The following information is based solely on fact and sourced within.

This essay is an addendum to my documentary film, “Lethal Injection: The Story Of Vaccination“. It is of utmost importance that you read this entire article and spread it indefatigably.

What you are about to read may very well be the largest combined cover-up of the confederated government, ranching, meat-packing, medical, and pharmaceutical industry’s history – a collaborative effort to hide the true nature of what can only be called the human race’s modern plague of neurological and other degenerative diseases, from Alzheimer’s to AIDS.

The virtually unknown and under-discussed scientific and medical topic of what is called “xenotransplantation“, as well as human protein ingestion – including injection (vaccination) of other animals and human cells into the human body – is now a practice as prevalent as the consumption of aspirin. From flavor enhancers labeled as “natural ingredients” or “natural flavors” to oral and inject-able pharmaceutical drugs ranging from insulin to human growth hormone to anti-blood clotting drugs to seasonal vaccines, the human race has unsuspectingly been transformed into a species that consumes itself “for medicinal purposes“.

Be it consumed orally, injected (vaccinated) through the skin to bypass the body’s natural defenses, or purposefully “xeno”-transplanted via surgical procedure, the deadly zombie-creating prion we are about to expose is officially undetectable, ineradicable, untreatable, irreversibly fatal, and unless good people take immediate action and demand public exposure and immediate research, unstoppable!!!

There is a distinct difference between animal and human consumption, both in application and in function. But the dangers in both cases are equally deadly – as in always deadly, without exception, meaning 100% fatal! The reasons for this fact will become inescapably apparent and self-evident as we read on…

–≈–
What is Xenotransplantation?
–≈–

The FDA explains Xenotransplantation as:

Xenotransplantation is any procedure that involves the transplantation, implantation or infusion into a human recipient of either (a) live cells, tissues, or organs from a nonhuman animal source, or (b) human body fluids, cells, tissues or organs that have had ex vivo contact with live nonhuman animal cells, tissues or organs. The development of xenotransplantation is, in part, driven by the fact that the demand for human organs for clinical transplantation far exceeds the supply.

Currently ten patients die each day in the United States while on the waiting list to receive lifesaving vital organ transplants. Moreover, recent evidence has suggested that transplantation of cells and tissues may be therapeutic for certain diseases such as neurodegenerative disorders and diabetes, where, again human materials are not usually available.

Although the potential benefits are considerable, the use of xenotransplantation raises concerns regarding the potential infection of recipients with both recognized and unrecognized infectious agents and the possible subsequent transmission to their close contacts and into the general human population. Of public health concern is the potential for cross-species infection by retroviruses, which may be latent and lead to disease years after infection. Moreover, new infectious agents may not be readily identifiable with current techniques.

(Source: http://www.fda.gov/BiologicsBloodVaccines/Xenotransplantation/default.htm)

–≈–

The FDA also has this information page regarding xenotransplantation:

Information and recommendations for Physicians Involved in the Co-Culture of Human Embryos with Non-Human Animal Cells

The U.S. Food and Drug Administration (FDA) wants you to know that the co-culture of human embryos with nonhuman animal cells raises health concerns for the recipients of such embryos, the offspring resulting from such embryos, and the general public. The use of nonhuman animal cells, tissues or organs in the treatment of human medical conditions is called xenotransplantation…

Co-culture of human embryos with nonhuman animal cells fits the second part of this definition (xenotransplantation, defined above). During co-culturing, human embryos and nonhuman animal cells are maintained together outside the body, in ex vivo contact. Thus, the woman into whom the co-cultured embryos are transferred is a recipient of a xenotransplantation product.

A serious concern regarding the clinical use of xenotransplantation is the potential for the transmission of infectious disease from nonhuman animals to humans. Scientists believe that the potential for transmission of an infectious disease from the animal source to a human is of concern either when live nonhuman animal cells, tissues or organs are implanted directly into a human, or when human cells are exposed to live nonhuman animal cells by ex vivo contact. Experience with organ allotransplantation has shown that diseases such as human immunodeficiency virus (HIV) infection, Creutzfeldt-Jakob disease, hepatitis B virus infection and hepatitis C virus infection can be transmitted from the human donor to the recipient. Similarly, xenotransplantation poses concerns for infection with recognized, or as yet unrecognized, infectious agents from nonhuman animals. These concerns may extend beyond the recipient to the general public because of the potential for subsequent transmission of an infectious agent to the recipient’s contacts and to the general population. Infections originating from animals that have been known to infect and be transmitted from human to human include, for example, HIV and swine influenza. Many viruses exhibit latency, so that the lack of symptoms at the time of the embryo transfer, or in the short term, does not alleviate all concern.

The U.S. Public Health Service has published guidelines on infectious disease issues in xenotransplantation.  These guidelines, as well as FDA guidance documents, can be found at the website http://www.fda.gov/cber/xap/xap.htm, or obtained from FDA. They recommend, for example, that:

• You should inform recipients of xenotransplantation products that they and their intimate contacts should defer from donation of blood and other tissues.
• You should inform patients that they have been treated with a xenotransplantation product and of the risks involved.
• You should archive patient samples, such as blood, to allow future monitoring for potential infections.
• You should follow patients for their lifetimes and counsel them to be alert to any unusual symptoms.
• You should archive samples of the xenotransplantation product. In this case, the nonhuman animal cells used for the co-culture process should be archived.

We would be happy to discuss any questions you might have about these recommendations. The nature and level of our concerns may vary depending on the species of nonhuman animal used in the co-culture technique and the source of the culture cells. We plan to have further public discussion of this topic with an appropriate federal advisory committee. At this time, FDA plans to enforce investigation new drug application (IND) requirements for investigations involving further production of embryos co-cultured with live nonhuman animal cells. However, currently it is not our intent to take enforcement action based on the transfer of already existing embryos created by co-culture with live nonhuman animal cells.

(Source: http://www.fda.gov/BiologicsBloodVaccines/Xenotransplantation/ucm136532.htm)

–≈–

Has anybody considered that the growing of human body parts on animals is a gateway for new and more dangerous mutation of prion development and transmission? After all, the animal circulatory system will be directly fused during growth, and transferred during xenotransplantation into or onto the human host.

