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INVESTIGATION: Three days before Dr. Bradstreet was found dead in a river, U.S. govt...

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100% of West Coast bluefin tuna are now radioactive Analysis: Chipotle victim of corporate sabotage by GMO industry

INVESTIGATION: Three days NaturalNews.com


1,631,573 likes

before Dr. Bradstreet was found


dead in a river, U.S. govt. agents Like Page

raided his research facility to seize a


breakthrough cancer treatment
called GcMAF
Monday, July 27, 2015
by Mike Adams, the Health Ranger
Tags: Dr. Bradstreet, GcMAF, cancer therapy

(NaturalNews) The history of the Tweet 593


Most Viewed Articles 85K 922
suppression of medical science in America is
Today Week Month Year
a long one, filled with true accounts of
ANALYSIS: Chipotle is a victim of corporate
sabotage... biotech industry food terrorists are pioneering doctors and clinicians being
planting e.coli in retaliation for restaurant's anti-
GMO menu threatened, intimidated and even
assassinated in order to bury emerging
Oregon man serving prison sentence for
collecting rainwater on his own property cures and keep the "sick care" industry in
control. (The American Medical Association,
Statin scam exposed: Cholesterol drugs cause
rapid aging, brain damage and diabetes for example, has been found guilty by the
Russia taking McDonald's to court, threatens U.S. federal courts of a conspiracy to destroy
countrywide shutdown
the chiropractic industry, by the way.)
California to throw adults in JAIL if they refuse
government-mandated vaccines
Over the last few days, we've learned that
Health News
ALL bluefin tuna caught off West Coast are before being found shot in the chest and
radioactive
floating in the river, pioneering medical ANALYSIS: Chipotle is a victim of corporate
sabotage... biotech industry food terrorists are
More proof that Obama is a sleeper cell: FBI researcher Dr. Bradstreet was working with a planting e.coli in retaliation for restaurant's anti-
agent ordered to shut down investigation into
GMO menu (Naturalnews.com)
Islamic terrorists little-known molecule that occurs naturally in the human body. Called, "GcMAF", this

NJ cops bust teenagers shoveling snow without


molecule has the potential to be a universal cancer cure for many people. It has also Marijuana use could prevent weight gain, study
a permit shows (Naturalnews.com)
been shown to reverse signs of autism in the vast majority of patients receiving the
Eyewitness claims Las Vegas vehicle attack treatment. Top 10 health lessons from the Japanese diet
carried out by Muslim woman screaming 'Allahu (Natural.news)
Akbar'... media blackout... HOAX or ISIS?
While GcMAF is perfectly legal as a treatment in dozens of advanced nations around the New study labels obesity as inflammatory
Healthy 12-year-old girl dies shortly after disease to be treated with pharmaceuticals
receiving HPV vaccine world, the U.S. Food and Drug Administration has outlawed it, calling it an "unapproved
(Slender.news)
drug." It is with this designation -- an effort to suppress the forward progress of medical
Irrefutable proof we are all being sprayed with
science -- that the U.S. government conducted a raid on Dr. Bradstreet's clinic, specifically Reduce your cancer risk; eat more cherries
poison: 571 tons of toxic lead 'chemtrailed' into
America's skies every year (Fresh.news)
seeking to confiscate GcMAF in order to shut down his research and halt his treatment of
How to make a nutritious superfood for survival patients. Meanwhile, Big Pharma gets special permission to unleash untested, Tropical diseases surge in America while
that lasts decades Obama leaves borders open to illegal
experimental drugs on the public as long as those drugs earn sufficient profits. immigrants (Medicine.news)
600 strains of an aerosolized thought control
vaccine already tested on humans; deployed via
air, food and water In this article, I summarize the videos, articles and documents covering GcMAF and the
Unbelievable scam of cancer industry blown mysterious death of Dr. Bradstreet. An exhaustive investigation needs to be pursued
wide open: $100 billion a year spent on toxic
chemotherapy for many FAKE diagnoses...
on this matter, possibly involving private investigators. The timing and manner of Dr.

