Yayamem Posted October 3, 2024 Posted October 3, 2024 Okey guys, Im reaching out for help for the first time in this. Im protracted 3,5 years out after 2,5 years of ssri-use. Im in a place where a lot of things are better, they truly are but the waves are as bad as ever. Just hade one for a month, not sure if im out, probably not but Im hitting rock bottom. I just cant make myself do this anymore. Im done. No resilience. Usuually I can distance myself and force myself forward. But i cant this time. I think it has to do with that i really hoped and sonewhat ecpected that I would feel better by now. Im trapped in more or less constant dpdr, have had akathisia now non stop for 3 weeks. Im hammered. I dont know what im supposed to do. I cant live like this. Sorry for the negativity but I really need some help. June 2018-december 2020 on Setraline. First year 150 mg, then tapered down to 25 mg for maybe a year, the quickly down to 12.5 and stopped by Christmas 2020. Symptoms started to intensify around 3 months after quitting and skyrocketed summer 2021. Basically bedbound for a few months, 1,5 years on complete disability. Now working part time, Windows and waves.
Moderator Catwoman73 Posted October 7, 2024 Moderator Posted October 7, 2024 Hi @Yayamem, and welcome to SA! We are a community of volunteers providing peer support in the tapering of psychiatric medications, and their associated withdrawal syndromes. Thank you for completing your drug signature. I'm so sorry for your ongoing suffering. I've been where you are- seven years of protracted withdrawal with my last cold turkey stop. It's not an easy journey. Please don't apologize for the negativity- there's nothing remotely fun about this journey, and it's hard not to feel hopeless. It looks like you tapered very quickly, which does put you at risk for protracted withdrawal. As you may have discovered, here at SA, we recommend tapering at a rate of no more than 10% of your current dose, no more often than every four weeks (so, as an example, 10mg, 9mg, 8.1mg, 7.3mg and so on). This is known as hyperbolic tapering, and is designed to minimize acute withdrawal symptoms, and minimize the risk of protracted withdrawal by giving the nervous system time to undo all the biochemical and genetic changes that have occurred as a result of the presence of the drug. The nervous system is a notoriously slow healer. You can read more about hyperbolic tapering here: Why taper by 10% of my dosage? Since you have been off your meds for so long, reinstatement is not really an option for you. The good news is that you will heal. I did once before. It took 7 years, but it did happen! And if you are having windows and waves, that's a great sign. You are well on your way... I know it doesn't feel like it when the waves hit, but it's true- you are healing, whether you feel like you are or not. I'm a big believer in controlling what you can, and learning radical acceptance for the rest of it. You are in protracted withdrawal, but there are some things you can do to help yourself along. Some of it is intuitive. Eat a balanced, whole foods diet, stay very well hydrated (this was huge for me), engage in gentle exercise, and get as much rest/sleep as you can. Avoid all neurologically active substances, such as caffeine, nicotine, alcohol and recreational drugs. These things are like pouring gasoline on a fire- they typically make things much worse. And don't take any other psychiatric medications to deal with the withdrawal effects of psychiatric medications- when in withdrawal, the effects of these meds are not predictable, and can make you feel worse rather than better. In terms of supplements, we only recommend two around here- magnesium, and omega-3 fatty acids. Do be mindful though- when in withdrawal, it is very common to develop hypersensitivities to all sorts of things- medications, supplements, and even foods! So if you wish to try a supplement, even those we recommend here, start with a very low dose, and see how you fare. You can always increase slowly over time, if you tolerate it. I have found it very helpful to keep a symptom journal, and include information on the foods I eat and the activities that I participate in. This has helped me identify several things that do trigger waves. Not all waves have triggers- sometimes they just happen- but many people do have things that trigger them. Figuring this out can make the journey easier, by allowing you to avoid your triggers. For me, symptoms are triggered by coffee (even decaf), chamomile, refined sugar in even moderate amounts (tiny amounts seem ok), intense exercise, and magnesium (yes, it's supposed to relax you, but it causes brain zaps and insomnia for me). I never would have figured this out without my