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Hi, all. I’m new here and thought I would do an introduction. Im a 42f mom of 3. I’m fortunate to have found this forum thanks to the Lexapro support group on FB and mentions in subreddits before I started my taper. in December of 2023 I was going through a time of heightened stress and anxiety that sent me into panic attacks, agoraphobia, and extreme anxiety and depression. I’ve always had moderate anxiety but this was on another level. I went to my primary doctor out of desperation and she immediately suggested Lexapro, and she stressed that it has hardly any side effects, easy to come off of etc. I wish I had educated myself better but I was desperate at the time. I went on 5mg. It maybe helped slightly, but not much. In January she upped my dose to 10mg. I was still having extreme anxiety and panic frequently, but things were slightly better maybe. I started researching more and decided I don’t want to be on these meds anymore. I have been on it for a total of 11 weeks, 6 weeks on 10mg. I want to start tapering slowly asap but I am nervous. I still don’t feel like I’m stable, I still have heightened anxiety although not as bad as the beginning. I am absolutely EXHAUSTED, to the point where i can barely function. I don’t know if these meds even “work” for me and if I’ll ever stabilize on them enough to start my taper. I was planning on maybe waiting until I’ve been on 10mg for 8-12 weeks to see if I’m more stable at that point. Does anyone have any suggestions or advice? I am also in therapy, take supplements (fish oil, vitamin d, b12, multivitamin, l theanine, and magnesium), I exercise daily, eat healthy, no caffeine, meditation daily, and go to acupuncture monthly. Happy to have found this site, it’s an amazing resource.

I was prescribed Lexapro 10 years ago following the death of my daughter. I was started on 10 mg, eventually increased to 20mg due to anxiety issues. 3 months ago I decided that I wanted to stop taking this medication. I felt blunted most of the time, and wanted to see how I would do off of it. This was discussed with my family practitioner. We halved the dosage for a month and then halved it again for another month. At that point I was down to 5mg daily and doing ok. I then went to 5mg every other day x 2 weeks, and then stopped. I have been experiencing brain zaps and parasthesia daily. Its extremely uncomfortable and has made me withdraw from social activities. I force myself through the work day, then come home and get into bed. Last week I spoke to a Psychiatric NP and asked about Prozac as an adjunct to help with these symptoms. This is day 4 on Prozac 10mg which has helped maybe 20% with the head zaps. I'd appreciate input. This is miserable.

Hi I’m mark. I spent an hour trying to make my signature , but it wouldn’t allow it because it was to long. Tried cutting it down significantly, still to long , gave up. Basically I’ve been on a million drugs on and off , and didn’t ween off any of the em correctly except lamictal and seroquil. I can make a extremely generalized timeline . Starting with cymbalta 16-17 years ago. cynbalta -2007 1 year 2012 -1 month wellbutrin-2007- a few days xanax-2012- 1mg, recreationally 10-15 doses klonopin-2013 1year .25-1mg lexapro-1-2 months 10mg topamax-2weeks small dose lamictal— 2015 7 years- doses(25-400mg) Seroquil- 2015 5 years -15-100mg ketamine-2019 -10 iv treatments gabapentin-2020- 300mg- 2 months litrhium-2020 1200mg-1 month ambien-2020 5-10 mg 3 months Propalanol-2023 10mg -2 weeks I’ve had several med trials for past 10 years trying to address symptoms that came out of nowwhere in 2013, which I now realize we’re most likely issues from taking cymbalta at an early age , not weening off then going into more rec drug use and Xanax . past ten years of my life were terrible , Constant doctors , trying meds , psych ward visits from bad reactions , not knowing what was wrong , more meds , even was convinced I had lymw and did antibiotic protocols , hyperbaric chamber , etc. also multiple shoulder surgeries from bad shoulders , one of which was a botch job and caused terrible nerve damage furthering my issues . started realizing psych drugs were the problem in late 2021. Got off everything for about a year I got hit with a severe life threatening bout of insomnia in 2022 June , and after being off of drugs for nearly a year , had to resort back to trying things , and things spiraled quickly . While I always have had the hypersensitive nervous system symptom, i I started developing this at a new level . super sensitive to sounds ( even not loud soundslike fridge clicking on, car door in distance , anything etc). Can’t watch most movies emotions trigger symptoms . Constant tinnitus . Can’t exercise , sex release , can’t go to the store without flare .) nighttime adrenal surges / jolting . even then I STILL was seeing psych and trying meds because I was not familiar with kindling . How would I know ? I was member of benzo buddies and knew something was going on drug related but was suffering and didn’t know how else to try and fix it . Then I finally learned of kindling , and found this site . I’ve been off everything for 6-7 weeks . I see people with exact symptom profiles and I see a lot of people that don’t seem to show improvement with the hyper arousal especially from sounds . ive already suffered most of my life , and it’s been ten years and I’m not even close to better , in fact way worse. I guess what I need is a success story, for people with similar countless (to long to list) drug trials , that had the hyper arousal from sounds , lights , emotions , etc and eventually showed improvement . I don’t want to break any rules by saying how I truly feel , but this basically isn’t doable . I saw one lady that said she has the auditory arousal issues seven years later .. what?????? No.. can’t, sorry, I’ve already been in hell for 10 plus years . any success stories or other who had this issue and showed improvement WOULD help. I can’t really find any though . thank you for allowing me in the group and for reading

Diagnosed with panic and adjustment disorder 1987. Experienced 3 situational depressions (1 was postpartum). SSRI for 30 yrs. Just RI Lexapro to 5 mg after a failed 4 day discontinuation from 2.5 mg. Seems to be helping in waves and windows. Dr appointment next month but he has told me that if I stop Lexapro, protracted w/d possible with treatment resistant depression surfacing. Advises that I should consider staying on for life. I am afraid of both staying on and discontinuing. I've read about severe, untreatable akathisia, protracted w/d and all other horror stories. I am worried that one or two months out from discontinuing, symptoms will return that can't be treated. 1. Will a gradual slow microtaper from 5 mg. (after stabilization) prevent a protracted w/d? 2. What if I experience another situational depression, how to treat it then? 3. What are risks of staying on a low dose SSRI 2.5 or under? 4. Is that better than risking protracted and untreatable w/d? Last situational depression 8 yrs ago, Dr switched SSRIs and now I realize what I went through was was w/d on top of the depression. Had to rely on Lorazepam for 3 months and did a gradual successful taper off. I believe I was very fortunate given the horrific Benzo stories.I cannot fathom relying on Benzos again and would rather stay on Lexapro low dose than risk benzo dependence. I would appreciate thoughts on the above. Thank you!

I’m a 63 year old woman and my first antidepressant use was in 1997. I saw antidepressants as mood cosmetics: an adjustment to my anxious, sometimes irritable and depressive personality that would help me get ahead and live more boldly. I didn’t stay on for long and I quit cold turkey. I broke up with my boyfriend and fell into a deep depression, which I attributed to the breakup. 2003, I found myself in a challenging job as I started having premenopausal irritability. My gynecologist put me back on Prozac, but at some point (2006?), my gp switched me to lexapro. I stayed on it until 2015. (I had post nasal drip with fluoxetine, which led (I think) to numerous sinus infections; that’s why I asked to switch) 2015, I realized I’d missed many doses and I felt fine, so I just stopped, but started having zaps, emotional lability, anxiety etc. I kept wanting to get through it, thinking the symptoms would abate sooner or later. After many months like this, I complained to my gp about hot flashes—not recognizing them as a withdrawal symptom. When she suggested lexapro as an off-label solution to that problem, it felt like a message from god and I resumed lexapro. 2021, I honestly felt there’d be no easier time in my life to taper. Never mind the pandemic, I thought my life was great, which presently seems blunted and delusional. 11/30, I started reducing my doses, and proceeded carefully for 254 days, listening to my body and making reductions after zaps stopped and I felt stable at the lower dose. My last dose in 8/2022. Tardive withdrawal symptoms started in September or October. They seem episodic but mostly, they’re present; I’ve had just a few multi-day breaks from symptoms. Writing this in mid-February 2023 and wondering if I’ll ever feel better. Dealing with loneliness, aging/dying parents and money issues are added, unavoidable stressors. of the four doctors who’ve prescribed ssris for me, one was a gynecologist. The others were GPs! Very grateful to friends who are willing to listen. what helps: —I used to take my Ssri with a fistful of supplements and I found it easy to lose the habit of taking supplements when I stopped the drugs. Now I’m careful to take supplements and they seem to help, but I’m not qualified to advise. (Everything I take: Fish oil, magnesium, b6, b12, calcium citrate, C, D3) —I take valerian to help with sleep. I like solaray because it has standardized active ingredient. Topical melatonin, also for sleep; sometimes kava tea for daytime calm —seldom drinking any alcohol —switching from black tea to green and limiting it to two cups in the morning —seldom watching any news at present —asking myself “what is the best way to take care of myself right now?”—especially when I’m symptomatic —I pick up a lot of good tips from YouTube channel “therapy in a nutshell”… not specific to drug discontinuation but useful techniques for staying calm I’m here to learn as well as to support and I welcome comments to improve my approach to recovery may we all be well, Mary

#1 Help. I was on lexapro 8 years. Tapered off lexapro onto Effexor in sept 2021. Couldn’t handle it. Stopped taking after 5 days. Started Zoloft. Lasted 30 days. Side effects were bad. Tapered off to pristiq. Lasted 10 days and my psychiatrist said to just stop. I was trying to give my body a break so I could start a new med. 8 days later I went back to lexapro. Took it tonight. I’ve been having slight confusion lately, mental fog, poor concentration and not in touch with reality. I’ve always had panic attacks but what I experienced was not. My brain started to get warm and I almost wanted to pass out following extreme confusion with my heart/pulse racing incredibly fast. It’s like my brain was shutting down. I was so scared thinking i was having a brain aneurysm, stroke or seizure. I called 911. Went to hospital where I got a ct scan of my head. They ruled out a tumor, stroke or seizure: they didn’t check my blood sugar or run blood work. This happened at 10pm tonight. Got back home almost 2AM and went to bed extremely scared. I woke up an hour later in state of confusion to this happening again. The docs say it’s from the meds. I’m so scared I can’t sleep bc I don’t want it to happen again. I feel like it’s more than this and I’m actually going to die from whatever this is. It’s like my brain is broke. I was perfectly fine a few months ago. Idk why the docs couldn’t find an answer to what I was experiencing. I’m so scared this is something else. I’m 34, male, good health.. active

