Supporting and Treating Officers In Crisis Act of 2019

Introduced by Republican Missouri Senator Josh Hawley, the “Supporting and Treating Officers In Crisis Act of 2019” (S. 998) was signed into law by President Trump on July 25, 2019.

This bill reauthorizes and expands certain Department of Justice grant programs to provide mental health, stress reduction, psychological services, suicide prevention services, and training for identifying, reporting, and responding to officer mental health crises and suicide, for law enforcement officers and their families. The bill authorizes up to $7,500,000 in appropriations each year for fiscal years 2020 to 2024, a maximum total of $37.5 million.

This sounds eminently socially acceptable, and indeed the bill was widely supported by Congress and various national advocacy groups.

The Real Crisis in Mental Health

While society certainly owes significant consideration and support to law enforcement officers (LEOs) and their families, we can’t help noting that in today’s environment, “mental health and suicide prevention services” really means psychiatric drugs and other harmful psychiatric treatments.

The real crisis in mental health care today is not officer stress, but psychiatric fraud and abuse.

While the bill specifically calls for evidence-based programs, the evidence actually shows that psychiatrists don’t know what causes mental trauma, are unable to predict violence or suicide, and cannot cure any mental disorder they claim to treat.

Psychiatric Fraud

By their own admission psychiatrists cannot predict violence or suicide, and often release violent patients from facilities, claiming that they are not a threat. In 1979, an American Psychiatric Association’s task force admitted in its Brief Amicus Curiae to the U.S. Supreme Court that psychiatrists could not predict dangerousness. It informed the court that “‘dangerousness’ is neither a psychiatric nor a medical diagnosis, but involves issues of legal judgment and definition, as well as issues of social policy.” In addition to not being able to predict violent behavior, psychiatrists certainly have no cures for it, a fact that even they admit.

Psychiatric diagnoses are not based on science, but opinion. Psychiatrists do not have any scientific or medical test to diagnose a person’s mental condition and rely upon faulty observation and opinion of behavior. They admit to not knowing the cause of a single mental disorder or how to cure them. The error in their opinions is enormous — they condemn the innocent, release the dangerous, induce violence in others through drugs and commit people who are not in need of help or turn those away who may genuinely be in need of it.

Recommendations

Rather than training psychiatrists and psychologists about LEO mental health, the grants should be used to train LEOs, security personnel, teachers, coroners, and other professionals to recognize that irrational, violent and suicidal behavior could be caused by psychiatric drugs.

Click here to download and read the CCHR report “Psychiatric Drugs Create Violence & Suicide — School Shootings & Other Acts of Senseless Violence.”

Click here to download and readPsychiatrists Cannot Predict or Cure Violence.

More About Psychiatric Drugs Causing Violence and Suicide

Reference:

Antidepressant-induced akathisia-related homicides associated with diminishing mutations in metabolizing genes of the CYP450 family
by Yolande Lucire and Christopher Crotty
Pharmacogenomics and Personalized Medicine, 1 August 2011
[doi: 10.2147/PGPM.S17445]

This research paper details patients who had been referred to Dr. Lucire’s practice for expert opinion or treatment. More than 120 subjects were diagnosed with akathisia [a neurotoxic psychosis often characterized by a feeling of inner restlessness and inability to stay still] or serotonin toxicity [extremely high levels of serotonin causing toxic and potentially fatal effects] after taking psychiatric drugs that had been prescribed for psychosocial distress. Akathisia has been known to be associated with suicide since the 1950s and with homicide since 1985.

They were tested for variant alleles in cytochrome P450 (CYP450) genes, which play a major role in the metabolism of all antidepressant and many other drugs, indicating ultrarapid metabolism due to allele duplications. This seems to be strongly associated with a large number of deaths from intoxication and suicide. High or fast-changing levels of psychotropic substances can cause unpredictable toxicity leading to violent behavioral effects, including akathisia. [An allele is one of two or more alternative forms of a gene that arise by mutation and are found at the same place on a chromosome.]

