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  1. Nuttinanna

    Nuttinanna

    Hi I am a 71 yr old nana who has had Lupus for 30+ years. I have been on Fluoxetine for approx 14 yrs. Started on 40mg. In 2013 reduced to 20 mg. After tons of therapy and other improvements in lifestyle I now believe that Fluoxetine is not doing me any good and am trying to stop. Started 8 weeks ago skipping doses every 4 days which had no effects after 2 weeks. So skipped one every 3 days and after a week started with withdrawal symptoms that have intensified. This has been going on for 6 weeks now and showing no sign of stabilising. Am now thinking I should go back and start again more slowly and get the liquid form. will be talking to Doc but although a great doctor she knows less about withdrawal than I do. Any feedback or advice would be appreciated. Also take Hydroxychloroquine, Ramapril, Bendroflumathiazide, Omeprazole,Thyroxine, Cod Liver Oil, Multivitamins. Many thanks
  2. Hi Guys. I have been on every SSRI over the past 2 years, apart from Paroxetine. This all started from some situational anxiety at work. Each time i took a medication i was on them for about 3 month without any benefit at all. I would loose time at work, cold turkey and return back to work. Each time i did this i was getting worse and worse. I would then return back to the doctor and ve started on something else. This has basically gone on for 2 years. All this time i have got worse. I have now come to understand withdrawal and the fact i could have well been prescribed numerous medications due to an illness been mistaken for withdrawal. 8 weeks ago after stopping my second attempt of Escitalopram for 3 months i decided to stop for good with a fast taper. I feel anxious, dizzy, fatigued, poor cognition and inability to focus. I know if i take a dose of SSRI that this will improve however i will return to the Zombie state of meds. I am finished with medication!!! On reflection my problems i encountered prior to any medication was far easier than the problems i have had the past 2 years on medications. I think i have been a victim of Psychiatry! I dont think i ever needed medication! My chemical imbalance was created by meds! If i had no knowledge of this i would be stuck in Psychiatry! I just want to know ppls experiences and can i still be in withdrawal at 8 weeks after 2 years of messing about with meds. Thanks Lee
  3. Hello, Recent online articles have brought me to this site, and after reading several topics I now realize that I experienced Withdrawal Syndrome when I tried to quit Fluoxetine a couple of years ago. My doctor and I had accepted at the time that I needed to go back on Fluox for the rest of my life, but now I see that it's possible to slow taper and eventually my body will heal. In a way, it's a relief to know the truth and if I had known then, it may have helped greatly with my anxiety. Here's a short summary of my AD history: Prescribed 20 mg Fluoxetine in 2011 (age 35) for symptoms of insomnia, depression and anxiety (I always considered insomnia to be the worst symptom, causing the others to rear up) Quickly tapered off Fluoxetine in spring 0f 2016 at the suggestion of my primary doctor (who was not the original prescribing doctor). Felt great over the summer, started to feel uneasy in the fall. Reinstated 20mg of Fluoxetine. Crashed in December, upped Fluoxetine to 40 mg and started 100mg of Trazadone for severe insomnia Withdrawal continued to be severe in early 2017, but I started seeing a therapist, going to a support group, MIND diet, light exercise, positive cognitive behaviors, etc. I also accepted the condition I was in and that it would be hard, long work to get better. Spring of 2017 I started to feel stabilized. A consistent, day-to-day "blah" feeling since then. This year I decreased the Trazadone to 20 mg with no detriment to my sleep so far. I informed my doctor, and she accepted that but cautioned me not to decrease anything further. I would like to slow taper the Fluoxetine. My to-do list: inform my husband, my doctor (possibly find a specialist), gather supplies for tapering if I have to make my own doses.