Hi friends... When SSRI's came into my life, they saved me. Through most of my life (teens and twenties) I had successfully lived with my mental health struggles using tools such as exercise, time outdoors, and an ever changing and stimulating lifestyle as one has during this time of their life. When I moved in my early 30s, completely upending my life as I had never lived anywhere else, I was no longer able to deal with the depths my depression took me to. After failing to find relief from Wellbutrin, I reluctantly decided to try Lexapro. It truly saved me when I was at my lowest point until then. I knew about some of the side effects, weight gain, lower libido, which is why I hesitated. But, as I was no longer functioning, something needed to change. And, it did. What I did not know, was how horrific it was going to be to try to get back off of this drug. I understand myself better now, and I've created an environment in my life that should help me to thrive. But then there is this drug. It is like a veil. More subtle than the depression was, but still something that keeps me from living fully. It keeps me from feeling fully. In 2019, I was ready to come off of the drug. With a new psychiatrist (not the one who initially prescribed SSRI to me), I expressed that I was ready to come off of Lexapro. She told me to cut the dose in half for a few weeks, then in half again, then for a few more weeks, then I would be off the medication. After 5 days at half dose, I was having flu-like symptoms, crying whenever I moved more intensely than a walk, not sleeping....it was too much. I told my doctor and she said to go back to the full dose and we could try again slower at a later time. Then, she retired, and I moved to help my Mom go through cancer treatment. Not a good time to remove your antidepressant. In April 2023, my Mom went into remission, I had the best job, I lived in a place that was good for my soul, and I had so much support around me that I was ready to try again. I did not have a new doctor by now to support me, but I had learned the first time that I needed to slow the tapering process down. I thought I could do it. I reduced my dose by only 25% for 2 weeks, then again to half dose for 1 day. After not sleeping for 4 consecutive nights in a row in addition to the previous WD symptoms I had the first time, I went back to full dose. I was angry and sad. I felt like I had no control and my inability to come off the drug made me want to come off it even more. Why don't doctors tell you about this before they put you on it???? Yes, I've gained weight, my sex life has suffered, but not being able to stop taking this little pill is appalling. I didn't sign up to be dependent on a life-numbing drug for my entire lifetime!@@ My Mom did pass away this last year. The last thing I've needed since April is to take away this crutch when my heart has been more broken than it ever has before. But I am healing, and I think part of that healing process is to take back full ownership and control over my mind and body by getting off Lexapro. I have a two new doctors who are going to support me through this, and I have this site!!! I am so incredibly thankful for the resources and stories about people's journeys going through the same process I will. Thank you all SO MUCH for this site. My new doctors have prescribed me some additional psychoactive drugs to support this process: Lamotrigine and Bupropion. I am taking these to help alleviate WD symptoms from tapering off Lexapro, but I am very anxious about becoming dependent on these as well. My goal is to come off all psychoactive drugs to see where I am in navigating my mental health without chemical support. We will see...

Hey everyone! I just recently found this site and I think I'm starting to finally have some answers. I was on antidepressants for about 10 years and then went cold turkey when I found out I was pregnant last year February 2023. I was fine for a while when I was pregnant, but then one day I started having major panic attacks, anxiety, and depression. I thought at first it was due to the pregnancy and the hormones and added stress so I just wrote it off as so. I was also having trouble sleeping with sensitivity to light and sound and waking up every couple of hours or so, which I also attributed to the pregnancy. I had my baby in November 2023 and have had worsening symptoms. Of course, anxiety and depression can come postpartum and so I attributed all of my issues to this and just to the general stress of having the baby and being new at parenting. But now, it is starting to feel like there is something more than just postpartum depression and anxiety. I have been having severe panic attacks and have trouble dealing with my emotions. When I get overwhelmed, my mind just shuts down and doesn't know how to comprehend thoughts or emotions. Could this be linked to a long-term withdrawal from my antidepressants? And if so, is there anything I can do?

Hi all, First off I am grateful for this forum, thank you for letting me join. My journey began with trying to address some confusing health issues that put an end to a career that I dearly loved. Anxiety and overwhelm with my situation took over and it was recommended by my therapist that I try an antidepressant. Since my father took escitalopram without issue (going on or off) I decided to try it. My mother and I are sensitive to medication and I was very, very resistant to going on an antidepressant. My GP prescribed 10 mg of escitalopram and hydroxzine for sleep. At this point I had been taking 50 mg of Trazodone for sleep. The first weekend of taking those meds changed everything. After the first dose I woke up dizzy and disoriented, nearly falling out of bed. The derealization and confusion from that was incredible. The panic and anxiety intense. After that weekend I stopped the hydroxyzine I asked to step down to 5 mg and did that for a month, eventually going to 7.5 because I was told that my body would adjust (under my doctors direction by alternate taking 5 and 10 mg every other to reach 7.5mg). By the fourth month at 10 mg I was having severe waves of body agitation followed by waves of peaceful calm, extreme eye strain, evening concussive headaches, sweating, fluctuating eye sight, trembling, contstipation, and derealization. The waves of body agitation were the worse but at least at that time I could lay down, ride it out and have moments of peaceful calm. I was told by my psychiatrist that most of my symptoms couldn’t be from the meds and had more with my aversion to taking it. After seeing several specialist and testing it was determined that I have acquired spontaneous nystagmus and an inner ear caused balance. Based off of my timeline of symptoms the balance issue thought to be most likely caused by long covid. At four months on escitalopram I tapered down over 2 weeks from 10 to 5 to 0 mg. Reviewing information on this site I realize now that may have been too fast. However, a lot of my symptoms did improve until I started vestibular therapy where they suggested that an ssri has sometimes been found to be beneficial. So, after 1 month of being off of escitalopram I started fluoxetine at 10 mg. Trembling started again with more headaches and brain fog. After two months of fluoxetine I’d had enough and was told that I could go off it cold turkey because it was “self tapering”. I have been off of fluoxetine for a month and was told that it would be out of my system at that point. Still I’m left with feet tingling, headaches and a constant feeling of derealization with brain fog, headaches, concentration issues and unsteadiness. Now true to form my physiatrist wants to try other things like Viibryd, Lamictal or Gabapentin. I can’t see getting hooked on benzo’s or going back on another psych med unless it’s going to be able to address my other issues. Of course nobody except my audiologist wants to go down the long covid route. Looking at past immediate AD reaction post it appears to me that I may in fact have had an adverse reaction to escitalopram and may have deregulated my nervous system further starting fluoxetine? Admittedly I am anxiety ridden over my situation regarding my nystagmus, inner ear balance (long Covid) issues but the brain fog derealization is the worst of it. I feel I may have made things worse by switching around with the meds, the way I took them and went off of them. I am being told that I wasn’t on the meds long enough or at a high enough dose to cause lingering withdrawal symptoms. I’m now basically bed ridden, unable to work or drive. I have looked through the supplements recommendations and started fish oil. I have taken vitamin C and D and a probiotic for ever. Thanks for being here and any insight that you can give me

Hi everyone, I'm Stanislav, 24 years old and I've been suffering from constant depersonalization/derealization for almost 7 years, triggered by a weed induced panic attack. My symptoms include feeling unreal, confused in the world, racing thoughts, excessive symptom monitoring, memories don't seem like my own, loss of sense of self, apathy, anhedonia, lights are bright and "tunnel vision" (a kind of visual processing problem where I don't seem to percieve all of my FOV at once). Two years later I was curious about medication since my symptoms haven't improved despite cbt therapy and time passing. In January 2020, I went to a psychiatrist, briefly described my situation and he instantly prescribed me Lexapro 10mg, which was supposedly really safe and unproblematic. I started taking it and felt changes in the next months. I cared much less about the intrusive thoughts but also had more anhedonia, was even less prone to laughing, was always feeling a bit tired and it was more difficult to reach orgasm but for me that was fine, since I had issues with premature ejaculation. Anyway, shortly after I met my boyfriend (the light of my life) and I continued the use of Lexapro for 2 years. Often times only taking half a dose, in hindsight it was irresponsible to be doing this. My dpdr symptoms have not improved but they were easier to live with and ignore. I want to emphasize that I didn't have a close connection to my psychiatrist and basically only went there for a new receipt where he asked if everything was fine and I said yes. Having no idea that tapering after prolonged AD use is supposed to be really slow, even though 5mg is the minimal tablet dosage, I quit cold turkey in 2022 for a month from 5mg because it wasn't helping with dpdr, not thinking much of it. I began experiencing great anxiety and depression and wanted to try wellbutrin, which helped for some people. So I was on wellbutrin for 2 weeks and had to quit it because it made me extremely tired and not much else. I then restarted Lexapro 5mg and later went up to 10mg for another 1 1/2 years. It was similar to the first time I took it. Then in January 2023 I decided to get off the drug and really work on my anxiety to recover from dpdr, which had been ruining my inner life. (Outwardly I was doing fine, got a Bachelor's degree in mathematics, while being dissociated 24/7, working on my master's degree right now) Without talking to my psychiatrist, whom I didn't trust that much anyway and he was changing offices too, I quit Lexapro 5mg cold turkey about a year ago. I really did not think much of it. I was really convinced the drug was relatively harmless. Stupid of me, I now know better. My withdrawals started after a week and I suffer them until today, a year later. They're not as bad as some people here have them but they are still debilitating and include: Waking up with and suffering from strong anxiety and incessant racing thoughts and uncontrollable worries, depressed mood, heart beating fast, not being able to breathe in deeply, I also have anhedonia which I had before but now it's worse and I miss laughing. At first I was telling myself it was relapsing or that my dpdr was improving because I was feeling more anxiety, so my emotions were less dampened but just last week the realization hit me that I was not just suffering from dpdr but also from having been on Lexapro. At this point I wish I never took it. The last few days have been especially bad with me not being able to calm myself down and feeling like a hopeless case. The withdrawal symptoms have not improved at all yet. I've been going to the gym for 2 months and I will continue to do so. One thing that sometimes helps is a diaphragmatic breathing meditation, Doing this I can feel the anxiety subside sometimes. I am struggling at work and university but I hope that I will improve in the next year. Do you guys think there is hope for me? I know I ***** up but after a year, I don't want to start taking the drug again to taper it more slowly. I was thinking about doing rTMS for depression and anxiety and I am also in therapy for the last half year. Would appreciate any kind words and thoughts. Cheers

