i got brain damage from electroconvulsive therapy.

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In 2005 I was given 22 lots of electroconvulsive therapy. It left me with brain damage that means I will never work again. I was lucky because I got support from a neuropsychologist who allowed me to understand and come to terms with my problems. ECT can be used to great effect. However some people like myself end up severely and permanently affected. I want to use this place to link up with those like myself. So that we can support each other.  I don't say ect shouldn't be used. But people thinking of it should understand what can happen. The Information given about ECT side effects doesn't go into details, they talk about memory problems. Actually it affects far more than that. It causes cognitive impairment. 10 years on I need 12 hours of home help a week to help me care for my 3 kids. I tire very easily and some days I am able and feel intelligent. Other days if I have pushed myself and not been able to have a midday nap I struggle to do the most basic of tasks. Some days I'm not well enough to drive at all. Other days I will drive short distances. I was a doctor and well never work again. 

Please let me know if you have had similar problems. Or if your thinking about ECT please make sure that you understand what could happen to you. It could mean permanent I'll health on top of your existing problems.I am no longer depressed. It wasn't stopped by the ECT but by psychological input to support me out of my coercively abusive marriage.

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  • Posted

    I was awake for one of my 14 ECT sessions. It caused the person I was to die and left me completely lost and pretty much useless as a functional human being. I remember it in... too much detail. I feel like something is really wrong with me neurologically, like there's an electrical storm firing on my head all the time. Am I having seizures? What did they do to me? Who do I talk to, how do I find one or pay when I've hardly been able to work since? How do I learn who I am after experiencing death of the self?

    I deeply wish I could talk to someone else that's been shocked. I feel like I lost my humanity, like other people can't understand me and I can't relate to them. I feel so alone.

    • Posted

      Hi ri05263, 

      I am so sorry you are suffering. I am shocked (and horrified) that you were awake for a “treatment” and I am wondering if that was a mistake by an anesthesiologist or on purpose for some reason I cannot think of? Also I am wondering when you had the last ECT?  

       I am not sure where you live, but to answer your question: I suggest you try and find a neuropsychologist. This is a person who is trained to do more extensive cognitive testing, not a regular psychologist. If you are able to get this type of tests done, you will have a better understanding  of cognitive deficits, and where you have weakness and strength still, etc. It will also give you a better baseline, and “medical proof” of cognitive deficits that you can show other doctors, therapists, etc. as well as if you apply for any type of disability compensation.  I live in the States, and it took several months to get in to see a neurophysiologist, but it was greatly helpful, for me to understand better my deficits as well as for applying for disability and maybe most importantly for getting referred to different types of rehabilitation therapies. Personally, I went through several months of speech/cognitive therapy. I was also able to find a talk therapist who only sees patients with brain injuries. Primarily he sees people who have had strokes, as well as TBI and ABI- I was his first post-ECT patient. I have been seeing him for over a year, and it has been extremely helpful in attempting to understand the crazy emotions and intense grief that has come with brain injury. He has also helped me with the PTSD I have around this, and it sounds like (or I imagine) that your experience would cause a fair amount of mental and emotional trauma. I also recommend trying to find support groups, there is a local one in my city, but it meets later in the eve, and that is too late for me, but there are online groups, both for traumatic brain injuries and ECT specific brain injury. I was recently also referred to an opthomologist who does cognitive/eye testing and visual therapy (one of my many issues is reading, and my gaze shifting, etc.) So I am looking into starting that. I will say that through my husband’s union I do have good private insurance and I realize not everyone has medical coverage. None of the above suggestions are cheap, and I don’t know your coverage situation. Knowing more about that I may have suggestions for helping w/the financial side. I am a little over two years out from the last ECT I had. I had 27 “treatments”, in two different rounds. I will tell you that the first few weeks and months were extremely difficult. It is not uncommon in any type of brain injury to experience extreme anxiety within the first few weeks and months post injury. I had a 6 week long anxiety attack, 24/7 that started about 2 weeks after last ECT. It was horrible, but I made it through. Leaning on anyone you are close with who is willing to help you find answers and understand or try to understand is very important. Lastly, I would recommend finding a doc that is, if not fully understanding what happened to you, and least willing to believe that you have changed and help you find some of the above mentioned resources. This can be difficult, esp when it is hard to trust doctors after an experience like yours or mine. And please believe, if you can, that the brain is changeable, yes for the worse, but also through training and plasticity to make improvements too. No one can tell you-no one, how much you will heal from this, but there WILL be some healing. 

