Comments by Ann Bracken

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  • The lies about ECT are legion—I think doctors simply cannot see that “treatment resistant depression” is simply showing that they are using the wrong treatment. My mother endured 37 ECT “treatments” in the 60s and 70s, and the doctor did them in his office. I am just sickened at the thought of what she went through. I had several ECT treatments in the 90s because I was depressed and kept telling the doctors that I couldn’t feel anything, so I wanted to die. I now believe I had a clear case of psychic numbing, and the doctors should have recognized the symptoms. But they remain locked in their model of more is better and force is the ultimate way through. Stay far away from psychiatrists.

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  • Banning, thank you for sharing your story with Amy and all of us at Mad in America. I was heartsick reading about your treatment, especially the insane chair sitting in a corner and the girls tied to the bed for 18 months. I simply cannot imagine carrying out those kinds of actions which so obviously harm a fellow human. But I come from working in special education where many folks have a very limited understanding of behavior management. When people resort to extreme punishment, they employ “command and control” rather than understanding and compassion—both of which take much more skill and time.

    I am glad that you wrote your book and are speaking out about the troubled teen industry. I also worked in a school in a psych hospital and my heart breaks whenever I think of the kids I worked with and what they must have endured. It was a dark place on many levels.

    Blessings to you in your wonderful work as a guide. Yosemite is a magical place, and I’m sure it’s healing for many folks to work with you. I love you story of crossing the river—so true.

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  • Thank you, Amy, for letting me and my readers know about this initiative . What a great thing to do with opioid settlement money. I going to read more about Goldfinch Health. So many people think the only victims of the opioid crisis are those who become addicted or who overdose…..but so often, that road starts with a prescription for post-surgical pain. Love the proactive approach!

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  • Dear Miranda,

    I greatly appreciated your help in writing my essay for Mad in the Family last year, and I’ve been impressed with all the work you contributed to MIA. You will be missed, but I look forward to learning about your newest ventures. Sadly, I’m not on Twitter or Mastadon, but I’m sure I’ll find you along the way!

    All the best,
    Ann Bracken

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  • Thank you, Bob and Ole Andreas, for this enlightening interview. Even though the hospital is in some jeopardy, you’ve done a magnificent job with helping people to recover and live productive and happy lives—which is more than our hospitals can boast. I’d love to see more hospitals like the Lake Hurdal Recovery Center proliferate around the world, and I understand the complexities of starting and maintaining such facilities. But every day I have friends and relatives who have family members in need of the care you can provide, but instead, they are consigned to harmful drug regimens, locked wards, and generic forms of therapy. With your work and this interview, you’re shining a light on what’s possible. Thank you both!

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  • HI Kathleen, Thanks for sharing your story, and I’m so very sorry to hear about the harm ECT has done to you. You’re so right–that the very drugs you were taking numbed you out and even likely caused suicidal thoughts and feelings. The willfull blindness of doctors to their patients’ stories and their refusal to consider other ways of treatment lead them to rely on the brutality of running electrical currents through the brain. Just once, I’d be so grateful if instead of labeling a patient as “treatment resistant”, the doctor would say “Maybe we’re using the wrong treatment.” Yes, the drugs and the brutal treatments like ECT, TMS, and ketamine infusions are the problem. Keep speaking out and thank you for your thoughtful essay and for your clear voice as a psych survivor.

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  • Thank you, Angie, for your thoughtful and well-written essay. Yes, you get to the heart of the matter when you say that the psychiatric community has long ignored deprescribing as a strategy—-it’s mind boggling how doctors never seem to consider that maybe the drugs are causing harm rather than helping people. Yes, we need psychiatry to get on board with deprescribing and with more responsible tapering, but I am so grateful all of the online forums exist and that you are out there working to guide people through the process of getting off psych drugs. Kudos to you for your work!

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  • I don’t know where this idea came from–giving kids “tickets” and fines for what are usually considered routine behaviors and used to be handled in-house by the admins, teachers, and parents. We should not have any law enforcement officials involved in routine school discipline, and even though I never personally witnessed a “school resource officer” –AKA a cop–discipline students in the high schools where I taught, I know such events happen routinely all over the country.

