Neurodegenerative disease is the fastest-growing cause of death in the world. The global spike in autism—a neurodevelopmental disease—began to surge at the same time in the wake of suppression, denial and deception. This global epidemic could have been prevented and it can be corrected.
An unstoppable neurotoxin is responsible for much, if not all, of the carnage. This neurotoxin is known for migrating, mutating and multiplying. It kills mammals with unparalleled efficiency. There is no cure for prion disease, which is a spectrum disease with few identical cases.
Unfortunately, misinformation and mismanagement by governments and industry are fanning the flames, shading the truth and obstructing reforms that can protect billions of people from Alzheimer’s disease, Parkinson’s disease, Creutzfeldt-Jakob disease and the forms that afflict other mammals, including mad cow disease and chronic wasting disease. It’s a criminal conspiracy at the highest levels.
The suggestion of a reliable species barrier against thousands, if not millions, of mutations is ludicrous. Regardless of the species impacted, prion disease causes memory loss, impaired coordination, abnormal movements and overall wasting of the mind and body. Victims become prion incubators and distributors. So do wastewater treatment plants.
Unfortunately, millions of victims are going undiagnosed, while millions more are misdiagnosed. Millions of other diagnoses have been suppressed. We don’t have accurate statistics to fully track the scope or the trajectory of the epidemic. Answers begin with the truth, which has been buried for years.
Scientists have finally confirmed that Alzheimer’s disease and other forms of neurodegenerative disease are forms of prion disease, which means that they are highly infectious diseases. Caregivers, family members and billions of innocent people are caught in the crossfire of this explosive epidemic.
Alzheimer’s disease alone is taking the lives of 50-100 million people around the world now. Millions will die of the disease this year, while many millions more will be diagnosed, misdiagnosed and undiagnosed. The epidemic is more severe in some countries than others. Supposedly, no one knows the scope of the problem. The evidence swept under the rug and the global misinformation campaign suggest otherwise.
Until recently, few have considered the possibility that Alzheimer’s disease is a transmissible disease. As it turns out, all evidence suggests that it is a prion disease (infectious disease). There is no evidence to the contrary. This denial and misinformation has been fueling a public health crisis around the world for years. It’s gaining momentum.
Prions (PREE-ons) are a deadly and unstoppable form of protein that migrates, mutates, multiplies and kills with unparalleled efficiency. Prions cause fatal neurodegenerative disease in humans and other mammals by converting the cellular version of prion protein into a toxic form that erodes the brain and body. Prion disease often is described as a wasting disease that causes a loss of body mass and brain mass.
A variety of factors can trigger neurodegenerative disease, including genetics, head trauma and neurotoxins. Exposure to infectious prions is a significant part of the equation. For example, spouses of those with Alzheimer’s disease are 600 percent more likely than others to contract the 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. Important reforms to policies to protect public health, however, have been elusive.
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. TSE is a spectrum disease that varies in severity and symptoms. The diagnosis depends on which region of the brain is impacted first and by what prion mutation. Few cases of prion disease are identical in terms of symptoms and pathology.
Millions of people have CJD, which is clearly an aggressive prion disease. CJD has not been declared a reportable disease across most nations. When the presenting symptom is memory loss, the diagnoses flow along the following chart.
According to neuroscientists Dr. Laura Manuelidis, at least 25 percent of Alzheimer’s diagnoses are actually Creutzfeldt-Jakob disease (CJD), which is further up the prion spectrum. 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.
Prusiner’s most recent study confirms that Alzheimer’s disease is a prion disease, which means that millions of people with Alzheimer’s disease (and millions who died ahead of them) are highly infectious. Alzheimer’s disease is currently defined based on the presence of toxic protein aggregations in the brain known as amyloid plaques and tau tangles, accompanied by cognitive decline and dementia.
“I believe this shows beyond a shadow of a doubt that amyloid beta and tau are both prions, and that Alzheimer’s disease is a double-prion disorder in which these two rogue proteins together destroy the brain,” said Stanley Prusiner, MD, the study’s senior author and director of the UCSF Institute for Neurodegenerative Diseases, part of the UCSF Weill Institute for Neurosciences. “The fact that prion levels also appear linked to patient longevity should change how we think about the way forward for developing treatments for the disease. We need a sea change in Alzheimer’s disease research, and that is what this paper does. This paper might catalyze a major change in AD research.”
“Alzheimer’s disease (AD) is the most common neurodegenerative disease in humans and will pose a considerable challenge to healthcare systems in the coming years,” Prusiner said.
