Citizens Commission on Human Rights® of Colorado

Relatives and friends across 22 countries describe memory loss, cognitive decline, disability and death following electroshock “treatment,” with many saying their loved ones’ lives were permanently destroyed.

The U.S. Department of Health and Human Services announced its intention to shift the standard of care toward prevention and a more holistic approach to mental health.

In a landmark shift in mental health priorities, the U.S. Department of Health and Human Services (HHS) yesterday launched an action plan designed to de-emphasize the prescribing of psychiatric drugs, ensure fully informed consent, support patients’ tapering off the drugs, and promote evidenced-based nondrug approaches to mental health.

In announcing HHS’s new direction, HHS Secretary Robert F. Kennedy, Jr., said: “Today, we take clear and decisive action to confront our nation’s mental health crisis by addressing the overuse of psychiatric medications—especially among children.  We will support patient autonomy, require informed consent and shared decision-making, and shift the standard of care toward prevention, transparency, and a more holistic approach to mental health.”

A stated aim is to curb the prescribing of psychiatric drugs.  “Through a multipronged approach including education and outreach, program and policy actions, and research-to-practice efforts, HHS is working to prevent the unnecessary initiation of psychiatric medications and support the tapering and discontinuation for patients not experiencing clinical benefit,” HHS announced.

HHS intends to bring more scrutiny to the harms of psychiatric drugs and the benefits of alternative mental health treatments.  “HHS agencies are bringing together their collective expertise and aligning to evaluate prescription patterns for psychiatric medications, their benefits and potential harms, and elevate the role of nonmedication treatments and scalable, evidence-based solutions to improve mental health.”

In a so-called “Dear Colleague Letter” published yesterday to notify mental health providers of this seismic shift in orientation towards mental health treatment, HHS wrote that it was “emphasiz[ing] the importance of ensuring that treatment planning for mental health conditions includes meaningful access to evidence-based non-pharmacological interventions.”

Continue reading…

A new large-scale study scrutinizing psychiatric prescribing finds clinicians continue to give high-risk drugs to Medicare dementia patients—most of the time with no documented justification at all.

WARNING: Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. —Food and Drug Administration

For decades, clinical guidelines have warned against prescribing brain-altering drugs like antidepressants and antipsychotics to dementia patients. Yet the practice persists.

And a new study published in the Journal of the American Medical Association (JAMA) reports that clinicians prescribe these drugs to roughly 25 percent of Medicare beneficiaries diagnosed with dementia.

That means one in four elderly Medicare beneficiaries with diagnosed dementia take pills known to carry serious risks, which can leave older adults drowsy and confused, unsteady on their feet and more prone to falls.

In the worst case, antipsychotics can even cause death, according to FDA warnings.

Clinicians were about twice as likely to prescribe psychotropics when there was no documented reason whatsoever than when there was one.

The study found doctors prescribed these drugs to over two-thirds of patients without any documented justification—no condition, symptom or circumstance that would justify prescribing the drugs—despite their known dangers. In other words, clinicians were about twice as likely to prescribe psychotropics when there was no documented reason whatsoever than when there was one.

“You would think it would be the opposite,” said Harvard Medical School’s Anupam Jena, a professor of health care policy.

No kidding.

The study’s senior author, Dr. John N. Mafi, was even more direct. Authorizing dangerous drugs without even so much as a purported justification to such a wide population of often helpless individuals can constitute, as he puts it, “inappropriate and harmful prescribing.”

These are “not trivial drugs,” he added. Some “actually have an FDA black box warning because they almost double the risk of death in patients with dementia.”

As people age, their ability to metabolize drugs changes, and they become more “susceptible to the toxicities of drugs,” Mafi explained. Older adults also tend to take multiple medications, increasing the risk of dangerous interactions.

Continue reading…

Researchers tracked more than 1,000 Australian infants and found children whose mothers used antidepressants in the last three months of pregnancy had up to nine times higher odds of developing autism.

At two months old, he didn’t babble or laugh or respond to any affection.

At 6 years old, he stared through you while you were talking, or fixed his eyes on some distant point above and beyond as if he were watching a plane passing by.

At 8 years old, he often flapped his hands or rocked back and forth for no apparent reason, ignoring attempts to intervene.

This is autism—a condition affecting brain development that can influence communication, social interaction and behavior.

It can also break a parent’s heart.

The message is clear: If you want a healthy baby, don’t take antidepressants during pregnancy.

And now, an Australian study reveals that a mother’s choices during pregnancy can dramatically increase the odds that her child will become autistic. Mothers who used SSRI or SNRI antidepressants during the last three months of pregnancy gave birth to children with nine times higher odds of autism compared to those who did not use the drugs.

