Caregivers At Risk In Battle Against Brain Disease

Spouses Of Those With Brain Disease More Likely To Contract Brain Disease

Millions of people are becoming caregivers for friends and family members with Alzheimer’s disease. It’s a silent epidemic that’s creating family crises around the world. In addition to the shock of the sudden dependency, at least some caregivers (family members and professionals) are being misinformed and exposed to deadly pathogens that can spread the disease.

“A good caregiver who understands the disease, its symptoms and progression is crucial to the overall well-being of people with Alzheimer’s disease,” said Dr. Fred Kobylarz, a dementia expert at the Robert Wood Johnson Medical School at Rutgers University. “Alzheimer’s has become pervasive in the United States and around the world. It affects people in all walks of life,” Kobylarz said. “It is a problem that needs action and attention.”

Memory problems are typically one of the first signs of cognitive impairment related to Alzheimer’s disease. Some people with memory problems have a condition called mild cognitive impairment (MCI). In MCI, people have more memory problems than normal for their age, but their symptoms do not interfere with their everyday lives. Movement difficulties and problems with the sense of smell have also been linked to MCI. Older people with MCI are at greater risk for developing Alzheimer’s disease, but not all do. Some may even go back to normal cognition.

The first symptoms of Alzheimer’s disease vary from person to person. For many, decline in non-memory aspects of cognition, such as speech, vision, and impaired reasoning or judgment, may signal the very early stages of Alzheimer’s disease.

Alzheimer's disease treatment

Researchers are studying biomarkers (brain images, cerebrospinal fluid, and blood) to see if they can detect early changes in the brains of people with MCI and in cognitively normal people who may be at greater risk for Alzheimer’s. Studies indicate that such early detection may be possible, but more research is needed before these techniques can be relied upon to diagnose Alzheimer’s disease in everyday medical practice.

For instance, people early on might show signs of memory loss that don’t affect their ability to function day to day. “Some memory loss can also be a sign of the normal aging process,” Kobylarz explained.

“Families should look for memory impairment and trouble managing aspects of their daily lives — like paying bills or taking their medication,” he said.

It’s also important to know your family history and share that with your doctors, Kobylarz said. Though older age is the biggest risk factor for Alzheimer’s, he explained, genetics and family history also play a role.

If you notice worrisome changes in an older family member, talk with a doctor, he said.

Scientists don’t yet fully understand what causes Alzheimer’s disease in most people. There is a genetic component to some cases of early-onset Alzheimer’s disease. Late-onset Alzheimer’s arises from a complex series of brain changes that occur over decades. The causes probably include a combination of genetic, environmental, and lifestyle factors. The importance of any one of these factors in increasing or decreasing the risk of developing Alzheimer’s may differ from person to person.

Alzheimers disease epidemic

To diagnose Alzheimer’s, doctors often:

  • Ask the person and a family member or friend questions about overall health, past medical problems, ability to carry out daily activities, and changes in behavior and personality;
  • Conduct tests of memory, problem solving, attention, counting, and language;
  • Carry out standard medical tests, such as blood and urine tests, to identify other possible causes of the problem; and
  • Perform brain scans, such as computed tomography (CT), magnetic resonance imaging (MRI), or positron emission tomography (PET), to rule out other possible causes for symptoms.

These tests may be repeated to give doctors information about how the person’s memory and other cognitive functions are changing over time. If the diagnosis is Alzheimer’s, beginning treatment early in the disease process may help preserve daily functioning for some time, even though the underlying disease process cannot be stopped or reversed. An early diagnosis also helps families plan for the future. They can take care of financial and legal matters, address potential safety issues, learn about living arrangements, and develop support networks.

In addition, an early diagnosis gives people greater opportunities to participate in clinical trials that are testing possible new treatments for Alzheimer’s disease or other research studies.

Alzheimer’s disease can be definitely diagnosed only after death, by linking clinical measures with an examination of brain tissue in an autopsy.

People with memory and thinking concerns should talk to their doctor to find out whether their symptoms are due to Alzheimer’s or another cause, such as stroke, tumor, Parkinson’s disease, sleep disturbances,side effects of medication, an infection, or a non-Alzheimer’s dementia. Some of these conditions may be treatable and possibly reversible.

Alzheimer’s cannot yet be cured, but medications and lifestyle changes can often help slow the progression of the disease, Kobylarz said. This requires the doctor, patient and family to work together to develop a plan to maintain cognitive function, he added.

Caring for a person with Alzheimer’s disease can have high physical, emotional, and financial costs. The demands of day-to-day care, changes in family roles, and decisions about placement in a care facility can be difficult. There are several evidence-based approaches and programs that can help, and researchers are continuing to look for new and better ways to support caregivers.

Becoming well-informed about the disease is one important long-term strategy. Programs that teach families about the various stages of Alzheimer’s and about ways to deal with difficult behaviors and other caregiving challenges can help.

Prion disease and Alzheimer's disease

Which Forms Of Neurodegenerative Diseaese Are Contagious

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 (PREE-ons) and prion disease, also known as transmissible spongiform encephalopathy (TSE). The operative word is “transmissible.” Prions are a deadly and unstoppable form of protein that migrates, mutates, multiplies and kills with unparalleled efficiency. Prions cause fatal neurodegenerative diseases in humans and animals by converting the cellular prion protein PrPC into aggregation-prone PrPSc.

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. Misinformed caregivers, family members, healthcare workers and others are caught in the crossfire of a deadly contagion known as a prion.

