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Sleep in WD

Featured Replies

Sleep in withdrawal

 

Sleep problems affect most of us in withdrawal, experiencing an adverse reaction or tapering off our Antidepressants to one extent or another. Sometimes it comes just before or part of a fresh wave of symptoms and goes with a window, for others it’s a regular feature of their recovery.

 

Melatonin and Cortisol levels (the sleep and wake hormones) can be disrupted leaving a signature list of sleep disruptions.

 

In the acute initial phases of healing, sleep can be very challenging with users often reporting just a couple of hours a night or even no sleep at all.

 

We sleep in ‘cycles' of around 1.5 hours dropping down through the stages of sleep in the first cycle to stage 4 deep sleep and lifting to the REM stage, the nearest one to awake. It’s here you may find yourself waking up when a ‘normal’ person would just continue onto the next cycle. As the cycles progress throughout the night, the depth of the sleep reduces and you spend more and more time in REM stage, which further increases the chances of waking and can eventually lead to great difficulty getting back to sleep.

Its often reported there is a ‘ceiling’ of around 5-6 hours where after sleep is much harder to achieve and if it happens its more broken and fragmented.

 

You may find the need to urinate during the night increases. This is again possibly due to changes in hormone levels the body normally makes to reduce urine production overnight so the body can sleep.

 

Initiating sleep is a common problem. With Melatonin production reduced, actually getting to sleep can prove difficult. Other symptoms can add to this frustration:

 

-Hypnic Jerks (Where you wake suddenly just as you drop off)

-Hot Sweats or a general lack of ability to regulate your temperature

-Out of character thought rumination

-Nocturia (Constant need to urinate)

-Sensitivity to light and sound

 

Sleep quality is greatly affected with sufferers experiencing very light, possibly nonrestorative sleep and no dreams or even the opposite extremely vivid dreams.

 

Others have found that they wake up very early when they do sleep. As well as early awakenings, it’s not uncommon for folk to wake to a surge of energy, panic or find waking triggers symptoms such as anxiety. Others feel their symptoms improve as the day goes on, only to restart all over again after a sleep ‘reset’.

All of this is likely caused by too high Cortisol levels (the body’s natural awake hormone) produced unhelpfully early in the morning making further sleep impossible and creating these chemical symptoms.

 

We don’t know exactly what happens during sleep, but we know it is important to the healing process and our wellbeing so it’s vital to get as much rest as you can. It’s often observed in the community that sleep is one of, if not the last, of the symptoms to resolve.

 

Getting enough sleep we can see is a challenge but there are some things we can do help ourselves.

 

 

Sleep Hygiene

 

Creating good routine in WD is one of the keyways to cope whilst we taper and heal from injury. An important part of this is our bedtime regime. Finding habits that help us and sticking to them is very important.

Some examples might be:

 

-Low temperature in the bedroom at night.

-Using your bed for just sleep can help teach your brain that it’s time to go to bed.

-A regular bedtime and awake time to help encourage our natural circadian rhythm.

-No eating or drinking 2 hours before bed. The later can help with middle of the night calls of nature!

-Avoid foods that are high in histamine levels particularly later in the day.

-Reduce or eliminate caffeine intake

-A relaxing bedtime routine, a nice bath, shower, a good book or perhaps a bit of meditation, whatever gets you relaxed and ready to sleep.

-Cutting out screen time an hour before bed or at least utilising blue light filters or glasses to reduce the impact our devices can have on our systems natural sleep/wake cycles.

-Eye masks and black out blinds can be great to stop the early morning light or interruptions from outside such as cars and streetlights etc.

-Ear plugs to reduce the levels of distracting sounds that are not conducive to getting off to sleep quickly and staying there.

-Some people find white noise machines effective so worth considering. There are even apps you can download.

-Weighted blankets or a light blanket to keep you cosy but not too hot! Having a second or third laid out next to you to pull over as the night gets chillier is also a very good system!

 

 

Light levels

 

Our brains naturally respond to light, this stems from caveman days where we didn’t have much in the way of supplemental light. The nighttime was for sleep, and the daytime was for everything else.

