

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I would argue Mike, that everyone has flu like symptoms. Flu like symptoms are

related to the immune system fighting something, yes. However, tell someone

that

they're HIV positive and they'll go back in their history and be able to

recall...

there was the time when... I thought I knew when I had seroconverted, and it

ended

up being Mono. Not to mention the fact that everyone I had been with tested

negative

and I had just tested negative one month before. However, virus or no, I still

don't think it's the cause of AIDS. It's a good point though. I'm still

straddling

the fence on whether there's a real retrovirus or not. Since 100 billion

dollars

hasn't produced one piece of solid evidence, I'm thinking not. However, I don't

know enough to completely refute Dr. Duesberg's hypothesis. Caer

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  • 2 years later...

T cells are a major player in your immune

system. In general, MS, cancer, and all other autoimmune diseases face

the same battle. Your immune system cannot cope with the onslaught of

disease. What you need to do, if you have not already been doing this is

to consider massive dietary change for openers. Please understand I am

looking at this from a cancer perspective, I do not have MS, ALS, etc…

But diet is a critical factor. Were it me, I would start by doing a

candida albicans (yeast) flush. I would also want to do a mild liver

flush to get the toxins out of my system that can trigger an attack. ALA (alpha lipoic acid)

at about 600 mgs per day and Ester C to bowel tolerance daily for a month along

with the liver flush. I would then maintain the Ester C at 4,000+ mgs per

day past the first month.

Limit meats to 10% or less of your diet

and get rid of all dairy with the possible exception of occasional cream (does

not have sugar of any kind in it). Get rid of ALL

vegetable oils and restrict your usage to flax seed oil, coconut oil, and olive

oil only. Increase you seafood intake for the additional Omega 3

oils. The key here is not to just take more Omega 3’s, but to

actually do away with the other oils, margarine, etc… that are heavy in

omega 6. Simply adding additional Omega 3’s does no good.

Just taking fish oil caps, for instance is worthless if you do not restrict the

other bad oils. Probably would not hurt to add some evening primrose oil

also to your supplementary intake.

Get rid of all processed sugars and

bleached flours in your diet. Avoid all fried foods and caffeine laden

foods. Severely restrict anything with gluten (gluten in flours requires

immune system action to digest it and you do not need to take away from your

immune system’s ability to fight your disease. Get all artificial

sweeteners (aspartame, etc…) out of your diet and eliminate all

MSG. Severely restrict or do away with all pectin laden candies such as

gummy bears, jelly beans, etc…

Strongly consider juicing green vegetables

such as listed on our NUTRITION page. The phytonutrients/biflavinoids

found in vegetables are very, very potent immune boosters. Also taking a

powdered green food supplement for 4 to 6 months would help to balance out your

system. Something such as Garden

of Life Green Food listed

on our SUPPLEMENTS page. (NOTE: we do not sell anything, just recommend

what should be considered.)

There is a lot more were it cancer that I

would be doing, but this should be enough to see and increase in your T cell

level.

Regards,

Bruce Guilmette, PhD

Survive Cancer Foundation, Inc.

Http://survivecancer.net

Therefore do not worry about tomorrow, for

tomorrow will worry about itself. Each day has enough trouble of its own.

Matt 6:34 (NIV)

From: low dose naltrexone [mailto:low dose naltrexone ] On Behalf Of Aristidis

Sent: Monday, February 06, 2006

3:41 AM

low dose naltrexone

Subject: [low dose naltrexone]

T-cells

Hi every one

I'm in the group for 15 months and I never come

across to the matter

of T-cells.

Since I was diagnosed, I'm fighting to bring those

in to balance, and

use LDN for this purpose. Not seeing any mention

of this, I'm

wondering if I do the right treatment. I'm having

tests for T-cells

every month, and I see no improvement. Any comment

will be

helpful.

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In a message dated 2/6/2006 12:19:05 PM Central Standard Time, wjkeeman@... writes:

--- In low dose naltrexone , "Aristidis" <aristalle@...>

wrote:

>Aristidis, what were you diagnosed with, can you provide more

information on your treatment? Do you take LDN and for how long? How

long have you been having your T-cells measured?

