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Overstimulation: Increased sensitivity to light, noise, sound, exercise etc


machawolf

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I just wanted to add my experience to the thread.

 

I have a disturbing inability to watch anything on TV, or read almost anything on the internet or in books. When I attempt to do these things, I get the most irrational fear washing over my brain, and my brain goes into almost full meltdown. I can't accurately describe what happens, but it's terrifying (and that's not hyperbole).

 

I have a select few shows I can watch in reasonable safety, namely British comedy panel shows, and only a single web site I can read (other than this one) that is about virtual reality (a subject/hobby I love, but can no longer participate in, other than reading about it).

 

Also, I absolutely cannot listen to music...it also sends my brain into a tail-spin.

My previous drug history was confusing, so I deleted it in favour of the following summary, as best I can recall:

2017 - Jun 2019: olanzapine, dose erratic, ranging from 1.25 to 2.5mg per day.

2017 - Jun 2019: klonopin, dose erratic, ranging from 0.0625mg twice a day to 0.25mg twice a day.

2017 - Jun 2019: gabapentin, dose erratic, ranging from 200 to 300mg per day.

Date uncertain: Lamotrigine, small amount for two months, C/T.

Jun 2019: admitted to hospital after months of severe rage (which I am certain was caused by akathesia, but no doctor caught it). Doctors cold-turkeyed all drugs, I submitted to 10 courses of ECT, and was put on 50mg of seroquel at bedtime.

Jul 2019 - Feb 2020: reduced seroquel sporadically from 50mg to 18.75mg.

Apr 19, 2020: Reduced seroquel from 18.75mg to 16.5mg.

 

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  • 2 months later...
  • Moderator Emeritus

I've discovered noise cancelling headphones and they are great.  At work I sit near an old, noisy air conditioner and they block it out really well.  I must look really crazy, sitting at the computer with my large (brown framed not black thankfully) blue light over glasses (they are much larger than my Cancer Council over glasses sunglasses) and my headphones.  The external walls of the building are full glass and there is a lot of glare and of course the fluoro lights.  The only issue I have is trying to get the arms of my prescription glasses and blue light glasses in the correct position so they don't interfere with the ear cups.

* NO LONGER ACTIVE on SA *

MISSION ACCOMPLISHED:  (6 year taper)      0mg Pristiq  on 13th November 2021

ADs since ~1992:  25+ years - 1 unknown, Prozac (muscle weakness), Zoloft; citalopram (pooped out) CTed (very sick for 2.5 wks a few months after); Pristiq:  50mg 2012, 100mg beg 2013 (Serotonin Toxicity)  Tapering from Oct 2015 - 13 Nov 2021   LAST DOSE 0.0025mg

Post 0 updates start here    My tapering program     My Intro (goes to tapering graph)

 VIDEO:   Antidepressant Withdrawal Syndrome and its Management

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  • 1 month later...
  • Mentor
On 7/9/2016 at 1:10 AM, Petunia said:

I've always had problems being under fluorescent lighting, at first its a subtle feeling like my perceptions are a bit wrong, there's a slight shift in the way things look and sound. Over time it makes me tired and irritated, then I get anxious and usually end up with a headache...

I have finally learned that this is exactly true for me. I was at an AA conference in LA... thought I could do it. Yesterday was in fluorescent lights with stale air for several hours. Left early with nausea and a migraine. Almost vomited and had to lie perfectly still for over 12 hours except for a bit of EFT tapping when I could muster movement.  Today spent most of it outdoors and drinking pu-erh tea. Definitely better if not baseline.

  • Prozac | late 2004-mid-2005 | CT WD in a couple months, mostly emotional
  • Sertraline 50-100mg | 11/2011-3/2014, 10/2014-3/2017
  • Sertraline fast taper March 2017, 4 weeks, OFF sertraline April 1, 2017
  • Quit alcohol May 20, 2017
  • Lifestyle changes: AA, kundalini yoga

 

"If you've seen a monster, even if it's horrible, that's evidence of divinity." – Damien Echols

 

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  • 4 weeks later...

I thought that I would just update on my situation with the noise sensitivity. In many ways it’s been the most disruptive symptom of my withdrawals. It’s so strange. When I have it, I am absolutely convinced that my neighbours are the noisiest neighbours in the world!! I have to watch tv with wax earplugs in and with the subtitles on . This can go on for 2 or 3 weeks and then it just goes. I will be sitting there, actually waiting for the noise and it doesn’t happen. For the first couple of nights , I will be convinced that they are out , then, I go to the wall, put my ear to the wall and I can just about hear it !!  It’s unbelievable the difference in noise intensity from one period to the next. At the moment , I haven't got it andI always promise myself that I will be prepared for when it happens again but it always takes me by surprise. 

Quote

Dosulepin 75 mgs per night since 1993.           Dosulepin March 16  2018   75mgs and 50 mgs alternate nights.             Dosulepin. March 30. 2018.  50 mgs per night

Dosulepin. May 2. 2018. 50mgs and 25 mgs alternate nights

Dosulepin. May 27 2018. 50 mgs per night ( increased )

Dosulepin. July 11 2018. 45 mgs per night

Dosulepin. August 13 2018  40 mgs per night

Dosulepin  October 10 2018. 37.5 mgs per night

Dosulepin. October. 24 2018. 35 mgs per night

Dosulepin. December 5 2018. 32.5 mgs per night

Dosulepin.  January 2. 2018  30mgs per night   February 14 2018  29 mgs per night

Dosulepin February 27  28 mgs per night

 

 

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  • 3 weeks later...
On 6/4/2016 at 8:26 PM, tntd said:

I find that a lot of motion around me causes my anxiety to escalate. Sometimes my husband comes around a corner and it scares the heck out of me. Or if he touches me and I'm not expecting it. Noises also increase my anxiety. 

 

I have this too. Describes exactly . Motion of all kinds and wind ?? causes me to feel fear. Cloudy weather and cold  weather also frighten me. Also, when the sun goes in I feel fear. It’s like the sensory changes act on the cns and instigate the fight or flight response. I realise not only does noise cause pain but fear too! It’s all related. Someone mentioned it all then contributing to DR/DP. Get this too.