http://www.naturalnews.com/050553_Dr_Bradstreet_GcMAF_cancer_therapy.html 12/24/2015
INVESTIGATION: Three days before Dr. Bradstreet was found dead in a river, U.S. govt... Page 2 of 14

National Cancer Institute's shocking admission


affects millions of patients
Bradstreet's death seems highly suspicious, especially in light of the many other holistic
doctors who have recently been found dead under mysterious circumstances. (Dr.
Natural News announces recipients of 2015
Celebrity Hall of Shame Awards Nicholas Gonzalez died just days ago...)

Republicans and Democrats have MERGED: It's


all one big, police state party of insanity now!

Truvia sweetener a powerful pesticide; scientists Motive to murder medical researchers and suppress a
shocked as fruit flies die in less than a week
from eating GMO-derived erythritol promising cancer treatment breakthrough AlternativeNews.com
The independent news source for free
thinking people
New York Times quietly edits article to delete Is there a motive for the murder of pioneering cancer researchers working on a possible
embarassing statements Obama made about
terrorism universal cancer cure? Of course there is... it's the most common motive in the world:
MONEY. GoodGopher.com
Search for more articles like this one a
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Popular on Facebook A universal cancer cure would destroy the profitability of the highly lucrative cancer for news and information.

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INVESTIGATION: Three days didn't need. See the article Cancer doctors 'fess up to making false diagnoses just to
85K before Dr. Bradstreet was found
dead in a river, U.S. govt. agents make more money.
raided his research facility to seize
a breakthrough cancer treatment
called GcMAF
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doctor who helped thousands heal
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http://www.naturalnews.com/050553_Dr_Bradstreet_GcMAF_cancer_therapy.html 12/24/2015
INVESTIGATION: Three days before Dr. Bradstreet was found dead in a river, U.S. govt... Page 3 of 14

government seized GcMAF from Dr. Bradstreet's research clinic:


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Yet another doctor was just found murdered inside his home here on the East Coast of
Florida. This makes six doctors to be found dead in the last month just from this region of
Find a Doctor Near
the country alone. Four out of the six were found dead here in Florida. We lost the holistic
You
Dr. Teresa Sievers, MD, who was found murdered in her Florida home just weeks ago.
opioiddependence.com
Opioid dependence treatment in We've also lost the alternative Dr. Jeff Bradstreet, MD, who was found in a river with a
the privacy of a doctor's office gunshot to his chest. He'd recently moved to Georgia from Florida. We've also lost the
Osteopath. Dr. Riley, who was found in Georgia at her home; just a few hours from the
Florida border. She was found with a gunshot wound to her head.

Now we've lost Dr. Schwartz MD, who was found murdered in his home, on Sunday, July
19th, 2015. This was four weeks to the day after the death of the first physician: (Dr.
Bradstreet MD) who I broke the story on a month ago. His family is still seeking answers
as to what happened to him and they're some of the kindest people I know. The latest MD,
Dr. Schwartz, in the picture above, lived just north of the fit, healthy, holistic Dr. Hedendal;
who was the second doctor to be found dead this past Father's Day, in Boca Raton. This
was the same day that Dr. Holt died at the age of 33. Both were fathers; and again, both
men died here in Florida on June 21st, 2015.

SCIENCE.NaturalNews.com entry describing the extraordinary benefits of GcMAF in a


published study:

Stepwise incubation of purified Gc protein with immobilized beta-galactosidase and


sialidase generated probably the most potent macrophage activating factor (termed
GcMAF) ever discovered, which produces no adverse effect in humans...

After about 16-22 administrations (approximately 3.5-5 months) of GcMAF, these patients
had insignificantly low serum enzyme levels equivalent to healthy control enzyme levels,
ranging from 0.38 to 0.63 nmole/min/mg protein, indicating eradication of the tumors. This
therapeutic procedure resulted in no recurrence for more than 4 years.

