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  1. Hello! I am new here. Please forgive how long this is, but I’m trying to be as concise as possible from the beginning for the moderators (and have a bad habit of digression, ha!). I so appreciate this page. I’ll try to add on my drug signature. But if I don’t do that correctly at first, I apologize in advance, as well as, for any repetitiveness, since my brain isn’t always on par and I just may not feel like overly editing any repeated information in different sections below. Please see my “thoughts about this forum” below “my history and withdrawal symptoms” further down the page here. Again, I am so grateful for this website and realize my situation is not nearly as extreme as many, but it is all relative on bad days I suppose ;). From everything I have read, it appears time is the KEY with all of this withdrawal malarkey. I am trying to be patient and positive and do have faith all will be ok in time, but I must admit I am totally blown away that I continue to have symptoms (sometimes new ones or variations on old ones) at 8 months out, after my last Zoloft, which I was on for only 2.5 months (25 mg and only the full 25 mg for the first 2 weeks – see below). Holy crikey Batman! And yes, I do know how quickly SSRI’s can start to change the pathways, etc. So, back on point… Please see below. AND THANK YOU so much in advance for all your help and my thoughts, heart and well wishes go out to all of those suffering FAR MORE than I am. This is enough for me. I can’t imagine some people’s hell in all this, though I’ve read enough on here to know I am grateful that, so far, I am not in that level of hell. SSRI HISTORY: I am currently 49 years old (2017) 1992-1998 (+/ - a year: in my early 20’s) - 20 mg Prozac (no major side effects, SE’s, and quit CT with no problems) 2001-2002 (+/- brief period of time after divorce: in my early 30’s) - 10 mg Prozac (again no major SE’s and quit CT no problems) I just didn’t like how Prozac kind of flat lined me and I didn’t like the idea of staying on anything when I really didn’t feel like I needed anything. THEN… RECENT LIFE EVENTS… 2017 April 27 - Start 25 mg Zoloft (generic sertraline) very reluctantly (after the passing of my mom in October 2017 and a VERY PAINFUL bad relationship break-up only a few months later. My doctor thought Zoloft would help break my cycle of poor sleep and anxiety and sadness – though I really just wanted to try a sleeping pill of some kind. Though in hindsight, benzos can be difficult too and I am apparently pretty sensitive to many drugs. Weeks prior to Zoloft, she gave me some trazadone, which I realize is not a benzo and, holy crap, hell no, never again. One pill and I WAS NOT MYSELF. Quit immediately and returned to normal, other than my original circumstantial sadness, anxiety and insomnia.) 2017 May 15 - Start cutting the Zoloft down to about 15-20 mg of Zoloft (because OMG it is wiring/amping –akathisia?- the crap out of me and not helping me sleep and I’m having fuzzy eyes and head off and on. I could have cleaned a house with a toothbrush. It got me motivated, but I was still edgy and couldn’t sleep on that crack feeling.) 2017 May 26 - Start 12.5 mg of Zoloft (because still SE’s of bleary eyes, extreme jaw clenching at night, mild fuzzy head with pressure – brain fog, still some anxiety and sadness) 2017 June 30 - Start 6.25 mg (because still a lot of jaw clenching, paresthesia – including prickling and burning, body vibrations – like every cell in my body was wired) 2017 July 10 - Stop Zoloft completely (because I suddenly developed tinnitus in my left ear and I was like “Eff This I’m done!” Yes, I know, now that that was probably too fast of a taper, but my doctor and the pharmacist insisted should be fine and quite frankly, I was having such a horrible paradoxical reaction to it while I was on it, I doubt anyone could have made me understand to stay on it longer at the time to wean off more slowly. It is what it is now. THEN WITHDRAWAL (WD) SYMPTOMS: In a nutshell… Immediately after stopping had painful neuropathy for a few days in some places, mostly my left arm. (I am familiar with neuropathy because I experienced it for several weeks years ago after only 1 dose of Cipro – won’t touch