We can mimic this by adjusting the exposure we have to different light qualities throughout the day.

Start by getting as much natural day light as possible first thing to signal the new day to your brain. Try getting a walk in first thing and letting your system experience the sun rise!

As the evening approaches reduce the use of ‘big lights’ in exchange for smaller side lights. The colour of the light matters too. White isn’t white. You can buy ‘white’ lights at different ‘kelvin ratings’. Go for ‘tungsten’ lights around 3200k for that warm cosy feel. Avoid the higher daylight balance 5600k bulbs in the evening but these might work well as supplemental light first thing on those dark winter mornings.

Dr Mark Horowitz has said he uses LED colour changing lighting in his house which change as the evening progresses mimicking a sunset! Brilliant!

 

 

Supplements

 

Some people choose to not use any supplements or find them too activating and are generally to be avoided. There have however been others who have found the following helpful during their recovery.

 

-Melatonin, our natural sleep hormone. Not available everywhere as a supplement but some have found it works very well. Little seems to be the key. Starting with a very low dose of perhaps 0.25mg. Others have reacted badly to taking this so caution is advised.

-Magnesium. Calms our nervous systems and many have found this to be a vital part of their bedtime routine. Again, start with a low dose and see how you get on.

-Omega 3 Fish oil

-Epsom Salt Baths

 

It’s worth mentioning that, as with all these things, some have seen no benefit and others have even reported reactions to the above so please bare this in mind.

 

 

Mindset

 

Our nervous systems are in a heightened and sensitized state during WD and tapering so we must do what we can to reduce the impact we have on it. This is especially important when it to comes to sleep. Most nondrug insomnia is caused by anxiety and its crucial we do what we can to not add to the sleep issues we face by overthinking or worrying about it. Its counter intuitive. The more we worry about sleep the less we sleep. It’s worth remembering that when you go to bed your only job is to relax and enjoy a rest. You can’t choose sleep, but your body knows how to get it. Remind yourself of this when sleep onset is challenging. It’s not your fault and you will sleep as much as your body needs!

 

How much sleep should I be getting?

 

This varies for everyone. As discussed above in acute stage, sleep can be scarce. But as we heal our sleep duration and quality increases, the body will always strive to achieve min sleep of around 5.5 hours. This can be a challenge in WD but trust your body knows how to do it and how much it needs. Some people naturally need less than others but 5-6 hours in WD is good. More is better!

 

What do I do if I can’t sleep?

 

Conventional sleep therapy suggests a technique of sleep limiting rather lying in bed for hours at a time. During WD we should perhaps be a little gentler than this. Where possible perhaps allocate a period of time for sleep each night and include a little more than you would like to get. This allows for any potential difficultly getting to sleep and stops the worrying at the start of the night. It also allows for some more sleep later on should onset be a challenge.

If you find it hard to sleep and or waking early, just resting in the dark and staying relaxed is in itself beneficial and it’s often possible to grab a few extra bits and pieces during these resting periods. Also, our brains will ‘secret sleep’ without us knowing. By staying in bed (if you can) for a set period of time you maximise the amount of sleep/rest your body will get and lay down the ground works for better sleep as you heal.

 

 

Napping

 

Some find an afternoon nap essential and, honestly, get the sleep where you can if that works for you. Others either can’t or find they wake to a feeling their sleep was somehow ‘toxic’ and perhaps choose to avoid. Overall trying to encourage a ‘normal’ sleep cycle is the goal.

I’m not a medical professional and cannot offer medical advice. I only offer my thoughts as support. Please speak to your health practitioner about your care. This is a peer site where we support each other on our taper/recovery journeys. 

 

If you are from the UK please make sure you fill in a 'Yellow Card' report for the MHRA. It is you doing your bit to help make a difference.

Please take the time to do it today 🙂 https://yellowcard.mhra.gov.uk

For US members details here.

  • Chippy unlocked this topic
  • 2 weeks later...

I recently learned a very helpful trick - when you wake up at night with terrors - my prominent symptom in the beginning - putting a cold compress (cold pad) on your forehead for 15 min allows to fall asleep quickly instead of ruminate.