TSE is a spectrum disease also known as prion disease. The spectrum includes Alzheimer’s disease, Parkinson’s disease and an extremely aggressive version known as Creutzfeldt-Jakob disease. Prusiner claims that all forms of TSE are caused by infectious prions. The prion spectrum varies in severity. It also varies depending on which region of the brain is impacted first. When the presenting symptom is memory loss, the diagnoses flow along the following chart.

prion disease spectrum

Prion disease causes memory loss, impaired coordination, and abnormal movements. Abnormal proteins are now associated with autism. In fact, it appears that the biggest difference between the neurodegenerative disease spectrum and autism spectrum disorders is age. Both spectrums share common environmental causes and pathologies.

Caregivers Misinformed

It’s not known which patients with brain disease become infectious or when, but both CJD and Alzheimer’s patients are being mismanaged. Informed neurologists won’t touch patients with these symptoms because of the risk of transmission. They are making diagnoses from across the room.

“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 Alzheimer’s diagnoses are not Alzheimer’s disease. These misdiagnoses are actually 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 in 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 disease. Misdiagnosis and misinformation regarding prion disease is a matter of life and death. The disease is now striking young people, including teenagers, with much greater frequency. It’s also killing clusters of people in the same communities with greater frequency. The mismanagement doesn’t end here.

Studies confirm that people and animals dying of prion disease contaminate the environment around them because infectious prions are in the urine, feces, blood, mucus and saliva of each victim. These infectious bodily fluids are contributing to the rapid spread of Alzheimer’s and other mutations of 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. “In fact, this ability to transmit an abnormal conformation is probably a universal property of amyloid-forming proteins (prions).”

Alzheimer's disease research

Caregivers and other stakeholders are caught in the crossfire of misinformation and mismanagement. At the most basic level, this means that a sneeze, a drinking glass and eating utensils are permanent pathways of disease transmission. Anything that ever comes into contact with the bodily fluids of a victim is impossible to sterilize.

On a larger level, it means that entire communities and watersheds are at risk of permanent contamination from just a single victim, not to mention thousands of infectious victims. Alzheimer’s disease is an environmental nightmare–it’s a real-world version of Pandora’s box.

A 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 adds to the claim. Meanwhile, there is absolutely no evidence to the contrary. Even wildlife are contracting brain disease from people because of the dumping of infectious waste on farms, ranches and forests.

Surgical instruments infected with prions, 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 prions 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.

More Mismanagement Of Prion Disease

When the U.S. government enacted the Bioterrorism Preparedness and Response Act of 2002, it classified prions as select agents that pose an extreme risk to food, water and much more. Only two labs in the U.S. were allowed to handle them for research purposes. Unfortunately, the CDC quietly took prions off the list because the regulation criminalized entire industries and several reckless practices.

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.

land application sewage sludge

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 it’s antiquated sludge rule crafted back in the dark ages. It does, however, consider prions a “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 deactivate 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 is dumped.

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 pathogens, pharmaceutical residue and chemical pollutants found in sewage sludge are taken up by plants and vegetables.”

TSEs also include mad cow disease and chronic wasting disease in the deer family. Few, if any, mammals are immune. 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. 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.

biosolids land application

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 in sewage sludge absorb prions and become infectious. We’re all vulnerable to neurotoxins and 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.

Alzheimer's disease public relations firm

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.

Patients With Neurodegenerative Disease Produce Infectious Waste

Caregivers Caught In The Crossfire Of Misinformation, Mismanagement

Neurodegenerative disease is the fastest-growing cause of death in the world. Alzheimer’s disease alone is taking the lives of 50-100 million people now. Despite millions of Alzheimer’s-related fatalities annually, experts suggest that the prevalence of the disease among the living will quadruple by 2050, if not sooner. Some advocates are warning that the surging epidemic could bankrupt entire nations.

Unfortunately, there is a growing stack of evidence that Alzheimer’s disease is a transmissible disease, which means that millions of caregivers, friends and family members are at risk.

The epidemic is more widespread than anyone knows. A groundbreaking study suggested that Alzheimer’s disease causes six times as many deaths than official statistics indicate. The Centers for Disease Control and Prevention estimated that, in 2010, Alzheimer’s disease caused almost 84,000 deaths in the United States, a number derived from death certificates in which Alzheimer’s disease was listed as the main cause. 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. The study was led by researchers at the Rush University Medical Center in Chicago and published in 2013 in the medical journal Neurology.

Prions and Alzheimer's 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 (PREE-ons) and prion disease, also known as transmissible spongiform encephalopathy (TSE). The operative word is “transmissible.” Prions are 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. 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. Misinformed caregivers, family members, healthcare workers and others are caught in the crossfire of a deadly contagion known as a prion.

TSE is a spectrum disease also known as prion disease. The spectrum includes Alzheimer’s disease, Parkinson’s disease and an extremely aggressive version known as Creutzfeldt-Jakob disease. Prusiner claims that all forms of TSE are caused by infectious prions. The prion spectrum varies in severity. It also varies depending on which region of the brain is impacted first. When the presenting symptom is memory loss, the diagnoses flow along the following chart.

prion disease spectrum

It’s not known which patients with brain disease become infectious or when, but both CJD and Alzheimer’s patients are being mismanaged. Informed neurologists won’t touch patients with these symptoms because of the risk of transmission. They are making diagnoses from across the room.

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 Alzheimer’s diagnoses are not Alzheimer’s disease. These misdiagnoses are actually 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 in 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 disease. Misdiagnosis and misinformation regarding prion disease is a matter of life and death. The disease is now striking young people, including teenagers, with much greater frequency. It’s also killing clusters of people in the same communities with greater frequency. The mismanagement doesn’t end here.

