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  1. Hi guys, sorry this may be a long post, I think it is okay to share my story on this. I am 21 years old, a college student about to graduate, and I have been on an SSRI for about 5 years now. I was diagnosed with ADHD and GAD when I was about 12, I have always been somewhat anxious and had issues with regulating my emotions. In 2013 my girlfriend broke up with me and I was really sad and feeling hopeless. After a few months of being down and also anxious, my doctor (pediatrician) decided to put me on 5mg of Lexapro. The Lexapro seemed to help (I think?) and I recovered somewhat quickly. Over the next few years, however, my doctor fluctuated my dosage quite a bit. I would get anxious, he would up my dosage, and then I would become a zombie and he would lower it. It did seem to blunt my emotions on a high dose. Other than that it was fine. However, the summer after my freshman college, I became extremely anxious and had an existential crisis, prompting my doctor to change me over to Zoloft and Trazodone. When starting Zoloft, I took 50mg and worked up to 100mg. It possibly helped my anxiety but my emotions became blunted again (or maybe it was depression?). I did not feel hopeless or sad, but I kind of lost the ability to have pleasure over simple things. After going through a hard time on Zoloft and Trazodone feeling empty and dull, my doctor and I decided to taper off to see if that would help. Every time I tapered, we would allow three weeks to go by to see if it helped. I went from 100mg to 75mg to 50mg to 25mg and eventually to nothing. Every time I lowered, I felt a little more in touch with my emotions. With the Trazodone, I stopped cold turkey on a dose of 50mg. When I went completely off of the Zoloft and Trazodone, I started having crying episodes, brain zaps, insomnia, anxiety, occasional anhedonia/brain fog, and severe social anxiety. After a month or two, all of these symptoms went completely away (except sometimes the anhedonia/brain fog). I was doing good and feeling very in touch with my emotions. After a few months off of the Zoloft though, the school year was coming back around, and the girl I had been dating for 2 years broke up with me unexpectedly. It devastated me and left me feeling sad and hopeless. I was crying all of the time, I was thinking about her all of the time, losing the ability to feel pleasure, and had anxiety because I still saw her every day. This continued on through the semester and I went home for winter break feeling depressed and anxious. I was feeling brain fog/anhedonia, and lost overall enthusiasm for life. It got bad enough that I knew I needed help, so I started talking to a therapist (I had seen a few before this one) and it was helping. I still was depressed, but was slowly improving. I started taking Adderall again to study for a certification exam over the break and this helped boost my mood tremendously. It cleared my mind, helped with the brain fog/anhedonia, and made me feel a little more peaceful inside (less racing thoughts). My psychiatrist decided he wanted me to take Trintellix and put me on a 5mg dose. I went back to school feeling down and anhedonic again. All the progress I made during seemed to start disappearing. I stopped taking the Adderall, and once the Trintellix seemed to start working I started becoming extremely anxious. I felt extreme depersonalization, started having weird sensory problems (visual snow, eye floaters, tinnitus, and my body started fluctuating between feeling tingly and numb) and was scared. My doctor upped my dose of Trintellix to see if that would help. I ended up taking Ativan to help with the anxiety. I was feeling less anxious but still had the sensory/depersonalization problems. Not to mention, my emotions went away again. The Ativan lowered my anxiety but made me feel completely dull and emotionless. I ended up tapering off of it and feeling better after a few months, but having a lot more anxiety/sensory issues. Since this (which was earlier in the summer), I started taking Adderall because I read a lot and it seemed my problems were kind of related to Adult ADHD. I always feel internally restless and have a hard time focusing, and taking therapeutic doses (20 mg or lower) seem to calm me down and clear my mind. Not to mention, it helps with my emotional regulation problem. Overall my academics and state of mind are improving. I have lowered the Trintellix from 20mg to 10mg over two months. I have had more sensory problems and anxiety since lowering the medicine, but it seems my emotions are slowly coming back. Every now and then, I get a nostalgic feeling that reminds me of what life used to feel like. It gives me hope. But I have been so up and down for the past 5 years, I am sick of feeling so unstable. I want to have emotions again and not deal with brain fog/anhedonia and anxiety for the rest of my life. I didn't have the former problem until taking medicine. I want the sensory problems to be gone. They only started after I started taking Trintellix. I need help with tapering off I think. Does anyone have any advice for me? I want to learn to treat my depression and anxiety in natural ways, and learn to regulate my emotions better. I want to believe I can live without taking medicine for these issues, because they only seem to exacerbate them. Do I have any hope of being stable again? I always feel uneasy inside and am constantly trying to distract my mind from this. I am sick of being anxious about these weird symptoms, everyone thinks I am crazy and writes me off. Will slowly tapering help this? I long for a day that I am not constantly thinking about being better, and can handle life's ups and downs. I am not wanting to be perfect, just to be able to not always think and worry about my mental health. I am always worrying about exercising enough, meditating enough, sleeping enough, eating well enough, and lowering stress enough. I think my issues could be related to tons of different things, but it is so hard to tell when you are put on medicines that only seem to compound the issue. School has been a big source of stress/anxiety and I am almost done, so I really want to take the time to improve my physical/mental/emotional/spiritual state of mind so life is not always this rocky. Thanks for listening, sorry this was so long.
  2. I have been on citalopram since 2009 then it stopped working. The Dr put me on citalopram and mirtazapine combination which worked for a while then that stopped working. The Dr then put me on mirtazapine and Venlafaxine 150mg XL combination which workes for a while again ans then stopped working. The Dr put me on amitriptyline 50mg saying thay would be the best drug for me while i took 8 months to slowly remove each bead from Venlafaxine capsule to come off it. As soon as I took my last beed i went into crazy angry depression. The dr increased my dosage of amitriptyline from 50mg to 150mg but the side effects were horrible and at this point i got sick of these meds and decided to quit CT. I had horrible withdrawal symptoms and i started acting like a child and not being able to walk, had balance problems. I reinstated back to 50mg amitriptyline since april 2018 and i have been getting worse. I cannot sleep. My vision is so badly affected that i have grainy vision and floaters have increased dramatically . I see after images and it's as if the lights have been turned off. When i begin to fall asleep, i start to have dreams before i actually fall asleep and my brain keep. Waking up just before i am about to sleep. I cannot follow conversations, I mishear things all the time. I am totally dependant on others and i feel people think i have gone crazy. I don't know what to do i am getting worse and worse. I often trip, lose my balance. I hardly have any short term memory and cannot do simplest of things. I cannot even watch anything on TV as i cannot follow.it I'm having major concentration problems. I don't know how. I'm writing this. I cannot work or drive. Please you have no idea how i am putting these sentences together. I need urgent help. Please advice. I have no energy, no appetite. If I'm posting this in the wrong place, please accept my appology as I can hardly read and understand things. P
