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MAF 314 (probiotic gcmaf)

Dr. Cheney will show the results of 1 month trial of maf 314 on CFS/XMRV infected patients on the 22-25 september Ottawa conference (http://www.iacfsme.org/)

Prof. Ruggiero 27 e 29 sept a Padova http://www.siai2011.azuleon.org/

due to the extraordinary results professor ruggiero and the other scientists involved agreed to explain people on how to do maf314 in our home kitchens

we know that first weeks of maf 314 made a rise of cd4,cd8 and nk cells in aids and healthy subjects...much more potent than chemical gcmaf i am doing now
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http://m.youtube.com/index?desktop_uri=%2F&gl=US

Here is the video with dr.enlander info.
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Is there a transcript or video of Cheney and Ruggerio presentations online?  If so, where? I went to the links below but did not find anything...

Dr. Cheney will show the results of 1 month trial of maf 314 on CFS/XMRV infected patients on the 22-25 september Ottawa conference (http://www.iacfsme.org/)

Prof. Ruggiero 27 e 29 sept a Padova http://www.siai2011.azuleon.org/
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Dr. Enlander in NY has MAF 878  Starter kit. There is more information on his website at
http://www.enlander.com
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it sure is and i bet that money is not going to fund more research on it
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5000 for six months. Boy these guys are sure nice guys! :)

I saw the prices for Cheney clinic in north carolina. And all i can say it is outrageous! They dont take health insurance.
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no they just show you how to make it urself in ur kitchen just like if it was a biolab, there is no market for this and it can t be made in powder or pill anyway, the live bacteria lasts 5days only and has to be alive

there is doctor in new york helander or something who said copied maf and sell it on ebay but i dont think it works, CFS cheney clinic in US charge 5000USD for a 6 month supply
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They don't have it ready in a pill or powder form?

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i got maf314 from dr santos konig in vienna, the cost for 6 months probiotics is 1000€, you have to add 300€ for the visit at their clinic and the cost of colostrum which is about 250€ for 3 months

you end up with a probiootic which costs about 5-6 euro daily and enough for 2 persons, so not that expensive in the end but you need help to make it, it is hard and complicated (many bacteria strains to add at different times and mix in special order).the probiotic can be shared with endless people just need to add more milk and colostrum
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lets just say I was told this by somebody involved in the research with this stuff. As for toxicity you should worry more about taking nucs. whatever interferon does is reversable.
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Where can we buy this? Is there a video on how to make this?

As far as political pressure goes all these inventors and researchers need to do is post their ideas on the forums and have a small website with donate button where they can accept donations via paypal.
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just 2 reports from patients with chronic hbv but not acquired from birth, this is too little to say it can work on hbv
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I mean the injectable GCMAF.
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I mean do you think GCMAF work for hep B?
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Hi studyforhope

Can you also provide your view about GCMAF?

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Hi stef

What about the injectable GCMAF?  Do you think it works for hep B?

Also have you tried alinia with simvastatin?  Is there any interaction?  I am not familiar with alinia.  I have to import it from progressiveRX as you suggested and check it purity.
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Avatar universal
Nice preach VeteranB ..
the light side that the GS9260 can remove HBsAg in 3 months .. great ..

the component that you mentioned it .. Imiquimod .. is it availble by any means .. tablet .. syrup .. capsules .. injection ..

do u have any idea about the toxity of gs9260?

is there any known person .. that take gs9260 in the trials phase?

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Avatar universal
Yes they are blocking cures.. For HBV for sure. Till 2017 they will continue to feed us antivirals..

Things are really bad, the system wants to get rid of very sick people and make money while they are at it. But do it slowly. I walked that road. Still do. In America it is the worst of ALL industrialized nations how they treat us. The Doctors, the hospitals and of course the health insurance companies that still continue to not provide health insurance coverage for very sick people. You have HBV you have to pay 3 or 4 times as much as  a healthy person or you get no health coverage at all. Or they put you into a high risk insurance pool (Obama care) that has 75,000 yearly benefit cap. And then what? When one day in the Hospital here just the bed costs $10,000 So that is why many good doctors that really like to bill health insurance really don't want to deal with people like us. $75,000 for these business guys is nothing.