–≈–

In my film, “Lethal Injection: The Story Of Vaccination”, I covered in great detail the disturbing fact that cloned DNA from human aborted fetuses and other animal proteins are used in the production of vaccines and in the growth of cell substrates for vaccine cell growth (free to view on YouTube, –> here). Some viewers mistook this information as an attempt to promote a “pro-life” political standpoint, indeed missing the very real point that we are literally being forced into eating, injecting, and applying as cosmetics ourselves (other humans) with our unborn aborted children in the name of “medical science” and “beauty”. Thus, to say that “Soylent Green is people” is truly an understatement in modern medicine, food, and cosmetics. Indeed, everything is a choice.

Before we proceed, we must understand exactly what it is that gets directly injected into the human body via the vaccination process. Here is an incomplete list of human and non-human animal proteins and ingredients that are used in the vaccine and other inject-able drug markets. Note that these are listed as “ingredients” of different vaccines:

-residual MRC5 proteins – human diploid cells from aborted fetal tissue – including DNA and proteins
-human albumin, albumin from human blood
-sucrose human albumin
-chicken embryo
-chick embryonic fluid
-chicken protein
-monkey kidney cells
-phenol red rhesus monkey fetal lung cells
-rhesus monkey fetal diploid cells
-rhesus monkey rotavirus
-3 rhesus-human reassortant live viruses
-guinea pig embryo cells
-mouse serum proteins
-gelatin (collogen – animal proteins, especially flesh and connective tissues. Aborted human fetal material also used in cosmetics)
-lactose (animal milk derived – also added to pills as a cheap “filler”)
-vesicle fluid from calf skins
–calf serum
–bovine fetal serum
–bovine extract, US sourced
–bovine gelatin and serum “from source countries known to be free of bovine spongioform encephalopathy” (Note: this is an impossible claim to prove.)
-Mycobacterium bovis
-polysaccharide from Salmonella typhi Ty2 strain
-recombinant protein (OspA) from the outer surface of the spirochete Borrelia burgdorferi kanamycin – a tick-borne pathogen that causes Lyme disease

(Older) List of vaccines with aborted fetal tissue (cloned):

(Link: http://www.silentvoices.org/vaccinechart.html)

These human and other animal proteins are all but impossible to filter out of the final inject-able product (vaccines), and are being introduced at an alarming rate into the human and animal population of the world with the advent of the popularity and profit-potential of vaccination on a world (United Nations) scale. While the moral implications of this barbarous and unethical practice are more than obvious and should seemingly be enough to defeat the ego when choosing whether or not to vaccinate ones self or ones children, there is a much more sinister and unknown danger in this practice that needs a bit of light shown upon it…

Introducing, the prion…

–≈–
The Indefatigable Prion
–≈–

–≈–
Deadly Feasts
–≈–

I am seldom one to promote a book or movie, and yet I feel compelled to share this one with you – a 15 year old warning that has gone unheeded by the corporate and government profit machine, ignored by the media and medical community and as a result the conditioned and ignorant people, and brushed aside out of public view in an effort led by the WHO and the U.S. FDA and CDC.

“Deadly Feasts: Tracking The Secrets Of A Terrifying New Plague” was written and researched by Pulitzer prize winning author and researcher Richard Rhodes, published in 1997. I recomend that this book be on your “to read” list, if only to understand what is potentially the worst continuing outbreak of avoidable, man-induced disease in the history of the world.

If you’ve ever been vaccinated or eaten any type of meat or dairy products, you should really pay attention here…

The Introduction to the book, entitled “To The Reader”, states:

“The threat of Ebola virus has haunted our nightmares since Richard Preston published his “terrifying true story” The Hot Zone in 1994. Ebola hides in the African rain forest, but a deadlier disease than Ebola has begun killing young people in Britain and France. Ebola is a terrorist: it sickens people quickly and spares at least one out of ten. The new disease is a stealth agent: it incubates silently for years and kills every last victim it infects. Ebola is a sickness of fever and bleeding, no worse than cholera, a quick if not a merciful death. The new disease is an atrocity of destruction – a headache, a stumble, and then hallucination, palsy, seizure and coma drawn out horribly for months. Victims’ brains go spongy; their minds dim; they lose the ability to walk, to talk, to see, to swallow; they die slowly, drowning in pneumonia, or they starve to death.

Ebola can survive outside of the body for a few days at best. Sunlight kills it. Ultraviolet light kills it. The new disease agent refuses to die. Assault with pressurized, superheated steam in the autoclaves that hospitals use to sterilize instruments for surgery barely slows it. It remains deadly after hours of intense bombardment with hard radiation, months of soaking in formaldehyde, years of burial, decades of freezing. It survives even the fiery furnace of a seven-hundred-degree oven.

How Ebola spreads is still uncertain, but scientists know it’s a virus. In time, a vaccine will protect us from its threat (author’s note: I disagree with this vaccine statement, as is self evident in my film and research). The new disease turns up no virus in victims’ brains. It creeps past the barriers of species and immunity. Evidence accumulates that it’s a bad seed, a mistake of protein, a misshapen crystal that forces the brain to poison itself. If so, it’s a new kind of disease agent that can never be eradicated.

How the new disease spreads is known: it spreads in the cannibalism of animals by animals, it spreads in the industrial cannibalism of animal remains fed to animals, it spreads by the eating of beef…”

Deadly Feasts then discusses the cannibalistic rituals of the Fore tribal people who lived in New Guinea. More specifically, the “revenge” of the female members of the tribes who consumed (ate) the parts of their husbands and menfolk together with vigor and ritualistic joy – the result of the less than loving matrimonial customs of the Fore people. Each internal organ was extracted with care and precision, and then served with various plant sides, sweet potatoes, and other forest condiments.

