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  1. Hello, I am new here. I really appreciate everyone posting their stories, struggles or successes. It helps me understands what I have been through WAY better. I was on paroxetine(20 mg) for 11 years for social anxiety. I was told by my psychiatrist that it would be "a vitamin I take for the rest of my life". Little did I know it would rob me off all my emotions in life. Over the last 11 years I have had a decent amount of "we dont know why this happens" health conditions. I now look back and blame alot of it on this drug. Since coming off of this drug my health conditions have improved, but some of the withdrawal symptoms kick my butt here and there. Reading the success stories, I know these will get better with time. So I am keeping my nutrition dialed in and my attitude positive. Thanks!
  2. Hi, I just wanted to share my experience of this drug and what I am going through. I was put on seroxat at 18 due to messing with recreational drugs. I was fine on 20mg for the next 17 years living life to the max!!! However, due to the birth of my son i wanted to be drug free, and had not had any symptoms for 12 years! I went to the doctor and she said to come off it over a few weeks and I'd be fine. This was not the case, after 7 weeks post taper and about 3 weeks off totally I had a total nervous breakdown. Dr put me back on 20mg, this was 4 months ago. Since then my nervous system is in complete meltdown, im suffering RLS, hand tremmors, depression, anxiety. The Doc suggests trying higher dose of Paroxetine and / or Mirtazipine. Has anyone experienced this, what did you do? Word of advice do your own research and read Shipko, and Healys work on SSRI discontnuation syndrome before you decide to come off it, especially if you have been on it for many years! Don't make my mistake and just trust your Dr!
  3. Hi, I was initially put on 37.5 mg paroxetine during a postpartum depressive episode in June 2016. My pdoc suspected the dose to be too high and reduced to 25 mg. I held on 25 mg for almost a year, and then my pdoc and I decided to try a dose reduction to 12.5 mg. I had a few brain zaps, but nothing serious, so I held there for a few months. My pdoc and I decided to drop to 0 mg in October 2017 (by taking 12.5 mg alternate days then zero). Again, only brain zaps were experienced. Four months later, at the beginning of March 2018, severe protracted withdrawal kicked in. I had not discovered this forum, so I immediately jumped to 12.5 mg at the recommendation of a doctor friend, and several days later jumped to 25 mg at the recommendation of my pdoc. When I experienced what I now know is a wave, I thought the paroxetine dose was not high enough, and my pdoc increased it to 37.5 mg. I have been on this dose for May and June, but now I have developed really loud tinnitus, and I suspect that the 37.5 mg dose might be too high. My pdoc supports my reducing to 25 mg. However, I don't want to destabilise my system. I have tried to work out the pharmacokinetics of the controlled release tablets, to see how to 'spread' my reduced dose over 24 hours, but have not found much on the internet. My intuition would be to take my 25 mg controlled release in the morning, along with 5 mg immediate release, so that I would have a peak and then a gradual dose over 24 hours. This would reduce my dose from 37.5 mg over 24 hours to 30 mg over 24 hours. Since I strongly believe that my system is flooded with serotonin, I think that this step won't destabilise me as there is an accumulated 'stash' of serotonin floating around my system. Any advice from the seasoned taperers out there? Thanks for hearing my story, Bee5
  4. Hi all - so so I tried to withdraw from 2.5 paxil while increasing my zoloft from 25 to 50. What a disaster! The 50 zoloft made me manic so I went back down to 25 but went off the 2.5 paxil in two weeks. Pure chaos ensued with crazy agitation and insomnia and practically convulsions! then I went down to 12.5 zoloft and after 5 days the crying began. Reinstated to 25 and feeling the reinstatement effects. Just wanted to connect with others!
  5. Moderator note: link to benzo forum thread - Miko789: Xanax withdrawal/tapering Hi, I'm new to the forum, I have some questions I want to ask. My doctor prescribed effexor for depression, in 2009. Now I'm free of symptoms and I managed to come off with withdrawal symptoms though. That's with the antidepressant. Now I'm on Risperdal consta from November 2013 and seroxat 10mg. My doctor prescribed with risperdal consta 3,3mg/day long acting injection every two weeks. From February 2015 he lowered the dosage to 25mg/every 2 weeks equals 1,66mg/day. I tried to lower the seroxat 10mg but after 40-45h I have withdrawal symptoms vertigo, dizziness. Is it possible to cut down seroxat? How about the Risperdal consta (long acting injection). Has anyone tapered off completely without withdrawals? I read about the 10% harm reduction procedure to taper off and I'm going to tell my doctor and follow. thanks in advance
  6. Amanda167

    Amanda167

    Hi. I've been on Paxil for 22 years with a few unsuccessful WDs in the past. I finally learnt that I was going way to fast so began during the 10% method from 15mg, everything was going well until I got to 7mg. I noticed that my last few prescriptions, I was constantly given a different generic and im sure my severe reaction was not only WD, but from being given yet another generic that I'd never has in the past ( paroxetine made by Milamed) as it coincides with the start of my severe WDs that started at the beginning of Feb 2019, I tried desperately to ride the storm but it got so severe with an endless list of symptoms that left me bedridden and had to give up work. 3 months of insomnia, anxiety, intrusive thoughts, panic, severe chest discomfort, etc left me wanting to end my life and I was taken to ER 3 times, they wanted to admit me to the psyche ward and I refused so each time, I went back home. From the 14th of May, 3 new meds were added.... Zoplicone.. to which I was grateful because i hadnt slept in months so have been taking half 375mg since. Quietiapine 25mg... to which I took for 5 days, then got scared and started tapering down and now on 8mg. Valium... I've been taking anything from 0.50mg daily to 4mg daily to try and take off the edge but obviously hasn't done much as mainly only taken 1 to 2mg on average for the past 4 weeks and now trying to taper that as to scared to just stop. On 1.3mg and trying not to keep switching doses. The only reason I kept switching as I never intended them to be permanent so wasn't paying much attention. As you can probably guess, I'm extremely cautious and trying so desperately not to rely on other meds and have a strong hate to big pharma. To add more confusion to what was once only 10 to 15mg of Paxil daily, I now have 3 other meds in the mix. And now it gets complicated... After hitting severe WD on the generic paroxetine from the 8th of Feb 2019, I updosed as follows... 