In other words, the administration of GcMAF eradicated tumors and left patients
cancer-free for 4+ years with no additional treatment!

http://www.naturalnews.com/050553_Dr_Bradstreet_GcMAF_cancer_therapy.html 12/24/2015
INVESTIGATION: Three days before Dr. Bradstreet was found dead in a river, U.S. govt... Page 4 of 14

Both U.S. and UK governments desperately seizing all


supply, shutting down clinics, even as millions die from
cancer every decade...
UK govt. admission that GcMAF was on track to being commercialized as a pioneering
cancer treatment, so they had to confiscate it!

GcMAF (Globulin component Macrophage Activating Factor), a blood product, claims to


treat a range of conditions including cancer, HIV and autism...

More than 10,000 vials were seized at this site and production of this unlicensed medicine
has now ceased. These products were sold through various European websites and UK
patients may have bought it from one of these websites. We are working with colleagues
in other countries to alert them to the potential risks. Our investigations are ongoing and
we have received no reports to date of side effects caused by this product.

That same page lists some of the websites where GcMAF had been available for
purchase:

www.GcMAF.eu
www.immunobiotech.eu
www.immunocentre.eu
www.petgcmaf.com
www.firstimmune.fr
www.firstimmune.de
www.firstimmune.it
www.gcmaf.gr
www.gcmaf.se
www.gcmaf.es
www.gcmaf.ru
www.gcmaf.pl

GcMAF is readily available as a medical treatment in Japan. This site explains:

GcMAF (Gc Protein derived Macrophage Activating Factor) - Gc MAF treatment is a highly
effective macrophage activating therapy, used to stimulate the immune system and
activate macrophages so that they can destroy cancer cells and other abnormal cells in
the body.

From the FAQ page of the treatment clinic:

What exactly is Second Generation GcMAF?


High Dose Second Generation Gc-MAF is produced using our new Patent Pending
process which was developed here in Japan by Saisei Mirai in collaboration with Dr
Hitoshi Hori and Dr Yoshihiro Uto at the University of Tokushima who have been studying
GcMAF for over 20 years. Studies on GcMAF began at the University of Tokushima in
1992, after they were introduced to Dr Nobuto Yamamoto's work and a collaboration
began...

Second Generation GcMAF is made using a new and improved 2nd generation method of
Gc-MAF production which is 10-20 times more concentrated and is more active and stable
than other GcMAF that is currently available. Importantly, this much higher concentration
GcMAF has been clinically demonstrated to be largely free of any side effects in the great
majority of patients and is much more stable because it is resistant to oxidation.

That same site describes Oral GcMAF as follows: "Oral GcMAF is a form of GcMAF
produced from bovine colostrum by Saisei Mirai which was developed in collaboration with
Tokushima University."

http://www.naturalnews.com/050553_Dr_Bradstreet_GcMAF_cancer_therapy.html 12/24/2015
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It also lists the following health conditions as being treatable with GcMAF, potentially a
"universal cancer cure" substance:

Gc-MAF and/or oral Colostrum MAF macrophage activation therapy is indicated in the
treatment of any diseases where there is immune dysfunction or where the immune
system is compromised, such as:

Cancer
Autoimmune diseases
Epstein-Barr Virus (EBV)
Hepatitis B virus (HBV)
Herpes Simplex virus (HSV)
Cystitis
Hepatitis C virus (HCV)
Multiple sclerosis (MS)
Urinary tract infection (UTI)
Autism Spectrum Disorders (ASD)
Rheumatoid arthritis (RA)
Endometriosis
Chronic Fatigue Syndrome (CFS)
Lyme disease (Lyme borreliosis)
IgA deficiency disorder
Myalgic Encephalomyelitis (ME)
Mycobacteria infections
Parkinson's disease
Tuberculosis
Fibromyalgia
Human papillomavirus (HPV)
Lupus (Systemic lupus erythematosus, SLE)
HIV AIDS
Dengue fever
Pneumonia infection
Warts caused by viral infection
Norovirus
Malaria Influenza virus (flu)
Herpes simplex virus (HSV)
Q fever (Coxiella burnetii)
Polycystic ovary syndrome (PCOS)
Chicken pox (varicella zoster virus)
Psoriasis
Respiratory tract infections
Ulcerative colitis, Crohn's disease
Type 1 diabetes (T1DM), insulin-dependent diabetes (IDDM)
Type 1.5 diabetes, Latent autoimmune diabetes of adults (LADA)