1999:  Paroxetine (20mg). Age 16. 2007-2008: Fluoxetine (Prozac) for 1.5 years (age 25) Citalopram 20mg 2002-2005, 2009: Escitalopram (20mg), 2 weeks, (age 26) (adverse  reaction)/*Valium 5mg/Temazepam 10mg 2010: Mirtazipine (Remeron)( do not remember dosage) 2010, 5 months.                     2010-2017: Citalopram (20mg) (age 27 to 34) 2016: i.1st Sept- 31st Oct Citalopram 10mg , ii.1st November 2017-30th November 2017, Citalopram 5mg iii.1st December 2017- 4th February 2018, Citalopram 0mg, iv.5th February 2018- March 2018 Citalopram 5mg (10mg every other day) 28th February- tried titration of 5mg ( some adverse effects)

2018: 1st March 2018- 1st June Citalopram 10 mg (tablet form) /started titration 8mg , then 7 mg.2018: June 15th- 10th July Citalopram 10 mg pill every other day 2018: 10th July - 13th Sept Citalopram- 0mg  (CBD oil first month of 0mg, passiflora on and off) 2018 13th Sept Citalopram  2mg ,  approx 16th Sept 4mg , approx 25th Sept 6mg held.  2019: 11 Feb 19: 7mg (instant bad rxn) 12 Feb 19 6mg held 1 May 19 5.4mg held 5 Oct 19 5.36mg 22 Oct 19 5.29mg 30 Oct 19 5.23mg 4/NOV/19 5.18mg 12 Nov 19 5.08mg 20 Nov 19 4.77mg 7 May 22 2.31mg 17/09/2023 0.8mg

(Herbal/Supplements since 1st September: Omega Fish Oil 1200mg, 663mg of EPA- 2 tablets a day, magnesium and magnesium bath salts)

I did not die, and yet I lost life’s breath
- Dante
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On 6/8/2018 at 8:21 AM, alyheartsux3 said:

I went to an audiologist to see if I have hyperacusis, and she insists that my hearing is normal and I don't. She says that it is my limbic symptom that is messed up and I have normal functioning ears. 

That’s really interesting . Need to find out more. It’s like my vision is disturbed by light sensitivity but I have been tested and have 20/20 vision.

1999:  Paroxetine (20mg). Age 16. 2007-2008: Fluoxetine (Prozac) for 1.5 years (age 25) Citalopram 20mg 2002-2005, 2009: Escitalopram (20mg), 2 weeks, (age 26) (adverse  reaction)/*Valium 5mg/Temazepam 10mg 2010: Mirtazipine (Remeron)( do not remember dosage) 2010, 5 months.                     2010-2017: Citalopram (20mg) (age 27 to 34) 2016: i.1st Sept- 31st Oct Citalopram 10mg , ii.1st November 2017-30th November 2017, Citalopram 5mg iii.1st December 2017- 4th February 2018, Citalopram 0mg, iv.5th February 2018- March 2018 Citalopram 5mg (10mg every other day) 28th February- tried titration of 5mg ( some adverse effects)

2018: 1st March 2018- 1st June Citalopram 10 mg (tablet form) /started titration 8mg , then 7 mg.2018: June 15th- 10th July Citalopram 10 mg pill every other day 2018: 10th July - 13th Sept Citalopram- 0mg  (CBD oil first month of 0mg, passiflora on and off) 2018 13th Sept Citalopram  2mg ,  approx 16th Sept 4mg , approx 25th Sept 6mg held.  2019: 11 Feb 19: 7mg (instant bad rxn) 12 Feb 19 6mg held 1 May 19 5.4mg held 5 Oct 19 5.36mg 22 Oct 19 5.29mg 30 Oct 19 5.23mg 4/NOV/19 5.18mg 12 Nov 19 5.08mg 20 Nov 19 4.77mg 7 May 22 2.31mg 17/09/2023 0.8mg

(Herbal/Supplements since 1st September: Omega Fish Oil 1200mg, 663mg of EPA- 2 tablets a day, magnesium and magnesium bath salts)

I did not die, and yet I lost life’s breath
- Dante
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On 3/5/2019 at 7:02 PM, Steve61 said:

I thought that I would just update on my situation with the noise sensitivity. In many ways it’s been the most disruptive symptom of my withdrawals. It’s so strange. When I have it, I am absolutely convinced that my neighbours are the noisiest neighbours in the world!! I have to watch tv with wax earplugs in and with the subtitles on . This can go on for 2 or 3 weeks and then it just goes. I will be sitting there, actually waiting for the noise and it doesn’t happen. For the first couple of nights , I will be convinced that they are out , then, I go to the wall, put my ear to the wall and I can just about hear it !!  It’s unbelievable the difference in noise intensity from one period to the next. At the moment , I haven't got it andI always promise myself that I will be prepared for when it happens again but it always takes me by surprise. 

@Steve61This is fascinating. I’ve had no let up and I feel tortured by my upstairs neighbour. But though they do bang around I experience it like a building site. I have nothing to compare it to since no let up but suspect what you have proven with your own windows. I put ear plugs on when she walks around. Some weeks back I was also sending messages to my family from the guest room because they were talking in the hall way “so loudly”. Apparently, they were just talking normally but they sounded like they were shouting to me. It’s great you get respite. I wonder what helps it shift for you?

1999:  Paroxetine (20mg). Age 16. 2007-2008: Fluoxetine (Prozac) for 1.5 years (age 25) Citalopram 20mg 2002-2005, 2009: Escitalopram (20mg), 2 weeks, (age 26) (adverse  reaction)/*Valium 5mg/Temazepam 10mg 2010: Mirtazipine (Remeron)( do not remember dosage) 2010, 5 months.                     2010-2017: Citalopram (20mg) (age 27 to 34) 2016: i.1st Sept- 31st Oct Citalopram 10mg , ii.1st November 2017-30th November 2017, Citalopram 5mg iii.1st December 2017- 4th February 2018, Citalopram 0mg, iv.5th February 2018- March 2018 Citalopram 5mg (10mg every other day) 28th February- tried titration of 5mg ( some adverse effects)

2018: 1st March 2018- 1st June Citalopram 10 mg (tablet form) /started titration 8mg , then 7 mg.2018: June 15th- 10th July Citalopram 10 mg pill every other day 2018: 10th July - 13th Sept Citalopram- 0mg  (CBD oil first month of 0mg, passiflora on and off) 2018 13th Sept Citalopram  2mg ,  approx 16th Sept 4mg , approx 25th Sept 6mg held.  2019: 11 Feb 19: 7mg (instant bad rxn) 12 Feb 19 6mg held 1 May 19 5.4mg held 5 Oct 19 5.36mg 22 Oct 19 5.29mg 30 Oct 19 5.23mg 4/NOV/19 5.18mg 12 Nov 19 5.08mg 20 Nov 19 4.77mg 7 May 22 2.31mg 17/09/2023 0.8mg

(Herbal/Supplements since 1st September: Omega Fish Oil 1200mg, 663mg of EPA- 2 tablets a day, magnesium and magnesium bath salts)

I did not die, and yet I lost life’s breath
- Dante
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On 12/29/2018 at 8:15 AM, ChessieCat said:

I've discovered noise cancelling headphones and they are great.  At work I sit near an old, noisy air conditioner and they block it out really well.  I must look really crazy, sitting at the computer with my large (brown framed not black thankfully) blue light over glasses (they are much larger than my Cancer Council over glasses sunglasses) and my headphones.  The external walls of the building are full glass and there is a lot of glare and of course the fluoro lights.  The only issue I have is trying to get the arms of my prescription glasses and blue light glasses in the correct position so they don't interfere with the ear cups.