    • Posted

      Thank you so much for replying. It's extraordinarily uplifting hearing from another person who's been through it, I've been feeling so alone.

      As far as I know I was awake by mistake, because I was still given both the muscle relaxer and the anesthetic before that particular treatment session. I did go under, but I guess not enough. Afterwards, when I woke up, I remember trying to explain that I'd dreamed I'd been struck by lightening.... Except you don't dream under anesthetic. I'd never had a seizure naturally at that time, so I didn't know what an aura looked like. They agreed it was a dream and moved on.

      My last session would have been in June of 2016. My shock doc "practices" out of Houston, Texas. I live in Denver now, because my family disowned me after the after-effects got too much to ignore. It's a lot easier to believe a 22 year old doesn't want to work out of laziness or selfishness than to accept something really f****d up happened to them.

      It's been two years since my last shock, and I haven't felt right the whole time, but I only just found out something seriously was going on. After shock I'd continued psychiatric treatment up until I was forced to flee my family for my own safety, and I kept telling every clinician I had I didn't feel right and something was wrong, but no one really did anything with that information.

      Seriously. Imagine a patient ran the full course of an IOP listing "twitching" and "brain fog" and "mental static" as their chief side effect complaints for the entire course of the program. and the appropriate solution is HEAVY anti-psychotic medication and sedating mood stabilizers. "I keep spacing out," "i can't focus," "I feel like I can't think," "someone filled my head with molasses...."

      Now, I'm pretty sure my symptoms match those described in post-ECT seizures, but I've lost my insurance and am having a f*****g hard time working. I've tried reaching out to some doctors and medical resources here, and I've been told I need an EEG, but no one can work with me and I'm completely overwhelmed trying to figure out any benefit program applications. I don't have my records, my memory is like Swiss cheese.

      I actually don't know what to do. At all. They told me "any side effects are purely temporary." The most f****d up part is that going in, I had no clue something permanent might even happen. At least for major surgery you know before hand that some serious s**t can go wrong and you have full knowledge of all those possibilities and can evaluate fully, make peace with negative odds... not when you don't know about them. I'm 22 and I feel f****d for life, like I never even had a f*****g chance.

      I'm at the end of my rope. I am so exhausted to my core, there's so much emptiness inside. My rage and apathy are stronger than they were for any suicide attempt, and my emotions seem basically unable to regulate properly anymore. I feel like i don't have control over myself anymore and if I didn't have an amazing partner with me through this I do not believe the struggle would be worth it anymore.

      Nothing ever hurt more or made me question my own life than ECT.

      Nothing ever made me more sure I wanted to die than ECT.

      The only reason I'm still here is because I'm having to choose every day to keep fighting, and that's f*****g s**t. If anyone reading this has a family member considering ECT, know that they will almost certainly have to face the same choice later, and it is not an easy one to make.

      This is not treatment. This is rewriting patients to make them easier to deal with.

      To anyone considering this for themselves or a loved one:

      Having been conscious for one procedure, I can tell you in vivid detail what it feels like. Because I have gotten stuck inside this flashback so many times, there is no forgetting or moving away or escaping from it.

      Before ECT, I would have said the single worst sensation I'd ever experienced was unwanted climax during forced sex. ECT blew that out of the water.

      Imagine you're in a dark, quiet place. It's a lot like being asleep, except you're not dreaming, not thinking, it's just... quiet. The next instance, your whole awareness is filled entirely up with what looks light light. It's every moment you ever lived, every memory you ever formed, and every neural connection you ever bridged lighting up at the same time. Every single point in your head lit up, connected, overloaded, exploding....

      It's the most intense neurotransmitter dump you could ever experience. In the same sense that an orgasm or drugs cause neurotransmitter dumps. Imagine the sensation of cumming, except 100x more intense and inside every cell, every part of you. There is no dissociation, no going away, no pretending to be somewhere else. Your body starts jerking, the muscles moving in disorganized rhythmic jerks, and it is the most disgusting sensation because they've pumped you full of muscle relaxers. So you can't even convulse properly, you're just aware of your body's limpness and inability to stop what is happening.

      We're talking minutes between the shock and when the ECT seizure stops. Minutes of being trapped in this sensation of horror.

      But there's even more than the physical sensation. Inside, your awareness knows you are dying. You can feel everything you ever were being unmade, and that is not a f*****g metaphor. It is a very real, literal, visceral sensation of finality, of being unmade, of the weight resolution.

