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Vision symptoms: floaters, snow, blurred/dimmed vision, twitching, dry eyes and pain


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1 hour ago, Ahms said:

I have some information for you for visual problems and visual snow. I came across a poster by one of the neurologists based in London who recommends Riboflavin/Vitamin B2 400mg daily, magnesium citrate 600mg daily and coenzyme Q10 350mg daily. He has seen some improvement in visual snow in some of his patients by using these supplements. Of course, consult a doctor first before you take them. Also, look at visual snow initiative website - a group of researchers trying to find a cure for visual snow. Visual snow is a potential hyperexcitability of neurons in the visual cortex in the brain. There is nothing wrong with your husbands eyes. It's the brain/neurological problem. Very few doctors or even neurologists know about visual snow or even heard if it. 

Die-hard thanks for that!!!

Took prozac 40 mg for 20 years.

January 2017 started cutting down prozac by 12.5% a week. End of February 2017 completely off prozac and withdrawals began.

Currently taking Levothyroxine 75 mcg, Magnesium citrate 200mg,Sage leaf 50mg daily

Amlodipine: October 2017 , discontinued 26 Feb 2019; Candesartan:  26 Feb 2019, 4mg.

Discontinued magnesium citrate 200mg Apr 3rd 2019

Reinstated prozac:  14 Jan 2019, 1mg; 26 Jan, 1.5mg; 4 Feb, 2mg; 16 Feb, 2.5mg; 2 Mar, 3mg; 5 Mar, 2.5mg, 23 Mar, 3 mg; 6 Apr, 3.5mg, 14 Apr 4mg, 23 Apr 5mg, 10 Jul 8mg, 1 Dec 20mg, 1 Apr 2020 40mg 

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On ‎9‎/‎12‎/‎2018 at 6:40 PM, gn11 said:

I wonder if anyone has been diagnosed with cataracts. There appears to be a connection between SSRIs and the development of cataracts.

I had a cataract removed in January,the other one is still pretty mild...I am 63 but is it a coincidence that it occurred after taking Paxil and had adverse reactions to it?

IDK.

went on Prozac 1994-99,60mg.poopout ct  back on 2001-2002,prozac weekly 2002,not working,Effexor 75 mg.?2003-mar.2004 gaining weight 8wk. taper,wellbutrin 150 mg.mar. -may 2004 ctmedfree til july 2005 back to Prozac gaining weight again,back on wellbutrin jan.2006150-300 mg.bad constipation.also was taking aygestin(hormone)perimenopausal irregular bleeding.back on Prozac around sept,?2006,hysterectomy jan30.2007(adenomyosis)off&on Prozac til 2009,citalopram about 1 mo, April 2010 no effect,Effexor again may -mar, 2011.ct,Prozac aug,-dec, 2011 &sept-nov 2012,paroxetine oct,23 2013-may 4 2014 20 mgs.tapered 6 wks.-failed RI in Oct.2014-in protracted WD.started 10 mgs. Fluoxetine May 25 2021 .Stopped fluoxetine May 2022 at 5 mgs.

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  • 1 month later...

Found this thread via Google. I am a 20 year sufferer of Visual Snow and all the fun and games that come with it. What AHMS describes is exactly what I have. When my problems began in 1999 I searched all over the internet, and could find nothing, I would describe it as "static vision" to my doctors, along with everything being like I am looking through a window all the time, not quite as clear and bright and crisp as things should be, they shrugged their shoulders. Later I found it to be known as visual snow. (mod note:  please see this post) I have not been on antidepressants but I am due to go on to venlafaxine this week. Can you describe to me your visual snow in detail ? Did it only begin after medication and what dosage ? Thanks !!

 

Edited by ChessieCat
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  • Administrator

Hello, Zammo. Almost everyone on this site has had an adverse reaction to psychiatric drugs such as venlafaxine. This topic is about visual symptoms that started when the person went on the drug or went off the drug and got withdrawal symptoms.

 

Please be aware that your doctors don't know what will happen when they prescribe venlafaxine for you. They are hoping that it will help, but it may not. It may cause other symptoms or worse visual 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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  • Songbird changed the title to Vision symptoms: floaters, snow, blurred/dimmed vision, twitching and pain
  • 3 weeks later...

Has anyone, literally one person had floaters disappear after withdrawal's over?

No prior history

2018 -

July - 3 x 5 mg tablets of Diazepam halved into 2.5mg at a time as needed

August - 5 x 5 mg tablets of Diazepam halved into 2.5mg at a time as needed

September - 17 x 10mg doses of Escitalopram before ct

October - 10 x Roxithromycin antibiotic for a 3 week flu

November - fish oil, magnesium, flax-seed oil, Coq10 supplements

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  • 2 weeks later...
On 10/17/2018 at 6:38 PM, Zammo said:

Found this thread via Google. I am a 20 year sufferer of Visual Snow and all the fun and games that come with it. What AHMS describes is exactly what I have. When my problems began in 1999 I searched all over the internet, and could find nothing, I would describe it as "static vision" to my doctors, along with everything being like I am looking through a window all the time, not quite as clear and bright and crisp as things should be, they shrugged their shoulders. Later I found it to be known as visual snow. (mod note:  please see this post) I have not been on antidepressants but I am due to go on to venlafaxine this week. Can you describe to me your visual snow in detail ? Did it only begin after medication and what dosage ? Thanks !!

 

Zammo, I developed visual snow after I came off Venlafaxine and not to mention the disabling withdrawal symptoms I had where I was bed bound for months. It's a horrible horrible drug. I would stay away from it personally. Even when I was on it, I had major personality changes. I still have visual snow/staticky vision along with palinopsia (afterimages). It's been 7 months. 