This made me chuckle so much 

1999:  Paroxetine (20mg). Age 16. 2007-2008: Fluoxetine (Prozac) for 1.5 years (age 25) Citalopram 20mg 2002-2005, 2009: Escitalopram (20mg), 2 weeks, (age 26) (adverse  reaction)/*Valium 5mg/Temazepam 10mg 2010: Mirtazipine (Remeron)( do not remember dosage) 2010, 5 months.                     2010-2017: Citalopram (20mg) (age 27 to 34) 2016: i.1st Sept- 31st Oct Citalopram 10mg , ii.1st November 2017-30th November 2017, Citalopram 5mg iii.1st December 2017- 4th February 2018, Citalopram 0mg, iv.5th February 2018- March 2018 Citalopram 5mg (10mg every other day) 28th February- tried titration of 5mg ( some adverse effects)

2018: 1st March 2018- 1st June Citalopram 10 mg (tablet form) /started titration 8mg , then 7 mg.2018: June 15th- 10th July Citalopram 10 mg pill every other day 2018: 10th July - 13th Sept Citalopram- 0mg  (CBD oil first month of 0mg, passiflora on and off) 2018 13th Sept Citalopram  2mg ,  approx 16th Sept 4mg , approx 25th Sept 6mg held.  2019: 11 Feb 19: 7mg (instant bad rxn) 12 Feb 19 6mg held 1 May 19 5.4mg held 5 Oct 19 5.36mg 22 Oct 19 5.29mg 30 Oct 19 5.23mg 4/NOV/19 5.18mg 12 Nov 19 5.08mg 20 Nov 19 4.77mg 7 May 22 2.31mg 17/09/2023 0.8mg

(Herbal/Supplements since 1st September: Omega Fish Oil 1200mg, 663mg of EPA- 2 tablets a day, magnesium and magnesium bath salts)

I did not die, and yet I lost life’s breath
- Dante
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  • Moderator Emeritus
25 minutes ago, India said:

This made me chuckle so much 

 

I hadn't realised how big my glasses were until I forgot to take them off one day and went to the bathroom and saw myself in the mirror.

 

However, I don't care about how I look so long as I'm more comfortable.  But I'm used to it.  I get some funny looks when I'm travelling on the train and take out a miniature storage box (like a lunch box with no lid) to use as a foot stool.  I have short legs and if I don't sit with a stool I get sciatica.  But I've also had people say to me what a good idea.

* NO LONGER ACTIVE on SA *

MISSION ACCOMPLISHED:  (6 year taper)      0mg Pristiq  on 13th November 2021

ADs since ~1992:  25+ years - 1 unknown, Prozac (muscle weakness), Zoloft; citalopram (pooped out) CTed (very sick for 2.5 wks a few months after); Pristiq:  50mg 2012, 100mg beg 2013 (Serotonin Toxicity)  Tapering from Oct 2015 - 13 Nov 2021   LAST DOSE 0.0025mg

Post 0 updates start here    My tapering program     My Intro (goes to tapering graph)

 VIDEO:   Antidepressant Withdrawal Syndrome and its Management

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@ChessieCat yes, it’s a great idea. Who knows, it might take off. In the part of London I live in (lots of artists) there is a general anarchy in respect to what is worn. You can literally wear anything and no one cares. Ive been out in my silk pyjama bottoms  and all sorts. It’s that kind of neighbourhood. I just chuckled because I like it. Wear what you want and what you need! It’s for you! I had been walking around city with silicone earplugs! Next purchase: ear cancelling headphones ! 

1999:  Paroxetine (20mg). Age 16. 2007-2008: Fluoxetine (Prozac) for 1.5 years (age 25) Citalopram 20mg 2002-2005, 2009: Escitalopram (20mg), 2 weeks, (age 26) (adverse  reaction)/*Valium 5mg/Temazepam 10mg 2010: Mirtazipine (Remeron)( do not remember dosage) 2010, 5 months.                     2010-2017: Citalopram (20mg) (age 27 to 34) 2016: i.1st Sept- 31st Oct Citalopram 10mg , ii.1st November 2017-30th November 2017, Citalopram 5mg iii.1st December 2017- 4th February 2018, Citalopram 0mg, iv.5th February 2018- March 2018 Citalopram 5mg (10mg every other day) 28th February- tried titration of 5mg ( some adverse effects)

2018: 1st March 2018- 1st June Citalopram 10 mg (tablet form) /started titration 8mg , then 7 mg.2018: June 15th- 10th July Citalopram 10 mg pill every other day 2018: 10th July - 13th Sept Citalopram- 0mg  (CBD oil first month of 0mg, passiflora on and off) 2018 13th Sept Citalopram  2mg ,  approx 16th Sept 4mg , approx 25th Sept 6mg held.  2019: 11 Feb 19: 7mg (instant bad rxn) 12 Feb 19 6mg held 1 May 19 5.4mg held 5 Oct 19 5.36mg 22 Oct 19 5.29mg 30 Oct 19 5.23mg 4/NOV/19 5.18mg 12 Nov 19 5.08mg 20 Nov 19 4.77mg 7 May 22 2.31mg 17/09/2023 0.8mg

(Herbal/Supplements since 1st September: Omega Fish Oil 1200mg, 663mg of EPA- 2 tablets a day, magnesium and magnesium bath salts)

I did not die, and yet I lost life’s breath
- Dante
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Did anyone have hyperacusis as a withdrawal symptom?  Im 3 months off and it keeps getting worse? Can it get better? 

December 2017- start 15mg mirtazapine

March 2018 - reduce from 15 to 7,5mg then after 2 weeks reduce tot 3,75mg

April 2018- going back to 7,5mg

July 2018-tapered 1mg off every 2 weeks.

September 2018- 4,5mg 

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On 12/29/2018 at 10:15 AM, ChessieCat said:

I've discovered noise cancelling headphones and they are great.  At work I sit near an old, noisy air conditioner and they block it out really well.  I must look really crazy, sitting at the computer with my large (brown framed not black thankfully) blue light over glasses (they are much larger than my Cancer Council over glasses sunglasses) and my headphones.  The external walls of the building are full glass and there is a lot of glare and of course the fluoro lights.  The only issue I have is trying to get the arms of my prescription glasses and blue light glasses in the correct position so they don't interfere with the ear cups.

 

 

I use also noise cancelling headphones, I believe they are the same sony 660 model

2011 protracted withdrawal symptoms from Effexor, managed to come off
2013-2015  risperidone consta 50 mg, started tapering from March 2015 to 1,66mg/day and from 02/2015 started seroxat 10mg/day

01/17 Seroxat 2,0mg,olanzapine 5mg,risperidone consta 25mg/every 15days

05/17 Seroxat 1mg,olanzapine 5mg,risp.consta 25mg/every 15days

06/17 Seroxat 2drops,olanzapine 5mg,liquid risperidone2mg

07/17 Seroxat 1 drop,olanzapine 5mg,Risperidone 0mg, 10/17 Seroxat 0mg,olanzapine,5mg,Risperidone 0mg, 12/17 Seroxat 1/2 drop, olanzapine 5mg,  04/18 Olanzapine 1,25mg, 04/18 xanax 0,5mg

24/06/2019 doc said to take 10mg olanzapine for 13days and down to 5mg
 been taking 10mg for 14 days, 5mg for 8 days  and  tapered to  3/4quart. 5mg  for 14 days, 1/2 for 14 days,

01/08/19 2,5mg

08/2021 5mg olanzapine

Supplements Omega 3, Turmeric, Bacopa monneri, Mucuna Pruriens

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  • Altostrata changed the title to Overstimulation: Increased sensitivity to light, noise, sound, exercise etc
  • 4 months later...
On 3/24/2019 at 10:21 AM, Gth27 said:

Did anyone have hyperacusis as a withdrawal symptom?  Im 3 months off and it keeps getting worse? Can it get better? 

