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  1. In july I was diagnosed with psychosi due to ptsd. I was in an abusive relationship. I started the resperidone 3mg in july and I am supposed to be tapering off in June, and Im a little nervous about the withdrawal and other things. Im just curious has anyone been successful in tapering off risperidone? All I have read are horror stories. I am supposed to taper off this drug and I wont be put on any other drugs, and I was just curious if anyone has come off risperdone without being put on any other meds? Are you able to feel emotion again? Did the psychosis return? Did the mask-like face go away? Will I return to normal I guess is my question.
  2. Hello, my name is Manny. I was diagnosed 0CD and schizophrenic in 2008, but I been taking benzos and amiptriptiline since 2005. Currently,taking abilify 20mg,risperidone 2mg,cymbalta 60mg,biperiden 4mg. I am tapering klonopin down to 0,27mg from a dose of 1,25mg. I went to see my doctor this week because a blood test that I did. He said my hepatic transaminases are high because of the medication that I take. I am assuming the APs that I take. What can I do to get my liver function well? I know, quitting the APs, but I can t cold turkey. Any advice,please.
  3. just want to thank everyone here who posts. I am managing my daughter's withdrawal. She doesn't speak much so i have to gauge her withdrawal by her eating and sleeping habits as well as when we 'see her old personality' show up for a few minutes a day. When she can concentrate on a video or a movie, play Uno, or listen to her spotify.....we know she is feeling better. THe tapering is so slow and i want her off this med, but watching her body is my only key. It is an amazing process to see this sweet child who has no idea why this is happening, go through this process. Those of you who can speak and share are my light. Peace
  4. Hi all, I'm a new member here and I'm starting this introductory post as a recovery journal. I'm recovering from risperidone (aka risperdal) and tried magnesium to help with anxiety and overall disassociation. I took a 250mg pill yesterday after dinner and went to bed. Woke up with severe back pain. Anybody else have the same effect while starting magnesium? On the plus side, my mood feels a lot better and I've been feeling much more productive so this feels like a body/mind tradeoff.
  5. Hello Folks, my name is LNY4ever and i am from Germany In the month of July in 2016 I decided to finally take LSD at a Party in the woods close to the town where I study. A few weeks later i think i had a flashback from this LSD trip and i started to wander around town. I would think that exposure to the outside world would keep me from getting insane, since i think I had some auditory hallucinations as well After 3 Days of roaming I couldnt take it anymore because i was so anxious about everything that I committed myself to the psych ward of our town. Because I freaked out in the ward, people tackled me to the ground and fixated me and sedated me with Haloperidol. I was diagnosed with a drug-induced psychosis and was court-ordered to stay there for 6 weeks, which was alleviated because of the fact I behaved quite nice and commited myself voluntarily. I cannot really recall the first week of my stay there, but i have been drugged with some benzos, Olanzapine and Risperidone. After 3 weeks (in August) I was released from the psych ward and went to my families place ( which is in another town, a few houndred kilometers from where I study). Because I was taking two antipsychotic medications, my mum and me decided to drop the Olanzapine (10mg/day) and just go for the Risperidone (1.5 mg/day at that time). After i quit Olanzapine cold turkey( because i was feeling very strange, very numb), i had some weird feelings when lying in bed, basically like dissolving or continious falling. Waaaay later i learned that quitting cold turkey is quite dangerous. In late August I really got bored out of my pants where my family lives (mostly because of the anhedonic adverse effects of the antipsychotic medication, which at the time i did not know about) and decided to go back to the town where I study, because I thought life should go on now. After a week i became intensly anxious and supposively psychotic again (probably because i quit Olanzapine) and decided to quit the medication because it made me feel even more weird, so i went to another psychiatry (where my family lives) this time for a weekend. This time i really had lost all grasp on reality because I think i was withdrawing from Risperidone. I was given RIsperidone ( this time 4mg/day) and was basically in a dream like zombie like state and I didnt know what the heck was going on. My father visited me and saw the wicked state I was in so my parents, who live apart, decided to take me home again. I stayed at my fathers place for a month and went after that to the place where I study again. I then got an appointment with a psychiatrist whom i told that the medication makes me very resless (akathisia), makes my legs move unvoluntairily ( dyskinesia) and i was feeling dull and not perceiving any form of enjoyment whatsoever(anhedonia). He agreed to taper the Risperidone So I went form 4mg --> 2mg --> 1.5mg-->1mg-->0.75mg-->0.5mg-->0.25mg-->0.125mg(broke Tablets in half)-->0mg from Oktober 2016 to January 2017. I held the dosage for around 2/3 Weeks and then went on a lower dose. Since then i am feeling waaaay better, because in January 2017 i was feeling very socially inapt, emotionally blunt, couldnt come up with a conversation topic because every spark of creativity was removed from my brain,still had to move my legs all he time due to restlessness. I still think there is a good amount of recovery to do since i think i was more inspired and more outgoing and more active before my little tango with drugs and medication. Yet I can feel good feelings again and have more energy to do things. Thats my journey until now, i hope the post hasnt become too long. Are there any other people around here with similar experiences? With best Regards, LNY
