Jump to content

Search the Community

Showing results for tags 'clonazepam'.



More search options

  • Search By Tags

    Type tags separated by commas.
  • Search By Author

Content Type


Forums

  • Support
    • Read This First
    • Introductions and updates
    • Tapering
    • Symptoms and self-care
    • Finding meaning
    • Relationships and social life
  • The commons
  • Current events
    • Events, controversies, actions
    • In the media
    • Success stories: Recovery from withdrawal
    • From journals and scientific sources

Find results in...

Find results that contain...


Date Created

  • Start

    End


Last Updated

  • Start

    End


Filter by number of...

Found 73 results

  1. I was given 20 mg of Prozac back in 1997 for depression. I was still technically a minor back then. I had an initial "high" from the Prozac which was mistaken for me not being depressed anymore. A few months later, Prozac stopped working and I had completely lost my sexual functioning. I told my doctor about this, so I was switched to Effexor. I kept on being switched from medication to medication in an attempt to achieve the initial "high" of the Prozac and to reverse the sexual functioning but things just got worse. One day I was put on a medication called Wellbutrin and that caused a manic episode from the first dose which caused me to have to be put into an inpatient facility. I was now switched from just being depressed to having bipolar disorder. I was put on Depakote which stopped the manic episode. Depakote caused me a lot of suffering, so I decided to cold turkey the medication about 6 months later. This led to another inpatient hospitalization and now I was polydrugged with Depakote and Zyprexa. This was the first polydrug combination I was on. This combination of medications was even worse because I was sleeping at least 16 hours a day. After another 6 months or so, I cold turkeyed both of these medications and that led to another inpatient hospitalization. I was fortunate in some ways to have the Zyprexa removed and be able to function somewhat ok on just Depakote and now Klonopin. I stayed on Depakote for years but my sexual issues were never solved and I had a lot of other side effects from Depakote such as multiple sclerosis and Parkinson's disease like symptoms. In around 2005, I discovered the first person who had described the same sexual issues I experienced. It was called Post SSRI Sexual Dysfunction. I discovered forums similar to this one, and consumed books by people like Dr. Breggin. In 2007, I was able to successfully withdraw safely from all medications by switching over to lithium and valium and using a compound pharmacy to taper down. I felt a lot better and recovered from some of the damages caused by the medications. I began social drinking in 2008 because I felt like I missed out on such a big part of my life. About 6 months later, I completely lost my ability to sleep probably due to the alcohol damaging what the benzos had already damaged. I was forced into a state psych ward and given a diagnosis of bipolar NOS, psychosis, anxiety etc. After 3 or 4 months in the state psych ward, I left on a combination of Depakote ER and Ativan. I had to eventually updose the Depakote ER and switch to Klonopin again. So for the last 3 years or so, I've been on 1250 mg of Depakote ER and 3 mg of Klonopin. While I am not suffering nearly as much as I did when I was bombarded with antipsychotics like Haldol and Geodon, life isn't nearly as good as I know it could be. That's why I want to get help in coming off of the Depakote ER and Klonopin safely. My confidence level is a bit low because I feel like I may be damaged beyond repair due to being on dozens of psychiatric medications and due to the past experience with insomnia I freak out when I cannot sleep and that is what is happening now. I started to taper off of Depakote ER on 11/24/2014 and I'm on 750 mg Depakote ER now and 3 mg of Klonopin. That's my intro but I'm not sure what to do next...
  2. Kristine