Hello, @Gth27. though I have other symptoms and not fully healed yet, I can report my hyperacusis is significantly better. This happened so gradually, until yesterday I realised how far i’d come. 

 

Every noise struck terror into my heart. It was as if every noise was amplified and no discrimination. It was tortuous. Any noise would cause pain. I also got what I call ‘Superman hearing’ or the inability to distinguish distances of sound so sensitive was I to noise. Honestly, I developed a seemingly superhero  the ability to hear conversations normally out of earshot, this might have been fun if it were not so painful. I wore ear plugs all the time, inside and outside. 

 

Now I may get a relapse for a day if other symptoms bad but now I can tolerate most noises ( though still sensitive ), sirens, motorbikes, children crying in an extreme way, noise from the wheels against rails when underground (subway) windows are open are the only thing that trigger it, but I usually just put my fingers in my ears til it passes. 

 

It reminds me to be grateful.

 I noticed that sustained  peaceful environment and rest helped me with this symptoms . I feel like it was tied to cortisol response.

 

@emilie @Harriet8 @Hisame

 

1999:  Paroxetine (20mg). Age 16. 2007-2008: Fluoxetine (Prozac) for 1.5 years (age 25) Citalopram 20mg 2002-2005, 2009: Escitalopram (20mg), 2 weeks, (age 26) (adverse  reaction)/*Valium 5mg/Temazepam 10mg 2010: Mirtazipine (Remeron)( do not remember dosage) 2010, 5 months.                     2010-2017: Citalopram (20mg) (age 27 to 34) 2016: i.1st Sept- 31st Oct Citalopram 10mg , ii.1st November 2017-30th November 2017, Citalopram 5mg iii.1st December 2017- 4th February 2018, Citalopram 0mg, iv.5th February 2018- March 2018 Citalopram 5mg (10mg every other day) 28th February- tried titration of 5mg ( some adverse effects)

2018: 1st March 2018- 1st June Citalopram 10 mg (tablet form) /started titration 8mg , then 7 mg.2018: June 15th- 10th July Citalopram 10 mg pill every other day 2018: 10th July - 13th Sept Citalopram- 0mg  (CBD oil first month of 0mg, passiflora on and off) 2018 13th Sept Citalopram  2mg ,  approx 16th Sept 4mg , approx 25th Sept 6mg held.  2019: 11 Feb 19: 7mg (instant bad rxn) 12 Feb 19 6mg held 1 May 19 5.4mg held 5 Oct 19 5.36mg 22 Oct 19 5.29mg 30 Oct 19 5.23mg 4/NOV/19 5.18mg 12 Nov 19 5.08mg 20 Nov 19 4.77mg 7 May 22 2.31mg 17/09/2023 0.8mg

(Herbal/Supplements since 1st September: Omega Fish Oil 1200mg, 663mg of EPA- 2 tablets a day, magnesium and magnesium bath salts)

I did not die, and yet I lost life’s breath
- Dante
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  • 2 weeks later...

Definitely still have the increased sensitivity to exercise, exertion, lifting weights, sports, etc. Other things have improved vastly, as I don't have the food sensitivities that I used to, nor do I have the chemical sensitivities to the extreme. Other things have relaxed as well, but the exertion malaise, sensitivity is still there. It's improved, but still there. .. which is tough, as I used to lift weights, play basketball, work hard, etc.

 

That's pretty normal eh? If I were to lift weights and work out right now, I'd no doubt for the next week feel a sharp increase in mood issues, very high anxiety and tremors, cognitive problems, increased akathisia and agitation, and be exhausted and in pain. It's just not going to happen right now.

Took Accutane in 2007 at age 19 and a severe reaction to it threw me into Psychiatry's dirty hands. Suffered through a number of c/t's, rapid tapers, drug switches, reinstatements before finally figuring out what was happening to me in 2012 after checking out of psych hospital with a prescription for Ativan and Prozac. (Went in because was unknowingly in Xanax c/t wd and dying at the time from it).

 

May 2016 - Last dose of Valium after 2 year long taper from 15mg

June 2017- Last dose of the corticosteroid Hydrocortisone after taper

July 2019- Last dose of Prozac after 2 year long taper from 30mg

 

Was on Accutane, Lexapro, Celexa, Xanax, Ativan, Prozac, Hydrocorisone, Valium, and thyroid meds when none of them were needed. Still recovering to this day and hope to be healed in the coming months, but taking it one day at a time.

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  • 3 months later...

Hi everyone. I am 19 months into withdrawal and one of the toughest things I am experiencing (which is not abating) is an extreme sensitivity to screens (phone/laptop/TV). Like a vampire exposed to light, my head goes crazy when I pick up the phone or try to look at any screen (TV or laptop). I get strange sensations in my head and it even impacts my speech slightly. Like my nervous system slows down and I can't speak properly after I look at a screen for more than a few minutes. I am struggling to type this message (which I am doing indoors with sunglasses on to alleviate the strange sensations) but I need some information/reassurance from anyone. Is this a withdrawal symptom? I have a host of other symptoms but they are common WD ones so I can easily attribute them to WD. But this bizarre symptom. Anyone heard of it? 

Summer 2016 - summer 2018: put on Lexapro, going from 5 mg up to 20 mg over the span of the 2 years (had visited shrink for help with obsessive thinking, was not diagnosed with anything in particular, just prescribed Lexapro 15 mins into first session)

Summer 2018: tapered down by 2.5 mg every few weeks

Protracted withdrawal ever since. 0-14 months began with a massive panic attack that landed me in ER, followed by prolonged anxiety, mental fog and a skin rash on my back. Was regularly consuming alcohol as did not know I was in WD. From then onwards, hit with worse myriad symptoms. Currently at 22 months and have electromagnetic sensitivity, brain zaps, brain fog, memory problems (especially name recall), twitch in right eyebrow, daily waking up at 3 or 4 a.m. with fast heartbeats and "sticky" negative memories, suicidal thoughts, rage episodes, temperature dysregulation, physical numbness & weakness, libido loss.   

 

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Anyone? 

Summer 2016 - summer 2018: put on Lexapro, going from 5 mg up to 20 mg over the span of the 2 years (had visited shrink for help with obsessive thinking, was not diagnosed with anything in particular, just prescribed Lexapro 15 mins into first session)

Summer 2018: tapered down by 2.5 mg every few weeks

Protracted withdrawal ever since. 0-14 months began with a massive panic attack that landed me in ER, followed by prolonged anxiety, mental fog and a skin rash on my back. Was regularly consuming alcohol as did not know I was in WD. From then onwards, hit with worse myriad symptoms. Currently at 22 months and have electromagnetic sensitivity, brain zaps, brain fog, memory problems (especially name recall), twitch in right eyebrow, daily waking up at 3 or 4 a.m. with fast heartbeats and "sticky" negative memories, suicidal thoughts, rage episodes, temperature dysregulation, physical numbness & weakness, libido loss.   

