Thanks to Richard Presser for reprinting Dr. Rima Laibow’s post on his blog.
Dr. Rima Laibow, well-known natural health doctor is speaking out openly on this issue of holistic doctors being assaulted and killed, and spelling out the enormity of what is going on — on several fronts — with the industry-led suppression of GcMAF, an immune factor vital to our immune system health. Please visit her website for her article, excerpted here: These Dead Doctors Told No Lies, Is That Why They Are Dead?
She has also set up a series of solutions we can all engage in, reprinted below–calling for vaccine-tests, prosecutions, investigations, and truth-telling–please visit her links and sign the petitions. She also recommends that we stop taking vaccines now, until they are fully tested for the presence of Nagalase, which she is embarking on. (To understand better what GcMAF/Nagalase are, and the Vitamin D connection, also see this recent explanatory post here, which also touches on many of the subjects in Dr. Laibow’s post.)
“Take a deep breath. What I am about to share with you is, as I see it, negligent at a level so breathtaking that its magnitude is literally hard to wrap my mind around. It appears that the very companies that make a profit from every illness we experience, have been adding something that they KNOW will cause autism, cancer and a wide variety of other diseases into the vaccines that they – and their complicit criminals in our regulatory agencies, the FDA, CDC, etc.- claim are “safe and effective” — while the science shows what the Supreme Court said, vaccines are “unavoidably unsafe.” . Yes, they make tainted vaccines. That didn’t stop when the SV40 cancer-causing virus was removed from the polio vaccine (after infecting 98,000,000 Americans). We pay for these vile brews and infect them into ourselves and our children and then they make a ghastly blood profit from the needless suffering that they have induced.
Although drug companies have been granted an insane level of insulation from tort liability from their unavoidably unsafe vaccines there is one area in which they still are vulnerable: they are still liable for damages if they are found to have engaged in willful negligence. Putting poison into vaccines without announcing that fact on the label constitutes willful and negligent behavior. . Denying us the “informed” part of Informed Consent constitutes a crime against humanity.” Please visit her website to read the whole article.
Second excerpt, and her list of Actions We Can All Take:
“Without GcMAF, the entire cascade of immune actions cannot be initiated. So getting rid of Vitamin D AND introducing Nalgalase assures,absolutely guarantees, that there will be huge numbers of cancers, autism cases and illness and death at every hand from viral and other diseases. . Oh, yes. The only company manufacturing GcMAF has been shut down. Can’t have people getting cured, now can we? . Here’s what we need to do: . 1. Create a huge demand for a complete moratorium on vaccination of any type immediately Do that here: http://TinyURL.com/VaccinationISViolation Share this link WIDELY . 2. Test six vials of currently available vaccines for Nagalase immediately (write to me if you have vials available and we will coordinate this test and make the results available world wide). . 3. Join us in calling for an Independent Special Prosecutor to investigate the murders of the doctors and the adulteration of vaccines with Nagalase. This Special Prosecutor must be acceptable to us as well as to the Politicos and the Big Pharma companies they serve. . 4. Support Informed Consent by taking this Action Item demanding the FDA honor US and International Lawhttp://TinyURL.com/InformedConsentPetition . 5. Support our FDA petitions and litigation:http://www.GoFundMe.com/FreeHealthSpeech . 6. STOP TAKING VACCINES NOW . 7. Like our FB page, NaturalSolutionsFoundation, and ask all of your contacts to do the same. We’ll be spearheading this action through this page and the information will be there. I can promise you that we’ll be facing a huge amount of opposition but we have the capacity to win this and end the decades of damage that the Pharmaceutical industry and its bought-and-paid-for co-conspirators have done to all of us. . Yours in health and freedom, Dr. Rima
This is such a terrible story in itself–but could it be there’s even more here to become aware of? What is it about the healing practices, research, and treatment protocols of these doctors that caused them to suddenly become missing or dead? What is it about GcMAF and Nagalase that’s causing such an extremity of violence aimed at holistic/alternative medical practitioners?