Orignal full title before shortening: 2 Months of lowest dose Mirtazapine, sufferin now for over 2,5 months of withdrawal I would set my signature up properly, but I just can't remember anything. Remeron/Mirtazapine withdrawal still leaves me with such a messed up memory that remembering only 2 things at a time causes me great problems. I can't tell which month I took my Effoxor back then, I'm not even sure about the year. Though I keep great track of the Remeron withdrawal, so at least I can tell that. If you don't want to read the whole story, I categorized the "drug" part in the Drugs section below. There is still some life story though. For the start, I'm currently 18 years old and a female. I was twice in mental hospitals seeking help for a problem that was solved with - you won't believe me - one sentence by my mom. One sentence just cured my whole condition. It may sound incredibly ridiculous, but seriously all of this that you'll read wouldn't have happened if somebody told me this one sentence at the very beginning. And I'm incredibly mad because of this, as I suffered and endured so much pain through the years because everybody was so desperate to prove that I had depression. At 13 years old I had a panic attack caused by a certain phobia which I mistook for suicidal thoughts. I admitted myself to a mental hospital to stay safe, as I was greatly scared that I would harm or kill myself. I spend there 1,5 months and they diagnosed PCOS-Syndrome (hormone problems) and "mild depression". They said I should spend more time with peers, as seemingly it was caused by having an inactive social life (I was quite the outsider at school and would remain. Not because I was shy or something, I was just always such an emotional-artist personality and had interest in completely other things than others my age, so I couldn't connect. Famous people or make-up didn't bother me at all.) On the contraceptive I felt much better, though it made me sleepy, but I needed, need and will probably always need it for without it my body completely breaks down, as the hormone imbalance is severe (more on that later). The phobia-episodes stayed away, emerging randomly for a few minutes sometimes but very rare, until age 15. I think the episode lasted there for half a year and little longer? They acted like panic attacks, up to 3-4 times a day and some days I was free from it. But I endured it, and though it may sound scary, looking back it actually wasn't so bad as I made it out to be when I went through it. At age 13 the panic attacks were much more rarer, you'll see why. So when I had those panic attacks, and I wondered why they were there, they seemed to have no cause, I blamed it on the contraceptives. So I was switched to another one, but I got very irritable on it and punched a wall for the first time ever in my life (I'm quite the peaceful person). The gynecologist didn't want to switch me on another contraceptive (as she was paid by this certain brand to only sell this one - literally posters of this contraceptive brand and calendars and cards everywhere in her place), so I stopped taking it. After few months, not many, my body began breaking down. I was dizzy most of the time, nauseated, I was constantly, literally constantly hungry, didn't have appetite though for anything, I was so fatigued I would sleep literally nearly the whole day, couldn't go to school, couldn't do anything really, and had quite the anhedonia. That was the worst, the anhedonia. Hormones can really, really do lots. Didn't have period for the whole year of no pill either. When my panic episodes (that I always called mistakenly suicidal episodes), returned I seeked help again desperately - and was admitted to a mental hospital again which mas psychosomatic in kind and didn't treat cases like bipolar disorder or schizophrenia. 4,5 months there and no improvement, in fact, I got worse there. The therapist there was also a complete idiot and made just everything worse. He blamed my condition on the family (he'd wish he'd have such a deep bond with his mother), he blamed it on literally everything and called it "depression" all the time, though at the end of 4,5 months they still had no diagnosis because I literally did all paper tests they had and in all of them came out a very low scale of depression. They couldn't identify the cause at all. At first they thought Cyclothymia, then bipolar II, then depression, then this, then that, 4,5 months later we haven't got anywhere. Funny thing is, the therapist wasn't even fully licenced yet. He attended "further education" about psychotherapy. He barely knew anything. The psychiatrists there neither, because they told that "hormones can't do such a thing". Haha. I can attest they really, really do. I should have noticed he was not alright in the head after a few weeks when he told me I had sexual problems because I wasn't interested in sex enough. "Normally, people your age try around their sexuality with friends or so..." no thank you, I'll have my dignity. Next, I had an "oversensitive mother". She "worried too much." Who wouldn't about their child that has been unwell so long? "Normally people your age should go partying at night, and your mother doesn't let you..." first, I don't want to go thank you, second, yes, partying until 01:00 am somewhere in somewhere seems very safe and plausible. But my father who didn't care about me my whole life is the best one! The therapist tried to get me away more from my mother so I would get closer to my father and forgive him for not knowing "how to be a father", which I didn't do which again frustrated my therapist, and with every session he grew more frustrated that he couldn't manipulate me. Everything I spoke about in therapy I told my parents (especially mom), and everything that she spoke about with him in visits she told me. My therapist said he can't do proper therapy with me if I tell everything my parents. He sees a lack of "privacy" in this family. Everyone should have "secrets". What was unnormal to him is that we only have locks on bathrooms and on no other door. "I should be able to lock my door", he said. Which, if he really thinks I have depression, is the most stupid thing you can say. I won't even mentoin the documents I got when I got out of the hospital that he wrote, seriously you wouldn't believe what is written on it. -------------------- Drugs So after 4,5 months of no getting better, no improvement but worsening, they placed me on 37.5mg Effoxor which I responded to extremely quickly and really, really well. Within a few hours nearly my whole condition was gone. Even they were surprised that it acted so quickly, and that already the first one suited me so well, as usually people have to try around to find one that is good for them. Whether placebo or not, it did the thing it was supposed to do - so well that pharma companies could show me as an example of "miracle drugs". (I'm very sensitive to medications/caffeine etc., so I'm not surprised that a low dose works so strong on me). I had also very few side effects. I was placed a few days later on 75mg, and then my whole condition was gone. When I asked if antidepressants really numb feelings, the lead doctor said "no, the depression does that." Tells about everything you have to know about him. On my last visit to my therapist I told him they did nothing, only the drugs helped me. That he didn't like of course and in the documents I was counterargumentet that I "eagerly took part in all of their offered therapies". Yes, it was so boring there that I attended even courses that others couldn't go to and I went in their place instead. If we hadn't any courses - music, physiotherapy - I would take hour long walks with the others because else I woulg go crazy sitting there and doing nearly nothing. They wanted to keep me longer there, but I said "no", as fast as possible out of this place, they were all not alright in the head. And I got really fast out because my mother stormed in and shoved such arguments up their faces, especially my therapist, that he started shuddering. The locks, the "sexual problems", she had no mercy with words. Twenty minutes later I was out. A very few months later we went to another gynecologist, who is a fantastic one. There the PCOS syndrome was diagnosed again, and I was put on contraceptives again (my third) - I responded very well to this one. Unlike the first one, which was good too, this one didn't make me sleepy and I can function to this day without midday sleeps, which I needed on the first one. After half year of Effoxor I had to see my psychiatrist again, as the longer I was on the pill, the greater the "freezing headache" and numbing of the antidepressant came to light. Theory I strongly believe in, again THEORY - this was because the more I gained hormonal balance, the greater the serotonine etc. production functioned again and my body functioned more normally again - meaning, I didn't need the effoxor anymore and it started doing a little more harm than good now. So I was put off it, I was told to taper, but stupid me wanted so badly the numbing to go away that I did cold turkey. And compared to other cold turkeys I read, this one wasn't so bad. Dizziness, very strong headache, a bit of vomiting, that's all. On the second or third day though I took a 37.5mg pill again and tapered this time, opening the capsule and putting the little tablets out of it until only one of the little was inside. Then I had a week or two of mild withdrawal and it was over. As I said, poster girl for pharma with this drug. This year, 2022, on February my "suicidal episode" came back - and it didn't came back like before - this time it hit, at the same time, with such a panic attack that I hyperventilated so badly I got severe twitches and my eyes rolled up and teeth shuddered etc. an ambulance had to be called. They knew it was hyperventilating and I was calmed down with reduced breathing, because too much oxygen. It worked. But now I was left with such anxiety that I became extremely sleep deprived. When I visited my psychiatrist again (I had to wait 2 days for the emergency visit to him), he wasn't able to offer much help besides "taking up an antidepressant again". I said no, no antidepressants anymore. I asked for sleeping aid, so I would get a bit of rest after being much sleep deprived for two-three days. So he gave me a sleeping pill. Without telling me it's an antidepressant. Later I found out it is an antidepressant. Thank you very much. So I was given Remeron/Mirtazapine 7.5mg. When I started it, I became greatly suicidal, with urges to kill my myself and immense hopelesness that was drug-induced. During this time I seriously thought about assisted suicide (and still a bit traumatized because of it, as I never, never had before sucidal thoughts - the suicidal episodes were mistaken, I'll explain later.) I wanted to stop it after two days, but my mom said they need a bit of time to settle and then it'll get better. And it did, the suicidality vanished. I slept much more on it, not very much as since years I had disrupted sleeping, but this time only once a night and I fell asleep quite fast after that. Now, what is important to mentoin as it happened during the taking of mirtazapine, and I had one of those "suicidal episodes" my mom told me - this was the one sentence that cured me - "that it seems like I'm not depressed or anything, but scared." Boom. Done. It all went away. As I googled later, I found out what I had all the time was "Suicidal OCD - an intense fear of suicide and intrusive thoughts about suicide which leave the individual disturbed and distressed." This was also why the episodes got more intense and frequent in time - the more I was scared of it, the more intense it became. When I was distracted, it wasn't there. I remember when blood was taken from me it would disappear for a while, I remember the more hopeful I was the more it disappeared. All in my head. Ones own head, illusion can cause such suffering... fascinating. And indeed, the second I realized this was only a fear and not actual suicidal thoughts, all disappeared. And didn't come back. A few weeks later I would know the difference between this and actual sucidal thoughts. I was very alright on Mirtazapine, had feelings and so on, was myself pretty much. Problem was, the longer I took it the more paranoid-anxious I became (along with more and more damaged short-term memory), which would make me stop it after 2 months - and also by another event. I took CBD oil (I consulted it of course with my psychiatrist first), for it to help me further as maybe this would help my sleeping problems and I could get off mirtazapine. And I took the two together, and mirtazapine didn't react well to it. Got extremely anxious and with semi-suicidal feelings, kind of like when I first took it but half so bad- so I stopped the oil after three days of no improvement, but fast forward a half week later and the symptoms don't go away. So I had to stop taking mirtazapine, on 4th April. At first I became a bit hypomanic, my senses were sharp as never before, adrenal-like, nothing negative much. It went away after two days and was replaced by huge anxiety. It was lowering continuously over the course of one month, and I thought "not so bad", at the end, at first it was bad, but it was going away. 6th of May, it hit, and it hit really, really hard. I never felt this suicidal, it was like when I started taking it but 3x worse. It was accompanied by dizziness, intense nausea, extreme brain fog, anxiety, memory was non-existent, hopelessness rose to 900%, apathy, no feelings. Half of the day I thought about suicide and the other half of the day I was flat, kind of existing. The suicidality was intense, I could think about nothing else - it was nothing like the OCD I had, now I could really, really distinguish between illusion and actual suicidal thoughts. I felt, and still feel such regret of ever taking any antidepressant, I never was so scared about my future before, never regretted something so much. After one, two weeks it started gradually falling and the suicidality went kind of away, along with nausea, etc. What was left was the brain frog, numbness, impaired memory. But it got better over time, and I knew from the beginning it was withdrawal else I would probably have got psychotic about this. Now, a few days ago, second wave hit. Suicidality (but half so bad this time), now I have weird skin sensations sometimes, still much numb (I can cry very well though, I just don't feel the sadness, but the feelings are still there, hidden somewhere.) Brain fog, short-term memory still doesn't exist. Again, intense regret, I'm still so scared it won't end or I will suffer permanent damage, even though it was just 2 months and the lowest dose. What is optimistic though, for the first time since these 2.5 months I responded emotionally to music which opened a window, and I was cycling recently between withdrawal-window-withdrawal. But the fear of no end and permanent damage is still there, and thinking only about the slightest good memory from childhood makes me tip over into intense crying, as I'm so afraid that I lost now everything. There are so many things I still want to do, finish school, a good university etc., and I will only be able to forgive myself and forget if it all ends well, with as little damage as possible. Reassurement of "it was only such a short time, such a low dose, it won't damage you..." leaves me only with a bit of hope. In the past month I read so much about neuroplasticity and learned so much about the true face of psychiatry (especially through "Anatomy of an Epidemic"), and it left me in bewilderment and anger. Had I knew, then I would have never taken it. Never, no matter what and I never will take anything of it ever again. I only found about long-term use damage, so I guess from 2 months and lowest dose I will recover? I found in the Anatomy book that for antipsychotics, the rule is 2 months recovery for 1 month use, and only at the period of over a year or so it might cause permanent damage. I hope it is better for antidepressants, especially since I read so many horror stories I cried about with immense fear, and many I read with hope who came off after 20 years of various antidepressants and recovered well to 100% themselves. Often the knowledge about neuroplasticity, neurogenesis and success stories keep me sane. Incredible what 2 month use of the lowest dose can cause. If it shall end in 5 months, I will endure. I'm extremely endurable, all my life I've proven it. But there is this uncertainity, and it won't let me sleep at times.