29th April 19.... updosed to 8.5mg 07th May 19.... updosed to 9.5mg 14th May 19.... updosed to 10.4mg 29th May 19.... switched from generic brand to GSK Seroxat Paxil and stayed at 10.4mg and holding. The reason for my switch was because I had to decide on one brand and stick to it after finding out that generics can vary and I was so mad that my pharmacist kept giving me different generics. I strongly believe that the last one was bad and aided massively to my severe WD. Well, since switching to the GSK Seroxat Paxil, a new kind of hell broke lose, it felt so much stronger my head felt it was going to explode. It has been absolutely horrendous and I'm struggling to hold on and to make things more complicated, I don't know if the added meds are making things even worse. I'm so desperate to reach some stability and now know that messing with the other doses have probably not helped at all but was so desperate not to rely on other poisons. I don't know what to do to make things better, it's been a month since updosing but only 2 weeks on the GSK paxil and it's not working. Please can someone advise me??? Help me??? I feel like I've had an adverse reaction and being given more meds on a sensitized nervous system only complicated matters further... so desperate to know a way out. I would of given up if I didn't have an amazing 14 year old Son. I'm so sorry for the complication of my story and would truly appreciate if someone can offer some advise. I so wish I'd just held but I was so so desperate. Thank you so much for reading, I appreciate that others are going through hell too and it's such a lonely frustrating painful journey x
  7. Hi, in march I decided to go to a shrink after dealing with depression/anhedonia for a couple months. I was put on paroxetine 30mg and olanzapine 2.5mg. During my last visit with my previous doctor I told her I still had anhedonia, to which she replied: "let's increase the olanzapine to 5mg, you'll sleep better". I told her: "I dont think blocking my dopamine receptor further will resolve my anhedonia". Anyways, I decided to find another doctor who told me I could just cold turkey the current 2.5mg because I don't need it. I also started venlafaxine 75mg to see if it alleviates my anhedonia. Any advice regarding the olanzapine? Thanks in advance for the replies, and sorry if my post is not very organized, I am not very good at writing.
  8. I've been taking 20mg of paroxetine for more years than I can remember...I would like to taper off and would like to make a list of supplements that will help with serotonin production. The only supplement on my list are B complex vitamins. Has anyone tried 'Genius Joy - Serotonin Mood Booster'? I plan on reducing 10% every month or 6 weeks depending on how I feel. Exercising and eating well. Does anyone have any other suggestions? The main reason I want to go off of the drug is the relationship of pharmaceuticals to dementia. Any thoughts on that topic? Thank you for any information. I feel like I'm about to climb a mountain.
  9. Hello! Finding myself in a temporary reprieve from debilitating apathy, I thought I would introduce myself here as I've been lurking for a while. Like many of you, I'm currently battling a severe withdrawal reaction from paroxetine. During the fall of 2014, I decided to chart a course to discontinue medication I was on (Paxil 60-100mgs for a decade for OCD, Buprenorphine of opiate dependency and mild chronic pain). Unfortunately, as seems to be common, my psychiatrist was entirely unaware of discontinuation symptoms and had me taper from 60mg to zero in the course of a few months. Strangely, I felt zero withdrawal effects during the taper and for approx four weeks afterwards. A few days after the last dose of paxil, I took some time off from work to recover from the foreseen mild opiate withdrawal and stopped taking the buprenorphine. For two weeks I went though a normal opiate withdrawal (cold sweats, chills, aches, etc). However, a few weeks later, my entire world was turned on its head by a new set of symptoms. Severe anxiety, panic attacks, loss of balance and coordination, crying spells, suicidal ideation, debilitating muscle pain, constant overstimulation, derealization, mild paranoia, memory loss, confusion attempting the simplest of tasks, poor word recall and communication ability and a host of other cognitive problems. Along with that horror came a wonder I hadn't experienced before -- akin to being instantaneously launched out of a lobotomy and the removal of years of emotional anesthesia. Everything and everyone in my life had meaning and emotional attachment. I was able to connect with friends and loved ones (and strangers) on a level I didn't heretofore remember experiencing. Music... oh how splendid it sounded. Sunsets and walks in the woods were mesmerizing. Exercise and sex felt fantastic. Empathy and concern for the plight of others was overwhelming. A lifetime of painful memories and grief bubbled uncontrollably to the surface. Due to the timing and the lack of capable professional help, I assumed this was a severe case of post-acute withdrawal from the buprenorphine and had no basis to connect it to paxil. Months into this lovely process, I decided to restart a low dose of paxil for the hell of it. Within 36 hours, the worst of the withdrawal symptoms vanished as if by magic and I suddenly knew something was very wrong. Although the SSRI withdrawal was greatly attenuated, restarting the paxil brought a total loss of affect, inability to experience emotions, severe apathy and anhedonia. These symptoms had been experienced somewhat during the decade of treatment, but at a much less significant level. Having a short college background in neuroscience, I spent weeks reading the latest research on SSRI withdrawal (turns out there is very little) and modulation of dopamine (crap shoot) and with the help of a confused, but helpful psychiatrist, attempted to abate the new symptoms. I tried: Other SSRIs (same lobotomy effect as paxil) Serotonin modulators like Viibryd (zombie state again) SNRIs (massive anxiety, didn't help withdrawal) Wellbutrin augmentation (no change) MAOIs (didn't prevent withdrawal) Low dose antipsychotics (no change, or exacerbated withdrawal) Selective Ht2c serotonin blockers (exacerbated withdrawal) In the end, I realized that, at least for me, I was on a wild goose chase and I might as well dig in the for the long haul and re-instate paxil (without any augmentation) in order to taper slowly. I restarted at 20mg and have been tapering since the beginning of the year. I'm down to 12mg now, and find myself stuck in a partial withdrawal / mostly lobotomized state. I'm very unmotivated and can't seem to squeeze any enjoyment out of life, friends, exercise, music, hobbies, etc despite my best efforts. I've become quite anti-social, and my days have been reduced to working, sleeping, eating and laying on the couch. At the beginning, despite knowing it was a dangerous idea, I would take 3-4 day breaks just to feel human again. I considered crashing off of it again and moving to a warm foreign country to spend a year or more recovering, but unfortunately I don't have the money to not be working right now. Thankfully, even on a steadily declining dose, I have started to have these short windows of time when I seem to awaken out of the haze, and suddenly feel the sun and the breeze, with music and socializing feeling great. It'll last for a few hours before it fades back into the abyss. Exercise, when I can force myself to do it, seems to increase the frequency and duration of these. I don't have advice for anyone, other than to keep pushing through... Even when it's rough and awful. Between the stories I have read here, and knowing that the brain is capable of amazing things, I'm quite confident I will recover. It may take another year to remove this poison from my brain in a responsible and safe way, but I will be so grateful when the time comes to feel alive again. I wish everyone luck with their own journey through this torture...
  10. Hi! I'm so glad to be here😊 I've been reading a lot of valuable info here and look forward to your insight and help! I'm a 30yo female, Med history as described in signature. Progressively more symptoms as I taper, mainly panic attacks and anxiety attacks that I haven't had in years, GI problems and heat / stagnant air / high humidity severe intolerance, morning cortisol spikes mild insomnia, more painful pms and BIG sensitivity to any stressor. Most of it wasn't even present when I was on 8.1mg ... For that reason I thought it would be good to hold for a while starting from 29/09/19 and so I did. So far cortisol morning spike is what has almost resolved. Others have improved. Still, about very other day I'll have a few hours of great discomfort from GI mainly I have a severe issue accompanied with panic attacks. It immediately triggers intense nausea for me that if not immediately taken care of progresses to vomiting. This unfortunately happens for any big stressor or even excitement now. This is the only lingering problem from my CT attempt in 2013 which I never had before that! To my unfortunate luck, I've had to deal recently with a big stressor, mimicking just the same environment and symptoms of the CT attempt and back then the solution I chose was to leave the situation and return home which gave me comfort. I could easily stabilize and continue with my taper if this stressor wasn't present, but I'm afraid I can't deal with both, aggravating each other and I'm so afraid itll become an uncontrollable spiral. So at this point I would like to ask for the best solution to an immediate relief. Yes, in the best scenario it would be just to leave the house that's causing the stress, but moving away will trigger panic attacks until I settle down and I'm so dreadful of that. Funny that this time it's the opposite solution for the CT attempt I had. Leaving instead of returning to my house. My options: Right now I can control the nausea with phenergan 12.5mg but the agony in waiting for it to work (1-2 hours) is big. I'll need this for perhaps a couple of months until things will settle down in my current house situation together with my stress sensivity. Powerful drug so not a very nice solution IMO. Other option I'm thinking about is to updose by 2.5%, just to make me less sensitive to stress I guess? I saw that this is what @Altostrata has suggested 2 days ago to my friend @embd with the option to divide the dose due to fast metabolism in the lower doses. So how do I go about that divide? I just dont know what my best shot is here so i would appreciate a moderator's advice. I have some interesting general questions prepared from a while before the stressor even begun, I'll save those for later as they're not urgent. Thanks For reading thus far 😚. Looking forward for your replies.
  11. Hi Everyone - I was put on Paxil 16 years ago, when I was 19, for generalized anxiety. I tried to get off it once, when they tapered me off 20 mg over two weeks after I had been taking the drug for a year. This was, clearly, a disaster, and I never tried again. Now I am deeply, deeply regretting not starting the taper earlier. I had NO idea how long it would take. I was thinking *maybe* a year. It seems like this will not be the case for me. I started at 15 mg in February 2018, and I'm now down to 8.8 mg, or rather 4.4 mL, as I've switched to liquid. I started by tapering 1 mg a month, which went fine for the first month. However, the next month I started experiencing panic attacks - even though I had never experienced a panic attack before. So I did some research and switched to tapering at 0.5 mg every two weeks. Once I went to liquid, because of the measuring syringe I had, I switched to tapering 0.2 mL (0.4 mg equivalent) every two weeks. This went fine until I got to 4.2 mL. I was rendered non-functional - so dizzy, couldn't remember ANYTHING for more than a few seconds, forgetting words, etc. It was horrible, and I couldn't do my job. So I went back up to 4.4 mL, where I have been for the past two weeks. I need to figure out what to do next. On a side note, but a super important one, I'm freaking out about how long this is going to take because I was thinking maybe I wanted kids, and I can't have kids on Paxil. I'm not sure what to do about that. I'm 35, and I don't have five years to try to get off Paxil and then have children. Maybe I can cross taper to Zoloft? I have no idea. So I'm lost. And looking for support. Already super excited about the information I've found here. My psychiatrist is not super helpful, and I've developed the schedule myself. She originally suggested a much faster one. Sigh. Thanks for reading!