Citalopram 20-30mg for 19 years, came off over 5 months, had to reinstate and taper over 6 years. 

Thank you so much for this! Insomnia was always the reason I reinstated in the past. But something good came out of it:

 

Lots of mainstream "advice" is full of horror scare stories about all the bad things that can happen to you if you don't get "enough" sleep. I won't list them. You've all heard them, I'm sure.

 

I'm here to tell you: none of those stories are true. I didn't sleep at night FOR MONTHS. I got maybe 20 minutes in naps during the day. I was in a lot of psychic pain, but I never lost it.

 

So, mindset is really important. 🙂

January 2001: klonopin, depakote, wellbutrin. Was experiencing overload from: getting married, selling my house, quitting my job, taking care of one grandmother as my other one died. All in the same year.  Asked Dr. for support and got called "mixed bi-polar" cuz I didn't have real bi polar symptoms.  AND I ACCEPTED THAT. UGH

 

Always felt sick on the meds so I would taper off. Then I would get EXTREME insomnia which I tolerated for several months before I would reinstate some combo. I've done this about 8 times. I'm extremely sensitive so I take really low doses. Still I feel sick.

 

Currently tapering off 1.4 mg paroxetine. Started at 20. Also on prasozin, 1 mg, Trileptal, 75, seroquel 50.

5/6/26 now on 2 mg paroxetine.

7/15/26 1.4 mg paroxetine

I absolutely agree @mars. I am not a fan of my GP in general but when I was panicking in the beginning that I couldn't sleep (I still don't sleep well) - he reassured me that I would be fine. I, of course, argued - how dare he, I will surely have a psychotic break. But he was right. Once I accepted that fact my sleep actually improved. I think sleeping longer is still better but I would also like to be a billionaire, I would like people to work for peace and for me to live on a beautiful tropical island - we rarely get what we want :) 

Citalopram 20-30mg for 19 years, came off over 5 months, had to reinstate and taper over 6 years. 

Lol. You sound quite mature in your radical acceptance. It has taken me a long time to recognize my need for that. 

And AMEN to spreading the word that insufficient sleep won't kill you or break you. Not ideal, but that's life. 

Thanks for sharing your  story

January 2001: klonopin, depakote, wellbutrin. Was experiencing overload from: getting married, selling my house, quitting my job, taking care of one grandmother as my other one died. All in the same year.  Asked Dr. for support and got called "mixed bi-polar" cuz I didn't have real bi polar symptoms.  AND I ACCEPTED THAT. UGH

 

Always felt sick on the meds so I would taper off. Then I would get EXTREME insomnia which I tolerated for several months before I would reinstate some combo. I've done this about 8 times. I'm extremely sensitive so I take really low doses. Still I feel sick.

 

Currently tapering off 1.4 mg paroxetine. Started at 20. Also on prasozin, 1 mg, Trileptal, 75, seroquel 50.

5/6/26 now on 2 mg paroxetine.

7/15/26 1.4 mg paroxetine

Oh no, not at all, I regularly throw mental tantrums when things are unfair. But sometimes there is no other way but to accept.


OMW

Citalopram 20-30mg for 19 years, came off over 5 months, had to reinstate and taper over 6 years. 

  • 3 months later...
  • Author

I’m not a medical professional and cannot offer medical advice. I only offer my thoughts as support. Please speak to your health practitioner about your care. This is a peer site where we support each other on our taper/recovery journeys. 

 

If you are from the UK please make sure you fill in a 'Yellow Card' report for the MHRA. It is you doing your bit to help make a difference.

Please take the time to do it today 🙂 https://yellowcard.mhra.gov.uk

For US members details here.

  • 1 month later...
On 2/4/2026 at 11:41 PM, mars said:

Thank you so much for this! Insomnia was always the reason I reinstated in the past. But something good came out of it:

 

Lots of mainstream "advice" is full of horror scare stories about all the bad things that can happen to you if you don't get "enough" sleep. I won't list them. You've all heard them, I'm sure.

 

I'm here to tell you: none of those stories are true. I didn't sleep at night FOR MONTHS. I got maybe 20 minutes in naps during the day. I was in a lot of psychic pain, but I never lost it.