  4. Introduction Hi everyone. I have been lurking here since last year but decided to start my thread as my waves are getting more frequent. I am trying to stabilize at 20mg of generic Prozac (fluoxetine) daily, and have been taking it for 6 months. I thought stabilization was finally happening in January this year but waves are now weekly. I am here to see if anyone can shed light on why my horrible waves are more frequent now. I've read “The windows and waves pattern of recovery” (http://survivingantidepressants.org/index.php?/topic/82-the-windows-and-waves-pattern-of-recovery/). Maybe I'm missing something? I'm not feeling very bright since WD hit me! Wave and window frequency Stabilization seemed to work right away and my intense waves were about every 14 to 21 days (3 to 4 weeks). Last month and this month, waves have increased frequency to about every week and last 2 to 5 days, with a window inbetween. Currently working on a graph based on my daily notes to visualize my stabilization journey. WD waves This is how I recall them now but I will update this description when I consult my notes next during a window. A headache and dizziness accompany a vice-like tightness around my head. I then get intensely irritable, depressed, and quite sleepy. I then get akathisia, mostly in the legs. I have tried pushing through it but I find it very hard to concentrate on anything and I just can’t bring myself to talk or interact with anyone. Any conversation or touch terrifies me and I just have to dismiss myself and apologize to whoever is around me at the time and hope they don’t take my sudden departure personally. I then go to sleep. When I wake, I feel better but the wave is still there. I tend to get better over the next day or two, only for the cycle to repeat as mentioned above. Aside from sleeping the only relief I get, for but a moment, is when my rescue cat comes home and deigns to grace me with her presence on the bed next to me or in my chair. This WD has meant that I can no longer keep many commitments, I can only work on a casual basis (i.e. I put in a few hours a day in a window), and my relationships have become skeletal. My life is slowly falling apart and I am now dependent on my partner. She is understanding of my withdrawal, having been on SSRIs herself but luckily avoided a protracted WD. Sadly though, I just feel so guilty and frustrated at how I am now a slave to this window and wave cycle, and largely a useless partner. Windows (something positive) I am myself: productive, fairly positive, happy, thoughtful of others, and able to tackle my anxiety properly. I still live in fear of waves but I am learning to try not to ruminate on them. I feel a willingness to connect with people. I am starting to put too much pressure on myself to do everything during a window and that is leading to problems. To be fair to myself though, my waves are iatrogenic and I must forgive myself for feeling wretched, even during a window, because SSRI withdrawal is the worst thing I’ve ever experienced and it has ruined my life. Why are my waves more frequent? I will share some of my hypotheses below regarding why my waves are more frequent. If anyone has any thoughts please let me know, I’d love to hear them. I’ve learned so much from SA already. As mentioned in my signature I am working on compiling all the daily data I have into a graph so I can get a better picture of my stabilization journey (and what proceeded it). I don’t know when that will happen as my windows are now spent doing all the things I put off in my waves and just improving my loosening grip on the good things in life. I know though that I have to finish this data processing as soon as I can in case the waves merge into one big, long one. 1. My SSRI history during the last two years is peppered with ignorant tapering attempts, maybe it is catching up with me? 2. The optimist inside me is hoping that the frequency is increasing because it could be a pattern that occurs prior to a period of flatter frequencies (perhaps the ebbs and flows of homeostasis). I am perhaps just fantasizing but I imagine that if the frequency increases so much, like in a radio wave, the peaks and troughs (waves and windows) will be indistinguishable, which could be what homeostasis looks like. I am laughing at this hypothesis as I can see I am desperate for some good news XD 3. Maybe my reinstatement/stabilization dose was a little too low (considering I was on 40mg daily for the longest time) and I am catching up with the WD that it would have caused in recent months. If this is the case, I can’t see any benefit in updosing now anyway. Sure, it could always get worse but I think it would definitely get worse if I start guessing at an updose level. I could be wrong. 4. Some of my family wish to visit me later this month for a few days. I haven’t seen them in years. They planned it during one of my windows in December and I felt positive about it all. I also felt optimistic that given about 6 months of trying to stabilize, my waves would be a thing of the past, or a rarer occasion. I tried to get them to postpone but they can’t change their plans without losing all their money. I don’t want them to stop their holiday for me but as the reason for travelling is to see me, I have warned them that I may be in bed, only able to talk to them for a few minutes. I hope I have a window when they are here but I think I’ve had a huge amount of stress about the visit because I just don’t need the guilt I will undoubtedly feel when I am only able to see them for a few minutes. In other words, perhaps stressors and other factors in my life are making waves more frequent. My expectations for stabilization and my tapering plan I didn’t expect stabilization to take this long but after reading “After reinstating or updosing how long to stabilize” (http://survivingantidepressants.org/index.php?