  12. Hello everyone, I am a first time poster, long time Paxil user. I have been on Paxil for about 12 years or so, prescribed by my doctor to combat anxiety. My anxiety was never severe, I just fell down the slippery slope of Paxil use after what should have just been a bump in the emotional road for me. Long story short, I've decided to taper off of the Paxil 20mg (down from 40mg a couple years prior). This year my doc advised me to cut from 20mg to 10mg. (I know now, way too much and too fast). I had brain zaps, irritablilty, and vivid dreams (which I actually don't mind since they are usually pleasant) and some dizziness. After a few weeks I was feeling OK enough to go from 10mg to 5mg. I was good for about 3 weeks. But the next two weeks I suffered from severe anxiety - unlike any kind of despairing feeling I've ever had in my life! I suddenly became an emotional wreck and was just at wits end. So I went from 5mg Paxil back up to 10mg. A week or so later - hives. Hives, - small ones, on my neck or forearms. They'd go away after a couple hours so I didn't put too much worry into it. Then a week after these small hive appearances, I had a really bad outbreak of hives on my legs, which I thought was just a heat rash. I didn't take an anti-histamine, I hate the way they make me feel. Big mistake. I ended up waking up at 4 in the morning, itching terribly all over my body. I was searching for Benadryl downstairs when my wife found me - at which point I was getting dizzy and nauseous. I was going into anaphylactic shock. My wife and I both thought I was dying, my children sobbing as they waited by the front door for the ambulance to arrive. I've never had allergies really. I am allergic to cats, it turns out, but I've had my cat for 3 years (a Persian which I found to not feel allergic reactions to in the past- and who has since been living with my brother till this all gets ironed out). So this anaphylaxis was not something I was prepared for. An amulance ride later, they told me I had some kind of allergic reaction. A few weeks later, after seeing an allergist, he suspected my bizarre reaction to be caused by a medicine (not a food or other allergen). I only take Paxil, and Propecia. (which I've stopped last week to try to rule that out as a cause of the hives). I still get small areas of redness on my skin, primarily when I wake up in the AM. And for now I'm on antihistimines, which I dislike greatly. I am wondering if the traumatic, despair-like anxiety feelings I suffered, and then yo-yo-ing back to a higher dosage of Paxil did a number on my body and made me overly sensitive to histamines, or my cat. Since my allergist suspected Paxil as a possible cause of the hives/anaphylaxis, I have since tapered back down to 5mg, and three days ago down to 2.5mg. I suspect its not the actual Paxil causing the hives, but the withdrawal itself, the toll it takes on my body and mind. Just hoping putting my story out there, if anyone can relate to such a physical reaction like what I experienced, and if they too, think it is related to the Paxil withdrawl. Thanks for reading. Cheers
  13. Admin note: link to benzo forum thread - Panicpax: Back on clonazepam Dear all i am happy im not alone, i have read many posts and see that at least in this world i am....not alone. 3rd attempt to taper 20mg paxil.... almost 2 years now and stuck at 3.6 using liquid paxil. my way was 0.2mg every week till now is great but as i reached 3.4 for a few days anxiety creeped , insomnia and waking up sweating and panic . my problem is even updosing 0.2mg which i did makes me feel a different worse.( agitation weird thoughts half the day. immediately updoased 3.5 and was back to normal only 2 days but still not enough so went to previous ( 10 days back 3.6 mg and hoping to stabalize here somewhere. then hold 2 weeks if im ok and then resume slower starting from this dose as i know SERT occupancy is telling my brain whops here is another drop ( had 1 same enstance at 9.2mg ) aggressive running, getting a cold or any fever makes me need to wait and gives WD symptoms. i have no physical WD just panic anxiety and insominia mild depression... usually only feeling down on day3 of a drop and first 2 days sleep is crappy. im interested in the cortisol thing i truley believe its the cause that WD symptoms i have ( awaking in panic and sweating and anxiety waves and windows) this past week trying to stabilise..... so...... vit C 1g and baby ASpirin at bedtime as the pubmed mentioned . an endocrinologist told me L-carnitine too. will start aspirin first and see it lowers in after a week of use ( 1.5mg per kilo so maybe 2 aspirins in 1 week if it didnt work. i get scared when i read some people have extreme trouble after 1mg .... if my experiment works ill still go slower and listen to my body but it feels like im crossing 2 building roofs on a thread holding a pole in my hands to balance.. cant go up or down right now without feeling it big time. any suggestions???
  14. (mod note)link to teePeer1's benzo forum thread: https://www.survivingantidepressants.org/topic/19092-how-to-taper-the-used-as-needed-benzo-or-sparing-benzo-use/ Dear all, I gradually tapered to 10 mg of paxil from 40 and also tapered off benzo (3mg to 0) both slowly over a period of months. Long story short, I thought I was near the fonish line. However, when I taperedd to 10 mg from 15 mg paxil and stopped a doze of less than .25 benzos things got rough after two weeks. My issues are mostly related to night:severe anxiety, hyper alertness, pounding heart. It was so bad a couple of nights that I resorted to taking a small dose of lexatonil. Now I am afraid of what strategy to follow next. My experience with psychiatrists have been pretty bad during my taper and I am afraid if I go back they will put me on more meds. Should I go back to 15 mg paxil from 10 and is it safe to use half a tablet of benzo at night to brave through the night? (Though i am afraid of benzo withdrawals too) I would appreciate any suggestions on how to stabilize my situation at this stage and dosage?