Do you see yet why the medical establishment must SUPPRESS GcMAF and
destroy all knowledge of its clinical applications? This one substance holds the
potential to render numerous vaccines and pharmaceuticals utterly obsolete.

GcMAF protein described at NaturalHealth365.com:

Researchers and practitioners have demonstrated that GcMAF can reverse diseases that
attack the immune system such as: chronic inflammation, bacterial and viral infections,
chronic herpes, chronic acne, Lyme disease, fibromyalgia osteoporosis, Hodgkin's, Lupus,
MS, Parkinson's and remarkably autism.

A clinical study out of Italy on 94 children with autism showed that 83 of them made

http://www.naturalnews.com/050553_Dr_Bradstreet_GcMAF_cancer_therapy.html 12/24/2015
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considerable progress while on GcMAF. The most common reported improvements


involve:

Cognitive abilities including attention and focus, learning and understanding,


receptiveness and awareness of the environment and both receptive and expressive
language gains.

Social Skills including willingness to interact and communicate with peers.

Behavior including less hyperactivity, less stereotypical behaviors and improved


cooperation and compliance.

In another study of 1500 children with autism, 85% had high levels of viruses and a
compromised immune system. All 1500 received weekly GcMAF injections and 70% of the
children responded to the treatment with reduced symptoms and another 15% made full
recoveries. The other 15% did not respond.

It was stated that the reduction of autistic symptoms is permanent provided that GcMAF
has been taken long enough for the body to produce its own GcMAF which typically takes
24 weeks.

The systematic suppression of medical science to


protect the lucrative cancer treatment industry
(chemotherapy, oncology, radiotherapy, etc.)
ANH-EUROPE.org covers the systematic suppression of advanced cancer treatments and
cures:

Back in 1993, Nobuto Yamamoto, then working at Temple University School of Medicine
in Philadelphia, PA, USA, first described a remarkable molecule. His paper reported the
conversion of vitamin D3 binding protein (DBP, known in humans as Gc) into a potent
macrophage-activating factor (MAF), known as Gc-MAF. Macrophages are a key part of
the human immune system with two roles: to engulf and destroy pathogens and cellular
debris, and to recruit other immune cells to respond to the pathogen.

Gc-MAF hasn't had the benefit of a single patent owner as a natural molecule, it cannot
be patented without being modified with the will and resources to push it under the
noses of the public and health authorities. Dr Yamamoto has run small human trials in
breast, prostate and colorectal cancers, with promising results.

David Noakes might just be the person to bring Gc-MAF into the mainstream. He's the
CEO of Immuno Biotech Ltd. and spokesperson for First Immune Gc-MAF, a project he
describes as, "PhD and BSc biochemists and biomedical scientists... with external
doctors, oncologists and scientists who kindly provide advice, committed to bringing some
of the increasing number of published but relatively unused medical cures to as many
people as we can." At the moment, Noakes and his colleagues are supplying Gc-MAF to
30 countries where it is legal, via a network of "around 300" doctors. Their Gc-MAF is
made to extremely high standards, and is being used in ongoing clinical research by
Noakes' collaborators and others. Their ultimate goal is to, "Build the case that GcMAF is
effective for various illnesses, which will help to make it available to the public".