/topic/4244-after-reinstating-or-updosing-how-long-to-stabilize/?hl=%2Bhow+%2Blong+%2Bstabilize) I realize it could take a long time, maybe years based on how much damage my ignorant tapering did in the past. When I stabilize (I suppose I have to believe that I will) I plan to do an SA taper, spanning years, with water titration (I have done a few trial runs of it and it’s very easy to get accurate doses this way). I have the syringes ready but it could be a long time before I get to use them! My current plan is to keep plodding along at 20mg until I can get a more stable window and wave frequency. I don’t expect my waves to disappear completely but this increase in frequency means I am questioning things and hope that someone out there may have an idea about what’s happening and what I may expect to happen for the next 6 months. Lifestyle As for my lifestyle, I am healthy, eat well, and exercise most days. I take some supplements but I don’t think they’ve made much of a difference either way. I will list them later when I can manage it but they include B12, magnesium, and fish oil. Sadly, during waves I mostly lie in bed as it provides me some relief. One of the side effects from fluoxetine is sleepiness and lethargy, which I've always had, so that contributes to me lying about a lot. It took so much out of me to write this but I am glad I did it now! Good luck to you all and I wish you the best, regardless of what stage of withdrawal and recovery you are. Kittygiggles
  5. Bluebird2009

    Bluebird2009

    Hi 8 am from the UK and was on Prozac for 18years but had been unwell and having physical problems the past few years but tests where all clear. I realised it was the drug that was the problem. I was taken off too quickly and my body went into shock and I have been in protracted withdrawal ever since which is 9months now. Every month I'm getting new symptoms and really struggling with living. I can't tolerate even a pain relieve tablet without a reaction. I have awful lung and chest pain, blurred vision, severe headache which has just started this week and feel like I'm dying. I feel I maybe shouldn't have came of but then maybe it's better to get the poison out of my body. Really need some positive vibes at the moment and if anyone else in UK can help please do as I'm frightened that I'm going to die.
  6. Hi everyone! First of all, I want to appologize for my english ....Im mostly french!😉 I have been reading here since a little while but first time I write. I have anxiety since 12 years. I am 40 yrs old female. Been on meds since 11 yrs. I have been on almost every ad. Lots of them didnt suit me. Never been able To stay more than 4 yrs on one med cause it pooped out. I starter feeling really dizzy a year and a half afp (was on lexapro at that time ). Anxiety and fatigue game back. So tried different meds again with always many side effects even at low dose. So back in march (On prozac 20mg) I decided that maybe or was time for me To try my life without meds. Juste To say, or is a big step for me cause I have thaught that I was meant To be on this for life. Si since the beginning or april, I slowly decrease from 20mg To 5mg (now). I have the liquid form. Still take my clonazepam 1/4 of 0.5mg at night. The more I decrease, dizziness decreased also. People tells me I look more alive ! Cause I always felt kinna stone. I still had anxiety but it was manageable. But since a week, I feel more anxious and short of breath. I feel sometimes near To have panic attack over the fact that Im not breathing correctly. I put si much focus on that. Since 2 dans, I cry more also. ... What the heck is going on with me????? Does that mean I wont ne able To live without it ??? Psychiatriscian had no clue how To wean us. That fustrate me. I was the one who did the withdrawal plan and ask Her for liquid form. Now she almost laugh at me saying Im not suppose to feel any withdrawal symptoms with prozac and mostly at 5mg. She tells me its probably the anxiety coming back !? So what do you think? Also....is Ltheanin good for my withdrawal? Someone refered me that? Thank you again! Lolita
  7. 9 months ago today I took my last Prozac and I am still dealing with withdrawal. I took 15 mg of Fluoxetine for 12 years from PAR pharmaceuticals. In July 2015 the fluoxetine I received from the pharmacy was from TEVA pharmaceuticals, apparently PAR pharmaceuticals discontinued the tablets I was taking. Well, my body did not react well to the TEVA brand. I started having nausea and tremors. After a couple of days on the TEVA brand I switched to the MYLAN brand but nothing changed. Realizing my body was not going to handle the change I decided to taper but it seemed pointless because my body was in withdrawal from the PAR pharmaceutical fluoxetine my body was use to taking. On August 27th 2015 I took my last pill. From July to November I dealt with nausea and tremors and then all hell broke loose. On top of the nausea and tremors I developed a bad smell in my nose that only I can smell, internal shaking that is constant, the nausea got much worse, I started having hot flashes, night sweats, insomnia and chills. I also have cried almost every day since November. In December I had a gastric emptying study done due to the nausea and lack of appetite. I discovered I now have delayed gastric emptying. To date I have lost 44 pounds from the nausea and not being able to eat. I have also had a CT scan and an MRI for the tremors and internal shaking. Those results were normal. I have seen an ENT for the bad smell in my nose, but they can find nothing wrong. I have noticed that I am feeling a tiny and I stress tiny bit better but I still have the internal shaking, nausea, bad smell in my nose and crying. I have read about internal shaking in withdrawal but how long does it go on. I was put on Prozac for panic attacks and the constant internal shaking is making me feel panicky and anxious. Does anything help with it? Has anyone else experienced a bad smell in their nose or heard of anyone having a bad smell in their nose during withdrawal? Thank you for any advice or help anyone can offer me.