  15. I'm another refugee from PP....I was so shocked when I logged in and found it gone! Very upsetting. I found a few people whose names I recognized from PP so that was nice. I'm currently in month 14 of my cold turkey WD.....I was too far out when I found out I should have tapered....PP was a wealth of information and support for me and reading the uplifting posts that "This too shall pass" was so encouraging in the thick of things. I am here if anyone needs an ear, wants to ask what my experience has been like, etc. My name is Gina and I am from Canada
  16. Gidday everyone. I am an ex-Paxilprogresser and when it closed I was very sick of the long horrible process, so I didn't join everyone here back then, but I finally paddled over to the U.S. from Australia. I have to keep reminding myself that the turtle got onto the ark by just keeping going, one step at a time! I started to have some decent days because I found a herbal remedy that has brought my headaches and migraines from 20 a month to 2 over a 12 month period. This means I can actually DO SOMETHING and is a wonderful relief. On those good head days, I always wonder how my old friends are going, so I intend to look you all up! I have decided to put up my history, a bit at a time, or it would be too laborious to read, so that's where I will start.
  17. Hi everyone, So glad to have found this forum in my journey weaning off Paxil. Because of severe withdrawal symptoms during my doctor's recommended tapering schedule, I'm weaning off Paxil painstakingly slowly (liquid prescription, with a syringe). I have a question about tapering at smaller doses. I accidentally missed a dose (just 1.2 mg.) on January 17. Anyone who has taken Paxil knows that you do. not. skip. a dose. I don't know how it happened, but I forgot to take it one night (for the first time in about ten years). For the next TWO WEEKS, I was nauseous, had trouble eating, had mood swings, and worst of all, had some very scary depersonalization (feeling like I was in a dream or on LSD). Very scary. So, this can really happen from just missing a tiny 1.2 mg. dose? I called my doctor and they said this "isn't because of Paxil." Lol. Thanks so much! (This is why I'm so grateful for this forum--people actually dealing with the reality of tapering off these medicines.) Wouldn't tapering get easier as I get down to lower doses? ? What am I going to do at lower doses? The 10% method sounds good in theory, but yikes -- it will take forever just to get off 1.2 mg. My eventual goal is to get off Paxil and Zoloft, but my primary goal is to stay alive. I appreciate your thoughts and opinions! Thanks! I ran out of room in my signature for my quite-lengthy history, so I am expanding it here since this is my intro post: On Paxil since 1996--anxiety and depression. It worked for a while, but had to keep increasing it. 20 mg --> 40 mg --> 60 mg. For years I've wanted to get off it -- it wasn't working anymore, but very difficult to come off. Early 2013--Getting treated for sleep apnea (with CPAP) eliminated about 75% of my anxiety. Who knew?!?!? How long had I had sleep apnea, but treated anxiety with meds? March 2013: Feeling so good with CPAP treatment that I started weaning off Paxil about 10 mg/month: 60mg to 50 mg to 40 mg (NO negative effects whatsoever--if anything, I just felt better and better.) July 2013-- went from 40 mg to 30 mg. Some dizziness; nothing major. Starting a new job; paused taper. June 2014, began Paxil taper again, going from 30 to 20 in one week. (I can't believe that a medical professional actually advised me to do this.) This was very, very bad (dizziness and suicidality--the first time in my life--very scary), so went back to 25mg. Stayed at 25 mg. for another year. Not looking forward to going back down and continuing taper! In June 2015 started a cross-taper while adding Zoloft--went from 25 mg. Paxil to 20, to 10, to [this was the most difficult one] 5.) The cut from 10 to 5 mg gave me akathisia; nausea; suicidal thoughts; rage; and severe anxiety. Most of my time was consumed in dealing with Paxil tapering effects. August 2015 -- obtained a prescription for liquid Paxil. September: 4 mg Paxil October 2015: Suicidality -- doctor advised me to go up on Zoloft; I did so to save my life. Now at 100 mg Zoloft. (But it's not working -- my exercise, eating, meditation, acupuncture, and supplements are.) October to December 2015: 4 mg Paxil --> 3 mg --> 2 mg --> 1.6 mg. Symptoms are tolerable at this rate; the worst is a feeling of being intoxicated for several hours a day. But going this slow makes me feel like it will take forever to get off! ! ! Currently: 1.2 mg Paxil. Also: Vitamin D; Vitamin B complex; magnesium; plenty of protein; exercise; acupuncture; meditation/mindfulness; working with a naturopathic doctor.
  18. Benzo topic: pinkfairy-in-ad-withdrawal-possibly-zopiclone-and-now-benzo Hi everybody am new around here....right here goes!i need some advice an help.am a single mum to a nine year old with no family or support.in janurary I was taken off Paxil which I was taking at 40mg...I had no clue about tapering,they took me off in 4 weeks I was on it for 3 an half years.they then gave me diazepam to stop the with drawals...so now am also in the process of weaning off this at 10% a month.have now educated myself on this one!!am in a right state an I feel like am in a deep dark hole!have got real bad depression but they can't get another AD into me,probably because my CNS is in a mess....am I too late to reinstate Paxil?or would you guys keep on going.any help would be amazing!!am really struggling xx
  19. 2010- Two years of severe headaches. Bad vision in one eye. Muscle pains. The doctors did not say anything. 2012- anxiety appeared. the first drug sertaline - a paradoxical reaction. I got depression, ss thoughts and other bad symptoms. 2012- 2016 paroxetine - - I tappered slowly, but I did not know yet that it should be stopped more slowly. 3 months without paroxetine and withdrawal syndrome appeared. Return to the drug worsened the matter. I crashed. Bridge with fluoxetine. A year passed. at the end of September 2016 I was diagnosed with Lyme disease. I did test in two different laboratories. 08/08/2016-now fluoxetin 20 mg 01/05/2016- now- triticco / trazadone 75 mg clonozepam - 04.03.2017. from 20.11.2017 I started tapper from 0.5 to 0.125 mg- when I got some relief from Lyme treatment. Now I am treated with ILADS ( Lyme and bartonella) and also tapper psycho drags. I want to not rule out the syndrome and stop the drugs safely. I am asking for support and exchange of experience, especially people who suffer from Lyme disease. I need to make plan. How to discontinue: clonazepam 0,125 mg, fluoxetine 20 mg and trazadon 75 mg How I feel now: Antibiotics have sustained discomfort from the urinary tract and improved the results of cytology. I have more windows, but I still experience strong hits of depression and pain in small joints, a specially neck. Through complicated diagnostics of Lyme disease and the syndrome, I do not know which symptoms are from what. Thank you for your attention, sorry for mistakes.