A tradition that was started by the women of the tribes in the 1930’s, this cannibalism resulted in mass outbreaks of disease locally called “Kuru”. Kuru was thought by the women of the Fore tribes to be nothing short of witchcraft by the menfolk, whom were thought of as “sorcerers” in many Fore tribes. The native word “Kuru” literally meant shivering- in cold or from fear. And once the sorcery of Kuru took hold, the “bewitchment” would, without exception, lead to death.

Kuru’s symptoms are described as if taken straight of Night Of The Living Dead:

The symptoms of Kuru are broken down into three specific stages. The first, ambulant stage, exhibits unsteady stance and gait, decreased muscle control, tremors, deterioration of speech and dysarthria (slurred speech). In the second stage, sedentary stage, the patient is incapable of walking without support, suffers ataxia (loss of muscle coordination) and severe tremors. Furthermore, the victim is emotionally unstable, depressed, yet having uncontrolled sporadic laughter. Interestingly, the tendon reflexes are still normal at this point. In the final, terminal stage, the patient is incapable of sitting without support, suffers severe ataxia (no muscle coordination), is unable to speak, is incontinent (unable to restrain natural discharges/evacuations of urine or feces), has dysphagia (difficulty swallowing), is unresponsive to their surroundings, and acquires ulcerations (sores with pus and necrosis). An infected person usually dies within 3 months to 2 years after the first symptoms, often because of pneumonia or pressure sores infection.

(Source: http://anthropology.ua.edu/bindon/ant570/Papers/McGrath/McGrath.htm)

Please note that the symptom called “necrosis” is defined as:

Necrosis: The death of living cells or tissues. Necrosis can be due, for example, to ischemia (lack of blood flow). From the Greek “nekros” meaning dead body.

Now, despite the fact that the hairs on your back of your neck may be standing up in fibrous nervousness about now, we haven’t yet begun to uncover the zombification of the world yet.

“Deadly Feasts” begins its story in Papa New Guinea with the true story of cannibalism and its cost:

“Men lived separately from the women and children, following their wives into their gardens to copulate, sharing the big men’s lodge with the older boys. Men believed contact with women weakened them. They resented the fecundity of women. Men seldom ate the dead and then only the red meat, surreptitiously…”

“The women at their mortuary feast butchered and cooked down in the garden, but they ate in private, carrying the steaming bamboo tubes back to their separate woman’s houses, sharing the feast with their children…”

“They ate every part of the body, even the bones, which they charred at the open fires to soften them before crumbling them into the (bamboo shoot) tubes. The dead woman’s brother’s wife received the vulva as her special portion. If the dead had been a man, his penis, a delicacy, would have gone to his wife…”

“Eating the dead was not a primordial Fore custom. it had started within the lifetime of the oldest grandmothers among them, at the turn of the century (1900) or not long before…”

“Women bewitched with Kuru staggered to walk, walked with a stick and then could no longer walk at all. Before losing the ability to swallow they got fat and the flesh of those who died early of pneumonia was rich meat…”

“Nevertheless, the damage Kuru caused to the brain was similar to the damage caused by the rare condition known as Creutzfeldt-Jakob disease (CJD).

Towards the end of the book, Mr. Rhodes discusses the phenomenon and likely scientific folly of xenotransplantation in an interview with Dr. David White, the cofounder and medical director of a company called Imutran:

“Pioneer xenotransplantation has already begun: in 1984 in the U.S., a baboon heart kept Baby Fae alive for twenty days: a baboon liver was transplanted in 1994; San Francisco AIDS patient Jeff Getty received a baboon-marrow graft in 1995 to shore up his immune system. Advanced biotechnology that may make xenotransplantation routine is under development in the United States and in Britain. Lines of transgenic pigs are being bred for use initially for hearty transplants. Pig blood types are more like human types than those of other animals, but a strong immune response known as hyperacute rejection normally destroys pig tissue grafted into primates in a matter of hours.

I investigated Imutran, a company based in Cambridge, England, that leads the world in xenotransplantation technology, and learned that it has cloned human genes that defeat hyperacute rejection and inserted them into pig embryos.  Imultran has bred hundreds of pigs carrying these human genes. Rejection of transgenic pig hearts still has to be controlled with drugs, just as rejection of transplanted human hearts has to be controlled with drugs. In 1995, Imutran demonstrated that even without such immunosuppressive drugs, monkeys implanted with its transgenic pig hearts survived for five days – well past the time when hyperacute rejection would have destroyed an ordinary pig-heart implant. Implanted monkeys treated with immunosuppressive drugs survived up to sixty days. That achievement led Dr. David White, Imutran’s cofounder and medical director, to predict routine pig-heart transplants in humans before the turn of the century. “The big debate now,” White told the media, “is, do we currently have the skills to keep the hearts functioning in people for a long time; and the only way to answer that question is to put them into people and find out.”

I interviewed White at Imutran’s headquarters in Cambridge in April 1996. He was enthusiastic about his work. “Right from the beginning,” he explained, “our approach was to ask how can we genetically engineer the pig, not how can we treat the patient. From there, we realized that a possible approach would be to put these human regulators into a pig. And the smartest thing I ever did was to take out a patent on the process. Because that’s what pays all the bills.” Although I didn’t know it at the time, White had just sold Imutran to Sandoz Pharma, Ltd., a major drug company.

I will put my career on the line,” he told me, “and say that hyperacute rejection as we know it is dead, gone, finished. You take an organ from one of our pigs and transplant it into a primate and it will go for days without any treatment at all, routinely. We’ve done kidneys, islets [i.e. pancreatic tissue which secretes insulin, to correct diabetes], hearts – I don’t even know the number now, sixty or seventy. Now all we have to do is immunosuppress the monkey in order to achieve long-term survival. We did our first baboon transplant a couple of weeks ago, and on the same day that we successfully transplanted a baboon with a pig heart, one of our patients died waiting for a human heart.”

I came to the point of my visit: “Are you concerned with BSE?”

***Note that BSE stands for bovine spongiform encephalopathy (i.e. Mad Cow Disease).

“Fortunately,” White countered, “pigs don’t get BSE.”

“I think there’s evidence they do.”