      It felt like I was in my death throws and they'd given me a muscle relaxer to make it less traumatic for them to watch me cry out and die without doing anything to help.

      That is what it felt like in the moment.

      I woke up remembering only the lightening. The person I was before ECT had a history of trauma and sexual abuse since childhood, and had a preexisting skill for memory repression. It wasn't until more recently that I was forced to fully deal with what had happened.

      For the love of God I hope someone reads this and takes it seriously. The person I was born as died during shock, and does not exist anymore.

      It would have been more humane to f*****g shoot me in the head than to shock me like that.

      I don't understand why this outcome was seen as more positive for me than suicide.

      They made me die either way, but now I'm stuck with a brain damaged on a cellular level.

  • Posted

    Hi Sue, I typed a reply to you earlier but I don't think it went through. In the mid 90's I had 9 ECT treatments. I had a severe complete burnout from working constant long hours in a high stress work environment managing a very unrealistic high caseload of work-injured clients as well as raising 2 daughters on my own with no help nor support. This burnout completely spent me physically, mentally, emotionally, cognitively as well as actively brought to light trauma symptoms from my childhood abuse I had buried, never dealt with. I was diagnosed with major depression, ptsd, anxiety, chronic fatigue syndrome, fibromyalgia, sleep disorders, low thyroid & disassociative episodes; some more uncommon, not recognized nor accepted well in the medical community back then took longer to get diagnosed (with the help of my own persistence of many hours of research in other countries & finding a physician elsewhere who had that knowledge). For the first few years, I was covered through my work place disability plan as far as income & counselling. My symptoms continued, not being able to work, I had my savings that I used to live on & pay the bills. Eventually that ran out & I had to go on welfare (poverty) & claim bankruptcy for a small amount of debt I couldn't afford to make payments on so all this was a real loss of pride for me. My children (just barely teens; their hardest years) as well now majorly suffered in so many ways; it was like they had lost their mother, the person they knew & could always count on, their strong & only caretaker, their sense of security, the home they knew, monetary level of comfort. I fell apart & so did they to an major extent; our family dynamics & relationships majorly fractyred & affected. No one offered to intervene, support or help us individually nor as a family unit. Now in poverty my only choice was to seek help from a psychiatrist, reluctantly. He denied me counselling, overdrugging me majorly with too many kinds of meds, for a long time period, some meds. for psychiatric diagnosis's I didn't have. With the overdrugging, I was constantly drooling at the mouth, seeing things not there, at.times getting lost with a blank mind for long periods, constant heavy sleeping states for which he chastised me when sleeping in for morning appointments (I had to take transit buses too to get there). I ended up sicker after going to him. Nothing he did seemed to help my depression so he recommended ECT treatments stating they do not cause any long-term memory nor cognitive impairment. Many months after my ECT's I tried to convince this psychiatrist that these treatments seemed to majorly increased my problems with cognitive & memory issues but he didn't believe me. I was afraid I would be cut off disability if I stopped seeing him & of course not thinking clearly with a cloudy brain. He still had me overdrugged & sent me for some type of academic-IQ testing that I'd been asking for done by a psychologist done over a 2 day period (which I never remembered having done). He told me my I had an extremely low IQ functioning at a borderline mental retardation level (his exact words) & he said that I had this low IQ before I had got sick & this was the cause of my burnout because of the stress of not being smart enough to do my job . Shocked, I told him I functioned at a high academic level in life & at my jobs successfully with promotions & I had the paperwork to prove it. I then took my chances & stopped seeing him, as well as majorly reducing or stopping the medications he had me on. I eventually got my medical file from his office & once reading it, I felt so angry with all the inappropriate & incorrect unsupported diagnosis's, negative labels & comments he had written & I saw the psycologist's written concerns at the time he was conducting the psy. IQ. academic testing in me that I was drooling at the mouth, appeared to be heavily medicated & of my disassociative episodes. Just unbelievable. He gets paid a very high income to abuse his patients making them sicker & So Wrong, as 20+ years later I still suffer with major depression (on an anti-depressant) & cognitive impairment of short & long-term memory loss, problems with confused, fragmented thinking, responding, understanding, communicating, learning, retaining, slowed functioning, spacing out with major time planning difficulties, late or missed appointments & functions no matter how hard I try to plan my time leaving people mad at me even though they are aware of my medical issues; balance problems & not walking straight; spacial awareness difficulty, clumbsiness, not remembering important or fun things I just did or an enjoyable movie, poor sense of direction & trouble with figuring out where things are around me when out & about (getting my bearings). The medical community that I've dealt with don't seem to accept my cognitive problems as relating to ECT nor take me seriously nor seen to care enough to refer me for neuropsychology testing nor anything else. I've felt like I have a true brain injury without the hit in the head & a childlike functioning mind in an adult body. And, without that hit in the head, I am not taken seriously. I feel so angry, powerless, stuck, unable to get better & move beyond my symptoms & limitations that keep me in poverty & sick. I have found the government here, the medical community, society, employers, landlords renting their properties, & even the ones closest to you like family or friends (if any anymore) walk away, criticise, have little patience nor tolerance, take it personally like you don't care enough, don't offer help, support nor understand or care or really want to with having these limitations. I feel it is criminal, unethical & immoral concerning how my psychiatrist & alike & the government here treat mentally ill people. Shame. It is refreshing to have run across your discussion online site on this topic as I so agree ECT causes brain damage . I applaud you for speaking out. I've never heard of his book but I intend to find it to read. Also, I'd be interested in viewing any documentaries or media episodes etc on this if you can share how I do that? Thank-you so much to all here.