 

 

Citalopram 30mg 2008 - 2015
Citalopram 30mg + Mirtazapine 15mg 2015 - 2016
Venlafaxine 150mg + Mirtazapine 15mg then 30mg 2016 - 2017
Venlafaxine 150mg + Amitriptyline 50mg January 2017. Coming off Venlafaxine took about 8 months 
March 2018 stopped venlafaxine. Increased amitriptyline to 150mg over two weeks end of March. Couldn't tolerate side effects. CT for 5 days then went back to 50mg amitriptyline since 8 April 2018

 

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  • 1 month later...

I developed Visual snow and light sensitivity after one single dose of 37,5 mg Effexor XR pill.After 1 year and 2 months I am still suffering.Please stay away from Venlafaxine

 

Is there any member that recovered from SSRI induced visual snow?

 

I am praying day and night for recovery 🙏🏻🙏🏻🙏🏻

 

 

 

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On 1/6/2019 at 7:17 PM, JasonK said:

I developed Visual snow and light sensitivity after one single dose of 37,5 mg Effexor XR pill.After 1 year and 2 months I am still suffering.Please stay away from Venlafaxine

 

Is there any member that recovered from SSRI induced visual snow?

 

I am praying day and night for recovery 🙏🏻🙏🏻🙏🏻

 

 

 

JasonK, have you tried anything of visual snow? VS seems to be permanent. Along with VS, I also have palinopsia, BFEP, nyctalopia and excessive floaters. All this started when I came off Venlafaxine. 

 

 

Citalopram 30mg 2008 - 2015
Citalopram 30mg + Mirtazapine 15mg 2015 - 2016
Venlafaxine 150mg + Mirtazapine 15mg then 30mg 2016 - 2017
Venlafaxine 150mg + Amitriptyline 50mg January 2017. Coming off Venlafaxine took about 8 months 
March 2018 stopped venlafaxine. Increased amitriptyline to 150mg over two weeks end of March. Couldn't tolerate side effects. CT for 5 days then went back to 50mg amitriptyline since 8 April 2018

 

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Hi Ahms,

 

No I have not.I am trying to accept it and hoping my brain will manage to reach homeostasis at some point.In addition, I am following some visual snow groups online, to keep myself update in case of a cure .

 

How many years you were taking Venlafaxine?

 

Best Regards,

 

Jason

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  • ChessieCat changed the title to Vision symptoms: floaters, snow, blurred/dimmed vision, twitching, dry eyes and pain
  • 1 month later...

Has anyone experienced extremely dry eyes. It's totally random and has a sudden onset. I don't have any allergies that I know of and it all started after three Lexapro incident. It goes away quickly as well.

-Lexapro 10mg March of 2017 for about 7 days. Insane panic  upon first dose.

-Clonazepam 1mg daily to counter the insane panic from Lexapro. March of 2017

-Reduced Clonazepam from 1mg to .75mg over 5 months. December 2017-April 2018

-Buspar October 2017 to August 2018. Discontinued due to rare side effects. Extreme withdrawals

-Switch to Valium in June 2018 from Clonazepam.  15mg daily. 

-Current meds, 15mg Valium daily. Pretty sure I hit tolerance.

 

-Tried low dosage Lexapro again mid October 2018. .5mg daily for one week, then 1mg daily for the second. Made it almost two weeks before madness ensued. 

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  • 1 month later...
On 6/9/2018 at 12:49 AM, deejay said:

I had a complete visual change on roughly 7th March this year. It is so hard to explain, at first I thought it was the sleeping tablets I had been taken but it has remained the same for the last 3 months. I'm not talking about just being a little blurry, I'm talking a complete and utter change, The only way I can describe it is if I'm seeing the world in 3D. I am also constantly seeing vertical and horizontal white lines in y visual field when staring at a hard surface like the ground or the wall. Dark patches at times which come and go. Light trails. After images. That's just when I'm awake, when eyes are shut I see all this weird stuff also. Sometimes a colour will come which I am seeing while eyes are shut for a few seconds. Asif I'm awake and looking at a bright red surface, but my eyes are closed. If I stare at something and focus on that object, other objects in visual field will disappear/reappear.

 

NOTHING showed up abnormal when I had an eye test a week after it happened so it's in my brain. And if it has remained this way for 3 months, I'm assuming it's permanent.

 

It's like my eyes are straining to see and cannot really focus as well. I have extreme trouble reading now due to this plus concentration issues. it's gotten to the point where I'm just seeing every single individual word

how is your vision now?

Took prozac 40 mg for 20 years.

January 2017 started cutting down prozac by 12.5% a week. End of February 2017 completely off prozac and withdrawals began.

Currently taking Levothyroxine 75 mcg, Magnesium citrate 200mg,Sage leaf 50mg daily

Amlodipine: October 2017 , discontinued 26 Feb 2019; Candesartan:  26 Feb 2019, 4mg.

Discontinued magnesium citrate 200mg Apr 3rd 2019

Reinstated prozac:  14 Jan 2019, 1mg; 26 Jan, 1.5mg; 4 Feb, 2mg; 16 Feb, 2.5mg; 2 Mar, 3mg; 5 Mar, 2.5mg, 23 Mar, 3 mg; 6 Apr, 3.5mg, 14 Apr 4mg, 23 Apr 5mg, 10 Jul 8mg, 1 Dec 20mg, 1 Apr 2020 40mg 

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  • 3 weeks later...
On 9/8/2018 at 10:32 AM, Ahms said:

Has anyone recovered from visual snow, afrer images and dimmed vision? 

 

Hi, I don't know if you are still having this issue but, I had after-images at times that would linger quite a while and they did clear up.  

I am not a medical professional and nothing I say is a medical opinion or meant to be medical advice, please seek a competent and trusted medical professional to consult for all medical decisions.