    Surveilling kids and throwing them into the court system does nothing to help a kid learn self-management skills or deal with the reasons why they’re so disaffected in the first place. Our schools need to be more nurturing and welcoming. Time for a paradigm change!

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  • So someone who is feeling depressed or anxious is considered mentally impaired? And telling untrue stories is standard practice in psychiatry? What hubris. I had to keep reading to see if you were actually serious. I found your defense of psychiatric drugs smug and self-serving.

    “And telling stories they know are or may be untrue has become standard practice in psychiatry. After all, we are dealing with mentally impaired patients; we know better than they what is best for them.”

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  • So many things I could comment on….but as a reader and someone who values supporting an argument with research, I’d say your writing and report win over anything the APA has to say. One thing that makes this debate about informed consent and revealing the absolute truth about the research on drug & ECT/TMS efficacy is that as a medical specialty, psychiatrists have more power than any other kind of doctor. They can forcibly have you committed to a facility, make you go to court to be released, and drug you and give you ECT without your consent. I find all of that power terrifying and believe we need to seriously hold psychiatrists and the APA to account for all the harm they have done.

    Lastly, you are absolutely correct about your rhetorical analysis of the APA website and the use of the statistic in one PP followed by a paragraph on antidepressants. The word treatment in the 1st PP paired with the statistic is misleading and many people would believe the success rate is due to medication, without the APA directly saying it.

    Keep up the great work!

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  • Bob Whitaker, thank you for another stellar article and for the call to action on putting together a class action lawsuit. I’ve written my story and my mother’s of psychiatric mistreatment and would be happy to join in such a lawsuit. How dare psychiatrists try to dismiss the notion that they ever told us we had a chemical imbalance in the brain which caused depression, anxiety, bipolar, etc. Many of us here on MIA were repeatedly told this lie and though we may not have a written record of it, we well remember the experience.

    What I fail to understand is that if there is no evidence of a chemical imbalance in the brain leading to mental health issues, why do psychiatrists continue to prescribe antidepressants which then disrupt brain chemistry? And why do they support brain-damaging “treatments” such as ECT and TMS? Oh, yes, I’m all in!

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  • While I commend Jim Phelps for his more progressive views on the state of psychiatry and the use of the DSM and mind-altering drugs, I have not found his views to be widespread based on recent experiences of family and friends. I know many people who are still being drugged with numerous drugs and told to stay them forever due to “damaged brains” and “chemical imbalances.” And if indeed “most psychiatrists” believe as Jim Phelps does, then why do they continue the extensive use of drugs, ECT, TMS, and Ketamine? It seems to me that as a field, psychiatry continues to hold on to the view that depression and other states have a biological basis and one of their magic bullets is bound to work—-or else the patient is labelled as having a “treatment resistant” condition.

    My psychiatrist told me I had a damaged brain and would be chronically ill if I refused medication. I’m happy to say he was wrong, and I’ve been drug and depression free for over 20 years. Lastly, I know of no friends or family members who have ever been given fully informed consent when told to take psych drugs. One friend who was recently hospitalized asked me “What’s informed consent?” That’s why so many of us are here at MIA—we’ve experienced the dark side of psychiatry and are happy to explore other options.

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  • HI Sera, Thanks for your very thoughtful and informative critique of the comments on the NYT article. I was actually quite happy to see them print something that tells a different story about meds and hearing voices. The comments seem to reflect how thoroughly brainwashed people are about “dangerous” others and what a good job pharma has done with obscuring the facts about their poisons.

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  • Dear Ryan, Bravo for you and your courageous journey. Your determination and fortitude got you out of the hell of turning to shrinks for help……and I do think anyone who would give someone over 100 ECT treatments is negligent. I’m glad that you’re writing and think you did a wonderful job chronicling your story. Here’s to finding your way out of the psychiatric hamster-wheel…….

    I have a story of overmedication and recovery that will be out in the fall. What I discovered in going through my mother’s records is that the drugs the docs gave her most likely kept her locked in depression and anxiety for over 40 years. This madness has gone on for far too long.

