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  1. I'll try to keep this kind of short. I've finally decided to post an intro today after reading posts on this site for a few years now which has helped a lot with understanding what's going on since most doctors just told me my SSRI discontinuation/withdrawal symptoms-which were unlike anything I'd ever experienced before and physically and emotionally worse than I'd ever felt-were a return of my depression & anxiety or possibly a bipolar disorder according to one doctor. I knew for a fact that it was not my original anxiety & depression, but I had no idea what was happening in the beginning or how to explain it. I had social anxiety, depression, & general anxiety since age 12 and was not allowed to drive/take the bus/go out or do much by myself other than going to school (because everything was too dangerous) by controlling, religious parents with their own high anxiety and agoraphobia. I was never allowed to receive counseling for these issues & when I went off to college, it was an extremely difficult struggle going from not being allowed to do almost anything to suddenly being responsible for figuring everything out on my own. I was also not great with time management skills & knowing how to plan ahead. (I actually relate to a lot of symptoms of ADD & Asperger's, which both greatly affect social skills & ability to get through college and would explain a lot of problems I've had. I have learned more about them in the past year, but can't afford to get diagnosed right now so I've just been looking at support groups for days when my nausea is lessened.) I felt overwhelmed all the time and all my negative thoughts worsened severely. I didn't see the free counselor at college during this time either because I was embarrassed about everything and about asking for help. I finally decided I wanted to try to make a change and try counseling the summer after sophomore year of college at age 20 and was at rock bottom, desperate to not feel depressed. I knew someone who said their antidepressant helped them, so I asked a doctor for medicine and they prescribed sertraline. After taking the first pill, I had a surge of anxiety and racing thoughts that made it impossible to concentrate. Within the first couple days on 25 mg of sertraline, I was gagging and dry heaving over and over for at least 20 minutes as soon as I ate anything. I would also throw up multiple times in a short timespan after one snack or meal. I called my Dr & was told to skip a dose and then change the time I took the dose from morning to night. After a week of this (dry heaving & vomiting all meals) on 25 mg, and another call to the doctor, I was told that digestive issues are a possible starting symptom and to increase to 50 mg. As soon as I increased, the gagging & vomiting increased even more. After 6 days of this, I called the doctor again and was told I could stop taking it altogether since it had been such a short amount of time on it. And to come in for a different medicine Rx after the weekend. The very first day that I didn't take the sertraline, I felt the worst nausea I had ever felt in my entire life. I ended up asking a friend to drive me to the ER because I felt so sick. I told the Dr how I had just stopped sertraline. The doctor said that my pupils were dilated and my reflexes were overactive. Then, he listed off illegal drugs & asked if I had taken those. (No, I've never tried any drug before). He said "You need to tell me what else is going on because the antidepressant couldn't have caused this." And I said "I don't know" and started crying. I do know that people in my family are highly sensitive to medicines and have since found out I have a gene that causes me to metabolize slowly so things build up for longer in my system. Anyway, the Dr left the room and at one point I was given Ativan in an IV by the nurse which did ease the nausea. When the Dr came back, he told me I had SSRI discontinuation syndrome, (he didn't explain what that meant), that I could never try another SSRI, and gave me a Rx for a small bottle of Ativan. My mom said he mentioned something on the phone to her about serotonin syndrome which dilated pupils and overactive reflexes are symptoms of, but I don't remember him saying anything about it directly to me. He also mentioned reinstating a small amount might help but my mom didn't pass this on to me until much later because she didn't want me to take it. After that, I experienced: -more dry heaving which gradually lessened in frequency -random times of vomiting after eating and after exercising when I wasn't sick & the food wasn't bad (or sometimes nothing was left to vomit & only a small amount would come up) -continuing debilitating nausea & dizziness -olfactory hallucination (putrid smell that wouldn't go away, would intensify around strong scents such as soap & car exhaust) -uncontrollable crying at every tiny thing (neuro-emotion, not regular