Studies confirm that people and animals dying of prion disease contaminate the environment around them because infectious prions are in the urine, feces, blood, mucus and saliva of each victim. These infectious bodily fluids are contributing to the rapid spread of Alzheimer’s and other mutations of 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. “In fact, this ability to transmit an abnormal conformation is probably a universal property of amyloid-forming proteins (prions).”

Caregivers and other stakeholders are caught in the crossfire of misinformation and mismanagement. At the most basic level, this means that a sneeze, a drinking glass and eating utensils are permanent pathways of disease transmission. Anything that ever comes into contact with the bodily fluids of a victim is impossible to sterilize.

Alzheimer's disease diagnosis

On a larger level, it means that entire communities and watersheds are at risk of permanent contamination from just a single victim, not to mention thousands of infectious victims. Alzheimer’s disease is an environmental nightmare–it’s a real-world version of Pandora’s box.

A 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 adds to the claim. Meanwhile, there is absolutely no evidence to contrary. Even wildlife are contracting brain disease from people because of the dumping of infectious waste on farms, ranches and forests.

Caregivers are being misinformed about the risks associated with exposure to people with Alzheimer’s disease and Creutzfeldt-Jakob disease. 

Surgical instruments infected with prions, for example, are impossible to sterilize. 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 prions 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.

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 and biosolids were prepared before the world of science knew about prions. The agency continues to cling to it’s antiquated sludge rule crafted back in the dark ages. It does, however, consider prions a “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.

wastewater treatment plant

“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,” 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.

biosolids land application sewage sludge

Pedersen also found that sewage treatment does not inactivate prions. Therefore, prions are lethal, mutating, migrating and multiplying everywhere sewage is dumped.

Unfortunately, prions linger in the environment, homes, hospitals, nursing homes, dental offices and beyond infinitely. Prions defy all attempts at sterilization and inactivation. Answers begin with the truth.

Alzheimer's disease public relations firm

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.

Is Alzheimer’s Disease Contagious

Science, Evidence Proving That 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.

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, includingAlzheimer’s disease, are caused by prions.

Prions and Alzheimer's 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. 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.

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.

Alzheimer's disease and caregivers

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.

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.

wastewater treatment plant

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.

joel pedersen prion research

“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.

biosolids 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,” said the 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

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. There is no species barrier.

mad cow disease

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. It’s time to demand reforms on many levels to safeguard caregivers, family members and our food and water supplies. Despite all of the warning signs, government and industry are insisting that we waste more time, money and lives studying these issues to death. The infection is real. The body count is real. The denial is disturbing.

Alzheimer’s Disease Research via http://crossbowcommunications.com/is-alzheimers-disease-contagious/

Alzheimer's disease public relations firm

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.

Neurodegenerative Disease A Global Epidemic

Neurodegenerative Disease The Fastest Growing Cause Of Death

Death rates from heart disease and cancer are dropping globally due to advances in nutrition, medicine and disease management. Meanwhile, neurodegenerative disease is exploding because it’s highly contagious in most cases.

In the U.S., deaths from Alzheimer’s disease increased 71 percent from 2000 to 2013, while those attributed to heart disease decreased 14 percent. Similar trends are emerging around the world. Unfortunately, the global spike in autism shares the same timing and trajectory as the surge in neurodegenerative disease. It’s not just a coincidence. The correlation is real thanks to reckless policies and practices. It appears that the biggest difference between autism and classic forms of neurodegenerative disease is age of onset.

The actual epidemic is larger than anyone knows. Physicians are withholding 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. The same suppression is likely at work in most countries. Meanwhile, millions more go undiagnosed and misdiagnosed. Women face an elevated risk of Alzheimer’s disease.

Prions and Alzheimer's 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 (PREE-ons) and prion disease, also known as transmissible spongiform encephalopathy (TSE). The operative word is “transmissible.” Prions are 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. 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.

TSE is a spectrum disease also known as prion disease. The spectrum includes Alzheimer’s disease, Parkinson’s disease and an extremely aggressive version known as Creutzfeldt-Jakob disease. Prusiner claims that all forms of TSE are caused by infectious prions. The prion spectrum varies in severity. It also varies depending on which region of the brain is impacted first. When the presenting symptom is memory loss, the diagnoses flow along the following chart.

prion disease spectrum

Prion disease is a spectrum disease that varies in severity. It also varies depending on which region of the brain is impacted first. It affects most, if not all, mammals. Prion disease causes memory loss, impaired coordination, and abnormal movements. It’s not known which patients with brain disease become infectious or when, but both CJD and Alzheimer’s patients are being mismanaged. The most savvy neurologists won’t touch patients with these symptoms because of the risk of infection. They are making diagnoses from across the room. Unfortunately, caregivers aren’t warned accordingly.

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

According to neuroscientist Laura Manuelidis, at least 25 percent of Alzheimer’s diagnoses are not Alzheimer’s disease. These misdiagnoses are actually CJD, which is further up the prion spectrum. CJD, without dispute, is extremely infectious to caregivers and loved ones. 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 disease. Misdiagnosis and misinformation regarding prion disease is a matter of life and death. The mismanagement doesn’t end here.

Prions are now the X factor and they are not being accounted for by industry or government. Prions are an infectious form of glycoprotein that can spread throughout the body.

“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 recent study published in the journal Nature also renews concern about the transmissibility of Alzheimer’s disease between people. A second study by the same scientist in early 2016 adds to the stack of evidence. There is no evidence that Alzheimer’s disease is not infectious to other mammals.