Psychiatric drugs are metabolized in the liver by cytochrome P450 enzymes in order to be eliminated from the body. Abnormal CYP450 metabolism, either ultrarapid and/or diminished, can lead to the drug or its metabolites reaching a toxic level in hours or days, correlating with the onset of intense dysphoria [unease or generalized dissatisfaction with life] and akathisia. A person genetically deficient in these enzymes, or who has an ultrarapid drug metabolism, or who is taking other (legal or illegal) drugs that diminish CYP450 enzyme activity, is at risk of a toxic accumulation of the drug leading to more severe side effects.

Eight of these cases had committed homicide and many more became extremely violent or suicidal while on antidepressants. Ten representative case histories involving serious violence are presented in great detail in the paper. None of the ten subjects described had any history of mental illness; none had been violent before. All recovered from akathisia after stopping the medication without assistance or supervision and, frequently, against medical advice.

Akathisia suicides and homicides, particularly when they involved children, gave rise to the first antidepressant suicide advisories by the FDA in 2004.

Personal, medical, and legal problems can arise from using psychiatric drugs and experiencing the resulting toxicity from these metabolic effects. The results presented in this paper demonstrate the grave extent to which the psychiatric industry has expanded its influence beyond its ability to cure.

As the authors state, “In all of the cases presented here, the subjects were prescribed antidepressants that failed to mitigate distress emerging from their predicaments, which encompassed psychosocial stressors such as bereavement, marital and relationship difficulties, and work-related stress. Every subject’s emotional reaction worsened while their prescribing physicians continued the “trial and error” approach, increasing from standard to higher dose and/or switching to other antidepressants, with disastrous consequences. In some cases the violence ensued from changes occasioned by withdrawal and polypharmacy. In all of these cases, the subjects were put into a state of drug-induced toxicity manifesting as akathisia, which resolved only upon discontinuation of the antidepressant drugs.”

“It is the authors’ contention that prescribing antidepressants without knowing about CYP450 genotypes is like giving blood transfusions without matching for ABO groups [the classification of human blood].”

In general, the psychiatric industry pushes psychotropic drugs without regard to these CYP450 cautions, but this is the direct result of the unscientific psychiatric diagnoses perpetrated by the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) which fraudulently justifies prescribing these harmful drugs for profit in the first place.

Recommendations

1. Practice Full Informed Consent by asking your doctor for information about possible side effects and benefits, ways to treat side effects, and risks of other conditions, as well as information about alternative treatments.

2. If your doctor diagnoses a mental disorder and prescribes a psychiatric drug, ask to see the clinical lab tests proving the diagnosis. (There won’t be any.)

3. All treatment options should include checking for real underlying medical conditions that could cause a patient’s mental or emotional duress.

4. Write your state and federal legislators to establish rights for patients and their insurance companies to receive refunds for mental health treatment which did not achieve the promised result or improvement, or which resulted in proven harm to the individual, thereby ensuring that responsibility lies with the individual practitioner and psychiatric facility rather than the government or its agencies.

5. The Diagnostic and Statistical Manual of Mental Disorders (DSM-5), psychiatry’s billing manual for mental disorders, is the key to false escalating mental illness statistics and psychiatric drug prescriptions and usage worldwide. Untold harm and colossal waste of mental health funds occur because of it. It is imperative that the DSM diagnostic system be abandoned before real mental health reform can occur.

6. Patients, doctors and insurance companies should report all instances of adverse side effects from psychiatric drugs to the FDA.

7. The pernicious influence of psychiatry has wreaked havoc throughout society, especially in hospitals, educational systems and prisons. Citizens groups and responsible government officials should work together to expose and abolish psychiatry’s hidden manipulation of society for profit.

FDA Reclassification of Electroconvulsive Therapy Devices

A new rule by the Food and Drug Administration (FDA) went into effect on 12/26/2018 that reclassifies certain uses of ECT machines from Class III (high risk) to Class II (moderate risk).

Although the FDA solicited comments regarding the use of ECT, many of which described the harm done by ECT and were against the reclassification of ECT devices, the FDA does not consider such comments to be valid scientific evidence, and basically ignored them.
Contrary to the psychiatric community’s position, the FDA is supposed to recognize “reports of significant human experience with a marketed device” as a form of valid scientific evidence.