  8. Cigarettes at age 11. Alcohol periodically from age 13 to age 30. Valium episodically from age 18 to age 27. I have been on myriad anti-depressants since 1982 for major depression and generalized anxiety. Imipramine, desyrel, ativan. Off drugs from 1984 till 1995. Started Prozac 1995 till 2014 (did well from 1995 to 2011). Tried Wellbutrin, Cymbalta. Abilify and Trintellix from March 2014 till August 8, 2017 (depression free). Had to withdraw due to cervical dystonia and tremors which still persist. Terrible experience withdrawing from Abilify and Trintellix. Started Wellbutrin 150 mg. and Prozac 10 mg. for one week to help with withdrawal. Then increased Wellbutrin to 300 mg. and experienced ringing in ears; stopped the Wellbutrin and increased Prozac to 20 mg. (10 in A.M.; 10 in P.M.) Now on Prozac 20 mg. per day, occasional Propranolol for tremors (doesn't help). I've read that coming off Abilify can take up to 3 months or more, and it has been 2 months so far. I feel like I've spent (wasted) my entire adult life trying to feel better, first by self-medicating, then by psychiatric medicating. I'm 72 years old. I wonder if there is any hope for me.
  9. I tapered of Prozac in early 2014. I tapered over 4 weeks by taking every other day so basically ct. I had taken Prozac for 17 years for anxiety and depression. It took almost 4 months to get very bad by which time Drs had prescribed me sertraline and citralopram both of which exacerbated things tremendously. I only took a single dose of each. It never occurred to me or Drs to put me back of Prozac and by this time I was too terrified to take anything. The last 3 years have been horrific, losing my husband, my health and my income. I was unable to work for 2 years and now work part time from home which I still struggle with. I'm diagnosed with cfs fibro and severe depression all caused by protracted withdrawal. Iv seen dr Healy a few times and a neuropsychiatrist who both back my cause. I haven't taken a drug in 28 months but am about to start imipramine on their advise. I hope to get some relief from the crippling depression and pain and then hopefully taper off. I know this is a risk but desperate times call for desperate measures. I have terrible tinnutus caused from the destabilising effect of ct Prozac. I also have vertigo and chronic insomnia, especially early morning waking and sleep maintence. I use magnesium glycinate and lactium but Iv not noticed a noticeable difference. I have learned to not panic too much during extreme anxiety, instead of it breaking me completely like in the old days, I open the door and invite the beast in. This also helps with odd flare up of akathesia that was relentless in the beginning. I'm completely amazed at the lack of knowledge from Drs about the dangers of drugs but I have also found at leat 3 who are well very knowledgable. It gives me hope at least that we are not completely alone.
  10. Hi everyone I withdrew cold turkey from Fluoxetine around a year ago and I've been suffering from visual snow for 7 months now . My question is can ssri induced visual snow go away or am I gonna be stuck with this forever?