So, if that’s what happens if you consume these drugs in the last three months of pregnancy, is it safe to take them during the first six months?

Only if you consider a 6.43 times higher risk of autism for your baby “acceptable.”

Researchers arrived at their conclusions after analyzing data from the Barwon Infant Study, an ongoing long-term research project that follows more than 1,000 children born in the Barwon region of the Australian state of Victoria between 2010 and 2013, tracking their health outcomes over time.

The data leaves little room for doubt. Higher antidepressant use during pregnancy is consistently linked to dramatically higher rates of autism.

And the message is clear: If you want a healthy baby, don’t take antidepressants during pregnancy.

The researchers, however, are cautious. They identify a series of other potential factors that could also influence their findings—including nutrition, air pollution and vinyl flooring.

But the numbers tell a different story.

A US Department of Health and Human Services press release last spring declares, “Autism Epidemic Runs Rampant.”

The article continues: “One in 31 American children born in 2014 [is] disabled by autism. That’s up significantly from two years earlier and nearly five times higher than when the CDC first started running autism surveys in children born in 1992. Prevalence for boys is an astounding 1 in 20, and in California, it’s 1 in 12.5.”

The obvious conclusion is that if autism has nearly quintupled since, then whatever was an active factor in creating autism must also have nearly quintupled over the same period.

Did the vinyl flooring industry boom nearly five times over since that year?

No, but something else did.

That “something else” entered the psychiatric armory in the late 1980s and exploded in popularity almost overnight: “modern” SSRI antidepressants.

Continue reading…

Long‑term use of common psychiatric drugs like Xanax and Valium can trigger a newly recognized condition that leaves users with years of fatigue, anxiety and cognitive damage.

Xanax, Valium, Librium, Ativan, Klonopin, Restoril.

On the street, they’re called “benzos”—psychiatric drugs that promise to reduce anxiety by slowing brain activity.

Considered “minor” tranquilizers (unlike antipsychotics, which are “major”), they are so culturally ubiquitous that in the Burt Reynolds film Starting Over, a character asks, “Does anyone have a Valium?” and every woman pulls out a pill bottle to offer one.

But benzos are no laughing matter. Only recently have researchers begun to document the extent of the prolonged and often devastating symptoms some users experience after stopping benzos.

“It takes everything in me to appear normal.… It was a nightmare. My brain has not been the same.”

A team at the University of Nebraska Medical Center recently reported a new disturbing condition resulting from long-term use.

They described a 57-year-old man with a 40-year benzo habit—originally begun to manage alcohol addiction, depression and anxiety. When he finally quit, he suffered debilitating fatigue, brain fog, uncontrollable anxiety, overwhelming emotional distress and panic far beyond the typical two-week withdrawal window.

His condition set off alarm bells for researchers, who recognized they were seeing benzodiazepine addiction as well as persistent damage to the nervous system, which they refer to as Benzodiazepine-Induced Neurologic Dysfunction (BIND).

BIND is real, underdiagnosed and dangerous. “While acute benzodiazepine withdrawal is well characterized, typically emerging within days and resolving in under two weeks, some patients experience prolonged symptoms such as fatigue, impaired concentration and anxiety that persist well past this time frame,” researchers wrote.

For patients trying to leave benzos behind, the road is long and grueling, The New York Times reported: “Many then get cut off from their medication or taper too quickly, and face dangerous and potentially life-threatening withdrawal symptoms that can linger long after the drugs are discontinued.”

The American Society of Addiction Medicine recommends lengthy tapering procedures, sometimes lasting more than a year, with monitoring even after the drug is fully stopped. Yet weaning millions of Americans off benzos is daunting: The FDA reports over 92 million prescriptions filled in 2019 alone.

Going cold turkey is often neither effective nor safe.

The human toll is severe. Tasha Hedges quit Xanax after 20 years and suffered hot flashes, cold sweats, restless legs, shaking and teeth grinding. Years later, she said: “It takes everything in me to appear normal.… It was a nightmare. My brain has not been the same.”

A University of Colorado Anschutz Medical Campus survey of 1,207 benzo users—63.2 percent still taking, 24.4 percent tapering, 11.3 percent fully off—found shocking results: 54.4 percent reported suicidal thoughts or attempts. Symptoms often lasted over a year, including low energy, memory loss, anxiety, insomnia, sensitivity to light and sound, digestive issues, muscle weakness and body pain. Over 40 percent reported 17 or more ongoing symptoms at least a year after quitting.

Dr. Christy Huff, one of the researchers and a former benzo user herself, explained: “Patients have been reporting long-term effects from benzodiazepines for over 60 years.… Even though I took my medication as prescribed, I still experience symptoms on a daily basis at four years off benzodiazepines.”

Continue reading…