sadness) -uncontrollable rage (neuro-emotion) -intrusive thoughts & floods of bad memories which I "word vomited" in texts to my sisters -didn't want to be around people who I associated with bad memories because it would greatly intensify neuro-anxiety. (I'd guess the feeling is similar to what people mean who talk about experiencing bad drug trips and how it's important to be with people you trust) -nightmares -paranoia/suspicion/distrust (felt like my mom & sister were not really my mom and sister even though logically, I knew it was them. Things feel creepy & sinister -almost like a horror movie sometimes. A post I read here compared the sinister feeling to a bad LSD trip. I have never tried LSD, but I understood what they meant & is the closest way I found to describe it. -cognitive fog (thinking, processing speed, & reaction time is noticeably slower) (I was a slow thinker/processor before, but it feels like I have brain damage now) -memory problems (I was somewhat forgetful before, but am even more so now) -depersonalization ("it feels like the medicine changed who I am & I don't have an identity/sense of self which I still hadn't fully formed before sertraline) -derealization (feel emotionally disconnected & distant from people/atmosphere. I know things are real, but they don't feel real. Sometimes it feels like consequences won't matter or there is no sense of helpful anxiety even in a potentially dangerous situation. Logically, I know they do matter and still want to do the right thing) -anhedonia/apathy/emotionally numb (don't care about things or have the same amount of passion for interests or feel empathy for other people's emotions or feel spiritual even though I had some spiritual beliefs before. Couldn't feel hopeful about anything/future or feel love towards or from anyone. These emotions have slowly returned to a certain degree since then & levels of ability to feel them have changed at different courses of time) -blurred/cloudy vision (when DR was at most intense, vision was different. Hard to explain) -eye floaters ( random black specks & lines) Didn't notice these until a year after DC-ing -constant yawning/air hunger -stomach/digestion issues -burning, tingling, itching, numbness, redness in feet -brain zaps/"crackles" (sometimes annoying, sometimes painful, but my most tolerable symptom) -head pressure/tightness, feels like head is being squeezed -headaches There was also a period of 6 months where I thought certain symptoms were over and after that period, the dizziness returned. Those are most of the symptoms I've experienced in the past approx 3.5 years. They're not in order. I'm 24 now. A few have gone away for the most part (vomiting, olfactory hallucination, yawning) and most are less intense. I have really improved a lot, I don't mean to sound overly negative. But, I still have the issues I went on the SSRI for & I have trouble accepting where I am & worrying about where to go from here & the uncertainty of how long this lasts because it has put lots of areas of my life on hold (I wasn't able to go back to college, I hope to someday) and ended up making things harder to deal with when I was told it would make them easier. (BTW, I am now seeing a counselor). I don't understand why people say SSRI's are not technically drugs when they have this much of an effect on your mind, mood, & perceptions. Sorry if I have over shared, I might need to post a shorter version of this at some point that's easier to read. And I'm still figuring out the layout of the website & where to post about certain questions & topics. I just know that sometimes other people's explanations made me feel better because I had some understanding of what was happening & words to describe feelings I'd never had before and didn't know how to explain. I've also had other stress & health issues and a few (physical health) medicines that have affected my withdrawal progress, but I guess that's a topic for a separate forum. Any advice, similar experiences, recommendations, tips for using the site, or insight into what happened to my brain is appreciated if anyone feels so inclined :)
  2. My story appears to be similar to many folks here on this forum. Reading all of these accounts has helped me accept my symptoms as a result of Zoloft, which has at least given me some piece of mind. Before I explain my timeline and struggle with getting off Zoloft, I want to bring to the forum’s attention something my psychiatrist informed me of which I have found no evidence of elsewhere. Hopefully someone can verify this. My psychiatrist explained the following: The FDA allows for a 30% upward or downward margin of error on Zoloft pills. He explained that a 50mg Sertraline (Zoloft) may have up to 65mg or as low as 38.5mg. Another example, a 25mg Sertraline may have have as much as 32.5mg and as low as 17.5mg. Can anyone validate this? If this is true, it is unimaginable. My story: I started 50mg of Zoloft in 2012 for general