Infectious Waste Fueling Alzheimer’s Disease, Autism

Reforming Policy, Practices Can Save Millions Of Lives

Neurodegenerative disease and autism have been surging around the world for the past 30 years. A man-made disaster is creating a public health disaster that’s still unfolding.

Neurotoxins are driving the epidemic more than age–in some countries than others. Teenagers are now dying of Creutzfeldt-Jakob disease–the most severe form of brain wasting disease.

Alzheimer’s disease alone is taking the lives of 50-100 million people around the world now. As millions die, even more will be diagnosed. Millions more are suffering in silence with a misdiagnosis or no diagnosis. Misinformation and mismanagement are fanning the flames.

Despite millions of deaths, experts suggest that the prevalence of the disease will quadruple by 2050, if not sooner. Unfortunately, there is a growing stack of evidence that Alzheimer’s disease, Parkinson’s disease and other brain diseases are transmissible. There is zero evidence to the contrary. Victims also are being misdiagnosed and undiagnosed at an alarming rate.

 

Prions

A variety of factors can trigger neurodegenerative disease, including genetics, head trauma and neurotoxins. Deadly, self-replicating proteins appear to be one of those neurotoxins.

Prions (PREE-ons) are a deadly and unstoppable form of protein that migrates, mutates, multiplies and kills with unparalleled efficiency. Dr. Prusiner coined the term as a contraction for proteinaceous infectious particlePrions cause fatal neurodegenerative disease in humans and animals by converting the cellular version of prion protein into a toxic form that erodes the brain and body. Prions migrate, mutate and multiply. They get stronger as they move up the food chain. At the top of the food chain, humans are highly vulnerable to prion disease. The prions shed from humans are the deadliest and most aggressive. Mismanaging human prions is a big mistake.

Alzheimer's disease and prion disease

Dr. Stanley Prusiner, an American neuroscientist from the University of California at San Francisco, earned a Nobel Prize in 1997 for discovering and characterizing prions and prion disease. President Obama awarded Prusiner the National Medal of Science in 2010 to recognize the importance of his research. Unfortunately, Prusiner’s science is being ignored and we all are facing a public health disaster because of the negligence and reckless disregard for public health.

Prions are a formidable threat. When the U.S. government enacted the Bioterrorism Preparedness and Response Act of 2002, it included a provision to halt research on infectious prions in all but two laboratories. It classified prions as select agents that pose an extreme risk to food, water and health systems. Unfortunately, the Center For Disease Control quietly took prions off the list about two years ago because the classification criminalized multi-billion dollar industries and many industry practices.

Prion Disease

Prion disease also is known as transmissible spongiform encephalopathy (TSE). The operative word is “transmissible.” Prusiner claims that all forms of TSE are caused by infectious prions. Prion disease often is described as a wasting disease that causes a loss of body mass and brain mass.

TSE is a spectrum disease that varies in severity and symptoms. It depends on which region of the brain is impacted first and by what prion mutation. Few cases are identical in terms of symptoms and diagnoses. When the presenting symptom is memory loss, the diagnoses flow along the following chart.

prion disease and CJD

In humans, the prion spectrum includes Alzheimer’s disease, Parkinson’s disease and an extremely aggressive version known as Creutzfeldt-Jakob disease. The difference between these diseases is very slight and often indistinguishable to neurologists. For example, millions of people have been told that they have Alzheimer’s disease, when, in reality, it’s CJD–where it’s clearly infectious.

“It is well known that CJD is transmissible via surgical or medical procedures involving prion-infected brain tissue. Our finding of infectious prions in skin is important since it not only raises concerns about the potential for disease transmission via common surgeries not involving the brain, but also suggests that skin biopsies and autopsies may enhance pre-mortem and post-mortem CJD diagnosis,” said Wenquan Zou, Associate Professor of Pathology and Neurology and Associate Director of the National Prion Disease Pathology Surveillance Center at Case Western Reserve School of Medicine. “The level of prion infectivity detected in CJD skin was surprisingly significant, but still much lower than that in CJD brains. Further investigation is necessary to determine whether extra precautions should be taken during non-neurosurgeries of CJD patients, especially when surgical instruments will be reused.”

Prion infectivity is highly concentrated in brain tissue, but it’s also in all bodily fluids and tissue. CJD transmission has occurred after patients were exposed to surgical tools previously contaminated by CJD victims. It’s also happening due to many other pathways.

According to neuroscientists Dr. Laura Manuelidis, at least 25 percent of Alzheimer’s disease diagnoses are actually CJD.

CJD, without dispute, is extremely infectious to caregivers and loved ones, but it has not been declared a reportable disease across the U.S. and many other nations.

Millions of cases of deadly CJD are being misdiagnosed as Alzheimer’s disease. Millions of patients and caregivers are being misinformed, misguided and exposed to an aggressive prion disease.

Read The Full Story About the Neurodegenerative Disease epidemic.

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Prion Disease Continues To Threaten Food Supply

Mad Cow Disease Spreading With Infectious Waste

Mad cow disease has again raised its ugly head in the United States. Thanks to misinformation and mismanagement by government, the problem will persist.

Government and industry representatives announced yesterday that an 11-year-old beef cow in Alabama tested positive for prion disease. Also known as bovine spongiform encephalopathy (BSE), the disease is always fatal and a major concern for producers and consumers alike.

It was detected after the cow showed clinical signs of sickness at an Alabama livestock market. This animal never entered slaughter channels and at no time presented a risk to the food supply, or to human health in the United States, the U.S.D.A. said. Unfortunately, this producer did attempt to sell a very sick animal to an unsuspecting buyer. He obviously has a farm or ranch that is contaminated. The sick animal added to the contamination on the farm with its urine, feces and saliva. It also infected the livestock auction site. Sun and oxygen do not deplete prions. In fact, they can mutate and multiply in some soil and migrate away via the wind and water runoff.

Alzheimer's disease and prion disease

The Problem With Prions

Each prion victim is a symptom of a much bigger threat to food safety, water quality and public health. Prion disease has been detected in livestock around the world.

Of the five confirmed occurrences of BSE in cattle in the United States, this is the second in Alabama., but the vast majority of beef and dairy cattle are not tested thanks to intense lobbying from cattle producers and food companies.

Unfortunately, livestock producers, farmers and other land owners are being duped into a false sense of security and many are unwittingly participating in high-risk production practices that expose livestock, wildlife and people to deadly prions. To purge the threat of prion disease from the food supply, it’s time to manage prion pathways like we handle all biohazards. It’s time for government agencies to stop spreading misinformation and stop promoting risky production practices, including the dumping of infectious waste on farms, ranches, golf courses, parks and playgrounds. Cities are now dumping their highly infectious sewage sludge, also known as biosolids, on open land across the U.S.—especially in rural areas. It’s bioterrorism. It’s fueling the spike in Alzheimer’s disease, autism, Creutzfeldt-Jakob disease, chronic wasting disease and mad cow disease. It’s also fueling cancer, endocrine disruption and more.

A Spectrum Disease Among Mammals

Neurodegenerative disease, including prion disease, is the fastest-growing cause of death in the world. Misinformation and mismanagement are fueling the epidemic among people and wildlife. Unfortunately, we have no idea how pervasive the disease is among livestock because 99.9 percent of the animals are not tested, even though many are being exposed to prion contamination on a daily basis. Infected animals are contagious long before they start to stumble, drool and fall down. Therefore, our food and water supplies are at risk.

The technical term for prion disease is transmissible spongiform encephalopathy (TSE). The operative word is “transmissible.” In addition to mad cow disease, TSE includes scrapie in sheep and chronic wasting disease in deer, elk, moose and reindeer. TSE has been found in many mammals, including dolphins, cats, mink and elephants. It’s likely killing whales and other sea mammals, since most mammals appear to be vulnerable to deadly prions.

In humans, TSEs are known as Alzheimer’s disease, Creutzfeldt-Jakob disease (CJD) and kuru. There is little, if any, difference because prion disease is a spectrum disease that’s only distinguished by the severity of symptoms. Diagnoses are usually a shot in the dark based only on visible symptoms.

Dr. Stanley Prusiner, an American neuroscientist from the University of California at San Francisco, earned a Nobel Prize in 1997 for discovering and characterizing deadly prions and prion disease. He claims that all TSEs are caused by prions–a deadly and unstoppable form of protein that migrates, mutates, multiplies and kills with unparalleled efficiency.

President Obama awarded Prusiner the National Medal of Science in 2010 to recognize the importance of his research. According to Prusiner, TSEs all are on the same disease spectrum, which is more accurately described as prion (PREE-on) disease Creutzfeldt-Jakob disease is at the extreme end of the spectrum. Prusiner’s science is being ignored and we are facing a public health disaster because of the negligence.