  6. Hello Everyone, I am relieved to find this site, because I have been dealing with problems from my medications alone for a long time, and it's a relief to find a support system, and a place where I may be finally be able to be helpful. For context, I grew up in an unstable home. My parents were upper middle class and had no serious problems (like drug abuse), and were caring in many ways - but not in others. My mother withheld food for every reason in the book (misbehavior, being too busy, not believing I was hungry, trying to teach me a lesson about different things, like patience, and making sure I stayed super thin, and making sure I enjoyed the food she cooked more) and I was hungry all the time, though never became too unhealthy because I never exceeded 24 hours without food. But it made me extremely hunger phobic (which I still am today.) I developed insomnia and generalized anxiety at the same time. And no one in my family took it seriously - they were all disappointed in me. However, when I developed depression, my parents constantly took me to doctor's and tried numerous medications - Hydroxyzine, Prozac, Lexapro, Zoloft, Clonidine, Welbutrin, and Abilify - all to no avail. During my depression, both parents became extremely emotionally distant from me, which made things worse. Finally, my doctor prescribed Mirtazapine and convinced my parents to feed me more regularly, and my depression and insomnia went away. However, I was also prescribed Risperidone. I was told that its mood-stabilizing effects would be beneficial in helping regulate my emotions and would prevent me from overindulging in my internal fantasy world (that became a crutch for me during my depression. I was not psychotic or bipolar - my official diagnosis was major depressive disorder and I never had mania or hallucinations. Risperidone was at a low dose, .5 mg, although I was only 14. She also wanted Risperidone to be a short-term drug. However, we had to abruptly switch to a new doctor (my parents had split up, and we had to find a doctor closer to their new houses). He seemed to think Risperidone would be fine as a long-term drug; I suppose he thought it was needed to keep my depression at bay alongside Mirtazapine. Here's when the trouble began. Mirtazapine was fine (I'm still on it.) However, with Risperidone, I had to fast regularly to test for insulin resistance. This aggravated my hunger phobia, but my parents didn't take it seriously. It also exacerbated my anxiety tenfold. I became so afraid of bugs that by the the first year I was on it, I was too afraid to leave the house during the summer. Sleeping was hard because I was terrified a bug would crawl into my bed. Some of my childhood fears came back and became huge an irrational - I was terrified of vomiting and lound sounds, to name a few. My family didn't take this seriously - they didn't believe it had gotten worse; they told me I was always this anxious. My doctor mostly believed them and gave me Xanax rather than examining my medications. After six months on the drug and for the rest of my time on Risperidone, I began waking up twice during the night by extreme hunger, unlike anything I ever felt (around midnight and again between three and four in the morning) which was disastrous for my mental health because of my phobia. (I think the only way I survived was because the hunger was so extreme that it felt fake, but it hurt like hell.) I couldn't go more than two hours without getting extremely hungry, and became afraid of taking standardized tests in high school (because food wasn't allowed) and couldn't go to social outings because I was afraid my friends wouldn't stop for food. Sometimes, no matter what I did, I couldn't feel full. I stopped doing the fasting blood draws because of my phobia, despite the potential consequences. I started cutting to deal with the constant threat of hunger. My family still didn't take my deteriorating health seriously and even threatened not to feed me to get to do what they wanted, and mocked me for being scared all the time. The only thing that stopped them from not feeding me was my doctor. He told them to feed me, but he didn't take me off the drug despite the hunger-induced insomnia and anxiety. I had prolactin troubles. It gave me an intense sex drive. However, it stopped my puberty almost entirely. I had menstrual periods once every three months, but when I did have them, they could last for two weeks and were very heavy, though I had no cramps. I also began to look different - I look younger in my senior yearbook photo than I did in my eighth grade middle school photo. People who saw me around high school who didn't know me well enough asked if I was a freshmen all junior and senior year. My parents blamed me for some reason - they just said I should wear more makeup and said I got bad "genes" from the other parent. After three years on the drug, I started having serious problems with my gut. For the first three years, I had bad constipation on and off, getting progressively worse as the years went by. After the third year, I had an episode where I was constipated for ten days and had to use powerful laxatives four times to finally get some relief. After that, I had to use those laxatives regularly. I also developed an immense, cramping pain in my gut. It would get so bad that sometimes, during class I couldn't do my work at all. I had to sit there, motionless, for the full hour because the pain was so bad I couldn't move. I had trouble standing for this same reason. This was my senior year, and the intensity of and the frequency of which the pain occurred and the need to use laxatives increased. At the same time, I started having psychotic episodes. I would switch between "positive" episodes, where I had delusions that the teachers and students in one of my classes were forming a conspiracy to humiliate me, that everyone I knew was trying to collect information about my weaknesses (hence my refusal to tell anyone about the pain in my gut), that other teachers were reading my thoughts, and so on. I became terrified of small noises and believed that whispering people were always talking about me. I had a perceptual difficulty where the world looked too shiny and glass-like. In between were "negative" episodes, where I couldn't make facial expressions, everything looked gray, and I moved very slowly and either felt immensely sad or nothing at all. teachers and friends tried to help me but I was scared of them and wouldn't let them. My family be angry with me. I was living with my dad, and would accuse me of abusing my Xanax drugs when I had negative episodes, and would yell and once hit me when I got scared of him during positive ones. I didn't live with my mom at all because her abuse was worse. After graduation, the laxatives just weren't