  3. Hello everyone. I'll try to organize this as best as I can. There is a lot going on. I was on benzos from age 17 to 36 and on Cymbalta from age 35 to 36. Went off both together for a 2 year nightmare. Absolute pure hell. I wont get into the details and symptoms of that withdrawal in this post as it is it's own little novel. Some things improved during those 2 years and I feel I've beat the benzo part of the nightmare even still, but at age 38 I was still suffering enough that I agreed to go on Lexapro to see if I'd improve. I did improve hugely but it stopped working as well after 3 years and I was switched to Prozac. I have taken the Prozac ever since and it felt like it was failing around 4 months ago. I missed a lot of doses around 3 months ago and just tried to stop CT for just over a week around a month and a half ago. I started feeling withdrawals so I went back on and the withdrawal feeling is still getting worse. My memory and focus went first, then the inner restlessness and anxiety started and dizziness. I am also having the disconnected dream like feeling 24-7. I am so depressed and fearful all of the time. I've been taking the Prozac without missing a dose for over a month again and this is still happening to me. It's as if the combo of Prozac tolerance and coming off for the short time has started a withdrawal that even going back on can't stop. My doctor wants to take me off the Prozac after a slow taper and start me back on the Lexapro. The hope is that since it worked before and I've been off of it for almost 3 years that it could pick me back up and end this nightmare I'm back in. I am really considering just tapering the Prozac and staying off all ssris; so no going back on Lexapro in that case. I am so afraid of entering back into a nightmare like a was in coming off benzos and Cymbalta. My current state is terrible but the previous experience was truly worse; being benzos and Cymbalta together. It is really hard t say what withdrawal symptoms were coming from which pill. There were so many. I am so terrified of how I am feeling right now, but mostly for the days to come. If I come off the Prozac entirely I know my current state will worsen. I will be thrown back into a situation similar to the first nightmare. If I taper the Prozac and go back on Lexapro and it actually works, I'll still be doomed because I'll be back on another pill waiting for it to stop working again and most likely going through it all again. If I go back on the Lexapro and it doesn't work I will just aggravate my current symptoms with throwing more chemicals on my already hurting brain. The first time around withdrawal I had terrible akathisia and I am already feeling it brewing and I am still on the Prozac. I don't want to go through this again! Also from what I've been experiencing this month it seems a lot of what I assumed were due to the benzos were possibly due to the Cymbalta withdrawal as it's so similar. Also, I forgot to mention that I am on 500 mg of Depakote XR as well. I was put on this a couple of months after the Prozac as I felt a bit agitated. It helped but I got worried about my liver and quit it after 4 or five months and had a mild withdrawal from that but it passed. Just a couple of weeks ago after my current situation started I went back on the Depakote to see if it would help and it hasn't. I'll most likely be stopping it again as well. I had an account on Benzo Buddies during that ordeal and it gave me an outlet and some hope. I've set this account up here and got my story out in advance as I am leaning towards just stopping the meds and I'll be needing all of the support I can get! I'm seeing my doctor on January 3 so whatever I decide to do it will be starting then.
  4. Hi All , I need your help ! I was on low dose of Amitriptyline ( 10 mg ) from Sept 29 th to Nov 9th , approx for 1 month. Was given this for low grade vascular headache Now I am 2 months off the drug , but still have issues. Approx 2 weeks post stopping the drug i started having severe tinnitus in both ears and still have it now , light sensitivity , brain fog , difficulty in concentration I had anxiety which I feel has been reduced since beginning of January. I got my tests done for MRI and all health tests everything came out clean , visual tests and macula degeneration tests also done Opthamologist message : Amitriptyline is neuro and ototoxic : your body will wean it eventually , he said it will take a month and I was actually getting better but BAM ! Jan 3rd week I was down in dumps again November Post stopping the drug : No Changes , just little bit of fogginess , headache Dec 1st week to 2nd Week : Muscle pain /drowsiness dec 3rd week to Dec 4 th week ( worst ) : i had grainy vision ( visual snow ) only on walls may be and then night vision was pathetic , brain zaps I was miserable was in dumps . Jan 1st week to 2nd week : On Jan 2nd when I work up my anxiety was gone ( its been better ) and getting better and my grainy vision I felt had subsided , I continued to move on ahead with the tinnitus and less snow Jan 3rd week to now : Suddenly I felt my vision dimness has got better ( I could feel this ) , the places i thought was previously dim was bright , and along with this the snow also became more , for example I an see sparse dots in day light and also when I look at my computer screen , and the walls have gone bad, not sure why this happened, shoulder pain , eye fatigue , dizziness , like when I close my eyes I see patterns and circle , when I m in REM braiz zaps after images ( both negative and positive)[ the symptoms I faced in Jan was not faced before in my life ] All the above symptoms Never had them in months of Oct, Nov Tinnitus : More Muscle Pain More Due to which : I'm nervous and anxious Issues I have now : Tinnitus more on left now , previously more on right , afterimages , vision snow ( bothers me the most ) and I know its not more than many of ul here , lil bit anxiety due to all this issues Disclaimer : I didn't know amitriptyline was an antidepressants until the 7th day of me taking it , I forgot to check it up online . Never done drugs in past , not smoked , no alcohol , I was a independent girl doing things on my own but now I'm so dependant on my family for everything I hope I get over this , I'm only 29 never had issues like this .
  5. I have successfully stopped using SSRI's (Celexa 40mg daily) and Benzo's (Xanax/Klonopin 3-4mg daily) for three years now after using them for 16 years. I tapered down from the Benzo’s first over a period of four months and then tapered down from the SSRI’s over the next four months. Of the nine subsequent withdrawal symptoms, I experienced since stopping both medications, three years later I am down to three symptoms that are lingering. Specifically: Sleep problems (waking up every 1-2 hours – inconsistent patterns) Elevated blood pressure (high-norm 140’s over 80’s) Ringing in the ears My PCP recommended I see a neurologist and he advised that the lingering symptoms are a result of the damage caused by the SSRI's and in time they will go away. Does anyone know when these lingering symptoms will leave and is there any recommended treatment I can utilize until they are gone? Thanks in advance for any suggestions.
  6. Hello Everyone, Let me introduce myself. You can call me Sebas (38), i'm from Amsterdam. Hope my English is okay. I was diagnosed with anxiety issues around 2004 and then started using Seroxat, I believe it's called Paxil in the US. I'm aware by now of all the problems this medicine is causing. In other words, i've read a lot, and i mean A LOT about it. I can almost graduate about the subject After several attempts to stop, I found out in 2015 or 2016 about the 5-10% reduction rule. That helped me from 20 mg (10 ml) tot 12 mg (6 ml) in about 1,5 years (estimated). I'm using the fluid suspension and some squirts for accurate dosage. From 6 ml down to 5,8 took me 5 weeks to feel allright, then i stabilized for a week and went back down from 5,8 tot 5,6. All the usual withdrawal symptoms occur during tapering periods such as illness, nerve system problems, visual, fatigue, stomache cramps and also i'm countering eye circles. Since the last dosage (from 5,8 tot 5,6) i've been feeling bad for 9 weeks already. Especially my stomache and my energy. So i'm now wondering what to do, wait (and wait...), go back to 5,8, go back to 6,0 of try to switch to another AD. Cause this one is really @#$%&* mainly cause of the fast half-life period. I've read about a cross tapering method. I asked my doktor for a psychiatric consult about it. Or...could it be my body (and mind) is telling me this dose is beneath the minimum that i just need for my personal wellbeing. I'm familiair with magnesium, omega 3/fish oil and multi vitamin for support. I'm looking forward fto exchanging some knowledge. Bye Sebas
  7. WuGang

    WuGang: hello all

    Hello, I am new to this website. A little about me; I suffer anxiety, panic attacks and was diagnosed depression. Many years ago, when I was around 14-15 years old, I was placed on antidepressants (Seroxat). I was later put on Fluoxetine and Amitriptyline for close to 20 years, I'm now 33. This year I made the decision I didn't want to keep taking these drugs and arranged with my doctor to slowly stop them, one at a time of course. It took a couple of months in total with his instructions. It's now been around 2 months off the Fluoxetine and a month off the Amitriptyline. I have been struggling with the side effects since. On and off sleeping difficulties, wild mood swings, constantly angry and easy to temper, and a really bad temper! Depression. But also, problems with my mind, brain fog, difficulty concentrating. It's really hard to explain, I feel dumber since stopping the meds, I know my mind, know how it works and I can tell it just isn't right. I don't recognize my own mind anymore. I struggle to enjoy anything that I used to, struggle to understand or concentrate on the things I used to like. And to be honest, it's been scaring me, I've been really tempted to go back on the drugs just so that I can be me again. Still struggle with anxiety and panic attacks. Anyway, that's a little about my story.