Is GcMAF actually a key to curing a whole host of illnesses that allopathic medicine tells us it’s impossible to find a cure to–cancer, autism, AIDs, auto-immune diseases, neurological diseases like Parkinson’s and Alzheimer’s and Multiple Sclerosis, etc.? Some researchers think so–and maybe there’s more than one industry here–not just the cancer industry or the vaccine industry–that’s beginning to panic and lash out.
There’s already a tremendous amount of interest online in this story–and I actually think that is a good sign, because it means people are waking up to the horrors of what is going on around us--until we wake up and make dramatic changes in how we live and how we govern ourselves, we’re going to keep turning a blind eye to these atrocities that are mounting against us, for they’re not stopping–and frankly, when wonderful, caring, compassionate, intelligent, dedicated healers in our midst are killed, we Need to wake up.
I also get the feeling this story is going to just keep growing–and watch how mainstream media tries to tear it down (with talk of “conspiracy theories” )–but maybe instead it will become a launching-off point to bringing a huge number of issues together.
The other two doctors she mentions are Dr. Nicholas Gonzales, and Dr. Jeffrey Whiteside–her article is detailed and well worth the read. Dr. Gonzales died 4 days ago–July 21–of apparent cardiac arrest, even though he had been in excellent health. Two days ago–July 23–Dr. Whiteside, earlier reported missing, was found dead with a .22 by his side.
This is happening right now, as we speak–these latest deaths happened This week!
It’s absolutely atrocious, and it needs to stop. We need to openly challenge these reported stories of supposed-suicides which in every way announce themselves clearly instead as covert homicides.
There’s one point I want to make here, which will come as no surprise to those aware of Electromagnetic Radiation/Sonic Weapons in our midst: It’s entirely possible several of these doctors were killed with a Remote Heart Attack Weapon, a Directed-Energy Weapon (DEW) currently in use under classified protocols by our military and Intel agencies, and possibly, just possibly also sanctioned for use on “Targeted Individuals” illegitimately labelled “Domestic Adversaries” by our Department of Justice. It’s entirely possible that gunshot wounds, gunshot residue, and guns planted at their side were planted to cover up any hint of death by DEW, and to create externally visible material evidence (since many DEWs would just destroy organs internally).
The Remote Heart Attack Weapon is a classified technology that absolutely exists–and that can cause sudden cardiac arrest. Please research what information is openly available on it.(For more on “Targeted Individuals,” which explores what many Americans (including this writer) are currently experiencing, by way of covert assault with remote radiation neuroweaponry (DEWs), please see this post. Dr. Nick Begich, in his book Earth Rising, The Revolution: Toward a Thousand Years of Peace has written extensively of Directed-Energy Weapons, and also documented how the development of certain Directed-Energy Weapons, also euphemistically called Non-Lethal Weapons, has proceeded in the USA via secret Memoranda of Understanding between the Department of Justice and the Department of Defense–in order, apparently, to permit their use domestically. This is being explored currently via FOIA requests at Muckrock. And if you’re a journalist or researcher, please also research and FOIA-request this too.)
Understanding GcMAF and Nagalase
The best and most readable and compelling source on this subject that I’ve found is The GcMAF Book, by Dr. Timothy Smith, copyrighted 2010 and fully available online–he posted it online as an interactive resource, permitting reader response and comment. It’s an English major’s dream, since it spells out the intricacies of highly technical molecular-biologist-speak in plain English, and takes a creative writer’s routes via metaphor and story and poetic license to do so–it’s a compelling read. (He wrote this before GcMAF was manufactured and available for use as a treatment protocol; now of course, the company making it in Europe has been forced to shut down.)