effective anymore, but I kept using them, more and more, to try and get their effect. This caused bizarre symptoms (I think.) I slept for 14 hours a day, and had trouble moving after I took one. My heart would go extremely fast for hours after taking them. At the time, I started to worry they were killing me. I knew that both Risperidone and Mirtazapine caused constipation. The hunger was bad as it had ever been, and I was having delusions based around that, and I knew that Risperidone and Mirtazapine caused increased appetite. I finally decided that I needed Mirtazapine more because it had relieved the depression symptoms first, and Risperidone was only ever supposed to be for emotional regulation help anyway. Deciding I could do without it, I quit it cold turkey. I wouldn't have done this if I was thinking straight, but I was psychotic and no one was offering any help. Within hours, my constipation was relieved and NEVER came back. My appetite dwindled within a few days, as did my anxiety about bugs. For the first time in years, I walked out into the summer heat without fear of bees, and slept without hunger. I had a wonderful feeling in my body that I can't even describe. My psychotic symptoms being to ebb immediately, and were gone entirely after a month. However, other troubles popped up. First off, I've been mildly depressed and isolated since what happened. I feel awful about how I treated my friends and teachers when I was psychotic and thought I had to protect myself from them (which usually meant rudeness or shutting them out). I reconnected with some of my friends, and they really understood. However, not with others. Also, my family is the most distant they've ever been. They don't understand what I've been through, what I'm dealing with now, or why I treated them the way I did. They think I over-exaggerate and seem to regard me as unstable and don't have a sense of the recovery I've made, they only see the shortcomings I still face. I feel like a burden to everyone - I always need something, like money for doctor's visits or emotional support. I haven't yet been able to offer much in return, and it's profoundly upsetting. There's always something going on with me and I just wish I could help others for once. Two moderate shortcomings are communication and driving. Talking has become very difficult - I'm always forgetting what I should say (like "have a nice day') and am frequently lost for words - I either stare off into space or say "um" multiple times when asked a question. My words come out jumbled. Only a couple of friends have been patient enough to learn how to communicate with me. My family says I'm less intelligent than most people my age, and my peers and professors tend to think I'm weird or rude. I'm getting better though and my writing has remained fine and is a good communication tool for me. I also still can't drive. On Risperidone, I was too afraid to drive. Now, my nutrition is bad (I'll talk about that more below) and so it makes it hard to focus on different things at once (like car speed and lights) but I'm working on it. It's slow going though because I need to get away from my family. One of those is my menstrual periods. They are regular now, but the cramps they give me are intense. So bad that they make me sick to my stomach. Sometimes so bad that I almost faint and/or see stars. The cramping extends down my legs. I experience some of the psychotic symptoms I had on risperidone, along with confusion and sometimes even hypomania (like rapid talking and over-spending.) I now take Xanax exclusively for this because it's the only way to drown out the pain. Worse, I have terrible problems with my gut. I had acid reflux for a year after quitting Risperidone, though it's now mostly gone. Risperidone may have increased my appetite, but when I quit it, I lost my appetite almost completely. I became at one point nearly ten pounds underweight. I usually ate one small meal a day with a snack. I became so underweight that at one point I had problems breathing and climbing staircases. I had strange pains in my legs and made very poor decisions. I got sick all the time. I was cold all the time too - I had the space heater running in the summer. My felt pain in my bones all over my body and sitting on hard floors was excruciating. My family noticed none of this. At one point, I had to go to the urgent care once for dehydration. But of course, the doctor and my family wrote it off as anxiety, though the doctor mentioned I needed to put on some weight. I can't eat breakfast anymore I have symptoms of severe IBS daily, and used to vomit if I didn't get enough sleep (though this has since lessened to heartburn.) I still have malnutrition problems on an off. I alternate between a week of eating normally, eating less, and then eating almost nothing at all. Doctors and family say it's anxiety, but my anxiety has been virtually gone since quitting Risperidone. On that note, I HAVE made improvements. My anxiety is the lowest it's ever been my whole life (I can pick up spiders in my bare hand!). My hunger phobia, for better or worse, is more manageable now that my appetite is unreliable. I am in college. Socializing is hard and my roommate also became verbally abusive, making fun and belittling my health problems more actively than my family. However, I've made some light acquaintances and am helping a professor with research. I'm in the honors program at my school and I have a job. Despite my pain and eating problems, I go to class and have learned to be tough about it. I'm thinking of writing a book about my experiences with Risperidone. I'm keeping hope and positivty. But to be honest, it's hard. I don't have anyone to talk to about what I've been through. The nutrition problems are bad, and no one takes them seriously. I have a better doctor now, prescribing Mirtazapine and Trazodone (for sleep), and does recognize my weight issues are a problem, but I have trouble paying for her on a regular basis, and she can't do much for me when it comes to helping the nutrition/weight problem - I need a nutritionist, which I also can't afford. And so my poor health continues to get in the way of a lot of things, but I don't many solutions and sometimes the only thing I can do is hide them and manage them the best I can without guidance. And so, I am so grateful to anyone who has read this long and personal post, and I greatly appreciate any support and want to offer all I can in return.