I have been on 20 mg of Lexapro for about 20 years for Generalized Anxiety Disorder. I have had breakthrough anxiety several times during the period and recently it seems to have quit working. My doctor did a genetic test which showed that I was not a good match for Lexapro do to being an ultra rapid metabolizer of the drug. Two weeks ago he did a direct switch from the 20 mg of Lexapro to 40 mg of Prozac. Since the switch I have been getting progressively worst having extreme anxiety, feeling sick, and having trouble with concentration. Really unsure of what to do as the symptoms are pretty severe. Any suggestions on what to do to help with the symptoms, should I reinstate the Lexapro or continue going forward with Prozac. Thanks in advance

Hello all, I am a 26 year old male living in the midwest of the United States. I had my first bout of depression when I was about 14. It’s been pretty up and down since then. I had been struggling for a while to adjust to the stresses of college and I kept getting beat down with anxiety and depression so I finally reached out for help to my GP. I was prescribed 50mg of Zoloft in October of 2017. I started with half a dose and it really did seem to lift my spirits and give me confidence I really noticed when talking to other people. Anxiety and shy/insecure feeling when talking to others is something I have always felt, and this was exciting to see a change in. I went up to 50mg after a couple weeks and after a couple more weeks there decided to go back down to 25mg as it started to make me apathetic. I also lost libido and interest in the opposite sex which was a scary feeling to me as a young college student. The Zoloft began to make me extremely lethargic and fatigued to the point where I could barely get out of bed, and I felt like my body was just heavy and weak. This annoyed me for a couple weeks then I went cold turkey off of it in January 2018. I was on it for a total of about 4 months. I experienced acute withdrawal for around 2 weeks and had brain zaps along with extreme irritability, but it passed and I was fine withdrawal wise. I still suffered from anxiety and depression, however, and in October 2019 I tried again to take Zoloft 25mg but quit again after about two weeks as it just made me too fatigued. In July of 2020 I was really depressed and went back to the dr. This is when I was prescribed Lexapro 10mg. The Lexapro really helped me, and my overall contentment was up, anxiety/depression were down, and I was doing pretty well. This lasted for around 7 months (till January 2021), where I realized that I was once again apathetic and more tired than usual but not bed ridden. The sexual side affects were strong as well, and having a girlfriend at the time, this bothered me a lot. I was apathetic enough around this time to stop caring about her as much and although there were other problems with our relationship I attribute the meds to a large part of the reason I broke up with her. I went down to 7.5 mg and gained some libido and energy. I was doing pretty well for the next few months although the breakup was hard. In October 2021 I went down to 5mg and stayed there until about December of 2022. I had been extremely fatigued once again and blamed the Lexapro, so I started to taper but very quickly - I went down to zero in around a month (January 2023). I started to experience panic attacks and feeling like I was going to pass out. I felt completely out of control of my own body and it was terrifying. I tried Buspar for about 2 weeks to help with this but gave that up as well. I went back up to 5mg Lexapro until April and tapered down to Zero over the next two months. June 6, 2023 was the date I fully got off Lexapro. I have been suffering since. My main side effects are extreme anxiety and depression, feelings of utter hopelessness, feelings of intense fear, shakiness, cold intolerance, panic attacks, and muscle aches in my arms, chest, neck, and legs (feels kind of like growing pains). I do experience the windows and waves, although the windows are not “normal” feeling, just patches where I am doing better rather than worse.

Hello- as my topic title shows, I have been on anti-depressants for 24 years (20mgs Lexepro, 175 mgs Wellbutrin). It is hard to face. After the birth of my first son, I began having acute anxiety. When I told my gynecologist he told me it was common after giving birth because of hormonal changes. In such cases, he recommends about six months of medication to help with the symptoms and recommended a psychiatrist that he works with for patients such as me. I'm sure none of you are surprised to know that, as is all too common, I never got off the drugs for very long. Each time withdrawel symptoms were interpreted as my illness returning. My mother suffered from anxiety and depression all her sad life, so it wasn't hard to believe that I was ill. Yet, I still tried a few times to stop the drugs. Interestingly, once it became clear how difficult it was to get off the drugs, I knew with certainty that I needed to stop taking them. I Thought I would put if off until I was retired, so I would have less stress, etc. to deal with the WD, but when I learned about the10% taper it gave me hope that I can be AD free by my 60th birthday! I will start with the Lexepro. Getting myself a scale and using a spreadsheet to calculate the decreases. I'm getting my yoga and walking on, and continuing meditation for success! I'm so glad to have this site for reference, information and support!