anxiety, social stress and general dissatisfaction. My psychiatrist at the time said “It was about as harmful as taking an aspirin.” In 2013 we increased my dose to 75mg. My psychiatrist retired in 2015 and I continued at 75mg through my general doctor’s refills. In 2018, I felt I was in a good place and tried to go cold turkey. After a couple of weeks of torture, I returned to 75mg. After learning that I should taper, and also feeling I was in a good place, I decided to reduce my dose to 50mg in July of 2019. Two weeks of intense symptoms ensued but by the end of the second week things became more manageable. I wanted to reduce the symptoms and requested (it took some convincing of my new psychiatrist) a liquid form of Sertraline in August. I reduced to 45mg but felt like I was not getting a consistent dose (sticking to the glass) and it was difficult to swallow even when mixed with water. My psychiatrist recommended that I switch to a 25mg pill + a half and a quarter of another 25mg pill bringing me to 42.5mg in September. I stayed at 42.5mg for September and October and was distracted by a series of sinus infections (antibiotics and 2 rounds of prednisone). Thinking I was ill from the infections, I did not realize most of my symptoms were Zoloft related. All of my symptoms were rationalized but my general doctors. Dizziness, light headed, extreme head pressure, headaches, persistent neck pain, fogginess, loss of appetite, ear pops and pings, jittery, imbalance, loss of equilibrium, flu-like symptoms and tingles in hands...doctors all rationalized them as symptoms of sinus/ear infection and the steroids. This went on for almost 2 months, while somehow I was still functioning. Until I called my psychiatrist last week and he informed me that it might be because we switched to a smaller pill which may have 30% less than is listed on the bottle. He prescribed the 50mg for me and within 2 days I felt somewhat improved, but noticed some brain zaps and the continuation of symptoms. My psychiatrist said that 50mg may not be enough to counteract a withdrawal and that we may need to go up to 75mg to stabilize. This past Sunday (10/27) I upped my dosage to 75mg. I am feeling some improvement, but still not feeling right: light headed, light sensitivity, headaches, fogginess, inconsistent appetite, ear pops and pings, jittery, imbalance and tingles in hands... So I am back where I started, 75mg, and hopefully stabilizing soon. Lots of information here from fellow “survivors” but I am scared. Shouldn’t I feel totally better? Could a couple months of enduring withdrawal make stabilizing more difficult? And most importantly, is the 30% margin of error that my psychiatrist shared with me true?? If so, we need to change that! Thank you for your time.
  3. Hi everyone, After a week of lurking here, I was motivated to join to ask for some advice for my particular situation. Everyone here is so helpful and supportive, and I'm hoping that someone has some insight into what's been happening to me! I think most of the main information is in my signature, but in short, I've been taking 5mg escitalopram intermittently since 8/2017 for bad PMDD symptoms. I start taking it at D14 of my cycle, and continue until the next one begins. It has been helping me deal with depression and mood swings quite well until recently. The last cycle I thought it may not be working, and would that I had just stopped then!! This past cycle, I again stopped taking it at the usual time, and about a week later felt like I was hit by a truck - vertigo, balance issues, blurry/double vision, nausea. After a few days of suffering, I realized that maybe this was withdrawal, so I reinstated back at 5mg on 6/26, a few days earlier than I normally would have. The vertigo has been more tolerable, but the other symptoms remain in force and are dramatically interfering with living my life. I feel like I walk around drunk and half blind the majority of the time. I'm due to stop taking them again in another week, but I'm so lost on what to do next.. 1- should I take them continuously from here on out & begin to taper if/when everything stabilizes?? or.. 2- stop taking them in a week & just see what happens? or.. 3- modify the dose up/down? I have had multiple blood tests and nothing abnormal has been found, and am waiting on an appointment with a neuro-ophthalmologist referred to me by my PCP. The double/blurry vision is the scariest symptom for me - I have had glasses for years so I'm comfortable with my poor eyesight without them, but this is awful!! I'm worried that it won't get better, even though I know its only been a little over a week. Thank you for taking the time to read all this, and I would love some advice on the best path forward ☺️ -jbird