Many factors are contributing to the epidemic. Unfortunately, it appears that Alzheimer’s disease and Parkinson’s disease are just as infectious as Creutzfeldt-Jakob disease. 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.

Alzheimer's disease infectious disease

Not only are homes, hospitals and nursing homes exposed to the deadly prion pathogen from those with prion disease, so are entire sewage treatment systems and their by-products. Wastewater treatment plants are prion incubators and distributors. The sewage sludge and wastewater released are spreading disease far and wide. 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.

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.

joel pedersen prion research

“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.”

Each victim becomes an incubator and a distributor of the Pandora-like pathogen. 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.

biosolids land application sewage sludge

Sewage from hospitals, nursing homes, slaughterhouses, morgues, mortuaries, veterinarians and other high-risk places enters the same sewage system. Thanks to more and more people dying from TSEs, sewage systems are more contaminated with prions than ever. Wastewater treatment systems are now prion incubators and distributors.

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 it’s antiquated sludge rule crafted back in the dark ages. It does, however, consider prions a “emerging contaminant of 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,” said the Toronto Department of Health, November 2004.

Researchers have more questions than answers about brain disease, but we know that neurotoxins, head trauma and genetics can all trigger neurodegenerative disease. Unfortunately, that’s where our knowledge gets fuzzy.

When the U.S. government enacted the Bioterrorism Preparedness and Response Act of 2002, it classified prions as select agents that pose an extreme risk to food, water and much more. TSE surveillance is important for public health and food safety because TSEs have the potential of crossing from animals to humans, as seen with the spread of mad cow disease. TSEs also have the potential of being transmitted from humans to animals. The most common example is chronic wasting disease among deer species. Deer, elk, moose, reindeer and many other animals are being exposed to infectious waste in sewage.

Prions are unstoppable. The pathogen spreads through the bodily fluids and cell tissue of its victims. The blood, saliva, mucus, milk, urine and feces of victims are infectious. Wastewater treatment doesn’t touch prions. In fact, these facilities are now helping incubate and distribute prions via solids and wastewater released.

biosolids land application contaminates food water

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.

Prions shed from humans are the most deadly. They demand more respect than radiation. They’re being ignored by regulators and industry alike. As such, food and water sources are being contaminated with the deadliest forms of prions. Homes, nursing homes, hospitals, clinics and restaurants are other examples of public places that are being contaminated by prions from victims of prion disease.

The deadly prion spectrum also includes mad cow disease and chronic wasting disease among deer. Scientists have shown that infected tissues can transmit prion disease between animals. There is no species barrier.

Although there are many causes and pathways contributing to prion disease, many pathways are being mismanaged around the globe. Not only are homes and hospitals exposed to the prion pathogen, so are entire sewage treatment systems. Wastewater treatment plants are prion incubators. Sewage sludge and wastewater pumped out spread the disease.

wastewater treatment plant

Sewage treatment plants can’t detect or stop deadly prions. Just ask the U.S. EPA. Dumping sewage sludge (biosolids) from billions of people on land and at sea spreads prions far and wide. It also spreads heavy metals, radioactive waste, carcinogens, pharmaceuticals and more. It’s time for the truth. It’s time for reforms that can safeguard us from this public health disaster.

Read more about the correlation between Alzheimer’s disease, autism and sewage mismanagement. http://alzheimerdisease.tv/autism/

autism population

Background On Sewage Sludge

In 1972, world leaders admitted that dumping highly toxic sewage sludge into the oceans killed entire underwater ecosystems and threatened public health. Some nations stopped the dumping immediately and started dumping it on land or burning it in incinerators. The most responsible cities started putting sewage sludge in landfills. Meanwhile, the United States allowed cities to keep dumping sewage sludge at sea for another 20 years. It finally passed the Ocean Dumping Ban Act of 1988, when beaches along the east coast were forced to close because of high levels of pathogens from sewage that washed up on shore.

land application sewage sludge and disease

The law prohibited all dumping of industrial waste and municipal sewage sludge into our oceans after December 31, 1991. It did nothing however, to keep cities such as Boston and Los Angeles from dumping millions of gallons of raw sewage directly into the oceans every day, but with the help of the U.S. EPA, the Act did redirect millions of tons of deadly toxins and pathogens from our oceans to farms, ranches, national forests, city parks, golf courses, playgrounds, fair grounds, race tracks, sport fields and beyond. From there, the pathogens began contaminating food, water and air as they were soaked up by crops, swept away by rainwater and picked up by windstorms, tornadoes and hurricanes and dumped on innocent citizens where they live, work and play. The runoff still contaminates our oceans after it filters through our creeks, lakes and rivers.

After the 1991 ban on ocean dumping, the EPA instituted a policy of sewage sludge reuse on agricultural land. It hired a PR firm to spin a new brand for the death dirt. They crafted the clever name “biosolids” to help disguise the hazards. The EPA promoted biosolids recycling throughout the 1990s. Unfortunately, the risk assessments were severely biased and flawed. The proof is in the pudding.

This new form of sewage dispersal has sparked a public health disaster that’s still unfolding in the form of autism, Alzheimer’s disease, west Nile virus, Zika virus, chronic wasting disease, meningitis, hepatitis, and other threats to public health. The risk assessments for these practices failed to account for heavy metals, pharmaceutical residue, radionuclides, carcinogens and a deadly form of protein known as a prion (which was unknown to the world of science at the time). The practice sparked a public health disaster in exchange for healthier oceans and a very profitable new industry. The EPA even took its show on the road and convinced other nations to use its faulty risk assessments to justify multi-million dollar contracts for these new corporations. Countries such as Canada took the bait hook, line and sinker and never conducted its own risk assessments.