  20. I have been on Paxil for 20 years. I was originally put on it for reactive depression from getting fibromyalgia . I don't need it now. I am not depressed anymore. My problem is that there is no liquid Seroxat /Paxil available here. I first tried bridging to Prozac. I found that moving from Seroxat to Prozac was too hard. I then tried dissolving it in water but my Seroxat tablets do not suspend or dissolve in water. They sink to the bottom of the glass. Does anyone know a reputable online pharmacy that sells liquid paxil and ships to Israel? There was a suggestion of using "Ora Plus" suspension liquid on this forum to dissolve insoluble tablets. I can easily buy Ora Plus from ebay with international shipping. What puts me off is that all the reviews of that on Amazon involve people using it to suspend tablets they give to their dogs and cats! It also contains some nasty sounding chemicals. The shipping cost is crazy too. But that doesn't worry me as much as the other two reasons. I take the gsk - glaxo smith kline version of Seroxat. I take 3/4 of a tablet - 15mg. It's the same tablet distributed to the whole of the European Union. Has anyone here successfully tapered off that without the liquid Seroxat? If so how did you do it? Anyone know an online pharmacy that sells liquid Paxil that ships to Israel?
  21. Well I have always had some sort of anxiety my whole life. Of course, nowhere NEAR as bad as the anxiety WD has caused me. I missed school a ton growing up cause it just made me anxious to be around a lot of people and I was very shy. Just the thought of having to go to school gave me a nervous stomachache. This led to me actually dropping out for a while in high school. Thankfully I was able to enroll in an alternative high school with very small classes where we could go at our own pace and make our own hours. I was able to graduate and get my diploma in under 2 years. I've also had OCD for as long as I can remember. I was tormented by my intrusive thoughts and thought there was something very wrong with me or I was possessed. When I was around 11 or 12 I was looking in a psychology book for some answers and when I read the description for OCD I had a Eureka moment. "That's me!" I was so happy I started crying. So I guess I diagnosed myself but it was later confirmed by a child psychologist. Around 1998 (when I was 18 years old) is when I started seeing commercials on TV for Paxil. Again, when I heard the description I thought it sounded a lot like me. I had just been broken up with by a guy for being "too shy". I was hating how reserved I was and my "social anxiety." It had been getting even worse as now I was getting very nervous and racing heart when in restaurants or standing in line at the store. So I went to a psychiatrist and told him I wanted this drug, Paxil. After a LONG questionnaire and hearing my symptoms he agreed it might help me. I asked him if I could stop taking it any time I wanted and he said "Yes." LIE. That was the day I made the worst decision of my life and I will always regret taking that first pill. So I started the Paxil at 20mg and had no start up effects that I can remember. A few months later I took a trip by myself on a bus half way across the country. So I gues the Paxil was "working." I also missed a couple of doses and that is when I found out about the horrible WD. Zaps, crazy sensitivity to noises, nausea, etc. It scared the crap out of me. Felt like I was stuck on this poison. The years start to pass and I begin to become numb to everything. I gain 30 pounds, which doesn't sound like much but on someone 5'2" with a small frame it definitely shows. Although I was in a relationship I became more and more disinterested in sex. My favorite hobby was sleeping. I had zero ambition and zero motivation. In 2002, my BF at the time finally convinced me to try to get off this drug. I started taking 2.5mg drops every month or so from 30-40mg (cant remember exactly). As I got lower my interest in sex returned and I felt good. I decided to go on birth control. Two weeks after starting it I crashed completely. I was at about 10mg of Paxil at that time. One morning I woke up to nausea, some vomiting, a horrible burning sensation everywhere in my body, horrible anxiety, and the dreaded akathisia which was by far the worse symptom. I became suicidal and made an emergency appt. with a psychiatrist (not the one who initially prescribed it) who talked to me for 15 minutes and said this was proof I needed to be on the drug for the rest of my life. She proceeded to up my dose back to 30mg. I slowly started to feel better and the experience was enough to scare me away from attempting to taper off for several years. In Dec. 2006 after I get out of that relationship I feel something needs to change in my life. I was very unhappy with who I was. So I once again start to taper from 37.5mg. In 2008 I make it 20mg and decide to take a break. I go out with friends, I drink ALOT. Sleeping, smoking pot, eating, and drinking alcohol are my favorite activities. The break lasts for a whole year. In 2009 I commence my taper, but I notice it's getting a lot harder, which would make sense since besides the crash in 2002 I have never been on a dose lower than 20mg. I have to reduce my drops to less than 5%. At around 15mg in Aug. 2009 I get a part time job I love but I'm so scared of having WD at work that I take even smaller drops. In a year at that job I drop about 3mg. In 2010 I start to have stomach problems and anxiety increases. I have to stop eating red meat completely as I notice it makes my stomach problems worse. I carry a bottle of Pepto Bismol in my purse with me everywhere I go. Stomach problems give me anxiety and vice versa so it's a vicious cycle. Finally in Aug. 2010 I'm spending most of my time at my job in the bathroom so I decide to quit the best job I ever had. Probably just as well as about a month later is when the crap really hits