“If you take contaminated brain from a mad cow and inject (vaccinate) the neural tissue directly into the brain of the pig it will get spongiform encephalopathy. But they’ve been feeding infected brain to pigs for five years no and none of the pigs has the disease.”

That was true.

“You have to appreciate that BSE is not an infection. It’s a very curious toxicity really.”

I told Dr. White I’d looked into it.

“Well,” he responded, “then perhaps you can tell me how the hell the bloody thing works. I don’t understand it.”

I tried to explain abnormal protein crystallization (caused by prions).

He listened. “Yes, that could work,” he said finally.

“Your pigs are isolated and presumably not fed meat-and-bone meal,” I prompted him.

“Oh no,” he confirmed. “Disease transmission is an area of considerable concern.” He left his desk and returned with a proprietary study as thick as a telephone book. “We put together a group of the world’s leading experts on pig disease and on the diseases that transplant patients get.” He opened the book. “I’ll just read you some of the headings. ‘Microorganisms Known To Be Pathogenic.’ ‘Microorganisms Pathogenic In Humans.’ ‘Microorganisms Known To Be Pathogenic In Pigs Bt Not Pathogenic In Humans.’ Microorganisms Not Known To Be Pathogenic But Similar To Microorganisms Pathogenic.” And so on. Porcine RNA viruses, porcine DNA viruses, exotic porcine RNA viruses, exotic porcine DNA viruses, a special section on the human measles viruses. Porcine bacteria – the gram negatives, the gram positives – and it goes on and on. A basic risk assessment of them all. A list of pathogens of most concern.” He closed the book. “So when you’ve done all that, you’re left with one problem, which is the retroviruses. We’re currently doing research on our primates to answer the question, will these pig retroviruses jump across the species barrier and recombine with human retroviruses? We haven’t finished, but we think the probability is extremely remote.”

***Author’s note: In my film Lethal Injection: The Story of Vaccination, we see various patents for using Porcine Zona Pellucida (pig ovaries) as inject-able vaccination birth control methods, for use in both animals and humans. The foreign ovary proteins cause an “immune response” in the vaccinated patient and the body’s natural defenses develop “antibodies” inadvertently for the body’s own (human) reproductive functions, while attempting to fight the foreign reproductive ovary or other proteins. This is but one example of xenotransplantation designed to control population growth in animals and humans…

“The pigs wont go to the hospital, White continued, The patient will come somewhere near the pigs. “That is,” he explained, “you will have a few dedicated specialist centers which do xenotransplantation. Those centers will have a sterile pig-production unit nearby. The patients will come there. It is ludicrous that you have to wait for fit, healthy people to die so that you can treat sick people. With a pig, you can come in and the physician will say, ‘I think you’re going to need a heart transplant. ‘You wouldn’t be at the end of the road. Maybe three months, maybe six months away. And we would modify your immune system so that you won’t reject pigs.

It occurred to me that we might be talking about more than hearts. “Are you planning to transplant other organs and tissues from the pig?”

“The heart, the lungs – all those former smokers, the market is huge – the kidney. Possibly the intestine. The substantia nigra is an area of great interest.”

I said: “What?”

“Bit of the brain,” White said. “For the treatment of Parkinson’s disease.”

I knew what substantia nigra was, I just couldn’t believe that a brilliant and innovative physician-businessman who had admitted he didn’t understand what causes spongiform encephalopathy (who does?) was planning to implant pig brain directly into the brains of humans.

In July of 1996, the Committee on Xenograft Transplantation of the U.S. Institute of Medicine, part of the National Academy of Sciences, endorsed xenografting on the grounds that the potential benefits outweigh the risks. “When the science base for specific types of xenotransplants is judged sufficient,” the committee concluded, “and the appropriate safeguards are in place, well-chosen human xenotransplantation trials using animal cells, tissues and organs would be justified and should proceed.” The committee cited “ample evidence,” however, that infectious agents could be transmitted from animals to humans, which indicated a danger “unequivocally greater than zero” that xenotransplantation could transfer new and deadly viruses across the species barrier. And it specifically mentioned transmissible spongiform encephalopathy (Mad Cow Disease).“

Most importantly, in analyzing the age-specific incidence of both bovine BSE and sporadic human CJD, Dr. Richard Kimberlin states:

“The shape of the age-specific incidence curve… implies that infection with a common strain [of CJD] occurs in childhood or adolescence, and that the median incubation period is 40 to 50 years.” German researcher Dr. Heino Diringer similarly defends and infectious cause: “It seems more than likely that… the sporadic cases of CJD always originate from direct or indirect transmission from animals to man.” In 1996, Deringer reported finding small virus-like particles in scrapie hamster brain…”

“Carleton Gajduserown freeze-dried a sample of scrapie brain, sealed the sample into a glass ampule and baked it in an oven for one hour at 360 degrees Celsius (nearly 700 degrees Fahrenheit). Reconstituted, the sample still transmitted scrapie to a hamster.”

At the end of his book, Richard Rhodes leaves us with these words (note: there are no spoilers here, just facts):

“I remember something he (Nobel-laureate virologist D. Carleton Gajdusek) asked me at our first meeting, late in 1995, before the British reported out the beginnings of what may be their new Black Death.

“You know the bone meal that people use on their roses?” Gajdusek asked me then. “It’s made from downer cattle. Ground extremely fine. The instructions on the bag warn you not to open it in a closed room. Gets up your nose.” The Nobel-laureate virologist who knows more than anyone else in the world about transmissible spongiform encephalopathy looked at me meaningfully. “Do you use bone meal in your roses?”

I told him I did.

He nodded. “I wouldn’t if I were you.”

The final blurb of Deadly Feasts is an article from the London Daily Telegraph, dated April 4, 1996:

“Gardeners have been reminded by the Royal Horticultural Society to wear gloves and a dust-excluding mask to avoid any risk of BSE when applying a spring dressing of blood and bonemeal to roses and shrubs.

Demand for beef is recovering steadily. At London’s Smithfield wholesale market, the trade in better quality cuts of British beef has recovered from zero a week ago to just over half the normal .