  7. How to taper less than .01mg at a time

    I am tapering liquid Risperdal and am trying to make a smaller cut than .01mg at a time. I am currently at 1.10mg. This is what I usually do: 1. Measure out 1 mg with a 2 ml syringe and at it to 1/2 cup water per directions from medication insert 2. Measure out .10ml with a .50 ml syringe (1ml of liquid = 1mg of Risperidone) 3. Stir then drink right away Is there a way that I can measure out an amount of liquid and then pull an amount that will give me a .005ml/mg cut? If so, can anyone provide he water to drug ratio as to how to go about making a cut this tiny? the smallest cut I can make with the .50ml syringe is a .01ml. Thank you all for your help!!
  8. Tiggy: Is it withdrawal or bipolar depression?

    Quick general question: What is the advice in the case of someone who has only been on 2.5mg Risperidone for a week? The conundrum is if they do a standard 10% / 3 week taper it'll take almost a year to reach 0.5mg, or two years to reach 0.05mg. During this time the duration may outweigh the risk of doing a much faster taper now. I am anticipating actually advising someone, and hopefully they won't delay much longer in asking for the schedule which may change the longer they're on it. So generally speaking I'm curious about the sliding scale of relative risks and tapering advice in this regard. At the lowest extreme someone who has only taken it once could probably safely stop cold turkey, or something approaching it, the next day, right? At the other end, at what point does the 10% / 3 week guideline become applicable?
  9. Hello, im from eu, sorry about my english. i'm going to taper my medication which is risperdal 1mg. I have had it about 1,2month. I have been taking 0,5mg for few days now so.. My earlier meds were abilify, zyprexa, truxal and levozin. I had my boozepsychosis about 7 months ago. how slowly do i need to manage with risperdal?
  10. New to the community. Joined after reading Schizor's (forum member) story. I'll try & make this short. Hospitalized twice. (For "psychosis"). Once for a month in psych ward (Oct - Nov 2016), second time for a few weeks. (Feb 2017) For the first time, forced to take Risperidone & Abilify. Approx 10mg. After complaining it was gradually decreased down to 1mg. Upon release from ward, through trial & error, stopped one drug, tried the other & vice versa. Eventually went cold turkey off both drugs. Second hospital stay was given a shot of Invega. It seems you guys know the drill .... Zombie like feeling, loss of balance, stomach pain, pounding headache, face numbness, involuntary muscle movements, aches, sore eyes, insomnia etc ... After constant arguments, battles & calls to local pharmacists ... Decided to go off the drugs cold turkey. Again it seems you guys know the drill .... After constant nights of bad withdrawals ( a few weeks or so), kinda - sorta made it through only to still have major insomnia, lack of motivation, no energy, weird thoughts, sensitivity to lights & noise, jerky movements, aggression, a bit of sexual dysfunction & so on. Ladies & gents ..... What now ??? I feel exactly like Schizor did. Only wanna sleep but can't really, only wanna eat but don't feel satisfied, lack of emotion & stone cold thoughts, loss of character etc ..... On top of all this I have legal issues & may face jail time. A nightmare is almost an understatement when it comes to these drugs. It's also caused me to become completely paranoid of any doctor diagnosis, (psychosis !?? ... More like psychosis induced) psychiatrist, hospital, medical help of any sort. Thanks for reading (if ya did).
  11. I'm new to the forums - currently taking 225mg Effexor, .25mg Klonopin, and .25mg Risperdal. My psychiatrist noted that the Risperdal is temporary (will be taking it for about 3 months), but after reading about withdrawal from this particular drug, I'm wondering if I shouldn't begin going off it sooner than that. It's worth noting that the depression and anxiety that I was experiencing even with Effexor and Klonopin did subside almost immediately after beginning Risperdal. At any rate, I already know I'll be beginning a taper off Klonopin soon, after successfully dropping from .5mg to .25mg without any side effects after 4 weeks - I think I got lucky there. I've been on Risperdal for 28 days, so my natural question, given that withdrawal from psychiatric drugs can occur for anyone taking them for "1 month or longer" is whether I should just stop immediately, since it's been just shy of one month and my dose is low, or if I should taper. I understand that I shouldn't expect a definitive answer to this, but I'm very interested to hear what others think and, quite frankly, very scared about what I'm about to face, given the need to taper from two different drugs. My psychiatrist will undoubtedly tell me to just stop taking it after I've been on it for 3 months, as she seems to believe that there are no withdrawal symptoms from any psych. drugs. So I kind of have to go it alone on this decision without guidance from her. Any thoughts would be much appreciated.