 

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how long did it take to clear up?

Took prozac 40 mg for 20 years.

January 2017 started cutting down prozac by 12.5% a week. End of February 2017 completely off prozac and withdrawals began.

Currently taking Levothyroxine 75 mcg, Magnesium citrate 200mg,Sage leaf 50mg daily

Amlodipine: October 2017 , discontinued 26 Feb 2019; Candesartan:  26 Feb 2019, 4mg.

Discontinued magnesium citrate 200mg Apr 3rd 2019

Reinstated prozac:  14 Jan 2019, 1mg; 26 Jan, 1.5mg; 4 Feb, 2mg; 16 Feb, 2.5mg; 2 Mar, 3mg; 5 Mar, 2.5mg, 23 Mar, 3 mg; 6 Apr, 3.5mg, 14 Apr 4mg, 23 Apr 5mg, 10 Jul 8mg, 1 Dec 20mg, 1 Apr 2020 40mg 

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20 hours ago, thecowisback said:

how long did it take to clear up?

 

To be honest, I don't recall. It was years ago now I had it, and that time is mostly a blur. 

I am not a medical professional and nothing I say is a medical opinion or meant to be medical advice, please seek a competent and trusted medical professional to consult for all medical decisions.

 

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it's good to hear that some of the symptoms do eventually go.

 

Took prozac 40 mg for 20 years.

January 2017 started cutting down prozac by 12.5% a week. End of February 2017 completely off prozac and withdrawals began.

Currently taking Levothyroxine 75 mcg, Magnesium citrate 200mg,Sage leaf 50mg daily

Amlodipine: October 2017 , discontinued 26 Feb 2019; Candesartan:  26 Feb 2019, 4mg.

Discontinued magnesium citrate 200mg Apr 3rd 2019

Reinstated prozac:  14 Jan 2019, 1mg; 26 Jan, 1.5mg; 4 Feb, 2mg; 16 Feb, 2.5mg; 2 Mar, 3mg; 5 Mar, 2.5mg, 23 Mar, 3 mg; 6 Apr, 3.5mg, 14 Apr 4mg, 23 Apr 5mg, 10 Jul 8mg, 1 Dec 20mg, 1 Apr 2020 40mg 

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  • 2 weeks later...
On 10/4/2011 at 12:52 AM, stan said:

hoi Tramond,

 

dry eyes are common symptoms of withdrawal from antidepressants and benzo, i have it and also dry mouth, withdrawal inhibits saliva or/and eyes water; hope it will go away,

Stan did your dry eyes and mouth get better and if so how long did you have it before it went? 

I have had this problem for a few months and it’s very distressing. 

Didn’t have it prior to withdrawal. 

Nov 2018 Pregabalin 2x50 mg a day to help with Paxil WD. Aug 2019 2 x 25mg a day, April 2020 45mg, May 40mg, June 35mg, July 30mg, end July 25mg, Aug 24mg, June 2021 14mg, Jan 2022 14mg (2x7mg a day), Oct 10mg, Nov 5mg, December 25th 2022 0mg 🎈

 

Oct 2004 - Oct 2018 Paxil 20 mg, Nov 15mg, Dec 10mg,  Feb 2019 7.5mg crashed, Feb 8.5mg, Nov 8mg, March 2020 7.2mg, April 6.5mg, May 5.9mg, June 5.4mg, July 4.8mg, Dec 4.5mg, Jan 2021 4mg, Feb 3.6mg, March 3.2mg, April 2.9mg, Aug 2.7mg, Sept 2.4mg, Oct 2.2mg, Nov 2mg, Dec 1.8mg, Feb 2022 1.6mg, March 1.4mg, April 1.2mg, May 1.0mg, June 0.8mg, July 0.6mg, Aug 0.4mg, Sep 0.2mg, October 6th 2022 0mg  🎈

 

December 25th 2022 drug free 

 

these dates are approximate 

 

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On 6/17/2015 at 2:46 PM, katieb said:

I have been experiencing blurred vision, dry red eyes and also runny eyes.The blurry vision is for me the worst.

Hello there did your blurred vision and dry eyes go away ? If so how long did it last ?

i Have this st the moment and find it very difficult to cope with 

Nov 2018 Pregabalin 2x50 mg a day to help with Paxil WD. Aug 2019 2 x 25mg a day, April 2020 45mg, May 40mg, June 35mg, July 30mg, end July 25mg, Aug 24mg, June 2021 14mg, Jan 2022 14mg (2x7mg a day), Oct 10mg, Nov 5mg, December 25th 2022 0mg 🎈

 

Oct 2004 - Oct 2018 Paxil 20 mg, Nov 15mg, Dec 10mg,  Feb 2019 7.5mg crashed, Feb 8.5mg, Nov 8mg, March 2020 7.2mg, April 6.5mg, May 5.9mg, June 5.4mg, July 4.8mg, Dec 4.5mg, Jan 2021 4mg, Feb 3.6mg, March 3.2mg, April 2.9mg, Aug 2.7mg, Sept 2.4mg, Oct 2.2mg, Nov 2mg, Dec 1.8mg, Feb 2022 1.6mg, March 1.4mg, April 1.2mg, May 1.0mg, June 0.8mg, July 0.6mg, Aug 0.4mg, Sep 0.2mg, October 6th 2022 0mg  🎈

 

December 25th 2022 drug free 

 

these dates are approximate 

 

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On 11/12/2015 at 6:18 PM, direstraits said:

my eyes have been terrible lately,blurry ,burning,sometimes I can hardly read this site.I know I've had times where they've been much better(few and far between tho :( ) so must be WD related I guess.

Hello there has your dry eyes and blurry vision got better if so how long did it take? 

Ive had this problem fir a few months .  