 

So, mindset is really important. 🙂

Thank you @mars I needed your post. It's really helping me since I have been struggling with sleep and sometimes like today I haven't slept at all and stressing about it and overthinking it and recollecting horror stories really doesn't help. So thank you ❤️ We will get through this!

I used to watch a lot of this channel and it gave me a lot of hope and support:

https://youtube.com/@thesleepcoachschool8192?si=e1ns2ZTX0-Jn6HKU

I was actually able to get good sleep last year after following a rigorous naturopathic treatment. Then I stopped the naturopathy treatment and went back to this horrible allopathy hospital which drugged me up and my sleep was bad again (because I was so foolish and naive then and trusted the therapist I worked with then, have since broken up with that miserable hospital and therapist.)

Edited by PomogranatePi

Between 2012 to 2023: On and off Sertraline primarily. Lithium, Gabapentin, clonipin, thorazine tested on me.

December 2023 to mid 2025 was on sertraline 200 mg, desvenlafaxine 200mg, clonapin, antipsychotics. Stopped anti psychotics under physicians guidance since May, sleep medications tapered off since July 2025.

July - August 2025: tapered down to 75 mg sertraline

September 2025: Given lumiteperone (don't remember the dosage)

October 2025: Lumiteperone removed. Sertraline ard 100 mg added.

November 2025: Given a host of medications that I can't remember (I will look it up and add it,) but included lumiteperone

December 2025: removed off November meds and kept on sertraline and aripriprazole added.

Feb 2026: cold turkeyed off sertraline and aripriprazole.

May 2026 to present: Put on 40 mg Duloxetine

  • 2 weeks later...

Thanks for letting me know my words helped a little.

I recently let my prescriber/de-prescriber (I'm training him, LOL) HAVE IT, because of all the suffering his profession has caused me and THOUSANDS OF OTHERS. It's not only that they hand out these drugs without caution. It's that when we report that we're suffering, they BLAME US instead of informing us that yeah, these drugs cause lots of side effects.

But anger only gets me so far. Meaning, I did what you so wisely did: I fired most "mainstream"/legacy doctors. I'm very careful who I see with any aspect of my help. We live in times where finding fully informed, decent medical care is difficult. It takes research, work, and even losing some money by trying out doctors who look good on their website, but turn out to be more a YouTube star than a doctor.

Anyway, I feel your pain. And I join you in celebrating the growth! We are pretty awesome. The pain of getting off the drugs is worth it.

All that to say, your post really helped me remember why I'm doing this. Bless you!

January 2001: klonopin, depakote, wellbutrin. Was experiencing overload from: getting married, selling my house, quitting my job, taking care of one grandmother as my other one died. All in the same year.  Asked Dr. for support and got called "mixed bi-polar" cuz I didn't have real bi polar symptoms.  AND I ACCEPTED THAT. UGH

 

Always felt sick on the meds so I would taper off. Then I would get EXTREME insomnia which I tolerated for several months before I would reinstate some combo. I've done this about 8 times. I'm extremely sensitive so I take really low doses. Still I feel sick.

 

Currently tapering off 1.4 mg paroxetine. Started at 20. Also on prasozin, 1 mg, Trileptal, 75, seroquel 50.

5/6/26 now on 2 mg paroxetine.

7/15/26 1.4 mg paroxetine

  • 3 weeks later...

Can anybody commiserate with me or offer hope for people who actually DO have severe consequences from sleep deprivition? I read/hear so many talking about how they didnt go crazy and made it through etc etc. the last time i stayed calm and just allowed the insomnia to run its course I actually did end up with mild psychotic symptoms and cant help but feel like i posed permanent consequences because of that.

I feel awful i am popping some lyrica and other sleep meds prn but it just seems like for me, no sleep isnt just more resistance in mt day, my dysautonomia and gut and perception are all messed up. I just wish i knew how others weathered the storm of insomnia psychosis and came back.