    Kristine: Not alone

    Moderator note: link to Kristine's benzo thread - Kristine: Protracted clonazepam withdrawal? Hello, I am new to this site and would firstly like to extend my gratitude to all the people who have shared their stories and support. I now know I am not alone. My story is long and complex so I will attempt to condense it. I am 43 years old and was introduced to antidepressants 10 years ago after being diagnosed with MDD, GAD and PTSD (l do not feel comfortable with labels) by my psychiatrist. During the first 8 years of treatment multiple antidepressants and other psychotropic medications were prescribed. I will fast forward to October 2015 when I attempted to end my life (I had never been suicidal prior to taking antidepressants). I had to resign from work and was hospitalised for 1 month. At the time I had been taking citalopram for a number of years and had reached the maximum dose. My intuition told me it was not helping. I wanted to stop this medication and my psychiatrist was supportive of this decision. However, it is obvious to me now that she was inexperienced and uneducated with this process. The citalopram was ceased over one week and due to severe anxiety I was commenced on seroquel and diazepam. After leaving hospital I managed to taper off the seroquel and diazepam but became increasingly unwell both mentally and physically. My psychiatrist convinced me that my mental illness had returned and I was commenced on Parnate which was increased in dose over 3 months. Instead of improving my mental and physical ailments worsened and my psychiatrist sort a second opinion. I was hospitalised again in May 2016 under the 'care' of another psychiatrist. This was the beginning of an indescribable hell where I was treated like a human lab rat. Looking back the medications he prescribed were beyond belief and I was the victim of poly pharmacy without adequte professional rational. Unfortunally, like so many others, I was vulnerable and trusted his guidance. He treated me as both an inpatient and out patient over a one year period. Over this time I was prescribed over 14 psychotropic medication some of which were abruptly ceased and crossed over with other medications. If this wasn't enough I was subjected to 15 sessions of unnessaccery ECT. Not surprisingly, I was in a zombified state, unable to function and unable to return to work. My anxiety and depression was not alleviated and I was plagued with tremors, nausea, vomiting, fatigue and migraines. By April 2017 I ceased my appointments with this psychiatrist (he had little belief in withdraw symptoms or side effects of the medication he prescribed - he resorted to blaming me) and returned to my previous psychiatrist. Over the past eight months I have the mammoth task of withdrawing from multiple medications. These include escitalopram (completed reduction), Lithium (competed reduction), clonazepam (partial reduction), bupropion (completed reduction), seroquel (completed reduction), dexamphetamine (partial reduction) and fluoxetine (no reduction). My withdrawal symptoms are horrendous and relentless. My psychiatrist has been unable to advise me along a comfortable path. She appears to be in denial and her support has mostly evaporated. I feel abandoned, alone and frightened. I was forced to seek information independently (for which I am grateful), which continues to be a hideous realisation that for years I was in a constant state of drug withdrawal, side effects and drug interaction. I also feeling very angry about my treatment. I am tapering at the 10% rate now (one medication at a time) but even though I know road ahead will be long and rocky, I feel a sense of empowerment from educating myself. What I am experiencing is common and I am finally breaking free from the clutches of psychiatry.
  3. Moderator's note: link to benzo thread - Rabe: questions re how ro navigate clonazepam, viibryd, and amiloride Hi, I am new on the site having been so impressed with the knowledge and personal experience that I have read as I continue my journey of tapering psychiatric medications. I have been on Clonazepam for many years for a severe panic disorder with agoraphobia and had no problems with it until I moved, had surgery, was exposed to environmental toxins and my doctor doubled the dose. I broke out in a weeping rash and was so very ill. I tried tapering on my own and became very very ill, lost weight, muscle and fat and was extremely depressed. My children brought me to a treatment center to get help with the tapering but instead I was put on an antidepressant. I am now finding myself tapering the Clonazepam and the Viibryd with a doctors help, but his knowledge seems quite limited. We did taper the Viibryd to 10mg in the spring and it was not too bad. I tried tapering by about 10% now and had horrible HA, nightmares, depression, stomach upset, agitation, anxiety, headache, electrical feelings in my head, weakness... I saw the doctor today and he would like to split the dose to 5 in AM and 5 in PM to help in tapering. My concern is that I take Premarin and the larger Clonazepam dose at night and I am concerned about having to eat that late d/t GERD, about less anxiety coverage during the day as well as the sleepiness from both the Viibryd and Clonazepam together at night. I was wanting to get any thoughts or experience on this if possible. Thank you so very much. This has been such an overwhelming and physically and mentally draining experience with little support for almost 2 years. I am grateful to be here!
  4. Hello, my name is Manny. I was diagnosed 0CD and schizophrenic in 2008, but I been taking benzos and amiptriptiline since 2005. Currently,taking abilify 20mg,risperidone 2mg,cymbalta 60mg,biperiden 4mg. I am tapering klonopin down to 0,27mg from a dose of 1,25mg. I went to see my doctor this week because a blood test that I did. He said my hepatic transaminases are high because of the medication that I take. I am assuming the APs that I take. What can I do to get my liver function well? I know, quitting the APs, but I can t cold turkey. Any advice,please.
  5. Hello, New member here. Had been on Klonopin for 15 months for insomnia caused by hypothyroidism. Been off K for 10 months now, with the help of 75 mg Trazodone for sleep. About 2 months ago, T was losing its effectiveness and I decided it's time for a drug-free me. I went from 75 mg to 50 with no problems; at 50, withdrawal hit hard. Insomnia (of course), shakiness, anxiety, you name it. I did a fast taper as I did not have it in me to go through another long taper after the K experience. In 2 months, I went from 75, down by 1mg every night to 50, to 25 for 2 weeks, 12.5 for another 2 and finally off. I have been off for only about 3 nights. Withdrawal after quitting seems manageable so far, although it is too early to tell if it will get worse. My main issue is with insomnia. I feel if I can manage this, I will be OK, especially after the horrific K withdrawal. My question for those who have used Trazodone: how long did it take for sleep to return after quitting trazodone? Please include how long you had been using T and the dosage. Thanks for your input and hope we all survive the trials of psychotropic drugs. Survivor1
  6. ...and still dealing with anhedonia. Is that what you'd call this? It's not nearly as bad as it was back in 2012. The first few years off prozac were a nightmare. I was a total robot, unable to feel present, to empathize, etc. I could barely compose a facebook status, even that required too much focus. (You can tell how much better I'm doing by the fact that I'm FINALLY POSTING IN HERE.) I had a job but didn't do much. The weird thing was, whenever I got my period, I would kind of "come alive" - at least somewhat. It was like a wall went down and I was able to connect with myself again. I could feel my feelings (kind of), feel more present (kind of). Even though the switch wasn't perfect (didn't get all the way back to "normal"), the change was always very drastic. I would feel like this during the first day or two of my period, when I was bleeding heavily. Immediately I would get online and start researching, trying to figure out WHY I felt better on my period... and then the bleeding would end and I'd go back to being a robot... At some point I thought that perhaps my serotonin was too high (isn't your serotonin supposed to be "low" on your period? so maybe my period brought my serotonin down to "normal"?) - like the SSRI had increased my serotonin too much and left my brain kind of stuck that way. The only thing I figured I could try to drastically lower serotonin was to take MDMA - simply for the serotonin crash/reset the next day. I was able to try it in early 2015 and it did exactly what I'd hoped it would do. The CRASH felt like heaven. The wall went down. I was suddenly able to concentrate. I could stand outside and look up at the sky and feel the breeze and watch the birds and just be still and present. That day I curled up and read half a book - something I had been unable to do for years. My therapist noticed a difference in me right away - how I seemed more connected and present. I don't think she believed in my prozac story (I mean, it sounds crazy to me as well - why would I still be messed up YEARS LATER???), but she did agree that I had changed. After this, my life started moving forward much faster... but I still wasn't completely myself. I still felt more myself on my period, which meant I was still somewhat out of it and disconnected the rest of the time... But at this point I had become so used to the anhedonia, or whatever you want to call it, that I just accepted that that was how I was. And then... last year, I tried a benzo for 2 months, for stress. Obviously a big mistake. I had only taken prozac for 6 months, and I still feel strange 5 years later... Why the hell would I try another psych med??? BUT I did. So anyway. The benzo withdrawal nightmare lasted a good 6 months...and a little longer than that to get all the way back to normal, which I feel like I am now. At least the benzo didn't cause permanent damage. Anyway, what I wanted to say is: twice during benzo withdrawal, when I was on my period, I felt COMPLETELY, 100% NORMAL. The "normal" I had once felt before prozac. Totally emotionally with it. Had totally fluid social interactions. And so on and so