fluoroquinolones again either). After stopping the zoloft still had inner vibrations (or what some may call minor akathisia at night…?) and paresthesia, mostly at night, but some paresthesia during day as well. About a week after stopping developed severe brain fog. Off and on quite severely for several weeks, but still with tinnitus and paresthesia. Totally messed with my menstrual cycle for about 4 months in terms of missing one and then crazy flow (perimenopause, maybe, but now a wee more normal again and it was NEVER like that before Zoloft). And as an Update – totally missed one in Feb 2018. Perimenopause possibly happening as well, but fun times to have both withdrawal and that. Makes it hard to distinguish some things. However, the crazy brain fog, internal tension and vibrations at night at times, the paresthesia and burning skin (not painful, but not normal), neuropathy at times (is painful), muscle weakness at times (not extreme, but notice when doing certain exercises), tinnitus, weird muscle tightness and head sensations at times, especially when trying to sleep and just overall, not quite me feelings at times… ah, yah, I’m gonna go with SSRI withdrawal on all that, because I was premenopausal prior to Zoloft and did not have any of those symptoms, other than some peri anxiety. Plus, I find it quite fascinating that almost all people have many of these symptoms across the board no matter what SSRI they were on. Coinkydinky…??? Hmmm, not as far as I’m concerned thank you very much. Ooooppps… I digress again… J Anxiety off and on, but some of that could be residual from prior losses mentioned above. FAST FORWARD TO… End of September 2017 to January 2018 to present… 2017 October - So to recap, I think I had a bit of a Window in some things in end of Sept and through October 2017. I was not “right”, but definitely felt better in some ways, even with some symptoms, felt more “normal” and hopeful. And the inner vibrations or mild akathisia while on the drug at night seemed to be gone. And the jaw clenching had stopped not long after stopping the drug. 2017 November - some things came back with a vengeance, like more sadness and anxiety and tinnitus more prevalent again. (Tinnitus changed from just left ear to a more of a high pitch in head or both ears off and on, which I still have, off and on, and especially in bed at night and first thing in the morning as of today March 2, 2018. I had had moments off and on in past months of the high pitch not being there at all and just some tinnitus in left ear from when originally started at end of Zoloft. But the high pitch, almost ringing in head-ish as well as both ears, has been present consistently for over a month now. Sigh. Just keep hoping eventually it will go away in time.) December 2017 - Same as November but with Stupid Crazy Brain Fog Awfulness again, like cotton head, and couldn’t do cognitive things for diddly and still sometimes have moments where if I think too hard my brain just says, whatever, pack up and leaves the room. This went on and off until around January 12, 2018. AND AT THE END OF DECEMBER - THE FIRST TIME I think I had the beginnings of mild akathisia since when I was the Zoloft, but it felt a bit different with some weird “internal tension in my chest and head and arms and just uncomfortable weirdness. And sometimes coupled with neuropathy in arms. I swore I might be having a heart attack and realized, nope, just more new withdrawal BS. Nov – present (ongoing at times)… Muscle weakness and weirdness (not extreme, but not normal to me) At some point in this time frame, I started to notice an overall muscle weakness feeling at times when exercising (weight bearing exercise and cardio), but I still do as much exercise as I can anyway for my sanity AND because at my age I can’t afford to lose any more of my fitness and tone. It’s just too hard to get back and I don’t have that much to begin with. I am grateful I can exercise at all (even if it flares a symptom or two at times, but mostly I’m ok), because I have read on this site how many can’t do that yet. 2018 Jan 12-19th – POSSIBLE MINI WINDOW…? About a week of almost “normal me mood” feeling Jan (though off and on all this time, still some tinnitus and minor paresthesia at times). 