Re: Cancer Cure- By Bill Sardi and Hubbell

[Guest guest]

Very interesting. Here's the whole article posted at National Health Federation.

http://www.thenhf.com/article.php?id=633

[Moderator's note: The article ends with this information:

" Addendum: Sadly, the treatment you have just read about is not available

anywhere..... " -Bill Sardi ]

This page has archived articles by Bill Sardi, 11 about Cancer.

http://www.lewrockwell.com/sardi/sardi-arch.html

Bill Sardi's website

http://www.naturalhealthlibrarian.com/

" D. " <parisd2002@...> wrote:

>

> I normally do not post but am curious to hear if someone knows more about the

following:

>

> Cancer Cured For Good - By Bill Sardi and Hubbell October 2008

>

> It works 100% of the time to eradicate cancer completely, and cancer does not

recur even years later. That is how researchers describe the most convincing

cancer cure ever announced. The weekly injection of just 100 billionths of a

gram of a harmless glyco-protein (a naturally-produced molecule with a sugar

component and a protein component) activates the human immune system and cures

cancer for good, according to human studies among breast cancer and colon cancer

patients, producing complete remissions lasting 4 and 7 years respectively. This

glyco-protein cure is totally without side effect but currently goes unused by

cancer doctors. Normal Gc protein (also called Vitamin-D binding protein) , an

abundant glyco-protein found in human blood serum, becomes the molecular switch

to activate macrophages when it is converted to its active form, called Gc

macrophage activating factor (Gc-MAF). Gc protein is normally activated by

conversion to Gc-MAF with the help of the B and T cells (bone marrow-made and

thymus gland-made white blood cells). But, as researchers explain it themselves,

cancer cells secrete an enzyme known as alpha-N- acetylgalactosaminidase (also

called Nagalase) that completely blocks conversion of Gc protein to Gc-MAF,

preventing tumor-cell killing by the macrophages. This is the way cancer cells

escape detection and destruction, by disengaging the human immune system. This

also leaves cancer patients prone to infections and many then succumb to

pneumonia or other infections. The once-weekly injection of minute amounts of

Gc-MAF, just 100 nanograms (billionths of a gram), activates macrophages and

allows the immune system to pursue cancer cells with vigor, sufficient to

produce total long-term cures in humans. Nobuto Yamamoto, director of the

Division of Cancer Immunology and Molecular Biology, Socrates Institute for

Therapeutic Immunology, Philadelphia, Pennsylvania, says this is " probably the

most potent macrophage activating factor ever discovered. " A MACROPHAGE

OVERCOMES AND EATS A CANCER CELL.

>

[Guest guest]

ParisD-

I spend much of my day, week on the internet posting in cancer forums,

looking for articles and studies to post on peoplebeatingcancer.org- I

have done this for the past several years and I have never heard about

the National Health Federation or the cancer cure that is talked about.

Having said this, I don't claim to know all in the cancer world. I

will keep my eyes open and try to learn more about this organization

and the cancer therapy they discuss. Like all cancer survivors I will

cross my fingers and hope.

Emerson

cancer survivor since 3/94

founder, director of the Galen Foundation and peoplebeatingcancer.org

http://peoplebeatingcancer.org/

_____________________________

" skpounds14 " wrote:

>

> Very interesting. Here's the whole article posted at National Health

Federation. http://www.thenhf.com/article.php?id=633

>

> [Moderator's note: The article ends with this information:

> " Addendum: Sadly, the treatment you have just read about is not available

anywhere..... " -Bill Sardi ]

_________________________________

" D. " <parisd2002@...> wrote:

>

> I normally do not post but am curious to hear if someone knows more about the

following: Cancer Cured For Good - By Bill Sardi and Hubbell October

2008

[Guest guest]

The NHF just reposted the article and I don't know about them either, I just

posted the whole article for people to read.

About the Original posters question, it may related to Mr. Sardi's cancer book

at http://www.thecancerbook.com/ It kind of sounds like it, could email him and

ask.

Other Cancer info by Mr. Sardi and verified by 2 books is a fairly inexpensive

supplement called IP-6.

The Overlooked Cancer Cure From Japan

http://www.lewrockwell.com/sardi/sardi39.html

IP-6 Cleanse & Benefits

http://www.life-enthusiast.com/index/Articles/Sardi/Cleanse:_Rice_Bran

-SOURCES-

Swanson brand is the best priced with few fillers.

http://www.swansonvitamins.com/SWU286/ItemDetail?n=0

iherb, vitacost, vitaminshoppe and others carry IP-6. Reviews at iherb,

vitacost.