forth. Colors were actually BRIGHTER and DEEPER. My vision literally changed!!! My palms were sweaty - random, I know, but usually my skin is SO dry - that was just one of the things I noticed, and I want to document it here. One night I laid in bed and started listening to music and I just cried and cried because I could FEEL AGAIN. And it was so ******* sad because I knew my ability to feel would slip away yet again... So, anyway, a good 4 years later I finally had real genuine windows...pretty depressing, right? I'm sorry to anyone reading this...I'm sure most people don't take this long to recover. My brain is ridiculously fragile, I guess... I had a bit of a window this month on my period, too (not as amplified as the windows from a few months ago, but I still felt way more normal than usual)... I'm not sure what all of this means. Maybe the recovery my brain had to go through after getting off klonopin helped to further heal whatever change happened in my brain from prozac? At this point, at least, I'm convinced that I don't have "brain damage" (which for years I figured I must have, and so I avoided this forum and avoided thinking about it because it was so terrifying). I guess there IS some kind of slow gradual healing going on. Maybe at this point it comes down to a hormonal or mineral imbalance of some kind? I don't know. I'm terrified to go to a doctor and ask for help about this, I assume they'll just laugh. I can never take another medication again after all of this, anyway...I'm scared to even try something like birth control. I don't know. Anyway. It's been many years and I wanted to finally admit to myself that this is actually going on by joining this forum... I have had some hope lately that I can find myself again after all of this. Oh, and another awful thing is prozac made me lose all sense of gender. I think because of that, for these past few years, I have identified as trans... and just in the last few weeks I have had moments where I look at myself in the mirror and feel a strong connection to myself (rare) and I "realize" I am not trans...and it's just that I couldn't feel my gender for a very long time... It's ******* horrifying. But I wanted to write that down here. I need to admit this. My period just ended the other day, which is why I'm thinking about all of this at all. I'm sure these feelings will slip away soon... I'm seeing how long I can hold onto myself this time. I'm hoping I will keep posting here and not give up. Thanks for reading. P.S. I've read about inositol resensitizing serotonin receptors - not sure how true that is, but I have started taking large doses of it. I'm not really sure what else to try at this point. So I guess we'll see how that goes. God I feel nuts writing about all of this.
  7. hi i'm new at this forum and i'm brazilian, 20 years old, started effexor when i was 18 for depression, stayed on it for 8 or 10 months, with almost no side effects, after this tried going cold turkey , since then have been dealing with all possible kinds of side effects, i tried reinstatement on january of this year (after 4 months of wd) obviously didn't worked, stayed on them for more 5 months, went to rehab. tapered effexor there and started trazadone and seroquel. now i've been taking 150 mg of trazadone and 25 mg of seroquel, was kind of "ok" so tried to reduce trazadone to 100 mgs, wasn't able to sleep for 3 days, went back on 150 mgs, and added 2 mg of klonopin to use when needed, but since that abruptly quitting of effexor i haven't been the same, dealed with EXTREME anxiety (never was a problem before), SEVERE imsonia, sometimes 5 days without any sleep, chronic pain and numbess and poor coordination on the right side of my body. the left side seems ok, i have no idea why. derealization, poor memory, poor concentration, diahrrea, akastisia, poor stress tolerance, emotional numbess, brain zaps and brain fog, anyway i have been dealing with pretty much all the symtoms you can come up with, pretty hopeless, desesperated, regreted, scared, feeling like it will never be the same. i really want to know what you guys think, is there any hope for me ever being the same again?
  8. 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?
  9. Hello, I am 24 years old, and am currently going through what I think are Lamictal withdrawals. My story is rather long and complicated, so I will try to sum it up as best I can. If anyone wants me to explain anything further, I can do that as well. I was diagnosed Bipolar II in 2010 at 18 yeara old, and was prescribed Lexapro, Seroquel, Vyvanse, and Klonopin. I immediately felt like a zombie, and stopped taking everything but the Lexapro. Fast forward to May of 2016, I am only on 5mg of Lexapro now and feeling rather depressed. My new psychiatrist wants to try a mood stabilizer (I have always fought against doctors wanting to add new drugs to my cocktail). Unfortunately, my parents convinced me that a new pill would be the answer, and I started up on 25mg of Lamictal. For two weeks I took that and felt alright, a slight improvement I guess. Two weeks later I bumped up to 50mg and started noticing a decent improvement, but also some pretty noticeable side effects. Two weeks later, I upped the dose to 100mg, and the next day felt absolutely horrible. I got terrible flu like symptoms, rash on my hands and feet, swollen glands, spread throat, stomach pains, etc. I went to the hospital and they said it was just a virus. I continued to take 100mg of Lamictal. Two days later, the rash had now spread to my whole body and was extremely itchy. I went back to the ER, and again they said it was just a virus and had nothing to do with Lamictal. I took it upon myself to stop taking 100mg that day (June 5, 2016). The rash went away almost immediately, but the withdrawal symptoms were unbelievably overwhelming so I reinstated 50mg three days later when I couldn't take it anymore. I stabilized for two weeks on 50mg, until I got yet another itchy rash, this titem accompanied with a very dizzy headache and a lot of cognition problems. I stopped cold turkey again, and made it three days before needing to reinstate 25mg as the withdrawal was too much to handle. I then stayed on 25mg for a week (still feeling absolutely horrible the whole time). I experienced insomnia (jerked myself awake every time I was about to fall asleep), rapid heart beat, extreme anxiety, worse depression then I've ever had before, zero appetite (lost 13 pounds and am already underweight), dizziness, terrible brain fog, confusion, memory loss, dp/dr, shakiness under the skin, back and neck pain, extreme fatigue, bouts of crying, extreme anger, and much more. After trying to stabilize at 25mg for that week, both my pDoc and GP told me just to stop the 25mg as it wasn't making anything better and I was past the worst of it. They also prescribed me 2 weeks of Klonopin as I basically hadn't slept the past week. I took my last pill of Lamictal on July 1, 2016. It's now been two weeks since taking my last pill, and I'm not sure if I feel any better. One moment I feel alright and think I can push through, the next minute I feel like it's going to last forever and I should reinstate a small dose and try to stabilize there first. Then I think I've already made it through 14 days with no pills, and my symptoms are not nearly as bad as they were when I was taking 25mg of Lamictal at the end of the taper. The first week after stopping Lamictal I felt rather depressed, but somehow still hopeful that things would get better. I still had a very rapid heart rate, trouble sleeping, dizziness, and feeling generally uneasy, but it wasn't too bad at all. This second week has been somehow harder though, and I feel like I don't know what to do. I am now pretty dizzy all the time, my loss of appetite is back, and I usually feel pretty depressed and hopeless about the future. I also have almost no interest in anything that used to bring me happiness. It's getting somewhat overwhelming and I don't know what to do anymore. Should I just keep fighting? Both my mother and my pDoc think that I should keep pushing through and eventually things will get better. I want to believe that but I feel like my hope is fleeting me each day that I wake up and feel the same. I also am very addicted/dependant on Marijuana, and use it to sleep, eat, stop anxiety, feel better, etc. However, after this whole issue whenever I smoke it makes everything a million times worse. Unfortunately, when I don't smoke, all I can think about is smoking pot and that it will make me feel better. So I then proceed to smoke, feel worse, and then painfully sober up until I go through the whole process again. I want to stop smoking altogether, and have tried hundreds of times, but have never made it more than a few days before I feel like I'm losing my mind. I was taking .25mg of Klonopin 2x/day these past two weeks, but have decided to stop that now as I don't want to become dependant on it. I have also been meditating, eating healthy (when I do eat), trying to stay positive, trying to exercise and stay busy, got myself on a sleep schedule, and want to start taking some supplements. None of these things I was doing before all of this. I also scheduled an appointment with a talk therapist (as I feel I have some deep rooted issues causing my anxiety/depression) and with a Neurofeedback Center (in hopes of lessening my anxiety/depression, reducing pot addiction, and resetting my brain to its natural state). If anyone could offer any insight or advice or experience with anything I've been going through I would be extremely grateful. Right now I have so many concerns I don't even know where to start. Should I continue pushing through the Lamictal withdrawals in hopes the symptoms will reside soon? Should I reinstate any amount of Lamictal to stop the withdrawals symptoms? But couldn't that cause worse symptoms like it did when I was on Lamictal in the first place? Should I keep taking the Klonopin to help with anxiety/sleep or should I stop? Should I just cold turkey stop or try and taper down the Klonopin? Is it possible to already be dependant on Klonopin after only two weeks? I feel as though I may be dependant on it to sleep. Sorry for the long post, I'm not sure if that's alright, but I've been holding this in for a while and am not really sure where else to turn.
  10. Celen