  • Posted

    Hi Sue

    My name is Sandi. From 2009-2013 I endured approx 140 ECT treatments. Some unilateral & some bilateral. 12 were voluntary but the rest were forced under the Mental Health Act which my family and I fought.

    We definitely noticed the memory loss early on but was were told it would improve. Not only did it not improve, It worsened. In time I didnt recognise my own daughter which was so distressing for her. We noticed my cognitive ability was quite badly affected. Sadly this has persisted and my neuropsychologist feels it is akin to having early onset dementia. I have always been a very active mentally alert and competent woman working manager in a disability support service. Despite my employers every effort to keep me working, I resigned from my job in 2013. I struggle with so many domains of life.

    My adult daughter tries to help but my needs are more than she can cope with. I find learning new things very difficult especially things like reading and following instructions, using the internet/media, phone, sequencing, telling time/date, paying bills, managing medication, as well as coping with some emotions like anger, frustration & excitment etc.

    Because my symptoms are pervasive & persistent I cannot work. I do receive a pension but do not qualify for NDIS to recieve the support I need to just maintain the skills I still have. I feel so cheated!

    • Posted

      I'm so sorry to hear this.

      Is such a common story.

      Here in the UK in trying to bring change.

      Where are you?

  • Edited

    Hi Sue my friend, a former nurse had ECT several times many years ago for deep depression. He now has trouble forming sentences, can’t spell and has anger issues . He is very “black and white”  in his reasoning and sometimes seems almost child like. He is insistent on having his own way and lacks empathy or much insight. I noticed these are like frontal lobe damage issues. He was quite depressed when I met him but Tryptophan has helped a lot. It seems to me he has cognitive damage from the ECT. Can you tell me any more about this?  
    • Edited

      Sue is busy preparing for the Maudsley debate on ECT on 19th September 2018 - 'This house believes that electro-convulsive therapy (ECT) has no place in modern medicine.’.

      Yes ECT causes brain damage though this is not on leaflets given to patients. Search for 'ECT brain damage'. Unfortunately, I cannot give extensive links here as the post will be deleted.

    • Edited

      Yes, ECT does cause brain damage. Doctors and psychiatrists will deny this, but all decent research on the topic shows that it does cause brain Damage. 
    • Edited

      Also visit the 'Mad in America' website for excellent articles about ECT and also the terrible story of Garth Daniels in Australia which sadly is still ongoing

  • Posted

    Please see the New discussion group I started ELECTROCONVULSIVE THERAPY.

    I had a large number of ECTs back in the 1970s. I have always searched to discover who brought me back from the OTHER SIDE . As the decades passed my theories changed.

    As you may know immediately after the electricity travels through your frontal lobes your brain FLATLINES for about 45 seconds. During this time YOU ARE BRAIN DEAD. Something or someone brings your soul back to your brain.

    Since everything but your brain is still functioning at the end of the 45 seconds reanimation is easy (at least it occured everytime for me),

    As you may also know, for reasons the doctors do not know; the face of a person for those first 45seconds displayes the expression of EXTREME PAIN. It is worse than just about any other event causes a human face to express, yet the Shock Docs say the patient feels no pain at all. Indeed after every ETC when I woke up I could not remember any pain . Of course I could not remember ANYTHING!