The new rule is somewhat complicated, and has some “ifs, ands and buts” that require some explanation. Here is the actual rule:

The FDA reclassifies the electroconvulsive therapy (ECT) device from Class III to Class II for use in treating catatonia or a severe major depressive episode associated with major depressive disorder or bipolar disorder in patients age 13 years and older who are treatment-resistant or who require a rapid response due to the severity of their psychiatric or medical condition; and requires the filing of a premarket approval (PMA) application or a notice of completion of a product development protocol (PDP) for all other uses of ECT.

Practically speaking, Class III means that a device presents a high risk of illness or injury to the patient and requires a premarket approval or product development protocol. A PMA is documentation which demonstrates the safety and effectiveness of the device before it can be sold and used. A PDP is documentation which demonstrates the clinical evaluation of a device and the development of necessary information for marketing approval; it may not involve actual clinical testing.

Practically speaking, Class II means that a device presents a moderate risk of illness or injury to the patient, and may require special labeling. Powered wheelchairs, x-ray machines and condoms fall under this category. Special labeling for ECT machines includes warnings that “ECT device use may be associated with: Disorientation, confusion, and memory problems” and “When used as intended this device provides short-term relief of symptoms. The long-term safety and effectiveness of ECT treatment has not been demonstrated.”

While the FDA acknowledges that the individuals for whom ECT therapy may be prescribed are at significant risk for complications, they are effectively ignoring these complications at the urging of the psychiatric industry, and doing so with a lot of psychobabble and pseudoscience, and the expectation that putting warning labels on the devices is protection enough.

Here are some facts which the FDA does not want you to know

In the forty years that the ECT device manufacturers have had the device on the market they have never conducted a clinical trial to support its safety and efficacy from which they have profited.

The procedure administers up to 460 volts of electricity through the brain causing a grand mal seizure.

Adverse effects from ECT include: irregular heartbeat; heart attack; stroke; cognition and memory impairment [sometimes permanent]; dental or oral trauma and physical trauma; manic symptoms; prolonged seizures; worsening of psychiatric symptoms and death.

Based on a 0.3% death rate found with ECT administered in Texas, an estimated 300 people receiving ECT may die each year in the U.S. and 3,000 worldwide.

Claims that ECT is safe and effective are not supported by clinical science and its use remains a theoretical practice with no conclusive mechanism determined to prove how ECT works. We have repeatedly suggested that psychiatrists stick their finger into an electric wall socket to see how well that works. So far, we have no takers.

ECT is not a cure. There is a high failure (relapse) rate within six months of receiving ECT, requiring more electroshock that creates more damage. Called “continuation” and “maintenance ECT,” antidepressants and/or other psychotropic drugs continue to be administered — the very drugs said to have failed, “requiring” ECT. A person might as well smack their thumb with a hammer, since this will take their mind off their mental troubles with less permanent damage than smacking their brain with electricity. (We’re not actually recommending this! Please do not try this at home!)

We do, however, recommend that a person consult a competent, non-psychiatric medical doctor for a thorough physical examination to determine whether an underlying, undiagnosed and untreated physical problem is causing the mental condition.

Pregnant women are electroshocked as late as their third trimester, despite adverse events that include miscarriage, premature labor, stillbirth, fetal heart problems and malformations.

In some countries children aged six and younger (U.S., Australia, and Canada) are electroshocked, damaging their developing brain and body. Psychiatrists are continually pushing the boundaries on whom they can shock. One of the current efforts is called external Trigeminal Nerve Stimulation (eTNS), where an electric current is sent into the brains of children as young as 7 years old.

A 2017 published review of more than 90 ECT studies since 2009 showed they remain “methodologically flawed” and “Given the well-documented high risk of persistent memory dysfunction, the cost-benefit analysis for ECT remains so poor that its use cannot be scientifically, or ethically, justified.”

In 2005 and again in 2015, the World Health Organization (WHO) warned against electroshocking children, and reported: “In addition to inappropriate use of medication, children with psychosocial disabilities in institutions around the world are subjected to other severe forms of inappropriate treatment such as electroconvulsive therapy (ECT, also known as electric shock therapy). WHO has stated that there are no indications for the use of ECT on minors, and hence this should be prohibited. The United Nations Special Rapporteur on torture and other cruel, inhuman or degrading treatment or punishment has remarked that ECT without anaesthesia, muscle relaxant or oxygenation amounts to torture. However, monitoring efforts worldwide continue to uncover instances of ECT being administered to children and adolescents.”