    Celen

    Hi I am 43 and have been on numerous psychiatric drugs for over 20 years. I’ve been diagnosed with so many different mental health labels and have been on psych drugs for all. Over the last 8 years I have been basically bedridden. During the past two years I’ve had to fend for myself when I decided I wanted off all these pills. They have only made me worse. 2 yrs ago I came off cold turkey Abilify, Latuda and 20 mg of fluoxetine. I felt great until 3 weeks in the withdrawals set in. I haven’t felt well since but have managed to wean off 70 mg of vyvanse, 1 mg of clonazepam, 15 mg diazepam and 10 mg of fluoxetine. I am now working on the last 10 mg of fluoxetine. After that I’ll start tapering my trazadone or more of the benzos. All-of this has been a nightmare, nausea,vomiting, headaches etc. I can not leave my house most of the time because of debilitating anxiety. I guess what Im looking for here is information, support, and ideas on diet ( no gallbladder and severe GERD) and tips on helping withdrawal symptoms. I feel like I can’t think properly,my memory is shot and right now I really need some hope. Also I’ve gained 70 lbs.
  11. I was on Prozac and Clonazepam since October of 2015 due to a few traumatic things that happened that summer. I had a lot of anxiety, jaw clenching non-stop, nightmares, and sleep paralysis/hypnagogic hallucinations. My doctor added in 10 mg of Buspirone sometime in 2017. I weaned off both of them in the span of 3 days per my doctor as we just found out we were having another baby. Taking Prozac in the first trimester can cause cleft palate and cleft lip. Since the end of February, I have had the following issues and I cannot tell if they are getting better: - Dizzy/Faint/Lightheaded - In somewhat of a daze (I never felt like that when even on the meds) - Hands feeling like they are going numb - Numb lips/gums and sometimes my tongue - Feeling weird/off I am having a hard time just doing life right now. If that even makes sense. This is the first time I have ever come off of anything like that. Many times that I get up I feel like I may black out. From what I have read using Dr. Google it sounds like the withdrawals are most likely from coming off the Prozac. My question is, and I know this can range from person to person, has anyone else here been through this, and if so, approximately how long does it last? I am still on the 10 mg of Buspirone once a day because it is supposed to be okay during pregnancy. I have a friend who said it made her feel dizzy all the time. I am wondering if it could be prolonging the way I feel right now. I was a huge gym rat and I have gained 10 lbs in a month almost. I am having a hard time doing much of anything bc of how crappy I feel. I can barely stand to even use a treadmill right now and I have got to get out of this funk. It is awful.
  12. Hi. I hope I'm in the right place because antipsychotic drugs and antidepressants and benzodiazepines have caused permanent brain damage and I have trouble navigating on this sight. Is it possible to taper off geodon before gabapentin? I have read in the Road Back Program that I must taper off gabapentin and clonazepam before I can finish tapering off geodon. I am terrified of antipsychotic drugs. I want to get off it after I finish tapering off clonazepam. I successfully completed tapering off trazodone and propranolol and have tapered the clonazepam to 1 mg and have tapered the geodon down to 80 mgs. I was misdiagnosed as having schizophrenia and now am working with a team of doctors to taper me slowly off the drugs that robbed me of my memory and pleasure and motivation. I am desperate to get off these terrible drugs. Especially the clonazepam and geodon. I'm tapering off slowly the clonazepam right now. I have read that if you taper off geodon before gabapentin and clonazepam it increases the clearance time of clonazepam and gabapentin by as much as 50% causing you to go into clonazepam and gabapentin withdrawal even without lowering the dosage of the clonazepam and gabapentin. However, I have also read in the book "Psychiatric Drug Withdrawal" by Peter breggin md that you should make it a priority to get off the antipsychotic drug first especially if you are non psychotic. My doctor thinks I can just stop taking the geodon but I know that is wrong. I appreciate any help you can give me.
  13. Really enjoyed reading the information by the administrator on this site. I too was sold on the idea that I needed to reduce a benzo Clonazepam before the Nortriptylene but have had little success. When I read that its best to taper off the activating AD first it made total sense. I'm currently holding at 1.5mg clonazepam and have recently started reducing the AD, dropped from 25mg to 23mg over the last two weeks using the water titration method from this site, what I did was put the 25mg capsule of Nort into 25 ml of water and shook the combination and drew out 2ml of the combination for a 2mg reduction. Lat night after two weeks I dropped to 20mg. My question is do I continue to reduce by 2mg all the way to zero or use some different % ratio. Thanks and glad to be connected with this group,
  14. Hi, I just wanted to take the time to introduce myself and ask for some advice I have been on various ssris for 11years and about 7 months ago I decided to wean myself off celexa which I had been on for the last 5 years at 40mg. I weaned of to fast over the course of about 3 months and was off for a total of 1 month when I crased hard with anxiety, fear and depression. I went back on 40mg of celexa after being off for a month but got panic attacks and weird sensations in head. After 2 weeks the doc than got me off that and put me on Paxil for 2 weeks which only made things worse with bad anxiety and feeling dissacated with everything and my cns was all messed up. They than put me on celexa at 20 mg and a low dose of remeron for 3 weeks but no relief and was getting electrical sensations and burning sensation in body. I than checked myself into the hospital where the cold turkeyed me off the celexa and put me on neurontin. I was off celexa again for a week but I gave up all other medications and put myself back on 5mg of celexa for the last 3 weeks and have also been on .05 a day of klonopin now for 2 months. My current symptoms are. Severe anxiety Inability to concentrate Muscle tension Akathesia Tremor Burning sensation in chest and pain from time to time Vision problems Brain fog Some anadonia Some nausea And sensitive to sounds and some foods and vitimins My questions is what do I do from here? Man this is no fun just looking for some words of encougement if nothing else.
  15. Hello all, I`m new here. I`m also a member of benzobuddies.org forum. English is not my first language so I appologize for possible grammar mistakes in advance. The reason I joined your forum is that I`d like to come off Mirtazapine and Buspirone asap. I`ve been suffering from anxiety disorders since I was a teenager (I`m 37). I was diagnosed with GAD and SF. In the course of time a depression developed too, but nothing serious. In June 2013 I started to attend a psychotherapy due to social phobia which helped me much. My issues with psych drugs started after a renal colic followed by a surgery in April 2015. In May 2015 I first saw a psychiatrist in my life. I was looking for some relief. A huge mistake! She prescribed me Zoloft 50mg. At the very first night I got a horrible panic attack which I`d never had before. This repeated next night. I went to ER next morning and got prescribed Rivotril 0.5 mg twice a day. I had to stop taking Zoloft two weeks afterwards and got another antidepressant called Trittico (trazodone) which had no positive effect. I tried to come off Rivotril after two months, tapering 1/4 of the pill every week. I had terrible withrawal symptoms. I only survived a few weeks without Rivotril and then started to get panic attacks at night. So I began to take Rivotril again, this time only 0.5 mg divided into two daily doses which was sufficient for me. It was last September. I also went to another psychiatrist`s. We`ve tried severeal meds like escitalopram, moclobemidum, venlafaxinum, olanzapin, lamotriginum, mianserin so far to help me get rid of Rivotril. Only venlafaxinum (Olwexya) helped me with my depression, but it had side effects like restless legs and bad sleep with severe sweating so I had to stop taking it after six months (at the begining of April). I made three unsuccessful attempts to come off Rivotril while I was taking Olwexya. My depression returned, I started to feel drowsy and tired all day. I started my next taper attempt at the end of June. I took one 1/4 of the pill in the morning and 1/2 of the pill in the evening. One week later I took 1/4 of the pill both in the