  8. Hello! I started on 2,5mg escitalopram in december 2018 for GAD and severe clinical depression by my GP. I gradually increased the dose up to 7,5mg and was on this dose for a couple of weeks (until january 7th) I then decided to taper down again, as the drug made me careless, emotionally numb, impaired my cognition and significantly decreased my libido. So I stopped it after 2 months (last 2,5mg pill taken 8th of february). Since stopping I suffered two weeks of accute physical withdrawal (flu-like symptoms, nausea, dizziness etc) but I thought that it would be over and I would go back to «normal», but now it is clear to me that I also suffer from protracted withdrawal (permanent brain damage) and the symptoms are scary and debilitating. I suffer from parasthesia, brain zaps, tinnitus, severe derealization, emotional numbness and extreme apathy to a point where I can’t force myself to get up and eat. I feel completely braindead and my cognition is ruined, the past month has gone by in a haze and I can’t remember or recollect much of it. This is extremely terrifying and almost worse than the original depression. I feel dead, even tho I’m alive. I am a masters student and I can’t function and have no support in my student town. My GP seems to be totally oblivious to the fact that this can happen. I am very distressed (logically, because I can’t really FEEL it) and I would be very grateful if someone here could come with some advice or similar experinces on lexapro that has «recovered» or gotten significantly better and how long it took them. Thank you in advance.
  9. I took paxil 12.5 mg for 10 months due to problem of panic attack in closed spaces. then i slowly withdrawn from it in 1 month. I am not taking any medication for 7 months except due to some depressive events i took paxil 12.5 mg for 10-15 days 2 months back. Now i have heart palpitations and stomach cramps. I had headache but now that has gone away in one week since i started eating walnuts. I hope slowly my other physical symptoms will also go away. The only thing which makes me sad is anxiety sometimes due to emotions and also the fear of relapse. Please tell when will i become emotionally stable. I have heard that after 3 months situation starts improving. Is it true?
  10. Hi guys, I’ve been doing some research into histamine since I believe it plays a very key role in the withdrawal process--at least from the medications that I’m on. I will summarise what I’ve found below as well as the potential impact it could have on managing the withdrawal from antipsychotics such as Zyprexa/Seroquel. I searched this forum but couldn’t find any good overview or discussion, so hoping this can help people. Many of the popular antipsychotics such as Olanzapine/Zyprexa and Seroquel/Quetiapine have a very powerful antihistamine effect: only a very small amount of these medications are required to block the H1 Histamine receptor. Zyprexa, for example, has a Ki(nM) of 0.65–4.9 according to Wikipedia, which is incredibly low (the lower the Ki(nM), the smaller the amount of a medication is needed to block a certain receptor). Therefore, withdrawing from histamine-blocking medications (Zyprexa/Seroquel) is associated with increased histamine (as the blocking effect is reduced, histamine levels become elevated). Certain groups of people might have even had a histamine intolerance and/or high histamine before going on psych-drugs (and both histamine intolerance and high histamine--also related to under-methylation--have been linked to psychosis and other psychiatric disorders), so coming off histamine-blocking medications can also exacerbate this pre-existing imbalance, on top of the effect described in the point above. Histamine is a neuromodulator of the adrenals, so elevated histamine can make the adrenals release a lot more adrenaline, instigate ‘fight or flight’ mode in the body and cause severe anxiety. There is also a strong link between histamine and sleep; having high histamine can cause insomnia. Interestingly, histamine levels naturally peak around 3am/4am, which is when many people experience cortisol spikes and unwanted adrenal activity. Sound familiar? All of these symptoms are very common in the withdrawal process, as we unfortunately know. When withdrawing from histamine-blocking medications, you can take steps to bring down histamine levels to help manage the adverse effects mentioned above. I’ve found anecdotal success stories online from the world of integrative medicine; Alice Lee (MD) says: “If you ever want to successfully reduce a medication that blocks histamine receptors, you will need to know how to lower histamine levels.” Lowering histamine levels can be done through a combination of diet and supplementation: 1) Follow a low-histamine diet (google it for more info!) 2) Through supplementation - taking a histamine digester that ‘chews up the histamine in food’ - Alice Lee recommends Histazyme (by Dr. Amy Myers, MD), but I’ve also seen Daosin 50 and other brands which all contain the same ingredient, Daimine Oxidase 3) Supplementation - natural histamine blockers like Allqlear by Integrative Therapeutics, Histaplex A-B by Biotics Research, or Opsin II by DesBio. Avoid xenobiotics for antihistamine support, such as Benadryl, because the body will react with an inflammatory response to a xenobiotic. I know that this kind of integrative approach is generally a dirty word on this forum, but for me it makes too much sense to ignore. Most of this advice comes from Alice Lee, who is a “holistic psychiatrist” who actually went through the withdrawal process herself, and reports impressive success stories weaning her clients off all kinds of medication (APs, ADs), just check the testimonials on her website TL;DR: I’m going to try a low histamine diet (being more careful around the time when I make a cut to my medication), as well as adding some of the anti-histamine supplements and histamine digesters. I will still be tapering using the 10% method. If anyone else has research or real experience in this area, I would be very curious to hear it. I think it is a very under-recognised factor and understanding more could potentially make for a smoother withdrawal. I'm also conscious that it's only one piece in the puzzle, and there are other receptors to tackle too. But for insomniac, Zyprexa-dependent folks like myself, it could be really key. More reading and links to the success stories can be found here: http://www.holisticpsychiatrist.com/viewpoint/2018/6/7/understanding-histamines-connection-to-mental-health and http://www.holisticpsychiatrist.com/medication-withdrawal/ https://beyondmeds.com/2014/07/13/histamine-psych-drugs/ and https://beyondmeds.com/2013/01/07/histamine-intolerance/ from around 33 mins https://www.mthfrsupport.com.au/dao-deficiency-and-histamine-the-unlikely-connection/
  11. "I've come to the unfortunate conclusion that I am in a state a protracted SSRI withdrawal. One of Alto's articles describes me perfectly in terms of a completely dysfunctional nervous system and paradoxical responses to most meds and even some supplements. The exaggerated alerting only allows me to sleep 3-4 hrs a night and my startle reflex is out of control (a bird chirping will send shivers down my spine). The most terrifying and unnerving symptom to me is derealization. It's as if I am in a dream 24/7. It breaks my heart not being able to truly connect with my wife, kids, family, and friends. The derealization has created a secondary self-sustaining anxiety/panic loop which compounds my other withdrawal symptoms. I feel trapped because no medicine seems to help (except for benzos which scare me) and I literally feel like I am dead waiting this out in hopes that I heal. " quoted from another member I could ever be a mother ( since there is no long term evidence on risk to unborn child). This seems laughable now. I live in complete dissociation and I'm unable to function. My depression is so bad I have hardly been able to leave my bed (psychomotor retardation). One psychiatrist said it was a relapse. But it is a different kind of despair.my nerves grated on - and a feeling that I cannot even describe. I only once tried to come off my meds, 2 years ago, my high-functioning partner said I should do without them. I couldn't function and felt constant emotional pain/sadness so went back on. I know it is hard to exctricate what is withdrawal and what is not. I went on them, off the back of mirtazipine and a depressive relapse ( from a traumtic indcident). I was still getting depressed on citalopram. This feels like a very different type of feeling. I feel pretty frightened that there is so little evidence about their long-term use. I have come off ssri's 3 times-- once at 17, once at 22 ( after 3 years) and do not remember symptoms like these. I feel, at 34, if I don't get off them now I never will but how long will this hell go on for? It's such a trap. It makes me think of the documentary of the same name, "The Trap" by Adam Curtis. He talks about antidepressants in it. Different family members of different generations have always been sceptical of the medical profession and especially drugs/pharmaceuticals. I think they had wisely, seen drugs introduced and then eventually recalled from the market and the medical professions role in this. I feel like I willingly went along with being a 20th century guinea pig. It always plagued the back of my mind that the drugs had been on the market for so little time, no-one really knew the long-term implications/behaviours of the drugs. We have no controls, I will never know what I would have been like living through my mid twenties to mid thirties without these drugs. I don't know if this nervous breakdown is due to the "truth" of my emotions repressed under the drugs or if this is withdrawal. It's scary to know that it may become protracted. I can't live like this- it's hell. I can't read up enough on pharmapsychology because I am so dissociated. I have been told that ssri's don't involve structural changes but like Joanna Moncrieff states, "we just don't know". Any help/ideas/comments??????????