Preface- The GCMAF Book, Timothy Smith, MD
Essentially, if you’re afflicted with an illness like cancer or a virus infection, GcMAF, a body-manufactured protein, jump-starts your whole immune response by activating macrophages–your immune-system warrior cells–and sending them off to destroy cancer cells and viruses. How is GcMAF manufactured by the body? By way of a precursor Gc Protein, linked to Vitamin D and sunlight: a Vitamin D-Binding Protein, DBP. What Nagalase does is sabotage this precursor–it zooms in and prevents the Gc Protein or DBP from manufacturing GcMAF by attacking its base structure. (Yes, there’s another, deeper story here: even minus Nagalase–without D Binding Protein, without Vitamin D, without sunlight, which fixes Vitamin D in our bodies, we wouldn’t have GcMAF–in other words, a macrophage-inciting superhero to jump-start our immune systems. Sunlight’s at the core here. And what are chem trails doing today--apart from delivering heavy-metal nanoparticulates that destroy our air, water, soil, and lungs, and delivering nanobots to attach to our nervous systems? Blocking sunlight. Isn’t that interesting?)
From The GcMAF Book:
“How GcMAF works: GcMAF is the protein that activates macrophages and jump-starts the entire immune response. To sabotage the immune system and put the macrophages to sleep, all cancers and viruses make Nagalese, the enzyme that blocks production of GcMAF. In the absence of GcMAF, cancers, HIV, and other viruses can grow unimpeded. Dr. Nobuto Yamamoto demonstrated that GcMAF administration bypasses the Nagalese blockage and re-activates the macrophages, which then proceed to kill the cancer cells and HIV viruses.”
Nagalase–much like our current television culture afflicting the general populace–literally puts GcMAF, our Immune System Superheroes, to sleep. Also not unlike our television culture with its baggage of subliminal advertising and mind-control, which seems to seep out from covert Mass Control mavens–and covens, Nagalase seeps out from cancer cells and viruses. Elevated levels of Nagalase have been found in patients afflicted with cancer and autism. Dr. Timothy Smith, like many other doctors, believes in the importance of Nagalase screening as an early screener for cancer and other diseases.
Nagalase has become a recognized early-marker of cancer in the body, and Nagalase screening tests exist, as this site, Nagalase Blood Tests demonstrates.
Dr. Yamamoto, who discovered the GcMAF/Nagalase mechanism in the body performed and reported on several clinical trials using GcMAF on cancer patients. This research is reported in Dr. Jeffrey Dach’s July 2013 article at Op-Ed News, Cancer ImmunoTherapy from Dr. Yamamoto.
From the beginning of the article:“This article explores the work of Dr. Yamamoto, who discovered the Macrophage-Activating Factor (GcMAF) in 1990 at the Socrates Institute in Philadelphia (4). Since then, Dr. Yamamoto has published three human clinical trials showing remarkable results for breast (5), colo-rectal (10), and prostate cancer(11).
What is MAF — Macrophage-Activating Factor?
MAF is a protein that activates our macrophages, the microscopic white cells that kill invading microbes and cancer cells. MAF is made from a precursor protein called the Gc protein.
Cancer is Clever — It Inactivates Our Immune System
In a way, cancer cells are clever little devils because they disable our immune system in order to enhance their own survival. Dr. Yamamoto discovered that cancer cells do this by secreting an enzyme called Nagalase, which prevents the precursor protein Gc from being converted to MAF. This Nagalase-enzyme activity can actually be measured in cancer patients, and greater tumor burden corresponds with higher Nagalase enzyme activity (as one would expect). Elimination of the tumor results in reduction of Nagalase activity to lower, more normal values. (5)
Dr. Yamamoto devised a technique for restoring Gc-protein activity, which creates the most potent macrophage-activating factor ever discovered, having no adverse effects. He called it GcMAF. Macrophages treated in vitro with GcMAF (100 pg/ml) are highly effective at killing breast-cancer cells.