-BOOKS-

IP6: Nature's Revolutionary Cancer Fighter: Nature's Revolutionary

Cancer-Fighter by Abulkalam M. Shamsuddin

http://amzn.to/hLq6lQ

Nature's Ultimate Anti-Cancer Pill: The IP-6 with Inositol Question and Answer

Book by L Coles

http://amzn.to/fc4aNI

2 time cancer survivor (2002,05)

>

> ParisD-

>

> I spend much of my day, week on the internet posting in cancer forums, looking

for articles and studies to post on peoplebeatingcancer.org- I have done this

for the past several years and I have never heard about the National Health

Federation or the cancer cure that is talked about.

>

> Having said this, I don't claim to know all in the cancer world. I

> will keep my eyes open and try to learn more about this organization

> and the cancer therapy they discuss. Like all cancer survivors I will cross

my fingers and hope.

>

> Emerson

> cancer survivor since 3/94

> founder, director of the Galen Foundation and peoplebeatingcancer.org

> http://peoplebeatingcancer.org/

[Guest guest]

dear david and skpounds14,

I do not know and not trying to know about National Health Federation (not my

post), it could really be a fake federation, simply a name taken by a website.

I am intrigated by GcMAF results, if you google it there are lot of information

on it.

What worries me is that those promoting this treatment considered the success by

looking at the dropping nagalase serum (not the PSA in case of PCa) claiming

that Nagalase is a perfect indicator of the cancer tumor burden. This is

something new to me, dont know if this is true.

" skpounds14 " wrote:

>

> The NHF just reposted the article and I don't know about them either, I just

posted the whole article for people to read.

>

> About the Original posters question, it may related to Mr. Sardi's cancer book

at http://www.thecancerbook.com/ It kind of sounds like it, could email him and

ask.

>

> Emerson <daviddecemerson@> wrote:

> >

> > ParisD-

> > I spend much of my day, week on the internet posting in cancer forums,

looking for articles and studies to post on peoplebeatingcancer.org- I have done

this for the past several years and I have never heard about the National Health

Federation or the cancer cure that is talked about......

[Guest guest]

it has been on the net for a good number of years. just google

Yamamoto, cancer and you will find some information but you will also find this:

do not contact Dr Yamamoto. He cannot help you.

[Guest guest]

I looked into this one a bit.

A good discussion here:

http://scienceblog.cancerresearchuk.org/2008/12/03/cancer-cured-for-good-gc-

maf-and-the-miracle-cure/

It seems that the research is good, though not comprehensive.

" Gc-MAF

I have extensive knowledge on Gc-MAF. First of all, the lack of " side

effects " as per Dr. Yamamoto is relative to the harsh side effects of

chemotherapies and antiretrovirals. The fact is, Gc-MAF results in high

levels of TNF-alpha production and other cytokines which in effect cause

side effects such as severe fatigue, feverishness, and depression in some

patients. Basically, " sickness behaviour " . This is due to the immune system

activation, no different from taking strong immune boosters or

pharmaceutical interferons. The Gc-MAF made in the western USA and shipped

to Europe is PURE, and as a matter of fact, the scientist who participated

in its production is one of the top researchers in Gc-MAF from southeast

Asia, who was retained to help produce it. The deleterious side of Gc-MAF is

well known in the scientific community by those researchers who are working

on synthetic mimics of Gc-MAF who are working on tweaking the protein to be

able to induce macrophage activation without the production of

pro-inflammatory cytokines. Therefore, all patient's using Gc-MAF that is

currently made in the USA and shipped to Europe experience fatigue and

distress during therapy. I can only predict that CFS sufferers will feel

miserable during such therapy and should be supervised by doctors. "

http://www.prohealth.com/me-cfs/blog/boardDetail.cfm?id=1379980

A descrioption on that page:

" Dr. Yamamoto's discoveries are related to the role of the macrophage in

the immune system. The macrophage, of course, is the Field Marshall of the

immune system. In a healthy human body, damaged cells release the components

of the cell membranes into the interstitial fluids and thence into the blood

stream. These are lysophospholipids. They serve as a cytokine (or chemical

activator) for the B cells.

The B cells produce an enzyme called beta galactosidase in response to the

lysophospholipids. The enzyme is located on the surface of the cell

membrane.

There is a protein in the blood stream known as " Vitamin D Binding Protein "

or " Group Specific Component " or " Gc. " We'll use Gc here.

At one specific site on the protein, there is a three-sugar entity attached.

The first sugar is attached to the protein, and the second and third sugars

are attached to the first. In Dr. Yamamoto's papers this is described as a

dibranched trisaccharide.

The B cell's enzyme cleaves sugar #3, and an enzyme on the cell surface of

the T-cells (always resident) can then cleave sugar #2. (If you want all the

names, read the Prostate Cancer paper published in Translational Oncology at

http://www.transonc.com/pdf/manuscript/v01i02/neo08106.pdf.)

The Gc protein is then left with only sugar #1 of the original three. That

resulting molecule is what activates the macrophages. Dr. Y states that it

is the most powerful macrophage activating factor ever discovered.