The Misinformation

Despite Dr. Prusiner’s crowning achievement, he has remained too silent on policies and practices that are contributing to the spread of prions in our daily lives. Government and industry spokesmen have stepped forward to cast smoke and mirrors over productive conversations about reforms to protect public health. Despite attempts to gag and censor Prusiner and other prion scientists, they have painted the landscape of the problem. It’s up to critical thinkers to connect the dots and demand change.

beef tongue recalled over mad cow risk

For example, Jimmy Holliman, a spokesperson for the National Cattlemen’s Beef Association in Denver went on record to say that BSE is not contagious. That’s the equivalent of saying that an infectious disease is not infectious. The comment demonstrates incompetence, negligence or contempt.

“USDA’s ongoing BSE surveillance program has tested more than one million cattle since the program began,” Holliman said. “The incidence of BSE in the United States is extremely low, and will remain so.”

That’s quite an admission. It only takes one infected animal to create a perpetual prion pathway that will infect live animals, carcasses at the slaughterhouse, meat markets and kitchens.

In the spirit of full disclosure, I worked for the National Cattlemen’s Association, the predecessor of Holliman’s organization, between 1988 and 1992. My father worked in the meat industry all of his life. I grew up in rural Colorado with many beef and dairy producers. I’m not an enemy of the beef industry. I’m trying to lead them out of this mess before government lies explode in their face.

Prion disease is a complex topic. Even the world’s top scientists don’t fully understand the dynamics, yet. All that we need to know is that prions + pathways = victims:

  1. Prions: Impossible to neutralize completely in laboratory or surgical setting. Even more impossible to halt in the open-air experiments that are taking place all around us.
  2. Pathways: The key to prion management is pathway management. The bodily fluids, feces and cell tissue of prion victims are highly infectious. Prion victims (especially people) contaminate the world around them. Although prions can migrate via many pathways, some of the largest and most obvious threats are being ignored. We examine the major pathways below.
  3. Victims: If we know that we have prions and pathways, there will be victims—an endless supply of victims will spawn new mutations and new pathways.

First of all, prion disease is prion disease. There are now thousands of mutations of prions. No two cases of prion disease are identical because some prions are more aggressive and pervasive than others. It also depends on which region of the brain is impacted first.

The best way to refer to this spectrum of maladies is just “prion disease.” It makes it much easier to keep score and cut through the misinformation. There is no evidence of a species barrier, but some species appear to be more resistant than others. Some people are more resistant to prions than others.

Since prions migrate, mutate and multiply, any official attempt to characterize prion disease as a non-event is reckless, incompetent and fraudulent. There are now thousands of prion mutations–not just two or three. The mutations are becoming more aggressive and more lethal every day as they spread throughout our world (naturally and unnaturally). Victims are getting younger and younger.

People and animals dying of prion disease contaminate the environment around them with the prions in their urine, feces, blood, mucus and saliva. It spreads throughout the entire body. Each victim becomes an incubator and a distributor of the Pandora-like pathogen.

Not only are homes and hospitals exposed to the prion pathogen, so are entire sewage treatment systems and their by-products (wastewater reclamation and sewage sludge). The human prion is resistant to both heat and chemicals. It’s reported that prions released from people are up to a hundred thousand times more difficult to deactivate than prions from most animals. Sewage from hospitals, nursing homes, slaughterhouses, morgues, mortuaries, veterinarians and other high-risk places enters the same sewage system. Wastewater treatment plants can’t detect or neutralize deadly prions.

Prion Mismanagement

Industry spokesmen are again trying to calm the minds and markets around the world. The official story is that the animal had an “atypical” form of the disease, which is one of many red flags regarding the misinformation and mismanagement of prion disease.

As stated earlier, prions can migrate via many pathways. Unfortunately for us all, some of the largest and most obvious prion threats are being ignored. In fact, I argue that humans, wildlife and livestock are exchanging prions back and forth now via food, water and air. The primary pathway is infectious waste from humans that is dumped on open spaces (more detail ahead).

land application sewage sludge

TSE among humans is much more prevalent than government and industry admit. However, just like the example with cattle above, it only takes one prion victim to spread the contamination far and wide. Unfortunately, we have had millions of people in the U.S. alone who have TSE or have died of it over the past century.

As stated earlier, Creutzfeldt-Jakob disease and Alzheimer’s disease are both part of the prion spectrum. Without dispute, CJD is highly infectious and extremely aggressive. It’s much more prevalent than reported. In fact, it’s now killing teenagers. 

“Creutzfeldt-Jakob disease behaves like Alzheimer’s disease on steroids,” said Dr. Jennifer Majersik, an associate professor of neurology at the University of Utah.

According to neuroscientists Dr. Laura Manuelidis, at least 25 percent of those who have been diagnosed with Alzheimer’s disease actually have CJD, which is further up the prion spectrum. Millions of cases of deadly CJD are being misdiagnosed as Alzheimer’s disease. None of these patients are being quarantined, which means that they are putting family, caregivers and entire communities at risk. It appears that the milder version, Alzheimer’s disease, is equally infectious.

Alzheimer's disease epidemic

Read The Full Story About Mad Cow Disease. The Vectors Of Transmission Are Numerous.

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Crossbow Communications specializes in issue management and public affairs. Alzheimer’s disease, Creutzfeldt-Jakob disease, chronic wasting disease and the prion disease epidemic is an area of special expertise. Please contact Gary Chandler to join our coalition for reform gary@crossbow1.com.

Alzheimer’s An Infectious Disease

Alzheimer’s A Transmissible Disease

If you think that you and your family are immune to the surging epidemic of neurodegenerative disease, think again. Neurodegenerative disease, including Alzheimer’s disease, is the fastest-growing cause of death in the world. It’s getting worse every day thanks to mismanagement and misinformation.

Infectious proteins known as prions are involved with most forms of neurodegenerative disease. Prion disease is known in neurology as transmissible spongiform encephalopathy (TSE). The operative word is “transmissible.” The global epidemic has more to do with the prion contagion than age. In fact, it appears that the autism epidemic has more in common with Alzheimer’s disease than previously thought.

Dr. Stanley Prusiner, an American neuroscientist from the University of California at San Francisco, earned a Nobel Prize in 1997 for discovering and characterizing deadly prions and prion disease. Prusiner claims that all TSEs, including Alzheimer’s disease, are caused by prions.

Alzheimer's disease and prion disease

President Obama awarded Prusiner the National Medal of Science in 2010 to recognize the importance of his research. According to Prusiner, TSEs are a spectrum disease. Creutzfeldt-Jakob disease, which is extremely aggressive and extremely transmissible, is at the extreme end of the spectrum. Unfortunately, Prusiner’s science is being ignored and we are facing a public health disaster because of the negligence.

Neurologists are just guessing when they make a diagnosis on the prion spectrum. If the patient exhibits memory problems, they are labeled with Alzheimer’s disease. If they have a movement disorder, they are diagnosed with Parkinson’s disease. If the person exhibits extreme symptoms of both, they are diagnosed with Creutzfeldt-Jakob disease (CJD). It’s far from a science.

prion disease spectrum

According to neuroscientist Laura Manuelidis, at least 25 percent of Alzheimer’s diagnoses are wrong. These misdiagnoses are actually CJD, which is further up the prion spectrum. CJD, without dispute, is extremely infectious to caregivers and loved ones.

Neurologists don’t know where along the spectrum the disease becomes transmissible. The entire spectrum could represent a transmissible disease. Unfortunately, neurologists are not warning these patients and their caregivers about the risks of exposure. Even those with Creutzfeldt-Jakob disease are not quarantined. They are sent home, where they can infect friends, family, caregivers, clinics, dental offices, restaurants and entire communities.

“There has been a resurgence of this sort of thinking, because there is now real evidence of the potential transmissibility of Alzheimer’s,” says Thomas Wiesniewski M.D. a prion and Alzheimer’s researcher at New York University School of Medicine. “In fact, this ability to transmit an abnormal conformation is probably a universal property of amyloid-forming proteins (prions).”

A study published in the journal Nature renews concern about the transmissibility of Alzheimer’s disease between people. A second study released in early 2016 by the same scientist adds to the stack of evidence.

Studies confirm that people and animals dying of prion disease contaminate the environment around them with prions because prions are in the urine, feces, blood, mucus and saliva of each victim. Each victim becomes an incubator and a distributor of the Pandora-like pathogen. Victims are contagious long before they exhibit clinical symptoms.

Alzheimer's disease epidemic

At the personal level, this is very bad news for caregivers, especially spouses, who are 600 percent more likely to contract neurodegenerative disease from patients (Duke University and Utah State University). A cough, sneeze, utensils and drinking glasses all become lethal pathways. Once an item is contaminated, it’s impossible to sterilize. The human prion is resistant to both heat and chemicals. It’s reported that prions released from people are up to a hundred thousand times more difficult to deactivate than prions from most animals. Prions are not alive, so they can’t be killed.

Wastewater treatment plants are collecting points for prions from infected humans. The sewage treatment process can’t stop prions from migrating, mutating and multiplying before being discharged into the environment where they can kill again. The bad news is that the prions are being released back into the environment and dumped openly on land. The wastewater is being reclaimed and used for irrigating crops, parks, golf courses. It’s even being recycled as drinking water.