Nov 2018 Pregabalin 2x50 mg a day to help with Paxil WD. Aug 2019 2 x 25mg a day, April 2020 45mg, May 40mg, June 35mg, July 30mg, end July 25mg, Aug 24mg, June 2021 14mg, Jan 2022 14mg (2x7mg a day), Oct 10mg, Nov 5mg, December 25th 2022 0mg 🎈

 

Oct 2004 - Oct 2018 Paxil 20 mg, Nov 15mg, Dec 10mg,  Feb 2019 7.5mg crashed, Feb 8.5mg, Nov 8mg, March 2020 7.2mg, April 6.5mg, May 5.9mg, June 5.4mg, July 4.8mg, Dec 4.5mg, Jan 2021 4mg, Feb 3.6mg, March 3.2mg, April 2.9mg, Aug 2.7mg, Sept 2.4mg, Oct 2.2mg, Nov 2mg, Dec 1.8mg, Feb 2022 1.6mg, March 1.4mg, April 1.2mg, May 1.0mg, June 0.8mg, July 0.6mg, Aug 0.4mg, Sep 0.2mg, October 6th 2022 0mg  🎈

 

December 25th 2022 drug free 

 

these dates are approximate 

 

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16 hours ago, Longroadhome said:

Hello there has your dry eyes and blurry vision got better if so how long did it take? 

Ive had this problem fir a few months .  

Hi,Longroadhome

it turned out part of my blurry vision was due to a cataract,which I think could have been caused by ADs but I still struggle with vision problems after 5 years off the drugs.

sometimes it's better,than worse again.  

went on Prozac 1994-99,60mg.poopout ct  back on 2001-2002,prozac weekly 2002,not working,Effexor 75 mg.?2003-mar.2004 gaining weight 8wk. taper,wellbutrin 150 mg.mar. -may 2004 ctmedfree til july 2005 back to Prozac gaining weight again,back on wellbutrin jan.2006150-300 mg.bad constipation.also was taking aygestin(hormone)perimenopausal irregular bleeding.back on Prozac around sept,?2006,hysterectomy jan30.2007(adenomyosis)off&on Prozac til 2009,citalopram about 1 mo, April 2010 no effect,Effexor again may -mar, 2011.ct,Prozac aug,-dec, 2011 &sept-nov 2012,paroxetine oct,23 2013-may 4 2014 20 mgs.tapered 6 wks.-failed RI in Oct.2014-in protracted WD.started 10 mgs. Fluoxetine May 25 2021 .Stopped fluoxetine May 2022 at 5 mgs.

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Thank you for your prompt reply Direstraits. Much appreciated. 

Nov 2018 Pregabalin 2x50 mg a day to help with Paxil WD. Aug 2019 2 x 25mg a day, April 2020 45mg, May 40mg, June 35mg, July 30mg, end July 25mg, Aug 24mg, June 2021 14mg, Jan 2022 14mg (2x7mg a day), Oct 10mg, Nov 5mg, December 25th 2022 0mg 🎈

 

Oct 2004 - Oct 2018 Paxil 20 mg, Nov 15mg, Dec 10mg,  Feb 2019 7.5mg crashed, Feb 8.5mg, Nov 8mg, March 2020 7.2mg, April 6.5mg, May 5.9mg, June 5.4mg, July 4.8mg, Dec 4.5mg, Jan 2021 4mg, Feb 3.6mg, March 3.2mg, April 2.9mg, Aug 2.7mg, Sept 2.4mg, Oct 2.2mg, Nov 2mg, Dec 1.8mg, Feb 2022 1.6mg, March 1.4mg, April 1.2mg, May 1.0mg, June 0.8mg, July 0.6mg, Aug 0.4mg, Sep 0.2mg, October 6th 2022 0mg  🎈

 

December 25th 2022 drug free 

 

these dates are approximate 

 

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  • 3 weeks later...

Hello I am looking for help regarding my visual problems. I am very distressed, depressed and frustrated about my visual issues because doctors haven't been able to explain them, and I see more visual disturbances appear as months pass, this is very hard to take in, not knowing whats happening or whats gonna happen. Additionally I have been suffering a horrible illness / syndrome since I discontinued Effexor in May 2018, I know its being referred as post acute withdrawal syndrome, I couldn't even write a post until recently but I wont get deep into that in this post, although its may be related. Attached on my post are images that explain some of my most distressing visual problems. 

 

During 2016 while I was on Effexor and Clonazepam I started to notice visual disturbances on my vision field, very small and subtle, something would pop up every 6 - 12 months, similar to the blurry spots on my drawings but very small. I started to blame effexor so I eventually discontinued effexor and keep taking clonazepam ( still taking it ). By May 2018 I was completely off effexor, on May - June 2018 while my withdrawal was getting worse I started to notice bad / blurry vision, coming and going, then problems seeing at night, also the visual disturbances increased in number and frequency. As the withdrawal got worse so did the visual disturbances, on July 2018 withdrawal became unbearable and in parallel vision problems also skyrocketed, I was seeing all type of distortions and stripes on my visual field, all type of small scotomas or abnormal spots, all these phenomena is shown on my drawings that I have attached in this post. The parallel increase in withdrawal with my visual distortions was evident. I also was seeing very distorted. Everything was bent. These are not floaters, these are fixed distorted spots on my visual field that dont move. I was and am also seeing blurry or just plain bad.

 

My vision problems have fluctuated, they did improve then got worse then improved again and now are worse again during the year I have been very ill and still am. Some of the spots or scotomas have remained permanent and some have improved, some appear and disappear others have stayed. While there is fluctuation on my problems the good vision days are in a very low ratio compared to the bad vision days. Many visual problems have come and got better including, visual static, visual snow, after images, things leaving a trail in visual field, bad low light vision, and innumerable visual phenomenon, most of which comes in waves.