You are right, I've been on this site longer than you and I've never

seen anyone mention their T-cell levels. You are probably the only

person posting here who can provide real blood-work information on

what LDN can do and if Dr. Biharis claims are correct.

+++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++

,

FYI...I have MS and a new doctor just had my TSH, T3 & T4 run. (He said that a TSH alone really tells a Dr nothing) I can't remember for sure, but I will find out, one of the numbers was too low, so he put me on 60mg of Armour Thyroid prescription. I have been on 4.5mg of LDN for over two years.

Marcie

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In a message dated 2/6/2006 12:19:05 PM Central Standard Time, wjkeeman@... writes:

--- In low dose naltrexone , "Aristidis" <aristalle@...>

wrote:

>Aristidis, what were you diagnosed with, can you provide more

information on your treatment? Do you take LDN and for how long? How

long have you been having your T-cells measured?

You are right, I've been on this site longer than you and I've never

seen anyone mention their T-cell levels. You are probably the only

person posting here who can provide real blood-work information on

what LDN can do and if Dr. Biharis claims are correct.

+++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++

,

FYI...I have MS and a new doctor just had my TSH, T3 & T4 run. (He said that a TSH alone really tells a Dr nothing) I can't remember for sure, but I will find out, one of the numbers was too low, so he put me on 60mg of Armour Thyroid prescription. I have been on 4.5mg of LDN for over two years.

Marcie

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In a message dated 2/6/2006 1:22:13 PM Central Standard Time, jaynbeth@... writes:

Marcie,

Are you happy with LDN? Have you taken the CRAB drugs in the past?

+++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++

,

Very happy with LDN. Some symptom improvement. I took Avonex for two years but quit over 6 years ago. Did nothing for me. I had my 3 mercury amalgams removed and cavitations cleaned out. I chelated by IV at that time (2001). I am currently chelating with a product called Chelex. It contains DMSA, EDTA, Chlorella, Cilantro, and something else that I can't recall.

Marcie

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By Dr. Bob Lawrence from the UK who has MS & uses LDN himself

Initially, MS occurs due to a reduction in the activity of the controlling

influence of the suppressor T-cells within the immune system. During an acute

relapse, the overall number of T-cells is reduced, the normal balance of helper

T-cells and suppressor T-cells is disrupted and the damaging helper (CD-4)

T-cells tend to predominate. This is the situation most pronounced during an

acute relapse but occurs similarly, but to a lesser extent, in chronic

progressive MS. Under the influence of LDN there will be an expected increase in

the overall numbers of T-cells but, because the CD-4, helper T-cells tend to

predominate at this time, an increase in their numbers will expectedly tend to

increase MS symptoms. It is only when the numbers of suppressor T-cells

effectively catch up that the normal balance is restored and symptoms once again

diminish and improve.

When starting this LDN(Low Dose Naltrexone) therapy in the treatment of MS,

there may also be some initial transient, though temporary, increase in MS

symptoms.

Experience in using this method has demonstrated most commonly, such as

disturbed sleep, occasionally with vivid, bizarre and disturbing dreams,

tiredness, fatigue, spasm and pain. These increased symptoms would not normally

be expected to last more than seven to ten days.

Rarely, other transient symptoms have included more severe pain and spasm,

headache, diarrhea or vomiting. These additional symptoms would appear to be

associated with the previous frequent use of strong analgesics, which

effectively create an addiction and dependency, thus increasing the body's

sensitivity to pain. This temporary increase in symptoms may also perhaps be

explained when we consider the manner in which this drug is expected to work.

In addition, because LDN stimulates the immune system and many of the drugs

routinely used by the NHS in the treatment of MS further suppress the immune

system, LDN cannot be used in company with steroids, beta interferon,

methotrexate, azathioprine or mitozantrone or any other immune suppressant drug.

If there is any doubt, please submit a full list of the drugs you are presently

taking so that their compatibility may be assessed.