Claudio Soto, PhD, professor of neurology at the University of Texas Medical School in Houston, and his colleagues confirmed the presence of prions in urine. Soto also confirmed that plants uptake prions and are infectious and deadly to those who consume the infected plants. Therefore, humans, wildlife and livestock are vulnerable to prion disease via plants grown on land treated with sewage sludge and reclaimed sewage water.

Prion researcher Dr. Joel Pedersen, from the University of Wisconsin, found that prions become 680 times more infectious in certain soils. Pedersen also found that sewage treatment does not inactivate prions. Therefore, prions are lethal, mutating, migrating and multiplying everywhere sewage is dumped.

“Our results suggest that if prions enter municipal wastewater treatment systems, most of the agent would bond to sewage sludge, survive anaerobic digestion, and be present in treated biosolids,” Pedersen said.

prion research Joel Pedersen

“Land application of biosolids containing prions represents a route for their unintentional introduction into the environment. Our results emphasize the importance of keeping prions out of municipal wastewater treatment systems. Prions could end up in sewage treatment plants via slaughterhouses, hospitals, dental offices and mortuaries just to name a few of the pathways. The disposal of sludge represents the greatest risk of spreading prion contamination in the environment. Plus, we know that sewage sludge pathogens, pharmaceutical residue and chemical pollutants are taken up by plants and vegetables.”

Thanks to more and more people dying from TSEs, wastewater treatment systems are more contaminated with prions than ever. Wastewater treatment plants are now prion incubators and distributors. The prion problem is getting worse every day.

land application sewage sludge

The U.S. Environmental Protection Agency (EPA) has confirmed that prions are in sewage and that there has been no way to detect them or stop them. As such, the EPA has never issued guidance on prion management within wastewater treatment plants. Unfortunately, the EPA’s risk assessment on sewage sludge and biosolids were prepared before the world of science knew about prions. The agency continues to cling to its antiquated sludge rule crafted back in the dark ages. It does, however, consider prions a “contaminant of emerging concern.” Meanwhile, its outdated risk assessments are promoting a public health disaster.

“Since it’s unlikely that the sewage treatment process can effectively deactivate prions, adopting measures to prevent the entry of prions into the sewer system is advisable,” — Toronto Department of Health, November 2004.

Exposing crops and livestock to prions is a very bad idea. Plants absorb prions from the soil along with water and nutrient uptake, which makes the prions even more bioavailable and infectious to humans, wildlife and livestock.

chronic wasting disease caused by prions

Unfortunately, the damage is real. Deer, elk, moose and reindeer are contracting an unstoppable prion disease now. In deer, the government calls prion disease chronic wasting disease. In cattle, prion disease is called bovine spongiform encephalopathy (they might as well call it what it is—transmissible spongiform encephalopathy). Mad cow disease is the term that most of us know. The government pretends that there is a specific prion responsible for each of these diseases. The fact is that there are thousands of mutations of prions spreading in the environment and food chain now. Some kill quickly, while some are less lethal. The only thing that we need to know is that a deadly prion is a deadly prion. Prions shed from humans are the most aggressive and the most deadly. There is no species barrier.

If prion disease is killing these animals, livestock are not immune. Beef and dairy cattle are consuming these infected crops and the infected water supplies, too. Since humans are at the top of the food chain, and since we are often downstream from these infected farms, ranches and forests, our food and water supplies are being compromised. Wind and tornadoes transport the infectious waste even further.

So, is Alzheimer’s disease transmissible? There is absolutely no evidence to the contrary. The truth is your best defense against neurodegenerative disease.

Alzheimer's disease treatment

Preview and order the eBook now. Learn how to avert exposure to the Alzheimer’s disease contagion. Answers begin with the truth.

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Crossbow Communications specializes in issue management and public affairs. Alzheimer’s disease, Creutzfeldt-Jakob disease, chronic wasting disease and the prion disease epidemic is an area of special expertise. Please contact Gary Chandler to join our coalition for reform gary@crossbow1.com.

Wastewater Reclamation Based On Flawed Risk Assessments

Alzheimer’s Disease Fueled By Infectious Waste

Neurodegenerative diseases are the fastest-growing causes of death around the world. The mismanagement of infectious waste is contributing to the epidemic.

Dr. Stanley Prusiner earned a Nobel Prize in 1997 for his pioneering research on deadly prions—an infectious form of protein that connects a deadly spectrum disease called transmissible spongiform encephalopathy (TSE). The operative word is “transmissible.”

President Obama awarded Prusiner the National Medal of Science in 2010 to recognize the importance of his work. Unfortunately, this groundbreaking research is being ignored. This negligence is fueling a public health disaster around the world, as critical prion pathways are being ignored and mismanaged.

wastewater treatment plants and prion disease

In June 2012, Prusiner confirmed that Alzheimer’s disease, Parkinson’s, Huntington’s and even ALS are prion diseases similar, if not identical, to Creutzfeldt-Jakob disease. The primary difference being which part of the brain the disease attacks first. The other variable is that there are now an unknown number of prion mutations.

“There is now real evidence of the potential transmissibility of Alzheimer’s,” says Thomas Wiesniewski M.D. a prion and Alzheimer’s researcher at New York University School of Medicine. “In fact, this ability to transmit an abnormal conformation is probably a universal property of amyloid-forming proteins (prions).”

Mutations of these deadly prions also are the common denominator between human forms of the disease, mad cow disease in livestock and chronic wasting disease in wildlife. Several other species of mammals, including sea mammals, also are victims of the unstoppable epidemic. Much of the carnage is being swept under the rug as the problem escalates.

Although there are many causes contributing to prion disease, many people and animals are contracting it from environmental exposure (food, water and soil) and then contaminating the environment even more with their own bodily fluids. Victims of prion disease are walking time bombs. Creutzfeldt-Jakob disease (CJD) is the most deadly form of prion disease in humans. Without dispute, it is a very contagious disease that kills rapidly. There is no cure for CJD.

Alzheimer’s and CJD are often indistinguishable to neurologists and general practitioners. Misdiagnoses are common. It appears that CJD is caused by a more aggressive mutation of prion than Alzheimer’s, but a deadly prion is a deadly prion. There is no reason to believe that some prions behave differently than others in disease transmission and progression. There should be no difference in disease management.

Unfortunately, as more people contract these brain diseases, the more deadly wastewater streams become. Meanwhile, wastewater reuse is surging around the world in response to growing populations and dwindling water resources. Other by-products from the wastewater stream known as biosolids (sewage sludge) also are being used to fertilize crops, pastures for livestock, golf courses, playgrounds and gardens. Millions of people, including your family, are in harm’s way because wastewater treatment plants can’t stop prions. Regulators and industry are playing dumb as the body count keeps rising. It’s a deadly circle enabled by an outdated risk assessment. Modern science is being ignored.

Prion researcher Dr. Joel Pedersen, from the University of Wisconsin, found that prions become 680 times more infectious in certain soils. Pedersen also found that sewage treatment does not inactivate prions. Therefore, prions are lethal, mutating, migrating and multiplying everywhere sewage is dumped.

prion research Joel Pedersen

“Our results suggest that if prions enter municipal wastewater treatment systems, most of the agent would bond to sewage

sludge, survive anaerobic digestion, and be present in treated biosolids,” Pedersen said. “Land application of biosolids containing prions represents a route for their unintentional introduction into the environment. Our results emphasize the importance of keeping prions out of municipal wastewater treatment systems. Prions could end up in sewage treatment plants via slaughterhouses, hospitals, dental offices and mortuaries just to name a few of the pathways. The disposal of sludge represents the greatest risk of spreading prion contamination in the environment. Plus, we know that sewage sludge pathogens, pharmaceutical residue and chemical pollutants are taken up by plants and vegetables.”

land application sewage sludge

The largest prion pathway in the world is wastewater (infectious waste) from homes, hospitals, nursing homes, slaughterhouses, dental offices and other high-risk sources. The problem is that prions are in all bodily fluids and cell tissue of millions of victims who often go undiagnosed.

Alzheimer's disease epidemic

Their mucus, saliva, feces, and urine are flushed down millions of toilets and rinsed down sinks every day. Once inside the wastewater system, prions proceed to migrate, mutate and multiply. Reckless risk assessments enable wastewater treatment plants to spread these deadly agents far and wide. Deadly prions are building up and incubating in sewage treatment plants and then dumped openly on land. They are swept into the air by the wind. Now, water contaminated by prions is migrating into our rivers, lakes and oceans. It’s being injected into groundwater and it’s being recycled as tap water.

biosolids land application and disease

I used to support wastewater reclamation and reuse projects until I realized that the risk assessments were prepared decades ago—before Dr. Prusiner characterized prions and prion disease. These microscopic protein particles have converted sewage and its by-products a public health disaster.

Claudio Soto, PhD, professor of neurology and director of the George and Cynthia W. Mitchell Center for Alzheimer’s Disease and Other Brain Related Illnesses at the University of Texas Medical School in Houston, and his colleagues are the latest to find prions in urine. The study appeared in the August 7, 2014 issue of the New England Journal of Medicine. Recent studies are confirming the presence of prions in blood. The U.S. EPA and other regulatory bodies around the world are ignoring these risks.