GcMAF for Metastatic Breast Cancer — Human Trial
Dr. Yamamoto then studied his GcMAF in human metastatic breast-cancer patients with weekly injections of 100 ng of GcMAF (5). Dr. Yamamoto found that over time, as treatment with GcMAF progresses, the MAF-precursor activity of patient Gc protein increased, and the serum Nagalase decreased (5). After 5 months of weekly GcMAF injections, the cancer patients’ elevated Nagalase activity had returned to normal levels, same as healthy controls. Over the next four years, these sixteen treated metastatic breast-cancer patients remained cancer free with no recurrence (5). In 2008, Dr. Yamamoto published his landmark study on human breast cancer.(5)” Please visit Op-Ed News for the whole article.
According to Dr. Timothy Smith, it is possible to envision a time when Nagalase screening will permit the early detection of early stages of cancer, the best time to begin a successful round of GcMAF therapy, which he cautions may be most effective only in the early stages, and in cases where the “tumor burden” or size is fairly low, not high nor in an advanced state of metastases. But it is important to be open to a screening methodology that is molecular or biochemical rather than waiting for a tumor to materialize first.
From the GcMAF book:
In terms of cancer, the bottom line here is that practicing the best possible medicine will force us to dispense with the luxury of palpating the mass or seeing it on an X-ray. Lives will be lost if we stay stuck in that groove. The best doctors will be using newer biochemical techniques to find disease early.
When rising Nagalase levels expose these early occult cancers, the first line of therapy will be GcMAF (100 ng/week, intramuscularly), along with immune strengthening, anti-cancer nutritional medicines. If the GcMAF program works, the Nagalase level (which should be checked monthly) will go down and the doctor and patient can rest assured that the cancer is going away. We’ll sleep better at night.
As mentioned above, it may seem bizarre and surreal to be treating a cancer that is still invisible, but this is exactly what is happening—and it works.Dr. Yamamoto’s studies showed that with GcMAF it works 100% of the time.
Then there’s AIDS, and Dr. Yamamoto has successfully treated patients with AIDS using GcMAF:Nagalase as secreted by viruses is explained in this discussion of a Nagalase blood test: “Nagalase is an extracellular matrix-degrading enzyme that is (increased) secreted by cancerous cells in the process of tumor invasion. It also is an intrinsic component of the envelope protein of various virions, such as HIV, Epstein-Barr virus (EBV), herpes zoster and the influenza virus. Thus, it is also secreted from virus-infected cells..1,3,4.”
Next, Nagalase and autism: Dr. Jeff Bradstreet, who had become renowned for his research into various methodologies of treatment for autism, had become interested in the GcMAF mechanism, and conducted various studies where he discovered elevated levels of Nagalase in children with autism. He reported on these studies, and he wrote about his findings on his blog and elsewhere online.
Dr. Bradstreet, Nagalase, and the Viral Issue in Autism
Although my daughter is not a patient of Dr. Jeff Bradstreet I’ve always had an enormous amount of respect for the good doctor. I’ll usually go on his website once or twice a month to find out what has most recently attracted his interest. Often it seems we’re looking at similar questions; which either means great minds think alike, or we suffer from some of the same delusions.
In the past months Dr. Bradstreet has become interested in nagalese, which he describes as an enzyme “produced by cancer cells and viruses.” He thinks it unlikely that children with autism have undiagnosed cancers, and thus suspicion falls on a viral etiology. Dr. Bradstreet writes, “Viruses make the nagalese enzyme as part of their attachment proteins. It serves to get the virus into the cell and also decreases the body’s immune reaction to the virus-thereby increasing the odds of viral survival.”Read the whole article at Age of Autism.
The article by Dr. Bradstreet referenced above, An Update on the Viral Issue in Autism, can be found onAutismWeb, and is excerpted here:
“We have now evaluated approximately 400 children with autism for the viral marker, nagalase. From my perspective this is one of the most important developments in the clinical treatment of children on the spectrum that I have experienced in the last 15 years. The short story is nearly 80% of the children with autism evaluated have significantly elevated levels of nagalase.
But what does that mean?