  12. Hi All - I am glad I found this forum! I am currently dealing with severe Withdrawal symptoms following stopping Sertraline on 28th Oct 2018. I was on 50 mg dose and my taper was just for 5 week on 25 mg. Before I get into that a brief history - 16 Feb 2011 - 28 May 2012 - Venlafaxine 75 mg - I was put on Venlafaxine for anxiety disorder and panic attacks following a troubling blood work report showing high cholesterol. I was able to come off this drug very easily without any real Withdrawal symptoms. Next episode was in September 2013 when I again started having severe heath anxiety (cardiac health + infections) following the untimely death of a close friend. I tried to manage this without medication for 2 months but eventually started medication again - 15 Nov 2013 - Oct 2014 - Cipralex - did not work for me. There were days where I felt good but then it all went downhill. Nov 2014 - March 2017 Venlafaxine with one attempt of approximately 3 weeks in Oct 2016 to stop the meds. After stopping Venlafaxine in March 2017 i stayed normal for another 35 days and then the anxiety came crashing back. I tried to manage it with Yoga and meditation but eventually gave in an started on another SSRI - Sertraline 50 mgJuly 2017-Oct 2018 Sertraline 50 mg (tapered to 25 mg for almost 5 weeks before stopping)Nov and Dec went well but were extremely stressful on the personal side.And then on the 28th of December the anxiety came crashing back. It initially started with Overwhelming thoughts, racing mind, uncontrollable negativity and generalized worry about my health. It was intermittent with a few good days interspersed in between.But following a business trip that involved some alcohol on 4 consecutive days the anxiety is back for good since the 18th Feb and I am not having any good days any more. In fact symptoms are intensifying each day. Current Symptoms - Severe anxiety, shivering, waking up in the night with palpitations, insomnia, diarrhea, scary thoughts, racing mind, tightness in chest, shivering My Personal Conditions - I have just moved to a new property and have been through a very stressful time. On the personal side I am expecting my first child in June 2019 which makes it even more difficult as I have to be there for my partner. I have a moderately stressful job but have some other temporary stresses from some financial transactions. In the light of the above can you please advise - 1. Is this withdrawal or do I need to be on the medication longer? Any advise would be appreciated. 2. I did not know about this website and the tapering strategies mentioned here? Will it make sense for me to go back on the meds and then do a formal taper over a long period of time (2-3 years)? Can it reduce the chances or intensity of the Withdrawal syndrome? 3. Are there support groups here locally in London that you can introduce me to?
  13. Topic title: Lingering Symptoms I have successfully stopped using SSRI's (Celexa 40mg daily) and Benzo's (Xanax/Klonopin 3-4mg daily) for three years now after using them for 16 years. Of the nine withdrawal symptoms I experienced, I am down to three symptoms that are lingering. Specifically, terrible sleep problems, elevated blood pressure and ringing in the ears. My PCP recommended I see a neurologist and he advised that the lingering symptoms are a result of the damage caused by the SSRI's and in time they will go away. Does anyone know when these lingering symptoms will leave and is there any recommended treatment I can utilize until they are gone? Thanks in advance for any suggestions.
  14. Hello, After a couple of months of reading some of the posts on this forum, I have decided to join, because basically it seems that I have PSSD. As you will see from my signature strip, I have been on escitalopram at various doses for just over 7 years (finally came off in January of this year (2017)). My history on this drug probably looks a bit confusing. Basically I went on the drug late in 2009 for anxiety that I was suffering. I only intended to be on it for a short time – maybe 6 months – whilst I made some important decisions about my future. But my doctor at that time provided no guidance on coming off the drug. I came off very quickly and crashed. It basically took me about 3 attempts like this to finally realise I could not come off it quickly. In the end it has been a long and slow process with some bumps along the way, but finally I am off the drug – but it took 7 years. I am male and now in my mid-thirties. Anyway, whilst on the drug I suffered from sexual side effects, which from what I have read is very common. But it was in late 2013 that I found out just how much the drug was affecting me. I started a relationship with a girl who although I liked much, I could feel no deep emotion with. Basically I could not fall in love with her. At first I could not understand what was wrong with me, but one day shortly into our relationship I suspected the drug. After a simple ‘Google search’ I had the answer. This combined with the sexual side effects of the drug just made it impossible for me really and in early 2014 we split up. It was at this point that I realised no matter what, I had to get off the drug. It took 2 further attempts of slow tapering but finally I have managed it. I am now almost 5 months off the drug, but seems I have PSSD. At the end of December 2016 I reduced from 10mg every other day to just 5mg every third day. A few days after doing this I could feel something changing sexually – more normal feeling was coming back. And about a week later I had a couple of days of what I would say was completely normal function returning. However this only lasted a couple of days. Shortly after this I took the last tablet. I was now off the drug. About 2 weeks later I once again had a couple of days of everything returning to normal sexually. Again this only lasted temporarily. Then a period of 3 weeks of the numbness and erection difficulties. Then - 5 weeks after taking the last tablet - I again had a period of 2 days of normal functioning – this time I thought it was going to be for good, but unfortunately not. And that was the last time I experienced what I consider everything being normal. Since then I have returned to the numbness, lack of drive and erection difficulties that I had whilst on the drug. I have had the odd day or two in recent weeks where the numbness reduces a bit and there is a little bit of sensitivity, but only a very tiny improvement for a day or so. Then back to full numbness. Also I have developed a ache/pain in my testicles that radiates at times into the top of my legs and buttocks. I can’t remember exactly when this started but I think it was around 6 weeks after being off the drug. I also feel emotionally flat – I don’t think I could fall in love with somebody. I think that issue is still there. I can cry at times, but can’t feel any real happiness for anything. I guess like so many people here I feel the most desperate I have ever done in my life and just looking to talk with others in a similar situation. These past months have seemed like an eternity and every day is such a struggle. I am hoping somebody can give me some hope, because right now I can’t feel much of it. Also I do have a few questions which if anybody can give some sort of an answer to I would be so grateful. 1) Why did I have 3 separate periods of normal sexual function in the immediate period of coming off the drug (first 5 weeks) and then nothing further? 2) the ache/pain that I feel in the testicles – is this part of PSSD? 3) one of the things that really worries me is the fact that I noticed a change to my sexual function after taking just one tablet (God only knows why I did not stop taking them there and then) but as I only planned to be on the medication for a short time, it did not bother me too much. Does this immediate reaction to the drug combined with my long-term use of it mean it more likely my recovery will be a very long time, or worse still that I never recover? Thanks very much for reading.