2018 Jan 19th to present – ANOTHER WAVE - the beginning of low grade akathisia for several weeks with awful paresthesia, neuropathy – all worse at night. So far, this wave is not absolutely 24/7, but many days for most of the day, with a minor window of 3 days lessened aka/pare/neuro/jingly symptoms. And some more of the tinnitus high pitch at times, but very little brain fog. Just more of an “off” feeling. And overall sad and anxious feeling. Less upbeat like in the window week. 2018 Feb 26th to present … Ruh-oh, as of today, super Brain Fog day – Crap ability to think or focus and brain just super fuzzy. So add Brain Fog back in to the mix now off and on as well. But had a few days with less to no akathisia or neuropathy or paresthesia. BUT SUPER TIRED off and on for the last week, including today. AS A SIDE NOTE ON WINDOWS AND WAVES: Windows for me happen in a way that not ALL symptoms have ever ALL been gone, just marginally better at times and it fluctuates as to which symptoms decides to rise up more. During Windows, if that is what they are, I feel more “normal” overall in feeling like ME and my mood is pretty good, even if I’m having tinnitus or some minor paresthesia, etc. And windows may even just be a day in the midst of things, where I “feel” so much better overall, even if other symptoms still happening on a subtle level. What I consider Waves are when my mood is crap sad or anxious and I don’t feel as “normal”, and/or I have a bad bout of the physical things like Brain Fog and/or mild akathisia, and/or paresthesia/neuropathy and tinnitus ( the tinnitus hasn’t really ever gone away yet, though there have been “moments” when it seems to have, only to come back. Mine is not as severe as some peoples, but is DEFINITELY annoying at times and something I have never had before). MEDS, SUPPLEMENTS, SLEEP, EXERCISE, CAFFEINE, ALCOHOL, ETC.: Some things I have been on since before the Zoloft. Thyroid (23 years) EPA only about 500-1000mg day (started just before Zoloft) Mild multi-vitamin (Dr. Furhman’s women’s with 1000mg D3 – sometimes take an extra 1000mg D3). Started before the Zoloft I believe. Mg citrate (just before zoloft - anywhere from 200-300mg, depending on what I feel like a day) Quercetin (500-100mg day for years for another medical condition I’ve had for 20 years) Hydrolysed Collagen for my skin (just before Zoloft). Does help my skin (doesn’t seem to matter one way or the other with WD, but can make me sleepy at night). Biotin (1000mg) for my hair (lost a lot after mom passed, but it is coming back) Play around with NAC 500 mg a day for a few days a week (not sure it helps, doesn’t seem to hurt). Vit C every now and again (500 mg), but not always very regular about it. Play around with caffeine (had some of my best days on it and so it doesn’t seem to directly affect WD. But I do limit my caffeine accordingly at times. But I do limit my caffeine accordingly at times. I think I’m finding WD does whatever it wants to, whenever it wants to, and, in my case, seems to be mostly independent of anything I specifically do, eat, drink, etc at any given moment. I have experimented many times. As many on this forum have said, TIME AND PATIENCE ARE THE KEY FACTORS. I am currently 8 months out and may have months to go... Alcohol is a crap shoot and I rarely drink anyway (once or twice a month or not at all). Sometimes it has been helpful and sometimes, maybe not. But I mostly avoid it right now. Try to keep to a strict sleep schedule because though I do sleep finally some now (didn’t while on Zoloft or before due to the losses I had and anxiety) I rarely sleep all the way through the night But a broken 5-6 hours of sleep or so, is way better than 4 or less or none! I also have found that the collagen at night (it has a lot of glycine in it) along with some magnesium helps me. But too much magnesium at night can seem to do an odd paradoxical thing and agitate me, so I have to be careful. I have exercise class about 3 times a week (when I can). And I walk or hike when I can or the weather allows. Exercise has helped a lot. Though, when the chips are down, the chips are down, even with exercise. But I refuse to not exercise and should probably do more. But sometimes laziness/tiredness, lack of time, or withdrawal symptoms win. THOUGHTS