The FDA and state and federal legislators must put patient protection above the financial interests of companies that have failed to conduct clinical trials and provide a PMA for 40 years.

Write your state and federal legislators and tell them to ban ECT. For more information go to http://www.cchrstl.org/ect.shtml.

Shock and Awe – the Latest Psychiatric Abuse of Children

Shock and Awe is a tactic based on the use of overwhelming power and spectacular displays of force to paralyze an enemy.

Now the psychiatric industry is introducing electrical “stimulation” of children’s brains as a socially acceptable gradient to just plain shocking them into good behavior.

The U.S. Food and Drug Administration (FDA) approved on April 19, 2019 a medical device for so-called attention deficit hyperactivity disorder (ADHD). The prescription-only device, called the Monarch external Trigeminal Nerve Stimulation (eTNS) System from NeuroSigma, is for patients ages 7 to 12 years old who are not currently taking prescription ADHD drugs. It was originally developed at the University of California, Los Angeles, to reduce epileptic seizures. Research continues on using eTNS for epilepsy, depression, migraine, PTSD, and ADHD.

This device delivers an electric current to the brain (through the V1 branch of the 5th cranial nerve) with an electrode taped to the forehead. It costs about $900 to start, with additional costs for more of the electrode patches which are only used once each. It is not currently reimbursed by insurance.

While the exact mechanism of how eTNS is supposed to work is not known, one physical effect is apparently to increase blood flow in certain areas of the brain and decrease it in others. They recommend using it daily for up to four weeks before any significant changes are observed; we could not find any information about long-term effects or whether any changes are observed after treatment is stopped. It was clinically tested in 2017 in the U.S. for this FDA approval, paid for by a grant from the U.S. National Institute of Mental Health, on 62 children for four weeks. The most common side effects observed were drowsiness, an increase in appetite, trouble sleeping, teeth clenching, headache and fatigue.

Results were recorded during clinical testing by asking the child to answer questions on the ADHD Rating Scale (ADHD-RS) such as whether they have difficulty paying attention or regularly interrupt others. Ratings of ADHD symptoms on various rating scales are entirely subjective, as are the diagnostic criteria for ADHD.

A prior feasibility study in 2015 was performed with 24 children for 8 weeks, using the ADHD-IV Rating Scale. It did not establish the durability of treatment effects following discontinuation of treatment, either.

To be blunt, ADHD is a fraudulent “disease.” In 1987, ADHD was literally voted into existence by a show of hands of American Psychiatric Association members and included in the Diagnostic and Statistical Manual of Mental Disorders (DSM-V). Within a year, 500,000 children in America alone were diagnosed with this, and to expand the client base it has also been associated with Asperger syndrome and Autism spectrum disorder.

ADHD actually represents the spontaneous behaviors of normal children. When these behaviors become age-inappropriate, excessive or disruptive, the potential causes are limitless, including: boredom, poor teaching, inconsistent discipline at home, reading difficulty, tiredness, street drugs, nutritional deficiency, toxic overload, bullying, abuse, stress, and many kinds of underlying physical illness.

By making an ADHD diagnosis, we ignore and stop looking for what is really going on with the child. These children need the adults in their lives to give them additional attention and to find and treat the actual causes, rather than shock their brains to see if that “works.”

There are no workable ADHD drugs, either for children or for adults. This new “treatment” is supposed to be appealing because it does not use drugs, but guess what? They don’t know how it is supposed to work, either; and they haven’t tested it long enough to know the consequences of running an electric current into a child’s brain.

Aw shucks, no one denies that children can have difficult problems in their lives. Mental health care is therefore both valid and necessary. However, the emphasis must be on workable mental healing methods that improve and strengthen them by restoring personal strength, ability, competence, confidence, stability, responsibility and spiritual well-being. Psychiatric treatments are not workable; they are designed, with shock and awe, to overwhelm.