the fan. In late September I take a 4% drop from 11.8 to 11.4. I get a little depression after about a week. Two weeks after that I try to eat a bit of red meat and visit the website of someone I used to know and it makes me very anxious. Several hours later I begin to feel very nauseous and anxious. I finally make myself throw up and feel a little better. I sleep a lot the next two days. The day after that however I stop sleeping completely. My anxiety goes into overdrive. I have no appetite and can't eat. I feel shaky, and depressed. My brain has forgotten how to sleep all of a sudden although I have never had insomnia in my entire life previous to this. If I do pass out it is for less than a hour. For 9 days I sleep one hour every 3 days. I see weird cartoony things when I close my eyes. I hear things that I know are not there. Once I had an awful bloody image flash into my mind out of nowhere when trying to fall asleep that "woke me up" with a gasp. I try everything over the counter: Benadryl, herbal sleep pills, melatonin, valerian. Nothing works. Finally someone gives me some Xanax and Trazadone. I take .50mg of Xanax and 25mg of Trazadone. Instead of sleeping one hour I sleep two. The next day I am more groggy than the night before and I am FINALLY able to sleep 5-6 very broken hours. I also updose to 12mg. I start to feel a little better but this doesn't last long. Three weeks later my stomach starts acting up again and I am unable to sleep. Not only am I unable to sleep but now every time I am about to fall asleep my body violently jerks awake. It is torture. I decide to start dropping again. I find I feel a little better after a drop but it doesn't last long. I start to drop every 3 weeks. The depression is still so bad cause I don't know what's wrong with me and my body keeps jerking awake, usually all night. I become suicidal and try to suffocate myself one night. Then I realize, I DON'T want to die. I just don't want to keep living like this. By the grace of God I make it through. I lose about 15 pounds in 4 weeks. I guess this brings us up to present, fifteen months after that "rough patch" or "mini crash". I still have no idea what caused it. The jerks are still here and still drive me insane but thankfully they have weakened and are not as relentless (usually) as they used to be. My sleep has never been the same since. I take magnesium and melatonin every night to sleep. If I get even slightly stimulated good or bad I am unable to sleep. Even going out with friends stimulates me too much and I am unable to sleep. I can't exercise for even 10 minutes cause it makes my jerks worse. I am still not working. I have found it has gotten even harder under 10mg. I have gone from tapering every 3 weeks to every six weeks. From 4% drops to not even being able to do 2.5% drops. I taper .1mg every 6 weeks. At this rate it will take me 6+ years to get to off if I can at all. I read on the other forum about someone who was going as slow as me and she STILL crashed at 6mg. I'm very hopeless. I am so freaking sensitive to drops and can't imagine how I will ever get off this poison. It has been three years since I started tapering from 20mg and I'm not even close to being off. I'm too scared to switch to Prozac because of all the horror stories I've heard and the fact that it is notoriously activating. If I try to hold on a dose longer than 7 weeks I feel very bad. I feel like I'm damned if I do and damned if I don't. Really don't know how to proceed and if I will ever get my life back. I am 31 now and would very much be able to have kids someday. I'm single and have been for a long time cause I can't even go out anymore and meet people. When I do go out, I don't sleep like I said. So that's it. Thanks if you took the time to read this LONG, LONG introduction. I pray for all you guys and I hope you will pray for me too. XX
  22. hi,all been on &off antidepressants for 20 yrs but never felt this crummy.since stopping Paroxetine have had flu-like symptoms ,then fatigue loss of appetite,taste changes,eye problems(excessive blinking actually started while on it,that's why I quit).depression,anxiety,just miserable,wondering if I should reinstate or just try & hang in there.I was on it about 6 mos.stopped May 4 after about 7 wk taper.thanks for any suggestions
  23. Hi everyone, I'm Mark, living in Marseille, south east of France, I'm 36 yo. I began Paxil (Deroxat in France), in 1999, given for a "IBS" (irritative bowel syndrom)... 20mg a day (1999-2014). 2010-2014 were the best years of my life, friends, family, job, music, soccer, etc etc... Mid-2014 I decided by myself to reduce Paxil. So, I started to take 20mg a day, then 10mg next day, then 20, then 10 ... End 2014, jav/fev 2015, I took 10, 5, 10, 5.. then 5mg... 2 weeks after being at 5 mg / day, my life turned to hell. Many symptoms occured weeks after weeks : Nausea, dizziness, lightheadness, belly ache, loss of appetite, tinnitus, electric schocks when moving eyes... Then i thought about my paxil reduction... I re-start 10mg in 2015, then 20mg since january 2016, but my symptoms are still here... Now, I just wanna die with those awful nausea all day, dizziness etc... Sometimes I have 1, 2, 3 days where symptoms seem to reduce, then they retstart awfully... In 2015 I had all medical examination to exclude other problem : Colonoscopie, Pillcam (for small intestine), Ultrasound, 2 Belly MRI, 2 head MRI, tons of blood analysis, eyes tests, inner ears tests, etc, etc... Nothing found... I saw more than 20 doctors in 18 month (gastro, neuro, diagnosticians, ENT, opthalmo, psychiatrists...). None want to listen me, and all say that's not a problem with my paxil, because Withdrawal least no more than few weeks... I'm here, to claim for help. i really need somebody who understands me, who well knows withdrawal problems, etc... I don't understand why I don't feel better since I have re-taken 20 mg... Sorry for my bad english.