  4. Hello forum! Female, 33, Sweden. Have been on Paroxetine, 20mg, for more than 5 years. In April 2017 I had my first major panic attack and ended up in the ER. My life completely changed and I developed panic disorder along with some GAD. Though the GAD may have been the underlying cause of panic, I don't really know. Since September 2017 I have been reducing my dose of Paroxetine, and am now on 10mg. Somewhere in December I got down to 10mg and thought I'd wait until I'm stable at this dose before continuing my taper. I have been using the Claire Weekes-method of trying to completely relax in the face of panic, and I seem to only have smaller attacks now. Palpitations have lessened, and I am less startled by my nervous system signaling panic. I have lately been feeling very off-balance/dizzy and sometimes theres an intense feeling of anxiety and dread in my body. Feels like there are bugs crawling around inside. Weird buzzing nerves? Dizziness is so bad I have to lie down sometimes. Last night I was holding on to the walls when moving around in my house. Feels like I'm losing my balance all the time, even when sitting on the toilet, but I can stand on one leg and walk in a straight line. So it seems to be some sort of misinterpretation happening in my brain, rather than an actual problem with my balance. Now to my question: When I wake up in the morning I usually feel perfectly fine. It is after taking Paroxetine that all of the horrible sensations start, and they seem to calm down slightly in the evening. Is this normal during withdrawal? Or does it sound more like I'm having actual adverse reactions to Paroxetine? They sort of worked until I developed panic disorder. But I clearly remember growing increasingly fearful and illogical during several months before I had that massive panic attack. Thank you in advance.
  5. Hi all, This is my first post, but probably not my last unfortunately. I was taking Lexapro 10 MG for anxiety and dizziness of unknown origin for about 3 years. I have tapered off over a little less than 3 months. As of today, I am over 1 week off completely of the drug. I have had a whirlwind of symptoms most notably anxiety and dizziness. The dizziness has been unrelenting and it's very taxing on the mind and body to have to compensate for this. Generally, I feel disoriented and most of my dizziness centers around head movement. Some heart symptoms, but mostly attributable to anxiety (racing heartbeat, palps, etc.). I've had a history of PVCs which have been checked out before and OKed. I'm writing this specific topic to ask what your definition of a brain zap is? I've read over some time that most people seem to center around a brain zap as a sudden jolt of electricity throughout the head, or an electric like sensation. I feel like I may have been experiencing brain zaps but not necessarily in this sense. I don't feel an "electric" sensation, but I do experience sudden dizzy spells, where my head feels like it's about to fall over. These spells last maybe a few seconds and really take up that time (I.E. I can't do anything else, for those short seconds I'm in the spell). Does anyone else experience brain zaps as sudden dizziness/vertigo that subsides in seconds? Thanks for any input and good luck to everyone.
  6. Acta Otolaryngol. 2010 Sep;130(9):981-3. doi: 10.3109/00016481003602082. A possible explanation for dizziness following SSRI discontinuation. Smith PF1, Darlington CL. Source ABSTRACT Dizziness is the most commonly reported symptom of abrupt discontinuation from the selective serotonin reuptake inhibitor (SSRI) category of antidepressants. The reported dizziness is exacerbated by even slight head movement, and therefore is likely to be vestibular in origin. The SSRIs most implicated are those with short half-lives and which are most selective for serotonin (as opposed to noradrenaline), e.g. paroxetine and sertraline. Since the vestibular nucleus complex (VNC) has an abundance of serotonin receptors, the abrupt withdrawal from an SSRI is likely to have a substantial impact on the electrophysiological activity of neurons within it. Here we suggest that the abrupt withdrawal from an SSRI is likely to cause a sudden decrease in serotonin in the VNC, which will disrupt the function of VNC neurons bilaterally, causing dizziness without vertigo.
  7. Hi All, I have been a reader of this site for over two years and wanted to share my story and ask for suggestions / hope. I was put on 10Mg lexapro in fall of 2014 for anxiety and took it for 1.5 years. The drug greatly improved my anxiety and self confidence but destroyed my sex life and caused weight gain. I tapered over 4 weeks at my drs suggestions and suffered through 9 months of fog, depersonalization, confusion and dizziness (Hell). I ended up going back on 10Mg Prozac and immediately stabilized and stayed on for 6 months. I have been trying to taper at 5% increments over weeks but am still having extreme dizziness. Have tried everything from acupuncture to meditation to diet and exercise, all of which helps but doesn’t “carry the day”. Aside from slow taper and good lifestyle changes, does anyone have any recommendations? Thanks so much.