    One thing occured everytime I was waking up from ECT. My mother would be calling my name from the door to the little treatment room . David.... David.....David..... My first thught was not "WHO IS DAVID?" or "AM I DAVID?" or even "WHO AM I?" My first thought ALWAYS WAS>>>>>>>>>>: "WHAT AM I????"

    What d.oes this suggest? SOMEONE OR SOMETHING USHERED BACK WITH ME FROM WHERE EVER THE SHOCK HAD KNOCKED MY SOUL (ESSENCE, WHATEVER YOU CALL IT). This is what the Buzz about the CIA using ECT in the 1960s and 1970s to program a human has hinted at. I do not know anything about that and some things on the WWW are jokes. DRR

  • Posted

    Hello again ; in regard to the loss of memory and the inability to perform tasks that require concentration of the mind on a specific thing, i developed a technique to get around this problem which had developed as a side effect of my ECT treatments. I produced a METHOD for any task; by writing out in a listed format, steps to do, and memorized the list .

    With this technique, my mind could wonder all over the place and it would not be noticed. My work would be completed as if I was a NORMAL human and not one DAMAGED BY ECT.

    This same idea worked for taking college classes while receiving ECT. Taking copious notes from lectures and memorizing said notes, I was able to maintain a "B" average. As to the "RED ELECTRODE MARKS" , there was class in a History of the USA where I had to take a test only a few hours after an ECT treatment. Those MARKS were evident . Everyone was busy with the test and did not notice the marks.

    I have noticed what might be the result of ECT causing a sort of "SPLINTEING" of the frontal lobes into what might be visulized as "KINDLING or TINDER_. I have trouble focusing my thoughts on a single thing. My thought patterns are defocused. I see the BIG PICTURE and often get lost in conversations because of trying to explain and as it were PAINT THE WHOLE PICTURE of something that those around me can only take in and grasp as a LINEAR presentation . They cannot follow my TANGENTIAL presentation in which I try to paint a whole picture instead of just a small part of the canvas.

    Something to additionally consider: WHAT TYPE OF SHOCK MACHINE WAS USED ON YOU???

    DRR

    • Posted

      after i just suffer a repeat and reversing of my healing brain i have to progam my brain to put on a sock. move talk speak and can ont speak well i make mistakes im words seem illiterate and my memory is wiped out. like i have never lived here. and cant not learn. i lost all information was erased and i can not learn. my brain was at a perfect healing before i was set up and somene revsered it all on me. induceing a intentional damage to my brain as i had recover in full and was at apex of that to drive me into mental break down and trauuamtize me and greif. then torture me . i can not smell my sense of smell hearing and sight voice and means to thrive are removed.

  • Posted

    r=ect. at 18 i was munchasuen by proxy. my father a mentally ill md. prior to this iw as honors in art school had bulimia i diagnose and cure alone and art school not medical. my father? dysfunctional. angry food addicted came from ignorant and alchol and drug family sister and her children were drugs.. alchol. i had this issue got over it and was healthy. outdoors art and sports.

    my father did a terrible thing to try to keep me from being an artist. some 39 years later or so, it might finally got his wish and to induce and get a dr to diagnose me with anythign to keep me from school turned hysteria and a fake mental illness diagnosis put on me.. which lead for me to never be treated or remove from MSBP.

    i suffered CPTSD from this and ran and suffered tragic life and left a vulnerable adult who worked one to two months summer then m life was a turn from this easy and normal recovery and healthy alone without drs to madnness and confusion trauma and drama. my world torn apart and drs tossing ECT at people like candy. they did not care if it was needed or not. my father and mother were self convince to not face what he did to have me mentally ill was easier . i was lead to this and a tragic situation which left me traumatize toss around at 18 and to sick drs using this for money.

    i was coerced threaten if i did not do this is be sent to worse place than hell where i was. in another private place i was drag to off a fake diagnosis an insurance some Nazi like dr was using it on anyone. now i was being force to this and i was given 6 before something in me not beaten down by trauma said to stop and i ate chicken bones to not be able to get it. then i called a lawyer. who stopped and said i could refuse.. i did. after this one time i began to change and suffer . throwing up in a garbage pail and my life feeling i was raped and brain means that something had to be so painful damage to make u puke . my personality change and along with all trauma, i began to suffer the effects mentally of a damage life..