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  • Miranda, thank you for sharing a part of your story and for your thoughtful review and critique of the film Just Like You. My heart aches every time I hear someone on the news talk about the “teen mental health” crisis, and they act like problems with anxiety and depression come out of nowhere. There’s always a reason why someone becomes anxious or feels depressed and instead of offering compassion, careful listening, and support, our society tells people there is something wrong with their brains. At the rate this “brain disease” is sweeping across our country, it’s a wonder anyone is surviving.

    I experienced a traumatic event when I was a young teen and managed to push my way through the dense fog of depression and anxiety and move on with my life. As a teen, I would hear been devastated if a doctor had told me there was something wrong with my brain.

    Thanks for your continuing advocacy for kids and families and for your insightful and thoughtful writing.

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  • The hubris of this new diagnosis is almost impossible to fathom. And I knew a new drug–or use for a drug–would follow right behind the diagnosis. I say stay away from psychiatrists, find a kind and compassionate counselor, and surround yourself with loving friends and family. How dare they think they can determine how long anyone should grieve?

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  • Hi Kevin, thank you for your kind words about my essay. I’m so glad that what I had to say was meaningful to you. And I’m equally sorry that you had to endure being medicated with Ritalin during your developing years. We need to shift our perspective in how we view our children and our students. There is no one way to behave and learn that constitutes normal. The irony is that teachers are always directed to “individualize” lessons and create meaningful experiences. We need to see our students the same way–as young individuals with their own particular backpack of needs, worries, hopes, and challenges.

    I refuse to hand the drug industry a victory even though I am well aware of how thoroughly accepted medicating children has become. We need to change the environment to meet the children’s needs, not change the children to meet our needs.

    There are so many of us singing a new song, I just have to hold on to hope!

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  • Hi Rebel, I are with you that the stimulant drugs are dangerous no matter what we use them for and they should NOT be given to children. The mindset that says it’s OK to drug kids because they have “ADHD” and they won’t be harmed is the same as the mindset that says you can’t get addicted to opioids if you use them for pain. The drugs have certain fundamental effects no matter who is using them. Honestly, we need a wake-up call as a society—we need to stop looking for “easy” answers in the form of a pill.

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  • Dear Bradford, thank you for your vote of confidence in both my education and my teaching and mothering skills. I think now that I know so much more about the effects of stimulant drugs on both children and adults, I can’t believe how casually we used to recommend them to parents of kids who were somewhat distracted and didn’t finish work—as if those are real obstacles to achievement. To me, part of the problem is a lack of creative thinking.One day standing in front of a high school class, I realized we had tried to change everything but the actual classroom environment. I see kids with “ADHD” as the canaries in the coal mine, indicators of what’s not working in your classroom. It’s the job of the teacher to bring everyone along, and sometimes that means changing up your lesson plans and imagining new ways to deliver your lessons.

    I’m sorry to hear one of your teachers tied you to a chair, but glad that you slipped her trap so easily. What an awful thing to do to a child. We, as a society, need to lift the veil on our use of drugs–psychiatric and stimulants especially–and investigate their effects and all the harm they can do. If we had truly informed consent, I think we’d use far fewer drugs to “help” people manage their behavior or deal with life’s sadnesses.

    As for teaching in college–Alas, I never earned a PhD, so I can’t get hired as more than an adjunct—and that’s another essay. :))

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  • Thank you, yinyang. The more I think about my trajectory as a teacher–and what my daughter is now experiencing as a teacher–I’m struck by how boxed in we are in our thinking. Teachers need to be able to see the children in their rooms as little people who may need something different from sitting all day in rows and doing work on paper. That not all bright kids want to do their work–like my son Connor–who saw no sense in doing tasks he already felt he knew.
    But honestly, teachers and parents need a deep-dive into the effects of stimulant drugs and the actual results of using them. Bob Whitaker and all the folks at MIA are a wonderful resource for beginning that journey.

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  • Dear Lisa, Thank you for sharing your story and Marcello’s. It’s one of the most heartbreaking reads about using psych meds that I’ve come across. You detail the journey so perfectly–that as parents and patients, we have to trust people who seem uninformed themselves, and certainly, when they don’t believe patients, they disempower people.

    I totally agree with you that no one would be drugged against their will, and when people are “noncompliant” with meds, they must have a very good reason–probably self-preservation. No one should have to go through what you have as a family, and I am so sorry for Marcello’s pain. I wish that you’d send this essay to every doc and therapist who “treated” your son so they could face the awful harms they’ve inflicted.