But attempts to treat the disease by clearing out these proteins have failed. The new evidence that active prions could be driving the disease – published May 1, 2019 in Science Translational Medicine — could lead researchers to explore new therapies that focus on prions directly. Hopefully, it will lead to many reforms to safeguard public health.
Prions + Pathways = Victims
In humans, the prion spectrum includes Alzheimer’s disease, Parkinson’s disease and CJD–the most aggressive version. The difference between these diseases is very slight and often indistinguishable to neurologists. Prion disease has been found in many mammals, including camels, cats, cattle, deer, dolphins, elephants, elk, mice, mink, moose, reindeer, sheep and others. It has been described as mad cow disease, chronic wasting disease and other terms to help cloak the bigger problem. Prion disease is prion disease. No two cases are identical.
“I learned that scrapie, Creutzfeldt-Jakob disease and kuru had all been shown to be transmissible by injecting extracts of diseased brains into the brains of healthy animals,” Prusiner said.
Prusiner basically repeated the process with brain samples from those who died of Alzheimer’s disease to complete his latest study. As such, the disease was transmitted from one person to another.
“There has been a resurgence of this sort of thinking, because there is now real evidence of the potential transmissibility of Alzheimer’s disease,” says Thomas Wiesniewski M.D. a prion and Alzheimer’s disease researcher at New York University School of Medicine.
A previous study published in the journal Nature adds to the evidence about the transmissibility of Alzheimer’s disease between people. A second study by the same scientist in early 2016 supports the claim.
Unfortunately, the implications are profound because prions are in the bodily fluids and cells of victims—blood, urine, feces, saliva, mucus, skin and more. Victims are walking prion incubators and transmitters who can leave a trail of death behind for friends, family and entire communities.
Prion pathways threaten each and every person on the planet. The greatest prion pathway in the world is human sewage. It’s contaminating food and water supplies with deadly prions now. It’s been going on for years, but it’s worse than ever now.
Claudio Soto, PhD, professor of neurology at the University of Texas Medical School in Houston, and his colleagues confirmed the presence of prions victims. Prions infect the entire body and all bodily fluids of its victims, including blood, mucus and saliva. Caregivers for anyone with neurodegenerative disease beware.
“Our findings open the possibility that some of the sporadic Alzheimer’s disease cases may arise from an infectious process, which occurs with other neurological diseases such as mad cow disease and its human form, Creutzfeldt-Jakob disease,” said Soto. “The underlying mechanism of Alzheimer’s disease is very similar to the prion diseases. It involves a normal protein that becomes misshapen and is able to spread by transforming good proteins to bad ones. The bad proteins accumulate in the brain, forming plaque deposits (and inflammation), which kill neuron cells in Alzheimer’s disease.”
Soto also confirmed that plants uptake prions from the soil and water. The plants become fatally infectious to those who consume them. Even wildlife and sea mammals are contracting brain disease from people because of the dumping of infectious waste on farms, ranches and forests. Humans, wildlife and livestock are vulnerable to prion disease via crops and plants grown on land treated with infectious waste (sewage sludge, biosolids and reclaimed wastewater).
Prions are such a formidable threat that the U.S. government enacted the Bioterrorism Preparedness and Response Act of 2002, which included a provision to halt research on prions in all but two laboratories.
The U.S. government initially classified prions as select agents that pose an extreme risk to food, water and health systems. Today, governments don’t regulate prions at all.
As such, millions of caregivers are being misinformed, misguided and exposed to an aggressive prion disease. So are friends and family. 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 associated with Parkinson’s disease and Alzheimer’s disease have been reported in skin tissues of patients with these conditions. Skin could serve as a screen for early diagnosis, but also for monitoring the accumulation of the misfolded proteins in the brain of these neurodegenerative diseases. It also could be another pathway of transmission.
The Alzheimer’s/Parkinson’s epidemic is more widespread than anyone knows. Physicians have withheld millions of diagnoses from patients and their families. According to the Alzheimer’s Association, physicians in the U.S. only inform 45 percent of patients about their Alzheimer’s disease diagnosis. Similar suppression is likely at work in most countries to help shade the epidemic. Meanwhile, millions more go undiagnosed and misdiagnosed.
A groundbreaking study suggested that Alzheimer’s disease causes six times as many deaths as the official statistics indicate. In reality, the study said Alzheimer’s disease was the underlying cause in more than 500,000 deaths in 2010 that were often attributed to conditions, such as pneumonia, caused by complications of Alzheimer’s. Those numbers make Alzheimer’s disease the third-leading cause of death in the United States, behind heart disease and cancer. Researchers at the Rush University Medical Center in Chicago led the study and published their results in 2013 in the medical journal Neurology. Governments and industry are working diligently to keep prion disease off the public radar. The epidemic will persist. A cure does not exist. Ignoring the truth is making it worse.