Hi everybody, posting this here in hopes of some help with taking next steps. I was on 20mg/day escitalopram (aka lexapro/cipralex) for 3 years due to crippling anxiety that came out of nowhere (never had anxiety before), and despite taking good care of myself (sleep habits, nutritious diet, regular exercise, strong social relationships, etc), it persisted. So after 6 months, I decided to take the drug route. I didn’t notice any improvement with 10mg after a couple weeks so we upped it to 20mg (should’ve given 10mg more time). My anxiety was brought under control without any serious side effects at first. After being on it for 1-2 years, I started to notice that I was always pretty tired and increasingly apathetic despite my good lifestyle practices and having always been an energetic and motivated person. By the end of the 3rd year, I was exhausted all the time with no motivation/enthusiasm, brain fog, and would literally need a nap 3 hours after waking up from 10hrs of sleep (caffeine/stimulants didn’t make a difference). A hard workout (I am a bodybuilder (no steroids tho)) would leave me crushed for several days, like a constant hangover. I was just chronically exhausted and lethargic and, possibly by extension of that or as a separate issue, depressed and unmotivated. I did a 4-week taper from 20mg to 0mg without any issues at each reduction, spending several days at each dose to make sure I was stable before reducing again. I now know that was way too quick of a taper, but I didn’t have any adverse reactions to dose reductions, even after going down to 0mg, and my energy/mood seemed to improve at first. It has now been 7+ months since my last dose because I thought it was just a matter of time/toughing it out after you got all the way off. To make matters worse, my last doses were 10mg that I was alternating with 0mg, which I now know I shouldn’t have done. The only acute withdrawal symptom I had was some manageable vertigo, but the protracted withdrawal symptoms have been hell. Despite great life circumstances and maintaining a good quality diet, sleep habits, and exercise routine, I am now almost always: exhausted, sad/depressed, lethargic, spacey, unenthusiastic, apathetic/anhedonic, irritable, moody, and sometimes anxious (though not nearly as bad as the original anxiety that I started taking the SSRI for). I don’t really enjoy doing much of anything any more and I feel like I could sleep forever. I’m lucky to work a job that is flexible, so I don’t need to set an alarm usually and typically get 9-10hrs of sleep. I still wake up tired every day and often need naps despite never being a nap person before. My sleep quality is good (no insomnia really) My life is falling apart. I’m familiar with the waves and windows, and I’ve experienced one 2-week window, and the very rare goodish day here and there, during that 7-month period, but most days are crap . I have been tracking my mood/energy every day in a spreadsheet for last 3 months, and although I THINK I am doing a bit better now than I was during the first few months, it’s almost negligible, with awful days and chronic exhaustion still being the norm. Given that I am 7+ months in, I don’t want to quit while being so “far along”, and I know that reinstatement is less likely to work now or may even have adverse effects (kindling), but I am starting to consider getting back on a very small dose (<1mg?) to get stable again before executing a proper taper in hopes of avoiding continued PWS. I’m 25 and I’ve basically lost the last 2 years of my life, which I know is nothing compared to some of the experiences on this site, but I’m hoping to get some guidance or input here since my doctor is pretty out of the loop on SSRI PWS (his suggestion was to start taking wellbutrin/buproprion, which I would rather not gamble with). It seems to me that I’m basically deciding between the risk of reinstatement resetting my withdrawal progress and not working/making things worse OR toughing it out for who knows how long, maybe forever, and possibly getting new, even worse, withdrawal symptoms as I know there is a possibility of experiencing new withdrawal symptoms many months down the road. Some context notes: I am still able to consume most supplements (other than 5-HTP and melatonin) without any obvious adverse effects (for example, caffeine/pre-workout and nicotine gum/Zyn seem to be fine, although they aren’t as effective as they used to be) and I still lift weights very intensely since time away from training doesn't seem to help.Point being, I haven’t really been able to identify any trends as far as diet, supplementation, lifestyle habits, etc. causing waves, but perhaps it’s because I’ve been constant with everything. I also tried magic mushrooms (2g) and it had no effect acutely, although the following weeks were slightly better, that could’ve just been a natural “window”. Any insight would be greatly appreciated as I am feeling hopeless.

Hi all, LavaBat here and ready to get some support for tapering off of Lexapro. A little about me: I am located in midwest USA and am 27 years old. I love animals, exercise, reading, and watching tv/movies. I was put on Lexapro at the age of 14 for anxiety and panic attacks, I am now 27 and can't seem to get off. I do not remember the dosage back then, but do know the highest I ever took was 20mg. In my later teen years I was at 10mg. Around 19 years old I managed to get down to 7.5mg and have been at 7.5mg for the past 8 years with no luck getting lower. At 22, I was diagnosed with Autism, and have found that was the cause of my anxiety/panic as a child because I did not have the correct accommodations and support. Since I got the correct diagnosis and support, I have tried several times to wean off. The first attempt was several years ago and my doctor suggested half dose for a few weeks, then half of that, and then off. I tried going down to 5mg and within a week I felt the most severe panic that I had ever felt before. My doctor told me that meant I needed the medication because I clearly still had bad anxiety and the medication was needed to keep it at bay. So I went back to 7.5mg immediately and stayed there for another year or so. Then with a new doctor, I tried to wean off again. This time it was suggested to shave off a bit of the pill each week. I believe I was shaving off about 10% of weight each week. Around week 3 of shaving down the pill, my anxiety was back to being unbearable along with bad nausea and diarrhea. The doctor told me once again that meant I needed to stay on the meds as I still had bad anxiety without. I have not tried weaning since 2022 and am still at 7.5mg. I have also had issues with different brands and forms of the drug. When I picked up meds from a different pharmacy, after about a month I was getting very dizzy and lightheaded. Luckily I was able to get back to the other brand. Then last month, I found this site and decided to try to switch to liquid Lexapro to help the weaning process. I did 5mg pill and 2.5mg liquid for a few days. I had nausea, diarrhea, headaches, and anxiety so I went back to 7.5mg fully in pill form. And that is where I am now. My first question is, should I even bother trying to get off Lexapro? I have zero known side effects from taking it at my current dose and manufacturer. My partner asked me why I wanted to get off since it has been so hard and I don't have any issues with Lexapro. I couldn't come up with an answer other than I just want to and hate the idea of being so "addicted" to something. Is it possible that I genuinely need to be taking Lexapro? As for tapering, I am not sure where to go from here since the liquid Lexapro didn't work for me. If I were to make my own solution with the pill, I just worry that I wouldn't be getting an exact dosage each day and I would have to make it each day to stay potent. Shaving off by weight also seems a bit hard to get exact dosages with too. Any suggestions would be greatly appreciated! Since I tried the liquid Lexapro only a few weeks ago, should I not taper for a bit just to make sure I'm stable? And finally, I was looking at microtapering. Since I have had such bad reactions in the past and already know I am super sensitive to medications (not just Lexapro), I have been thinking of starting with literally 1-2% taper for this next try. I think that could help me perhaps get the smallest amount of withdrawal and ease my fear of a bad reaction. Thanks so much for taking the time to read this and for any support

Suffering from severe stress, overthinking and anxiety for over 15 years. Was on cymbalta for about 5 years. Then tried to withdraw from it using amino acids and herbs on my own. But had serious withdrawal symptoms and psychosis. Then I was prescribed Lexapro 20 mg and rexulti 1 mg. I was able to withdraw from rexulti after 2 years. But still currently on Lexapro 20 mg since 4 years. I want to wean off this time. I am so planning to get the SPECT scan done at the Amen clinics soon if it can be helpful. I am currently 35 years old and not going to give up this time. i tried to lower the dose by 15% (approx) 3 weeks back for 3 days and had severe withdrawal symptoms like fever, headache, muscle pain, sore throat, brain zaps, loss of control. I went back to my original 20mg dose and doing fine now since this week. Is it a good idea to take fish oil, multi vitamins, and other natural herbs while tapering off Lexapro so brain can produce new neurotransmitters?

Hi everyone. First time posting but I’ve been reading a lot of your stories over the last week. Thanks to you all for sharing, the mods for their feedback and the amazing resources that have been prepared. I’m 60 and have struggled with anxiety for most of my life but always felt like it was my own fault. I’m sure we’ve all been told that we need to be more resilient/less sensitive etc - as if that ever helped anyone, but I digress. My antidepressant journey began in 1995 when I tried Zoloft for post natal depression. It didn’t make me feel “better” but I didn’t want to kill myself anymore, so I guess it was better than nothing. Dr told me to get off it after 6 months so I did. Didn’t notice any changes. Quit my job and decided to move back to my home city and was prescribed Cipramil by a psychiatrist. When I first started it it honestly made me a bit manic I think and I decided to blow up my life further by splitting up with my husband. I went along happily on Cipramil for a while, got a new job and a new partner. Tried to quit cold turkey when I got pregnant again but was so loopy my dr told me the benefits outweighed the risks and I should stay on it through the pregnancy. My baby was born perfect in 2004 so all was well but my depression continued. At some point I had to stop Cipramil because of concerns about urination (one of those rare side effects). Psych tried me on Effexor because she thought the norepinephrine might help. I hated it and had to have a washout period of about 2 weeks before I could start a new something new. So about 2005 I started Lexapro. I was told it’ll be great cos it’s related to Cipramil and that worked well for me before. I can vividly remember the feeling as it literally hit my brain after the hellish washout period from Effexor. Such a relief. Started at 10 mg. In 2009 I got right into mindfulness meditation and it helped me immensely. I got healthy in body and mind and decided I was well enough to taper off Lexapro. By this time I was seeing my local dr (here in Australia we call them GPs or General Practitioners) for my prescriptions because the mindfulness had helped so much I stopped seeing the psych. But when I needed a new prescription to finish out my taper, I just got a lecture instead. That it was perfectly ok to stay on antidepressants long term and some people just need them. The amount I was taking at that time was well below the therapeutic dose and I should either stop or keep taking 10 mg a day. I liked my GP ( and he’d clearly drunk the coolaid) so I listened to him and went back up to 10 mg daily. Life happened and my mindfulness and fitness fell away and by 2017 I was falling back into a hole. My new GP told me to up my dose to 20 mg so I did, with minor improvements. By 2019 I was having suicidal ideation again. 2020 was rotten for everyone and I got burnt out at work and went on long term sick leave. GP tried me on 30 mg of Lexapro but it made no difference so I dropped back to 20. I started seeing a psychiatrist in late 2021 and he put me backup to 30 mg. Minor improvement and I’m a compliant patient. Late 2022 I stared reading about inattentive ADHD in relation to one of my daughters and realised the description fitted me to a t. I asked psych about it and he gave me a trial of dexamfetamine. I felt great and all my mood issues disappeared overnight. I forgave myself for all my “character flaws” (untidiness, lack of staying power, procrastination etc) cos they’re all just down to adhd. I cut myself back down to 20 mg of Lexapro almost immediately and it made no difference to me whatsoever. I still felt great.I stayed on that for about 6 weeks. Went back to psych and told him about my experience with dex and he upped my prescription of that and wrote me a prescription for a lower dose of Lexapro - 10 mg. So I dropped to 10 mg. First 7 days I was completely fine - getting back into yoga and mindfulness, keeping on top of my budget - fabulous. Then on about day 8, while doing yoga, I suddenly felt like I was gonna throw up and I was sweating profusely. Spent the next three days either on the sofa or in bed feeling dizzy and nauseous. My mood is still fine although I do find myself a little bit hyper vigilant. I used my time on the sofa wisely though and investigated discontinuation syndrome and came across this amazing site and realised that a drop from 20 mg to 10 was hopelessly ambitious. Even the Harvard guidelines for tapering suggest going from 20 to 15. So I’ve learned a lot in the last few days. I was so ill - just nonfunctional - that I decided to go back up. I took 20 mg yesterday to try and level myself out a bit and am planning to stick to 15 mg for a few days and see how it goes. That’s the main highlights of my antidepressant story. There are a couple of other bits that may be worth mentioning. I very briefly tried an MAOI in about 1998. Before it even had a chance to work on my mood, I took a sinus tablet and that was a disaster. Always read the label kids. I felt like I was literally going to explode both physically and mentally. Absolutely horrible. As I regularly get sinusitis and accompanying headaches, MAOIs were off my treatment plan immediately and permanently. The other thing I should mention is that a couple of times when my script has run out I’ve gone 4 days without any problems, but then suddenly on day 5, I’m irritable, weepy and get brain zaps. thanks for reading.