  12. My brain going into dream condition but not into sleep condition every night or day when ever I attempt to sleep I have believed the information about remote neural monitoring in all over internet and browsed internet 2 years heavily which resulted heavy thought process ,doubts and suspicion over near and dear. So I went to a psychiatrist and requested to bring me out of heavy thoughts.He made me use lorazepam for 10 days ,risperidone and trihexyphenidyl combination drug for 30 days.After 30 days my thoughts reduced so I did not go to doctor again.What a mistake ,I was ignorant of how psychiatry medicines work and slow tapering nor my doctor warned me while prescribing an anti psychotic.It is happened in july 2016. From then my brain going into dreams when ever I attempt to sleep.In october 2016 again I went to the same doctor and reported about the condition I am in.He prescribed olanzapine silently.I started using olanzapine ignorantly and innocently.When i was experiencing stomach upset that is when I researched in the internet about risperidone and olanzapine. Now this is june 2017 I have tapered risperidone and olanzapine safely and became drug free safely.But the thing is my brain still into dream condition and not allowing me to sleep when ever i attempt.My querry is what risperidone and trihexyphenidyl and lorazapam [10 days]did to my brain?what chemicals they blocked.Now stopping them cold turkey did what on my brain?what chemical i should take to get my sleep pattern back.?If I wait patiently with time will the brain correct its condition naturally?Any brain researcher please help.
  13. I have been on 3 mg of Risperdal for 13 years due to drug induced psychosis for meth. I decided to finally try to get off the med and have been tapering since December. I did 0.25 mg per month for 4 months but when I hit 2 mg insomnia kicked in for a couple weeks so I waited it out for 2 months and this time went down 0.10 mg for this month. It has been 5 weeks since my last taper and my only real symptoms are fatigue, feeling completely brain dead, and occasionally my vision feels all strange kind of like a very mild acid trip. I am sleeping 9 hours a night and everything is calm I just feel completely flat emotionally, brain dead, and tired for the most part. Would it be better to continue the taper or just hold since my symptoms aren't unbearable but they are just frustrating?
  14. Fair warning: my journey revolves around PMDD (my menstruation cycle). If this is not your cup of tea, turn back now. Hi! I'm so happy to be here! Here's the short version of my story... I was misdiagnosed with Major Depressive Disorder when in fact I had PMDD. At first, the symptoms were bearable, but after my last child, everything changed. Suddenly, I was not able to make myself or my children food, not showering, not able to pick my kids up from school. Not only that but my self-esteem was shot and anxiety soaring, and I had about one week a month where I could gather myself back up and try to heal before everything started all over again. This went on for over three years. I was completely broken. During all of this, my Psych started throwing meds at me to see what would stick. Unfortunately, nothing would work, and I ended up on 6 meds for depression and anxiety. Finally, I had had enough and approached my Psych and my Gyn about a full hysterectomy and BSO (ovary removal) to stop the fluctuation in my hormones. By this time I had tried all methods of care ranging from DBT to exercise, birth control to relaxation techniques, and so much more. Anyway, I had the surgery, and I felt (and feel) amazing. Like I had been missing out on living. Unfortunately, I was still stuck on all six meds. And so began the titration. I began titrating risperidone at the beginning of 2015. It is important to me to get off this med because I believe it to be the most dangerous. I started at 1 mg, and currently, I am at 0.18 mg. I am taking a break on my titration but intend to jump after my summer vacation and be done with this demon of a drug once and for all. Here is a list of my other meds: Morning: Zoloft 200 mg Wellbutrin XL 300 mg Lorazepam 0.5 mg and 0.375 mg ( also take around 3 pm) Night: Clonazepam 1 mg Trazadone 50 mg Risperidone 0.18 mg (liquid) StuckOnMeds
  15. Hello everybody, i hope everyone is well. i would like to thank altostrata for this website and i also want to thank whoever volunteers, so thank you. anyways, i am almost fully recovered from the harmful effects of risperidone. I did not think i would recover, all in all it took 14 months to feel "normal." Here's a link of my first topic if you want more of a perspective on how i used to be: http://survivingantidepressants.org/index.php?/topic/12502-risperdalhater-my-risperdal-story-and-how-it-has-affected-my-life/#entry234527 I took risperidone for about 3 weeks, i recall starting off with 2mg doses daily then after a few days i complained about drowsiness and feeling weird so they lowered the dose to 1mg then after a few more days they worked their way up to 3mg daily and a long with that i received a long acting 7mg injection which can be taken once a month (as i recall). towards the end of me taking the drug i started feeling very very drowsy and i recall saying in a pathetic weak voice "I don't like this, i want to stop", so i dumped the risperidone in the trash and never took it again, i stopped cold turkey. the next week and a half or so i went through the worst experience of my life until that point. i had: - constant shakiness - could barely sleep - extreme sadness - seemingly a complete absence of happiness - serious muscular fatigue and weak blood flow these all disappeared after that week and a half except for the muscular fatigue and weak blood flow. the sadness/blah feeling got better at an extremely slow pace. libido died of course (pretty common with risperidone). thankfully i did not grow breasts or lactate like some of the victims of risperidone, perhaps they took it longer or took a higher dose. month 1-10 i was a fatigued wreck, people asked me why i looked so sad, i had to force my smiles etc. month 8-10 or so (as i recall) got slightly better but nothing big, just slight improvements. month 10.5 = more slight improvements in energy. nothing to be excited about though. month 11-14 is when the healing starting picking up its pace. i was hopeless at one point. i don't care if you've been on the drug for years, i still sincerely believe you will get better, just get off of the drug. taking this drug is not how a human being is supposed to live. so i started supplementing with niacin and my blood flow was better, i know because when i was at the gym i could actually get a muscle pump again, it wasn't that great but it was there. when someone is lifting weights, their blood is supposed to flow and the muscle that you're using will get filled with blood and become more vascular, i did not have this except for before i took risperidone. i've been lifting weights for 5 years, gym rat level; that being said, i could tell something was wrong when my blood flow became weak. don't worry about libido, it will return as long as you avoid those crap drugs. i personally put any drug in the category of "crap" whether it is prescribed by a doctor or not. i heard that when you show low libido, zinc can be a link.... yes i did try to make that rhyme. get your blood tested, i have heard that medicines can deplete certain vitamins/minerals. again, please get your blood tested. recovery won't happen overnight no matter how many methods you use to help yourself. supplements that helped me: Natural vitality calm magnesium: it's a powdered form of magnesium and has worked better than any magnesium i've tried. Melatonin __________________________________________________________________________________________________________ if you need help or advice, feel free to message me. at this point it has been 14 months and i am recovered, everything is back to normal. check your blood, supplement with what you need, eat good food, exercise. thanks for reading everyone.