 

The main problems that bother me and impair me are just plain bad vision or blurry vision that comes with a sensation of huge eye strain eye pressure and discomfort, and also the visual distortion spots or scotomas on my visual field. I often have trouble seeing, reading, identifying objects but then some days its better, the scotomas remain there. I have seen several specialists, retinal specialists said retina is perfect, same neuro-ophthalmologist said he couldn't explain the issues, Visual field cant detect the distortions because it came normal. I however have trouble reading because of visual issues, have trouble seeing well objects and so on, so its a real problem. I was starting to take on some mental activities like programming but I had to stop on April because of this visual problems got so bad and also severe memory impairments and other stuff I wont bring up here.

 

So There are only 3 possible causes for my visual problems that I can think of:

1) The syndrome / illness from discontinuing effexor.

2) Clonazepam.

3) Just some rare non drug related illness I have.

I need help to understand what may be causing the problems, Please if someone has experienced similar problems and have a diagnosis or know the cause let me know your experience. Also How can I bring this up on the benzo forums ? in case this problem is being caused by clonazepam also I could really use feedback from people that know about benzos.

I appreciate all the help I can get on this.

 

IMG_5002.jpg

IMG_5003.jpg

IMG_5004.jpg

IMG_5005.jpg

IMG_5006.jpg

Effexor XR of 150mg from 2003 to 2008.

Zoloft 100mg from 2008 to 2011.

Prozac ?mg 2011 to 2012.

Vibrid ?mg 2012 to 2013. 

Effexor IR 200mg from 2013 to 2016.

Effexor XR 150 mg  for 6 months 

Clonazepam 1mg 2008 to 2018 ( Currently taking )

Tapered Effexor from 150 mg to 37.5 mg on 10 months

Effexor 37.5 to 0 in 3 months

Off Effexor since March 2018

Reduced clonazepam from 1 to .75 on 2016

Currently taking Clonazepam .75mg

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On 9/8/2018 at 10:32 AM, Ahms said:

Has anyone recovered from visual snow, afrer images and dimmed vision? 

I have "recovered" from visual snow, still comes occasionally in waves but less intense now, often there is no snow at all or i dont notice it. Visual snow in dim light makes it hard to distinguish objects, it has improved dramatically, dim vision also improves, it comes in waves now less frequently. I been having it during withdrawal, got worse when I took a reinstatement dose, now better. After images have improved too, I used to have like 20 images of things in my vision all the time because of stuff i just saw, but it improved a lot, i barely notice it now. I however have other visual issues now, specially just blurry vision in long waves and other weird stuff. In my experience many visual issues do improve, others stay. 

Effexor XR of 150mg from 2003 to 2008.

Zoloft 100mg from 2008 to 2011.

Prozac ?mg 2011 to 2012.

Vibrid ?mg 2012 to 2013. 

Effexor IR 200mg from 2013 to 2016.

Effexor XR 150 mg  for 6 months 

Clonazepam 1mg 2008 to 2018 ( Currently taking )

Tapered Effexor from 150 mg to 37.5 mg on 10 months

Effexor 37.5 to 0 in 3 months

Off Effexor since March 2018

Reduced clonazepam from 1 to .75 on 2016

Currently taking Clonazepam .75mg

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This started happening to me a couple months back. I can’t tell if it’s a sinus problem, an ongoing SSRI discontinuation problem, or both.

 

 

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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  • 2 weeks later...
On 8/30/2017 at 1:33 AM, Oran said:

Hello everyone

 

Am I the only one who is housebound by visual symtoms? My visual symtoms are so bad I cannot go outside anymore. I cannot determine depth, light, and everything looks disproportionate, much darker and distorted, too close or too far away. It's like my brain cannot process the input of my eyes and If I walk around outside for more than 5 minutes, all these visual symptoms gets much worse and by forcing myself to keep staying outside my other symtoms such as confusion and brain fog also gets much worse! No ophthalmologist has been able to find anything wrong and I am getting both extremely scared and really, really sick of this. Could this be something else than withdrawal? Some disease? I haven't been able to go or stay outside properly for several months now.. I am 9 months off Effexor..

I can relate, i have some vision issues too.Like things are moving too fast sometimes, laggy vision, blurry, can’t focus, depth vision is low, feeling of vision is not right at all

Lorazepam -2 weeks-1 week 3 mg.4 days 2mg, 3 days 1mg. 13-27 November 2018

Lexapro -2 months-6 weeks of 10mg, 2 weeks of 5mg 27 November 2018-27 January 2019

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  • Moderator Emeritus

merged similar topics

 

* 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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  • 2 months later...

Hello everyone,

I have struggled with blurry vision, dry eye, eye strain, for the past few years -and can absolutely say that has become worse since being on duloxetine in 2015, which I am now tapering. I also take clonazepam and lamotrigine (started in 2014) and gabapentin, which may also cause the visual disturbances.   Using a computer is nearly impossible on some days. Paper is also be a struggle. Magnifying glasses with lights help.

 

I use speech recognition on the computer and dictation software - which helps with some applications - particularly on a Mac. Has anyone tried this and found one that works well? The best font I have found for people with visual issues is Dyslexie. It is free and was developed for people with (obviously) dyslexia.

 

I see beyond mid-range and in the distance better (because I am then not looking at details). I have been to about 5 opthalmologists for the blurry vision, dry eye, and poor vision in general. Everything is negative and I wear eyeglasses. Medication causes have been suggested by 1 of the opthalmologists (and all have my cocktail of neuro meds). Interestingly I had been diagnosed with cataracts (between 1-2 so I was not a candidate a surgery) - but in a year they went away!!! Is this possible?