morning and evening. At night I had a nightmare, slept very bad. My withdrawal symptoms were: sleep disturbances, increased anxiety, social phobia, perceptual distortions, depression, poor memory and concentration, intrusive memories, weakness, fatigue, influenza-like symptoms, dizziness, nausea, diarrhoea, dry mouth, metallic taste, sweating, halucinations. My doctor said I couldn`t be phyzically addicted only on 0.5 mg. Very funny. At the end of July when I was on dose 0.2mg, I was hospitalized because I couldn`t go to work. They stopped giving me Rivotril almost immediatelly. I didn`t want to take any new pills. I just wanted some help to survive the withdrawal. I agreed with Buspirone because I considered it the least harmful. But later they tried to give me something to beat my insomnia - Atarax, Quetiapine, Valdoxan. Mitrazapine was the first one which alowed me to sleep. I didn`t feel any side efects besides horrible dizziness when I went to the toilet at night. Two weeks later they added Venlafaxine (California rocket fuel). I had many side effects including terrible panic attacks which I complained about. After all the meds my dizziness got worse. On September 9th I was released from the hospital. I agreed with my doctor to stop Venlafaxine 75mg within 10 days (I took it only for three weeks). Last Wednesday when I was still on 25mg withdrawal hit me. I had vivid dreams, influenza-like symptoms, mood swings and cry spells and terrible dizziness. It`s much better now except the dizziness. The dizziness is literaly ruining my life. I feel like I was constantly drunk. I can`t drive and I even refrain from walking. I suspect both Buspirone and Mirtazapine are the cause. I definetely can`t live with Mirtazapine because I sleep 12 hours day and still feell drowsy and tired all the time. I have no energy. They say my dizziness is somatized anxiety but I don`t believe it. Anyways, current medication has done nothing with it. I`d like to ask for your opinion which one I should start to taper first or whether I can taper them both at the same time? I`ve been taking them only for about two months. 10% taper a month seems very slow to me. I`ve never had big issues when coming of antidepressants. What do you think? Thank you.
  16. Sorry if you're posting this in the wrong place, I'm new here, I'm not fluent in English either. Please do not consider possible errors. I used clonazepam for three years, I tried to quit this twice and it was absolutely horrible experiences. I would like to understand how to do this safely, I was directed to this forum via Facebook, they said that I could get help here and that a moderator could give me access to benzobuddies. I can not sign up for benzobuddies. All email I submit for registration counts as invalid. My question is mainly aimed at understanding how I can measure the 10% decrease from previous dosage. When I heard that the correct thing would be to reduce the dose to 10% per month, I figured it was 10% of the initial dose. I use 20 drops of liquid clonazepam, how can I measure 10% of 18 drops? Is not that impossible?
  17. Hi to everyone and thank you for accepting me into this group. I was planning on tapering from my Wellbutrin after I had been stable on it for a couple of months. I have only been taking it since January but had been experiencing what I thought were just increased anxiety and agitation from it. I was inpatient at the time and the doctors told me that those weren't side effects and it was just my own anxiety. I have a long history of panic disorder which was under control until my husband and I decided to move to another city due to a job change. After I left the hospital it took a month to be able to get in to see a psychiatrist. Unfortunately she had a very strong accent and though I think accents are neat I have had trouble understanding people with accents since I had surgery to correct a badly deviated septum. So I had to wait another month to see a different psychiatrist. I was having a horrible time on the Bupropione the whole time but I was able to get some help from a mental health urgent care clinic.They increased my Buspirone from 30 mg to 50 mg which really helped with the anxiety I was experiencing from the Buproprion, I finally got in to see a new psychiatrist and the first thing she wanted to do was take me off the clonazepam. She wanted to cut my dose in half but I only cut it by a quarter. About five days later I was in full blown withdrawal and she wouldn't believe me. She said if I was in withdrawal I would be in the hospital. I have been going to a group and one of the facilitators told me I should go back to the mental health urgent care which I did the next day and they referred me to an addictionologist. He has been wonderful. He confirmed that I was indeed in withdrawal. I was pretty much through it by that time but at least he understood. It had been about three weeks since I had tapered down on the clonazepam and he recognized that the bupropirone was causing me problems so he told me to drop it to half. After my recent experience I chose to drop it by .25 again. I went straight into severe withdrawal and he reinstated the medication after only two days of a reduction. At this point I would wake up every morning with severe trembling and anxiety so I switched my night time clonazepam to the morning and that caused those symptoms to remit. I was feeling really good and enjoying my days. Getting out into the sunlight, walking my dog, mowing the lawn. It was great. Anyway I learned about a device called Cranial Electrotherapy Stimulation (CES) that is supposed to help you with anxiety and depression and since I want to get off my medications I discussed it with my psychiatrist. He thought it would work so he gave me a prescription for it. I started using it 15 days ago. The first two days were great. I woke up with no anxiety and I felt even better than ever. Then I started having increased anxiety on the third day. One of the things that the CES device can do is increase the effectivness of your medications, and their side effects. About a week into my use of the device the side effects from the Buproprion became intolerable. It turned out that the clonazepam had been disguising akathisia and the CES brought it out. Of course this happened over Memorial Day Weekend so I was left to my own devices and the wonderful counsel of my concerned husband. We decided to drop my Buproprian to 75 mg IR to see if that would help. Unfortunately it did not. I didn't seem to have any withdrawal symptoms either though. On Tuesday we went in to see my Dr and he recommended a beta blocker for the side effect. It worked wonderfully. Unfortunately it also caused me to become depressed. The Dr recommended that I go off the medication completely at this point. So starting the next day on June 1 I went cold turkey. The withdrawal symptoms started immediately. I have had crying spells and unending anxiety. I have continued to use the CES as it is reputed to help with withdrawal symptoms and to help prevent relapsing into depression. It seems to help but not as much as I would like it too. I know that my brain has to remodel itself and it will take time even with the help of the CES device. I have also been using L-theanine which helps a little. I am really trying to find some way to reduce the anxiety as it has turned me into a severe agoraphobic. I hide in my basement so I don't even have to look outside because that is anxiety producing in itself. The only way I have been keeping sane is to keep my brain occupied by surfing the net. I have also been reading The Mood Cure trying to find something that will help with the anxiety. I do have extra clonazepam that the Dr gave me and I have Baclofen but I don't want to have any more addictions than I already do. Once I get off the Buproprion I am planning a liquid taper of the clonazepam. I really feel like I am in between a rock and a hard place because if I reinstate the Buproprion at all then I have the akathisia to deal with and the medication for it makes me depressed. I would really love any input that anyone has for me. I have been thiking of trying some of the following for the anxiety. Lemon Balm Valerian Root Inositol Niacinamide (the Niacin makes me itchy from the histamine release) L-glycine Taurine Ashwaghanda I even read that someone coming off of Buprorpion had some success with L-phenalalanine but I have anxiety issues so I don't know if that would be counter productive or helpful becasue going off of the Buproprion is what is causing this. I'm also afraid of long term consequences to the cold turkey but I don't know what else I could have done. I would really appreciate any comments or suggestions. Thank you, and thank you for this wonderful group.
  18. AlanHarper