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  • Hi E. Baden, thank you so much for your honesty and your sincere attempts to help people with as few meds as possible. You might want to get in touch with the folks at Medicating Normal https://medicatingnormal.com–a film about the harms of meds with 4 compelling personal stories. Also, check out Adele Framer of Surviving Antidepressants https://www.madinamerica.com/2020/11/surviving-antidepressants-adele-framer/ Many folks who want to come off of psych drugs use her forums for assistance since so few doctors are either willing or able to help people withdraw safely.

    You are right about trauma–past and present–being one of the leading causes of feelings of depression and anxiety. If only more docs were of your mindset, but it’s so hard to go against the grain.

    You’ll find your tribe—and thanks for speaking out.

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  • Thank you, Bob, as always for your measured and thoughtful response to the issues. It is truly mind-boggling how MSM continues to pound away at the medication-is-the answer, despite mountains of evidence in the opposite direction. I will read the Harrow and Jobe study with interest. I have a few family members who carry a “schizophrenia” diagnosis and two of them are nearly completely disabled; the other cousin died a couple of years ago in a very debilitated state. The Irish have a saying that a thin veil separates this world and the next, and I think of that with the mainstream mantra of “drugs are the answer” in opposition to all of the books and research I’ve read. It’s a thin veil…..and how do we break through? I keep hoping, and I know MIA is part of that work. Keep up your wonderful writing and advocacy. Onward!

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  • Thanks so much for this powerful essay on the negative effects of ADHD drugs. What a frightening scenario, and I’m not at all surprised that the ER doc was in denial about the effects of the drug. Most people think if a kid can’t pay attention or is distractible, they need drugs. And most people believe the drugs are safe. We need informed consent around ADHD drugs as much as we need informed consent around psych drugs. And more people need to know about the very short-term usefulness of stimulant drugs. As a special ed teacher, I’ve often thought that we try to change the kid more than we try to change the environment. So often, the kid with ADHD is very bright, very bored, or very troubled.

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  • Sarah, thanks so much for your incredible work to bring the harms of ECT to a broader light. My mother and I both had ECT many times–because doctors told us it was the only way out. I’m fine–as far as I know–but Mom suffered terribly, mostly from memory loss. How anyone thinks provoking a seizure is a good idea is beyond imagining. Your bravery and persistence are much needed and appreciated. Blessings on your work.

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  • Dani, Your story made my heart ache. I’m so sorry for all of the pain you’re enduring and for the awful treatment you received from this psychiatrist. At the very least, you could register a complaint with the FDA adverse activity website—-not sure of the exact name, but TMS sounds an awful lot like ECT minus the seizures—and you had one. I bet seizures are out of the ordinary for adverse reactions. I hope you can find a good ally in your search for healing.

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  • Thank you, Bob, for another thorough and thoughtful essay. I have to say, reading all of this information about the corruption at the FDA as far as approving questionable and dangerous drugs, is it fair to assume that the same practices happen with other classes of drugs—-and vaccines? In relation to vaccines, most people I know are not eager to line up for the new Covid vaccine when it comes to market.

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  • Thank you, Phil, for this powerful and disturbing article about the distorted practices in psychiatry. The very idea of sedating people for weeks and subjecting them to ECT and other “treatments” is horrifying. Any doctor or nurse who would engage in such practices is truly operating outside of human decency. I have read about insulin coma therapy, which I thought was horrible, but this sleep therapy is beyond imagining. And the sexual abuse Bailey engaged in? Truly sick. I was just doing some research on doctors’ attitudes toward patients in the 50s and 60s and I came across a British psychiatrist who defended lobotomy as a legitimate form of treatment. My heart breaks even as I feel enraged.

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  • HI Gail,

    Thanks so much for writing this enlightening essay, and thank you for being a compassionate psychiatrist. It is beyond shocking that so many psychiatrists engage in the mind game of not believing patients because of course, someone who is “mentally ill” doesn’t tell the truth. My heart ached for the men you described, even as I raged inside at the stupidity and arrogance of the psychiatrists and courts. Many years ago when I told my psychiatrist I had stopped taking my meds, he told me I had a damaged brain and would get “sicker” than ever if I stopped the meds. So happy I was secure enough not to listen. To this day, I don’t reveal any past experiences of depression for fear of being boxed and labeled once again. Keep up your wonderful work!