In addition, because LDN will also block the analgesic effects of any opiate

drugs (includes codeine, dihydrocodeine, morphine, pethidine or diamorphine)

presently being taken, the use of LDN will initially greatly increase the level

of pain experienced. It is therefore advisable that any opiate-like drugs be

discontinued at least two weeks before this treatment is initiated. When

starting the treatment it is essential that any untoward or adverse side-effects

are reported immediately so that the treatment process can be further assessed

and, if necessary, modified.

Dr. M R Lawrence

posted by

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--- In low dose naltrexone , " Aristidis " <aristalle@...>

wrote:

>Aristidis, what were you diagnosed with, can you provide more

information on your treatment? Do you take LDN and for how long? How

long have you been having your T-cells measured?

You are right, I've been on this site longer than you and I've never

seen anyone mention their T-cell levels. You are probably the only

person posting here who can provide real blood-work information on

what LDN can do and if Dr. Biharis claims are correct.

> Hi every one

> I'm in the group for 15 months and I never come across to the matter

> of T-cells.

> Since I was diagnosed, I'm fighting to bring those in to balance, and

> use LDN for this purpose. Not seeing any mention of this, I'm

> wondering if I do the right treatment. I'm having tests for T-cells

> every month, and I see no improvement. Any comment will be

> helpful.

>

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Marcie,

Are you happy with LDN? Have you taken the CRAB drugs in the past?

On Feb 6, 2006, at 2:11 PM, marciemjm@... wrote:

> In a message dated 2/6/2006 12:19:05 PM Central Standard Time,

> wjkeeman@... writes:

>

>

>>

>> >Aristidis, what were you diagnosed with, can you provide more

>> information on your treatment? Do you take LDN and for how long? How

>> long have you been having your T-cells measured?

>> You are right, I've been on this site longer than you and I've never

>> seen anyone mention their T-cell levels. You are probably the only

>> person posting here who can provide real blood-work information on

>> what LDN can do and if Dr. Biharis claims are correct.

>>

>

>

> +++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++

>

> ,

>

> FYI...I have MS and a new doctor just had my TSH, T3 & T4 run. (He

> said that a TSH alone really tells a Dr nothing) I can't remember

> for sure, but I will find out, one of the numbers was too low, so

> he put me on 60mg of Armour Thyroid prescription. I have been on

> 4.5mg of LDN for over two years.

>

> Marcie

>

>

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> > >Aristidis, what were you diagnosed with, can you provide more

> > information on your treatment? Do you take LDN and for how long? How

> > long have you been having your T-cells measured?

> > You are right, I've been on this site longer than you and I've never

> > seen anyone mention their T-cell levels. You are probably the only

> > person posting here who can provide real blood-work information on

> > what LDN can do and if Dr. Biharis claims are correct.

> >

>

> +++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++

>

> ,

>

> FYI...I have MS and a new doctor just had my TSH, T3 & T4 run. (He

said that

> a TSH alone really tells a Dr nothing) I can't remember for sure,

but I will

> find out, one of the numbers was too low, so he put me on 60mg of

Armour

> Thyroid prescription. I have been on 4.5mg of LDN for over two years.

>

> Marcie

>

?????? Are you confusing T-cells and TSH? A TSH blood test tells a

doctor a lot. It determines if your thyroid gland is overactive,

underactive or normal. It's a very basic and reliable thyroid

function test.

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In a message dated 2/6/2006 3:22:14 PM Central Standard Time, wjkeeman@... writes:

> Marcie

>

?????? Are you confusing T-cells and TSH? A TSH blood test tells a

doctor a lot. It determines if your thyroid gland is overactive,

underactive or normal. It's a very basic and reliable thyroid

function test.

+++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++

,

I don't think that I'm confusing anything...I'm just telling you what my doctor told me. He said that the TSH alone is really not a very accurate indicator of the thyroid. The ratio of T3 - T4 tells more accurately, according to him, but maybe you know more about it than I.

Marcie

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  • 7 months later...

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