 

If anyone is working - what kind of work are they doing? I am not working - and when I was - a computer was the primary work tool. I would not do this today. I'd like to work part-time but don't know what I'd be able to do. 

 

There are also days when I don't  drive - and this is largely due to  vision and dizziness issues. 

 

Love to hear back from anyone. Sorry this is so long. Just found the vision thread...😎 😉

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  • 3 months later...

Eye problem

 

Hello,

 

I have one eye problem. I had this before blurry vision and feeling that somethings is in my eye and i saw halos when i looked in to the light source. I visited eye clinic they can't found nothing. Doctor told me wait. In a week this thing weaned off. I had maybe 10 episodes in 8 eyes. I was on full dose 20 mg Seroxat. Now I am tappering and i have similar simptoms but no halos in place of them eyelid twitching but not constantly bit in the morning and evening. And feeling that something is in my eye. I have this already 2 weeks.  What should i do? I can visit eye clinic but if they didn't found anything last time i don't want to pay again 400 euros for nothing. Last episode was year ago. I am so confused same eye so many years but always lasted week max and now i am scary...

Edited by ChessieCat
added topic title before merging with existing topic

AD: Seroxat since 2005 20 mg and tapering from March 2018 10% every 4 weeks.

15-11-2019 down to 5.5 mg 

28-12-2019 crashed really bad on 5.5mg 

01-01-2020 updose to 7mg

16-01-2020 Updose to 9 mg

 

Benzos: Bromazepam 1.5 mg daily since 2015

Quit CT Bromazepam 16-01-2020 No withdrawals 

Occasionally 1.5 mg extra

Last extra 1.5 mg 12-01-2020

 

 

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Sorry to hear this. I can't help but hopefully someone can advise you. 

Lexapro 10MG

Almost continually for 25 odd years 

Reduced to 5MG beginning July 2018-  end August 2018

August 2018 til now off completely 

 

 

 

 

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Mod note:  Titled Blurred Vision and Prozac/venlafaxine taper

 

During the past five weeks physical anxiety symptoms from wd have much receded. Heavy derealization fog and blurry vision remain. I went off Effexor in May 2019 and Wellbutrin 2 months later. On  moderators' advice I have continued throughout this withdrawal to continue taking 20 mg of Prozac / fluoxetine. Because recovery seems to be progressing, however at micro-speed, should I consider starting a very slow taper of the Prozac with expectation that that might help alleviate the vision problem. This issue with Prozac is well known. My vision is also compromised owing to the derealization (perceptual disconnection) and to esophoria, or double-vision, which is partially corrected with prisms in my glasses. Or would I be ill-advised to change the Prozac dose at all until my CNS is in better shape than it is so far? Prozac helped me for several years but pooped out six years ago. I tried it again as a replacement for the Effexor.  It might be helping me now by preventing even slower recovery, but I have no real evidence of that. I would, however, like to see better than I am now. Any comments?

Edited by manymoretodays
merged with existing topic, added title, also is in members introduction topic

Fluoxetine 1997-2014, 2015, 10-40 mg. GAD and DR symptoms returned  April 2013.

Bupropion 2013-14, 4 mos; Lexapro 2014; Cymbalta 2014. Gabapentin 2014; Mirtazapene 2014. Buspirone 2015.

Venlafaxine Dec. 2015 – May 2019, 150 mg, tapered to 0 in 3 weeks, May-June 2019

Bupropion Mar 2017 – July 2019 300 mg, tapered to 0 in 3 weeks, July 2019

Fluoxetine/Prozac May 2019 – present, tapered from 20 mg started Jan 2020, linear 10% every 4 wks.; tapered 6 to 4 mg June, 2, 2020; 4 to 1.8 mg Aug. 26, 2020; updose from 1.8 mg to 2.0 Nov. 16, 2020. Holding at 2.0 mg as of Mar 14,2021. April 14, 2021 updosed to 2.5 mg.

D3 2,000 mg; Omega 3 360 EPA/240 DHA; Magnesium Chelate 250 mg; Inositol powder started Nov 12, 2020; Theanine 400 mg; cranial electrotherapy stimulation device, self-treatments started Mar 14, 2021.

 

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  • 2 months later...
On 4/3/2015 at 12:09 PM, ten0275 said:

** floaters - which for me appeared to sometimes be little sparkling zig-zaggy things, or also bright spots that i could not see through.

 

all of these dissapated for me as my withdrawal symptoms decreased.

Hi,

 

I had an appointment yesterday with a new doctor (my doctor is on long sick leave) to get renewal of Amitriptyline which I reinstated Dec 21.  I told her I cold turkey'd Amitriptyline, and reinstated and had a mix of symptoms both of withdrawals and side effects, as I had a resistance to reinstatement, but I persisted and it is on its way to stabilize as I'm now sleeping 6 nights on 7.  FLOATERS on my left eye started Feb 2nd during a bad Wave (never have them before).  I also have a migraine (never had migraine before) that started after reinstatement.  FLASHES started at same time, on the extreme left of the eye if I look there, but they are quite rare.  My new doctor approve my reinstatement and taking my time to stabilize before tapering it very slowly.  But she said she never saw floaters and flashes as a symptom of withdrawal or side effect with Amitriptyline and she said I'm in great danger and must see an eye doctor urgently, as it could be a retina detachment.  

 

I found an eye doctor and awaiting it receives my new doctor's reference by fax, so I could have an appointment maybe next Tuesday since I said it was urgent as per my doctor.  I'm convinced it is a withdrawal effect, but feel I should have the eye doctor check it, but I fear anything he'll do to me, as my brain is hypersensitive because of the cold turkey and new reinstatement after only almost 3 months.  I don't even think I could suffer a surgery on the eye for the retina, as I've been told and read that it is quite painful, and remain painful for a long while, and it may not succeed and cause more problems.