“This is the first time that prions have been detected in human urine,” Dr. Soto told Neurology Today.

Soto failed to reference urine and blood studies performed earlier by Ruth Gabizon in 2001 and Reichl in 2002, which also detected deadly prions in bodily fluids.

sewage treatment plant and infectious waste

Wastewater Reclamation Hazards

As many hospitals have learned the hard way, deadly prions are unstoppable in the sterile confines of an operating room that has been exposed to someone with prion disease. Prions are totally unaccounted for in the high-volume streams at wastewater treatment plants. Prions migrate, mutate and multiply as they move through the environment and up the food chain. Prions from humans are the most aggressive and deadly. Wastewater treatment plants have been prion incubators and distributors for decades. The victims no longer fit under the rug of deceit.

Sewage treatment plants and their discharges are permanently infected. Once a prion reaches the soil, the soil is permanently contaminated and the entire watershed below that point is at risk forever. If your food and water is generated in that watershed, you and your family are exposed. We can’t afford to further contaminate entire watersheds – increasing the pathway to humans, livestock, and wildlife downstream.

chronic wasting disease caused by prions

Read the full story about the hidden hazards associated with wastewater reclamation and reuse at http://crossbowcommunications.com/wastewater-reclamation-reuse-based-on-outdated-risk-assessments/

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Crossbow Communications specializes in issue management and public affairs. Alzheimer’s disease, Creutzfeldt-Jakob disease and the prion disease epidemic is one of our special areas of practice. Please contact Gary Chandler to join our coalition for reform gary@crossbow1.com. Stop prion disease.

Sewage Sludge Spreading Brain Disease

Biosolids Spreading Brain Disease Among Mammals

In 1972, world leaders realized that dumping millions of tons of sewage sludge into the oceans killed entire underwater ecosystems. Some nations stopped the dumping immediately, while others did not.

The U.S., for example, finally passed the Ocean Dumping Ban Act of 1988. It required dumping all municipal sewage sludge and industrial waste on land. That meant dumping it into landfills or dumping it openly on land, including farms, ranches, national forests, city parks, golf courses, playgrounds, sport fields and beyond. The Act went into effect in 1992 and it sparked a public health disaster. The practice is spreading pathogens to people, livestock, wildlife and beyond every day.

Landfills designed to handle this toxic soup are extremely expensive. So, the dumpers hired a public relations firm to convince unsuspecting citizens that neurotoxins are fertilizer. The PR firm called this toxic waste biosolids. It’s even sold in bags at your local home and garden store as soil for your garden and potting plants. It should be called death dirt.

biosolids management land application

Since then, millions of tons of sewage sludge have been given to farmers as fertilizer every year. Those farmers and ranchers who don’t believe that “fertilizer” bullshit are being paid to dump it on their land and shut up. The farmers are held harmless if the infectious waste causes damage to people or property.

“There is now real evidence of the potential transmissibility of Alzheimer’s,” says Thomas Wiesniewski M.D. a prion and Alzheimer’s researcher at New York University School of Medicine. “In fact, this ability to transmit an abnormal conformation is probably a universal property of amyloid-forming proteins (prions).”

Unfortunately, the practice of dumping extreme quantities of sewage sludge on land has created an even bigger public health problem. It’s now killing wildlife and it still kills sea mammals. Livestock are not immune to the threat.

chronic wasting disease caused by prions

Prions are the protein-based infectious agents responsible for a group of diseases called transmissible spongiform encephalopathy (TSE). The operative word is transmissible. TSEs are more commonly known as:

  • bovine spongiform encephalopathy (mad cow disease) in cattle;
  • scrapie in sheep;
  • Creutzfeldt-Jakob disease (CJD) and Alzheimer’s disease in humans; and
  • chronic wasting disease (CWD) in deer, elk, moose and reindeer.

According to Nobel Laureate Stanley Prusiner, Alzheimer’s disease, ALS and Huntington’s disease also are on the TSE spectrum. All are fatal, neurodegenerative brain diseases.

Prions and Prusiner win Nobel Prize

Infectious prions are in the bodily fluids of its victims, including blood, urine, mucus, saliva and feces. These victims send prions to the municipal sewage treatment plant where they remain untouched. Wastewater effluent and sewage sludge recycles prions into the environment. Once dumped on open land, they remain infectious. Irrigation, precipitation and wind carry the prions into groundwater, streams, lakes, oceans and airways, including homes, offices and beyond.

Alzheimer's disease epidemic

Reckless wastewater treatment policies and practices are now fueling a global epidemic of neurodegenerative disease among people, wildlife and livestock. The risk assessments are based on fraud and outdated information. The risk assessments for the land application of sewage sludge (LASS) were developed back in the 1970s and 1980s–before we knew about prions and other killers in modern sewage streams, including many forms of infectious medical waste.

The risk assessments were questionable then and they are total failures now. Plus, these risk assessments do not account for the possibility of sewage sludge dumped on land going airborne. It’s much more than a possibility–airborne sewage sludge is killing people and animals. It’s dumping the toxins and infectious waste everywhere.

land application sewage sludge

Unfortunately, the U.S. exported these ridiculous ideas to other nations who proceeded to contaminate their food and water supplies with sewage. If hospitals can’t stop prions, neither can the brain surgeons at wastewater treatment plants.

The legislation banning ocean dumping was very explicit about the need to stop dumping potentially infectious medical waste into the oceans. Ironically, the current policy that promotes LASS ignores the risk of infectious medical waste and many other threats. It also ignores radionuclides, endocrine disruptors, birth control pills, antibiotics, flame-retardants and other toxins and superbugs. This toxic waste belongs in a lined landfill not our watersheds and food supplies. It’s time for immediate reforms.

The same sewage-borne toxins and pathogens are still contaminating our oceans. Now, they’re dumped in further upstream. Entire watersheds are now being infected—including the oceans. The body count among people, livestock and wildlife has been stacking up ever since ocean dumping began phasing out. Biosolids and other forms of sewage mismanagement are now fueling a global epidemic of neurological disease, including Alzheimer’s disease, Parkinson’s disease, autism, mad cow disease, chronic wasting disease, microcephaly and more. Industry and governments are scrambling to blame the global epidemic on anything but contaminated soil, water, food and air. They are playing dumb in the face of fraud and scientific suppression. Negligence is too kind of a word for these public servants.

biosolids land application and disease

Sewage also contaminates our food with listeria, e-coli, salmonella and other killers. In fact, scientists are scrambling to come up with new names for the growing list of sewage-related ailments, including Zika virus, West Nile virus, epizoic hemorrhagic fever, equine herpes, valley fever and others. Industrial disease is a more accurate label.

Crops contaminated by sewage sludge can uptake prions and deliver them throughout the plant. Plants then deliver the deadly prions to mammals that consume the plant. In fact, infected plants are spreading prion diseases to several species. When hamsters consumed infected wheat grass, the animals were infected with prion disease. Researchers also found deadly prions in plants exposed to infected urine and feces. The concept of a species barrier is a myth. A deadly prion is a deadly prion. They don’t discriminate among victims.

“These findings demonstrate that plants can efficiently bind infectious prions and act as carriers of infectivity, suggesting a possible role of environmental prion contamination in the horizontal transmission of the disease,” said Claudio Soto, the lead investigator from the University of Texas at Houston.

Killer prions are impossible to stop. Prions are contributing to the death of millions of people now. Victims produce and spread prions daily because they’re in the bodily fluids of all victims. Millions of people with brain disease are contaminating their homes and communities, while exposing caregivers and family members to the contagion. The sewage from these victims is contaminating the local wastewater treatment plant and everything that enters or leaves these facilities, including reclaimed wastewater and sewage sludge. Once dumped on open land, these contagions remain infectious as they migrate, mutate and multiply forever.

biosolids land application LASS

Prions demand more respect than radiation. They require containment and isolation, not distribution and consumption through air, food and water. These toxins demand lined landfills not reckless dumping on our dinner tables. Prions migrate, mutate and multiply, so dilution is not a solution. Prions are a nightmare.

The world has never done an effective job of managing its sewage. It’s an industry that drives by looking in the rear view mirror. It only swerves when the road is buried in body bags. After enough people get sick and die, new alternatives emerge. Today is no different. The bodies are stacking up. The prion contamination grows stronger and spreads further every day. It’s time to stop dumping sewage sludge on land because of the prion risk and many others that are not accounted for in the antiquated and fraudulent risk assessments. It’s time for citizens to defend our land, water and air–not just our guns.

chronic wasting disease caused by prions

Today, the land application of sewage sludge is killing mammals and more around the world. Pathogens in sludge are causing brain disease, cancer and death. Let’s take a meaningful stand for food safety. Just say no to biosolids in our watersheds and food supplies.

Take a free preview of our new eBook to learn everything that you need to know about the epidemic and the mismanagement. The rest of the book explains how to defend yourself with aversion and targeted nutrition. Please join our campaign for truth and reform.