Chronic wasting disease is now rampant among deer and elk in Canada and it recently jumped the Atlantic to Norway’s reindeer herd. It’s spreading across the U.S. like wildfire as we spread more pathogens and lies. Land application sites often involve locations where poverty is high and economic prosperity is low, which means resistance is low. Sludge tends to be dumped where minorities live, leading to allegations of environmental racism. Unfortunately, contaminated food and water make it back to the cities where the infectious waste originated.

Treated sewage sludge has been used in the UK, Europe and China agriculturally for more than 80 years, though there is increasing pressure in some countries to stop the practice of land application due to farm land contamination and public outrage. In the 1990s there was pressure in some European countries to ban the use of sewage sludge as a fertilizer. Switzerland, Sweden, Austria, and others introduced a ban to safeguard public health. Others should follow their example.

Alzheimer's disease treatment

Preview and order the eBook now. The truth can save your life.

public relations firm Alzheimer's disease

Crossbow Communications specializes in issue management and public affairs. Call 602-999-7204 or write to Gary Chandler to join our campaign and coalition for truth and reform. gary@crossbow1.com. Together, we can prevent Alzheimer’s disease and autism.

Caregivers Overwhelmed By Alzheimer’s Disease

eBook Offers Vital Tips For Caregivers, Patients

Neurodegenerative disease is the fastest-growing cause of death in the world. There are no vaccines to prevent it or cure it. Prevention is our best hope and nutrition offers the only proven hope for those who have brain disease.

Alzheimer’s disease is a member of an aggressive family of neurodegenerative diseases known as transmissible spongiform encephalopathy (TSE). As the name implies, the disease is transmissible and extremely difficult to treat.

The good news is that with the truth, caregivers can safeguard themselves and others, while treating patients with targeted nutrition that helps treat the symptoms of Alzheimer’s disease. Targeted nutrition also offers promise in preventing brain disease.

A new book by researcher Gary R. Chandler sheds light on tips for aversion and treatment of Alzheimer’s disease and other forms of neurodegenerative disease. The most common forms of neurodegenerative disease include Alzheimer’s, Parkinson’s and Creutzfeldt-Jakob disease–the most aggressive and infectious of them all.

Prions and Alzheimer's disease

According to Nobel Prize Laureate Stanley Prusiner, they are all part of the same disease spectrum—prion disease. It’s also known as transmissible spongiform encephalopathy (TSE). The operative word is “transmissible.”

TSEs are caused by a deadly protein called a prion (PREE-on). Prion disease is unstoppable. The pathogen spreads through the bodily fluids and cell tissue of its victims. Blood, saliva, mucus, milk, urine and feces carry deadly prions from the victim. All tissue is infectious.

Prions linger in the environment, homes, hospitals, nursing homes, dental offices, restaurants and many other places infinitely. They migrate, mutate, multiply and kill with unparalleled efficiency. Prions defy all attempts at sterilization and inactivation. Victims often become infectious long before they appear sick.

Prions kill everything in their path—man or beast. Prions are highly infectious and the bodies of victims become highly infectious long before they look or feel sick. Blood, milk, meat, urine, saliva, mucus, feces and other bodily fluids of victims are contagious.

According to research from Duke University, caregivers of someone with dementia are six times more likely to develop the condition themselves.

Even sophisticated healthcare systems have failed to grasp the severity of prion disease. Unfortunately, hospitals around the world have been sued for spreading CJD to innocent patients. Most health care systems are still misinformed and under-informed about the dangers that CJD patients pose to others. Therefore, these care facilities are exposing others and contributing to a global mismanagement problem.

Alzheimer's disease infectious disease

Only a decade ago, the idea that Alzheimer’s disease might be transmissible between people would have been laughed away. But scientists have now shown that tissues can transmit symptoms of the disease between animals. A new study published in the journal Nature raises additional concern about the transmissibility of Alzheimer’s disease between people.

Prion disease is a spectrum disease because of its many mutations and because some victims appear to have a genetic predisposition to resist the disease. Some prions can kill people within weeks of exhibiting clinical symptoms, while others can take years. Others may not fall victim to the disease, but can still carry the pathogen internally and externally. Victims become infectious long before they appear sick. Their bodily fluids proceed to contaminate the world around them with infectious waste.

Alzheimer's disease research

Since prion disease is a spectrum disease, doctors can’t tell the difference between Alzheimer’s disease and CJD. It’s a process of elimination and a shot in the dark. The only definitive diagnosis comes with an autopsy, which rarely happens with neurological disease (concerns over deadly contamination). All doctors are guessing with each diagnosis based on the severity of the symptoms. This problem also complicates the search for accurate statistics about the size and scope of the epidemic.

Alzheimer’s diagnoses are wrong at least 20 percent of the time. Unfortunately for caregivers and family members, the protocol for patient care and caregiver safety are vastly different for Alzheimer’s patients and CJD patients. The double standards put many stakeholders at risk. It’s reckless to try to distinguish between prion diseases on the spectrum. In other words, treat people with Alzheimer’s disease as though they have CJD. Assume the worst and hope for the best. A deadly prion is a deadly prion.

infectious waste and food contamination

Although there are many causes and pathways contributing to prion disease, many pathways are being mismanaged around the globe. Not only are homes and hospitals exposed to the prion pathogen, so are entire sewage treatment systems. Wastewater treatment plants are prion incubators. Sewage sludge and wastewater pumped out spread the disease.