 

  Is my attitude about it is correct?   cc, @Altostrata

1989, 25mg, Amitriptyline 1st prescribed for 1wk insomnia, 2020 october Cold turkey

20/12/21, 22.5mg reinstated; waited 1.5 year to start tapering

21/07/25, 20mg tapering started. 10% every 4 weeks

22/02/26, 9.5mg - Emergency surgery put chaos to tapering: chronic insomnia till May

22/04/11, 10mg tapering started. 10% every 4 week. Sleep came back but trickled away in Sep' 22

22/09/17, 5,1mg - 10/15, 4.6mg - 11/12, 4,1mg - 12/10, 3.7mg.  Too fast. Permanent symptoms.

22/12/28, 4,0mg - partial updose where I'll remain until perfect stabilizing

22/12/30, 4,0mg - started Melatonin 3mg, Maritime Pine Bark Extract am & pm

23/02/03, 4,0mg - sleeping well every night with dreams, symptoms are diminishing

22/03/20, 4,0mg - insomnia is back on some nights. Waves. Anxiety. My dog is sick.

Maritime Pine Bark Extract (Omega Alpha Labs) in capsules am & pm, Melatonin 3mg

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On 12/10/2019 at 9:21 PM, Edmunds said:

My vision is also compromised owing to the derealization (perceptual disconnection) and to esophoria, or double-vision, which is partially corrected with prisms in my glasses

 

3 hours ago, Sleepan said:

FLOATERS on my left eye started Feb 2nd during a bad Wave (never have them before).  I

 

3 hours ago, Sleepan said:

FLASHES started at same time, on the extreme left of the eye if I look there, but they are quite rare. 

 

3 hours ago, Sleepan said:

But she said she never saw floaters and flashes as a symptom of withdrawal or side effect with Amitriptyline and she said I'm in great danger and must see an eye doctor urgently, as it could be a retina detachment.  

 

3 hours ago, Sleepan said:

but feel I should have the eye doctor check it, but I fear anything he'll do to me, as my brain is hypersensitive because of the cold turkey and new reinstatement after only almost 3 months.  I don't even think I could suffer a surgery on the eye for the retina, as I've been told and read that it is quite painful, and remain painful for a long while, and it may not succeed and cause more problems.

 

Hi Sleepan

 

I am a fellow member here and when I saw vision related issues I couldn't help by swing by your thread.

 

I have had an abundance of these, including those you mentioned. I recommend being cautious and getting your eye checked by an opthalmologist to make sure it is healthy.  I had terrible tinnitis, etc.  - finally went to an ENT and his first question was 'are you getting off of ADs?'  He gave me an exam including audiology and it was negative for any irregularities.

 

Many MDs are unfamiliar with WD symptoms (that they exist at all!).

 

Notes about my vision first. In general, I have experienced diplopia and blurry vision priot to my WD as I take a high dose of lamotrigine (a known side effect) for a non-psych  issue. It is significantly worse during WD. This diplopia/blurry vision does not afffect looking at objects or in the distance so much - however reading is impossible - whether on a high resolution computer screen (futile). Reading paper is slightly better. I use a magnifying glass and it helps slightly. I did not get prism glasses.  Without the WD, reading is slow for me because of the vision.

 

About your other symptoms. I have experienced floaters, flashes less often, twitches of the muscle under the right eyelid, and maybe other things. 

 

I cannot comment about your meds and any potential surgery. My only comment is to take one thing at a time. I know it's hard to. All of this is overwhelming. I never had these ocular issues before, nor did I ever have a migraine.

 

I had cT f cymbalta in Dec 2018 and one prior in mid-2018. Floaters and flashes started in June 2019 and are mostly gone. Diplopia/blurry vision have been hanging around since the summer I think. Twitching eyelid started 2-3 months ago.

 

The good times keep rollin'.... 😉

 

Hang in there.

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7 hours ago, Sleepan said:

Hi,

 

I had an appointment yesterday with a new doctor (my doctor is on long sick leave) to get renewal of Amitriptyline which I reinstated Dec 21.  I told her I cold turkey'd Amitriptyline, and reinstated and had a mix of symptoms both of withdrawals and side effects, as I had a resistance to reinstatement, but I persisted and it is on its way to stabilize as I'm now sleeping 6 nights on 7.  FLOATERS on my left eye started Feb 2nd during a bad Wave (never have them before).  I also have a migraine (never had migraine before) that started after reinstatement.  FLASHES started at same time, on the extreme left of the eye if I look there, but they are quite rare.  My new doctor approve my reinstatement and taking my time to stabilize before tapering it very slowly.  But she said she never saw floaters and flashes as a symptom of withdrawal or side effect with Amitriptyline and she said I'm in great danger and must see an eye doctor urgently, as it could be a retina detachment.  

 

I found an eye doctor and awaiting it receives my new doctor's reference by fax, so I could have an appointment maybe next Tuesday since I said it was urgent as per my doctor.  I'm convinced it is a withdrawal effect, but feel I should have the eye doctor check it, but I fear anything he'll do to me, as my brain is hypersensitive because of the cold turkey and new reinstatement after only almost 3 months.  I don't even think I could suffer a surgery on the eye for the retina, as I've been told and read that it is quite painful, and remain painful for a long while, and it may not succeed and cause more problems.

 

  Is my attitude about it is correct?   cc, @Altostrata

About three years ago, before any wd issues started, I noticed a shadow on the bottom of my right eye. Because of a novel I had read in which the main character saw a shadow and got a diagnosis of detached retina, I almost immediately connected the ophthalmology department of my HMO. I was told to get over there pronto. Over the next four hours I had in-office repair of the retina. It was not painful at all.The major annoyance was that the doctor had to plant a gas bubble in my eye to stabilize the retina, and it remained visible for about a month, though not in my central vision. Eventually, it got smaller and disappeared. I know that a significant thickening of floaters, which I've had since age 18, can be a sign of a torn or detached retina.