For More Information About Food Safety and Water Quality, please visit http://crossbowcommunications.com/land-application-of-sewage-sludge-spreading-brain-disease/

public relations firm and public affairs firm Denver and Phoenix

Crossbow Communications specializes in issue management and public affairs. Alzheimer’s disease, Creutzfeldt-Jakob disease and the prion disease epidemic is one of our special areas of practice. Please contact Gary Chandler to join our coalition for reform gary@crossbow1.com. Stop prion disease.

U.S. EPA Spending Billions On Lawyers, Guns, Ammo

Whose Profits Are They Protecting With Weapons?

By Stephen Moore, Heritage Foundation

The Environmental Protection Agency spent millions of dollars over the last decade on guns, ammo, body armor, camouflage equipment, unmanned aircraft, amphibious assault ships, radar and night-vision gear and other military-style weaponry and surveillance activities, according to a new report by the watchdog group Open the Books.

The report raises questions about why EPA’s enforcement division employs well-armed “special agents” who appear to be conducting SWAT-type operations on American businesses and households it suspects of wrongdoing.

biosolids land application and disease

Illinois-based Open the Books scanned tens of thousands of checks written by the EPA and totaling more than $93 billion from 2000 to 2014.

The audit discovered hundreds of millions of dollars of questionable expenses, including high-end luxury furnishings, sports equipment and “environmental justice” grants to raise awareness of global warming.

It also revealed that seven of 10 EPA workers make more than $100,000 a year and that more than 12,000 of its nearly 16,000 employees were given bonuses last year despite agency budgets that were supposed to be constrained by budget caps and sequester cuts.

EPA’s $8 billion budget also found room for more than 1,000 attorneys, which would make the agency one of the largest law firms in the nation.

And more than $50 million of EPA funds since 2000 went to international organizations — dollars that flowed to countries such as China and Mexico. These activities appear to have little or no connection to the EPA mandate of safeguarding the air and water here in the U.S.

guns and ammunition bought by EPA

But the eye-grabber in the report is the agency’s ongoing military-type purchases. Some $75 million is authorized each year for criminal enforcement, including money for a small militia of 200 “special agents” that appear to be snooping on industry and preparing to use deadly force to enforce EPA edicts.

“We were shocked ourselves to find these kind of pervasive expenditures at an agency that is supposed to be involved in clean air and clean water,” said Open the Books’ founder, Adam Andrzejewski. “Some of these weapons are for full-scale military operations.”

Those who keep an eye on the agency have also been stunned by such outlays. “EPA has always been primarily an agency that is involved in analysis and regulation. Even its enforcement arm is mainly involved in litigation,” notes Marlo Lewis, who covers environmental issues for the Competitive Enterprise Institute.

“Since when did we start going down this road of allowing agencies of government to engage in military-style operations?”

In 2013, the EPA was involved in what many residents called an armed raid at a small town in Alaska where local miners were accused of polluting local waters. Fox News reported that EPA “armed agents in full body armor participated.”

The Justice Department has reported that there are now 40 federal agencies with more than 100,000 officers authorized to carry guns and make arrests. They include the Fish and Wildlife Service, the Bureau of Land Management, the National Oceanic and Atmospheric Administration and the Park Service.

EPA has numerous joint projects with the Homeland Security Department. In 1988 the agency’s criminal enforcement division was granted police powers.

The EPA website describes the activities and mission of the criminal enforcement division as “investigating cases, collecting evidence, conducting forensic analyses and providing legal guidance to assist in the prosecution of criminal conduct that threatens people’s health and the environment.” But nothing about the use of lethal force.

Asked for comment on the Open the Books findings, EPA said purchases of armaments are necessary for “environmental crime-fighting. For more than 30 years there has been broad, bipartisan agreement about the importance of an armed, fully-equipped team of EPA agents working with state and federal partners to uphold the law, protect Americans and access potential crime scenes as quickly as possible.”

One former EPA administrator with more than 30 years at the agency says of the Open the Books report: “EPA has been increasingly captured by the environmental left, and the purchases of military-style armaments has increased accordingly.”

The new report comes at a time when the EPA is under fire over a new regulation approved last week by the agency to tighten ozone emission rules. The National Association of Manufacturers calls it one of the most expensive EPA rules ever.

There’s also a fight in Washington over whether federal agencies can withstand another sequester spending reduction without jeopardizing vital services. The White House says further agency cuts would be disastrous.

But reports such as the latest by Open the Books are sure to be promoted by Republicans as evidence of rampant waste and misspending.

Read More At Investor’s Business Daily: http://news.investors.com/ibd-editorials-perspective/100815-774747-stephen-moore-does-epa-need-guns-ammo-to-protect-environment.htm#ixzz3pDKMEqgL

Chronic Wasting Disease Spreads To Ohio

Brain Disease Spreading Through Sewage Sludge

The first case of chronic wasting disease in Ohio was confirmed Thursday from a single buck on a deer farm in Holmes County.

Erica Hawkins, spokeswoman for the Ohio Department of Agriculture, said the deer was found at World Class Whitetails in Millersburg. The deer farm has been under quarantine since April 24 because it acquired deer from an operation in Pennsylvania that tested positive for CWD this year.

chronic wasting disease caused by prions

The farm was one of 43 captive-deer operations since April to be placed under quarantine for receiving about 125 deer from places in Pennsylvania that had the disease. More than 20 of the quarantines have since been lifted because the Ohio deer farm owners killed the deer in question and chronic wasting disease was not found. There is no way to test a live deer for the disease.

Farms under quarantine are not allowed to sell live animals or purchase any new ones — although deer can still breed, Hawkins said. The quarantine also does not prohibit the farms from allowing controlled hunts for the deer. All deer who die, whether from hunting or natural causes, are tested for the disease. Hawkins said since the quarantines have been in place, 770 deer have been tested from the captive operations and this case was the first one to test positive for the disease.

The state banned all deer imports from Pennsylvania, but that was largely lifted earlier this year. Now the state only bans importing deer from a five-county area in Pennsylvania where chronic wasting disease has been found.

Chronic wasting disease is among a family of diseases known as transmissible spongiform encephalopathies, which includes mad cow disease. The diseases are caused by “misfolded” rogue proteins called prions. Prions cause normal protein molecules to mimic their twisted, misshapen form, creating spongelike holes in the brain, a process that can take years. The diseases are always fatal. The human strains of prion diseases cause severe dementia and brain deterioration ending in death. When deer develop symptoms from CWD, they become disoriented and emaciated, literally wasting away.

land application sewage sludge

Scientists suspect the primary way the disease is spread is nose-to-nose contact (actually, the largest prion pathway in the world is sewage sludge, also known as biosolids). The prions, which can be passed on in bodily fluids (from humans and other mammals), are so hardy that they also can bind to soil and remain infectious for years, researchers say. It’s believed that deer can contract the disease by feeding in contaminated areas and possibly by inhaling prions in dust. No human has ever been known to have been infected by the disease.

The disease has now been found in deer farms in 14 states, according to the Chronic Wasting Disease Alliance. Critics of deer farms have said they are a perfect breeding ground for disease. Officials from the farm where the disease was found and theWhitetail Deer Farmers of Ohio could not be reached for comment Thursday afternoon.

It has also been found in wildlife in 18 states, according to the Michigan Department of Natural Resources, but Hawkins said she is “absolutely” confident the state has contained the disease.

prion disease epidemic

House Bill 389 in 2012 transferred much of the regulatory power over deer farms from the Ohio Department of Natural Resources to the Department of Agriculture. Hawkins said the law’s new licensing and record-keeping requirements allowed the state to contain a possible outbreak of the disease much quicker.

Scott Zody, chief of the state division of wildlife, said there is no reason to believe the chronic wasting disease has transferred to the state’s wild deer population.

“With hunting season in progress, there are no CWD concerns that should prevent anyone from enjoying wild deer hunting in Ohio or from consuming meat from healthy animals,” Zody said in a statement.

Source: http://www.bucyrustelegraphforum.com/story/sports/outdoors/2014/10/23/chronic-wasting-disease-found-ohio-deer-farm/17786995/

public relations firm and public affairs firm Denver and Phoenix

Crossbow Communications specializes in issue management and public affairs. Alzheimer’s disease, Creutzfeldt-Jakob disease, chronic wasting disease and the prion disease epidemic is an area special expertise. Please contact Gary Chandler to join our coalition for reform gary@crossbow1.com. Only the truth about biosolids and infectious sewage sludge can stop chronic wasting disease.

Sewage Sludge, Reclaimed Wastewater Spreading Alzheimer’s Disease

Biosolids, Reclaimed Wastewater Spreading Deadly Disease

A new study confirms that people and animals dying of prion disease are contaminating the environment around them with a deadly and unstoppable protein found in their bodily fluids, including their urine and feces. Wastewater treatment plants can’t neutralize the deadly form of protein known as a prion.

Claudio Soto, PhD, professor of neurology and director of the George and Cynthia W. Mitchell Center for Alzheimer’s Disease and Other Brain Related Illnesses at the University of Texas Medical School in Houston, and his colleagues recently found deadly and infectious prions in urine. The study has been published in the August 7 issue of the New England Journal of Medicine. Unfortunately, other researchers have found prions in all bodily fluids of victims, which is extremely bad news for caregivers, family members and others in the community who are caught in the crossfire.