  15. Hello Everyone, I always intended to return when I felt that my recovery was at such a stage as to be no longer the main focus of my existence. For me that was a sign of 'success'. I probably reached that point over a year ago. This was my original thread in 'Intro's and Updates'. Like others my withdrawal developed in clear stages:- Months 0-3: Nausea, sweating, increased energy etc Months 4 - 12: everything listed in my topic. Hell on earth. My topic doesn't do it justice. Months 12 onwards: The major symptoms (acute anxiety, suicidal ideation, chronic fatigue, intense rage, an inability to function at any level as a human being) are gone. Residual issues: my sleep is lighter and more broken than it was whilst on the AD's and pre AD's. Memory problems relating to name recall. Neither issue impacts my quality of life to any great degree. Today? I feel well, my pre-drug personality has been fully restored (for better and worse) and I deal with the emotional problems that first led me to the drugs with exercise and a well-practised shrug of the shoulders. If that fails the odd hour of stewing in a pot of my own self-pity never did me any harm! Those days are thankfully rare and are alleviated by a swift kick to my own ample arse😃 I always thought I'd write more in my 'success story' but my ordeal feels very much a part of my past now. Things have returned to normal... 'normal' in this case meaning being free from the maelstrom of chemically-induced madness that is acute withdrawal from an SSRI. Looking back that is the only way to accurately describe it. My only advice (if I may be so bold) is to never ever think what you are going through will stay the same. There will be deep despair and flickers of hope. There will be false dawns and genuine improvements. REGARDLESS, YOU WILL GET BETTER. It just takes time. As a wise-owl once wrote on here 'it takes at least a year' if you cold-turkey from these drugs after prolonged use. That's pretty much what it took for me to return to a sense of normality. The improvements in the 2nd year off the drugs were immeasurable. As Claire Weekes once wrote about recovery from nervous breakdown (and which equally applies to withdrawal-induced breakdown IMHO): "Once you are on the right road to recovery, recovery is inevitable, however protracted your illness may have been" If anyone has any questions I'm more than happy to answer them. I know how much I needed some perspective and reassurance when I was in the pit of despair. For those who supported me in my thread you will never know how much I needed and appreciated it. A huge heartfelt thanks. A huge thanks also to the owners and the mods who do such a selfless and brilliant job. . To everyone else. Keep going. It will come right. xxx
  16. Hi guys! Its been almost 7 months since I ct Lexapro, having only used it in 1 month om 5 mg. Its only now for the last weeks that the zaps, vertigo, flu-sympthoms and burning are starting, and becoming more severe by each day.. And I have a constant low fever since one month. (No virus.) Im burning all over my body, not sensitive to touch really.. Just feels like im on fire. And feels like breathing.. Sulfur. Not a refluxprob. (Also kinda blushing in face) All worse in my belly. Having attacks where it kinda knocks me with burning nerves all over and then goes back to constant medium-burning.. My cold sheets in bed is a blessing to naked skin! Also, notice aches and getting weaker in all my muscles.. 😕 Im so afraid! Whats going on! Have someone felt like this?
  17. Hi all, This is my I don't know, 6th? Maybe 7th? Time coming off of cipralex. I have been trapped over the last four years in a cycle of stopping and starting the medication and this past time taking it I became so suicidal that I had to stop cold turkey from 10 mg. I am also taking lithium which I will remain on until I have discussed being weaned off of it and reassessed with my doctor(I say my symptoms match PMDD and seasonal affective disorder with social anxiety more closely than bipolar disorder). Lithium makes me violently sick all night and morning almost every day for over a year now and the worst part is that it doesn't do anything useful for me as I've only experienced manic symptoms when taking antidepressants. I'm feeling frustrated the last few days. I had for whatever reason had this timeline for myself where I would be in the gym doing light exercise by now, getting some peer support and seeing friends. Meditating and living healthier. Instead my days are saved for napping to make up for how horribly I slept the night before. I have to keep cancelling appointments because sleep is more important. And I'm always in pain. I'm frustrated this process takes so long. Between the vomiting, the insomnia and the pain I don't even know how anyone makes it getting off these meds. The emotional spirals every day and cognitive problems.. I was staying positive but it's hard right now.
  18. Hey all, Looking for some advice and encouragement :(. Just to give you some dates and background. October-November 2016 - suffered sudden hearing loss that was treated with high doses of prednisone. Caused me to have severe anxiety and panic attacks, which I'd never had before. November 2016 - Went to a psychiatrist on encouragement of my doctor since I was having so many side effects from the treatment from my hearing loss. Psych told me to take 50mg Zoloft for 3-6 months. Upon starting Zoloft, I started feeling really depressed, jittery, anxious, fatigued, etc. Felt really terrible. January 2017 - Evened out on Zoloft and started feeling pretty good again. June 2017 - Was told my treatment was over and was told to just stop taking Zoloft. I was told just to quit cold turkey. June-August 2017 - Became very depressed (but was still functional), sensitive, crying spells, obsessive thinking etc. Things I never had before. Didn't know that I was possibly experiencing withdrawal and that I hadn't tapered. September 2017 - Doctor recommended I take 10mg Lexapro. On day 1 of 5mg, all my depressive symptoms went away, but the drug made me feel very anxious. Never went up to 10mg. Stayed on 5 mg for 2 months and then took 2.5 mg for 3 weeks and then got off. November 2017 - Stopped taking Lexapro entirely. Since then it's been a rough journey. Sometimes feel very depressed, sometimes very anxious, and sometimes fine. It makes me very angry because I didn't experience depression at all before I started taking the first anti-depressant. I'm doing what I think I should be doing to manage and let things take their course. I exercise, see friends, am working, etc. But there are some days it's just really tough. I don't want to go back on another drug because I'm 100% convinced that these drugs are the cause of these issues to begin with and I don't want to be on this crazy train for years and years. I know I took substantially lower doses of these drugs than other folks, but I'm generally extremely sensitive to all forms of medication. Is there anything anyone can recommend to help me get through this, so that I can help with my recovery? Is there anything else to do besides "just dealing with it?" Any supplements, herbal remedies, exercises, relaxation techniques anyone can recommend? I'm currently taking vitamin d, magnesium, and tumeric. Doing running, yoga, weighlifting, swimming. And trying to take it easy. Any love, support, and advice would be very much appreciated. All the best, Michael Try
  19. StillSinging

    My journey to be off psych drugs