  11. Hello everyone! I am a new user here. I've lurked around this site before but have yet to introduce myself. I was a Prozac user for a year from August 2015 - September 2016. I had taken it for social and general anxiety. I was on 20mg/day. Initially, I was actually doing fine and great emotionally but had side effects like massive fatigue everyday (not even 3 cups of coffee could wake me up!) and constipation every time I went to poop (sorry for TMI). I also felt like a zombie for a brief period in which I was neither happy nor sad. In May 2016, I decided to abruptly stop taking the Prozac by choice without consulting my doctor (bad move!) and had brain zaps and mood swings which I assumed as worsening depression. I then just asked my doctor to simply increase my dose because I thought I was getting worse (bad move again!). I was put on 40mg/day from June - August 2016 in which I was ok at first but then I was hit with a panic attack so severe I had to rush to the ER. For that week, I was having very severe symptoms. So I was instructed to go back down to 20mg/day. From then on, I decided to stop taking it a few months ago in September because I felt better and didn't want to rely on medication anymore to make me happy. I consulted with my psychiatrist who said for me to just take 10mg for one month and then I can stop. I did just that. Over the month of October I was fine and felt completely normal. However, I realized symptoms would come later once the month of November started. I have since felt every type of symptom under the sun including brain zaps, hot flushes, insomnia, irritability, tingling sensation of the skin, anxiety, shortness of breath, sweating, tremors, and slight vertigo. I have never felt these symptoms in my life til now! I've talked to my doctor and he doesn't believe in withdrawals. At this point I feel helpless. I am experiencing waves and windows in which I have waves of really bad flare ups and then windows of good normal days where I feel fine. But they keep cycling back and forth. I now have questions to ask: 1. Do windows of no symptoms mean that my body is getting better? 2. Should I reinstate the Prozac and taper off more gradually? Someone suggested I shouldn't because I've already been clean for 3 months now. But what do you guys think? 3. Will symptoms go away if I keep pushing cold turkey? 4. Should I try medical weed to help ease tthe symptoms? I want to try natural ways of healing
  12. Unsure if I'm posting in the right place but this is somewhat of an introduction. 1.5 years ago I started on 20mg of Prozac for OCD. There was restlessness with starting but it went away. Gradually I tapered down to 10mg of Prozac which I was on for a full year. 2 months ago, I felt the sudden onset of a a very severely agitated feeling. It was very vague but I can pinpoint the exact moment I noticed it -- I was sitting, doing nothing remarkable, and unstressed. I had felt something like this before throughout my treatment but it was very very temporary and felt more like an agitated depression brought on by external circumstances. When this feeling started I could not pinpoint anything else as the cause. Things were good in all parts of my life. I had not messed with the dosage of Prozac at all for a year. Is it still possible that the Prozac is causing this long term agitation/akathisia that I still experience today? A month into the feeling I decided to taper off Prozac completely. I experienced very little withdrawal...just mild headaches and dizziness. The akathisia didn't get worse or better. But it is still quite bad. And the longer it continues the more hopeless I become and probably the more depressed as well because I can't see a life without this agitation anymore. Started on some Klonopin to treat the restlessness and help me sleep. Has anyone else experienced akathisia without a dose change? And also only being on a low dose?
  13. Hi i wanted to ask if anyone in here experienced extreme fatigue ? All day I feel so tired and the only activity I can manage is an hour walk but even through walking I feel very weak.. the mornings are the worst when I wake up after 10 hrs sleep I have no energy my body just lies in bed but have absolutely no energy did anyone experienced something similar ? Thank you in advance
  14. i've been off 60mg 40mg (see Post #4) of prozac for 2 months after tapering very quickly over 2 months. i took prozac for 20 years. i have really bad headaches most days, something i never used to have before unless i was dehydrated. i have terrible mood swings - i shout at people in the street if they're badly parked, i get road rage when i'm driving, i scream at the kids and my husband. fatigue is a big problem - i can fall asleep at any point during the day and often do. i sleep all night but am still exhausted the next day. i have constant vivid dreams and nightmares. my ocd is creeping back (which is what i was prescribed the prozac for in the first place). i thought i had it under control until my kids told me i needed to stop posting on social media so much as it was dominating my life. i was also alienating people online. i have constant diarrhoea. i cannot stop eating -i'm constantly ravenous, especially for carbs - crisps and potatoes are my downfall and i've put on a stone in weight since stopping. i have lots of pains in my joints and limbs. i did have crawling under my skin, especially in my knees and feet but this seems to have subsided. i'm scared of seeing or talking to people. this has always been a problem for me but it is worse right now. i feel panicked when i think of all the things i have to do - chores to be done round the house, things i need to do with my kids, hospital appointments for my husband (he has an avm in his brain and had a traumatic bleed nearly 4 years ago which has left him with life changing disabilities. i am his full time carer). thankyou for listening if you made it this far. today is a bad day and i keep asking myself why i gave up the pills in the first place? i hoped i would have more energy, feel more emotionally, lose weight etc. but it was only after i stopped that i started to read up on protracted withdrawals. i had no idea it could be so bad to stop the drugs.