GcMAF suppliers fighting for survival against a global


medical monopoly that profits from disease
MUST-SEE website: http://gcmaf.se/

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INVESTIGATION: Three days before Dr. Bradstreet was found dead in a river, U.S. govt... Page 7 of 14

From the site:

The medical laws have been changed over the last 40 years so that all the brilliant
breakthroughs in cancer are denied to the British public. Lord Maurice Saatchi had to
watch his wife die, while his doctor told him the only thing he was allowed to prescribe her
was chemotherapy, which would shorten her life. He hopes to bring the Medical
Innovation Bill to Parliament, so instead of obeying a destructive government law, a doctor
will be able to prescribe whatever treatment is best for the patient...

Bad law kills, and Britain has the worst medical laws in Europe. The 1939 Cancer Act
makes it illegal to discuss the possibility cancer can be cured, which is partly why 160,000
people die unnecessarily of cancer in Britain every year. Science and treatments are
decades ahead of where the medical industry is today. The MHRA's job is to get life
saving treatments like GcMAF out to people as quickly as possible. Instead they block
them to protect billion dollar Big Pharma monopolies, who also fund the MHRA. Over a
hundred thousand lives could be saved every year if the 1939 Cancer Act were repealed,
and the MHRA were closed down.

There are 142 eminent scientists who have published GcMAF research papers on the US
National Library of Medicine alone.

From the how GcMAF works page:

Your GcMAF empowers your body to cure itself. In a healthy person your own GcMAF has
11 actions discovered so far, including two on cells, three excellent effects on the brain,
and 6 on cancer. Amongst these it acts as a "director" of your immune system. But viruses
and malignant cells like cancer send out an enzyme called Nagalase that prevents
production of your GcMAF: that stops its 11 beneficial effects, and neutralises your
immune system. So diseases become chronic, and cancer cells grow unchecked.

Minutes after a receiving a dose, 10 of the body's actions restart. In three weeks of two
GcMAF 0.25ml doses a week, your immune system is rebuilt to above normal strength.
You need two doses a week for typically 24 weeks for many diseases and early cancers,
up to seven one ml doses a week and a year for stage 4 cancers. Your body then takes
the disease down without side effects, and successfully in 80% of cases -depending upon
how well you follow the protocol under "Treatment Protocol" on this website.

What is GcMAF?
It is a human protein. One week's GcMAF looks like a small raindrop. If properly produced
it is perfectly sterile, and a most ethical course for doctors.

GcMAF is therefore a replacement therapy for those who can't make their own. Taking
GcMAF replaces the missing part of the immune system, and also acts as the body's own
internal medicine.

GcMAF is extracted and isolated; its a 24 step process, and at the end it must have tests
to prove its sterility and activity. (If it does not come with published tests, its probably not
GcMAF.) One GcMAF has been tested in universities, laboratories and clinics, where, as
a result of the testing, consistent activity and sterility have always been found, and been
the subject of 40 scientific research papers.

What does GcMAF do?


The GcMAF Conference 2013 showed GcMAF is a far more powerful molecule than
thought, both in terms of the science, and doctors' results. In stage 4 cancer, some
doctors who use the full protocol, listed on "Treatment Strategies," are saving every
patient (if they have not had chemotherapy.) Success can be achieved with all tumour
cancers including breast, lung, prostate, pancreatic and melanoma.

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INVESTIGATION: Three days before Dr. Bradstreet was found dead in a river, U.S. govt... Page 8 of 14

GcMAF can eradicate chronic inflammation and viral infections. It is better than antibiotics
in many areas, and 25% successful with Autism, 50% or more with Chronic Herpes,
Chronic Acne, Chronic cirrhosis of the liver, Chronic kidney disease, Chronic depression,
Colitis, Crohn's, Fibromyalgia, Hepatitis, Herpes, LMBBS, ME/CFS, Osteoporosis,
Periodontal disease, Psoriasis and various types of Immune dysfunction including
allergies. Research shows GcMAF can halt deterioration in Parkinsons, multiple sclerosis
(MS), dementia and ALS, and in its role of immune system regulator, can reverse
diseases that attack the immune system like Lupus and Arthritis. And is effective with
wound healing. Its successful with tumour cancers, and some others.