ABOUT THIS FORUM and just stuff in general: Thank goodness it exsists, ha! Thank you all for being here and for those who started it! My doctor didn’t think this withdrawal was a “thing”. I had to send her an article from Harvard Med Page showing that it is (but even the Harvard article doesn’t think it lasts this long). Have had 2 people, another doctor of mine (later into withdrawal) and one a psychologist confirm withdrawal or discontinuation syndrome is a “thing” and that it will take longer than I like or think it will. So, yay, I’m not crazy ;). My Withdrawal (WD) is far less that many people on here, but enough to definitely get my attention and still disturbing, despite that I am mostly functional, because I feel very “off” kilter. I refuse to believe it will not get better, but am a bit blown away that after only 2.5 months at 25mg or less of Zoloft (the generic), I would still be dealing with any of this, but of course, this forum proves this is definitely not unusual for some. Am getting on this site to just confirm that getting worse before better, etc, is “normal”, even for such a short period of time on the drug (yay, not the way I want to be “normal”, snort, but one must keep a sense of humor ). I will probably not “live” on this site because I am trying to just get on with it and give it time as much as I can and because I, so far, knock on wood, am not as severe as some people. But I am grateful for this site, as I have been on it many times for my sanity (but equally I try not to go down the rabbit hole too much with it either), and am in awe of those who have walked through hella worse. Despite a strong family history of anxiety and depression on my mom’s side, which I have subtly dealt with all my life (with some severe depression from situational events), I will do everything I possibly can to be happy and healthy without drugs. I know I was desperate for relief and sleep before this zoloft Sh*tstorm , but the bright side is I will have learned some valuable cognitive skills and behavior (I do have a counselor and have for a long while, but this is definitely making me up my game on my thought processes ;). And I will not take another SSRI again. I was going to go to Italy for my 50th this summer and hike in the Dolomites, but have decided to wait until WD is done. Stupid WD. Whenever I’m in a Wave I think I’m going to do a TED talk on all this Withdrawal stuff to help educate and save the world! And then I have a good day and think, heck No, I don’t want to spend any more time on this malarkey at ALL when it is all GONE for good! (so, I can see why there may not be more success stories actually online – people just want to get on with living). Again, I’m not nearly as bad off as some, but I also know I’m not supposed to feel all these side-effect-like symptoms. I know what “normal” feels like and WD most definitely is NOT IT! WOW. SORRY THAT WAS SOOOO LONG! And not very well written (I'm sure there all kinds of typos etc). But I just want to get this out into the ether, before I keep putting it off and then have a wave and wish I had done that, ha! Many thanks for this site. I may have questions in time, but for now, I’m just trying to get my basics on here in the event anyone or the moderators have any helpful words and affirmations and so that I can ask questions if I need to do so later. Also, I may have totally forgotten some things which I may add later on. IN ADVANCE, please do not feel I am being rude or slighting anyone if I do not respond should anyone post to me. I may just be getting on with things as best I can and not checking this site too often. But I still appreciate everyone on here and what everyone is going through. My best wishes to all! KimLou DRUG SIGNATUE (FROM ABOVE)... SORRY, I'M NOT SURE HOW I "ADD" THIS ON... SSRI HISTORY: I am currently 49 years old (2017) 1992-1998 (+/ - a year: in my early 20’s) - 20 mg Prozac (no major side effects, SE’s, and quit CT with no problems) 2001-2002 (+/- brief period of time after divorce: in my early 30’s) - 10 mg Prozac (again no major SE’s and quit CT no problems) I just didn’t like how Prozac kind of flat lined me and I didn’t like the idea of staying on anything when I really didn’t feel like I needed anything. THEN… RECENT LIFE EVENTS… 