Hello! Here is my story: Started taking Lexapro in 2012 and it really helped me to function in life during a stressful time. Decided to go off Lexapro in 2017. It was a fast taper, and I ultimately ended up staying at 5mg. Acute withdrawal symptoms were brain zaps, agitation, anxiety but they subsided after the first month, and over the course of the next 6-8 months, I slept a lot. I planned to ultimately finish the withdrawal process in the future. October 2020, I started putting a withdrawal plan together. Instead, I ended up going CT on Nov. 1 when I had a dental surgery and infection. This was an impulsive decision and a poor one. I thought that I just needed to get through the first month and then I would be okay. November 25, 2020, I got vertigo out of the blue and fainted/threw up. I thought this might have something to do with the withdrawal, so I kind of freaked out and took 2.5mgs of Lexapro. This knocked me out for 24-48 hours (headache/body aches/dizziness) and I stayed in bed. Everything checked out okay with the Doctor and when I asked if this was related to the Lexapro withdrawal, she said no, told me to throw away the pills. I received a diagnosis of Benign Positional Vertigo and was given a maneuver to do. The dizziness cleared up, it lasted 2-3 weeks Late December, work was stressful. I didn't eat really well and ended up with hives. I was taking Benadryl on and off. I took Allegra one day. There was one night the last week of the year where I didn't sleep at all and this was strange for me. Work stress seemed to be getting to me, but I pushed through. January 4, I started what was to be a month long meditation retreat at home, but something went wrong. I wasn't sleeping well, I was pushing myself, I had a lot of fear and resistance. I was crying uncontrollably. I was spinning out. By the end of the week, I decided to stop the retreat and now I'm in a very strange place. I'm super alert, anxious, fearful, tightness in my chest and I am not sleeping for more than 30 minutes at a time. I can't seem to calm down and I am not functioning well. I can't even imagine going back to work like this. Have an appointment with my Dr. tomorrow, and will try to possibly see a psychiatrist. My question - at just over 2 months out, do I try to reinstate at a very low dose of Lexapro, or should I try the sister drug Celexa (I think that is it)? I'm worried about how to present to my Doctor. I am trying to make the best of this, but am really very scared. Thank you for your time, Crochet

I am desperate for some help. My story is long, so if you read it entirely, I sincerely appreciate it. I was on SSRI's for about 18 years, since age 11. I added in wellbutrin for about the last 7 years to counteract the side effects of celexa and lexapro. Eventually I had to add in buspar because my anxiety was uncontrolled. I felt better for a while, but when it got worse, I decided to see a psychiatrist. My primary doctor had been prescribing my meds previously. The psychiatrist tried me on zoloft, lamictal, paxil, and abilify. At the end of it, I was on paxil, wellbutrin, and abilify. I had taken abilify for 10 days and had a night where I vomited 6 times; I had not vomited in about 10 years. My psychiatrist told me she felt I had serotonin syndrome and instructed me to discontinue all of my meds immediately. She gave me klonopin to get through withdrawal. I trusted her and did not know any better. I thought I would be okay. I had all of the typical withdrawal symptoms, but shortly after, started to experience new symptoms/injuries/illnesses. I started having panic attacks which I never had before. I started to have muted and painful orgasms, and then came pudendal nerve pain. I tried to reinstate antidepressants 4 months later, but they have only made me feel worse. I'm experiencing side effects I've never had before, even on AD's I've previously been on with no issues. I will attach a medication timeline and a symptom timeline. I have a new psychiatrist and he does not know how to help me except to keep trying me on medications. I'm terrified of them now, but all in the same, I know I can't stay this disabled for an indefinite amount of time. I lost my job due to dizziness/dysautonomia/swaying etc. If anyone has any advice for me, I would really appreciate it. I'm feeling very lost and alone and terrified. I saw numerous specialists who all told me I had anxiety and needed pills; not that my brain and body are injured and destabilized. As of today I am still on klonopin (0.25mg twice daily) and tapering off of lexapro 0.5mg every 4 weeks (currently at 1.5mg, experiencing withdrawal symptoms, set to decrease to 1mg on saturday 1/1/22). I cannot taper off klonopin until I'm done with the lexapro taper. April 29th- discontinued paxil (20mg) and Wellbutrin XL (150mg) May 2021- muted and painful orgasms May 2021- numbness/tingling in extremities May 2021- panic attacks started July 4, 2021- pudendal neuralgia/tailbone pain started July 2021- waves of depression started July 20, 2021- carvedilol increased from 1 q12h to 1 AM and 2 PM August 11, 2021- BPPV maneuver (half somersault)- PPPD started August 13, 2021- mouth twitching (due to Compazine) August 25, 2021- clonazepam prescribed by primary doctor August 31, 2021- jaw clenching (due to Trintellix prescribed by primary doctor) August 2021- hair falling out in clumps September 2021- dysautonomia/POTS started September 2021 (after reinstating Lexapro per psychiatrist)- RLS, migraines, tinnitus, ear ringing, constant music in my head again October 2021- rashes started October 2021- PPPD diagnosed after vestibular testing October 2021- left shoulder popping October 2021- brain fog, memory issues, trouble word recalling November 2021- muscle spasms (everywhere) November 7, 2021- left knee popping November 7, 2021- right shoulder pain November 11, 2021- right shoulder popping November 11, 2021- jaw popping November 12, 2021- cold sensation and nerve sensations coming from tailbone November 15, 2021- right shoulder pain and weakness November 16, 2021- decreased carvedilol back to 1 q12h December 9, 2021- blisters on top of hives December 10, 2021- cardiologist confirmed dysautonomia due to discontinuing antidepressants December 10, 2021- medial right knee pain December 24, 2021- pudendal neuralgia symptoms back to square one (pins and needles, burning, stabbing, hypersensitivity and severe pain) Celexa from 2003-2011 Cymbalta for 5 days in 2009- felt horrible like I was dying Celexa + Wellbutrin from 2011-2014 Lexapro + Wellbutrin from 2014- 03/2017 Lexapro + Wellbutrin + Buspar from 03/2017-2018 Lexapro + Wellbutrin + Buspar + Carvedilol (carvedilol introduced for physical forms of anxiety high BP high HR) from 2018-2020 Zoloft + Wellbutrin + Buspar + Carvedilol from Dec. 2020- Feb. 2021 Zoloft + Wellbutrin + Carvedilol + Lamotrigine (lamotrigine 2 weeks) Feb. 2021- lamotrigine caused stiff neck, increased anxiety, short term memory loss, overall floaty feeling in my head Zoloft + Wellbutrin + Carvedilol March 2021- zoloft helped with ocd and depression, but not anxiety Last dose of Zoloft April 1st Paxil + Wellbutrin + Carvedilol March 2021- April 2021- still had some anxiety with paxil April 15th, 2021- April 18th, 2021- trazodone 50mg April 19th-April 28th – Abilify added. On the 28th, up all night vomiting/diarrhea April 29th, 2021- discontinued meds cold turkey at Jaime Mendoza’s instruction (except carvedilol)- suspected serotonin syndrome 5/19/21-5/23/21 Seroquel (12.5mg)- made me very dizzy and I was already very dizzy from withdrawal (pre pppd) 6/22/21-6/30/21 Prozac (10mg)- heart was racing and pounding, chest hurt, increased blood pressure. Instructed to stop and see cardiologist: heart monitor and echocardiogram normal, cleared to take meds on 8/20 8/20/21- Pristiq er (50mg)- severe diarrhea, nausea, woke up at 1am having a panic attack, face green, eyes dilated, shaking, sweating and about to vomit 8/31/21-9/22/21 Trintellix (5mg)- jaw clenching, teeth clicking, brain zaps, increased dizziness, increased anxiety, nausea/vomiting, increased headaches, dry mouth, vivid and frightening dreams, increased panic attacks and pseudoseizures, itching, some blurry vision, gas, worsening depression, irritability 9/23/21-10/8/21 Lexapro (5mg)- Palpitations/pounding heart (mostly at night), Ear ringing, Tinnitus, Bad dizziness/off balance/increased 3pd, Nausea, Racing thoughts, Restlessness, restless leg syndrome 10/9/21-11/5/21 Lexapro (2.5mg) 11/6/21-12/3/21 Lexapro (2mg) 12/4/21-12/31/21 Lexapro (1.5mg) 1/1/21-1/28/22 Lexapro (1mg) 1/29/22-2/25/22 Lexapro (0.5mg)