Here is another example..  There is GS9620.. Imiquimod that works, very very promising drug. So they are doing "clinical trials" makes sense..

But they are very selective of who they take. I live within driving distance of San Diego. And just because I take Baraclude I cannot try this drug. Have to be on Tenofovir fro 3 months or more.. Does that make sence to you?

What is the difference? Both are the same group of drugs. Both do the same thing, both are toxic, and really dangerous drugs if you talk with HIV treating people - off the record. But it is still better to be on them, then not.. I am just saying..

So one can ask what kind of a research this is anyway? And what kind of research they are doing in the Antiviral Center there is SD if they test Corporate sponsored medication, according to the guide lines that Gelead has set up. This is not research, this type of research they over at Gelead could do them selves. When one think of research you would think doctors there would try pioneering treatments on patients that are willing, without any conditions attached.

So face 2 will be 2014 for GS9620.. and face 3.. yes you guessed right, right up there in 2016 :)

Yet everybody "wants to help" so they say.. BUT they won't give the medication to people that need it unless thy take an antiviral that from a specific drug maker that also happens to sponsor these  trials of their product. This is what this is. Product testing, and not really about helping people.. But they think we are stupid, from low income, and can be told some bs line and be quiet.

Here is what I was told about GS9620 off the record btw.. that they have data, that people Loose HBsAG.. on it over 3 months of this stuff. They just can't guarantee that it wont come back at some later point. I say this is very important, I think it should be available for people that want to try it so we can report it here and spread the awareness. This is the way to fight HBV for real.

The reason guys all the stuff is happening is because we are being quiet about it. That health care for profit hides cures from people. That medicine became an industry - somebody profits while others suffer.
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thanks Stefano. This is  very good info...
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Avatar universal

there is no prof it has an effect on hbv at all so i suggest not to use this for hbv now
maf314 can be bought in austria (dr Uta Santos-König vienna) and germany kassel (dont have the name of clinic now)
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Hi Stef

Where can i prurchase MAF314.  
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Thanks for the info. I honestly do not understand many things but anyway I'll follow this post as this is also one of the hopes of cure for us.....
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redlabs.com have also cytokine tests, this way we may have a clue of wht we do with gcmaf to immune system
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i just posted the most interesting parts of this last study because if we use gcmaf or maf 314 we can use cd counts and cytokine tests to see if maf or gcmaf are having an effect

for example in my case cd4/cd8 ratio was 0.4 while they say acute are usually 2:1 ratio.so with my gcmaf therapy i need to increase cd4 at least more than double
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Interferon-g findings

The data on IFN-g production by PHA stimulated peripheral blood mononuclear cells from the studied patients revealed a highly significant (P < 0.001) increase among the acute HBV group as compared to the healthy subjects and chronic cases (Table 6). However, IFN-g production among the chronic cases revealed a highly significant decrease (P  0.05) when compared to the controls (Table 6). The results published by Kakumu et al (1989) [22], Inowa et al (1989) [23], Fuji et al (1987) [24], Ikeda et al (1986) [25] and Abb et al (1985) [26] were in accordance with the present data. The findings of defective IFN production in patients with chronic HBV infection reported in our study and by other investigators had led to the hypothesis that this might be a primary defect which could have been instrumental in the early stages of infection in permitting continued viral infection. These have led to the speculation that a defect in the ability to produce sufficient IFN during acute viral hepatitis may lead to chronic infection. Our data enabled us to suggest that IFN levels were statistically highly correlated (P < 0.001) to IL-2 levels. Both cytokines increased in acute HBV cases and control subjects, and both decreased in the chronic cases (data not presented).

The release of IL-2 by Th1 cells seemed to be the main stimulus for the sequential synthesis of IFN-g . When exogenous IL-2 was added to peripheral blood lymphocytes (PBL) in culture, there was a significant increase in the amount of IFN-g [23]. When both cytokines were correlated to Th subsets they were statistically insignificant. This was explained by the fact that measurement of Th subset in the present study did not specifically identify Th1, the main inducer of IFN-g and IL-2.

So, not only the phenotypic analysis of Th subsets was a must but also their functional differences should be studied to confirm the hypothesis proposed that defective Th1 was the main element underlying viral persistence in chronic HBV infections.
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