  15. Hi folks, I've been on Zoloft (2000-2001) and tapered off over a period of 2 months (too fast and I suffered) then tapered off citalopram (2014) and this year, my doctor put me on prozac 20 mg for GAD and Major Depressive Disorder but I stopped cold turkey 8 days ago because it was making my depression and anxiety much worse and no one would listen to me when I asked about getting off the meds. Anyhoo, I found this message board while searching online for anyone else who might be trying to get off AD's and am glad to have found you.
  16. I have been on antidepressants 3 times in the last 14 years. Usually would take them for 6-8 months and then taper off with no problems. The last time I took them (2011), I needed the maximum dose of sertraline (200mg) to get an effect. After a year on it, I felt it was time to stop. The nurse insisted I had to keep taking or risked relapsing into severe depression. I tried several times to bring up the topic to no avail. After about 1.5 years on it, I cut the dose on my own to 150mg and felt ok for 2 weeks. But after I started having a dull headache that lasted hours, dizziness, serious cognitive difficulties and severe fatigue. I could not function and needed excessive sleep (12-14 hours/day). Tried increasing it again and the more severe symptoms got better, but the headache and flu-like malaise persisted for at least a week. I consulted with a psychiatrist. We tried effexor and cut on zoloft. Had no withdrawal symptoms, as I was cross-tapering. I was completely off the zoloft. Only took Effexor for about a month on a low dose (never past 150 mg) because it never helped with the symptoms of Atypical Depression I had. When I started tapering down the effexor, I got the dizziness and extreme fatigue again. When I would fall asleep, I found it extremely hard to get up. Literally felt pinned to the bed. Woke up more tired than I went to bed, even after 12 hours of sleep. Woke up dizzy and with a headache. I increased dose again and we're doing a slower taper over 21 days. The starting dose is 37.5mg. I experience dull headache that lasts hours, flu-like malaise, muscle tension, fatigue every day (with the occassional good day of no symptoms and the occassional day of much worse symptoms). I have learned to cope the best I can with these symptoms, but the fatigue gets unbearable at times. I sleep 12 hours at night and still feel tired and even drowsy during the day. I'm in grad school and it's hard and often impossible to study or even make it to class. I was supposed to decrease dose to 25 mg after 10 days on 37.5mg, but since I still have symptoms, I'll ask dr if I can postpone the decreasing... Im also concerned that the increasing apathy Ive had over the last 7 years might be due to antidepressant use. It could also be depression, but if it is SSRI use, its a very scary symptom that is not going away (has not gone away for more than 3 months in over 14 years since I started having depression/taking SSRIs). The only reason I can semi-function today is because I take nuvigil (a stimulant) 3 or 4 times/week. Without that, I can't do homework or clean or shower. Im extremely dysfunctional. I don't rely only on the stimulant though. I use it to give me energy and motivation and alertness that I use to do positive things, which improve my mood and further help with apathy.
  17. I wanted to introduce myself. I plan to taper off of Prozac, and I feel that this community will help me manage my titration. If you have any questions, let me know!