    I always took my medication without thinking really. I had a psychotic episode (due to insomnia, stress, and anxiety most likely) after Christmas in 2007. I was 13. I had been taking Lexapro for a few months. My M.D. prescribed it for me. I don't quite remember why. I think I might probably have been depressed and anxious. I only now realize that taking the Lexapro could very well have caused the insomnia and resultant delusions. Anyway, I had a breakdown. I was seen by a psych. She (Dr. S.) prescribed Lamotrigine. It seemed to quell the delusions. I was back at school, medicated and delusion free. Over the years I developed fatigue, irritability, and apathy. I kept taking the drugs. For fatigue, I was prescribed Bupropion (Wellbutrin). I can't remember if it helped or not. I did develop hypomanic episodes at some point which further supported my bipolar 2 diagnosis. I would also have bouts of depression. Not the crying kind. Just apathy and mild anhedonia. I say mild because I still did some things I loved such as piano, art, singing. I did eventually lose my passion for art though. It showed up now and then sometimes. I always was told by my mother "It will get better", and "It won't always be this way." It didnt comfort me much. Though, looking back, it did get better. Eventually. It took around a decade. But I'm not off meds yet. I moved with my parents to a smaller comfy house in 2014 and joined our local Orthodox Church, met some loving, supportive people and made a really good friend. It did get better. But I still didn't know that there was an alternative for taking medication. I took my meds. I needed them. Or I thought I did. So did my mother. Now, my mother really has been with me all way. She's taking psych drugs too since I was in first grade for depression and anxiety. I went to 2 mental institutes. Thankfully never the hospital psych ward. I know a lot of you on here have been. From what I hear it's not fun and can be traumatic. I remember the people I met at the institutes. Broken, struggling people trying to get by and looking for a little hope. I connected with them. I still miss them and hope they're still fighting. I have a long story so I'll cut it up some in chunks. This is my first post. I'll write later about my experience at college (traumatic) and other things. I have some funny memories too so I'll put those in there as well. Don't give up! Anyone's welcome to share their experiences and stories too. -StillSinging
  20. December 15 started lexapro 5mg for panic attacks and anxiety. One week after notice mild hamstring soreness two weeks after severe hamstring soreness, (maybe restless leg)?, and full body joint pain. I was basically bedridden and went to a clinic where they tested me for the flu, I tested negative. I quit taking the pills after two days of this. The symptoms subsided a bit over the next week then suddenly got bad again a week after discontinuation. I had Burning skin sensation, severe restless legs or hamstring pain, and joint pain that feels like theflu. Currently I'm a few days from three weeks after stopping and can barely sleep because the pain is so great. I'm terrified this is something else because no Dr will admit that this **** drug is poison and "there is no documented case of this happening" WELL ITS HAPPENING TO ME SO DOCUMENT IT! The pain I would describe is me, a 27 year old male, feels like I just turned 99 years old. I'm calling my mom daily crying about not being able to sleep and being in constant pain. Has anyone had anything like this after a short and low dose? I'm really afraid I have some other terminal illness. Besides anxiety about this pain, I haven't actually had a panic attack in a while.
  21. Hello all, after much reading and looking around I finally mustered the courage and concentration to post my account. It all Started around August of 2016. My doctor had put me on Viibryd due to the sexual side effects that I had experienced from being on Trintellix. I have to say, I really did well on Trintellix . Everything was coming together. I think I was in a really good place in my life and everything felt like it was going to fall into place sooner or later. During this period I remember having an overwhelming sense of optimism. So believing that antidepressants are harmless off I went onto my next one, Viibryd Boy, little did I know the hell that would ensue. Shortly thereafter I started to experience hair falling out. Then the hip, and joint paint. All the while feeling like a numb zombie the entire time. I talked to my doctor about the side effects. She stated the hair loss was not a known side effect of the Viibryd therefore it was not possible. The joint and the hip pain she said would go away just like the extreme gastro side effects I had in the beginning. She recommended I go to the “therapeutic” dose which was 40 mg. Me being the good little guinea pig I was, I obliged. This only spiraled into further and stronger side effects. The straw that broke the camels back was that one day I started to feel severe burns in my skin. It really felt like my skin was burning, not just an itchy rash but actual burning sensations. All over my arms, back, and scalp. I had enough! At this point I said to myself I would no longer take whatever this poison was, I simply couldn’t. I was terrified. So at that moment I decided that no withdrawal could be worse than the hell I had been through in the past 2 months of taking Viibryd. So I decided that the best thing to do was to quit all antidepressants, cold turkey. Boy do I regret that dearly. I think it was a couple of days after my last dose that I began to experience erectile dysfunction. I didn’t really begin experiencing any real withdrawal symptoms until after about 3 weeks. Then it all hit me hard like a ton of bricks. First was the eye problems/pain. For me I couldn’t see out of my contact lenses anymore. It’s almost as if my eyeball had swollen, I remember the contact lenses would just not fit, it felt like they were just dancing around my eye. I could not get them to stabilize and I just couldn’t see properly. I think for me, aside from the horrible anxiety, this was the most devastating symptom. I know I experienced at least a dozen symptoms simultaeously these are only a few of them. - Hair loss - Not being able to see in low light - dozens of eye floaters - sensitivity to loud noises - Seeing Halos - Erectile dysfunction - constant brain fog - memory loss - carpel tunnel like symptoms - pins and needles under my feet, legs, and arms - hand pain In the cold - dizziness/off balance And the the list goes on and on but these We’re the lasting side effects. I’m happy to report that most of these symptoms have greatly diminished. Had this been a couple of months ago I would’ve said many were completely gone. However, it appears that I was experiencing what is referred to on this site as a window. Fast forward 2 years and I was inpatient I’m the psych ward for suicidal ideation. This hospitalization further taught me that doctors really don’t know what the hell theyre doing, especially when it comes to psychiatry. It has been over 2 years since my last dose of Viibryd and I’m still dealing w/ the overwhelming withdrawals symptom till this day. Some days are better some days are worse, but I can definitely agree w/ the windows and waves. So here I am reaching out to you guys because I thought by now I would be completely healed. Sadly I have to report that I have not. Furthermore, I have to say I am so impressed w/ the layout, organization, and overall insight of those that contribute to this forum. I feel like I finally understand what is happening to me and I am compelled to share my experience. I also hope to find answers and serve as support for those going through this hellish journey! May we all heal and be restored to our previous lives.