–≈–
Creutzfeldt-Jakob Disease (CJD)
–≈–

Before we read the following report from the Mayo Clinic on CJD, and as we will see once again this clinic reiterating the fact that very few cases of CJD have been reported throughout the world (as has the FDA, CDC, WHO, etc…), we must begin to consider that on an international scale, “prion diseases” are being covered up – quite simply by means of diagnosing them as other diseases such as “Alzheimer’s Disease” – of which these same “organizations” claim not to know the origins or causes of.

In fact, on page 133 of “Deadly Feasts”, Dr. Carlton Gajdusek and Joe Gibbs are quoted as such:

“Gajdusek and Gibbs prepared a technical note for the Journal of Neurosurgery. They reviewed CJD transmissibility. They advised that it was reasonable to assume that the CJD agent was at least as resistant as the scrapie agent to heat, formaldehyde and ultra-violate light. “In particular,” the wrote, “one must assume the agent is not killed by boiling.” They pointed out that physicians often misdiagnosed CJD as Alzheimer’s disease, as the form of cerebral atrophy known as Pick’s disease, or as many other conditions including brain tumors and strokes. They recommended sterilizing instruments used on such patients in an autoclave – a machine used in hospitals that kills even hardy microorganisms with hot steam under pressure – for at least thirty minutes, twice the standard autoclaving time. They recommended treating all organs as infectious, even those fixed in formaldehyde. They had found only one chemical, chlorine bleach, that reliably killed the scrapie agent and they recommended using it to decontaminate floors and other surfaces where tissue might have fallen.

But before this technical note was published… from Deadly Feasts:

“Diseases doctors unintentionally cause are called iatrogenic, Greek for “physician-born”. The first known human-to-human transmission of spongiform encephalopathy outside the Fore was iatrogenic (by Dr. Arthor DeVoe, eye surgeon and chairman of the department of ophthalmology at the College of Physicians and Surgeons of Columbia University in New York)…

A donor became available, a middle aged man with a two-month history of memory loss and involuntary tremors who died of pneumonia. Down in the hospital morgue, an ophthalmologist harvested one of the man’s eyeballs, immersed it in sterile saline in a small jar and delivered it to surgery…

Holding the donor cornea like a contact lens, DeVoe lowered it over the hole in his patient’s eye. It fit perfectly. Meticulously, across the next hour, DeVoe joined the edges of the cornea and the woman’s eyeball together with stitches of fine nylon thread, burying the knots in the wound…

The eye healed. The woman could see again clearly through the dead man’s cornea and the operation seemed a success. But the optic nerve connects the eye directly to the brain, providing a channel for infection, and the brain of the man who died of pneumonia, who had not been autopsied until after his cornea was harvested, showed the characteristic damage of Creutzfeldt-Jakob Disease. A year and a half after her operation, the woman began feeling nauseated, had difficulty swallowing, came to drool and stumble and jerk, went spastic, went mute, gradually introverted into vegetable oblivion. Two years beyond her surgery, emaciated and bedsore, she mercifully died. On autopsy her brain looked like the brain of the man who had donated his cornea – like a sponge. If Arthor DeVoe had only known before the transplant operation. A sickness had oozed from the cornea he’d implanted and eaten holes in his patient’s brain.”

–≈–

Now, when we look at the description for “Alzheimer’s Disease”, which according to the preeminent Spongiform Encephalitis expert is actually a prion disease such as CJV, we see virtually the same symptoms listed.

Alzheimer’s Disease is the most common form of a whole class of diseases generically called “dementia”. There is no stated or listed cure for Alzheimer’s Disease, which worsens as it progresses, and it eventually leads to death without exception from one of the direct or indirect “symptoms”.

Like AIDS, Alzheimer’s is not a disease in and of itself within the medical books, but rather a description for the symptoms of a particular disease state that is not understood – and this is the case with thousands of disease states and their symptoms.

The NINCDS-ADRDA Alzheimer’s Criteria specify eight cognitive domains that may be impaired in AD: memory, language, perceptual skills, attention, constructive abilities, orientation, problem solving and functional abilities.)

Sound familiar?

Now let us consider the number of cases of Alzheimer’s worldwide, and the predictions for humanity’s future.

In 2006 the worldwide prevalence of Alzheimer’s disease was 26.6 million. By 2050, prevalence will quadruple by which time 1 in 85 persons worldwide will be living with the disease. We estimate about 43% of prevalent cases need a high level of care equivalent to that of a nursing home. If interventions could delay both disease onset and progression by a modest 1 year, there would be nearly 9.2 million fewer cases of disease in 2050 with nearly all the decline attributable to decreases in persons needing high level of care.

Interpretation: We face a looming global epidemic of Alzheimer’s disease as the world’s population ages. Modest advances in therapeutic and preventive strategies that lead to even small delays in Alzheimer’s onset and progression can significantly reduce the global burden of the disease.

(Source: “FORECASTING THE GLOBAL BURDEN OF ALZHEIMER’S DISEASE” – Johns Hopkins University, Dept. of Biostatistics Working Papers, Year 2007, Paper 130)

Suddenly, by taking into consideration only the Alheimer’s diagnosis’ worldwide as being an actual “prion disease”, the 1 in one million figure listed as supposedly confirmed worldwide cases of CJV becomes instead a true epidemic – the true black plague of humanity – of prion disease.

And Alzheimer’s is just one of the listed dementia diseases.