Here is my story. As an adolescent and college student, I suffered from anxiety and in particular social anxiety. I finally sought psychiatric treatment in senior year of college (year 2014) as I also started getting major depressive symptoms and was prescribed Zoloft (at 100 mg for 7 years, then tapered to 50 mg for the remaining time I was on it; I did not take any breaks, was always on it during this time; mainly had some sexual side effects, a bit of emotional blunting, but overall really manageable from side effect standpoint, nothing major). It was highly effective at treating the physical feelings of anxiety and healed me mentally as well, slowly improving and lowering social anxiety and my depressive symptoms. In late July of 2023, while on 50mg I decided I was in a good place and found a few of the side effects annoying, and (unfortunately) self-tapered off the 50 mg (50 to 25 to 12.5 over around 6 weeks) by mid-September. As I tapered, I felt no increase in anxiety or depression (and had not been feeling these in a significant way for a long time – in fact I was the happiest I had probably ever been in my whole life, which is what prompted me to think I did not need the Zoloft any more), or any of the symptoms I took it for the in the first place, and experienced minimal ‘discontinuation’ symptoms as well. Then, about 6 weeks after stopping, in mid-November I had several things pop up at the time I did not recognize as relapse/discontinuation, but almost certainly were (GI distress, nausea, constipation) – these were separate ‘episodes’ that occurred, and there was spacing in between them. December 10 is when the true full relapse began: I woke up in the middle of the night feeling uneasy, with chills, got bad night sleep / struggled to get back to sleep, following night at girlfriend’s had panic attack come out of nowhere- chills, shivering, feeling anxious not self, thought I was going to die- walked around and talked it out, died down in 20-30min… but for rest of night felt uneasy, struggled to sleep / got a bad night sleep. Following day woke up feeling full anxiety in chest, shoulders (adrenaline type feeling) and had racing/worrying thoughts, told primary care provider they refilled Zoloft 25 mg. I took the Zoloft 25 mg had a strong reaction (this was ~2.5 months after my last dose of 12.5mg), both positive in sense it did calm me down but with strong side effects (tingling, no libido, strange sensations (I experienced lower libido, but nothing like the strange sensations when on it before)—like an electric shock in lower body mostly, i.e., what I now know to be the ‘kindling’ effect and you can’t argue against this because human beings can’t natural produce electric shock sensations internally even as a manifestation of anxiety), deterring me from wanting to take it again, still got pretty poor sleep that night but not horrible. Did not take Zoloft Wednesday because concerned about side effects, still felt anxious / off and got poor night’s sleep again. I met with primary care thursday, at doctor’s office Thursday had a panic attack that did die down, they referred me to psychiatrist. On Friday took 12.5 mg Zoloft since they said it wouldn’t make a difference either way at that dose and felt more relaxed but again had weird side effects. The next day I started to feel weird, and took 12.5mg to take the edge off (in retrospect, not how Zoloft to be used but I was in an irrational, anxious state), made me feel calmer but still got a bad sleep. Sunday morning felt very off, like panic building so took 25 mg Zoloft initially calmer but panic attack did not stop ended up going to ER, had elevated BP/HR otherwise fine, and gave me low dose of lorazepam, talked it out, calmed down. Also trazodone for sleep, ended up sleeping very well that night for whatever reason. The next day felt a bit weird but also a bit recovered, around noon felt growing depression feeling so took 25mg Zoloft, then that night really struggled to get sleep, next morning also feeling off, had panic attack, ended up calling 911 evaluated in ambulance, just elevated HR and BP, calmed down, flew home that day (took Zoloft 25mg at noon because could feel growing depression feeling again). Had another panic attack and went to the ER one more time (this was last day I took Zoloft 25mg). I then started on my newly found psychiatrist’s (yea… unfortunately did not have one for a while) plan of 0.5mg/night clonazepam and 150mg Wellbutrin (since starting the 0.5mg clonazepam, no true panic attacks have occurred), unfortunately even with taking the Wellbutrin in the morning, I got no sleep that night (got hypnic jerks that kept me awake), told me psychiatrist, he told me to stop and we’d re-evaluate in a few days. Then following two nights no sleep, the psychiatrist kind of gave up on me, so then took a few days to find a new provider. Who started me on 5mg Lexapro (and continue 0.5mg/night clonazepam) – the main side effects were getting no sleep (down from 5-6 hours previous two nights) both nights I tried it and constipation (but other than that nothing bad). I took a break for a day and re-tried in the morning, then was able to get some sleep. Over a 5-week period, I vamped up from 5 to 7.5 to 10mg/morning Lexapro, and tapered down to 0.25mg/night clonazepam (tapered down regardless of impact on sleep because I did not want to become dependent). Since starting the Lexapro, there has been continued improvement in daily functioning, reduction in anxiety (in particular better control over thoughts), mood (continues to improve actually – in many ways getting back to old self despite being sleep deprived); I continue to feel I am approaching ‘normal’ / being myself more. However, there is still something major that is very off: I do not feel exhaustion/tiredness (OR anywhere near as much like **** as I should after a poor night’s sleep, I am also strangely am able to focus better and in a better mood than I’d be under normal circumstances) during the day (or a very limited amount of it), and continue to get poor night’s sleeps (I have not taken a single nap or dosed off at all since December 10… I even took 5mg ambien in the middle of the day (long story) and that failed to make me fall asleep). It is often challenging for me to both fall asleep, and guaranteed I will wake up at least 1-2 times throughout the night (and sometimes during these instances I cannot get back to sleep), and I can never sleep in past 7am. The worst nights are usually 1.5-2.5 hours, the better ones are in the 4.5-6 hour range (I had a streak of 0 hour sleep for 3 nights in a row after going down from .5 to .25mg Klonopin too early, then went back to 0.5mg and made taper more gradual). I have had several nights of 7-8 hour sleeps, but with only a few exceptions these have always been after taking a sleeping drug (and always the 0.25mg Klonopin as well). During the nights, I will sometimes wake up with a faster heartrate, night sweats, urinate frequently, when trying to fall asleep I have experienced minor hypnic jerks (though a lot less bad than the ones after taking the Wellbutrin) – a lot of these have admittedly declined in frequency (and some I think have been in reaction to taking certain sleep meds the night prior, e.g., Mirtazapine), but nonetheless my average amount of sleep has not improved that much, still waking up often and not getting very many hours (interestingly I also pretty much always remember my dreams). For awareness, I have tried Ambien (just 5mg) which did not work at getting me to sleep (did make me extremely drowsy though.. also felt depressed/anxious like 5-6 hours of taking it), Trazodone (25-100mg, it was effective, but started realizing it might be causing tachycardia and made me act weird in the mornings so stopped taking it), Mirtazapine (~4mg, probably the best sleep I’ve had during the whole experience slightly over 8 hours only woke up once, obviously made me extremely drowsy, but the next morning was a zombie, then in the afternoon started experiencing hypersensitivity and getting jolts of anxiety in reaction to things like dogs barking while on a walk), Lunesta (1mg – was effective 6-7 hours helped with falling and staying asleep, but did some GI distress, and felt causing some sort of mini-withdrawal since on the Klonopin / not advisable to take z-drug with benzo), and Hydroxyzine (25-75mg – this has been effective, I think become a bit less effective over time but still helpful, some side effects getting better, notable so want to avoid taking every night); for supplements I take 2mg melatonin, 300mg magnesium, vitamin D3, I try going to bed at consistent time, go on daily 30+ minute walks, employ diaphragmatic breathing, though admittedly have more to learn on sleep hygiene. All of this said, I would love to hear people’s thoughts on the following (and I am going to an online forum because I have brought some of this up to supposedly highly qualified Ivy League-trained psychiatrists who won’t really know what to do). (1) Is there any possibility I did not give re-trying Zoloft a proper chance, and getting back on it at some TBD dosage is my only chance to get back to normal? When I took it initially it did feel weird, but all of the effects I’d be willing to put up with if I got back to feeling normally and being able to sleep properly again (even though as I took it later in the week I noticed most decline in intensity). Additionally I took it incorrectly, starting on a Tuesday at 25mg, then taking 12.5mg on Friday, then 12.5mg Saturday, then 25mg for just a few more days before stopping. You may think, why on earth would he get back on that he still had panic attacks on them (and yes, they were potentially worse because I took it, but I took it improperly, which likely completely threw off my brain). In comparison to Lexapro, when I first took it it did not interfere with sleep like Lexapro did (two nights in a row with no sleep, and still after 5 weeks on Lexapro I am getting poor sleep, though some components may be improving). It did have a calming effect, did have a somewhat numbing effect and made me feel better than I should have (given the overtiredness), but still that was early days and towards the end 4th day or so of using that became less the case. a. I read in some cases if you react strongly to the initial dosage that is “kindling” and does not mean the drug will not work, but just you are extra sensitive to it. My brain clearly grew dependent on Zoloft over the 9+ years I was on it and may need the drug to get back to normal. I had not taken it long enough the second time (only 4-5 days) to tell if it could properly reduce anxiety, rebalance my brain so I could sleep properly. When I was having the panic attacks while taking it, it had not been long enough to prevent them (would take weeks…), I was also not eating nearly enough (something I realized during my final ER visit when I horsed down a bunch of mediocre hospital food). b. If I were to switch I am pretty sure I’d need to cross taper with Lexapro, because going to 0 on an SSRI I don’t think would be good for me at this point, in particular combining the withdrawal with the sleep deprivation. It would probably be wise to start with a very low amount of Zoloft (like 1 mg?) to minimize any risk of Serotonin Syndrome. c. While I don’t think they take a nuanced approach, and lack a sophisticated enough understanding of SSRIs, have been advised against this by several doctors. (2) Does it make sense to stick with Lexapro, at least for several more weeks, potentially at a higher dose. I am not concerned about the constipation, but obviously if it makes sleep worse that’s a no go. I have noticed continued improvements shifts to normality while on it just not the desired improvement on sleep. In some ways I am happier on it than I was on Zoloft, but still not the sleep improvement—and sleep is huge foe me. If I were to increase the dose I would start going from 10mg to 12.5mg. My GI system seems to be improving (gets less irritated after meals, getting more of real appetite/feeling hunger) a. The recent psychiatrist I saw recommend I try increasing the dose of Lexapro and see how it goes over the next month. (3) Could it make sense to try an alternative SSRI, such as Prozac or Celexa? The key here would be getting brain back to a state where I could sleep. Or a different antidepressant class, but those are second line and known for even worse side effects. (4) Some may say the Klonopin, especially in the context of tapering, is hurting sleep (which it probably is but I doubt that severely given I have held at .25mg for 3 weeks), and right now I am still suffering from the bad sleep deprivation, have lost 15 pounds – suffering through potential benzo withdrawal might not be something I can handle now. I have no desire to ever take a dose higher than 0.25mg, and eventually 100% want off of it, preferably as soon as possible. (5) In terms of other treatment options for the insomnia, I have not yet tried Seroquel but have reservations given I already have not had the best experiences with Trazodone and Mirtazapine – if I were to try Seroquel maybe like ¼ or ½ the usual starting dose of 25mg… Would rather try one of the alternative treatments, CBD/cannabis if those really do sometimes work. a. I have heard CBT-I, ketamine infusions, psilocybin microdose, CBD, cannabis, maybe be helpful – would love to hear anyone’s thoughts on any of these or other treatments