  22. Hi All, I've been reading this forum for a while and the topics here have been indispensable, especially regarding dealing with withdrawal symptoms as I prepare myself for a slow taper off of my remaining dose. Pre-backstory I’m in my early 20s and I just graduated college in late 2014 with a high GPA and a degree in Computer Science. I’ve got a strong resume with projects under my belt. I should be starting my career right now but can’t due to antidepressant withdrawal, but I keep telling myself that I will get better and it will happen, I just need some more time to heal mentally and spiritually. Backstory On January 1st of this year (2015) I suffered the first panic attack of my life. I’ve always had weird heart flutters and missed beats, so I thought I was having a heart attack and dying. The day that I had this awful panic attack, I didn’t get much sleep the night before and I didn’t eat much that day (triggers, I know). I also smoked pot regularly (I am clean now) which in retrospect I figure could be messing with my seratonin. I had bad depersonalization that day, basically forgot who I was for a few hours, and over the next month or so I was bedridden feeling shaky every day, suffering a chain of panic attacks in bed. I was immediately prescribed ativan (lorazepam) to help dull the panic attacks, and shortly thereafter, desperate for something to stop the chain of panic attacks, I was prescribed Lexapro. I took the Lexapro 5mg for the first week and 10mg for the second week, and basically over the next few months my panic attacks got generally better but my mental health got generally worse. My doctor upped me to 20mg Lexapro and I got so disoriented and out-of-it that my mom had to start walking me up to the door of my therapy appointments, because I didn’t feel like I could do it alone. I decided to taper down off the Lexapro because my panic attacks had basically vanished, the Lexapro was causing some bad side effects (at higher doses making me confused and disoriented all the time, at the lower doses mostly just preventing me from getting decent sleep, so I was feeling tired all the time). I felt like the panic attacks would probably not come back, since I was on a good new pattern of diet, exercise, supplements (fish oil, magnesium, probiotic and multivitamin), and I also stopped smoking weed completely, which I think may have been a big contributor to the initial panic attack. Anyways, I had miraculous success taking the dosage down from 20mg to 10mg, from 10mg to 5mg, and from 5mg to 2.5mg, with almost no withdrawal effects. The side effects improved steadily with each dosage decrease, and I’m very grateful that I had so little trouble getting down this far. The big trouble started happening about a month ago. I had thought that I had tapered down successfully from 2.5mg because I felt pretty great for 3 weeks on 1.25mg (¼ of a 5mg pill) with no discernible withdrawal symptoms (Sept 9 2015 to Sept 29 2015). On my psychiatrist’s suggestion, I dropped the lexapro completely (0mg) on Sept 30 and I felt worse and worse for about 4 days. On the 4th day I almost had a panic attack, and I felt so depressed and shaky that I took a small fragment of my pill to try to stave off the symptoms. Literally 15 minutes after taking the pill fragment I went from feeling terrible to feeling great, browsing the internet on my phone. So I stabilized again on 1.25mg after about 5 days, or so I thought. 1.25mg (¼ of a tiny 5mg pill) is terribly difficult to measure - there was one time I wasn’t sure if I even took my pill fragment or if it fell on the floor, since it was so small I couldn’t feel it on my tongue. So I started pushing it against the roof of my mouth so I could be sure it was actually in my mouth. But that made it start to disintegrate before it hit my stomach, so… basically I think that my true dosage was getting really uneven. I felt really tired some days and needed naps, and other days I felt mostly fine. So I figured I could get a more consistent dose if I switched to the liquid, which my psychiatrist prescribed for me. Latest Chapter So on 10/28/2015 I switched to the liquid. I figured that the liquid form would be much more readily absorbed by my body than the pill fragments and I was right. I started out with 1.2mg of the liquid and it felt like way too much (cloudy head, sleepy all day), so over the course of 2 days I lowered it to 0.9mg, which felt pretty fine for 5 days. I felt like I was getting better and that I could even start driving and running errands around town with my mom again if I just waited a few more days. On 11/4 I made a really, really stupid headstrong decision. I felt like I could reduce my symptoms even more if I just reduced the dose by a tiny bit further. So that day I cut from 0.9mg to 0.8mg (which in hindsight was a HUGE cut especially considering how recently I had changed the dose before that). The depression came back in such full force that I immediately had to put the dose back up to 0.9mg 2 days later, but reupping the dose didn’t help at that point. I continued to get worse and worse (more depression/anxiety) until my mom pointed out that I was only eating like 800 calories every day - I knew that my appetite was shot, but I had no idea I was eating so little. On 11/11 I started counting calories and now I’m getting at least 2000 per day, with an ultimate goal of 2500. I upped the lexapro from 9mg to 9.5mg daily and the crippling depression is partway gone now. Anyways now it’s 11/14 and I think I’m seeing some progress, but I can never be sure, and these symptoms are very difficult to work through every day. Today Over the last few days, every morning I wake up nauseous and depressed, and every night I get anxious and need to take a 0.5mg lorazepam to calm down. Progress is slow for me and I’m impatient, but I keep trying to remind (convince?) myself that my body is working very hard to right itself chemically, and that if I just hold this dose and don’t do anything else stupid with it, I will feel a little better by next week, and yet a little better by the week after. I could really use some reassurance though :/ My First Question I’m taking 0.95mg in 2 doses daily (0.475mg at 11am and 0.475mg at 1:30pm). On 0.95mg I feel like my seratonin levels are very unbalanced (depressed/hopeless in the morning, decent around noon, anxious by afternoon/evening). When I accidentally took my second lexapro dose at about 4pm one day instead of 1:30pm, that night I went into a drug-trip kind of sleep (almost like an alternate reality) which was a little scary but most of all exhausting and made me feel disoriented and confused and anxious the next day. As of the last few days, I wake up after vivid dreams exhausted, not at all rested, depressed, and with a burst of adrenaline. Will my body actually be able to get used to such a low 0.95mg dose taken mostly towards the beginning of the day like this? If I just stick it out for another week or two, my mood will start to level out again so that I’m not getting these big daily mood swings, right? If not, where do I go from here? Thank you everyone for your support.
  23. Hi guys! Im new here, im 30/f and its been 7 months since i ct from Lexapro (escitalopram.) And yes, I only took it for a month.. prior to that ive tried Setralin, Mirtazapin, Brintellix and Venlafaxin. Low doses. All in 18 months of a time, and I took each one for about a month since I had a pretty severe reaction to all of them and was always given something new to try from my doc. So, 7 months ago i started Lexapro, 5 mg. And an hour later my body felt like it was pushed forward when i sat still, when i walked it felt like someone dragging me backwards and my feet and legs were burning, not really dp or dr but and outer body feeling set in. After about 4 weeks my doc told me to upper the dose to 10 mg. I did. A few hours later walkin in the street i just collapsed, in cramps, my heart felt like it was on fire, a highwolt jolting thru my body.. and someone called an ambulance. I stabilized at the hospital, nothing really wrong. Got sent home. When i got home, i called my doc, shakin in fear.. and he told me to just quit it. Youll be okay. Dont take it anymore. Ah, yes.. so i didnt. First 2 months after ct - is all in a blurr, it was hell. No honeymoonphase here. I was insane, totally mad! Nothing worked. And felt like when someone looked at me they saw mr potatohead were nothing was were it should be. I would lie on my kitchenfloor just screaming in panic and anexiety, just feeing like i was slipping away, dying, my soul just left. From month 3 - I was able to leave my apartment a little longer than going foodshopping, without that haunting fear and ongoing panic. But still mostly on my floor feeling like a dead person. This is where the sweatin kicked in, totally covered in sweat all the time. From month 4 - The burning sensations stopped, the brain zaps stopped, the swaying feeling of being pushed and pulled also stopped, i begun to feel pretty good besides my sweat and mild flushes. Like i was back before the meds with my regular panic syndrome and anxiety, i was able to meet some friends, started a danceclass and going back to the gym. From month 5 - Back in hell. Everything went to sh*t, i got a severe case of candida and bv and was given fluconazol and itraconazol, and pretty severe reaction to those (and it didnt even help.. my doc wanna put me on antibiotic, ah hell no. Im to afraid.) And the burning started up again, but not in my legs or feet, but in my belly. Spreading each day to my whole torso, head, eyes, mouth, throat, ass and at last back to legs and then feet. So, the last 2 months since then ive been dealing with ZERO stresstolerance, even the tiniest little thing push me over the edge, shivers in my brain, pretty horrible DP on and off, dizzy spells, being stuck the flu and the burning.. i sometimes take epsom salt baths in relly hot water but sit there freezing and shivering.. (it really scares me when its burning in my throat btw, like breathing acid..), with icecolds spots on my arms, mucles feeling really weak and achy, and for the last week ive been having this pins and needle-feelings all over, like when your feet falls asleep and about to wake up? Thats my whole body! All the time! Warm things feels cold, cold things feel warm. Im flushing all the time. And also a new sympthom is this pain.. aching pain from my nerves, like ive been drinking vodka on empty stoach..(?) Everything hurts. And constant low fever and flu-sympthoms. White noise in my head. Im so tired! Get this buzzing feeling in my eyes of tiredness and "have to sleep now!" even do i slept 9 h and havent really done anything all day. Neuroemotions and panic attacks out of the blue here and there. Im mostly just lyin in beed feeling sick as f*ck and wonder if im gonna live another 5 minutes. Feel like an idiot when a friend wanna hook up and im "still in flu with fever.." And I cant eve describe how i feel during pms with all of this, its like having a psychosis for about 7 days.. 😕 My timeline doesnt match anything ive read on here, and I know were all different, but are there anyone who have felt like I do now? This wave is killing me, I dont think i cant handle it anymore, the only thing keeping me alive are all of you ..2 months of this, will it end?