Dementia includes many disease descriptions, including the symptoms of this partial list:

Huntington’s disease
Frontotemporal lobar degeneration
Alzheimer’s disease
SCA17 (dominant inheritance)
adrenoleukodystrophy (X-linked)
Gaucher’s disease
metachromatic leukodystrophy
Niemann-Pick disease type C
pantothenate kinase-associated neurodegeneration
Tay-Sachs disease
Wilson’s disease
cryptococcal meningitis
HIV
Lyme disease
progressive multifocal leukoencephalopathy
subacute sclerosing panencephalitis
syphilis
Whipple’s disease
dementia with Lewy bodies
corticobasal degeneration
progressive supranuclear palsy
encephalopathy
viral encephalitis
limbic encephalitis
Hashimoto’s encephalopathy
cerebral vasculitis
lymphoma
glioma
vascular dementia
antiphospholipid syndrome
CADASIL
MELAS
homocystinuria
moyamoya
Binswanger’s disease
Behçet’s disease
multiple sclerosis
sarcoidosis
Sjögren’s syndrome
systemic lupus erythematosus
Alexander disease
Canavan disease
Cerebrotendinous xanthomatosis
Dentatorubral-pallidoluysian atrophy
Fatal familial insomnia
Fragile X-associated tremor/ataxia syndrome
Glutaric aciduria type 1
Krabbe’s disease
Maple syrup urine disease
Niemann Pick disease type C
Neuronal ceroid lipofuscinosis
Neuroacanthocytosis
Organic acidemias
Pelizaeus-Merzbacher disease
Urea cycle disorder
Sanfilippo syndrome type B
Spinocerebellar ataxia type 2

Now what happens to all of these classifications/descriptions of disease states and their symptoms when we place them all into the same category of disease – prion disease? What indeed…? What if one thing is responsible for all of the above descriptions of the same disease?

The Mayo Clinic published this report on October 23, 2012:

–Begin report–

.

Creutzfeldt-Jakob Disease

By Mayo Clinic staff

Definition

Creutzfeldt-Jakob (KROITS-felt YAH-kobe) disease is a degenerative brain disorder that leads to dementia and, ultimately, death. Symptoms of Creutzfeldt-Jakob disease (CJD) sometimes resemble those of other dementia-like brain disorders, such as Alzheimer’s, but Creutzfeldt-Jakob disease usually progresses much more rapidly.

Creutzfeldt-Jakob disease captured public attention in the 1990s when some people in the United Kingdom developed a form of the disease — variant CJD (vCJD) — after eating meat from diseased cattle. However, “classic” Creutzfeldt-Jakob disease has not been linked to contaminated beef.

Although serious, CJD is rare, and vCJD is the least common form. Worldwide, there is an estimated one case of Creutzfeldt-Jakob disease diagnosed per million people each year, most commonly in older adults.

Symptoms

Creutzfeldt-Jakob disease is marked by rapid mental deterioration, usually within a few months. Initial signs and symptoms of CJD typically include:

• Personality changes
• Anxiety
• Depression
• Memory loss
• Impaired thinking
• Blurred vision
• Insomnia
• Difficulty speaking
• Difficulty swallowing
• Sudden, jerky movements

As the disease progresses, mental symptoms worsen. Most people eventually lapse into a coma. Heart failure, respiratory failure, pneumonia or other infections are generally the cause of death. The disease usually runs its course in about seven months, although a few people may live up to one or two years after diagnosis.

In people with the rarer vCJD, psychiatric symptoms may be more prominent in the beginning, with dementia — the loss of the ability to think, reason and remember — developing later in the course of the illness. In addition, this variant affects people at a younger age than classic CJD does, and appears to have a slightly longer duration — 12 to 14 months.

***Author’s note: Does this list of “symptoms” sound like a zombie to you? Sudden, Jerky movements with lack of reason or ability to think; an anxious monster unrecognizable as your mother, father, sibling, or friend due to “personality changes”, who when questioned can only utter guttural sounds due to “difficulty speaking and swallowing”?

Causes

The cause of Creutzfeldt-Jakob disease and other TSEs appears to be abnormal versions of a kind of protein called a prion. Normally, these proteins are harmless, but when they’re misshapen they become infectious and can wreak havoc on normal biological processes.

How CJD is transmitted

The risk of CJD is low. The disease can’t be transmitted through coughing or sneezing, touching, or sexual contact. The three ways it develops are:

• Sporadically. Most people with classic CJD develop the disease for no apparent reason. CJD that occurs without explanation is termed spontaneous CJD or sporadic CJD and accounts for the majority of cases.

• By inheritance. In the United States, about 5 to 10 percent of people with CJD have a family history of the disease or test positive for a genetic mutation associated with CJD. This type is referred to as familial CJD.

• By contamination. A small number of people have developed CJD after being exposed to infected human tissue during a medical procedure, such as a cornea or skin transplant. Also, because standard sterilization methods do not destroy abnormal prions, a few people have developed CJD after undergoing brain surgery with contaminated instruments. Cases of CJD related to medical procedures are referred to as iatrogenic CJD. Variant CJD is linked primarily to eating beef infected with bovine spongiform encephalopathy (BSE), the medical term for mad cow disease.

Risk factors

Most cases of Creutzfeldt-Jakob disease occur for unknown reasons, and no risk factors can be identified. However, a few factors seem to be associated with different kinds of CJD.

• Age. Sporadic CJD tends to develop later in life, usually around the age of 60. Onset of familial CJD occurs only slightly earlier. On the other hand, vCJD has affected people at a much younger age, usually in their late 20s.

• Genetics. People with familial CJD have a genetic mutation that causes the disease. The disease is inherited in an autosomal dominant fashion, which means you need to inherit only one copy of the mutated gene, from either parent, to develop the disease. If you have the mutation, the chance of passing it on to your children is 50 percent. Genetic analysis in people with iatrogenic and variant CJD suggest that inheriting identical copies of certain variants of the prion gene may predispose a person to developing CJD if exposed to contaminated tissue.

• Exposure to contaminated tissue. People who’ve received human growth hormone derived from human pituitary glands or who’ve had dura mater grafts may be at risk of iatrogenic CJD. The risk of contracting vCJD from eating contaminated beef is difficult to determine. In general, if countries are effectively implementing public health measures, the risk is virtually nonexistent.

***Author’s note: For anyone that is familiar with FDA standards and the meat packing and dairy industries, as well as the use of beef bone meal and other beef products to feed cattle (cow cannibalism) along with the use of inject-able bovine growth hormone (cow to cow vaccination) as a standard of practice by factory farms, and of course we mustn’t ignore the abhorrent health conditions of these beasts while kept in piles of their own excrement and infectious dung, this last sentence is no reassurance with regards to “public health measures” and the risk being “virtually nonexistent” from the FDA, especially with food now imported from China and other developing countries.