Caring For Someone With Alzheimer’s Disease

Nearly 15 million caregivers in the U.S. work with someone who has Alzheimer’s, and approximately 70 percent of Alzheimer’s patients are cared for by relatives and friends. In addition to the truth about transmissibility, these caregivers desperately need guidance on effective treatments. The search for cures has been a total washout.

Fortunately, targeted nutrition offers promise. Some foods increase your risk of contracting brain disease, while some foods help prevent it. Other foods offer the best hope for effective treatment. For example, the eBook explains how walnuts, coconut oil, olive oil, grapes, salmon and hundreds of other foods offer proven results to people with brain disease.

Alzheimer's disease Survival Guide

Order the eBook now and learn how to:

  • Avoid neurotoxins in food, water and the circles of life;
  • Prevent brain disease with targeted nutritional guidance;
  • Effectively treat brain disease with nutritional therapies. It’s the most logical and comprehensive nutritional advice available for neurological disease; and
  • Keep caregivers safe. Misinformation and misdiagnoses are putting us at risk.

treat Alzheimer's disease

Brain Disease The Fastest Growing Cause Of Death

More Than 50 Million People Have Alzheimer’s Disease

Neurodegenerative disease is now a global epidemic among many mammals, including humans. Advocates claim that mismanagement and misinformation around the world are fanning the flames and putting millions of people in harm’s way.

Anywhere from 50-100 million people around the world are dying of brain disease. Millions more will contract it this year, while just as many will go undiagnosed and misdiagnosed. Adding to the madness is the fact that physicians are withholding millions of other diagnoses.

Alzheimer's disease epidemic

Death rates from heart disease, cancer and other leading causes of death are steady, if not dropping, in most countries due to advances in nutrition, medicine and disease management. Unfortunately, neurodegenerative disease is the one glaring exception. It’s spreading exponentially. If we had accurate mortality statistics, we would likely find that brain disease is already the leading cause of death around the world. Some countries are at a higher risk than others.

“This will be the most important documentary ever produced about brain disease,” said Gary Chandler, president of Crossbow Communications. “Thanks to mismanagement and the widespread contamination of our food and water, brain disease has more to do with neurotoxins than it does with normal aging and genetics.”

The most common forms of neurodegenerative disease include Alzheimer’s, Parkinson’s and Creutzfeldt-Jakob disease–the most aggressive and infectious of them all. According to Nobel Prize Laureate Stanley Prusiner, they are all part of the same disease spectrum—prion disease. It’s also known as transmissible spongiform encephalopathy (TSE). The operative word is “transmissible.”

Prions and Alzheimer's disease

Prions are unstoppable. The pathogen spreads through the bodily fluids and cell tissue of its victims. The blood, saliva, mucus, milk, urine and feces of victims are infectious. Once unleashed on the environment, prions remain infectious. In fact, they migrate, mutate and multiply.

Not only are homes and hospitals exposed to the prion pathogen, so are entire sewage treatment systems and their by-products. Wastewater treatment plants are prion incubators. The sewage sludge and wastewater released are spreading disease far and wide.

Alzheimer's disease prevention and treatment

Sewage treatment plants can’t detect or stop prions. Dumping sewage sludge (biosolids) from billions of people on land and at sea spreads prions far and wide. It also spreads heavy metals, radioactive waste, carcinogens, pharmaceuticals and more. The risk assessments for biosolids and wastewater reuse don’t mention prions because there is no answer.

“Although there are many factors contributing to the global epidemic, millions of these deaths could have been prevented,” said Chandler. “In addition to dietary risks, it appears that Alzheimer’s disease is just as infectious as Creutzfeldt-Jakob disease. There’s no evidence to the contrary.”

  • Women are contracting neurodegenerative disease at twice the rate of men;
  • Caregivers are six times more likely to contract brain disease;
  • People from Finland, Iceland, Sweden and the United States have the highest death rates from Alzheimer’s; and
  • Smart nutrition is the best strategy to avoid brain disease and the only way to effectively treat its symptoms.

biosolids land application sewage sludge

There are many more questions than answers, but we know that neurotoxins, head trauma and genetics can all trigger neurodegenerative disease. Unfortunately, that’s where much of the knowledge gets fuzzy. Diagnoses, for example, are barely more than a shot in the dark.

According to Chandler, truth and targeted nutrition are the best defense against environmental contamination and brain disease. His company is producing a documentary that will help promote food safety, wellness and reform. It’s called “Food For Thought.” It offers the most comprehensive guidance available about prevention, aversion and treatment, including vital advice for caregivers and family members.

brain disease treatment

Preview and order the eBook now. It will:

  • Help you avoid neurotoxins in food, water and the circles of life;
  • Offer targeted nutritional guidance that can save lives;
  • Offer nutritional therapies that can make a difference. It’s the most logical and comprehensive nutrition for neurological disease available. It also has critical aversion strategies;
  • Inform caregivers about misinformation and misdiagnoses that put them in harm’s way;
  • Blow the whistle on industry practices that are contaminating food, water and other pathways; and
  • Advocate for food safety, water quality, wellness and reforms that can save millions of lives.

According to Chandler, pharmaceutical remedies are nonexistent, but nutritional strategies and tactics provide hope and relief from many symptoms. Unfortunately, there is no cure for brain disease, so prevention is paramount.