journal. You can use the following list of typical withdrawal symptoms as a template for a journal if you wish. Starting a journal and figuring this stuff out is definitely helpful in taking your power back, to the degree that we can. Control what you can, right? Daily Checklist of Antidepressant Withdrawal Symptoms (PDF) I'm not sure what kind of symptoms you are having with your waves, but we have lots of threads here on non-drug coping mechanisms. I'll link some below. It's really important to develop some strong habits to support your nervous system throughout this process. For me, developing a daily mindfulness practice has been hugely helpful in preventing emotional spirals. Using guided meditation/yoga Nidra, recordings of nature sounds helps calm my nervous system at night, and fosters a good sleep environment. I do a LOT of deep breathing, and use mantras to get through the bad times minute by minute. I have taught myself to recognize the negative thinking behind the negative emotions, and I've learned to challenge and replace those thoughts. This helps to rewire the brain to have a more positive outlook. And when all else fails, I love a good old fashioned distraction... find things that bring you joy (or things that once brought you joy), and do them regularly when you're feeling rough. I love watching different series on Netflix, swimming (I feel great in water!), dancing, cooking and working on all sorts of artistic projects. When I'm focused on these activities, I can't be focused on my symptoms, or ruminate about how long this is all taking. Non-drug techniques to cope with emotional symptoms Easing your way into meditation for a stressed-out nervous system Music for self-care: calms hyperalertness, anxiety, aids relaxation and sleep Ways to cope with daily anxiety "Change the channel" - dealing with cognitive symptoms Dealing With Emotional Spirals Important topics about symptoms, including sleep problems The importance of recognizing you're feeling good Tips to help sleep: so many of us have that awful withdrawal insomnia Path to Better Sleep FREE online for everyone from the US Veterans Administration Most of all, I really don't want you to lose hope. If you are having windows and waves, you ARE healing. I know it's a very long haul, and I know it's hard. But you will get well from this. And I have to believe we will all be better people on the other side- more compassionate, more patient, and less willing to tolerate living a life without joy. You will get there! I sincerely hope you will take advantage of the peer support model that this site offers, and read and comment on the intro threads of other active members. This journey is very lonely at times, and you may find some comfort in the knowledge that there are people out here who completely understand. I will definitely follow your journey, and help out wherever I can. ❤️🩹 This is your introduction topic. Each member gets one intro topic. Please post any updates or questions here, on this thread. Do explore the rest of the forum though- there's lots of good info here! And like I said, jump in and participate in the community if you like- it really is beneficial to have the support of those walking the same path as you. 1995- 2007- On and off multiple antidepressants (Prozac, Paxil, Effexor, Wellbutrin, escitalopram). Memory poor- can’t remember dates. Always tapered fast or CT. 2007- tapered Wellbutrin, zopiclone and escitalopram over one month to get pregnant. Withdrawal hell for many years. 2009- Daughter born 🥰 Post partum depression/psychosis- no meds taken. 2016- Back on escitalopram due to job change/anxiety 2022- Severe covid infection- Diagnosed with long covid 08/22. 2023- 01/23- Long term disability approved for long covid. Started taper under MD advice from 20mg: 11/23- 15mg. 2024- March-10mg. Started low dose naltrexone for long covid-5mg- terrible reaction, reduced to 0.5mg. April- 10mg escitalopram, 1.0mg LDN. May 1- 9.0mg escitalopram, 1.0mg LDN. May 15- 9.0mg escitalopram, 1.5mg LDN. June 12- 8.5mg escitalopram, 1.5mg LDN. July 8- Brassmonkey micro taper started. 8.4mg escitalopram, 1.5mg LDN. July 15- 8.3mg esc, 1.5mg LDN. July 18 8.3mg esc, 2.0mg LDN, July 22 8.2mg esc. 2.0mg LDN. July 29 8.1mg esc. 2.0mg LDN. Aug. 24- 8.0mg Esc. 2.0mg LDN. Aug. 30 7.9mg esc. Sept. 6 7.8mg esc. Sept. 13 7.7mg esc. Sept 21 2.5mg LDN. Oct. 4 7.6mg esc. Oct. 11 7.5mg esc. Oct. 18 7.4mg esc. Oct. 25- 7.3mg esc. Nov. 1- 3.0mg LDN. Nov. 15- Dec 27- 6.9mg esc. Supplements/other meds: Vitamin D, B12, Claritin, HRT PLEASE DO NOT PM ME! PLEASE ONLY TAG ME FOR URGENT QUESTIONS! Thank you! I am not a doctor. I don't even play one on TV. This is not medical advice, but based on personal experience. Please consult a medical professional.