Alzheimer's disease epidemic

The good news is that the research offers hope for earlier diagnosis among the millions of people impacted around the world. The discovery can promote earlier intervention and better disease management. It also can help develop screens to protect our blood supplies from donors with prion disease.

The bad news is that prions in urine and feces underscore the environmental nightmare associated with Alzheimer’s disease, Creutzfeldt-Jakob (CJD), Parkinson’s, Huntington’s and prion diseases among livestock and wildlife. Although there are many causes for prion disease, many people and animals are contracting it from environmental exposure (food, water and soil) and then contaminating the environment even more with their own bodily fluids. Once victims die, carcasses also contaminate soil and water.

Alzheimer's disease prevention

“This is the first time that prions have been detected in human urine,” Dr. Soto told Neurology Today.

Soto failed to reference urine and blood studies performed earlier by Ruth Gabizon in 2001 and Reichl in 2002. These studies also detected prions in bodily fluids. Despite that detail, Soto’s findings can help focus global attention on the exploding prion problem.

Dr. Stanley Prusiner earned a Nobel Prize in 1997 for identifying, naming and studying deadly prions. President Obama awarded Prusiner the National Medal of Science in 2010 to recognize the importance of his research.

prion disease epidemic

In June 2012, Prusiner confirmed that Alzheimer’s, Parkinson’s, Huntington’s and even ALS are prion diseases similar, if not identical, to CJD in people, mad cow disease in livestock and chronic wasting disease in wildlife. The variations in disease progression could be due to genetics in the patients or mutations in the prion, not different diseases entirely.

Additional research has determined that the prion pathogen spreads through feces, saliva, blood, milk, soil, water and the tissue of infected animals and humans. If a single person with prion disease discharges bodily fluids or feces into a public sewer system, that sewage system is permanently infected and the amount of contamination will multiply and intensify daily. Everything discharged from that sewage system—reclaimed water and biosolids—can spread the contamination even further.

Once a prion reaches the soil, that soil is permanently contaminated and the entire watershed below that point is at risk forever. If your food and water is generated in that watershed, you have a higher risk of contracting prion disease.

“There has been a resurgence of this sort of thinking, because there is now real evidence of the potential transmissibility of Alzheimer’s,” says Thomas Wiesniewski M.D. a prion and Alzheimer’s researcher at New York University School of Medicine. 

land application sewage sludge

With the help of weather, prions can migrate through wind and water. Rain and snow can rinse them into surface water, groundwater, streams, ponds, lakes, and oceans. Wildlife, livestock and humans can ingest prions from soil, water and food. We can’t afford to take the risk of further contaminating entire watersheds – increasing the pathway to humans, livestock, and wildlife downstream.

Because of these factors and others, we have an epidemic of prion disease around the world right now. The epidemic is worse in some regions of the world than others. For example, the death rate for Alzheimer’s disease is higher in Finland than any other country in the world. Iceland and the United States are runners up. In fact, the death rate for Alzheimer’s is higher in Washington state than any other known region in the world. Norway has the highest death rate from Creutzfeldt-Jakob disease (CJD). These vast discrepancies can only be explained by environmental factors, including food, water and air pathways. Sewage disposal that contaminates local food and water supplies is likely part of the problem.

The scientific name for prion disease is Transmissible Spongiform Encephalopathy (TSE). The operative word is “transmissible.” TSEs include Alzheimer’s disease, mad cow, CJD, chronic wasting, Huntington’s, scrapie and possibly Parkinson’s. This transmissible family of disease is unstoppable for many reasons. In addition, once items are exposed to victims of prion disease, they can never be sterilized again.

Prion News via http://crossbowcommunications.com/sewage-mismanagement-contributing-to-global-alzheimers-epidemic/

public relations firm and public affairs firm Denver and Phoenix

Crossbow Communications specializes in issue management and public affairs. Alzheimer’s disease, Creutzfeldt-Jakob disease, chronic wasting disease and the prion disease epidemic is an area special expertise. Please contact Gary Chandler to join our coalition for reform gary@crossbow1.com.

Chronic Wasting Disease Related To Alzheimer’s Disease

CWD Spread Through Sewage Sludge

A Colorado company says that hunters, landowners and many others are being misinformed about the dangers of chronic wasting disease. As such, public health and the health of entire water sheds are at risk.

Chronic wasting disease (CWD) is another form of prion disease. Prions also are behind the explosion in Alzheimer’s disease, Parkinson’s disease and Creutzfeldt-Jakob disease (CJD). We also know prions because they are the causative agent behind mad cow disease. The scientific name for this family of neurodegenerative disorders is Transmissible Spongiform Encephalopathy (TSE). The operative word is “transmissible.”

“There is now real evidence of the potential transmissibility of Alzheimer’s,” says Thomas Wiesniewski M.D. a prion and Alzheimer’s researcher at New York University School of Medicine. “In fact, this ability to transmit an abnormal conformation is probably a universal property of amyloid-forming proteins.”

prion disease epidemic

Dr. Stanley Prusiner, an American neuroscientist from the University of California at San Francisco, earned a Nobel Prize in 1997 for discovering and characterizing deadly prions and prion disease. President Obama awarded Prusiner the National Medal of Science in 2010 to recognize the importance of his research. According to Prusiner, TSEs all are on the same disease spectrum, which is more accurately described as prion (PREE-on) disease. He claims that all TSEs are caused by prions.

Prions are unstoppable and the pathogen spreads through the bodily fluids and cell tissue of its victims. Prions shed from humans are the most deadly mutation. They demand more respect than radiation. Infected surgical instruments, for example, are impossible to sterilize and hospitals throw them away. Prions are in the blood, saliva, urine, feces, mucus, and bodily tissue of its victims. Many factors are contributing to the epidemic. Prions are now the X factor. Industry and government are not accounting for them or regulating them. They are ignoring the threat completely, which violates the Bioterrorism Preparedness and Response Act of 2002 in the United States. Other nations also are ignoring laws developed to protect food, air and water.

“The species barrier between these diseases is a myth,” said Gary Chandler, president of Crossbow Communications. “Prion disease is an environmental disease. It spreads in many ways and to stop it we need to reform many policies around the world.”

Although CWD spreads through many vectors, the greatest pathway is sewage sludge, also known as biosolids. The U.S. alone dumps more than 700 millions tons of this infectious waste on land–farms, ranches, forests, golf courses, parks and school grounds. Once unleashed on the environment, prions remain infectious. They migrate, mutate and multiply as they infect crops, water supplies and more.

Unfortunately, prions linger in the environment, homes, hospitals, nursing homes, dental offices and beyond infinitely. Prions defy all attempts at sterilization and inactivation. If they can’t stop prions in the friendly and sterile confines of an operating room, they can’t stop them in the wastewater treatment plant.

Deer, elk, moose and reindeer are now contracting prion disease from humans. To help cloak the epidemic, it’s called chronic wasting disease (CWD). Deer with CWD are proverbial canaries in a coal mine. They are being killed by government sharpshooters to help cover up the problem. It’s insane.

Chandler says that sewage disposal practices are contributing the the outbreak among wildlife. He says the same threat is viable for livestock. The practice of spreading sewage sludge (biosolids) on cropland and pastures makes prions available to grazing animals. It also puts prions in a position to contaminate water supplies when irrigation and rain rinse the biosolids into groundwater and surface water runoff. This water runs into creeks, ponds, streams, lakes, rivers, oceans and our drinking water. 

biosolids land application and disease

Reused wastewater for drinking is reckless. Prions are in the bodily fluids of its victims. Sewage plants can’t detect or stop prions.

The risk assessments prepared by the U.S. EPA for wastewater treatment and sewage sludge are flawed and current practices of recycling this infectious waste is fueling a public health disaster. Many risks are not addressed, including prions and radioactive waste. They don’t mention prions or radiation because there is no answer. Most nations are making the same mistake. We’re dumping killer proteins on crops, parks, golf courses, gardens, ski areas, school grounds and beyond. Wind, rain and irrigation spread these contaminants and many more throughout our communities and watersheds.

Failure to account for known risks is negligent. Crops for humans and livestock grown grown in sewage sludge absorb prions and become infectious. We’re all vulnerable to Alzheimer’s and other forms of prion disease right now due to widespread denial and mismanagement. It’s time to stop the land application of sewage sludge (LASS) in all nations. Safer alternatives exist.