The film will be produced in both Denver and Phoenix. The producers are looking for testimonials and commentary from a variety of stakeholders, including family, caregivers, providers and advocates. For more information, please contact Gary Chandler at 602-999-7204 or visit our home page at http://alzheimerdisease.tv/

Crossbow Communications is a public affairs and issue-management firm headquartered in Denver, Colorado. The company is expanding to Phoenix, Arizona. The firm specializes in health and environmental issues. It has helped influence public opinion and public policy around the world. For more information, please visit http://crossbowcommunications.com/phoenix-pr-firm-alzheimers-disease/

Food For Thought About Alzheimer’s Disease

Alzheimer’s Disease Discussed In Upcoming Documentary

As you probably know, Alzheimer’s disease is no laughing matter. It’s killing more than 50 million people around the world right now. It’s probably impacting your family or someone that you know.

As death rates from heart disease, cancer and other leading causes of death are dropping around the world today, Alzheimer’s disease is the one glaring exception. Death rates from Alzheimer’s disease are skyrocketing around the world. Finland, Iceland and the United States have the highest rates in the world. Regional hot spots also exist, including the state of Washington in the U.S.

Alzheimer's disease treatment

Neurological diseases are the fastest-growing cause of death in the world today. If we had accurate mortality statistics, we would likely find that Alzheimer’s disease is already the number one killer around the world.

Alzheimer’s disease is the only major cause of death with no known prevention or cure. Its progression is unstoppable.

Dementia is a term used to describe a wide range of symptoms associated with the most common forms of neurological disease, including Alzheimer’s disease, Parkinson’s disease and Creutzfeldt-Jakob disease. They’re all part of the same disease spectrum—known as prion disease. The discussion is less confusing if we refer to them all as prion disease.

Prions are a deadly form of protein associated with several forms of neurological disease. Stanley Prusiner earned the Nobel Prize in physiology in 1996 for his pioneering work on prions. Unfortunately, his earth-shattering science has been ignored and a global health epidemic has ensued.

Prions and Alzheimer's disease

There are many factors contributing to the global surge in Alzheimer’s disease. Age and genetics play a role, but it’s smaller than you realize. Due to mismanagement and misinformation, people from some regions of the world are at a higher risk than others. These hot spots speak of an environmental disease not one driven by age and genetics.

cropped-Turmeric-Ad1.jpg

The good news is that many foods are promising treatments that can extend the quality of life for those who have Alzheimer’s disease. Stay tuned. Our documentary will shed light on the causes of neurodegenerative disease. It also explores ways that you can help prevent it and treat it in your family. We still have room for testimonials, sponsors and investors.

crossbow logo white1public relations firm Alzheimer's disease

Please spread the word. Please call Gary Chandler at Crossbow for more information. 602-999-7204 (USA). Thank you.

California Approves Death With Dignity Legislation

New Policy Unlikely To Impact Those Battling Alzheimer’s Disease

By Patrick McGreevy, Los Angeles Times

Caught between conflicting moral arguments, Gov. Jerry Brown, a former Jesuit seminary student, signed a measure allowing physicians to prescribe lethal doses of drugs to terminally ill patients who want to hasten their deaths.

cropped-Alzheimers-disease-treatment.jpg

Approving the bill, whose opponents included the Catholic Church, appeared to be a gut-wrenching decision for the 77-year-old governor, who as a young man studied to enter the priesthood.

“In the end, I was left to reflect on what I would want in the face of my own life,” Brown added. “I do not know what I would do if I were dying in prolonged and excruciating pain. I am certain, however, that it would be a comfort to be able to consider the options afforded by this bill. And I wouldn’t deny that right to others.”

California becomes the fifth state to allow so-called assisted suicide, following Oregon, Washington, Montana and Vermont.

The new law is modeled after Oregon’s. It permits physicians to provide lethal prescriptions to mentally competent adults who have been diagnosed with a terminal illness and face the expectation that they will die within six months. Those restrictions will likely keep people fighting neurological disease out of the equation.

The law will take effect 90 days after the Legislature adjourns its special session on healthcare, which may not be until next year. The earliest likely adjournment would be in January. The governor’s action caps months of emotional and contentious debate over the the End of Life Option Act, which divided physicians, ethicists, religious leaders and the Democratic majority in the Legislature.

“Abx2 15 is not an ordinary bill because it deals with life and death,” Brown wrote in his signing message. “The crux of the matter is whether the state of California should continue to make it a crime for a dying person to end his life, no matter how great his pain suffering.”

Brown said he carefully read input from two of his own doctors, a Catholic bishop and advocates for the disabled, as well as pleas from the family of Brittany Maynard, a cancer victim who took her own life. He said he even has received input from retired Archbishop Desmond Tutu.

“I have considered the theological and religious perspectives that any deliberate shortening of one’s life is sinful,’’ he wrote.

Most Republican lawmakers opposed the bill on moral grounds. Democrats who voted against it cited religious views or experiences in which family members given months to live by doctors had lived for years.

Californians have been debating such end-of-life legislation for more than two decades. State voters in 1992 rejected a broader proposal that would have allowed physicians to administer lethal injections to the terminally sick. Bills offering patients the right to obtain deadly drug doses failed in the Legislature in 2005, 2006 and 2007.

Alzheimer’s Disease News via http://www.latimes.com/local/political/la-me-pc-gov-brown-end-of-life-bill-20151005-story.html

Alzheimer’s Disease Puts Caregivers, Others At Risk

Prion Disease Unstoppable Among Mammals

There might not be a difference between Alzheimer’s disease and the more-feared Creutzfeldt-Jakob disease (CJD) at all. That is very bad news for millions of caregivers and community members around the world.

Alzheimer's disease infectious disease

Alzheimer’s disease and CJD are both members of an aggressive family of neurodegenerative diseases known as Transmissible Spongiform Encephalopathy (TSE). The operative word is “transmissible.”