2013

Initiated and quit citalopram /latuda for misdiagnosed bipolar (no withdrawal)

2021

Long covid symptoms began with dizzy spells, ringing ears, dpdr episodes, floaters

2025

March: Long covid became severe with insomnia, akathisia episodes, brain zaps, myoclonus in sleep, severe fatigue, tachycardia

April: diagnosed with “anxiety” and prescribed nortriptyline 20mg, cbti

Late april: discontinue nortriptyline cold turkey after presenting to Er with persistent symptoms and now chest pain and higher heart rate

May 6: begin taking 30mg cymbalta after prescribed cymbalta for “panic disorder” in er in april

June 29: Begin tapering cymbalta at 4-5 %every two weeks

(5% decrease every 2 weeks until below)

Dec 8 - 16 mg

Dec 22 - 12mg (big drop over break)

2026

Jan 5 - 7.5mg (big drop over break)

Feb 16 - 6.85ng

Feb 24 - 6.5

March 6 - 4.4

(Dropping by .175mg per week until may)

May 5 - 2.6mg

June 10 - 1.75mg

June 21 - 1.6 mg

June 25 - 1.4mg

July 1 - 1.2mg

July 22-25 - forced to temporarily go up to 1.3 bc of brand switching on work trip (forgot my meds at home had to acquire a different prescription)

July 26 - back to 1.2mg

  • 2 weeks later...
On 8/19/2026 at 12:28 PM, Jazzjunkie84 said:

Can anybody commiserate with me or offer hope for people who actually DO have severe consequences from sleep deprivition? I read/hear so many talking about how they didnt go crazy and made it through etc etc. the last time i stayed calm and just allowed the insomnia to run its course I actually did end up with mild psychotic symptoms and cant help but feel like i posed permanent consequences because of that.

I feel awful i am popping some lyrica and other sleep meds prn but it just seems like for me, no sleep isnt just more resistance in mt day, my dysautonomia and gut and perception are all messed up. I just wish i knew how others weathered the storm of insomnia psychosis and came back.

I’ve seen a few stories over on SA and some YouTube videos of people discussing insomnia. Granted I only like to read or watch success stories, but I’ve seen plenty where people actually got better and are sleeping again. Don’t feel guilty for doing what you need to do to survive. My primary complaint during WD has been sleep issues so I’ve been using a small amount of Unisom for almost 10 months now. I don’t see myself stopping it completely for a long time yet.

Drug History

December 2018 to July 2020:

Fluoxetine 10/20mg

July 2020-Nov 2025:

Celexa 10/20mg

June-December 2025:

Atenalol 25mg (for migraines)

December 2025-Current:

Unisom 12.5-6.25mg for sleep

Current Supplements:

Qunol Fish Oil 1,000mg

Olly Prenatal

Magnesium Glycinate 210mg

Temporary Use in 2026:

Vitamin D.

GABA

5HTP

B6

Methylated Folate/ B12

  • Author
11 hours ago, Sara said:

so I’ve been using a small amount of Unisom for almost 10 months now.

We respect members choices to do what they think is right. For the benefit of others reading this though, Unisom is psychoactive and taking it isn't advisable.

I’m not a medical professional and cannot offer medical advice. I only offer my thoughts as support. Please speak to your health practitioner about your care. This is a peer site where we support each other on our taper/recovery journeys. 

 

If you are from the UK please make sure you fill in a 'Yellow Card' report for the MHRA. It is you doing your bit to help make a difference.

Please take the time to do it today 🙂 https://yellowcard.mhra.gov.uk

For US members details here.

4 hours ago, Chippy said:

We respect members choices to do what they think is right. For the benefit of others reading this though, Unisom is psychoactive and taking it isn't advisable.

I’ve done my best to not take anything but after a year of not sleeping well, sadly it’s either that or be non-functional for my family. I’ve tried researching for better options and my doctor offered me amitriptyline and gabapentin, which I thankfully denied in hindsight. I kind of see it as the lesser of all evils at the moment, especially since I’m not even taking half a dose. Maybe it’s different for me because I’ve had to use it my pregnancies as part of the B6/Unisom protocol for morning sickness, so I’m less sensitized to it. I’m so discouraged as I’ve done all the recommended things: magnesium, earplugs, sleep hygiene, blackout curtains, not eating/drinking for hours before bed, no caffeine or high amounts of sugar. There is literally nothing else to try.