  8. Hi everybody! I started taking Lorazepam 0.5mg and escitalopram (Lexapro) 10mg for anxiety attacks back in Sep 2016 after 4 months of one-per-month short vertigo episodes, dizziness, imbalance and (unconfirmed later) misdiagnosis of Meniere's "Syndrome"). I never reached the prescribed limits started with 1/2 pill -> 3/4 pill of Lorazepam and 2.5 -> 5 ->7.5 mg of Lexapro. I wasn't feeling good. Constant dizziness, sometimes a bit of nausea and overall while feeling less anxious not feeling good most of the time (a bit dizzy in some situations like elevators or driving). Then, I think in Feb 2017 I decided to start tapering off scared by all the withdrawal descriptions I've read and no being able to have tests for my vestibular system. I bought mg scales, and I think for two months I tapered off Lorazepam, and then May 26 was my last day of escitalopram. For 2 weeks or more I felt more or less okay. Then, things started getting worse. In mid-July 2017, after a stress I felt really dizzy, and my anxiety attacks got back to me. I started having strange sensations of posture imbalance, like my feet were not in accordance with the rest of my body. I thought I have a chronic subjective dizziness, took some vestibular therapy (they said I have a perfect objective balance), it seemed to help, but still I was having difficulty concentrating, sitting in front of a computer, felt constant eye muscle pain and anxiety. Strange feet sensation / imbalance was more perceivable when I was standing. Then I started having sort of "excitement"/"dizziness" zaps in my brain like you are on a rollercoaster for a second. Then roughly 3 weeks ago it got gradually accompanied by tingling, numbness in my feet and also tingling/ hypersensitivity in my arms / body and all over the body. For a couple of nights I felt extremely fatigue and felt weakness in my leg muscles and overall body, went to bed 2 hours before my wife, woke up a couple of time in a cold sweat. I started thinking I was developing an MS and all that made me completely freaked out (not mentioning chronic subjective dizziness and prospective to taking ADs again). I'm doing MRI in a couple of weeks, MRI from Sep 2016 showed no lesions. A couple of days ago, maybe a week, I started feeling odd taste in my mouth, I searched for it and yes, the closest description is "metallic". These three months were the worst, I think I'm in depression now (my psychotherapist kind of shares my view), really preparing for the life with MS and, well, the joy of life has gone So I'd like to ask community a couple of questions and ask for support, because it seems my CNS is waving me a goodbye 1. Do you think I tapered too fast? 2. Was the dose good enough to "justify" what was going on? 3. Is all this more likely WD than suddenly appearing MS? 4. I'm taking Fish Oil, magnesium, Turmeric, taking St. John's Wort (800mg) right now. Should I add / remove anything from the list? 5. I'm doing yoga warm-up every day, try to visit yoga classes a couple of times per week With hope, citydweller.
  9. hi guys, Its been 10 days since I stopped Lexapro after 1.2 years 10 mg and tapering off for 2.1 months last dose 5mg . I got light on and off dizziness and mild anxiety after 1 week but I am able to do my job like going to gym working out . ihave no problem with it . every 6 years I get dizziness sensation while walking sitting or lying down . I had mri done twice , neurological examination twice , ent twice , cardiologist , blood tests everything completely normal even heart rhythm and paplitaions were normal. so they put it to anxiety related dizziness and was put on Lexapro . in the long run my parents thought medications are bad so I stopped after tapering as told by psychiatrist . my fear is will get greater symptoms or will I get better ? I don't want dizziness again I have enough of it . will iget more withdrawls later ? . please help . I am feeling anxious after reading many horrible online forums .