    my father was mentally ill and abuse and doing insane things out of his sickness passed the illness to me or was meant to . i would suffer 11 long years of abuse torture and not being removed from this and ran into streets where i suffered and had to try to cope with it and to survive and was a victim of some kind of hell attacks on me and abuse. then i put one foot out of it and escape the hell and walked away from what they wanted me to be back into who i was before i lost me. then 24 years of my rising up and trying to deal with all kinds of neurological issues and ptsd and taking it to top. autism and pains in head , and something damage that i ahd to compensate for all time. i did not want to think about what happen to me but not until i cut off family who wanted me to be this lie and drs did i make a right move forward. i wanted ideal for a dr to do this but never did. so i was left to do it alone and i was a good dr. from time i was less than 15 years old..

    i took my story and healing to levels of regain speech and other and to healing until 4 years ago . past list of abusers i regain talent and other and worked hard. at one point because i was constantly traumatized my life could not heal until i removed threats. and walked into a job trusting god who was there still some how and i began to recover . ideally a dr should have remove me and my father should been removed from me and others and him treated. i did my work of ptsd alone. i was going all way up, before i was intentionally induce what someone might wanted to reproduce things in my life and this time take me down with it. a very evil game to induce damage to my brain and reverse my miracle to heal and function, was induce on me four years ago by some abusers, and remove god and any means for me to heal. leaving me to suffer and induce a stroke or lobotomy's effect aggravate my healed damage and send me to depression by induce fatal brain damage mind erasing and to induce a break down and rape trauma on me to dose me with fatal to induce mental illness because no matter what persons did to me i kept keep healthy and get up. i was deprived abused tortured and i refused to break so they helped it along by cheat and removed part of my function and induce extremes on me and i went instantly to death and living hell and my 24 years of very artistic restoration of my life, began to reverse with some punks then induce torture on me and make me suffer and i was again a hostage of torture abuse and people. this time they induce damage in part of my brain that has to do with allow intelligent function and speech and life and basics and i began to die. i began to die and suffer and was left and am not a walking lobotomy's and catatonic and a sad state . i got to dr holding off my fate using repetition tactics of stroke victims and they did not remove me and stabilize and protect me but left me and forced me into streets and to reverse my progres as a person and talent an remove my life. pushig me and others pushing me down to get even with me for surviving them. i am now the opposite of who i was. i also ahve all the symptoms of brain damage of the woman. i suffered extreme brain damage and persons began to attack me as i had no defenses and no function and if dr had remove me and given me means to heal with my super effort to not lose it and not let devil have my soul i might outwit him and them again. instead i was damage and induce strokes on me and left in sick hard places not places to heal with someone sit and wait for me to die. not tell drs i was in distress and being mugged raped and damage.. with a sister who might be envious of me artisticly and a said story and my life turned to hell from a bright story of self recovery. i had issues where i could not learn and autism serizurs and onset of musculature issues. in time i removed myself to recover and i took 11 years of torture abuse. i had stil some lingering neuro and stroke like conditions. i felt if i worked hard i could over come and persons watching me to antichrist me.. now i suffer from fatal forms of what i overcome and not one person stopped it. if someone had felt for me and wanted to prevent me from lose talent and be a victim again. but instead they left me to suffer and abuse me. shut me up for what i saw and left me.. i did suffer also all of above and got better. until i was traumatized again. this is not a chronic thing. if ur leg is broken, it heals if a person comes along and found out it was broken and healed and break it again is not chronic. chronic is only when someone is not given means to heal.. my brain in three and half years awas damage and broken over and over and over. if i put up a fight to show life i was hit again and left in deep trauma and drs not care to much . until i have no sign of intelligence no music also , no sense,visual damage blind and senseless. and articulation and intelligence damage.

  • Posted

    Thanks for speaking out about your experience. I'm not even close to the gregarious person I was before. I have a day here or there where I can have hope and have fleeting moments of my brain back but it doesn't last. All my medical team work for the same major university and cover each others backs. My experience is that psychiatrists have more power and influence over anyone else and I'm stuck with life long brain cell damage. I see no hope but to try my best each day and try to move on from a procedure that made me much worse overall with no options.

    My family Dr has seen this before but he can't speak out. Are the anything special i can do. Going to a Nero psychiatrist sounds nice but they are in the same group and i can't afford to go out of network. Do you have any words if advice for this US injured patient?

    I hope you're still answering threads and successful in your new life! Thank you for the thread.

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