 

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Yes. I have very bad sensitivity to both screens and light. I don’t feel like I’m here sometimes. Dealing with it as I type this. I got a new TV in January and can barely watch it. I don’t know what you are coming off of, but I am about 17 months or so into this. 

Prozac (2007-2008), Zoloft (2009-2017) Paxil (2017-2018), Celexa (2018), Luvox (2018-Current) Average 50-200. Nothing as of January 2019

Lorazepam 2007-Current 2MG 3 times a day

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 Thank you for your feedback. I thought I was the only one. I started doubting that it's a withdrawal symptom but clearly it is since you're experiencing it too. It is listed as a symptom on the website of The Withdrawal Project. That's how I knew what this bizarre condition was even called. I came off Cipralex 19 months ago (had been taking it for two years) and at the beginning had a panic attack, anxiety and skin problems. Then about 5 months ago I was hit with a barrage of bizarre new symptoms including sensitivity to sound and extreme sensitivity to screens, speech problems, suicidal thoughts out of the blue, and muscle pain among others. I hope we all heal soon. 

Summer 2016 - summer 2018: put on Lexapro, going from 5 mg up to 20 mg over the span of the 2 years (had visited shrink for help with obsessive thinking, was not diagnosed with anything in particular, just prescribed Lexapro 15 mins into first session)

Summer 2018: tapered down by 2.5 mg every few weeks

Protracted withdrawal ever since. 0-14 months began with a massive panic attack that landed me in ER, followed by prolonged anxiety, mental fog and a skin rash on my back. Was regularly consuming alcohol as did not know I was in WD. From then onwards, hit with worse myriad symptoms. Currently at 22 months and have electromagnetic sensitivity, brain zaps, brain fog, memory problems (especially name recall), twitch in right eyebrow, daily waking up at 3 or 4 a.m. with fast heartbeats and "sticky" negative memories, suicidal thoughts, rage episodes, temperature dysregulation, physical numbness & weakness, libido loss.   

 

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At this rate I don’t think any odd symptom that seems to pop up is not related to withdrawal. Screens, light distortion seems to be one of the bigger ones. Might be related to the depersonalization. I’ve gone to ENT doctors for my bad right ear, eye doctors for my vision, a neurologist, had an MRI, went to dermatologist for my skin.  All gave me a response “There is nothing wrong.”

Prozac (2007-2008), Zoloft (2009-2017) Paxil (2017-2018), Celexa (2018), Luvox (2018-Current) Average 50-200. Nothing as of January 2019

Lorazepam 2007-Current 2MG 3 times a day

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Dr. Peter Breggin, known as the conscience of psychiatry, said that after stopping these meds people can pretty much attribute any symptoms they have to withdrawal.  I did CT scans and MRIs too months back because I was getting dizzy spells and strange sensations in the right side of my head in addition to my speech slowing down whenever I looked at screens for a long time. The tests came back saying "all normal." Psychiatrists said it's anxiety. "Some of those symptoms are unusual but anxiety can cause strange things, " my shrink said. But of course I didn't believe him. It's amazing how clueless they are. The first time I ever got a panic attack in my life alongside spells of anxiety was after stopping those diabolical drugs. Then the rest of the symptoms ensue. 

Summer 2016 - summer 2018: put on Lexapro, going from 5 mg up to 20 mg over the span of the 2 years (had visited shrink for help with obsessive thinking, was not diagnosed with anything in particular, just prescribed Lexapro 15 mins into first session)

Summer 2018: tapered down by 2.5 mg every few weeks

Protracted withdrawal ever since. 0-14 months began with a massive panic attack that landed me in ER, followed by prolonged anxiety, mental fog and a skin rash on my back. Was regularly consuming alcohol as did not know I was in WD. From then onwards, hit with worse myriad symptoms. Currently at 22 months and have electromagnetic sensitivity, brain zaps, brain fog, memory problems (especially name recall), twitch in right eyebrow, daily waking up at 3 or 4 a.m. with fast heartbeats and "sticky" negative memories, suicidal thoughts, rage episodes, temperature dysregulation, physical numbness & weakness, libido loss.   

 

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Hey, good topic.  Even now, 3 plus years out from many years, of many medications........I need to keep it all in a healthy balance.........the screens, the outside natural light, and how I do my reading and writing.

 

I suspect that some "normies" do need to do this as well.  Especially with the smart/Iphone, Kindles, I pads, and good old desk top screens.  Maybe this even includes those huge tv screens, often glowing all the time in peoples homes.

As a whole, we may well be just a bit more susceptible to the rays, those of us in some phase of WD or tapering now.

Our nervous systems are repairing, from dysregulation.

 

I've been working on reading some books lately, outside when I can.  And often print out longer documents or articles that I need to read.  Journaling on paper.  Etc.  Old school stuff.

As I do experience a weird fatigue, if I overdo on my screens.

 

I know we have a topic on fluorescent lights here too, and sensitivities to that. 

I've got to get screen free now though, or I'd look for it. B)  Going to get outside in some natural light and sunshine for at least a few now, as it's a very nice day, here, today.

 

It gets better.  It has for me.  And I can work around any sensitivities pretty well now.

Late 2023- gone to emeritus status, inactive, don't @ me, I can check who I've posted on, and I'm not really here like I used to be......thanks.

Started with psycho meds/psychiatric care circa 1988.  In retrospect, and on contemplation, situational overwhelm.

Rounding up to 30 years of medications(30 medication trials, poly-pharmacy maximum was 3 at one time).

5/28/2015-off Adderal salts 2.5mg. (I had been on that since hospital 10/2014)

12/2015---just holding, holding, holding, with trileptal/oxcarb at 75 mg. 1/2 tab at hs.  My last psycho med ever!  Tapered @ 10% every 4 weeks, sometimes 2 weeks to

2016 Dec 16 medication free!!

Longer signature post here, with current supplements.

Herb and alcohol free since 5/15/2016.  And.....I quit smoking 11/2021. Lapsed.  Redo of quit smoking 9/28/2022.  Can you say Hallelujah?(took me long enough)💜

None of my posts are intended as medical advice.  Please discuss any decisions about your medical care with a knowledgeable medical provider.  My success story:  Blue skies ahead, clear sailing

 

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On 2/27/2020 at 9:45 PM, manymoretodays said:

Hey, good topic.  Even now, 3 plus years out from many years, of many medications........I need to keep it all in a healthy balance.........the screens, the outside natural light, and how I do my reading and writing.

 

I suspect that some "normies" do need to do this as well.  Especially with the smart/Iphone, Kindles, I pads, and good old desk top screens.  Maybe this even includes those huge tv screens, often glowing all the time in peoples homes.

As a whole, we may well be just a bit more susceptible to the rays, those of us in some phase of WD or tapering now.