CJD is without question the most infectious and aggressive form of prion disease in humans. Unfortunately, doctors cannot distinguish between the two diseases and neither can anyone else. Meanwhile, the protocol for patient care and hazardous waste is vastly different. I argue that the protocols should be identical for many reasons.

Scenario One: When a person with CJD is diagnosed, they are walking disasters because they contaminate everything in their path. Everything in their wake is exposed. Hospitals will take great precautions when handling a confirmed CJD patient. All exposed equipment becomes disposable. Unfortunately, they don’t pass along this advice to family members and caregivers. These patients proceed to contaminate their homes, communities, sewers and beyond.

Scenario Two: When a person with CJD is misdiagnosed with Alzheimer’s disease, caregivers and the community at large put their guard down because transmission has never been discussed with Alzheimer’s disease. The patient continues to visit restaurants and dentists. They donate blood. They can donate organs in many countries. They discharge sewage. The contamination spreads.

Scenario Three: If there is no difference between CJD and Alzheimer’s disease, we are making many mistakes on many levels. I argue that a deadly prion is a deadly prion and there is no difference between any prion disease in any mammal. Any difference in symptoms and speed of decline is due to the mutation of the prion involved, diet and genetics of the victim. Therefore, it’s time to reform many protocols to safeguard health facilities, communities, caregivers and entire watersheds.

To make a complex story short, prion disease is unstoppable and the pathogen spreads through bodily fluids and cell tissue. Prions linger in the environment, homes, hospitals, nursing homes, dental offices and many other places infinitely. They migrate, mutate and multiply with unparalleled efficiency. Prions defy all attempts at sterilization and inactivation. People and animals with prion disease represent an environmental nightmare.

biosolids land application contaminates food water

Prions mutate as they move through the food chain, which puts animals at the top of the food chain, including humans, at greater risk. In fact, prions discharged from humans are much more voracious than those discharged from other animals. As such, we are recycling the pathogen that causes Alzheimer’s right back into our food and water via biosolids and reused water. We’re dumping these killer proteins on parks, golf courses, ski areas and school grounds.

Although there are many causes of Alzheimer’s disease and other forms of prion diseases, the epidemic is being mismanaged on many levels around the globe. This mismanagement is contributing to the epidemic.

There is definitely a connection between sewage and prion diseases. Deadly prions are in the blood, urine, feces, saliva and tissue of millions of infected people and animals. Sewage treatment cannot stop the prions discharged by these people every day, which means that deadly prions survive the sewage treatment process. They are pumped and dumped on golf courses and farms through reclaimed water and biosolids (sludge). This foolish practice also could be contributing to the spread of prion disease in wild and farmed deer–known as chronic wasting disease. It also could contribute to prion disease in livestock–known as mad cow disease.

food safety campaign

New research confirms that plants exposed to prions become contaminated and deadly carriers of the disease. Crops grown in sewage sludge and irrigation water that flows over these fields becomes contaminated. So does surface water runoff after rains and snows. That runoff carries deadly prions into streams, rivers, ponds, lakes and oceans. prions now threaten our drinking waters and much much more thanks to the surface applications of biosolids and reclaimed sewage water.

Adding to the insanity, deadly prions are destined for more and more taps around the world through reclaimed water and toilet to tap programs. By recycling disease with sludge and wastewater, the prion pathogen is making its way into drinking water and into food products. We have created Pandora’s Lunchbox with our sewage disposal practices alone. It’s time to reform these practices before the contamination spreads even further. Read more in the book and please advocate for the reform of sewage disposal practices to help stop the Alzheimer’s epidemic.

Alzheimer’s Disease A Form Of Transmissible Spongiform Encephalopathy

Alzheimer’s Disease Is Transmissible Through Many Environmental Vectors

Unfortunately, Alzheimer’s disease is a member of an aggressive family of neurodegenerative diseases known as Transmissible Spongiform Encephalopathy (TSE). The operative word is “transmissible.”

Alzheimer's disease treatment

TSEs include Alzheimer’s disease, Creutzfeldt-Jakob disease, Huntington’s disease and possibly Parkinson’s disease. TSEs also include mad cow disease, chronic wasting disease, scrapie and other related diseases in mammals. It appears that no mammals are immune from the epidemic.

There is very little difference, if any, between these diseases. There is no cure and there is no species barrier. Doctors and even neurologists can’t tell the difference between Alzheimer’s disease, Creutzfeldt-Jakob disease (CJD), Parkinson’s disease and Huntington’s disease. They’re guessing with each so-called diagnosis, which is really just a process of elimination. Once all other options are eliminated, it’s just a question of which of these TSEs they call it.

Unfortunately, the protocol for patient care is vastly different for CJD and these other diseases. CJD is handled with the respect that a prion disease demands. Hospitals and even coroners handle CJD with a wide berth, if at all. Hospitals that have erred have been sued for exposing other patients to equipment that cannot be sterilized. All TSEs, including Alzheimer’s disease, demand the same respect. Meanwhile, the epidemic spreads.

Alzheimer's disease infectious disease

TSEs are caused by a deadly protein called a prion (PREE-on). Prion disease is unstoppable and the pathogen spreads through bodily fluids and cell tissue. Prions linger in the environment, homes, hospitals, nursing homes, dental offices and many other places infinitely. They migrate, mutate and multiply with unparalleled efficiency. Prions defy all attempts at sterilization and inactivation.

People and animals with prion disease represent an environmental nightmare. These killer proteins are unstoppable. Public and private protocols demand the truth and reform to help stop the Alzheimer’s epidemic.

http://alzheimerdisease.tv/creutzfeldt-jakob-disease/