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  • Thanks, Peter, for your wonderful work on this article. As I was reading it, I kept thinking “How can we ever trust any drugs?” The corruption is good to know about, but as ordinary consumers who may need medication, what actions can we take? I remember hearing one researcher say to never take a drug that’s been out less than 5 years…..Any other ideas? Thank goodness for people like Amsterdam.

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  • I was in therapy for 20 years and had about 4 episodes of depression during that time. No one ever mentioned emotional /verbal abuse as a possible cause of the depression. According to what I’ve read in a few places, most of the field of psych workers didn’t recognize verbal abuse as an actual entity until about 1994. I divorced in 2000 and haven’t had an episode of depression since, despite losing both parents, changing jobs, and navigating relationships. Depression always happens for a reason and once you can address its roots, you can find a way out of the darkness.

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  • Thank you, Bob, for sharing Zel’s story. It is heartbreaking to know of his work and his dedication to science and his own suffering due to the drugs that so many of us have been told are the answer to our emotional distress. It is hard to imagine akathisia so bad that one cannot sleep, and that sounds like an awful way to try to live. MIA is doing great work here, and I wish doctors from all over the world would read Zel’s story and face the truth.

    Reading MIA and reading mainstream media info on psych drugs and their efficacy is like living in two different worlds—right next to each other, but so far away. Stories are a powerful way to get at the truth, and Zel’s is powerful, brave, and profoundly sad.

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  • HI Bob, Congratulations on all of the fine work that MIA is doing, and I have no doubt that you are having an impact for the better. This site publishes so many thoughtful and well-researched articles, and there seems to be no end of the variety of topics that are covered. And while some people are convinced to make a change once they learn facts, others need a combination of facts and personal stories, which you provide as well.

    I’m happy to read that the major medical journals are publishing pieces that challenge the old narrative, but in my dealings with friends, I find that kind of information hasn’t filtered down to the average person yet, nor do I see much of the new narrative in mainstream media.

    While the chemical imbalance narrative may have the sound of being scientific, its utter failure to deliver should render it powerless. I take comfort from the work of Masuro Emoto who wrote Messages in the Water. He talks about the idea of morphic resonance and how if something is happening in one part of the world, that energy makes it possible for the phenomenon to happen somewhere else. For example, if “medication-free” treatment is possible in Norway, it’s possible here as well. MIA is helping to build the critical mass that is moving us inexorably to a tipping point where great change can happen. I’m happy to contribute to the fine work everyone at MIA is doing. As I’ve told you before, your book saved my life, and I’m sure countless others as well.

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  • Dear Sam, Thank you for sharing your story with me and for your kind words about my mother, I think she did remarkably well, especially now that i know all she was struggling with. My mother was kind, creative, and courageous, and I so appreciate everything she did for all of us. Yes, I agree, women need a good support system, but that’s not how things were set up bak then—-even now for a lot of people. I agree with you about your dry skin story—OMG, psych docs ar esophaguses hubristic—–and usually don’t really have a clue about human beings.

    Thanks again for sharing with me. All the best, Ann

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  • I’m curious about the guidelines that say to use the antidepressants for nine months—–seems very arbitrary. Is it no longer than nine months or up to nine months? What is the source for this information?

    I agree that most people are very afraid to discontinue antidepressants—and I know many who have been taking them for 10-25 years. I just wonder what that stuff is doing to them. Some seem fine, others struggle with depression despite meds.

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  • Dear Amanda, Thank you so much for sharing your story of courage, resilience, and recovery. You are so right when you say that the psychiatric diagnosis overshadows anything you might say to a doctor about physical pain–you are not believed. It is criminal to dose people with powerful psychiatric drugs and at the same time, to be ignorant of the withdrawal process and associated problems. Many people resort to online forums for peer-supported withdrawal advice, and sadly, I can see why.

    You are incredibly courageous. Many of us join you in demanding answers. Unfortunately, I think most people working in the so-called “mental health” system believe all of the propaganda from the drug companies and only rely on the poorly designed and weak “studies” designed to get the drugs approved as quickly as possible.