  16. My question is: How much time (in an average estimation) do synaptic receptors (5-HT/dopamine) need to recover from atypical antipsychotics, such as risperidone or aripiprazole, at the standard dosage after a short amount of time taking them (let's say, 2-3 months)? If anyone has information about this subject, please do share. Thanks.
  17. i stopped risperdal 4MG "Cold Turkey" and because of that that i can sleep only 3 hours per night. i am wondering regarding 2 issues: 1. How long will it last without start again and tapering ? 2. Can it make permanent damage to the brain so even after slow tapering the problem will persist permanently? If someone did the same, couldn't sleep and can share with his experience it will be great! Thanks
  18. I've been off of this drug for about 8 months now. I was on 3mg for 4 months I have no drive, passion, or interest in anything. The zest of life is gone and I'm simply existing. I can't start a conversation much less contribute to one someone else has started. I'm trying to "fake it till you make it", but it's getting old. I don't remember the last time I truly laughed. Love and joy are things I see other people display and I am yearning to experience those emotions again. I have no sex drive. I hate to sound like I'm throwing a pity party, but I feel like my quality of life is ruined and I see no hope. Like, I'm afraid I'll be like this for the rest of my life and I'm only 29. How LONG does it take for you to get your emotions back? If ever? Someone give me some hope....please?
  19. do APs and/or anti-depressants deplete vitamins/minerals? i have heard that they have and i am beginning to believe that they do. any ideas?
  20. I began tapering risperdol Feb 2017. It's been about 6 weeks now. I taper 5% every week. My original dose was 1mg each night. I am now at .70mg. I have no physical symptoms but the mental symptoms are the same as the side effects only much worse. The side effects are derealization, severe brain fog, severe depression, emotional flatness and what feels like lowered I.Q. I am sleeping fine and my appetite is good. I didn't gain any weight while on this poison and instead lost quite a bit. I have been taking risperdol for 3 years. I started at 2mg and lowered the dose to 1mg about one year ago. I was told by my pdoc that I could go off of it and I jumped at the chance. He tapered me way too fast and I think I experienced a psychosis or extremely high anxiety. I reinstated at that time. (I hope this post makes sense. I'm not thinking too clearly.) My question is, will these side effects start to diminish while I'm tapering? Will this start to go away as I am ingesting less and less drug? I've read many horror stories online and I'm really reaching for some success stories. I'm very afraid that these side effects will last long after the taper is complete. I am so depressed and do very little but sit on the sofa. I have to force myself to do anything and I have no interest in anything at all. Nothing brings me joy and I cannot feel love anymore. I don't laugh and I don't cry. I am zombie like. It is completely miserable. I've lost everything since I started this med. I've made very bad choices and lost my relationship, my job and my home. I am now living with my grown daughter and her husband. Without them I'd be homeless. Any advice would be very much welcome and appreciated. Thank you.
  21. Hi I'm Kat At last after 25 years and after much begging my Mh team have said I can gradually withdraw from the cocktail of drugs I am taking. Starting a week on Friday. They have decided that the first med I should taper is the 30mg of Mirtazepine. They didn't explain why this particular drug should be the first to start with. They also didn't tell me what the lower dose will be. I take Diazepam, Risperidone, zopiclone and prn tamezepam. Any help would be appreciated so that I can make a decision whether to do what why MH team want me to do.
  22. I am 54 years old, and experienced my first manic episode, starting 1st November of last year, requiring a month of involuntary hospitalisation starting 14th November brought on by numerous stressors. I was on Lithium and Haloperidol, from the 15th Nov, then ±900mg Lithium and 0.5mg Risperidone from the 15th Jan . I started tapering the Risperidone from the Feb 16th. My last dose was 0.125mg on 15 March. How long will the withdrawal symptoms last? The reason why I'm asking is I'd also like to know if I am experiencing withdrawal symptoms or bipolar depression? The intense depressive feelings arrive and leave suddenly and unexpectedly, sometimes lasting a few minutes, sometimes a few hours, after which I feel mildly depressed again, which is a general state. I am able to be lifted, for example by gardening, good cooking, humour etc, during this general milder state. I have general anxiety about several factors which triggered the original mania, namely money (increased now, due to difficulty working), accommodation for my and my spouse's ageing parents who are both difficult to work with, those being by far the most major among other stressors. I have found that very carefully-considered and rare - perhaps twice a week - use of Diazepam can also return me to this state from the more intense state. I intended to start tapering the Lithium once I feel more stable and know myself better after this current tapering. I apologise if this has been covered before, but I find reading and writing about my condition extremely stress inducing, which is to say getting to this point has not been easy. I am eternally grateful in advance for the help.