In addition to rebuilding a depressed immune system, GcMAF:


Inhibits angiogenesis stops blood supply to tumours
Activates macrophages phagocytosis and destruction of cancer cells
Apoptosis suicide of cancer cells
Reverts the cancer cell phenotype to normal (Turns cancer cells into healthy cells)
Reduces the metastatic potential of human cancer cells in culture.
Increases energy production at the mitochondrial level ME/CFS
Improves human neuronal metabolic activity through cAMP signaling autism, ME/CFS,
MS, ALS
Counters toxic effects including cadmium ME/CFS

It abolishes neuropathic pain due to neuro-oxidative stress (stress due to the anti-cancer
drug oxaliplatin) in the lab. (neurodegenerative diseases and autism that have oxidative
stress as a pathogenetic mechanism)
It increases neuronal connectivity by promoting differentiation and the formation of
dendrites and neuritis (autism and ME/CFS, where there is a lack of connectivity between
neurons).

See the 31 research papers published, particularly Brescia, and the 60 published by
others listed under "The science".

80% of terminal stage four tumour cancers cases can be saved (40% if they've had
chemo), but usually when they are closely monitored, which is why residential Treatment
Centres are being run in Switzerland. If they have three months to live and have not had
chemo, almost no one needs to be lost.

The 180 scientists who have published papers on trials of GcMAF selected those in the
early stages of cancer and HIV, and reported nearly 100 percent success, with no
recurrence after many years. They did not attempt trials on people with large tumours.

Our trials are quite different: many people are over 50, some over 80, with advanced or
terminal cancers, with significant tumour mass. Most come to us when their doctors tell
them they can do no more.

The life of GcMAF is only six days you have to keep taking it until your disease has gone
(ie your nagalase is under 0.65 nmol/min/mg) then a further 8 weeks, or the immune
system gets shut down again.

How long should you take GcMAF for?


8 weeks for chronic herpes/acne, fibromyalgia, inflammation.
Allow 24 weeks plus of GcMAF for: Autism (85% improve, 25% eradication), CFS (70%
eradication), HIV, Lyme (8% respond, most appear to have the VDR gene blocked and the
viruses conceal themselves with biofilms) and stage 1 to 2 cancer, (80% respond).
Late stage cancer, if you follow "Treatment Protocol" again has 80% responders, but it
takes a year to 18 months to become cancer free.
Cirrhosis of the liver: 16 months

Remember everyone responds differently. We can't say how you will respond.

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The more minor the disease, the easier it is for GcMAF to eradicate. GcMAF needs
normal levels of vitamin D to function strongly (take 10,000iu a day). in low responders,
larger doses are required.

We have probably proved GcMAF can work for people up to age 90, and can destroy
large tumour mass. See "Participants experiences".

If you have your blood taken for monocyte counts, relevant markers and vitamin D levels,
and again for a nagalase test at the beginning, you should see on your next test after
three weeks that your immune system is back to full strength, and after 8 weeks
significantly falling nagalase will indicate the disease is losing its grip. Don't stop the
GcMAF until your nagalase gets below 0.65 nmol/min/mg, when it loses the ability to
prevent your body producing your own GcMAF, and then you no longer need ours. Even
better, get scans.

Autism children can improve at five weeks with substantial improvements at 8 weeks. See
"Participants experiences." But everyone is different.

The beauty of using your own immune system to attack disease or cancer is that it
remembers how to defeat it for the rest of your life: it doesn't come back. And unlike
chemotherapy, the side effects are trivial.

The only way you can tell if GcMAF is genuine and active is to test with living cells in a
laboratory. See "Quality and Tests of our GcMAF." To recap:

We put live macrophages cells and MCF7 breast cancer cells together; nothing happens.
Then we add GcMAF; in 72 hours the macrophages eat all the MCF7 cancer cells. We
then put only GcMAF and MCF7 together, and the GcMAF turns the cancer cells back into
healthy cells.