  24. Hello fellow AD wayfarers, I've been following this site for several weeks and am amazed at what we humans can endure. I do believe that in the process of withdrawing from these drugs, many of us have been to h###. I think we're a select group, and unless you've been there, you wouldn't understand. I feel for everyone here who is going through this dark night! 26 years on paroxetine 20 mg, and I've just finished transitioning to fluoxetine with the goal of totally transitioning off all ADs next year. I began Paxil in 1993 due to a history of depression and anxiety. It worked like a charm, and I was thrilled. After 2 years, I tapered down to 0 mg over just 3 weeks because my husband and I were ready to get pregnant. All was well at first but withdrawal kicked in about a month later. I white-knuckled my way through it and experienced two miscarriages during that time. I reinstated the Paxil the next spring, I think, and subsequently had 2 beautiful daughters. 🙂 Fast forward to 2009. I was feeling good and eating well and was ready to experience life again without ADs. My emotions were well-controlled but flat-lined, and I had put on 30 lbs. I enlisted a chiropractor and an acupuncturist to assist me with treatments over my 4 month taper. Not knowing any better, I tapered by cutting out the paroxetine one day the first week, two days the second week, and so on. Not sure how it took almost 4 months but that's what I remember doing. I started having withdrawal symptoms before the end of the process. The symptoms became intolerable. I remember spending a lot of time in bed with severe depersonalization (which I learned about here- I was so happy to find a name for it! Thought I was losing my mind!), not sleeping or eating for days due to severe anxiety and nausea, and very jittery with weak and trembling muscles. It was absolutely terrifying. Add to this the guilt of not being a great mother to my two girls at this time. Thank God for wonderful husbands. I reinstated the paroxetine after a couple of months and the symptoms abated. It never seemed to work as well, though. Fast forward again to this summer. Working with my psychiatric nurse, I spent 3 weeks going from 20 mg paroxetine to 20 mg fluoxetine. I know transitioning off fluoxetine is a much gentler process. Although I'd love to get off ADs sooner rather than later, I'm planning on holding here until spring of next year when I'll begin the process of tapering. I teach middle school and trying to do this during the school year would probably be a disaster. I was REALLY nervous about the switch but it's gone way better than I imagined! I've been on straight fluoxetine now for 2 weeks. My symptoms include persistent headaches, stiff and jerky neck muscles, blurry vision, trouble falling asleep, and minor anxiety upon waking. Nothing major at this point. I'm hoping and praying it doesn't get worse and that it improves before school starts. Most any physical activity is hard right now. I'm putting my intro out there now wondering if anyone has experience doing the same thing. I'm curious how long these symptoms will continue. The headaches are really annoying. Ibuprofen helps to a certain extent, but there's always some discomfort. I'm so grateful for all who work this site and contribute with their stories. Withdrawal involves such feelings of loneliness. This site is much needed! Thank you! xoxo
  25. Hi everybody, My name is Grégory, I'm french, 35 years old. Here's my story : I started Paxil (paroxetine in France) in 2002 because of anxiety, 40 mg for 5 years, and then 20 mg for 5 another years. In 2012 I tried a withdrawal in 1 month, and I started to suffer from pain and burning sensations in my legs, and depression. One month later I reinstated Paxil 20 mg, and after some weeks, I felt better. I stayed 2 years like this. In november 2013 I retried a withdrawal, 20 mg a day, 10 mg the next day, 20 mg again the next day etc during 3 months -> then 10 mg for 3 other months -> then 10 mg/5 mg/10 mg for 3 months -> then 5 mg for 3 months -> then 5 mg/2,5 mg/5 mg for 3 months -> then 2,5 mg for 3 months. During this withdrawal (a year and a half) I had some back pain, I thought it was my discopathy that got worse, and when I was in 2,5mg for 4 months, the pain in my legs suddenly reappeared strongly, and the depression. I tried to reinstate 5 mg for a week, but a morning I had been wake by a short ring in my ears. I made an anxiety attack and I felt so bad that my family send me to a psychiatrist that sent me to a psychiatric hospital. They gave to me a lot of medication, they stopped paxil and gave to me chlomipramine, abilify, tranxene and a sleeping drug (I forgot the name) I was like a zombie. So I decided to leave one week later. I suffered from akathisia, and a lot of side effects. It was really horrible. So I stopped all the drugs and I decided to go back to paxil, 20 mg because I thought it was the best for me. Of course it was a big, big mistake. I didn't made the connection with the short ring in my ears 3 weeks ago. 1 hours after taking the only pill, a constant tinnitus appeared in my ears... So I decided immediately to stop everything, and day after day the tinnitus decreased. 3 weeks later it was completely gone, it lasted one week. After that it reappeared slowly, it was 3 months ago. Since that the tinnitus increase slowly, sometimes I can't sleep. Because of that I have a nervous breakdown. The pain in my back and my legs are a little less intense but I have no windows since I stopped Paxil. I read a lot of information about antidepressant withdrawal, a lot of testimony, in particular in your forum, the tinnitus topic, the 'reinstating and stabilizing' topic, etc..... Now please could you give me your advice ? Because I think that the pains are withdrawal symptoms and the tinnitus an adverse reaction, isn't it ? But isn't it strange that an adverse reaction goes away after a moment, then reappears and increases ? It's more like a withdrawal symptom ! I'm really lost. Thanks for your help !
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