  23. Last year November, I was diagnosed with depression and given benzhexol along with risperidone. By December, I began feeling dependent on Benzhexol and could rarely do stuff without it especially reading, talking to folks around me,etc. I always felt too anxious without it,also I wouldn't sleep properly, then gradually my body begins to feel horrible, headaches along with a terrible body feelings, confusion. I knew there was a problem and complained about it to my Doctor. He dismissed it as I was becoming anxious, it's a mild side effect, etc basically I would be fine and he increased my dosage to take a tablet twice daily, then I felt better but only during the drugs. By January the drug wasn't making me feel better, I then began complaining further but this time I also tried stopping, I would stop for a few days, usually lying down thinking my discomforts would go away, it doesn't then I would use a pill, I could reduce my use to a pill, then half, I spoke to my doctor further, so now I'm taking half a pill daily, but it feels like hell and I often wish I never should have started using pill as I only feel worse.
  24. Hello. I am twenty years old and had been on antidepressants since I was ten. From then on through my teenage years, all I knew was I needed to take my medicine . Once I was diagnosed with high-functioning autism, my pediatrician referred me to a neurologist. The neurologist then put me on respiradone and strattera. I don't remember if I had any behavior problems or not, but my neurologist told me I would have to be on medicine for the rest of my life. I stayed on those two meds until I got into high school. My first two years of high school, I couldn't stop crying. I cried day and night. My neurologist put me on celexa. When that didn't work, my neurologist told me he could no longer help me and referred me to a psychiatrist. I saw the new psychiatrist my junior year of high school who told me I had depression and anxiety that needed to be treated. I was taken off respiradone and strattera and put on pristiq and adderall. When pristiq wouldn't work, I was switched back to celexa. So it went on, switching back and forth between antidepressants. There were so many different ones I can't remember many of them. Every time I asked my psychiatrist if the next time it would work, he assured me it would. There was no chance to talk when I saw my psychiatrist. It would result in a new prescription every time. During my senior year, I helplessly slept through every class, sometimes falling out on the floor asleep. I had a good school counselor who allowed me to pass because she knew it was the medicine and I got plenty of sleep. I also cried uncontrollably almost every day in front of everyone and it was very humiliating as I would stir up a lot of attention. My senior pictures of me showed a person with a puffed up and swollen face. I was switched to lexapro again and stayed on it my whole first year of college. Then the crying returned. During my second year, I was switched to Abilify for depression. I still trusted my psychiatrist as he again promised me it would work. Out of all my experiences with antidepressants, there is nothing that could ever have compared to this. As soon as I took the first dose of Abilify, my brain signaled to me something was very, very wrong. I began receiving no sleep. My psychiatrist put me on trazadone for that, but when I took it, my body fell completely limp, my heartbeat slowed down to almost nothing, and I went numb while my body shut itself down. I stopped it after two nights. Meanwhile, with abilify, I began spending all my time obsessing over things I would normally never touch. I believed I was an alien hybrid sent from outer space to save the planet. I also believed the human race are all aliens in disguise. Then I started going mad. I didn't want to be a human anymore. I wanted to be a supernatural creature with otherworldly capabilities. This was all extremely terrifying to me, but I couldn't stop myself. I lost my common sense as I believed these nonsensical theories. My mind was overpowering me with racing thoughts such as these listed. I couldn't think clearly. I was almost always in a state of rage. Reasoning had left me. For reasons I do not remember, I stopped Abilify by myself cold turkey. My psychiatrist had told me before that I never needed to worry about tapering because the antidepressants I took were all in the same family. He never mentioned stopping completely. Withdrawal symptoms didn't show up until a week later. My psychiatrist told me they would last 15 days. They were relatively minor, and I didn't worry much about them. However, nothing could have ever prepared me for the horror I underwent next. Every horror I could have never imagined bestowed me over the course of a month. I received no sleep. I was very lucky if I got one hour. The nights soon got from bad to worse. I developed REM sleep disorder. I was unable to tell the difference between being awake and asleep. As my mind was drifting, I jumped up in the air, screamed, swung at the air, and thrashed violently all over. In addition, my head would suddenly snap up and I would shout melancholy indistinguishable language and suck in sharp breaths. I was aware of everything, but I had no control over it, and it was very disturbing to me. Then came the uncontrollable muscle movements. My lips drew up on the sides, my mouth gaped open, my lips puckered and pouted, my teeth bared, my tongue stuck out, my neck extended, my eyes bulged, my eyebrows rose and lowered, my hands flapped, my arms swung, my knees jerked, my head jerked side to side, and my fingers extended. Shouts, grunts, moans, and gasps escaped my mouth. Several weeks went by as more horrendous symptoms appeared. Every day I was a zombie. I could only do basic human activities. I had no awareness of the passage of time. At night while drifting off, a dark shadowy presence swept over me. I was aware of where I was in real time while drifting, but I sensed a sudden danger. I jumped up alert every time. I heard a voice I believed to be God's telling me why I was like this and what I needed to do. It spoke to me relentlessly for days. When this occurred, an