We have GcMAF available for preclinical trials. See "Buy GcMAF".

You must read at least all of "Buy GcMAF" and "Treatment strategies" on the left if you
want to take this further. And you must be prepared to give us feedback.

Patent document on GcMAF


See the Yamamoto patent involving GcMAF:

Cancerous cells and HIV-infected cells secrete -N-acetylgalactosaminidase into the blood
stream, resulting in deglycosylation of serum Gc protein. This inactivates the MAF
precursor activity of Gc protein, leading to immunosuppression... When peripheral blood
monocytes/macrophages of 175 cancer patients bearing various types of cancer were
treated in vitro with 100 pg GcMAF/ml, monocytes/macrophages (phagocytes) of all
cancer patients were activated for phagocytic and superoxide generating capacity. This
observation indicates that patient phagocytes are capable of being activated...

Also see BetterHealthGuy.com coverage on GcMAF:

first heard about GcMAF almost a year ago. At the same time, I had first learned about
"nagalase", a blood test that is used to in part determine whether or not one might be a
candidate for GcMAF therapy. Nagalase is an enzyme that prevents Vitamin D receptors
(VDR) from being activated on the surface of the macrophage. As a result, macrophages
are not "activated" and our immune systems are not able to properly respond to invaders.

Here are some points that I have learned thus far on GcMAF:

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- GcMAF has reportedly been tested more for safety, purity, etc. than other human blood
products.
- Macrophages are cultured, destroyed, and the GcMAF receptors are purified.
- Treatment is via injection 1x/week for 8-20 weeks. Dose is titrated initially to avoid
exacerbation or Herx responses as much as possible.
- A commonly used dose is .25ml once weekly (a 2.2 ml vial should last 8 injections).
- The primary test used in looking at whether or not GcMAF may be a reasonable
intervention is nagalase.
- Nagalase inactivates macrophages.
- I personally would NEVER consider this option without having a baseline nagalase test.
Normal is < 0.95. Mine was 2.9.

The practitioner I worked with suggested that 2.9 was in the range of someone with HIV or
cancer in terms of the impact on the immune system. I'd like to hear from others in the
Lyme community as you get test results as well to see if there is a pattern of elevated
nagalase in those with Lyme disease. Whether or not Lyme itself has anything to do with
nagalase elevation is something I have not been able to find anything on. We certainly all
have underlying viral co-factors that are likely in play as well, but I suspect that Borrelia
may also play a role in nagalase elevation.

- In healthy college students, a nagalase 0.4 is not uncommon (the lower the better).

- At 2.9, my practitioner was surprised that I did not have more cognitive deficits such as
memory loss and other cognitive issues.

- It has been suggested that ongoing antimicrobial therapy without a working immune
system is like leaving the house with the door wide open inviting burglars in. By using
GcMAF to activate macrophages, nagalase drops, and one may regain a functional
immune system. The door is then closed to further invaders and we may no longer serve
as a microbe hotel.

- Maintenance therapy should not be needed once the immune system is once again
properly functioning.

- Activated macrophages only remain active for 7 days so any negative responses are
generally short-lived. That said, some people do have strong inflammatory responses that
are not believed to be typical die-off reactions.

- It has been indicated that in some cases, other medications may be needed in order to
manage the inflammatory response. This is another reason that one needs to be working
closely with a knowledgeable practitioner before considering GcMAF in my opinion. In the
CFS and GcMAF world, this more severe form of a die-off reaction is called IRIS.

- VDR genetics do not seem to play a role in predicting response as earlier thought
according to one practitioner that I have spoken with. That said, Vitamin D levels do
correlate with the positive response rate of GcMAF. Thus, Vitamin D supplementation may
be required in order to optimize outcome.

- Other than die-off reactions or activation of symptoms (inflammation), no other side


effects are generally expected.