  18. Hi folks, Just looking for a bit of advice. I'd been on Prozac, 25mg a day, for 9 months, for depression and wanted to come off them. I was advised by my doctor to take a 25mg tablet on alternating days for 1 month and then stop completely. I did this and have now been off for 4 weeks. Asides from some rather severe depression symptoms my main withdrawal issue has been PGAD (Persistent Genital Arousal Disorder), something which I suffered with 2 years ago. What I'm wondering is, does this mean I tapered off too quickly? I should also mention I have M.E. and tend to respond strongly to drugs. Is the best plan of action to just ride this out and hope the symptoms go or to go back on the Prozac and taper off again much slower? (my doctor did tell me if I go back on the Prozac I'd have to stay on for 2 years but I really don't want to do that.) Any advice appreciated, Thanks
  19. I wanted of prozac was on it 9 months last dose was 20 mgs off 30 days dr said ok to stop self tapper. I know i don't know if have wd from the from prozac or my slow tapper K pin after two months use 1.5mg to .125 mg i stopped to day after trying to get on another AD which was horrible experience
  20. ADMIN NOTE See ang's Intro topic with her earlier history here ☼ ang: help and confidence needed Hello Altostrata and friends. I now believe I am a success story. I am working, contributing and ENJOYING life again. I am 58, so I am grateful that I can enjoy maybe a few more years of my life. From the amount of drugs I was on, this is a miracle. Took me I would say, many years. Mistakes I made, so, so many, ........then in desperation .......... I found this wonderful lifeline Surviving Antidepressants. The pharma fraud, and psychiatric fraud, and $$$$ made destroying lives on these poisons, I can never forgive. I have not been able to update my own timeline, as I have been so happily busy. I do, however, wish to write my survival story, maybe in 6 months, when I am permanent in my job, and will update with all the things I have done in the last 6 months. Just wanted to say, is hard to revisit this site, remembering how ill and desperate I was. But I will, and I will contribute when I can. Yes, there IS a light at the end of the tunnel, for me the agony waxed and waned for a couple of years. Keep up the fight, never give in. Happy Easter Everyone. I am so hoping you may be able to enjoy, but I know how ill I have been, and family and friends were just too much to cope with. This easter, I cant WAIT to see my grandkids and family. Yes the brain recovers from these poisons. Cheers Ang
  21. Hi everyone, I'm new here. I figured I needed some support through this journey of exploration. I am currently on - Quetiapine/Seroquel 300 mg XR and 25 IR (used to be 300 XR + 100 IR half a year ago, I've been on it, just like the other meds, for more than three years) - Fluoxetine 40 mg - Dexamfetamine 3dd 10 mg I've been on psychotropic meds for 5 or 6 years now (I'm almost 21). I've been on different meds before this combination. The side-effect have taken it's toll on me (No matter how long I sleep, I wake up tired, tachycardia, tremors, constantly out of breath, I feel like an old lady) When I was prescribed my psych meds I was in a very bad place, I was suicidal. However, I feel like most of the reason I was in a bad place was bc I was living at home. Things weren't going well there, and I've had depressed symptoms and an eating disorder that went unnoticed since I was 13. I've had many diagnosis, it started with adjustment disorder, ADHD and asperger, adjustment disorder changed to depression NOS, then came the borderline and eating disorder diagnosis and now I finally have a diagnosis of PTSD and major depression and ADHD (which I agree with). I was originally given the antipsychotic for my "autism and hypersensitivity". anyway the new psychiatrist just coppied that medicine regime and now I figured I'm done with it. It helped me through **** times, but I've been living in a different place for 2 years now and that allowed me to make some process. The whole tapering of Seroquel isn't going easy though. The first 50 mg (in 25mg per 3 months) gave me pretty bad anxiety. I lowered 25 mg again 4 days ago, I've been able to get the anxiety under control with magnesium (3 times a day, 600 mg in total). Beside the mental discontinuation problems, the first 2 days it made my tachycardia go haywire and my tremors go nuts. It was quite funny, but not if that will happen with every 25 mg decrease. 3 and 4 day I was nauseous, vitamin C, camille tea and lemon juice made it slightly better. Anyway, I'm thinking about lowering and eventually quitting (if possible and healthy for me) my other medication. Also, I wonder if it's best to take 200XR, 50 XR and 25 IR or 200 XR 50 IR and 25IR for example. I'm not sure about what's better. Anyway, I'm gonna keep you guys posted. Ask questions if you feel like it, -E
