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GcMAF

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r,

did u start the b12 and nexavir at the same time as gc maf? if so, how can u be

sure what has helped?

do u have a sense on how others are doing on gc maf?

thanks,

jim

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Hi EveryOne,

I have not had any negative effects from the MAF Yogurt and some would think

that means it is not working. I do not think that is true, it may be because it

is delivered to the body in a much more natural form.

Some have claimed that the MAF Yogurt is more powerful than the injection but

without the negative side effects. I have no basis of comparison. Dr E just said

on a video that he feels the injection works better for many people.

Perhaps those who have issues with the injection might try the yogurt and maybe

one day I will try the injection. For now, I am happy with my progress on the

yogurt. It also might work better for people to start with the yogurt and then

switch to the injections once the body is used to it.

I have good levels of Vit D and B12 not sure if that matters but it might.

Peace, Love and Harmony,

Bev

>

> dr. de meirleir's gcmaf is 35 euro per vial (the same size vial that dr

enlander has, and it is also the same product made from the same source). but

you have to go to see de meirleir in europe to get gcmaf from him. enlander is

" only " in NYC. so enlander's gcmaf is much more expensive for the same product

($270 per vial), but it is not an int'l trip.

>

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Watching Dr. De Meirleir's presentation of Nov. 20, 2011, I found out I'm

not a candidate for GcMAF because I have autoimmune disorders.

Did you (or anyone else using it) have your levels of nagalase or LPS tested

before starting?

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Doesn't everyone with CFS have autoimmune problems?

Ellen

Re: gcmaf

Watching Dr. De Meirleir's presentation of Nov. 20, 2011, I found out I'm

not a candidate for GcMAF because I have autoimmune disorders.

Did you (or anyone else using it) have your levels of nagalase or LPS tested

before starting?

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i have severe CFS for 20 yrs but didnt show any autoimmune problems...normal

ANA, etc

________________________________

From: ellen <variegatedfoliage@...>

Sent: Thursday, May 24, 2012 3:40:51 PM

Subject: Re: Re: gcmaf

 

Doesn't everyone with CFS have autoimmune problems?

Ellen

Re: gcmaf

Watching Dr. De Meirleir's presentation of Nov. 20, 2011, I found out I'm

not a candidate for GcMAF because I have autoimmune disorders.

Did you (or anyone else using it) have your levels of nagalase or LPS tested

before starting?

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i had my soluble CD14 tested..i think that is connected to LPS.....they told me

it was normal (and they said it meant that gut dysbiosis is not a major problem

for me) but my friend had a similar value and was told it was abnormal at

another lab...and they found overgrowth of certain bacteria in her too. when she

took the prescribed antibiotics, her brain fog disappeared! but it came back

eventually.....then she got on gcmaf and is doing very well...

________________________________

From: Slater <diana_slater@...>

Sent: Thursday, May 24, 2012 2:57:50 PM

Subject: Re: gcmaf

 

Watching Dr. De Meirleir's presentation of Nov. 20, 2011, I found out I'm

not a candidate for GcMAF because I have autoimmune disorders.

Did you (or anyone else using it) have your levels of nagalase or LPS tested

before starting?

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hi jim. it is nice to get nk cell function tested but the only tests that are

necessary during gcmaf, i think, are the regular bloodwork tests (wbc liver

kidney etc), calcium, and both vitamin D's

some people get complement CD4a tested too, to see if the inflammation is

decreasing...but i dont think its necessary

________________________________

From: Jim <jims111@...>

Sent: Thursday, May 24, 2012 12:29:35 PM

Subject: Re: Re: GcMaf

 

does anyone know if testing CD57 levels during treatment is important? my lab

does not do this test, tho they do NK and CD20.

thanks.

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