Just ask the US EPA. Therefore, putting biosolids and recycling wastewater is more dangerous than injecting radiation into our watersheds. Radiation at least has a half life. With prions, it’s a question of how fast they double and triple their numbers. It’s safe to say that every sewage system in the world has been used by a person, if not millions, of people with Alzheimer’s and Creutzfeldt-Jakob disease.

land application sewage sludge

Approximately 50 million people around the world already have Alzheimer’s disease and other forms of dementia. The threat is so severe that health officials expect the numbers of people living with the disease to triple soon. Unfortunately, neurodegenerative diseases among people of all ages are rising around the world. As these numbers rise, our sewage disposal will become more critical than ever because the further it spreads, the faster it will spread.

chronic wasting disease caused by prions

Prions are associated with an entire family of neurological disorders that are killing people, wildlife and livestock around the world. These deadly diseases are known as Transmissible Spongiform Encephalopathy (TSE). The operative word is “transmissible.” TSEs include Alzheimer’s disease, Creutzfeldt-Jakob disease, Parkinson’s disease, Huntington’s disease, scrapie, chronic wasting disease and mad cow disease. The disease has killed many species of mammals including dolphins. Victims permanently contaminate the world around them with their bodily fluids. Once contaminated with prions, items cannot be sterilized.

For more information, contact the experts at Crossbow. http://crossbowcommunications.com/public-affairs-firm-phoenix/

public relations firm and public affairs firm Denver and Phoenix

Crossbow Communications specializes in issue management and public affairs. It’s also promoting forest conservation, reforestation, sustainable agriculture, and wildlife conservation through its subsidiary–Sacred Seedlings. Please contact Gary Chandler at gary@crossbow1.com to join our network.

Chronic Wasting Disease Fueled By Sewage Sludge

Brain Diseases Linked By Prions

By Martha Rosenberg

It’s been over ten years since Wisconsin endured a kind of deer holocaust. The terminal deer and elk disease, chronic wasting disease (CWD), descended upon its deer population with such vengeance officials declared CWD eradication zones in which fauns and does would be killed before bucks.

Thousands of deer carcasses were stored in refrigerated trucks in La Crosse while their severed heads were tested for CWD. If the carcasses were disease-free they were safe to eat (really?); if not, they were too dangerous to even put in a landfill. Why? Because “prions” (which also cause mad cow disease, scrapie in sheep, Creutzfeldt-Jakob and Alzheimer’s disease in humans) are not inactivated by cooking, heat, autoclaves, ammonia, bleach, hydrogen peroxide, alcohol, phenol, lye, formaldehyde, or radiation. They remain in the soil indefinitely. (They contaminate everything indefinitely.)

prion disease epidemic

Hunters in Wisconsin and other states were warned to wear surgical gloves when cutting up deer and to avoid exposing open cuts or sores on their hands. One hunter wrote the local paper after his buck tested positive for CWD — he was worried about the blood on his steering wheel and hunting clothes, which his wife handled.

There were also cross-contamination risks since deer processors do not usually sterilize their equipment after each deer. Food pantries in Wisconsin and their customers were warned about the risks and it became difficult to donate. (“If this meat is so safe why don’t you eat it?” the pantry patrons may have been thinking.)

land application sewage sludge

Department of Natural Resources (DNR) officials in Wisconsin and other states assured the public that deer meat was safe, even if it harbored CWD, as long as they avoided eating a deer’s brain, eyeballs, spinal cord, spleen and lymph nodes–the parts also implicated in mad cow disease. But scientific articles suggested most of the animal contained prions including its kidneys, pancreas, liver, muscle, blood, fat and saliva, antler velvet and birthing material.

Another reason to doubt DNR officials’ reassurances, calculated to keep their funding from hunting licenses flowing, is a 2002 Morbidity and Mortality Weekly Report from the CDC titled Fatal Degenerative Neurologic Illnesses in Men Who Participated in Wild Game Feasts —Wisconsin, 2002.

Many animal lovers have noted the hypocrisy of states citing deer “overpopulation” when they encourage deer breeding farms. What? Recently a four-part expose in the Indiana Star explores how “the pursuit of deer bred for enormous antlers and shot in hunting pens” on trophy farms is spreading CWD at an alarming rate. Deer breeding and “trophy farms” are a $4 billion a year industry and hotbeds of CWD thanks to their concentration of animals, “communicability window” (from trophy stock trading and escaped animals) and its unknown feed sources.

biosolids land application and disease

 

Like mad cow disease, widely believed to stem from the cost-cutting practice of feeding cows to cows, chronic wasting disease may also have man-made origins. In the mid-1960s, the Department of Wildlife ran a series of nutritional studies on wild deer and elk at the Foothills Wildlife Research Facility in Fort Collins, Colorado and soon after the studies began, however, Foothills deer and elk began dying from a mysterious disease. The CWD in the deer may have been caused by sheep held at the same facility which had scrapie, say researchers. (There are a few theories about the way that the disease arrived at CSU and spread outward from there. They all involve mismanagement of a biohazard that they completely underestimated.)

Since 2002, Wisconsin’s CWD eradication efforts have failed abysmally. The penned herd of 76 deer at Stan Hall farm has gone from one animal with CWD to 60 in five years writes outdoor reporter Patrick Durkin and in some areas, half of all deer now have the disease. “The world’s most ‘disturbing,’ ‘frightening’ and ‘unprecedented’ CWD case is growing next door to our capital and flagship university, and our government won’t crack a window to sniff it,” he writes.

chronic wasting disease caused by prions

Clearly using wildlife, which is held in trust by the state for the benefit of the public per the”Public Trust Doctrine”, to profiteer from hunters is unethical and harmful to animals. And despite DNR officials’ assurance, the spread of CWD may prove harmful to humans too.

Martha Rosenberg is an award-winning investigative pubic health reporter who covers the food, drug and gun industries. Her first book, Born With A Junk Food Deficiency: How Flaks, Quacks and Hacks Pimp The Public Health

Prions are associated with an entire family of neurological disorders that are killing people, wildlife and livestock around the world. These deadly diseases are known as Transmissible Spongiform Encephalopathy (TSE). The operative word is “transmissible.” TSEs include Alzheimer’s disease, Creutzfeldt-Jakob disease, Parkinson’s disease, Huntington’s disease, scrapie, chronic wasting disease and mad cow disease. The disease has killed many species of mammals including dolphins. Victims permanently contaminate the world around them with their bodily fluids. Once contaminated with prions, items cannot be sterilized.

Source: http://www.opednews.com/articles/Mad-Cow-like-Disease-Growi-by-Martha-Rosenberg-Cows_Deer_Disease_Disease-Virus-Epidemics-140601-640.html

public relations firm and public affairs firm Denver and Phoenix

Crossbow Communications specializes in issue management and public affairs. Alzheimer’s disease, Creutzfeldt-Jakob disease, chronic wasting disease and the prion disease epidemic is an area of special expertise. Please contact Gary Chandler to join our coalition for reform gary@crossbow1.com.

Four People Hit By Deadly Prion Disease Near Vancouver

CJD Cluster In Canada

Editor’s Note: As the following news story indicates, deadly prion disease (known as Creutzfeldt-Jakobs disease in people, mad cow disease in cattle, and chronic wasting disease in deer, elk and moose) has struck four people simultaneously in British Columbia. Based on government risk models, such an event is impossible.

The facts and stories are changing rapidly as one might have predicted. All four people apparently lived in the Fraser valley east of Vancouver. Additional cases of prion disease have been investigated over the past few months in the same area, but explained away with typical anti-flac rhetoric.

In the most recent cases, Canadian authorities again are exhibiting their immediate bias to protect the food industries more than the millions of consumers. Unfortunately, these victims could have all been exposed to prions in many ways, but for the government to make such bold, blind statements that it isn’t beef and it isn’t food is again reckless. All pathways should be pursued and all forms of prion mismanagement must stop.

land application sewage sludge

For example, these four unlucky souls could have been exposed by drinking water, dental instruments, blood transfusions, eating utensils, workplace exposures, gel caps, growth hormones, collagen in lotions and cosmetics and the list goes on. But they could have been exposed by beef or dairy products. They could have been exposed via infected venison. Do they live near parks and pastures where biosolids from the sewage plant are applied?

In other words, government and industry alike have opened the doors on prion exposure to pathways way beyond beef and dairy products. This pattern either suggests incompetence, negligence or criminality. All answers are unacceptable.

As further proof of the mismanagement of prions, let’s ask what precautions have gone out to the families of these victims. Have they been advised that their homes are hopelessly contaminated with deadly prions? Eating utensils, cups, glasses, tooth brushes, sheets, pillow cases, toilets and more? 

sewage treatment plant and disease

You see, deadly prions are released from the bodies of infected people and animals via their blood, saliva, urine and feces. People are infectious way before they start stuttering and stumbling. If you follow this logic, the local sewer system that serves the homes and hospitals of these victims has now been exposed to deadly prions (if they weren’t already). Now, we know that everything discharged from this local sewer system(s) is contaminated and will hopelessly and permanently contaminate the parks and cropland where the sewage sludge (biosolids) is spread as “fertilizer.”

The next time that it rains or the irrigation system is turned on, prions are washed from the sludge and into the groundwater and surface water. The prions migrate into streams,  ponds, rivers, lakes and oceans where they proceed to multiply (prions migrate, mutate and multiply. They kill everything in their path). 

Prions and Prusiner win Nobel Prize

Dr. Stanley Prusiner earned a Nobel Prize in 1997 for identifying, naming and studying deadly prions. President Obama awarded Prusiner the National Medal of Science in 2010 to recognize the growing significance of his discovery. In June 2012, Prusiner confirmed that Alzheimer’s disease is a prion disease like CJD and mad cow. In other words, every person with Alzheimer’s (and the rates are soaring) are contributing to this environmental contamination.

