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Re: Professor Basant K. Puri believes most cases are ...

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In a message dated 02/06/2007 20:17:37 GMT Standard Time,

dawnofthedeadhere@... writes:

cs

Professor Puri is a world expert on cfs and does have a clue i think

he has many patients that are well .-

Long-chain polyunsaturated fatty acids and the pathophysiology of

myalgic encephalomyelitis (chronic fatigue syndrome)

B K Puri

***Sorry - he is clueless.

Regards

CS

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ly, there's little point in even posting here with people like

you around.

There are a substantial group of sufferers who can't follow protocols

involving whey to raise glutathione levels, or follow a whole range of

others because of the reactions they experience.

So they need to seek alternatives. And Puri's approach is one of them.

If your suggestions were so bloody marvellous, boards like this

wouldn't be here.

>

>

> In a message dated 02/06/2007 20:17:37 GMT Standard Time,

> dawnofthedeadhere@... writes:

>

> cs

> Professor Puri is a world expert on cfs and does have a clue i think

> he has many patients that are well .-

> Long-chain polyunsaturated fatty acids and the pathophysiology of

> myalgic encephalomyelitis (chronic fatigue syndrome)

> B K Puri

>

>

>

> ***Sorry - he is clueless.

>

>

> Regards

> CS

>

>

>

>

>

>

>

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Thanks for posting this info on Professor Puri, I may try the vegEPA

myself. I've been taking Nordic Naturals fish oils for years which

contains DHA and would like to sample EPA without DHA for 3 months to

see if there is a difference.

I met several people many yrs ago with ME who benefited from Efamol,

for me I didn't feel any difference. But I believe fish oils are a

very important supplementation to our illness.

Nat

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Lipid therapy in neurotoxic conditions is a long studied and used

protocol coming from some of the most serious researchers and

clinicians. The subject is not as simple as Dr Puri implies. Some

people with CFS get great benefit from DHA some do not. Many lipid

researchers like Dr Kane believe that the EFAs (Essential Fatty Acids)

should be balanced according to the most advanced thinking on this

subject. We need a wide range of EFAs. Without lipid tests it is

impossible to know what lipids are deficient or in excess. Such tests

are available but expensive. So best take a wide range of lipids. The

EFAs are called essential because they are essential for life and

health yet we can not manufacture them and must get them from diet.

Some lipids that can be manufactured by the body are not properly

produced in case of many problems including chronic liver problems, so

we might need supplemetation with various lipids even the non

essential ones.

There are dozens of clinicians getting good results in CFS using,

lipid replacement therapy, methylation pathway error correction, Vit

D. So anyone saying that lipids do not have anything to do with CFS

are way behind the curve on this subject. Clinicians like Dr Shoemaker

and Dr Kane use the neurotoxic model of diseases like CFS and have

excellent results in a large percentage of patients. Lipids are

important for we PWCs to understand. Liz

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In the unlikely event after 3 months after taking EPA without any DHA

you feel no benefits have been noticed at all - it is worth having a

special red blood cell membrane fatty acid test - this will show up

whether or not the EPA and the omega-6 levels are in the normal range.

>

> Thanks for posting this info on Professor Puri, I may try the vegEPA

> myself. I've been taking Nordic Naturals fish oils for years which

> contains DHA and would like to sample EPA without DHA for 3 months to

> see if there is a difference.

>

> I met several people many yrs ago with ME who benefited from Efamol,

> for me I didn't feel any difference. But I believe fish oils are a

> very important supplementation to our illness.

>

> Nat

>

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Professor Puri like Dr Kane also does the special red blood cell

membrane fatty acid test- to measure the EPA and omega levels are in

normal range.

>

>

> Lipid therapy in neurotoxic conditions is a long studied and used

> protocol coming from some of the most serious researchers and

> clinicians. The subject is not as simple as Dr Puri implies. Some

> people with CFS get great benefit from DHA some do not. Many lipid

> researchers like Dr Kane believe that the EFAs (Essential Fatty Acids)

> should be balanced according to the most advanced thinking on this

> subject. We need a wide range of EFAs. Without lipid tests it is

> impossible to know what lipids are deficient or in excess. Such tests

> are available but expensive. So best take a wide range of lipids. The

> EFAs are called essential because they are essential for life and

> health yet we can not manufacture them and must get them from diet.

> Some lipids that can be manufactured by the body are not properly

> produced in case of many problems including chronic liver problems, so

> we might need supplemetation with various lipids even the non

> essential ones.

>

> There are dozens of clinicians getting good results in CFS using,

> lipid replacement therapy, methylation pathway error correction, Vit

> D. So anyone saying that lipids do not have anything to do with CFS

> are way behind the curve on this subject. Clinicians like Dr Shoemaker

> and Dr Kane use the neurotoxic model of diseases like CFS and have

> excellent results in a large percentage of patients. Lipids are

> important for we PWCs to understand. Liz

>

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In a message dated 04/06/2007 09:10:59 GMT Standard Time,

dawnofthedeadhere@... writes:

Professor Puri like Dr Kane also does the special red blood cell

membrane fatty acid test- to measure the EPA and omega levels are in

normal range.

********Kane does more than focus on lipids. She looks at the entire

picture.

There is no comparison.

Regards

CS

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There's a doctor (psy) in the lowlands that states the ratio of Omeag-3 intake

should be 3-4/1 (EPA/DHA)...

Liz A Hall <lizahallny@...> wrote:

Lipid therapy in neurotoxic conditions is a long studied and used

protocol coming from some of the most serious researchers and

clinicians. The subject is not as simple as Dr Puri implies. Some

people with CFS get great benefit from DHA some do not. Many lipid

researchers like Dr Kane believe that the EFAs (Essential Fatty Acids)

should be balanced according to the most advanced thinking on this

subject. We need a wide range of EFAs. Without lipid tests it is

impossible to know what lipids are deficient or in excess. Such tests

are available but expensive. So best take a wide range of lipids. The

EFAs are called essential because they are essential for life and

health yet we can not manufacture them and must get them from diet.

Some lipids that can be manufactured by the body are not properly

produced in case of many problems including chronic liver problems, so

we might need supplemetation with various lipids even the non

essential ones.

There are dozens of clinicians getting good results in CFS using,

lipid replacement therapy, methylation pathway error correction, Vit

D. So anyone saying that lipids do not have anything to do with CFS

are way behind the curve on this subject. Clinicians like Dr Shoemaker

and Dr Kane use the neurotoxic model of diseases like CFS and have

excellent results in a large percentage of patients. Lipids are

important for we PWCs to understand. Liz

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and so does Puri have you seen him ? what tests did you have done

for your cfs and what are your results ?

> ********Kane does more than focus on lipids. She looks at the entire

> picture.

> There is no comparison.

>

>

> Regards

> CS

>

>

>

>

>

>

>

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I had an RBC Fatty Acids test done a few yrs ago, just checking here,

my DHA was at 3.69 (3.20-7.04) and my Eicosapentaenoic is low at 0.40

(0.36-1.92).

Nat

> In the unlikely event after 3 months after taking EPA without any DHA

> you feel no benefits have been noticed at all - it is worth having a

> special red blood cell membrane fatty acid test - this will show up

> whether or not the EPA and the omega-6 levels are in the normal range.

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