The enzyme nagalase is produced by cancer cells and viruses. Since it is clear cancer is not feature of autism, it is most likely viral mediated enzyme activity (although in rare cases children with autism could have an undiagnosed cancer – this is unlikely). Viruses make the nagalase enzyme as part of the their attachment proteins. It serves to get the virus into the cell and also decreases the body’s immune reaction to the virus – thereby increasing the odds of viral survival.
As previously stated on this blog – the target of nagalase is the GcMAF or Vitamin D3 receptor. It is capable of inactivation of this cell receptor and reducing both Vitamin D function and immune function.
It is reasonable and likely that the nature of the immune dysfunction and the frequently observed autoimmune problems in autism are mediated by persistent, unresolved viral infections.”
Dr. Bradstreet’s study on Nagalase and autism titled “Initial Observations of Elevated Alpha-n-Acetylgalactosaminidase Activity Associated with Autism and Observed Reductions from GC Protein—Macrophage Activating Factor Injections...” can be downloaded as a pdf from this site.
So What is the Connection Between Nagalase and Vaccines?
As noted above, in light of all the studies on autism patients with elevated levels of Nagalase, the understanding among several researchers and analysts, as also Dr. Jeff Bradstreet, is that this elevation is due not to cancer but to viruses.
“Dr Jeffrey Bradstreet has now treated over 2,000 autistic children with GcMAF and the results are well established. In 15% GcMAF makes no difference. 85% improve, if only a little, and of them 15% have their autism eradicated. In all 3,000 children have been treated with GcMAF with similar results.
With Dr Bradstreet we ourselves published a groundbreaking paper in “Frontiers in Neurology” on the 2nd January 2014 where we identify, for the first time, the point in the human brain where autism resides.
In our opinion Autism tends to be caused by the MMR and other vaccines putting viruses and mercury into children. A shortage of lipids may contribute. Another Italian court has awarded €178,000 against the government to a family who’s child contracted autism from MMR.
These viruses sabotage the immune system by sending out nagalase to prevent the production of the child’s GcMAF, and therefore become chronic.
Autism is usually a viral disease to a greater or lesser extent, with viruses in the brain and the stomach. In 15% of children viruses are negligible, and GcMAF probably will not help. In 85% viruses are involved, and they will respond to GcMAF. In 15% of children autism is mainly a viral disease, and these children make full recoveries.
Children can begin to respond inside 5 weeks. If nothing happens in 16 weeks, their autism may not be viral. If they respond, GcMAF should be continued for typically 24 weeks, or 8 weeks after they appear to be recovered, to ensure the viruses does not return.
GcMAF has three excellent effects in the brain and rebuilds the immune system, which then attacks the viruses that cause autism. Improvements in the child are often seen as early as five weeks – about the same time it often takes to permanently eradicate the herpes virus.” More information at their site.
This issue, I’m aware, is controversial, and needs more research. But that’s the gist of it, that the live viruses in vaccines or viral material included otherwise have an impact on immune systems via the Nagalase that comes along with “the envelope protein” of the virus.
Isn’t all this eye-opening enough…but there’s more.
Could GcMAF Offer The Promise of A Cure For More Than Cancer and Autism?
GcMAF for the treatment of cancer, autism, inflammation, viral and bacterial disease by David Noakes
Human GcMAF, otherwise known as Vitamin D binding protein macrophage activating factor, holds great promise in the treatment of various illnesses including cancer, autism, chronic fatigue and possibly Parkinson’s. Since 1990, 59 research papers have been published on GcMAF, 20 of these pertaining to the treatment of cancer. 46 of these papers can be accessed through the GcMAF web site.
GcMAF is a vital part of our immune system which does not work without it; and is part of our blood. GcMAF stimulates the macrophage element of the immune system to destroy cancer cells. It also blocks the supply of nutrients to cancer cells by stopping blood vessel development to the site (anti-angiogenesis). Cancer cells are weakened and starved, making them more vulnerable to attack by the GcMAF stimulated macrophage system. Research has shown macrophage activation and stopping diseased blood vessel development can also help in various neurological diseases such as Parkinson’s, Alzheimer’s, rheumatoid arthritis, inflammatory conditions, and diabetic retinopathy.