Involuntary Commitment Under Another Name

The Acting Cook County Illinois Public Guardian filed a class-action lawsuit (Golbert et al v. Walker et al) December 13, 2018 on behalf of hundreds of children and teenagers in state care who have been held in psychiatric hospitals after they had been cleared by doctors for release, calling the practice inhumane and unconstitutional.

The lawsuit follows a ProPublica Illinois investigation that found nearly 30 percent of children in DCFS care who were sent to psychiatric hospitals between 2015 and 2017 were held there after doctors had cleared them for discharge.

It may not legally be Involuntary Commitment, but it has the same harmful physical and emotional effects. Some children were sexually exploited.

Every 1¼ minutes, someone in the U.S. becomes the next victim of involuntary incarceration in a psychiatric hospital. And there’s nothing they can do about it.

With health care eating up vast amounts of our national budget, the first spending cut to make is the cost of “treating” people who prefer not to be mentally treated or whose treatment is no longer necessary. Involuntary incarceration hikes federal, state, county, city and private health care costs under the strange circumstance of a patient–recipient who is not allowed to leave when treatment is over. ProPublica Illinois found that DCFS spent nearly $7 million on medically unnecessary hospitalizations between 2015 and 2017.

Read more about this here.

Knock Yourself Out with Spravato (Esketamine)

A nasal spray version of the anesthetic drug ketamine was approved by the FDA on March 5, 2019 for treatment-resistant depression.

Janssen Pharmaceuticals says that the cost for a one-month course of treatment for Spravato (generic esketamine) will be between $4,720 and $6,785.

Esketamine is the S-enantiomer of ketamine, which means that it is one of the two mirror images of the chemical structure of ketamine, S (for the Latin sinister) being the left image. It enhances glutamine release in the brain. Glutamine is an amino acid used in the synthesis of proteins, among other things. In the brain, glutamine is used in the production of neurotransmitters. It is believed that glutamine plays a role in raising or lowering aggression levels.

Treatment requires that doses be taken, in conjunction with an oral antidepressant, in a doctor’s office or clinic, with patients monitored for at least two hours, and their experience entered in a registry.

Because of the risk of serious adverse outcomes and the potential for abuse and misuse of the drug, it is only available through a restricted distribution system. At least you can’t take it home with you.

The Spravato labeling contains a Boxed Warning that cautions that patients are at risk for sedation and difficulty with attention, judgment and thinking (dissociation), abuse and misuse, and suicidal thoughts and behaviors after administration of the drug.

Basically, it knocks you out so you don’t feel so depressed anymore. You don’t feel much of anything, actually, since you’ve just taken an anesthetic in the snout.

There were four phase 3 clinical trials; two of them failed to show any statistical improvement, but the drug was approved anyway because it was on the Fast Track and Breakthrough Therapy paths.

A 9/5/2018 update from Consumer Reports said, “All these drugs [Ketamine, Phenylbutazone, Chloramphenicol] are prohibited in beef, poultry, and pork consumed in the U.S. Yet government data obtained by Consumer Reports suggest that trace amounts of these and other banned or severely restricted drugs may appear in the U.S. meat supply more often than was previously known.”

Note that “depression” is not an actual medical illness; it is simply a symptom of some undiagnosed and untreated condition. A diagnosis of depression is a prime example of psychiatric fraud.

Any form of ketamine used to treat so-called depression is unethical and harmful, since it precludes the patient from finding out what is actually wrong and getting that treated. Psychiatrists pushing ketamine or esketamine are shameful drug pushers who are making a buck off people’s misfortune.

Go here for more information about alternatives to drugs.

Human Rights in the Mental Health Care Industry

The United Nations Sustainable Development Goal number 3.4 says, “By 2030, reduce by one third premature mortality from non-communicable diseases through prevention and treatment and promote mental health and well-being.” This is certainly a laudable goal.

We are particularly interested in promoting mental health and well-being. The United Nations measures its success with this goal by reducing the suicide mortality rate. We think this is a useful measure.

Unfortunately, the current “standard of care” in the psychiatric mental health industry heavily promotes and prescribes harmful and addictive psychotropic drugs which are known to cause violence and suicide, exactly the opposite of this goal. How might we engage to counter this sorry state of affairs?