    AlanHarper: need help

    I am new here, although I did try to start an account awhile back. I am sure there is much on Paxil withdrawal. I cam off of 2mg of klonopin and still am on paxil which I wish to discontinue. I am using Alan Harper as pseudonym. Is there someone out there who is willing to help me in my desire to stop using paroxetin 20mg.? Thanks.
  19. Moderator note: link to Linus' benzo thread - Linus: Klonopin question Hi everyone, I like this forum, I think the moderators are sensible people who give good advice, compared to some other websites. I have already come a long way with regards to withdrawing from Escitalopram, from 30mg to 1.8 mg. It has been hell but hey here I am I know that by now even small cuts are problematic. My first question would be if anyone has a clue as to whether there comes a point in the withdrawal where things get easier (like at 1mg or 0.8 mg) or does it stay funky all the way down to zero?
  20. Been quietly observing and reading other peoples posts and finally decided to post my story. My path with AD started with a full blown panic attack. I had never in my life experienced a panic attack so it was very difficult at the beginning. Everybody's different. My panic attacks were debilitating lasting for several hours. Went to see my doctor and was quickly put on benzos. Started with xanax 0.5 mg and was quickly raised to 2.0 mg. Later it was switched out to klonopin 2.0 mg. It did control my panic attacks and my anxiety attacks. Later on I was told to add an AD to further control my panic attacks. This was the fun part where I became my own guinea pig where I had to "FIND THE RIGHT MED" for myself. Initially started with lexapro and was told that it could take up to 4 months for the drug to kick in. 4 months past by and it did nothing. lexapro had no effect on me. Tried viibryd, celexa, paxil, and prozac. Settled with paxil and klonopin for a long time. Towards the end made the jump to cymbalta and klonopin. If it wasn't for people around me telling me how I've changed, over the time frame that I was on these drugs, I would have probably continued taking these drugs. I've lost all emotions nothing in the world gave me any enjoyment. Started drinking heavily to the point where I was drinking every day. Spent money like money grew on trees. I had no apathy at all towards others. I became completely indifferent towards the entire world. I have so much respect towards people here that are maintaining their strict taper schedule. I tried to slowly taper from my drugs but I could never keep it myself. At the first sign of withdrawal I kept running back to my drugs. I decided to throw all my meds out and go the cold turkey route. I fell into a dark abyss. I didn't bother going to no doctor because I knew it was my fight and my fight alone. Woke up with severe panic and dread. It was as if all my nerves were fired up. Every person was associated with a flash back from the past with a very negative flash back from my past. For example, my dad was asking me how I felt and I had a really bizarre flash back from the past where my dad was not so kind to me when I was a kid. It was a memory from the past that I had forgotten for a very long time. This flash back resulted in me with a rage like emotion towards him. Pretty much everyone I met, that had an unkind past with me, brought up these negative flash backs. Entire body feels numb. Light/noise sensitivity. Blurry vision as if I'm surrounded by fog. All my muscles were sore, aching and shaking. Tingling burning sensation on the skin. Itchy anus. Joint pain like I've never experienced before. Difficulty breathing. Flu like symptoms. Severe headaches. Head felt really heavy as if there was a rock embedded in my brain. Messed up sinus. Weak legs. Weak neck. Difficulty speaking. Difficulty balancing myself. Coordination skills severely impaired. Severe tinnitus. Body feels heavy as if gravity increased. Severe dp/dr. One day I spilled my entire plate while eating and I could see my plate fall down in slow motion in 3-D. One day I was cooking and accidentally burnt my hand and I could feel the pain from my hand travel all the way to my brain. I'm pretty sure there were a lot more symptoms that I really can't remember them all. It's been six months now that I've gone cold turkey. I'm still a long ways from recovery but looking back sure as hell feels like I've made some progress. Going cold turkey put my body in full reboot mode and slowly one by one I get to feel parts of my body come alive one by one.
  21. Hello everyone, thank you for creating and building such a fantastic resource. It’s so helpful to read about the journeys of others here. I was advised by my GP to speak with a psychiatrist in April 2016. The GP suspected I had depression & anxiety. I met with a psychiatrist for an assessment. I’d been through a lot of stressful experiences in life. Life had dealt me a tough hand, and I was already quite vulnerable when I arrived in his office. At the end of the assessment, the psychiatrist diagnosed me with depression and anxiety and prescribed me Bupropion 300mg and clonazepam 2 mg+ per day. I was never keen on the idea of taking medication, but the Dr said I needed it as I had “disorders” caused by chemical imbalances, and that I was lucky to have made it this far without it. I don’t believe that for one moment and now feel I was misinformed. If I had been warned about the side effects, I would never have put them in my body. I’ve been through some hard times, but the medication has served me with the hardest and most agonising four months of my life. To make things worse, after a couple of months seeing him every few weeks the psychiatrist offered me a job. It was a slightly unusual series of events, but I felt lucky to have been given the opportunity. I worked hard, was often praised for it and I was given reassurance my role was pretty much permanent. I loved my job. It gave me purpose and a role in the world. My self-esteem rocketed as I felt I’d been specially selected for showing signs of promise, it changed everything. However, the different roles called for different protocols, and the roles of “therapist” and “boss” required disparate and often conflicting styles of relating. The Doctor providing me with a job and treating me outside of the clinic caused the boundaries between Psychiatrist and employer to become extremely blurred. Even though it was unorthodox, I pinned a lot of faith on the Psychiatrist, his advice and the job he gave me. He gave me hope and faith for the future. August 2016: Prescribed Sertraline 100mg due to depression remaining and increasing number of bad moods. October 2016: While at work the Psychiatrist commented he suspected I had ADHD. Despite not suffering from day to day symptoms I completed the DIVA ( ADHD assessment ) with him, He prescribed methylphenidate 10mg 2-3 times a day. Over time I didn’t feel any improvement in mood, so the dose was increased to 20mg x5 (up to 100mg+ per day). I asked the Psychiatrist about alternative ADHD treatments as I was apprehensive about taking more medication. The Psychiatrist informed me that there were no ADHD treatments in my area and even if there were he would not be prepared to enter into a shared care agreement. I believed treatment with him was my only option. I was told there were no services or specialists other than him and the only treatment available was medication. March 2017: The symptoms started with a lump sensation in my throat like there's some thing stuck, maybe it’s my thyroid. I went to the GP who said it was globus or anxiety and it was nothing to worry about, but I know it’s not anxiety as it’s there even when I’m not anxious. Next came tremors, dizziness and chronic fatigue. I was struggling to think, speak and walk. I felt as though a part of my brain had shut down. I had strong pains in my chest, dull aches that moved around my back and occasional shooting stabbing pains in my back and leg that stopped me in my tracks when I did walk. April 2017: The relationship seemed to work well initially but became very confusing until eventually I was dropped not only occupationally but therapeutically. My false sense of security was pulled from beneath my feet. I'm sorry to say last time the Psychiatrist, and I