Yayamem Posted October 7, 2024 Author Posted October 7, 2024 Thanks so much for your answer 🙏 really. Im so grateful. I know I tapered too fast but didnt have a clue back then. Wouldnt have believed something like this could happen. This thing with alcohol and nicotine, how is that after withdrawal? Are people able to have it when theyre through? How did you manage 7 years? Thats amazing. And crazy. I have all sorts of symptoms but would say those that bothers me the most is the akathisia, the extreme pain and depression that comes with it, the dpdr, feels like I Walk around in a cartoon very often... Completely disconnected. Dont feel anything good except from tiny moments. Extreme fatigue. A lot of cognitive problems. June 2018-december 2020 on Setraline. First year 150 mg, then tapered down to 25 mg for maybe a year, the quickly down to 12.5 and stopped by Christmas 2020. Symptoms started to intensify around 3 months after quitting and skyrocketed summer 2021. Basically bedbound for a few months, 1,5 years on complete disability. Now working part time, Windows and waves.
Yayamem Posted October 8, 2024 Author Posted October 8, 2024 @Catwoman73, forgot to tag youfor the answer above. June 2018-december 2020 on Setraline. First year 150 mg, then tapered down to 25 mg for maybe a year, the quickly down to 12.5 and stopped by Christmas 2020. Symptoms started to intensify around 3 months after quitting and skyrocketed summer 2021. Basically bedbound for a few months, 1,5 years on complete disability. Now working part time, Windows and waves.
Administrator KenA Posted October 8, 2024 Administrator Posted October 8, 2024 @Yayamem This month will be my 5 year mark from my CT. I consider myself 99 percent healed at this point. I'm able to enjoy alcohol again when I feel like having a drink. Also able to smoke occasionally as well. They don't affect me negatively at all. You will heal at some point and be back to living a normal life. Just have to let yourself heal and give it the time it needs You've got this! 2010-2011 - Tramadol - Can't remember dosage 2011 - CT Quit Tramadol 2011-2019 - St Johns Wart - Started out at 3 Pills a day (300 MG) and increased to 6 per day over the years August 2019 - CT Quit St Johns (Told by Hospital Dr to Stop Taking due to increased BP) September 2019 - Citalopram 10mg - Approx 2 weeks - CT Quit September 2019 - October 2019 - Clonazepam .5mg - Approx 3 weeks - CT Quit Drug Free Since October 5th 2019
Yayamem Posted October 8, 2024 Author Posted October 8, 2024 @Catwoman73 @KenA thank you so much for your reply! 🙏🌻 How bad was it for you in the befinning? Did you have akathisia? June 2018-december 2020 on Setraline. First year 150 mg, then tapered down to 25 mg for maybe a year, the quickly down to 12.5 and stopped by Christmas 2020. Symptoms started to intensify around 3 months after quitting and skyrocketed summer 2021. Basically bedbound for a few months, 1,5 years on complete disability. Now working part time, Windows and waves.