CCHR To The Rescue

The Citizens Commission on Human Rights® (CCHR) is a non-profit watchdog organization whose purpose is to restore human rights to the field of mental health by ensuring that criminal abuses are speedily investigated and prosecuted and that people’s rights are legally protected. CCHR was founded in 1969 by the late Professor of Psychiatry Emeritus Dr. Thomas Szasz and the Church of Scientology. The CCHR St. Louis chapter was incorporated in 1989 in Missouri.

The mission of CCHR is to investigate, expose and eradicate violations of human rights by the field of psychiatry. To be sure, CCHR’s investigations over the last 50 years have consistently shown that the field of psychiatry itself is a human rights violation.

By depicting those they label mentally ill as a danger to themselves or others, psychiatrists have convinced governments and courts that depriving such individuals of their liberty is mandatory for the safety of all concerned. Wherever psychiatry has succeeded in this campaign, extreme abuses of human rights have resulted.

Through the broad dissemination of CCHR’s internet sites, documentary videos, books, newsletters, booklets and pamphlets, more and more patients, families, professionals, lawmakers and countless others are becoming educated on the truth about psychiatric fraud and abuse, and that effective action can and should be taken.

Has Your Life, or The Life of Someone in Your Family, Been Affected by Fraud or Abuse in the Mental Health Industry?

Here are some examples of psychiatric fraud and abuse:

No Mental Health Help When Needed
ElectroConvulsive Therapy (ECT, Electroshock)
Harmful and Addictive Psychiatric Drugs
Suicide
Violence
Involuntary Commitment
Being Threatened with Involuntary Commitment or Punishment for Refusal of Treatment
Being Coerced into Hospitalization or Treatment
Treatment Without Prior Informed Consent
Medical Kidnapping
Forcible Removal of Children to Foster Care
Forcible Drugging of Foster Children
Misdiagnosis
Sexual Assault
Elderly Abuse
Insurance Fraud
Forcible Restraints
Psycho-Surgery
Transcranial Magnetic Stimulation
Deep Brain Stimulation
Vagus Nerve Stimulation

Tell us how this has affected you. Report psychiatric Abuse. It’s a Crime.

Press Release – CCHR STL Visits Missouri State Capitol

Jefferson City, Missouri – February 6, 2019

Citizens Commission on Human Rights, founded in 1969 by the Church of Scientology and the late psychiatrist Dr. Thomas Szasz, has been vigilant in exposing the lack of science behind psychiatry’s diagnostic methods and treatments that, left unquestioned for years by authorities and insurance companies, led to soaring increases in both health care costs and the prescription of dangerous and addictive psychiatric drugs.

It is time for the Missouri legislature to put an end to this lucrative scam and thereby help protect our citizens. Instead put our citizen’s money into proven physical health care and education, where it will produce real results. An example of a real positive result would be: patients recovering and being sent, sane, back into society as productive individuals. The introduction and passage of legislation designed to curb psychiatric fraud and abuse can contribute much to this effort.

To this end, CCHR St. Louis once again visited the Missouri State Capitol in Jefferson City February 5 and 6, 2019, and set up a display in the Capitol Building, talking to legislators and their aides about fraud and abuse in the mental health care system.

Volunteers personally visited with many Representatives and Senators, distributing packages containing the CCHR documentary DVD “Making A Killing – The Untold Story of Psychotropic Drugging” (MAK) and explanatory materials about harmful electroconvulsive therapy (ECT) and the over-drugging of foster children.

The MAK documentary exposes the problem of psychotropic drugs, the profits they generate and the harm they do. CCHR recommends investigating the link between psychotropic drugs and the sharp rise in violence and suicide.

Claims that ECT is safe and effective are not supported by clinical science and its use remains a theoretical practice with no conclusive mechanism determined to prove how ECT works. CCHR recommends outlawing this barbaric practice.

In Missouri as well as nationwide, there is a significant problem over-drugging foster care children with harmful and addictive psychotropic drugs. CCHR recommends legislation to develop explicit foster children’s rights.