spoke he was abrupt, abrasive, insensitive and rude. I’ve been left in shock, fear, trepidation and with more health problems than before I met the Psychiatrist. At the time I thought the stress of losing my job caused me to become unwell, but after discovering James Moores Mad in America podcast, listing to peoples stories and reading a little, I think I’d reached a tolerance point with the medication and started to have terrible side effects. By this point, I’d lost faith in the Doctor so felt I couldn’t ask him for help. I think part of me knew it was the medication as I went to my GP, firstly to find the Psychiatrist hadn’t been keeping my records up to date. I told the GP what I had been prescribed, and I was told it would be impossible to identify what was causing the problems. I naively agreed with my GP that the best option would be to stop taking all medication, however stopping without tapering has left me with a long list of withdrawal symptoms. I stopped taking sertraline, clonazepam & methylphenidate that day and cut my dose of bupropion in half for one week then stopped the following week completely. Every symptom I already had, got worse, tremors, dizziness, feeling unsteady, feeling like I might pass out, loss of coordination, back pain. The fatigue was so bad, I couldn’t walk for more than a minute or so which lead to me not being able to leave the house. My partner was having real trouble getting me out of bed in the morning, and after a few hours of being up, I’d need to go back to bed due to feeling exhausted. I think I was putting it down to severe depression, but I didn’t feel depressed, I just felt numb. After a couple of days of stopping I started to get really bad night sweats, I’d wake up stinky, drenched with my mouth tasting how I smelt, it was horrible. The chest & back pain continued to get worse and progressed to tingling and numbness in my arm. I’ve been to the hospital three times in the past four months in various states of feeling close to death but sent home every time. I’ve been to the GP many times as the side effects have left me with so many physical symptoms and feeling so ill. I had numerous blood tests and even though I felt like I’d been poisoned every test came back clear. August 2017: The fatigue has lifted slightly, the part of my brain that felt as though it had broken is slowly coming back, and I’m smelling much better :). I continue to have flu like symptoms and intense joint and muscle pain, mainly in my back, shoulder and arm and I’m not entirely sure if the pain will ever go away. I feel like a very rickety eighty-year-old. My GP finally acknowledged some of these side effects last week. They haven’t been able to give me much support due to stopping taking so many different medications at the same time and stopping cold turkey. The GP did frustratingly say some of what I’m going through maybe down to the return of depression and anxiety. I’m only depressed as I’m in so much pain and have anxiety as my nerves are messed up. I’m a little worried that the medication has caused permanent damage. I accept a return in my depression and anxiety, but I have so many physical difficulties that began following and since stopping taking the medication. I trusted the Psychiatrist and put my life in his hands. Looking back, I feel like I was led astray, betrayed and like I’ve been chemically assaulted. Before everything went wrong, I recommended the Psychiatrist to some friends who also became patients of his. They were given a similar diagnosis to the one I’d been given, told they also had chemical imbalances and they too prescribed a similar cocktail of medication including methylphenidate and told to contact him when they needed a repeat prescription. After a couple of months, they both began asking me why he wasn’t returning their calls or emails. When I spoke with him about this, he said they had contacted him last minute, and for that, he wasn’t going to reply right away as he didn’t do last minute. Eventually one of my friends requested to have her care transferred as she lost faith in him. The other works at one of his clinics, and is still having problems with him returning her emails and calls and providing her with prescriptions when needed. She has told me there'd been many occasions recently that other patients of his have called his clinic in tears as they are unable to get hold of him. I also know a woman who was under his care at the inpatient unit long before I met him. She said he had given her a combination of medications. She told me it made her feel like a zombie. For one reason or another, she was transferred to a different psychiatrist who questioned why she was on so much medication and immediately began to reduce her dose. No one was warned about side effects and withdrawals, supported, monitored or made aware they’d have to request prescriptions on the Psychiatrists personal terms. It was hugely irresponsible of him to tell people they need medication due to a medical condition and chemical imbalance and to encourage dependence on medication and not provide support, information, monitoring and often fail to provide the advised medication to patients dependant on it. I’m so happy to have found this incredible community and source of information, it's allowing me to start making sense of what I’ve been and am going through. It’s such a relief to learn I’m not the only one feeling this way. The support and compassion I’ve seen on this forum is incredible and a brilliant way of making good of what everyone here has been through. Trusting I’m going to get better and connecting with others isn’t easy at the moment, but I’m hoping it’s going to get easier. My heart goes out to everyone that has been through or who is going through withdrawal. x
  22. 8 months ago I was on. Primidone 500mg Vraylar 6mg Cymbalta 120mg Zoloft 200mg Clonezapam 2mg My kidney function had dropped to 42% and a certain NP for a award winning psychologist continued treatment after noticing major muscle movement disorder. After a few months of this she stopped vraylar 6mg cold turkey. I had a reaction within days of cognitive impairment. I could not handle ANY external input. For a month I could only stare at the ceiling in total darkness and no sound. No TV and food had to be something I could grab and eat in bed in the dark. I lost 40lbs in 3mo because of stomach issues and me being unable to get food for myself. When I confronted her about my problems she informed me it could not be medicine related and sent me to see her friend a counceller who agreed with her and added that my condition was totally " behavioral " I was still on everything except vraylar. That is when I started doing some research and quit seeing both doctors. I had a genesight survey which NP had access to that listed 3 meds she had me on as a high risk and I am a poor drug metabolizer. In the drug interaction checker I showed her 5 serious interactions which she ignored. I was in a state of total apathy, did not care if I lived or died. I could not find any help in the psychologist field. I could not even manage to keep myself fed or handle phone or internet. I begged several times a Dr I had seen before her to help me but she would not accept me as a new patient. Finally after 50 calls my mom had to make...because no doctors were accepting new patients or they did not take my insurance....i got an appointment with an neurologist/psychologist I had seen before. He was amazed the amount of medications I was on and recommended I start coming off them. However he could not manage my taper but did recommended a taper that I followed. I finally got into see a local psychologist who agreed on taper....which was basically drop one at a time by half every 2 weeks. Way to fast I believe after reading your site. I cannot get anyone to answer what happened to me. It's now been 7mos and I can at least type and watch tv.....i still have crippling anxiety and depression. I have came off Cymbalta, vraylar, zoloft, and halfed clonezapam. But I'm still having horrible symptoms I never had before. I've been on at least 12 antidepressants and antipsychotic medications over the past 8yrs for bipolar. Before that I was on nothing for 10 years with no problems. I did have issues in my teens. But it's been downhill ever since I had a nervous breakdown due to extreme stress that lasted years 8 years ago and I started trusting doctors that I needed medication. I had to go on disability 5 years ago due to medication side effects. Before the pills started I had a successful career and ran half marathons. I am thinking about contacting a lawyer. Does anyone have experience with such a drug combo, how long this will last? What happened? Or if seeing a lawyer may be a good idea?