However, both cancer and viruses release an enzyme (Nagalase) into the blood

stream that cleaves all three sugars in that entity. With all three removed,

there is no way the body can convert it to GcMAF, because sugar #1 must be

left in place.

Cancers and viruses disable the immune system by destroying

(deglycosylating) the Gc protein that is the precursor of GcMAF. With little

or no Gc protein, there is little or no GcMAF. With little or no GcMAF there

is little or no activation of the macrophages. With little or no activation

of the macrophages . . . .

Dr. Y extracts Gc protein from a healthy volunteer's blood and uses the two

enzymes found in B-cells and T-cells to cleave sugars #3 and #2, thereby

producing GcMAF in the lab.

That GcMAF is then injected into the vein of the patient and begins the

process of activating the macrophages. The dosage is 100 nanagrams (or one

ten-millionth of a gram). Increasing the dosage will not increase the

macrophage activation.

GcMAF has been tested at ten times the maximum effective dose (one millionth

of a gram) without any adverse side effects. Even in a healthy person, it

exhibits no side effects.

Within 4 hours the ingestive rate (phagocytic rate) of the macrophage

increases 30-fold. In about 4 days, the number of macrophages will have

increased about 40-fold. The amount of superoxide produced by the macrophage

increases 15-fold.

So, 40 times as many macrophages gobbling up things at 30 time the rate . .

.. . You do the math.

GcMAF is not disease-specific, because the macrophage is not

disease-specific. If there is a protein or organism in the ailing body that

the macrophages should be attacking, they will do so when GcMAF is

administered.

Curing CFIDS would probably take about 5 to 10 IV injections (at one per

week).

Sometime in the future, research will prove that CFIDS is a viral disease --

probably a recombinant virus formed by rubella fragments and a retrovirus.

But activated macrophages do not care where it came from. If it's not

normal, they'll destroy it.

That was the good news. What follows is the unhappy news.

GcMAF does have an Achilles Heel -- prescription drugs. Certain drugs

prevent the activation of the macrophages. They include all pain-killers

(even Novacaine), blood pressure meds, and steroids. There is no

comprehensive list of the drugs that interfere with macrophage activation,

so the safest course for anyone using GcMAF is to refrain from ANY drug use.

This is somewhere between difficult and impossible in some extremely

late-stage cancer patients.

Also, GcMAF is not available in the United States. Nor, to my knowledge, is

it available anywhere on earth. But I am hoping that it will be made

available somewhere within the next year.

There is a cancer clinic in the Bahamas that has been producing and

administering what they say is GcMAF, but their results have been dismal. I

have it on good authority that the product has been analyzed by a researcher

and found to have little or no activity.

Another counterfeit version is being sold by a fellow in the western United

States, but he is careful to only ship it out of the US. I have reliable

reports of adverse reactions to that product.

GcMAF is very, very difficult to make, requiring extremely exact laboratory

procedures. Only highly-qualified scientists with an intimate knowledge of

certain key steps are able to produce it, so it is unlikely to show up on

the black market.

Also, not all reagents and biologicals are the same, even though they have

the same names and formulae on the labels. More than one batch has been

lost, because of sub-standard reagents and biologicals.

I am not one of those who can produce it.

If I had CFIDS and could not get GcMAF, I would be investigating

photoluminescence, intravenous hydrogen peroxide, and intravenous

polymannans (extracted from aloe vera). I am sorry that I am not allowed to

post information on how to obtain those treatments. They are all legal. A

prescription for the polymannans must be filled by a compounding pharmacist.

I hoe you find this useful. If I can help you with anything else, let me

know. "

An opinion piece on 'cures':

" A " new concept " drug is said to cost over a billion dollars to get through

the (often needless) FDA testing. If you read Dr. Marcia Angell's book, you

learn that the entire testing approval process is corrupt.

One of the reasons that FDA testing costs so much is that they require such

large experimental groups. They require large experimental groups, because

(a) most drugs do not show much improvement over

(1) existing drugs or

(2) no drugs at all and

( most drugs are quite toxic.

To get statistically reliable data on a drug that shows only a slight effect

requires a large experimental population.

If GcMAF were evaluated on a purely scientific basis, it could be done with

fewer than a thousand experimental subjects in less than a year. The reasons

that I say that are that (a) GcMAF shows incomparable results (complete

cures) in nearly 100% of patients and ( has no toxicity.

But I seriously doubt that the FDA would even dream of allowing that.

In this case, if GcMAF were to be approved by the FDA, it would cause

unemployment in the health care industry that could be measured on a

seismograph and scored on the Richter Scale.

Getting such a revolutionary discovery to market would require the wisdom of

.

If you know how to do it, I'd love to learn how. And I bet Dr. Y would too. "