  22. I joined this site a couple of weeks ago. After finding that paxilprogress was no more. I was devastated. That site may have truly saved my life in some of my darkest moments. What is one to do? When essentially you've self-destructed in front of everyone you love; because of a nasty little "non-habit-forming" pill that's been shoved down your throat for decades. So here I am. Time (weeks really) has eluded me. I meant to reach out sooner. I'm just hoping I'm not reaching out too late. I feel like such a horrible failure. I know better than that at some level, know that maybe I failed but that I just have to pick up the broken pieces and keep moving forward. But I'm so I'll. I'm so weak. I'm so alone. And I feel so helpless. My life may not have been a picnic before the introduction of SSRIs. But this is one situation in which the grass was truly greener on the side of which I was already standing. Before popping that first "innocent" little pink pill, prescribed by a doctor who had seen me only once and only spent 10 minutes "getting to know me". I couldn't tell you who that doctor was, I never saw him again. Nevertheless he was the first in probably nearly a hundred who have insisted upon continuing the saga. And what better did I know? I was unhappy before the meds. I was often unstable on them. And I was clueless as to why I was saying and doing psychotic things (that I often didn't remember, or just have "snippets" of memory after the fact) and so violently ill when I decided I simply no longer wanted to take the pills. Or was even 12 hours late on a dose. (More about that and my travels down genetic testing road and CYP450 mutations later.) All that being said; Hello to all in these forums. I'm the antisocial one. The antisocial one that sometimes doesn't know when it's appropriate to shut up. Or how to appropriately ask for help. But if you've been through it (psych med-wise), I probably have too. And vice versa.
  23. Prince1924

    Prince1924: Prozac

    I have just read this advice about keeping a withdrawal programme Simple ie 3KIS. Not sure but there doesn't seem to be a support network like this in the UK? Only one I've come across is the Royal College of psychiatrists which is a in the form of a video). I've taken great comfort from all this advice as I makes me feel I can try and come off Prozac one more time.
  24. After 19 years of 10mg of Fluoxetine, I finally had the wherewithal to get off of it. I knew shortly after starting it that it wasn't doing much, if anything, to help my depressive symptoms, but each time I tried to get off of it I had horrible withdrawal and so, went back on. After my daughter graduated high school and went off to college I figured I could suffer through the withdrawal. I was 50 years old when I went off... 52 now and has been almost exactly 2 years. My main withdrawal symptom was really horrible depression accompanied by anhedonia, and anxiety. When I went off the dp's I also got really healthy. I eat really well (no sugar, no gluten, very few carbs, lots of OG veggies and meat, very high quality supplements (fish oil, a multi with methylated folate as I am compound heterozygous for MTHFR). I engage in moderate exercise often (run or hike 5 times/wk). No caffeine or alcohol for years now. I feel like I have done everything in my power to get through this. In May, I had what they used to call a "nervous breakdown" , ie. became completely dysregulated and ended up in the ER and then in an acute psych facility. This was never something I thought I would go through. I've always been "high functioning". But now I've come to see that the "high function" was just layers and layer of coping mechanisms that served to cover up the real psychological problems underneath. Fluoxetine just made it easier to add on more layers and not FEEL. When I got out of the psych facility I decided to try a promising treatment called rTMS that got FDA approval in 2008. My insurance didn't cover it so $10,000 went on my credit card. It took 6 weeks for the full treatment which definitely changed my brain function. I was having non-stop suicidal ideation when I went in and almost none when I finished treatment. I was waking each morning with the most dystopic feelings... and the feelings didn't seem to come from thoughts but were just in my body when I awoke. Those also decreased in intensity by quite a bit. Also, I could work through emotional issues much better and basically felt like life might be worth living (some day). That all sounds fairly optimistic... but now I'm in the waves and windows and I have no idea what's what. Some days I feel like I could go to a job and work but then I'll have 4 or 5 days where I feel like my function has dipped so low that I might never "participate" in the world again. It's helped reading your posts but it also fills me dread when I read about people who have been off dp's for 6.5 years and are just now feeling "normal". I don't feel like I will make it to year 6. Any words of wisdom are greatly appreciated.
  25. Moderator note - link to benzo forum thread - Spice81: Please help I’ve recently gone from years on fluoxetine to straight swap to citalapram for 5 weeks now straight swap to venlafaxine I’ve experienced bad diarrhoea nausea rapid weight loss due to no appetite and tingling burning knumb sensations in my hands anyone else experience this
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