Furthermore, this is not the first apparent cluster to emerge of prion disease. Close to 20 people have died in one county in North Carolina in just the past few months. In Washington state, two former workers at a hospital came down with prion disease within days of each other and both passed away within weeks. Plus, Washington state leads the United States in rates of death from Alzheimer’s disease (almost double the national average). Ironically, Washington state and British Columbia share a border and the Fraser valley is not that far from the state line. Marin County California had a handful of cases near the same time. I’m sure there are others that deserve mentioning, but you get the point. Environmental factors are playing a role in the spread of prion disease in people, wildlife and livestock. (Prion disease is ravaging deer populations in places such as Wisconsin, Wyoming, Colorado and parts of Canada).

So, with the floodgates wide open on prion pathways, maybe that’s why the government is so confident that food is not the source of exposure.By this afternoon, the official story will likely indicate that these people just had the flu.

CJD Cluster Hits Near Vancouver

blood

One of the largest outbreaks of human Mad Cow disease in decades has struck four people simultaneously near Vancouver, Canada. One person has already died and three others are in hospital with possible cases of Creutzfeldt-Jakob disease east of Vancouver, the Fraser Health authority has confirmed.

Creutzfeldt-Jakob disease is the human variant of bovine spongiform encephalopathy, or BSE, commonly called mad cow disease. But officials say they don’t believe these suspected cases are associated with eating beef, and say there is no risk associated with eating beef from the region.

B.C.’s Provincial Health Officer Dr. Perry Kendall said the cases were diagnosed by neurologists on Friday, but none have been confirmed because complete diagnosis can only be made on death.

“Every indication is that if it is Creutzfeldt-Jakob disease it would be the classic sporadic kind for which there is really no cause known,” said Kendall

He said B.C. gets between five and six cases reported a year, but what makes this situation unusual is to have so many cases reported at once.

Kendall said a beef-related outbreak in the U.K. between 1980 and 1996 caused about 250 cases of the human variant, but said he does not think it is related to beef in the B.C. cases.

“I would not worry about this being the beef-associated variant.”

Only two such cases have been reported in Canada — one in 2003 and one in 2011. Both cases are believed to have been contracted in the UK.

The Canadian Food Inspection Agency runs a surveillance program which Kendall says has ensured that no suspect beef has made its way into the food supply.

“This is not going to be a food-borne cluster of cases.” (because they can’t afford for that to be the cause).

Source: http://www.cbc.ca/news/canada/british-columbia/story/2013/06/14/bc-creutzfeldt-jakob-disease-fraser-valley.html?cmp=rss

Chronic Wasting Disease Ravaging Wisconsin Deer

Prion Disease Threatens Wisconsin Livestock

Editors Note: A deadly prion is a deadly prion. Hiding behind ignorance and special interests is doing no one any good. Prion disease is always fatal. There is not a cure. Prions migrate, mutate and multiply. Sick animals (including livestock and people) that have prion disease contaminate their environment with prions that are discharged via blood, urine, feces, saliva, and milk. These prions enter the soil and are carried into groundwater, surface water, streams, rivers, ponds and lakes. 

When people have prion disease, their bodily discharges contaminate entire sewer systems–forever. When biosolids and reclaimed sewage water are discharged from the sewage plant, that sludge is then applied to cropland across Wisconsin and the nation. In fact, few counties in Wisconsin have not been subjected to sewage disposal on cropland. Are prions in sewage sludge infecting the deer? If so, what’s to keep the prions from migrating and infecting Wisconsin’s multi-billion dollar dairy herd? The species barrier is a myth. Prion disease is prion disease and a deadly prion is a deadly prion. Don’t buy the spin about “no evidence of” or “species barrier will protect you.” That is pure BS to sell you a bill of goods that covers a lot of asses. 

land application sewage sludge

Further more, asking hunters to kill sick deer, dress it and process it without fear is reckless. As the following article illustrates, hunters are dressing and processing thousands of carcasses riddled with prions every year. In those cases, infected blood and tissue will permanently contaminate the hunter’s knives and saws and clothes and processing plants and beyond. If I dare cut through the spinal chord to remove the head for testing, my chances of prion exposure escalate. If the test comes back positive, I will throw out the remaining packs of deer burger. I should throw out my knife and burn my clothes. Unfortunately, those items have already been in my home and garage. Why isn’t the Fish & Game and Divisions of Wildlife giving hunters better safeguards? With mismanagement like this, eradicating deadly prion disease from deer herds and entire ecosystems is a pipe dream–or make that a nightmare. If you live in Wisconsin or any state impacted by chronic wasting disease, challenge them to hire me as a consultant on this life-and-death issue.

CWD A Lost Battle

The rate of chronic wasting disease (CWD) is on the rise among deer in Iowa County, Wisconsin and elsewhere across the state. CWD is a fatal, transmissible spongiform encephalopathy (TSE) similar to what is commonly known as mad cow disease that is caused by twisted proteins, or prions. For hunters, writes outdoors reporter Patrick Durkin, this means the disease might be affecting the herd now. For anyone who eats venison, this means greater chances that the disease could conceivably make the species jump and infect humans, according to Dave Clausen, a veterinarian whose term on Wisconsin’s Natural Resources Board expired in May.

chronic wasting disease caused by prions

About one out of every three male deer aged 2.5 years and older carries CWD in north-central Iowa County, as does one out of every six yearling male deer (1.5 years old), according to the Wisconsin State Journal, and the rates are climbing at about ten percent a year. As several experts told Durkin, the increasing rates are “unprecedented,” “frightening,” and “disturbing.”

Over 633,000 hunters purchased licenses to hunt white-tailed deer in Wisconsin in 2012, according to the Department of Natural Resources (DNR). The primary deer hunting season (for guns) runs for nine days in late November. An exact number of Wisconsinites who eat hunted venison is not known, although media reports indicate it is large. But testing of these deer for CWD is on the decline, even as infection rates rise. In 2002, over 40,000 deer were tested in Wisconsin, and .51 percent tested positive. In 2012, 6,611 deer were tested, and 5.13 percent tested positive.

As then-Natural Resources Board member Clausen wrote in a white paper on CWD and human health in 2012, the “ever-increasing number of CWD infected deer on the landscape . . . and the accompanying exponential increase of environmental contamination with CWD prion will result in increased inter-species, including human, exposure to the CWD prion. Under our current management strategy, human exposure will increase.”

prion disease epidemic

Less Testing, More People Eating Infected Venison In Wisconsin

One of the reasons why it is possible for CWD to make the species jump to humans is because of insufficient warnings to hunters by the DNR, Clausen says. The DNR website says there is “no strong evidence” that CWD can be passed to humans, but warns hunters to “minimize contact with the brain, spinal cord, spleen and lymph nodes” when processing deer.

But in 2010, the World Health Organization (WHO) changed its definition of infective tissue to include skeletal muscles from CWD-infected deer and elk. And a 2012 Centers for Disease Control and Prevention (CDC) study notes, “CWD prions are present nearly ubiquitously throughout diseased hosts, including in muscle, fat, various glands and organs, antler velvet, and peripheral and CNS [central nervous system] tissue.” It concludes that the potential for human exposure to CWD from handling or eating material from infected deer “is substantial and increases with increased disease prevalence.” Both the WHO and the CDC recommend that people avoid eating meat from CWD-infected deer or elk.

Unlike the WHO and CDC, Clausen said the Wisconsin Department of Health and Safety (DHS) will not publicly recommend against eating infected venison until there is hard evidence that someone has gotten Creutzfeldt-Jakob Disease (CJD, the human TSE) from eating infected venison. But he believes that the government should be operating on the precautionary principle — that “if something is plausible, that we should be erring on the side of caution unless we have absolute hard evidence that it’s not possible.”

chronic wasting disease and moose

But, Clausen adds, the “precautionary principle is bad for business.” If people become so concerned about contracting CWD that they stop hunting, it means a potential decrease in DNR revenue; and the federal government has stopped funding CWD testing and research in the last year or two. UW-Madison Professor Michael Samuel has seen federal research funds for studying “disturbing” new trends in CWD dry up. “There’s little interest in CWD these days, Wisconsin and nationwide,” he told Durkin.

With testing on the decline, the DNR “has tracked hundreds of cases” in which people have eaten infected venison and “knows that there are many more,” according to the Wisconsin Center for Investigative Journalism. As the rates of the disease rise — as the CDC notes — “the potential for human exposure to CWD by handling and consumption of infectious cervid material increases.”

Source: http://www.prwatch.org/news/2013/06/12144/chronic-wasting-disease-rise-wisconsin-deer-will-it-infect-humans

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Crossbow Communications specializes in issue management and public affairs. Alzheimer’s disease, Creutzfeldt-Jakob disease, chronic wasting disease and the prion disease epidemic is an area of special expertise. Please contact Gary Chandler to join our coalition for reform gary@crossbow1.com.