  24. Hello, my fellow men and women in this important battle. I'm 25, I live in Luxembourg and I've chosen to call myself EtaCarinae because that's a name that has always stuck with me. I'm fascinated by astronomy, astrophysics, space stuff. I was diagnosed with major depressive disorder at 16, but a recent diagnosis by a reputable service in the field has found that I am on the autistic spectrum. I have Asberger's syndrome, a "mild" form of autism. Sometimes, when my meltdowns get really bad, I may get suicidal if I don't have anyone to talk to, but my symptoms are not caused by depression, but rather by my autism. Anyway, this is the second time I'm weaning off escitalopram 10mg. First time was when I was 18, I had been on 10mg for 2 years during ambulatory therapy with a children's psychiatrist, and he advised me to halve the dose, to take 5mg daily for two weeks, then quit altogether. I, being the stubborn young man I am, decided to speed that up by a factor of two, so I took 5mg for a week, then I quit. This... worked really well for me. I experienced very mild withdrawal symptoms, all I can really remember is a feeling of derealization and some transient vertigo, all of which resolved within a week. This time, I admitted myself to a psych ward after two days of intense suicidal ideation (the exact context isn't really important, but I'll say my family played a role to put me into that situation), where I was put back on escitalopram 10mg. That was on new year's eve, and now, 3 months later, I've decided to throw out the pills again, as they never made me even feel any better. I plan on doing the 50% taper again (as a matter of fact, I've started my taper today), and I plan to alleviate any withdrawal symptoms with CBD oil (10%), which seems to take effect very quickly. I'm very aware that I can count myself lucky for being someone who can come off these meds without any large problems.
  25. Hey everyone, My name is Abby and I have been off Prozac for 3.5 months now. I'm currently experiencing intense withdrawal and the return of mental states I never thought I'd have to experience again, and I would really like to connect with others who are going through similar during this long, difficult process. Background info: I always had tendencies towards anxiety, depression and obsessive compulsive disorder (the Pure-Obsessional variety) since childhood. At 16 these symptoms very rapidly became so severe my whole life fell apart within a matter of days (Going on the contraceptive pill at this time may have been a contributing factor). I didn't have a full breakdown until I was 18, at which point I was taken to the doctor, put on Sertraline, and referred to psychiatry. The following 8 years consisted of several psychiatric admissions, different drugs including clomipramine, seroquel, mirtazipine, prozac, and possibly a few others for shorter periods. I lost pretty much everything, my obsessional fears were so strong that I attempted suicide more than once, developed a bad cocaine/mephadrone habit, was a constant worry to my family. There were times, however, where the medication would help a lot. At 60mg of Prozac I went through some periods of being functional - I went to work, got into a relationship etc. These were a great relief but I can't say I was truly happy as the fears were never properly dealt with. My last hospital admission was in 2014 when I was 24. I had attempted to come off medication as I believed I had to deal with the underlying problems, and I hated the weight gain side effects. Looking back, this was doomed to fail as I was still using cocaine regularly, drinking a lot, and didn't have any proper support mechanisms in place. I was fine for 6 months then crashed, was borderline psychotic with the OCD symptoms, depressed and anxious beyond belief and desperately wanted to die (and believed I deserved to). I was in a psych ward for just over 2 months before new meds kicked in - clompipramine and (randomly, I don't know why) Epilum, as I was told it 'balanced moods'. A year later I went back on to old faithful Prozac and also came off the contraceptive pill. I had always been told the same about it, that it leveled out moods, and don;t think it's a coincidence that my symptoms became much more manageable a few months after stopping it. I then managed to stay at 40mg for 2 years and my life changed drastically for the better. to myself and everyone around me it was like a miraculous recovery - I stopped taking drugs, began volunteering at a Buddhist meditation centre, got my dream job, published a novel, did newspaper interviews about my experiences, ...I pretty much had my dream life. It was like being reborn after thinking everything was all over...forever. It was in January 2017 that I decided to gradually wean off Prozac. Over the following 10 months I reduced until stopping completely in October. In these past 2 years I have done extensive mind training and spiritual exploration, which has probably been the main factor in this recovery. My life is pretty much dedicated to this practice now - I still volunteer at the meditation centre, go on meditation retreats throughout the year, and have also completed a Reiki Mastership. It was always potentially on the cards after exploring my mind with psychedelic drugs in the past, doing past life regressions and also taking Ayahuasca twice in ceremonies. It was around the time of the reiki mastership that I was weaning off the last of the Prozac. Things became challenging - but at first I welcomed it. I was in a strong place mentally, and my mental health hadn't plagued me intensely for a few years. I was made aware that the Reiki energy can churn things up to be healed, but I think that the combination of this, a massive flare up of a back issue that left me not able to walk for weeks, family pressures and intensive mind exploration during retreat that has led me to my current situation. Since December just passed things have been incredibly difficult. I have experienced a return of old OCD obsessions, to the point where I've had panic attacks for days that made my vision blur, heavy depression, crying all the time, existential fears and experiences which medically would look similar to psychosis (although I believe that term can pathologize important and natural inner processes), identity confusion etc. I knew it would be hard, I just never expected to feel this level of horror ever again. Having said that, I know things are different this time round - I have a level of insight gained through spiritual practice that is keeping me going. Energetically, I'm aware that I am creating this reality on various levels, and that I need to relax as much as possible to allow it to pass through the way it's supposed to. I'm no stranger to facing the darkest parts of the psyche, but it's still terrifying and I'm struggling to cope day to day. To make matters worse, my Mum has gone abroad for cancer treatment and I'm now caring for my little brother and sister 4 days a week which is incredibly stressful (I'm used to having my own space and being able to retreat when I need to). My CBT therapist has discharged me as she feels I cannot engage with therapy under this amount of stress, but encouraged me to come back when my Mum gets back. To be fair, she never taught me anything I didn't naturally learn in meditation and I was only seeing her regularly to comply with services. I have however started going for reiki treatments with the person who facilitated the course I was on last year - he is exceptionally intuitive, knowledgeable and takes an all round, individual approach. One session with him last week was worth a year of 'traditional' therapy. So I'm hoping that continuing with this will help. Anyway, sorry for the essay. I don't have many people to talk to about all this. It's also weird for me to ask for help now as I haven't needed it in so long - I'm usually now the one that helps everyone else. It's a scary and heartbreaking thing to go back to a place you thought you'd left long in the past, but I do believe deep down that I have done so in order to face my demons fully and emerge stronger in the long run. Thank you if you made it this far, I'm looking forward to connecting with others on this site. You are all incredibly strong to be doing what you're doing, no matter what stage you're at. Much love x
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