Administrator KenA Posted October 8, 2024 Administrator Posted October 8, 2024 My first 8 months I can only describe as pure torture. I don't like to think back on those days. But it slowly got better with time. That's the secret to this. Time time and more time. I had very very mild akathisia, but when it happened, I would just go for a long walk and wear myself out until it went away. 2010-2011 - Tramadol - Can't remember dosage 2011 - CT Quit Tramadol 2011-2019 - St Johns Wart - Started out at 3 Pills a day (300 MG) and increased to 6 per day over the years August 2019 - CT Quit St Johns (Told by Hospital Dr to Stop Taking due to increased BP) September 2019 - Citalopram 10mg - Approx 2 weeks - CT Quit September 2019 - October 2019 - Clonazepam .5mg - Approx 3 weeks - CT Quit Drug Free Since October 5th 2019
Yayamem Posted October 8, 2024 Author Posted October 8, 2024 @KenA allright.. What where your symptoms? Do you remember? June 2018-december 2020 on Setraline. First year 150 mg, then tapered down to 25 mg for maybe a year, the quickly down to 12.5 and stopped by Christmas 2020. Symptoms started to intensify around 3 months after quitting and skyrocketed summer 2021. Basically bedbound for a few months, 1,5 years on complete disability. Now working part time, Windows and waves.
Administrator KenA Posted October 8, 2024 Administrator Posted October 8, 2024 Over the course of my WD, I probably had more than 20 different symptoms. Big ones were Anxiety and Depression, DP/DR, muscle cramps and spasms, tinnitus, digestive issues, short term memory issues, cortisol bursts, insomnia, headaches, internal itching, skin burning, unable to concentrate. They all went away over time. 2010-2011 - Tramadol - Can't remember dosage 2011 - CT Quit Tramadol 2011-2019 - St Johns Wart - Started out at 3 Pills a day (300 MG) and increased to 6 per day over the years August 2019 - CT Quit St Johns (Told by Hospital Dr to Stop Taking due to increased BP) September 2019 - Citalopram 10mg - Approx 2 weeks - CT Quit September 2019 - October 2019 - Clonazepam .5mg - Approx 3 weeks - CT Quit Drug Free Since October 5th 2019
Yayamem Posted October 8, 2024 Author Posted October 8, 2024 @KenA Sounds like the classical ones. Thank you so much for you support. It really means a lot June 2018-december 2020 on Setraline. First year 150 mg, then tapered down to 25 mg for maybe a year, the quickly down to 12.5 and stopped by Christmas 2020. Symptoms started to intensify around 3 months after quitting and skyrocketed summer 2021. Basically bedbound for a few months, 1,5 years on complete disability. Now working part time, Windows and waves.
Administrator KenA Posted October 8, 2024 Administrator Posted October 8, 2024 Not a problem. Don't hesitate to reach out if needed. 2010-2011 - Tramadol - Can't remember dosage 2011 - CT Quit Tramadol 2011-2019 - St Johns Wart - Started out at 3 Pills a day (300 MG) and increased to 6 per day over the years August 2019 - CT Quit St Johns (Told by Hospital Dr to Stop Taking due to increased BP) September 2019 - Citalopram 10mg - Approx 2 weeks - CT Quit September 2019 - October 2019 - Clonazepam .5mg - Approx 3 weeks - CT Quit Drug Free Since October 5th 2019
Yayamem Posted October 17, 2024 Author Posted October 17, 2024 Can anyone relate to a deep deep soulcrushing depression - like pain that often pre-exists before outbursts of akathisia or dystonia? June 2018-december 2020 on Setraline. First year 150 mg, then tapered down to 25 mg for maybe a year, the quickly down to 12.5 and stopped by Christmas 2020. Symptoms started to intensify around 3 months after quitting and skyrocketed summer 2021. Basically bedbound for a few months, 1,5 years on complete disability. Now working part time, Windows and waves.
Yayamem Posted October 17, 2024 Author Posted October 17, 2024 Hi, also I wonder if anyone developed dystonia late in the process? Ive had a really bad wave for 7 weeks now, and its getting worse. Now I have dystonia - outbursts that I havnt had before. Im 3.5 years out. My beck and torso is pulling and I be d my arms and legs in twisted ways. Im really scared. June 2018-december 2020 on Setraline. First year 150 mg, then tapered down to 25 mg for maybe a year, the quickly down to 12.5 and stopped by Christmas 2020. Symptoms started to intensify around 3 months after quitting and skyrocketed summer 2021. Basically bedbound for a few months, 1,5 years on complete disability. Now working part time, Windows and waves.
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