Legislators welcome the contact, so contact them, let them know you appreciate what they do, and make specific suggestions to correct the egregious abuses of the psychiatric industry in Missouri. Subscribe to the CCHR STL newsletter so you receive our legislative take-action alerts.

The Truth About ECT

TruthAboutECT.org is a blog site created to bring about public awareness of the dangers of electroconvulsive therapy (also known as electroshock or ECT).

Most people don’t believe that electroshock is still being used in modern society. This is most likely because the mere idea of electroshock is so abhorrent that most people simply can’t believe it’s still being used.

Factually, ECT is one of the most brutal “treatments” ever inflicted upon individuals under the guise of mental health care. Yet approximately one million people worldwide, including an estimated 100,000 Americans, are given electroshock each year, including the elderly, pregnant women and children.

The Washington University in St. Louis psychiatrists at Barnes-Jewish Hospital give 2,000 shock treatments per year, including to pregnant women.

The articles on this website are written by those who have either experienced the damaging effects of ECT or those who are medical professionals who have seen the damage caused by it.

ECT is a Violation of Human Rights

On December 3, 2018, the Inter-American Commission on Human Rights of The Organization of American States published a Precautionary Measure calling for the Judge Rotenberg Educational Center in Canton, Massachusetts to immediately cease electroshocking children as a disciplinary measure, emphasizing that electroshock is a gross violation of human rights.

A November, 2018 Supreme Court decision in Victoria, Australia ruled that the forcible use of electroshock treatment violates patients’ human rights, saying “People with mental illness are highly vulnerable to interference with the exercise of their human rights, especially their right to self-determination, to be free of non-consensual medical treatment and to personal inviolability.” While the decision reinforces that electroshock given without consent is a human rights violation, the entire practice of ECT is a human rights violation and should be banned.

If you would like to report a psychiatric abuse, please fill out the abuse reporting form by clicking here.

If you would like to write about your own horrifying electroshock experience, click here.

For more information about the devastating effects of ECT, click here.

Shocking New Psychiatric Abuse – Deep Brain Stimulation

Would you let a psychiatrist poke wires directly into your brain and turn on the current?

Deep Brain Stimulation (DBS) is a process where electrical shocks are delivered directly into the brain by wires inserted into holes bored into the skull.

The psychiatrists conducting research on DBS say that this “reflects a move away from the long-held view that depression is caused by a chemical imbalance in the brain.”

In other words, some psychiatrists are now admitting that the chemical imbalance theory is bogus, and they are desperately trying to find other treatments, because too many people are now wise to the chemical imbalance fraud.

Unfortunately, DBS is just another harmful fraud, because “it’s unclear whether the stimulation can produce long-lasting changes,” and “Despite the widespread use of DBS in clinical and research applications, the mechanisms by which focal brain stimulation modulates network activity to produce complex behavioral changes remain largely unknown.”

In response to this alarming and abusive “therapy” the Citizens Commission of Human Rights calls for victims to report abuse suffered during this or any other psychiatric treatment.

No one denies that people can have difficult problems in their lives, that at times they can be mentally unstable. Unfortunately, not only do psychiatrists not understand the etiology (cause) of any mental disorder, they cannot cure them. In effect, psychiatrists are still saying that mental problems are incurable and that the afflicted are condemned to lifelong suffering.

Psychiatric treatments such as DBS, however, are unworkable and dangerous, and while they may temporarily mask some symptoms they do not treat, correct or cure any physical disease or condition; and by calling this a “treatment” they preclude finding out the real underlying causes of the condition and treating that with real, workable medical therapies.

New high-tech “treatments” for the brain will continue to be used to create the appearance of scientific progress, but in the end, psychiatry will be no closer to identifying any causes or effecting any cures; instead, their betrayal and brutality in the name of mental health continues. Psychiatry has proven only one thing — without the protection of basic human rights, there can only be diminished mental health.

Persons in desperate circumstances must be provided proper and effective medical care. The correct action on a seriously mentally disturbed person is a full, searching clinical examination by a competent medical, not psychiatric, doctor to discover and treat the true cause of the problem.

Click here for more information about the brutal reality of abusive psychiatric practices such as electroshock, deep brain stimulation, and psychosurgery.