Our nervous systems are repairing, from dysregulation.

 

I've been working on reading some books lately, outside when I can.  And often print out longer documents or articles that I need to read.  Journaling on paper.  Etc.  Old school stuff.

As I do experience a weird fatigue, if I overdo on my screens.

 

I know we have a topic on fluorescent lights here too, and sensitivities to that. 

I've got to get screen free now though, or I'd look for it. B)  Going to get outside in some natural light and sunshine for at least a few now, as it's a very nice day, here, today.

 

It gets better.  It has for me.  And I can work around any sensitivities pretty well now.

@manymoretodays thank you for your reply and reassurance. Yes in general we all need to cut down screen time but it's particularly pronounced in my case now because of WD. When I look at any screen, including right now, I get a strange sensation in the right side of my head and it makes me grit my teeth or reach out for chewing gum. One of the weirdest withdrawal symptoms I have. I can't stay long looking at screens. Haven't watched any movies recently because of this and had to take time off work because of the computer screen. I also have sensitivity to loud sounds and can't be near speakers. This affects my social life as I can't go to night venues or loud cafés. I'm hoping this will all dissipate soon. I try to spend as much as time as possible outdoors. And read paper books or listen to audiobooks. I wish you and I and everyone swift healing 🙏 

Summer 2016 - summer 2018: put on Lexapro, going from 5 mg up to 20 mg over the span of the 2 years (had visited shrink for help with obsessive thinking, was not diagnosed with anything in particular, just prescribed Lexapro 15 mins into first session)

Summer 2018: tapered down by 2.5 mg every few weeks

Protracted withdrawal ever since. 0-14 months began with a massive panic attack that landed me in ER, followed by prolonged anxiety, mental fog and a skin rash on my back. Was regularly consuming alcohol as did not know I was in WD. From then onwards, hit with worse myriad symptoms. Currently at 22 months and have electromagnetic sensitivity, brain zaps, brain fog, memory problems (especially name recall), twitch in right eyebrow, daily waking up at 3 or 4 a.m. with fast heartbeats and "sticky" negative memories, suicidal thoughts, rage episodes, temperature dysregulation, physical numbness & weakness, libido loss.   

 

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Yes I also have sensitivity to screens. But not as bad sensitivity than you have. It wasn't before I started to withdrawal. I recommend you to try omega-3 and magnesium l threonate. They may help.

Everything started 2015 and here's shortly how it went: Bad diet change --> health problems  -->  problems caused by medicines --> 5-6 months benzos --> about half year Mirtazapine for supporting sleep in benzo tapering (because I first tried to do it too fast) --> Mirtazapine caused more problems  --> 3 years Escitalopram (including tapering) --> 1 year tapering from 15 mg to 5,73 mg and then cold turkey from that dose in september 2019.

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49 minutes ago, Ismo said:

Yes I also have sensitivity to screens. But not as bad sensitivity than you have. It wasn't before I started to withdrawal. I recommend you to try omega-3 and magnesium l threonate. They may help.

Thank you @Ismo. I'm trying to get off all supplements and just focus on eating healthy and getting gentle exercise. I stopped taking omega 3 and magnesium. I'm currently tapering off Rhodiola Rosea. That's because I feel they relieve some symptoms in my case and trigger others. It's like walking in a mine field. But many people in WD say omega 3 and magnesium help them. Maybe after I'm off the rhodiola completely I can try readding them to my regimen. I'm also worried they interact with the rhodiola which is a powerful adaptogenic herb. I was told to wean off it and let my nervous system heal naturally without herbal intervention. Thank you so much for your advice. I hope we heal soon. Wishing you all the best. 

Summer 2016 - summer 2018: put on Lexapro, going from 5 mg up to 20 mg over the span of the 2 years (had visited shrink for help with obsessive thinking, was not diagnosed with anything in particular, just prescribed Lexapro 15 mins into first session)

Summer 2018: tapered down by 2.5 mg every few weeks

Protracted withdrawal ever since. 0-14 months began with a massive panic attack that landed me in ER, followed by prolonged anxiety, mental fog and a skin rash on my back. Was regularly consuming alcohol as did not know I was in WD. From then onwards, hit with worse myriad symptoms. Currently at 22 months and have electromagnetic sensitivity, brain zaps, brain fog, memory problems (especially name recall), twitch in right eyebrow, daily waking up at 3 or 4 a.m. with fast heartbeats and "sticky" negative memories, suicidal thoughts, rage episodes, temperature dysregulation, physical numbness & weakness, libido loss.   

 

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On 2/29/2020 at 12:00 PM, SolarPlexus said:

@manymoretodays thank you for your reply and reassurance. Yes in general we all need to cut down screen time but it's particularly pronounced in my case now because of WD. When I look at any screen, including right now, I get a strange sensation in the right side of my head and it makes me grit my teeth or reach out for chewing gum. One of the weirdest withdrawal symptoms I have. I can't stay long looking at screens. Haven't watched any movies recently because of this and had to take time off work because of the computer screen. I also have sensitivity to loud sounds and can't be near speakers. This affects my social life as I can't go to night venues or loud cafés. I'm hoping this will all dissipate soon. I try to spend as much as time as possible outdoors. And read paper books or listen to audiobooks. I wish you and I and everyone swift healing 🙏 

I'm still in widrawls, with intrusive thoughts

  • 13th of August 2019 started to take 20 mg citalopram
  • 😀24th of August 2019 down to 10mg stopped citalopram altogether on the 30th of August 2019
Quote

Short term citalopram

 

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18 minutes ago, Felisbela said:

I'm still in widrawls, with intrusive thoughts

@Felisbela Same here. My latest WD symptom is waking up at 4-4.30 a.m. daily (cortisol spikes I guess) with a wave of depressive thoughts. They linger around for several hours till I get on with my day. I have other symptoms too ongoing. May we all heal. May we all heal. I pray daily for this. 

Summer 2016 - summer 2018: put on Lexapro, going from 5 mg up to 20 mg over the span of the 2 years (had visited shrink for help with obsessive thinking, was not diagnosed with anything in particular, just prescribed Lexapro 15 mins into first session)

Summer 2018: tapered down by 2.5 mg every few weeks

Protracted withdrawal ever since. 0-14 months began with a massive panic attack that landed me in ER, followed by prolonged anxiety, mental fog and a skin rash on my back. Was regularly consuming alcohol as did not know I was in WD. From then onwards, hit with worse myriad symptoms. Currently at 22 months and have electromagnetic sensitivity, brain zaps, brain fog, memory problems (especially name recall), twitch in right eyebrow, daily waking up at 3 or 4 a.m. with fast heartbeats and "sticky" negative memories, suicidal thoughts, rage episodes, temperature dysregulation, physical numbness & weakness, libido loss.   

 

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  • 2 weeks later...
  • Administrator

Merged similar topics.

This is not medical advice. Discuss any decisions about your medical care with a knowledgeable medical practitioner.

"It has become appallingly obvious that our technology has surpassed our humanity." -- Albert Einstein

All postings © copyrighted.