2017 April 27 - Start 25 mg Zoloft (generic sertraline) very reluctantly (after the passing of my mom in October 2017 and a VERY PAINFUL bad relationship break-up only a few months later. My doctor thought Zoloft would help break my cycle of poor sleep and anxiety and sadness – though I really just wanted to try a sleeping pill of some kind. Though in hindsight, benzos can be difficult too and I am apparently pretty sensitive to many drugs. Weeks prior to Zoloft, she gave me some trazadone, which I realize is not a benzo and, holy crap, hell no, never again. One pill and I WAS NOT MYSELF. Quit immediately and returned to normal, other than my original circumstantial sadness, anxiety and insomnia.) 2017 May 15 - Start cutting the Zoloft down to about 15-20 mg of Zoloft (because OMG it is wiring/amping –akathisia?- the crap out of me and not helping me sleep and I’m having fuzzy eyes and head off and on. I could have cleaned a house with a toothbrush. It got me motivated, but I was still edgy and couldn’t sleep on that crack feeling.) 2017 May 26 - Start 12.5 mg of Zoloft (because still SE’s of bleary eyes, extreme jaw clenching at night, mild fuzzy head with pressure – brain fog, still some anxiety and sadness) 2017 June 30 - Start 6.25 mg (because still a lot of jaw clenching, paresthesia – including prickling and burning, body vibrations – like every cell in my body was wired) 2017 July 10 - Stop Zoloft completely (because I suddenly developed tinnitus in my left ear and I was like “Eff This I’m done!” Yes, I know now that that was probably too fast of a taper, but my doctor and the pharmacist insisted should be fine and quite frankly, I was having such a horrible paradoxical reaction to it while I was on it, I doubt anyone could have made me understand to stay on it longer at the time to wean off more slowly. It is what it is now.
  2. Zoloft withdrawal success - my story When I first decided to wean myself off of Zoloft, I searched the internet for stories about people who had successfully gotten off antidepressants and had trouble finding them so I promised myself that if I made it I would post my story. Tomorrow, will mark my "no Zoloft for one year" anniversary. In that time, I haven't used alcohol or any other mood altering substance either, and I'm doing fine. It hasn't been easy, and it took a while, but I made it and I was able to function, to work and to take care of myself throughout. Diagnosed with social anxiety and depression when I was in my mid 40s, I was put on Zoloft and stayed at 200mg per day for around 5 years. The Zoloft helped me. It took the edge off of my anxiety, and since my depression was the result of my anxiety, it helped with that as well. Another pleasant side effect was that I lost a few pounds. So why would I want to stop taking it? The Nurse Practitioner who prescribed the meds was puzzled. It works, why stop taking it? I can't fully answer that question, but I think it has something to do with the fact that I've struggled with addiction my entire life. Drugs, alcohol, food... maybe I felt like by taking the Zoloft I was avoiding dealing with one of the major themes of my life. Whatever the reason, I wanted to stop taking it. I'd tried twice using the NP's tapering recommendation, which was to decrease by 50mg every week for a month. I never made it past the first week because I'd have flashes of disorientation and dizziness (which I didn't mind) and then become anxious and depressed (which I did mind). She told me Zoloft didn't cause withdrawal symptoms, it was my natural state of anxiety and depression returning, so I needed to stay on the Zoloft. I knew I was having withdrawal symptoms, but they were so intense I couldn't function, so went back on the Zoloft. Then my mother told me that she had weaned herself off of Premerin by doing a very slow taper over the course of a year, so I decided to try that. My plan was to decrease the Zoloft by 25mg every month over a period of 8 months. The first month was fine. I'd have rough patches, but they were manageable. After 8 months I was off the Zoloft but a few weeks later, I started having withdrawal symptoms including what people refer to as "brain zaps." I called them "head rushes" because it felt like my brain was being flooded by