Do you think the Unisom will keep me from healing? I ask because my husband and I are unsure that we’re done having children. When I’m pregnant, I typically take multiple nausea meds that aren't recommended for people in withdrawal, yet I can’t wait years and years for complete healing. Trying to figure if this chapter is closed for good in my life has been heartbreaking. I understand that you, as well as many others don’t have every answer, but I’d love your opinion, Chippy.

Drug History

December 2018 to July 2020:

Fluoxetine 10/20mg

July 2020-Nov 2025:

Celexa 10/20mg

June-December 2025:

Atenalol 25mg (for migraines)

December 2025-Current:

Unisom 12.5-6.25mg for sleep

Current Supplements:

Qunol Fish Oil 1,000mg

Olly Prenatal

Magnesium Glycinate 210mg

Temporary Use in 2026:

Vitamin D.

GABA

5HTP

B6

Methylated Folate/ B12

  • Author
17 hours ago, Sara said:

I’ve done my best to not take anything but after a year of not sleeping well, sadly it’s either that or be non-functional for my family. I’ve tried researching for better options and my doctor offered me amitriptyline and gabapentin, which I thankfully denied in hindsight. I kind of see it as the lesser of all evils at the moment, especially since I’m not even taking half a dose. Maybe it’s different for me because I’ve had to use it my pregnancies as part of the B6/Unisom protocol for morning sickness, so I’m less sensitized to it.

I totally respect your choices here, and I know sometimes we sound like we are pill shaming, it isn't our intention, we are just trying to share the knowledge of the community in an attempt to keep people safe and give them the best long term outcome possible.

17 hours ago, Sara said:

I’m so discouraged as I’ve done all the recommended things: magnesium, earplugs, sleep hygiene, blackout curtains, not eating/drinking for hours before bed, no caffeine or high amounts of sugar. There is literally nothing else to try.

Like all drugs, tolerance is built up and the effectiveness or benefits will lessen over time.

Unfortunately your experience here with sleep is common in WD. We all do all the things that are supposed to help sleep as you mention above, the reality is these things do help but can't undo the injury that has happened to the sleep archiecture (knowone knows the actual mechanics of the injury, but it's clear to me it's very real), time is the healer here imo. Im still dealing with this to a lesser but signifcant degree 2.5+ years later. Main thing is to set the foundation for healing as we will have mentioned at the end of your intro post you recieved from us when you joined/started your personal topic.

17 hours ago, Sara said:

Do you think the Unisom will keep me from healing? I ask because my husband and I are unsure that we’re done having children. When I’m pregnant, I typically take multiple nausea meds that aren't recommended for people in withdrawal, yet I can’t wait years and years for complete healing. Trying to figure if this chapter is closed for good in my life has been heartbreaking. I understand that you, as well as many others don’t have every answer, but I’d love your opinion, Chippy.

I can't know that. I can say that taking additional substances that are psychoactive is seen as upsetting to a nervous system that is already sensitive. I would say that if you wanted to stop taking it, as you have been taking them consistently for a long time, I wouldn't stop CT. I would start to taper them with a set of scales and just reduce at your own pace over a period of time till your off. I would worry rebound insomnia might be a problem otherwise.

I know the timescales of healing are daunting, and I know it really messes with lifes plans. I can't tell you what you should or shouldn't do with your family planning or how long this will take to resolve. What I would say is that we all in WD have to accept the reality of what has happened and adjust our plans and expectations accordingly, keeping our mind on the day in hand and not thinking too much about what comes next. Acceptance is peace, peace calms the nervous system and helps it heal imo.

Chippy

I’m not a medical professional and cannot offer medical advice. I only offer my thoughts as support. Please speak to your health practitioner about your care. This is a peer site where we support each other on our taper/recovery journeys. 

 

If you are from the UK please make sure you fill in a 'Yellow Card' report for the MHRA. It is you doing your bit to help make a difference.

Please take the time to do it today 🙂 https://yellowcard.mhra.gov.uk

For US members details here.

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