Hello,this is my story (sorry for my English), Currently suffering a lot and don't have a good supporting system,I feel so alone and lost and don't know if this nightmare will ever end, any help appreciated. 01/2017-12/2022 ~6 Years on Generic Lexapro (5mg-20mg) because of repeataive panic attacks and anxiety that lead to depression.No idea about withdrawal,dr just said that it will be easy to stop them just like I started them .Just I have to do it slowly when I see myself better.My tapering was not tapering as i read here ,I consider it cold turkey because of wrong directionns of docs. I went from 20mg to 5mg in a short time(4-5 month) and and then 0mg. Withdrawal symptoms: 01/23-04/23 Low mood , anxiety at times, high energy, feeling uncomfortable some times.I was feeling that something is not going very well and something is coming but no idea that was from withdrawl as I thought this poison was already out of my system as I was told by doctors. 04/23-07/23 Lot more stress and anxiety, shortness of breath, higher heart rate, balance problem showed, several panic attacks, difficulties focusing, lower productivity at work as my cognitive skills started to go down,pssd.(Thought just ws high stress and anxiety who caused this maybe need some rest ,still no idea about withdrawal.) 07/23-31/09/23 The terror just started,all the above symptoms but in much more extreme which gradually worsened(I took maca for pssd for 4 days in the beginning of 07/23 possibly worsened my symptoms or just what came was supposed to happen ).In the beginning I couldn't talk , couldn't find the easiest words tos say to complete sentences.My cognitive skills just faded away (I was able to understand that because I used to be a good student at uni so I had great pc skills and was a smart guy high grades ) but my mind just stopped to cooperate.All of this gave me a lot ,a lot of stress I thought I was going insane and I just couldn't accept this.I stopped my work temporary for a month because I thought I need some rest because of anxiety i had and I just needed some rest but the worse was coming.My balance problems worsned a lot more ,and just one day I started to have a headache in back of my head ,It was like someone was burning my brain inside.Then everything went worse i started to have headaches in every part of my head , sometimes feel like there is missing part of my brain ,and i feel that parts of my brain are missing sometimes,Very sensitive to louds and sounds in general cand handle everyday sounds I feel paralyzed ,not able to communicate for a long time or focusing in the words someone says ro me because headache starts and just cant handle (it is like it triggers stressors and if i continue to hear or focus in conversations after the pain this goes me to a panic attack )The same happens if i see a vidio for lot of minutes ,feell like my brain is very sensitive maybe due to the fact that i had so much stress about what was happening.I found about this group accidentally as I was in 2psy docs who suggested that i had relapsing and wante ro give me cocktail of other drugs . I suspected that and started the searching on internet.In the beginning i found a group of pssd because this is a problem I have since my CT,and wanted to know about these other drugs they prescribed me ,then I saw @pugsuccess story which lead me to this amazing forum.And reading here about symptoms and everything about withdrawals things started to make sense ,but I was in shock (I found SA0 12/09/23).I didn't started to get these drugs they prescribed me but Im suffering a lot these days.Worth to mention that when my headache started I had a lot of pain on my brain (I thought I was going insane minute to minute )and I wa unable to tolerate it.My family went me In ER and they gave me sth no idea what it was however they told me to take Lyrica(pregbalin) and see how things will go.I took lyrica next day (50mg) and it helped me a lot to be honest my pain reduced and since then I continue it ,but im afraid as it is also addictive and dont know really in this moment it helps or puts more fuel to the fire,but im afraid to take it off because the terror I saw when i went in ER was out of this world.I don't work anymore as I am not able to concentrate on pc and my cognitive impairment is very low . I live with my family this moment as not able to take care by myself but they don't understand me they think that everything is just in my head and they expectthis to pass day by day putting some sort of pressure on me ,also my friends dont understand me,thay just have not ever heard about everything i say so doesn't make sanse ,Im not not able to seee them a lot because I cant handle conversation for lots o minutes with pepople it trigers me that pain in my head .I don't know what to do anymore,I cant go back to ssri the stole my feelings for years ,but im suffering a lot now and 2 month ( 9 months off srri).Apart from the fact that i dont function normally because of my brain I also have lots of stress daily which also cause high heart rate . My worts days are usually I'm bedridden and just a step away to go in ER(lot of pain inside in my soul like is screaming so loudly but only me can hear it , fatigue,not able to communicate, sensitive to light and sound,and dont know if i will make next hour or not).It goes after 6-7 hours some times takes all day and night but freaks me out.Some moments of the day I feel ok but ar less than the waves. My sleep is (4-5 hours per night) except from some days that I was no able to sleep at all .Try to eat 3xday even though some days i don't have appetite.Exerxice whenever Im able and not beddriden usually (30 -50min biking ride or walking/jogging ~8000steps )5/7 days a week . Im trying to fight this but in we deepest waves i feel so bad ,so weak and not imaggine to tolerate this for much time .I don't know if anything i said makes any sense because my symptoms are a little different from others with lexapro.I just want to ask the moderators if is a good idea to continue with lyrica or not? And what is the best thing to do when acute withdrawal hits because I cannot know if there will be strongers acute waves than these who passed just in case to be prepared.Would be a good idea any benzo or any other way either way? Any support and suggestions appreciated. #Thank you for reading my story.🙂

Hi guys I tapered Cipralex 10mg to 0.00625mg over 2 years, Everything goes nice until I smoke weed which I thought is a medicine to heal, From that day onwards I got Akathisia then healed after 10 months and I got depression, Awful Mornings, Insomnia, Racing Thoughts, Fear of abandoned, Visual Snow, feels like always high. I got Patterns like Awful Mornings and Depressive Evenings. Note. I takes Propranolol 5mg for Akathisia and I still continue the med, If I Stop the med my feel like always high become worse and Heart palpitate, But Most of Symptoms heals day by day Thank God for Healing me. But I can't tolerate somes supplement like fish oil which could tolerate in Cipralex taper. I can't even tolerate Pepper in food. I introduce myself what are the things I do and I don't in me.

Hey Everyone, I have been working on coming off of Lexapro for years and this is the closest I have ever been. Long story short, I have been weaning off lexapro after a couple of failed attempts of 20mg. I am currently at 5mg and having severe waves and windows of withdrawal. Looking for a little support that this is normal. I have a week or two where I feel phenomenal then suddenly a sharp drop where all the suicidal fake thoughts intrude. This also includes horrible chest pain, nausea, gastrointestinal issues, insomnia and just an overall feeling of dread. These last anywhere from two weeks to a couple of days. I am unsure about whether I should continue a taper, or if I should hold, but from what I am reading this is going to be a long arduous process. Any support or advise is appreciated. Been reading many of the articles on here and just now decided to try to become a member myself. Thanks so much.

Hello. I’m a 31 year old female. Straight, single, no kids. From California. I am alcohol-free since 1/1/18 and don’t smoke or use drugs. I was diagnosed with anxiety in 2001, depression in 2013, and have had moderate to severe emetophobia for as long as I can remember (this contributes to most of my anxiety). My first time being prescribed an antidepressant was at age 12. I was on a low dose of Paxil CR after being hospitalized for mysterious ailments that turned out to be anxiety-related. I’m not sure but I think I was on that med approximately six months. I don’t remember having any issues coming off it. In my last year of college (2013), at age 23, I started experiencing a worsening of anxiety and depression symptoms and ended up back on Paxil. Between then and early 2016 I was on and off Paxil, Zoloft, and Wellbutrin. I gained a lot of weight from the SSRIs which started negatively affecting my health. I was able to get off the combo I was taking (Paxil and Wellbutrin) in 2015(?) with tolerable and brief withdrawal symptoms, and was having great success managing my life with healthy habits and talk therapy. That all came crashing down when I decided to buy my first house. (A decision I now regret!) The stress of it all made me start having panic attacks at work so I decided to go back on medication. I started with Zoloft but the second time around it gave me terrible side effects. Next was Prozac which was just a week of misery. So I finally tried Lexapro. It worked. But over the course of the next several years I gained even more weight, and along with unhealthy lifestyle choices, ended up with a type 2 diabetes diagnosis. Along with the type 2 diabetes, my absolute worst struggle is fatigue. I have low energy every single day of my life. It got so bad that I was almost fired from my job for excessive tardiness; I’d sleep though alarms. I actually ended up quitting that job and selling my house because my mental and physical health were sinking to their lowest. I spent over six months on disability and moved back in with my parents. I eventually started working part time. And now I’m back to working full time and recently moved alone in a nice rented apartment. The constant, everyday, debilitating fatigue is still there. I tried everything to remedy it, even had a sleep study done. Nothing. The sleep doctor said that SSRIs can disrupt sleep patterns. So through process of elimination I’ve come to the conclusion that my chronic fatigue is because of the Lexapro. Between that, no sex drive (and thus being single for the past 7 years), and the metabolic issues, I’m determined to get off it. Which brings me here. I first tried getting off my 15mg/day dose in summer 2019. I took the bad advice from a homeopathic doctor to taper down 5mg every two weeks. It was hell and even after stretching that out a bit, I had to go back to the full 15 and eventually 20mg dose after six weeks. I’m now on my second attempt to taper. I easily got back down to 15mg in January 2020. In October 2020 I talked to my psych NP (who’s been managing my medication for several years now) and she prescribe me liquid Lexapro so I can start a slower taper this time. I started off going down 1mg each week, sometimes two weeks if needed. I didn’t have too many issues. The main symptoms were fatigue, nausea, dizziness/lightheadedness, and brain zaps. January 22, 2021 I got down to 3mg and that’s where I still am because for some reason I’ve been smacked on my a** with symptoms. I’m experiencing all the physical symptoms above, but worse; now along with crying jags, derealization, irritability, intrusive thoughts, and depressive mood. They’re not constant but they’re enough to really mess up my life right now. (Pandemic burn out is definitely a contributing factor as well.) So I’m here on this site to navigate this last leg of my taper. Feel free to drop a comment, give advice, ask a question, or just say hi. I’m using this site mostly on my phone so I’ll do my best to figure it out and add my signature line ASAP.