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  • HI Mike, thanks so much for posting about your experiences working for NAMI. I have not been involved with them on a personal level, but they offer many support groups in the Baltimore area and are highly regarded. I’m a real outlier when I talk about their relationship with Pharma as many I talk to still believe the story about chemical imbalances. I participated in a community event and engaged in a conversation with a NAMI volunteer, and the longer I talked to her, the more I noticed her jerky movements, eye-blinking, and head-shaking. She was explaining to me how much the drugs helped her bipolar disorder, but all I could think about was the possibility that she was experiencing akathisia from the drugs. Thank you for sharing your experiences with us. I abhor the idea of “mental illness” and wish we had a better term for the emotional distress caused by trauma and abuse or difficult life-circumstance. Bravo for your work.

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  • I am not a veteran, but I greatly appreciate you sharing your story. You detail the overmedication that happens to so many of us when we enter the mental health (?) system. I have often wondered about the role of overmedication in veteran suicides and am so glad you are speaking up and raising the issue that many might be unaware of. Thanks also for providing an alternative form of therapy. Bravo to you for your courage.

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  • Dear James, thank you for posting your compelling story about the great difficulties you are experiencing with getting off of psychiatric medications. My heart goes out to you and to everyone else who finds themselves trapped in the vortex of drug withdrawal. Stories like yours help others to know about the dangers lurking behind the simple directions to take pills to manage intense feelings of pain and despair. I will be sharing your story with many friends. Thank you and all the best with your journey.

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  • Lauren, thank you for sharing your story. You are very brave and are definitely doing the right thing to get off of drugs slowly and to tell your story. Everyone needs to know of the incredible harm that can come from taking psych drugs which are presented to us as benign pills meant to soothe and calm us or restore some kind of imbalance that was never there to begin with. Many blessings on your journey!

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  • Dr. Gordon seems to have experienced the game that psychiatry frequently plays with patients who question the treatment–his sanity is questioned and he’s told he’s unwell because of course, the drugs are good for him. He’s a truth-teller who is being discredited and marginalized by those who want to protect the status quo. Everyone deserves the choice of how they want to live—with or without medication–and should be believed when they report adverse effects. He’s got my full support for his courage and honesty.

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  • Thank you, Neils, for your honest and essentially hopeful story. You sound like you’ve found the correct answer to your anxiety attacks—that you are finally feeling all of the pain you couldn’t handle when you were growing up. I don’t know if the doctors and nurses can be helped, especially if they truly believe in their biological model. Keep ups your great work!

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  • Michael, I also wanted to say that schools do a very effective job of scaring parents, and so many teachers just accept the drugs as the way to go. In all the years I worked as a special ed teacher, I never had an in-serivce on the use of amphetamines for managing ADHD, but the drug’s use was very common in all the schools where I worked. Once I read Anatomy of an Epidemic, I became firmly opposed to using the drugs. There are so many better methods to offer to children and families–but it takes more time and more skilled people. Kudos to you for your work.

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  • This is one of the most frightening articles I’ve read in a vey long time. And the wording is so wishy-washy—-why do people fall for this crap? I was a special education teacher for many years and worked with a lot of students who were on medication before I knew of all the harm. Even then, I would often tell parents that pills would not “fix” the attention issue and that more was needed to help the child process what was going on inside. I believe that schools will change everything but the environment—-and then kids suffer because so many teachers don’t have the knowledge and training to offer appropriate guidance. But electrical current to the brain all night? I am heartsick over this. How did this ever get approved? Oh, yeah, same way Esketamnie did……

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  • Thank you, Rosalee, for your kind words. I am stunned that a psychiatrist would mock you for side effects and describe you as noncompliant. From all the reading and research I’ve done, I believe that they fully embrace their paradigm of chemical imbalance and therefore, chemical cure. They lose sight of the person across from them that has a real life with real pain and distress. I honestly don’t know what doctors don’t believe their patients–I think they are truly acculturated to believe that if someone objects to the meds, it’s because they are “crazy” and not in their right minds. For all of those reasons, when I discontinued my meds, I worked with my therapist to taper and never mentioned it to the doctor until I was off the meds. Believe in yourself and all the best to you!