chemicals. Then I became anxious and depressed again, so I decided to go back up to the lowest dosage where I felt good, which was 50mg. Then instead of tapering at 25mg per month, I reduced it to 10mg a month, and that is how I eventually got off the Zoloft. Whenever the withdrawal symptoms became uncomfortable, I'd go back up to a "comfortable" dosage then begin tapering in smaller increments, a "progressive taper," similar to what is recommended in the book "The Anti-Depressant Solution," and on this website. Eventually I had to buy a milligram scale (available on amazon), because the increments became so small. I was amazed how sensitive my body had become to the tiniest adjustments in dosage. The last month I was down to 5mg, and I stopped taking Zoloft completely February 1, 2014. One year ago tomorrow. I was on 200mg of Zoloft for 5 years and it took 2 ½ years to taper off completely. It took a long time, but I wanted to taper safely, physically and emotionally. And I did. During that time I was able to work and to meet all my social commitments. At the suggestion of the NP, I joined a social anxiety group which used Cognitive Behavioral Therapy. She warned that I shouldn't go off the meds without addressing the underlying cause, which made sense to me. However, I also believe that much of my anxiety and depression was situational, even though she maintained it was my natural state. When I first came to her, I was going through an extremely stressful period of my life. I was having problems finding work and didn't know how I was going to pay my rent or survive from month to month. I went on one job interview after another and I think social anxiety and depression were my way of trying to protect myself from more rejection and failure. So how do I feel now, one year later? I'm doing okay. I occasionally get a head rush, but it's very mild. I wouldn't today describe myself as either socially anxious or depressed, but I know that this is how I react to stress, and Cognitive Behavioral Therapy has helped me develop strategies for dealing with those tendencies. 12 step programs, self help books, spiritual practices like yoga and meditation, healing modalities like Reiki, and individual therapy have all been part of my healing process as well. On this journey, life has given me both challenges and assistance in dealing with social anxiety and depression. For example, as I was tapering I started dating someone for the first time in years, and we had a fun relationship which helped heal a lot of issues relating to social anxiety. Then, after two years we broke up, so that offered its challenges, but I didn't sink into depression, which was kind of amazing. At the time, I also had bed bugs which deprived me of sleep and sent my anxiety through the roof, but I survived that too. (The bed bugs did not.) My ex-boyfriend introduced me to hiking, which I loved, so I started going to hiking meet-ups and found a circle of friends who also love to hike which helped heal a different aspect of my social anxiety. Also, becoming more physically active probably helped with the depression... In other words, life went on. There were challenges and there were opportunities and often the challenges were the opportunities. The Zoloft helped me get through a very difficult period of my life, and I'm grateful for that, but I had no idea what I was getting myself into. But here I am, 8 ½ years later, and I haven't used Zoloft or any mood altering drugs, alcohol or coffee (all of which affect my anxiety and depression) for a year. Today, I feel optimistic and hopeful. I know life will have it's challenges but also that I have resources and strategies to assist me, and I am grateful to all who have helped me on this journey; therapists, teachers, friends, strangers, nature, and also to life itself, which Eckhart Tolle calls "the greatest guru of all." Do I have moments of fear and anxiety? Yes! Do I have moments of happiness and joy? Yes! Do I have moments of depression and sadness? Yes! Do I have moments of laughter and silliness? Yes! All of it, yes. What I was dreading is that it would be unending anxiety and depression, and that hasn't been my experience. Life is okay, with its highs and lows and all of it. Like Snoop Dogg says, "it's all good."