Complications

As with other causes of dementia, Creutzfeldt-Jakob disease profoundly affects the brain as well as the body, although CJD and its variants usually progress much more rapidly. People with CJD usually withdraw from friends and family and eventually lose the ability to recognize or relate to them in any meaningful way. They also lose the ability to care for themselves, and many eventually slip into a coma. The disease ultimately is fatal.

Physical complications, all of which may become life-threatening, include:

• Infection
• Heart failure
• Respiratory failure

…

Tests and diagnosis

Only a brain biopsy or an examination of brain tissue after death (autopsy) can confirm the presence of Creutzfeldt-Jakob disease. But doctors often can make an accurate diagnosis based on your medical and personal history, a neurological exam, and certain diagnostic tests.

The exam is likely to reveal such characteristic symptoms as muscle twitching and spasms, abnormal reflexes, and coordination problems. People with CJD also may have areas of blindness and changes in visual-spatial perception.

In addition, doctors commonly use these tests to help detect CJD:

• Electroencephalogram (EEG). Using electrodes placed on your scalp, this test measures your brain’s electrical activity. People with CJD and vCJD show a characteristically abnormal (brain) pattern.

• Magnetic resonance imaging (MRI). This technique uses radio waves and a magnetic field to create cross-sectional images of your head and body. It’s especially useful in diagnosing brain disorders because of its high-resolution images of the brain’s white matter and gray matter.

• Spinal fluid tests. Cerebral spinal fluid surrounds and cushions your brain and spinal cord. In a test called a lumbar puncture — popularly known as a spinal tap — doctors use a needle to withdraw a small amount of this fluid for testing. The presence of a particular protein in spinal fluid is often an indication of CJD or vCJD.

Treatments and drugs

No effective treatment exists for Creutzfeldt-Jakob disease or any of its variants. A number of drugs have been tested — including steroids, antibiotics and antiviral agents — and have not shown benefits. For that reason, doctors focus on alleviating pain and other symptoms and on making people with these diseases as comfortable as possible.

Prevention

There is no known way to prevent sporadic CJD. If you have a family history of neurological disease, you may benefit from talking with a genetics counselor, who can help you sort through the risks associated with your particular situation.

Preventing iatrogenic CJD

Hospitals and other medical institutions follow explicit policies to prevent iatrogenic CJD. These measures have included:

• Exclusive use of synthetic human growth hormone, rather than the kind derived from human pituitary glands

• Destruction of surgical instruments used on the brain or nervous tissue of someone with known or suspected CJD

• Single-use kits for spinal taps (lumbar punctures)

To help ensure the safety of the blood supply, people with a risk of exposure to CJD or vCJD aren’t eligible to donate blood. This includes people who:

• Have a biological relative who has been diagnosed with CJD
• Have received a dura mater brain graft
• Have received human growth hormone
• Spent a total of at least three months in the United Kingdom from 1980 to 1996
• Spent five years or more in France from 1980 to the present
• Received a blood transfusion in the U.K. between 1980 and the present
• Have injected bovine insulin at any time since 1980

***Author’s note: The American Diabetes Association lists the total number of official diabetics in the United States, as of January 2011, at 25.8 million people, or 8.3% of the population, with approximately 7 million of those listed as “undiagnosed”, and with 1.9 million new cases diagnosed in people aged 20 or older in 2010. It also lists an estimated 79 million more cases of “prediabetes”, the precursor symptoms to diabetes. This represents a whole lot of inject-able insulin shots.

Preventing vCJD

The risk of contracting vCJD in the United States remains extremely low. So far, only three cases have been reported in the U.S. According to the Centers for Disease Control and Prevention, strong evidence suggests that these cases were acquired abroad — two in the United Kingdom and one in Saudi Arabia.

In the United Kingdom, where the majority of vCJD cases have occurred, fewer than 200 cases have been reported. After its first appearance in 1995, CJD incidence peaked between 1999 and 2000, and has been declining since.

Regulating potential sources of vCJD

Most countries have taken steps to prevent BSE-infected tissue from entering the food supply, including tight restrictions on importation of cattle from countries where BSE is common; restrictions on animal feed; strict procedures for dealing with sick animals; surveillance and testing methods for tracking cattle health; and restrictions on which parts of cattle can be processed for food.

The risk of vCJD from the following sources is estimated to be extremely low:

• Vaccines. Some parts of cows, including blood, enzymes and amino acids, are used to grow the bacteria and viruses needed to make certain vaccines. Not all vaccines are grown in cattle parts, however, and the Food and Drug Administration (FDA) recommends that companies producing such vaccines use cattle parts only from low-risk countries. These recommendations apply to cosmetics as well. The FDA keeps a listing on its website of companies that use cattle from countries that aren’t classified as low-risk.

• Insulin. Insulin sold in the United States isn’t derived from cattle, but you’re allowed to import beef insulin from other countries if you follow specific guidelines. Because there’s no way to guarantee the safety of imported insulin, talk to your doctor about the best way to obtain insulin from sources outside the United States.

–End Mayo Clinic report–

–=–
“Woman with Mad Cow Disease donated her eyes”
–=–

The Associated Press reported in December of 1997 that:

LONDON – Scottish health authorities are investigating how tissue from the eyes of a woman who had suffered from the human form of `mad cow disease” was transplanted into three other people.

“We are aware there is a potential infection risk from tissue retrieved from a patient in Scotland,” a spokesman for the government Scottish Office said Saturday on customary condition of anonymity. “We do not know the full facts, but we are making urgent inquiries into how this could have occurred,” he said.

The 53-year-old woman suffered from lung cancer, but after she died a post-mortem examination showed she also had Creutzfeldt Jakob Disease. The brain-destroying disease is the human form of bovine spongiform encephalopathy, which afflicts cattle and is known as ‘mad cow disease’.”