  10. Hi! I'm Britt777. I joined this site to figure out what is causing me numerous symptoms. Here is my brief story: Took Lexapro for about 3 years or more, came off of it Tried Trintillex and Brintillex, didn't like the way it made me feel Doctor then tried Fluvoxamine 100mg and took that for 7 months. He decided to add Wellbutrin (Bupropion XL 150mg) along with it. A month later I ask to stop Fluvoxamine (Luvox) because I felt like I was experiencing "depersonalization" or pretty much felt like life was not real and was a dream. So, at that appointment he told me to stop the Fluvoxamine and upped my Wellbutrin to 300mg once a day. The first day from this switch I felt great. Then the second day came... had nausea, lightheadedness, dizziness, "brain zaps", increased tinnitus (ringing in the ears), blurry vision, feeling like I could pass out, headaches, head pressure, and crazy fluctuating heart rate. (Today I had a heart rate of 100 and dropped to 70 within 5 minutes without doing anything different.) This is day 7 since the switch. I just want to find out if it's withdrawal symptoms from the Fluvoxamine since he didn't advise me to taper or if it's a reaction to upping the Wellbutrin.
  11. Hi all, Checking in to ask a few questions about SSRI (Effexor) withdrawal. Basically, when I came off Effexor in August 2014 over 12 weeks after being on them for 4 years, I started to have stomach / digestive problems about 6-8 weeks after stopping. Always figured that it was due to coming off Effexor, never had anything like that in the past. But basically almost 1 year later in July 2015 out of the blue I developed this lightheaded / dizzy feeling 24/7 and a year later it's still here and my health has taken a major dive. I was given an antibiotic (clairithromycin) by my then gp just to see if it helped the dizziness, he thought it was a sinus infection, and it almost killed me and am still feeling the effects from it today. The best way for me to describe the experience is like trying to throw petrol on a fire to put it out. So right now I'm dealing with suspected Effexor withdrawal and also been floxed by the antibiotic, my body is a total mess. I wanted to ask here is it possible to get additional withdrawal symptoms 1 year later after stopping Effexor? I'm trying to figure out where this dizziness came from, I've had an MRI and came back clear. I'm trying to figure out if it could be connected to the Effexor withdrawal, but because it happened 11 months after I stopped it I'm thinking to myself is it even possible or connected to the Effexor withdrawal. That's why I'd like to speak to a few people on here and maybe see what they have to say about it. If anyone can shed some light on this, please comment or drop me a pm, really would like to get to the bottom of it. Thanks for reading.
  12. I really could use some advice I am not sure if what I am experiencing is from Effexor withdrawal or not. I was on 150mg for a few years I have been slowly tapering down for several months now (weighing beads on a micro scale for accuracy) on Friday 22nd I took my last dose which was 0.124g of beads (so very little actual drug). For months now I've had severe dizziness and nausea, and diarrhea too. Enough to keep me in bed a lot. Plus a strange sensation on the tip of my tongue. Now it's pretty much just dizziness but it's so bad. Previously when I was down to 0.5g of weighed beads I decided to take it back to 1.5g to see if my symptoms eased and go a little slower. I think things improved a little but I've not been symptom-free. I'm out of the drug completely now. I took 2-3 weeks to taper back down from that to zero. Slower than the first time. I thought my symptoms had actually improved because I bought a whole lot of natural remedies for giardia and tried them all and had relief within a day, but now I don't even remember if that's also when I took my dosage back up. I'm just not sure what's wrong with me. The doctors did a bunch of tests and gave me no answers. My family doctor told me to go off birth control and take naproxen every day. Well I'm doing half that... I'm not risking pregnancy just because SHE thinks I should have a baby. Yikes. It's been over a week since I stopped, still so dizzy I am wondering if I should go back on (I'd have to go refill the script) and if I do, what dosage? I would try the 10% taper every 3-4 weeks but I don't want to be doing this much longer. I hate taking it. And honestly I'm not totally sure if this is even the cause of my dizziness. I had no headaches or brain zaps or the other sensations I had when I missed a dose. But sometimes I am hearing sounds and I'm not sure if it's my head or the sounds are really there. I just don't want this diziness to go on forever and I feel like it's going to. But I also don't want to go back on Effexor if that's not even the reason I'm dizzy!