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  • 3 months later...

Hello folks, currently i am on sertraline and propanolol. 50 mg and 40 mg respectively.

Of lately i have noticed my eyelids covering more of my pupil almost droppy type although i dont feel like droopy.

I am also sensitive to white light which sometimes casts reflection and when i widen my eye all is normal. Am i imagining things or is this real?

I have no issues with vision. Just i seem to notice my eyelashes more often.

I am not going to call my doctor because i hardly doubt he was have a clue. Has anyone else had this?

 

cheers

February: 10 mg citalopram - for anxiety related to sleep ( getting adrenal surges on sleep onset )

March : Mirtazapine 15 mg as citalopram side effects unbearable - Mirtazapine prescribed for sleep. Stopped Citalopram cold turkey

April: Anxiety around sleep still bad put on Sertraline 50 mg - continued with Mirtazapine - 15 mg

June: Anxiety around sleep in good control and able to sleep well most nights. Stopped Mirtazapine 15 mg cold turkey based on Doctors advise

May 31st 2022 started 15 ml mirtazapine for sleep onset anxiety

june 30 2022 started paxil 25 cr stopped mirtazapine

dec 2022 reduced paxil to 12.5 cr based on advise from psych 

currently on paxil 12.5 cr tried to quit cold turkey with really bad symptoms reinstated at 12.5 cr 

 

 

 

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  • ChessieCat changed the title to What is this weird sensation related to eyes
  • Administrator

If you are light-sensitive, you might cut down on light stimulation by wearing sunglasses or blue-blocking glasses indoors and out.

 

It could also be the propanolol you're taking is causing you to be somewhat dopey.

 

Otherwise, it sounds like you're looking too closely at your eyes for symptoms.

This is not medical advice. Discuss any decisions about your medical care with a knowledgeable medical practitioner.

"It has become appallingly obvious that our technology has surpassed our humanity." -- Albert Einstein

All postings © copyrighted.

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  • 7 months later...

I'm wondering if this could be a symptom of iatrogenic damage and/or tapering. 

 

I think I notice this in myself only at work, where I'm already usually massively stressed out because my cognitive impairment constantly breaks my heart. 

 

There are often times when I don't understand what is said by people, and I usually have to ask them to repeat themselves. It's like something in my brain becomes jumbled, and doesn't hear and understand words. It feels like it's psychological, to me, because in those moments it's like I'm in a different world. 

 

Also when people nearby are discussing something I should be paying attention to, I usually don't understand or hear it, so I miss out on it. 

 

😢

2000: Paxil, low dose. 2001: Paxil, quickly tapered off. 2006: Zoloft, 25mg. 2007: Wellbutrin, low dose, discontinued after a week or a month. 2007-2009: Zoloft, increasing dose (up to 75mg). 2009-2011: Zoloft, failed withdrawal attempts (cold-turkey; fast tapering). 2009-2011: Trying out Cymbalta, Celexa, Prozac, Lexapro, Ambien, Ativan, and Xanax. 2012-2015: Zoloft, 100mg to 200mg. 2013: Trazadone for Zoloft-induced insomnia, 25mg to 50mg.  2015: Trileptal, dose?, withdrew; Bupropion, up to 200mg. 2016: Zoloft, 137mg, Bupropion, 150mg, Trazodone, 25mg.

05/21/16: Began Zoloft taper - 10% from 150mg - 137ish mg

06/23/16: Zoloft taper - 125mg

08/03/16: Bupropion XL taper - cut 150mg pill in crude half (mistake)

10/31: Zoloft successfully down to 100mg. Staying on 100mg for 2-3 months to let my brain rest.

11/09: Wellbutrin SR prescribed, 150mg once a day, for withdrawal.

12/11: Wellbutrin SR, twice daily - minus 18ishmg = 112.50mg

09/30/17: Off Wellbutrin SR successfully. Zoloft taper: 90ish mg (shaving it off). Trazodone: still at 50mg.

June 2018: Zoloft: 80ish (shaving off). Trazodone: 6mg. End of 2018: Off Trazodone.

01/20: Zoloft: 70ish?

08/20: Still around 80 or 70. Tapering by only 15 shaves each month.

04/2021: 50mg! 11/2022: 40ish mg

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  • 10 months later...
  • Moderator

Hyperacusis in withdrawal: exposure treatment or not?

 

Recently even low levels of noise have been bothering me - things that did not bother me before. In terms of decibels it is no higher than a whisper 30-32 dB (cars on the road from well insulated windows, fridge buzzing) but it feels almost painful and makes me irritable. This happened once in the beginning of withdrawal and resolved within a week and has happened periodically with very loud noises. 

 

I understand this is one of those hypersensitivity issues but the question I have is whether it requires the same treatment as regular hyperacusis. In regular hyperacusis, you don't want to go around wearing earplugs but instead want to keep exposing yourself to everyday noises to acclimate your nervous system. However, in withdrawal, this should theoretically resolve itself so will wearing these earplugs damage by sensitizing you even more? Any thoughts? 

 

Edited by ChessieCat
added topic title before merging with existing topic

"Nothing so small as a moment is insurmountable, and moments are all that we have. You have survived every trial and tribulation that life has thrown at you up until this very instant. When future troubles come—and they will come—a version of you will be born into that moment that can conquer them, too." - Kevin Koenig 

 

I am not a doctor and this should not be considered medical advice. You can use the information and recommendations provided in whatever way you want and all decisions on your treatment are yours. 

 

In the next few weeks I do not have a lot of capacity to respond to questions. If you need a quick answer pls tag or ask other moderators who may want to be tagged. 

 

Aug  2000 - July 2003 (ct, 4-6 wk wd) , citalopram 20 mg,  xanax prn, wellbutrin for a few months, trazodone prn 

Dec 2004 - July 2018 citalopram 20 mg, xanax prn (rarely used)

Aug 2018 - citalopram 40 mg (self titrated up)

September 2018 - January 2019 tapered citalopram - 40/30/20/10/5 no issues until a week after reaching 0

Feb 2019 0.25 xanax - 0.5/day (3 weeks) over to klonopin 0.25 once a day to manage severe wd

March 6, reinstated citalopram 2.5 mg (liquid), klonopin 0.25 mg for sleep 2-3 times a week

Apr 1st citalopram 2.0 mg (liquid), klonopin 0.25 once a week (off by 4/14/19- no tapering)

citalopram (liquid) 4/14/19 -1.8 mg, 5/8/19 - 1.6 mg,  7/27/19 -1.5 mg,  8/15/19 - 1.35, 2/21/21 - 1.1 (smaller drops in between), 6/20/21 - 1.03 mg, 8/7/21- 1.025, 8/11/21 - 1.02, 8/15/21 - 1.015, 9/3/21 - 0.925 (fingers crossed!), 10/8/21 - 0.9, 10/18/21 - 0.875, 12/31/21 - 0.85, 1/7/22 - 0.825, 1/14/22 - 0.8, 1/22/22 - 0.785, 8/18/22 - 0.59, 12/15/2022 - 0.48, 2/15/22 - 0.43, 25/07/23 - 0.25 (mistake), 6/08/23 - 0.33mg

 

Supplements: magnesium citrate and bi-glycinate

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This has been my question as well with regard to sensory exposure. Over time, I appear to have gotten more restrictive in my sensory exposure to minimize flare ups. Now I feel like I have to put in more work to retrain my mind and body to things that I was used to 

 

 

Chronic IBS since 1990

Former smoker (1992- Jun 2017)

Prescribed mirtazapine for sleep in Aug 2017 after IBS flare-up following Nicotine cessation.