  3. HollyHope

    HollyHope

    Hi all, Firstly, I am so grateful to have come across this site and I hope that by sharing my experience I might be able to help others and also gain some help and support in return . So, my story - I have suffered on and off with depression since my late teens, I have now just turned 30. I was first prescribed the antidepressant citalopram when I was 18, I took a low dose of this (can't remember how much exactly). I took this for about 6 months and then stopped as felt a lot more in control of my life and generally happier. I unfortunately relapsed about 5 years later and was prescribed citalopram again which I took for about two years. After a while I felt that it was not having much of an effect on me and my mood so my GP switched me to sertraline which I have been on since, about 4 years roughly at 50mg a day. Sertraline has worked very well me and I have been lucky that I have not suffered too many side effects while being on it. Over the years I have tried many therapies, CBT, counselling, human givens and acupuncture to help combat my depression. In all honesty I am not sure how much of an effect any of these things have had on my well being but I do find that having a safe place to talk things through in a non judgmental environment has been a blessing at times. I am currently trying Human Givens therapy with a lovely lady who I feel very secure to talk things through with. I made the decision about 2 years ago that I wanted to be, or at least try to be, medication free to give my body and mind a chance to cope alone. I first tried to taper off sertraline in March 2014, I did pretty well and got down to taking 25mg just three times a week (however, since then I have read that it is not generally a good idea to alternate the days that you take the medication as the levels of the drug are then not consistent in your body.... or something along those lines). Anyway, after splitting up with my then boyfriend in June, I had a major relapse and went back up to 50mg daily. In the summer of 2015 having been consistently on 50mg since June 2014 I decided that I wanted to give it another go and try and come off the sertraline. I have slowly tapered to 25mg over several months and I have been taking 25mg a day for the last week and a half. I am going to stay on this dose for at least one month to allow my body and mind time to adjust before making the next reduction. It has however not been smooth sailing to get to this point and I am now left feeling very anxious, agitated, unmotivated and generally quite dull (I have no sparkle!). If I had the choice I would probably chose to stay in bed all day and just sleep. Of course in realityt this is not possible as I have a full time job and bills to pay. I used to be a gym addictt and would exercise atleast 3 times a week which I found to be very good at helping to stabilise my mood. However, over the last two months I have no motivation or energy to go to the gym and feel anxious at the thought of going (I have never really suffered with anxiety before!) I know that if I start going it will probbaly help me on the road to recovery but I just feel so unmotivated. Also, over the last two months I have completly lost my libido and feel so sorry for my boyfriend who probably feels very rejected... I just have no desire at the moment and feel out of touch from my friends, family and boyfriend who have all had to put up with me being negative and agitated recently. Finally since making the reduction to 25mg I am suffering my bouts of diarrhoea almost every day . I can only assume that this is part of the withdrawal process as I did not feel like this before I began to taper. My only hope is that it will pass eventually. My symptoms are manageable currently but I know that I am not living life to the full which makes me feel pretty rubbish. I am also worried that as I further decrease the amount of sertraline I take, these things that I am feeling now will become more intense and I may not be able to cope. It is hard to discuss with my GP as she will say that I am relapsing and advise me to go back up to 50mg, I know that this is not a relapse. I have seen some people mention that it is easier to taper using liquid serttaline? I feel this may be helpful as I am unsure when the time comes how I will make the next reduction as I already half the 50mg tablet to give me 25mg and I think it would be impossible to half that tablet again without it crumbling to pieces. Does anyone know if liquid sertraline is a thing? and if so is it availabel in the UK? I would love to hear from anyone who is currently tapering or maybe you have successful got off sertraline? Is it possible? Will I ever feel okay again? This is me and this where I am currently at. Thank you so much for you time. R
  4. Im New to this forum. For many years I took 100-150mg sertaline and the only side effect was weight gain. My depression was moderated but not completely gone. Got a New doctor who recommended Pristiq. I've been taking 50mg for about 6 months. It was going fine. Suddenly I'm noticing frequent headaches, trouble remembering and nausea. Also increased anxiety. I'm not functioning and can barely get to the grocery store. I live alone and am scared. I've read about the symptoms of withdrawal and I seem to have all of them, except I have not changed my dose or time of day (night) that I take it. Has anyone else had this happen? I can't get in touch with my doc until 4 days from now.
  5. Anyone taking It? How do you feel about it because I have zero clue if it's a good thing or a bad thing for me after being on it for one year now...
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