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  • Thank you for writing this powerful article. I am deeply disturbed that now many people who don’t respond to two antidepressants are considered “treatment resistant” and immediately recommended for ECT. When I begged for it in 1995, I thought it was my last hope to get out of depression–now I cringe inside that I was every willing to subject myself to such a thing. But of course, everyone told me how safe it was. All of us need to join together and stop this horrendous practice.

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  • HI Lily Pad, thanks for your kind words. I’m very sorry you’ve taken multiple meds and experienced ECT multiple times–I did as well and it was quite terrifying. At the time I thought it was my only way out of depression, Now I think I felt so dead inside due to the multiple meds I was taking—they call is psychic numbing. I kept telling my doctors I couldn’t feel anything–none of them blinked ar told me that such a feeling could be due to the meds. I’m telling my story and my mother’s for all those who are on the same dark road. They deserve to know there’s another way out.

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  • Thanks, Julie. I’m so grateful to be able to tell my story and to offer hope for life after meds. I appreciate your story as well about your awful experiences with Lithium and look forward to your book. I think it’s vital that people know that choices exist to help with mood swings besides the dangerous drugs so often prescribed.

    When friends bemoan how some people with manic-depression don’t want to the the drugs–I tell them “With good reason” and then I describe my expires with Depakote—shaking, word-finding difficulties, weight gain, and feeling like my personality was weighted down with a wet army blanket. My doctor wouldn’t listen to me and kept me on Depakote for two years.
    Please send me a message on FB so we can talk off line. All the best!

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  • Dear Rachel, I’m so sorry to hear what happened to you with medication. Stories like ours need to be shared so that more people can begin to learn to ask serious questions about psych drugs. I also had the experience of doctors not believing me when I talked about drug effects. There are two kinds of people who are easy to dismiss: imprisoned people and people with “mental illness”–which I prefer to call emotional distress. We’ve got to work to change that situation. I hope you are doing better now. Blessings to you and thanks for sharing your story.

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  • Hi Catnight, thanks for you thoughtful comments. Both of my parents are dead and so are their siblings, so I am left with letters and memories. From all that I’ve discovered by looking at my dad’s files, he did the best he could to help my mother. The medical treatments of the time were crude and my mother and many people like her suffered at their hands. Doing the research on the treatments of the time (50s, 60s, 70s) was very painful for me. But my hope is that by shining a light on our stories, more people will seek an alternative path to healing.

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  • Hello Someone Else, thanks for your thoughtful comments. I’m sorry for the difficult road you’ve had to travel and hope that life is better for you now. I hope that by sharing my story, the issues of overmedication and iatragenic illnesses become more than ideas discussed in journals. Real people are harmed by drugs and by a model of care that neglects the human aspects of suffering.

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  • Dr. Coleman, I am so happy that I’ve found your work. I had the challenge of a lifetime about 25 years ago when I tried to tell psychiatrists that my severe migraine was a symptom of emotional distress—-instead of working with me, they dosed me with numerous drugs, including OxyContin and Methadone, alone with psych drugs. I was so over-medicated that I had two car crashes and finally found real help with an energy healer. The greatest help for me emotionally came from poetry–from the metaphors of dealing with darkness and having a fierce determination to keep struggling towards what my soul directed.

    I have not had any depression since 1997 and have been drug free since 2002. My last psychiatrist told me I had a damaged brain….luckily, I’d read Glenmullen;s book Prozac Backlash, and I did not listen to him. I’ve been fine ever since. But due to my awful experiences with overmedication and doctors not believing me, I have major skepticism when it comes to Western medical treatments.

    Keep up your great work and I hope more doctors will hear your words and wake up. Is there any way to email you offline? I am working on a book and would love to consult with you.

    Thanks for your work!

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  • Yes, ECT damages the brain. On the other side, no one thinks that people with epilepsy are helped by having grand mal seizures, so why should such a seizure help anyone with depression? The problem of emotional distress is not a malfunction of the brain—it is a problem of some kind of injury to the spirit. No electricity or drug can help that. Sadly, the medical paradigm is pretty solidly believed, except by some of us who have experienced it and come to believe in another way to wellness.

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