  23. Hello, all! I've been reading the website for the better part of an hour, now, and it seems to be an invaluable resource, a scientifically-sound one, for this complicated and severely-unstudied process of stopping medication. I've been diagnosed bipolar type 2 some 8 years ago, having been under some type of treatment every day since. My diagnosis came after visiting 4 different psychiatrists (as I would not accept the diagnosis, every time a doctor would say it to me). What I am currently prescribed: - morning - 15mg Aripiprazole - morning & evening - 2.5mg Oxybutynin - morning & evening - 40mg Propranolol - evening - 400mg Quetiapine - evening - 1000mg Sodium Valproate I also have access to Clonazepam, 2mg pills, for an as-needed dosing, but I haven't taken that in a very long time, now. Since this Monday, after an absolutely horrific psychiatrist visit, I've halved all my medication... Each dose, I take at the same time, but would break up the pill in half. I've been feeling great (to be honest, I've actually been feeling, which is an accomplishment), but I want to continue this down to 0mg of each substance. I've read the topics on polysubstance stopping, but it is not clear to me what best course I should follow, given the above cocktail. Can I cold-turkey the Oxybutynin and Propranolol, and after focus on tapering off the mood stabiliser, with an end goal of doing the same with the antipsychotics? My initial train of thought was to halve each week, and I was prepared in a few weeks' time to take a vacation from work, just so I could lay in bed with withdrawal symptoms. This is based on me stopping the Quetiapine in the past (OK, some 4-5 years ago), under doctor supervision, because I had been selected for a medical trial... That process took around 2 weeks, and even if I was prescribed Ambien to sleep, it would only "knock me out" for 2-3hr, after which I'd play video games, as I couldn't sleep at all. It was a painful process, during which I spent about a week in bed, but if the process can be the same this time, I'm ready to withstand all that pain, just so I could be myself, again. Thank you all for any contributions, in advance!
  24. Hi everyone, I have been on Klonopin since 2013 and started my taper in tolerance withdrawal this past February at 2.5 mg's a day. My method of tapering was to liquefy .5 mg's in 100 mL's of milk and reduce by 10% a month while taking the rest of my dosage dry. Things were far from good but ever since I've been at about 1.75 when I slowed to 5% I've been completely non functional. I'm extremely dizzy, have DP/DR, horrible morning anxiety, agoraphobia, bad gastro issues, insomnia, depression and many other symptoms that I'm sure many of you suffer from. I know that everyone is different and that a MT was not a guarantee to a smooth ride by any means but I at least thought it would be bearable. I don't work, I don't see my friends, my memory and photo-sensitivity are so bad that I can't really even watch TV/movies/sports and I honestly have no idea how anyone can live like this for a prolonged period of time. My prescriber is extremely unwise when it comes to benzos and attributes any worsening in my symptoms entirely to my "underlying anxiety disorder" while pushing drugs even though I've been seeing her for three years and have gotten MUCH worse as I unwittingly let her up my Klonopin dosage and try several SSRI's and other psych meds. I just don't know how to progress. I am at 1.5 mg's so I am just holding there and taking my full dosage dry for the time being but I don't know whether to try a cut and hold or find someone who will oversee a Valium crossover (which I've been looking for to no avail for a long time) or what. I just don't know if there's anything that I could be doing to limit the amount of suffering that I'm going through and I'm feeling very hopeless and confused. I don't ever seem to "stabilize" but I don't know how to proceed. I'm not sure what I'm looking for to come out of this but any advice you can offer would be greatly appreciated. Thanks.
  25. Hi everybody! I am Julz, a 33 year-old female - polydrugged to my eye-balls Ten years ago, I fell into anorexia and depression, soon unveiling terrible anxiety. I was referred to a psychiatrist (in France) who prescribed me medication and also gave me psychotherapy. Regarding the medication, different combinations and doses where tried and I eventually found myself on a prescription which seemed to suit my troubled mind (Escitalopram, venlafaxine, clonazepam and diazepam) - did it ever do anything? I still haven't got a clue. I trusted this doctor. This is my initial prescription: Escitalopram: 20mg 20mg 20mg - (yes, that is 60mg...!!!) Venlafaxine(MR): - - 75mg - Clonazepam: - 2mg - 2mg Diazepam: - - - 10mg Time passed and psychologically, a lot changed. I moved away from where I used to live, totally changed my environment, and went for a fresh start. But I was still taking my medication as prescribed. My General Practitioner (in charge of my prescription in my new environment) convinced me to lower the Escitalopram (on the grounds that it was "bad for my heart") and I managed, between 2011 and 2013, to come from 60mg/day to 15mg. How? By jumping 5mg at a time every now and again. I had no idea... again, I more or less trusted this doctor who was willing to prescribe me the drugs I was clearly physically dependent on. The withdrawals I experienced were uneventful. I did feel something was happening but within a few days, I always felt the same as before the drop. Between 2010 and 2014, a LOT had changed as I finally got an MSc BUT I had fallen into terrible exhaustion and had no life. How did I get my degree? A struggle every day. I then began to question this cocktail of drugs, I'd been on them for 10 years and was still taking them as prescribed because I was physically dependent. That was clear enough! It then hit me: my meds were probably incapacitating me rather than providing any help! The realisation came as in January 2013, after I managed to lower my Escitalopram intake from 20 to 15mg/day in a single 5mg step (...), I began to feel even more tired during the day, exhausted - I simply had to nap every single day. After some personal research, I went to my GP and told him I didn't believe in keeping our focus on the Escitalopram because it seemed that the more I decreased it, the more sleepy I'd get during the day, considering my benzo intake (at that point, I was taking 3 hours' naps), and I could not live like that! Fortunately, before I was able to drop a pill here and there as instructed by my GP, I found the BenzoBuddy website and managed to find a taper method to gradually come off clonazepam. From December 2014 to July 2015, I came from 4mg to 2mg and am now below 1.9mg and still tapering off successfully. I decided to join Surviving Antidepressants as I want off ALL any medication which alters who I am. I believe in other ways to manage my weaknesses - I am not ill, I have a tendency to be anxious and this is not new, I was an anxious child but I had emotions too. I'd like my emotions and my whole life back... I realise I know NOTHING about anti-depressants, I surely did not know about Escitalopram's potency and am still in shock from the news. My initial plans (supported by a psychiatrist I saw in February 2015) were to come off clonazepam (bz), then diazepam (bz), then Escitalopram, then Venlafaxine. In the light of what I read on this wonderful site, I wonder whether I should stay of Valium (diazepam) while at least tapering off Escitalopram, when I am done with clonazepam... I realise I need knowledge myself because sadly, doctors haven't been helpful at all... so far... Thanks for welcoming me on your wonderful Forum! Julz xxx
×

Important Information

By using this site, you agree to our Terms of Use.