Mirtazapine 7.5mg 8/17 to 5/18

Mirtazapine 3.75mg 5/18 to 1/19

Off Mirtazapine since 2/19.

Vit B, Vit D+K2 and Magnesium Glycinate as needed.

On Ayurvedic herbs for GI issues - Guduchi since Jul 2020, Indukantham since Oct 2020

On Ashwagandha 1g since Nov 2020

 

 

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7 hours ago, Onmyway said:

However, in withdrawal, this should theoretically resolve itself so will wearing these earplugs damage by sensitizing you even more? Any thoughts? 

 

I think where possible wearing noise cancelling headphones is a better option than ear plugs.

 

Because the sensitivity is related to the drug/getting off the drug, I think it is better to use things to reduce the exposure.  We need to try and keep our stress levels down, and exposure to noises etc adds stress.

 

I had light sensitivity for a while and was wearing blue light glasses at work.  Then I found that I didn't need them.

* NO LONGER ACTIVE on SA *

MISSION ACCOMPLISHED:  (6 year taper)      0mg Pristiq  on 13th November 2021

ADs since ~1992:  25+ years - 1 unknown, Prozac (muscle weakness), Zoloft; citalopram (pooped out) CTed (very sick for 2.5 wks a few months after); Pristiq:  50mg 2012, 100mg beg 2013 (Serotonin Toxicity)  Tapering from Oct 2015 - 13 Nov 2021   LAST DOSE 0.0025mg

Post 0 updates start here    My tapering program     My Intro (goes to tapering graph)

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On 12/3/2021 at 5:08 PM, tsranga said:

This has been my question as well with regard to sensory exposure. Over time, I appear to have gotten more restrictive in my sensory exposure to minimize flare ups. Now I feel like I have to put in more work to retrain my mind and body to things that I was used to 

 

 

It's a difficult question, isn't it @tsranga? My experience from this has been that it comes and then disappears and so it might be that we just do what @ChessieCat says without worrying that it is going to make things harder. Have you found that your sensitivities are getting better or change in the windows and waves pattern? 

"Nothing so small as a moment is insurmountable, and moments are all that we have. You have survived every trial and tribulation that life has thrown at you up until this very instant. When future troubles come—and they will come—a version of you will be born into that moment that can conquer them, too." - Kevin Koenig 

 

I am not a doctor and this should not be considered medical advice. You can use the information and recommendations provided in whatever way you want and all decisions on your treatment are yours. 

 

In the next few weeks I do not have a lot of capacity to respond to questions. If you need a quick answer pls tag or ask other moderators who may want to be tagged. 

 

Aug  2000 - July 2003 (ct, 4-6 wk wd) , citalopram 20 mg,  xanax prn, wellbutrin for a few months, trazodone prn 

Dec 2004 - July 2018 citalopram 20 mg, xanax prn (rarely used)

Aug 2018 - citalopram 40 mg (self titrated up)

September 2018 - January 2019 tapered citalopram - 40/30/20/10/5 no issues until a week after reaching 0

Feb 2019 0.25 xanax - 0.5/day (3 weeks) over to klonopin 0.25 once a day to manage severe wd

March 6, reinstated citalopram 2.5 mg (liquid), klonopin 0.25 mg for sleep 2-3 times a week

Apr 1st citalopram 2.0 mg (liquid), klonopin 0.25 once a week (off by 4/14/19- no tapering)

citalopram (liquid) 4/14/19 -1.8 mg, 5/8/19 - 1.6 mg,  7/27/19 -1.5 mg,  8/15/19 - 1.35, 2/21/21 - 1.1 (smaller drops in between), 6/20/21 - 1.03 mg, 8/7/21- 1.025, 8/11/21 - 1.02, 8/15/21 - 1.015, 9/3/21 - 0.925 (fingers crossed!), 10/8/21 - 0.9, 10/18/21 - 0.875, 12/31/21 - 0.85, 1/7/22 - 0.825, 1/14/22 - 0.8, 1/22/22 - 0.785, 8/18/22 - 0.59, 12/15/2022 - 0.48, 2/15/22 - 0.43, 25/07/23 - 0.25 (mistake), 6/08/23 - 0.33mg

 

Supplements: magnesium citrate and bi-glycinate

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6 hours ago, Onmyway said:

Have you found that your sensitivities are getting better or change in the windows and waves pattern? 

I haven't found any noticeable and consistent improvements, but I have noticed small signs of improvements especially in the fight/flight response that can kick in..  Many a time, I think its going to kick in, but it doesn't..  for the same symptom. 

 

Essentially the symptoms are still there and probably at the same intensity and frequency with reduced duration, but more often than not, I am able to experience them without making them worse by my fight/flight reaction.   Now the question is if I am doing that by avoiding/controlling my exposure to those triggers, which may be so,  but there are several instances where I am inadvertently exposed to a trigger and nothing happens eg. my shower suddenly going cold.. So the tolerance does seem to be improving..  

 

Touch/skin hypersensitivity still seems to be the most challenging compared to smell, sight or sound, severely limiting my choice of clothes/bedding. Ambient air temperature seems to contribute in a major way.

 

I am also finding that my symptoms have a circadian rhythm eg. sound and light sensitivity during the dawn/dusk times, skin/hot/cold sensitivity between 2PM-6PM and 10PM-2AM, which may be very normal for a human being given the changes in body temperature/hormones/daylight etc..  I can't change the sensitivity, so I am working on the fight/flight response.. 

 

 

 

Chronic IBS since 1990

Former smoker (1992- Jun 2017)

Prescribed mirtazapine for sleep in Aug 2017 after IBS flare-up following Nicotine cessation.

Mirtazapine 7.5mg 8/17 to 5/18

Mirtazapine 3.75mg 5/18 to 1/19

Off Mirtazapine since 2/19.

Vit B, Vit D+K2 and Magnesium Glycinate as needed.

On Ayurvedic herbs for GI issues - Guduchi since Jul 2020, Indukantham since Oct 2020

On Ashwagandha 1g since Nov 2020

 

 

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  • 2 months later...

I have a really loud 5 year old, she is constantly yelling, even when she talks she is loud. Having noise sensitivity issues atm giving me headaches. Not sure if there is anyway around this one 

10 years on various anti-depressants

5 years Effexor xr

tappered of 150mg in 6 months

nothing for two weeks

Reinstated 15 beads for 50 days

Tappered off then clean 2-3months

gradually went back up to 13 mg 3 years

bridged fluoxetine 10mg

2 week tapper

1 year clean

reinstated 5ml dispersed fluroxatine for 6months

 

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