  13. Hi everyone! I've just found this thread and I'm so happy I did. I'm 27 and have been taking klonopin 1.5mg daily for about four years. Last month I started seeing a new doctor and she put me on Zoloft with the hopes of tapering the klonopin. I took 25mg for the first week, 50 mg for the following 3 weeks and now have been on 100mg for the past 3 days. This medication is making me feel insane. On 50mg I felt more depressed. Now that I upped the dose I'm constantly anxious so I've been taking more klonopin. I'm dizzy, my eyes just start shutting constantly, nauseous, can't stop yawning (and the yawns make me sick to my stomach). Has anyone had similar symptoms? Did they go away? My doctor said to give it a few more days and if this persists we'll lower the dose. I honestly just want to stop the medication. Also, I haven't been able to sleep at night. It's pure hell. Someone please tell me I'm not the only one struggling with this. Has anyone stopped the medication after this amount of time and had minimal side effects? Because now I feel as if I'm stuck between a rock and a hard place. Medication symptoms or withdrawal symptoms. Thanks in advance!
  14. Hello all! I found your forum and figured I should ask for thoughts regarding my Lexapro withdrawal experience. I’ll post a brief overview paragraph, but if you have time or want to know more, I tried to be as detailed as possible describing my symptoms to see if they sound familiar to anyone here. Short explanation: I took Lexapro for around 2 years, maybe a bit longer. The dose was 10mg, but it’s possible it was a little higher for a short while. I lowered the dose to 5mg at some point in 2014 and was on that dose for a year. I then spent the bulk of a year tapering from 5mg to 0mg. The last dose I took was so small that it was a tiny piece of powder on my finger, which is what I had gotten it down to over time. I am on here because I have been off of the medicine completely for almost four months and still have some odd slight-dizzy/floating feelings sometimes, which typically aren’t very strong or long lasting, but I also have fatigue most days. I sleep very well and get 7-8 hours a night, but feel the need to lay down for a few minutes several times a day. I never had these issues until I started messing with my Lexapro doses. Thats the short story, but I can get more in-depth. Fatigue details: The fatigue used to be so bad a few months ago that I could easily fall asleep within 3 minutes; I would often take a few minute break at work and immediately fall asleep in my car and set a short 6 minute timer and wake up and feel a lot better. I would do that a few times a day especially after work. Now days I don’t instantly fall asleep, but resting my eyes for a few minutes helps. I take a 20 min nap at lunch and a 20 min nap after work and for both of these I fall asleep and jolt awake when the alarm goes off, but feel a lot better. When it happens, I can often feel the tiredness growing in a short period of time, often within an hour or even 15 minutes. The tiredness is usually just to the level of being annoying, but sometimes it becomes so strong that I literally just have to close my eyes at my office desk for awhile. When it’s really bad I notice I even close my eyes for a couple seconds when I am walking or doing simple things. This isn’t like when a driver starts closing their eyes without noticing it; I very purposefully close my eyes just for a second or two to get a vague feeling of minor relief. Usually I feel like my mind is actually still working and I am wanting to stay productive, but my eyes and head just get tired even though the rest of me seems to have energy. Its almost like a synthetic tiredness, as if my water was spiked several times a day without me knowing; it’s very different from a normal tiredness. Often if I am at home I will feel it kick in and just have to drop what I’m doing, lay down and set my timer for 5-15 minutes just to recharge and then get back up and continue what I was doing. Then it might kick in two or three hours later and I’ll have to do the nap/timer session again. Before I go out and do anything, such as meet a friend or go to a movie, I preemptively take a short nap to prepare my body. Also, when I wake up in the morning after a full 7 or 8 hours sleep, I am typically a bit groggy for awhile inevitably. Before I started changing my meds I would often wake up and have energy and used to love my morning time during the weekends. Now mornings aren’t horrible, but they aren’t really much to look forward to. On weekends I often take one of my quick naps within an hour or two after waking up because I get so groggy I just have to lay down. Dizziness details: My dizziness from time to time gets bad enough to become an issue that really bothers me. These periods where it is bad usually only last for a few days, but more often the dizziness is a very minor symptom and just makes me feel a bit “off” for a half hour or so. It’s hard to explain and there are actually several different feelings of dizziness