otherworldly and overwhelming sense of peace filled my every being. But it was always soon replaced by a terror so surreal I could not function. During this time, I could "see" my brain and I believed I was in control of what I allowed to be let in. After four days of this, I ordered the voice to "Get out!" It did and did not come back. Right after this, a veil suddenly covered my mind and I was disengaged from reality. I had no sense of where I was and I had no connection with my parents. I was always mad, crying most of the time, and my head was always jerking. I saw my psychiatrist for the last time two months ago. The doctor who had been nice to me all this time suddenly turned mean. He told me he refused to see me unless I got on medicine. By this time, I had found this site and many other websites about withdrawal. I knew I wanted to try living a better life and I was not backing down. I never took the newly prescribed anti psychotic he prescribed me. A week later, my parents, exasperated with how I was doing and on their last straw, called my psychiatrist. My dad told the psychiatrist I had read on the internet how long the withdrawal really is and the doctor spoke with me on the phone. My psychiatrist told me that the withdrawal symptoms I was describing were "all in my head" because the medicine would already be out of my system now six weeks later. He told me I needed to get on medicine right now because "I needed help". He told me my quality of life was not as good without the medicine. I was in another rage episode by this time, and unlike me, I confronted him. I said "Well why are a lot of these the same symptoms I experienced during the so-called withdrawal time?" He said he didn't know and preceded to ask me was I on drugs. I was in disbelief that anyone would ask such a thing. I have not spoken to that psychiatrist since. I am dealing currently with a lot of physical and mental symptoms but none I would describe as severe as that horrible nightmare of a month. (That month just happened to be timed perfectly with my Christmas break.) My mouth, head, and fingers jerk, but never as exaggerated as they were the first month. I dealt with extremely numb fingers, feet, and ankles up until two weeks ago. My ankles at times felt like they were hanging by a single nail. My feet, bluish-green, were so numb and swollen I had no feeling and shooting pains shot up my legs. I was extremely dizzy for so long. My gp told me I have low blood pressure. I started having panic attacks. Anxiety crept over me for no apparent reason. I cried a lot. I felt hopeless. I am dealing with apathy, anhedonia, akathisia, and cognitive problems. My memory has not been well during this whole time. I am not aware; I'm just wherever I am. I have lost perception of sight, hearing, and touch. I do things I'm supposed to do because I know that's what I've always done. I cannot connect feelings to memories; I have to rely on pictures and journals from over the years. I had to look back in my journal to refresh my memory of this whole experience which I happened to write down. I have been disconnected with myself...it was worse in the beginning. I would look at pictures of myself and couldn't connect that it was me. The whole first month of withdrawal my face was so puffed up I thought my skin would fall off. Sometimes things look bigger or smaller than they appear. My thinking ability is limited. I went to my gp again three weeks ago and I was low on vitamin D. I am currently on iron medicine, vitamin d supplements, allergy medicine, and multivitamins. Although the numbness has gone away, I am extremely faint and have weak tremors every day. At night I'm miserably exhausted. My heart is always beating fast and hard. I get chills and my body tenses up. I'm not sure if I should be concerned about any of this. I cold-turkeyed Abilify four months ago. I have managed to keep my grades up in college since then and so far have maintained a perfect attendance. Some days are harder than others, but I try to count my blessings as I've heard stories far worse than my own. I am only beginning to understand what I am dealing with. The last thing I would want is to ever take another antidepressant and hinder this process. I feel like I have a real sense of myself now and I feel more in control. I have no idea how long this will last or if it will ever go away but I try to maintain a positive attitude about it as things slowly get better. I have faced the fact that I can't change my past but I can certainly shape my future. I apologize for the long story. It is difficult to get my thoughts together.
  25. Hi all. I have been on a combo of Risperdal and Zoloft since 2012. I reached 3mg risperdal and 200mg zoloft in early 2016, tried to taper off both starting in June of that year, and had a bout of insomnia in November, at which time I reinstated along with an additional 15mg remeron. Adding the remeron, I've learned, was a huge mistake and most likely unnecessary. Since then I've slept at most 6 hours instead of my usual 8. For the first 2 months on remeron I avoided caffeine and tobacco. Then, after picking up both again, my sleep suffered, and I eventually had nights with 2-3 hours. I've since learned that caffeine and tobacco induce the enzyme CYP1A2, which metabolizes remeron, explaining this. By abstaining from both, my sleep has returned. I have also tried shaving a sliver off my 15mg pill with no luck...getting a full night without sleep. I would like to be able to drink coffee and smoke again. That leaves me with 2 options, get off the remeron (seemingly impossible) or tolerate the lack of sleep. If I do the latter, will my sleep eventually not recover even when abstinent due to repeated withdrawals? I had been planning to use coffee and cigs only sporadically, letting my sleep return before using them again, or using only on the weekends. If I that is not sustainable, then how do you recommend I get off the remeron, given my sensitivity to even a small dose decrease? My doc has suggested trazodone as a replacement, but that med interacts with my other meds and a post about it here scared me away. Thank you so much for your help.
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