- Nagalase should be monitored every 1-2 months while on treatment to determine the
required duration of the therapy. Target nagalase after treatment would be 0.4 to 0.6.

- Elevated nagalase has a profound detrimental effect on the immune system. Elevated
nagalase is often presumed to be related to microbes of viral origin or cancer. Viruses that
are nagalase producers open the door to chronic infections.

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- Hemagglutinin contains nagalase and is also found in flagella of some bacteria so it


could also be the case that some bacteria may produce nagalase.

- Parents with ASD children also often have elevated nagalase.

- A practitioner I spoke with likened Lyme disease to a "peat moss fire" burning below the
surface. Activating macrophages should help to deal with the fire.

- GcMAF should be helpful in dealing with other infections that are not of viral origin; for
example, Borrelia, Bartonella, and other infections commonly associated with Tick-Borne
Infections (TBIs). GcMAF is active against many cancers and many different kinds of
microbes.

- Neopterin is another test that is sometimes used as an indicator of immune suppression.


As macrophages become activated, neopterin may rise and later fall. If one is in the
normal range for neopterin and has an immune-related illness, this could be an indication
that the immune system is suppressed and not responding appropriately.

- People with autoimmune conditions can generally use GcMAF. However, GcMAF may
be contraindicated in people with Multiple Sclerosis.

- Reduction in nagalase is generally seen early in the course of treatment; within the first
3-6 weeks. In some studies, nagalase dropped by over 50% in less than six weeks.

- Cancer patients may initially feel as bad on GcMAF as they do on chemotherapy, but
often feel much better after the first month.

- Anti-inflammatories may limited the effect of GcMAF.

- Enzymes and biofilm-reducing supplements may have a negative impact on GcMAF


therapy and may be best avoided. It is still too early to know what the impact may be, but
one practitioner I spoke with feels that it is best to avoid these.

- One should not be on any immune-suppressing agents while on GcMAF as the immune
system must be partially functional in order to respond appropriately to the treatment.

- A common pattern is to see elevated lymphocytes, high nagalase, and low NK cells.
Once nagalase drops, it may be the case that NK cell function could be positively
impacted. CD57 is a type of NK cell. It is too early to know if this proves to be true, but it is
one of the things I'm quite interested in.

Watch this video presentation on GcMAF therapy to learn more.

Read about GcMAF from Alternative-Health-Group.org.

Read The GcMAF Book at this link.

Open the "Stop Fighting Cancer" PDF document and search it for "GcMAF" to read some
intriguing passages:

Researchers testing GcMAF stated it, "works 100% of the time to eradicate cancer
completely, and cancer does not recur even years later." (This was stated based on the
tested group of patients -nothing works 100% for everyone) The weekly injection GcMAF,
a harmless glyco-protein activates the human immune system which then can kill the
growing cancer. Studies among breast cancer and colon cancer patients produced
complete remissions lasting 4 and 7 years respectively. This glyco-protein 'cure' is totally
without side effect but currently goes unused and completely ignored by cancer doctors.

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Why? Maybe it is because there is little money to be made in selling it. For less than
$2000USD a cancer patient can obtain an adequate amount of GcMAC.

See the National Library of Medicine page Immunotherapy for Prostate Cancer with Gc
Protein-Derived Macrophage-Activating Factor, GcMAF:

When human macrophages were treated in vitro with 100 pg GcMAF/ml for 3 hours and a
prostate cancer cell line LNCaP was added with an effector/target ratio of 1.5,
approximately 51% and 82% of LNCaP cells were killed by 4 and 18 hours of incubation,
respectively [14,15]. This in vitro tumoricidal capacity of macrophages activated by
GcMAF led us to investigate the therapeutic efficacy of GcMAF for prostate cancer.
GcMAF therapy as a single remedy modality can eradicate metastatic breast and
colorectal cancers most effectively...

Click here to search for "GcMAF" on GoodGopher.com, the new search engine for truth
seekers.

Read this article from The Telegraph on how scientists are being assassinated because of
what they know.

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