No further details were given on the grounds of patient confidentiality. But the tabloid Sunday Mail said the post-mortem findings were not passed on to officials handling organ donor arrangements, and parts of her eyes, including the corneas, were transplanted into two men and a woman in her eighties.

Remember what the FDA stated from above?

“Currently ten patients die each day in the United States while on the waiting list to receive lifesaving vital organ transplants…”

Is it at all reasonable to assume that the FDA, Red Cross, AMA, ADA, or any other “association” out there can screen body parts for prions, including these CJD and other variants of “Transmissible spongiform encephalopathies (TSEs)”, also known as prion diseases, considering that they are undetectable without the victim being dead first?

The Red Cross blood donation guidelines website states:

Creutzfeldt-Jakob Disease (CJD)
If you ever received a corneal (eye) transplant, a dura mater (brain covering) transplant or human pituitary growth hormone, you are not eligible to donate. Those who have a close blood relative who had Creutzfeld-Jacob disease or who is in a family that has been told they have a genetic risk for Creutzfeld-Jacob disease are also not eligible to donate. Learn more about CJD.

Creutzfeldt-Jakob Disease, Variant (vCJD); “Mad Cow Disease”
See under Travel Outside of U.S. Learn more about vCJD and blood donation.

Interestingly, the supplied links to learn more information about CJD and vCJD do not link to anything, and a search on this Red Cross website for CJD turns up no search results.

(Source: http://chapters.redcross.org/ky/rivervalley/eligibility.htm)

–≈–
Prions And Cancer
–≈–

Prion related disease is not limited to brain functions, and is a virtually unknown field of research when it comes to the rest of the human body.

Science Daily reported in August of 2009:

Prion Protein Identified As Novel Early Pancreatic Cancer Biomarker

ScienceDaily (Aug. 18, 2009) — Mad cow disease is caused by the accumulation of an abnormal protein, the prion, in the brain of an affected patient. Outside of the brain, very little is known about prions. Case Western Reserve University School of Medicine, researchers have, for the first time, identified the prion as a biomarker for pancreatic cancer. Pancreatic cancer is one of the most deadly cancers in humans; the five year survival rate is less than 10 percent.

Chaoyang Li, Ph.D., Wei Xin, M.D., and professor of pathology, Man-Sun Sy, Ph.D., discovered the mechanism by which prions causes tumors to grow more aggressively. They published these findings in the September issue of the Journal of Clinical Investigation.

Unlike normal cells, in human pancreatic cancer cells the prion is incompletely processed and binds to a molecule inside the cell known as filamin A. Filamin A is an important regulator of the cell’s skeleton and its signaling machineries. The binding of the incompletely processed prion to filamin A disrupts the cell’s organization and signaling. As a result, the tumor cells grow more aggressively. On the other hand, when the prion level is reduced, the tumor cell loses its ability to grow in tissue culture and in animals. Most importantly, Dr. Li, et al. found that a subpopulation of patients had incompletely processed prion protein in their pancreatic cancer. This subgroup of patients had significantly shorter survival compared to patients whose tumors do not have prion.

According to Dr. Sy, “Currently there is no early diagnostic marker for pancreatic cancer. Detection of the incompletely processed prion may provide such a marker. Preventing the binding of prion to filamin A may open new avenues for therapeutic intervention of this deadly disease.”

Next, Drs. Li and Sy will look to determine if this type of prion protein expression is seen in other types of cancer.

There are other examples of truth seeping its way into the public’s eye…

Prions and cancer: A story unfolding

Prions, the causal agents of Mad Cow and other diseases, are very unique infectious particles. They are proteins in which the complex molecular three-dimensional folding process just went astray. For reasons not yet understood, the misfolding nature of prions is associated to their ability to sequester their normal counterparts and induce them to also adopt a misfolding conformation. The ever-growing crowd of misfolded proteins form the aggregates seen in diseases such as Parkinson’s and Alzheimer’s. Once misfolded, a protein can no longer exert its normal functions in the cell.

Now, a group led by Dr Jerson Lima Silva at the Federal University of Rio de Janeiro, Brazil, presents some new evidence that p53, a protein with the daunting task of suppressing tumor formation in the body, may show a typical prion-like behavior when mutated.

It has been known for some time that the buildup of p53 in the cell impairs the protein in preventing tumor growth. This has been observed in neuroblastoma, retinoblastoma, breast, and colon cancers. In a paper entitled “Mutant p53 aggregates into prion-like amyloid oligomers and fibrils: Implications for cancer” and published in the Journal of Biological Chemistry, the group shows that in breast cancer cell lines carrying the most common p53 mutation, the formation of amyloid-like aggregates of p53 proteins may explain the protein’s lack of function.

Whether this prionoid behavior in fact represents a relevant cancer-related mechanism remains to be shown. Development of novel and ingenious strategies to prevent p53 misfolding and aggregation may be just one way to find out.

“We are planning pre-clinical tests with synthesized nucleic acids in an attempt to prevent the changing in conformation of normal p53, and avoid aggregates of misfolded protein,” says Dr. Silva.

If successful, the strategy may help unveil unforeseen molecular mechanisms leading to tumor development. Considering that more than half of the cancers lose p53 function, this prionoid behavior may serve as a potential novel target for cancer therapy, dramatically transforming our way of thinking of cancer and treating cancer patients.

While radiation, heat, time, and chemicals will not destroy the infections nature of mutated prions, I believe that this most suppressed of technologies is the one thing not available or known about to those doing the testing.

Here’s the thing…

“The newspaper article provided here was included in a newspaper called The Planet and published February 1986 in Washington, D.C. It was delivered to every member of the U.S. House of Representatives and every member of the United States Senate. Not one representative, senator or staff assistant was motiviated sufficiently to investigate further.

The newspaper was also provided free to the George Washington University Medical School students and professors. Again, not one was motivated to investigate further. All while 7,000 to 10,000 Americans died weekly from cancer!

Good examples of public irresponsibility from people in positions of public trust or professions with public trust implied! Shame!

–Barry Lynes, September 25, 1999