In the case of autism, Dr. James Bradstreet has so far treated 1,100 patients with GcMAF with an 85% response rate. His results show a bell curve response with 15% of the patients showing total eradication of symptoms and 15% showing no response.
In addition, experimental and clinical evidence confirms that GcMAF shows multiple powerful anti-cancer effects that have significant therapeutical impact on most tumors including breast, prostate, and kidney. GcMAF is created in the body by the release of two sugar molecules from a GcProtein molecule.
However, tumors release an enzyme known as Nagalase. Nagalase degrades GcProtein to the point it is unable to become GcMAF. Since GcMAF only lives for about a week in the body, without continuous conversion of GcProtein the stores of GcMAF are depleted rapidly in the presence of Nagalase. However, Nagalase can only destroy GcProtein and not GcMAF. Thus the introduction of external GcMAF through injection into the body has been shown to be effective. Read the whole article at the FAIM website.
There’s discussion elsewhere online about the magical promise of GcMAF therapy in any kind of immune-system disorder, including auto-immune diseases.
“Further evidence supporting the GcMAF and nagalase story, which seems to be behind the elimination of several alternative medicine doctors has come forth in the form of a search warrant for Dr. Bradstreet and his offices. This search warrant was targeting GcMAF and those who have been treated with it.
Dr. Timothy Smith, author of The GcMAF Book, suggests that the reason this subject matters to every one of us, eventually, is the increasing pervasiveness of cancer. In his opinion, cancer could be eradicated virtually overnight by screening everyone for high Nagalase levels, and giving GcMAF to those with high levels, thereby jump-starting their own immune systems to attack the incipient or extant or proliferating cancer cells, instead of having these people (the majority of us in today’s EMF and pollution-riddled world?) just putter along toward oblivion with a deliberately deactivated immune system gifted by Nagalase secreted by beginning cancers or viruses in the body.
GcMAF Book – Chapter 4
Please share this information widely so more of us can fully understand what is at stake here–ruthless suppressions of cures for cancer and other diseases, ruthless silencing of our best and brightest researchers and healers who challenge the status quo–we shouldn’t stand for it.
Exclusive Reportage on Counter-Terrorism “Manufactured-Target” Targeting & Gross Human Rights Violations in Amoral Human Experimentation Crimes by Intelligence Agencies, Law (Lie) Enforcement, & US/NATO Military Divisions: Off-the-Charts Torture & Abuse of “Targeted Individuals”
GLOBAL BRAIN ENSLAVEMENT, DNA BIORESONANCE, & EXOTIC MILITARY TECH: TARUN RAVI REPORTS | REPORT 296 | At Bitchute | At Brighteon | At Odysee | At Rumble | Posted Oct 4, 2022
CARNICOM DISCLOSURE UPDATE 2022 – PANEL 2 | BIOTECH TRANSFORMATION VS RESILIENCE IN DIVINE CREATION | At all channels | Posted Sep 28, 2022 Report 295 | Michelle Ford/California Assembly on Restoring Your Status as American on Land & Soil | At Bitchute | Brighteon | Odysee | Rumble| Posted Sep 25, 2022
Free Keene’s web site/A peace-liberty-voluntarism project pursuing and promoting peaceful living in Free Keene, New Hampshire
Free State Project
Free State Project’s website/A Liberty in our Lifetime project in New Hampshire, pursuing liberty, community, and peaceful living
New Earth Project
New Earth Project website/Open platform to unite humanity and create initiatives to support the emergence of absolute freedom and sovereign creative expression for all
Public Intelligence Blog
Blog for Earth Intelligence Network, Phi Beta Iota the Public Intelligence Blog/Promotes hybrid transparent governance, collective intelligence, true cost economics, and whole systems understanding