I experience. “Dizziness” isn’t even always the best word, but its the only one that I can think of that fits. Often it is just a vague sense of feeling disconnected and unbalanced. Sometimes when I am showering I do literally feel slightly unbalanced, but it is a very minor feeling and I never *actually* feel like I am loosing my balance. Another feeling is almost like the whole room is spinning, but at such a very, very slow rate that it is just enough to make me feel slightly uncomfortable. Sometimes another feeling happens where I feel slightly cloudy headed and if I turn my head quickly, it takes a second for my brain to readjust. This usually doesn’t last very long, and in fact, most of these dizzy feelings come and go within a half hour and don’t interfere with my life very badly. Oh, and another one is a vague “floating” sense that I sometimes feel when I walk down a hallway, for example. Again, pretty minor, but just enough to make me feel a little off. I should also mention that sometimes the dizziness transitions into tiredness; the dizziness evaporates and I am left feeling like I need to lay down from sudden fatigue. Additional issues: When I first got off Lex completely, I had really sore muscles in my back and shoulder blades within a few days. One of those curved self massage sticks really helped with that. I used to also have a really bad pressure in my head during the tapering process (but went away after a few weeks of stopping lex) and the massage stick also relieved a lot of that head pressure that I used to get. I no longer have the tension in my back, but my shoulders themselves often feel like they get tense, like there is a “grip” on them. Sometimes this is combined with a slight feeling of dizziness. When I am around my father to give my shoulders a quick massage it relieves a lot of the dizziness as well as the tension. I have read that anxiety can cause tension like this, but I have had anxiety my whole life and never have felt this shoulder “grip” before. But it may be an indirect, subconscious anxiety causing this tension, as opposed to a direct result of lexapro withdrawal. Typically a short period of laying down helps with this also. Waves/Windows: I have read different parts of this forum and found them helpful. I feel that the “waves/windows” idea is in line with what I have been going through. I feel that I am getting better, and then all of a sudden I will feel way worse for several days or a week, then I will start feeling better again for a week or so. However, looking back on the whole process, overall I think I am improving in the big picture scheme of things. I went to the doctor yesterday and of course he told me it couldn’t have anything to do with Lexapro because I have been off of it for a few months. I also am having blood work done just in case it is anything else. I guess my big question is do these things sound familiar to others and will these symptoms go away over time?
  15. . My name is Kim. I'm new to the forum. I am trying to get off of escutalopram. I have been taking it since July of 2014. I currently take 10mg. I take two 5 mg. pills a day. I tried to lower my side awhile ago but I got terrible withdrawals--severe anxiety and headache. I cut it down 25%. After withdrawal effect I went back to regular dose. My psychiatrist is no help. He told me to just cut it in half. No way! He is clueless. I wonder what some of you have to say.
  16. Kilito12

    Kilito. New.

    Hey everyone. Not sure what I'm looking for here. I guess some reassurance about how things are going for me. Been reducing citalopram (40mg) since April and now not taking anything. Serious side effects. Worst being the dizziness and electrocution down my neck and necks every time I move my eyes. Insomnia too. Hence why I'm awake at 4:30am.
  17. Hello Everyone. I was on 20mg nortriptyline for 6 weeks. I tapered off the drug over a 1 week period due to it's side effects (increased heart rate, muscle spasms and hair loss). It's been 2 weeks since I stopped taking the nortriptyline and I am still having a very rough time dealing with withdrawal symptoms. I constantly have this constant rocking motion that I feel in my head as though I'm on boat that's bobbing up and down, left and right, forward and backwards. Although this seems similar to vertigo, things around me in the environment are not spinning. I just feel like my mind and head is always rocking ever so slightly with the beating of my heart. I should note that I had and am still dealing with constant rapid heartbeats throughout the day since I stopped taking the drug. This constant rocking motion in my head makes me feel dizzy and nauseated. And my head feels like a balloon all the time. Has anyone here experienced movement problems during nortriptyline withdrawal? If so, does it go away and how long does it take for it to go away? It's very bothersome. It greatly hinders my concentration and focus. I'd like to hear from anyone who's had this experience. Thanks.
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