Despite millions of deaths annually, experts suggest that the prevalence of Alzheimer’s 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. Deadly, self-replicating proteins appear to be one of the common threads. Similar proteins are now associated with the childhood cases of Creutzfeldt-Jakob disease. Abnormal proteins also appear to be related to the global autism epidemic.
The epidemic is worse in some regions of the world than others. Finland and Iceland were at the top of the list just a few years ago. Now, countries in the Middle East and Persian Gulf states have soared to the top of the list. As a result of the epidemic in the region, even the camels are dying of prion disease.
In the United States, for example, deaths from Alzheimer’s disease increased 71 percent from 2000 to 2013. During that time, deaths from heart disease decreased 14 percent.
Unfortunately, the CDC quietly took prions off the highly regulated list of select agents because the regulation criminalized entire industries and several reckless practices. It also opened the floodgates to prion mismanagement.
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. Wastewater treatment plants are spreading infectious waste far and wide because they are incapable of stopping prions. As such, all by-products and discharges from wastewater treatment plants are infectious waste, which are contributing to the global epidemic of neurodegenerative disease among humans, wildlife and livestock.
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 (biosolids) was 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 an “emerging contaminant of concern.” Meanwhile, its outdated risk assessments are promoting a public health disaster. The neurotoxins found in sewage, including heavy metals, also are contributing to the global spike in autism, which follows the same timing and trajectory as the spike in neurodegenerative diseases.
“Since it’s unlikely that the sewage treatment process can effectively stop prions, adopting measures to prevent the entry of prions into the sewer system is advisable,” said the Toronto Department of Health, November 2004.
Once unleashed on the environment, prions remain infectious. They migrate, mutate and multiply as they infect crops, water supplies, wildlife, livestock, sea mammals and humans. According to prion researcher Joel Pedersen at the University of Wisconsin, prions in soil become up to 680 times more infectious. From there, they migrate, mutate and multiply. It’s a real world version of Pandora’s Lunchbox.
“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.”
Pedersen also found that sewage treatment does not inactivate prions. Therefore, prions are lethal, mutating, migrating and multiplying everywhere sewage (biosolids) is dumped—including our food and water supplies.
Prions reach 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 pathogens, pharmaceutical residue and chemical pollutants found in sewage sludge are taken up by plants and vegetables.”
Thanks to the mismanagement of infectious waste, including sewage, the animal world is contracting prion disease from humans. They also are passing it among themselves via their own bodily fluids. When it comes to prion disease, species barriers are a myth.
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.
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 are 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. Stakeholders are being duped, while private companies are making billions spreading bioterror across the land. Even school grounds, ballparks and golf courses are being contaminated with prions, endocrine disruptors, radiation and more.
In 2018, the EPA announced that the risk assessments on biosolids (sewage sludge) are negligent if not fraudulent. Unfortunately, nothing has changed. It’s time to outlaw the dumping of infectious/toxic/radioactive waste on land. Dumping this crap into our watersheds, on our crops, playgrounds, sporting fields, golf courses, city parks, and forests has created a public health disaster—mostly in various forms of brain disease, but it also includes cancer, endocrine disruption and much more. Plus, that “soil” that we buy for our potting plants and gardens often has this toxic/infectious waste in it. It’s criminal. The following brain diseases are related to this reckless practice and it’s getting worse every day: Alzheimer’s disease, Parkinson’s disease, autism, chronic wasting disease, mad cow disease, zika virus, west Nile virus, equine encephalopathy, and others. All have emerged and/or spiked since the EPA blindly created a multi-billion dollar industry built on deceit and death.
Thanks to the land application of sewage sludge (biosolids) and antiquated/fraudulent risk assessments, we’re witnessing a public health disaster that’s still unfolding in the form of autism, Alzheimer’s disease, Parkinson’s disease west Nile virus, Zika virus, chronic wasting disease, mad cow disease, valley fever, meningitis, hepatitis, and other threats to public health.
Crops for humans and livestock grown in sewage sludge absorb prions and other neurotoxins. They become infectious. We’re all vulnerable to neurotoxins 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 to keep prions and other toxins out of our food, water and air. It’s time to stop spreading deadly pathogens and lies for profit. Sewage sludge is a prion super-highway. It’s killing more than our wildlife. If all else fails, it’s time to enforce the Bioterrorism Preparedness and Prevention Act. It’s time to defend the homeland from deadly pathogens and lies. Biosolids is a glorified term for bioterrorism.