Fluoxetine 1997-2014, 2015, 10-40 mg. GAD and DR symptoms returned  April 2013.

Bupropion 2013-14, 4 mos; Lexapro 2014; Cymbalta 2014. Gabapentin 2014; Mirtazapene 2014. Buspirone 2015.

Venlafaxine Dec. 2015 – May 2019, 150 mg, tapered to 0 in 3 weeks, May-June 2019

Bupropion Mar 2017 – July 2019 300 mg, tapered to 0 in 3 weeks, July 2019

Fluoxetine/Prozac May 2019 – present, tapered from 20 mg started Jan 2020, linear 10% every 4 wks.; tapered 6 to 4 mg June, 2, 2020; 4 to 1.8 mg Aug. 26, 2020; updose from 1.8 mg to 2.0 Nov. 16, 2020. Holding at 2.0 mg as of Mar 14,2021. April 14, 2021 updosed to 2.5 mg.

D3 2,000 mg; Omega 3 360 EPA/240 DHA; Magnesium Chelate 250 mg; Inositol powder started Nov 12, 2020; Theanine 400 mg; cranial electrotherapy stimulation device, self-treatments started Mar 14, 2021.

 

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2 hours ago, Edmunds said:

Over the next four hours I had in-office repair of the retina. It was not painful at all.The major annoyance was that the doctor had to plant a gas bubble in my eye to stabilize the retina, and it remained visible for about a month, though not in my central vision. Eventually, it got smaller and disappeared. I know that a significant thickening of floaters, which I've had since age 18, can be a sign of a torn or detached retina.

 

Thank you Edmunds.  I'm so pleased this retina re-attachment surgery has worked well for you.  You were not in WD at that time.  Don't you think I would imperil the stabilization of my reinstatement of Ami in its 10th week now if I had such a surgery?  

 

I do not think I'm strong enough to have such a retina re-attachment surgery.  I have strong withdrawal symptoms with my brain hypersensitive because of the cold turkey early October and reinstatement since Dec 21st.   It's not easy to stabilize as I have many side effects from a resistance I have with Amitriptyline now.  But there's progress, and I'm convinced and I'm determined to be well again.  My intuition tells me, rightly or wrongly, that I can't have such a surgery.  So I will go to this appointment next week yet to be confirmed but with no intention to accept a surgery at this time.  I have to know in advance, because I'm afraid otherwise I will do whatever the eye doctor tells me what is best.  Going to doctors is stressful right now.  I don't trust them blindly anymore.

 

6 hours ago, Giulietta said:

I have had an abundance of these, including those you mentioned. I recommend being cautious and getting your eye checked by an opthalmologist to make sure it is healthy. 

 

Thank you Giulietta.  I will have it checked.  I'm quite sure the zig zag I'm seeing are WD and not a separate health issue, so it will disappear with other symptoms.  Many members here have issues with their eyes.  However, if it is a retina detachment in progress on one eye, I would like to be re-assured that I can withstand such a surgery at this time.  My brain is fragile, hypersensitive, inflamed and it seems it is doing a pressure on my eyes.  I'm not ready right now for a surgery, yes?

 

 

1989, 25mg, Amitriptyline 1st prescribed for 1wk insomnia, 2020 october Cold turkey

20/12/21, 22.5mg reinstated; waited 1.5 year to start tapering

21/07/25, 20mg tapering started. 10% every 4 weeks

22/02/26, 9.5mg - Emergency surgery put chaos to tapering: chronic insomnia till May

22/04/11, 10mg tapering started. 10% every 4 week. Sleep came back but trickled away in Sep' 22

22/09/17, 5,1mg - 10/15, 4.6mg - 11/12, 4,1mg - 12/10, 3.7mg.  Too fast. Permanent symptoms.

22/12/28, 4,0mg - partial updose where I'll remain until perfect stabilizing

22/12/30, 4,0mg - started Melatonin 3mg, Maritime Pine Bark Extract am & pm

23/02/03, 4,0mg - sleeping well every night with dreams, symptoms are diminishing

22/03/20, 4,0mg - insomnia is back on some nights. Waves. Anxiety. My dog is sick.

Maritime Pine Bark Extract (Omega Alpha Labs) in capsules am & pm, Melatonin 3mg

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2 hours ago, Sleepan said:

My intuition tells me, rightly or wrongly, that I can't have such a surgery.  So I will go to this appointment next week yet to be confirmed but with no intention to accept a surgery at this time.  I have to know in advance, because I'm afraid otherwise I will do whatever the eye doctor tells me what is best.  Going to doctors is stressful right now.  I don't trust them blindly anymore.

 

Hi there,

 

I understand that going to the MD's is stressful. I can offer you only my personal opinion.

 

Given that I know nothing about retinal detachments and how long you may wait before they are repaired -  I would first want to know the risk of waiting for the repair and implications for my vision - vs. the impact of anesthesia on WD. I can answer neither of those questions. I would ask Alto about the anesthesia part.

 

I would personally prefer to postpone a procedure until I was at least stable unless it was medically necessary to have the procedure now.

 

Why do you have to commit to a procedure when you meet with the MD?  Even if you do, you have the right to change your mind.   😉  Might you also get a 2nd opinion?

 

I'm sorry you have to be contend with this now.

 

KR,

G

 

 

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If you have a torn or detached retina, you can't procrastinate at the risk of losing your sight in the affected eye. That loss can happen within a very short time of noticing symptoms. If you suspect a retinal problem, you should treat it as an emergency and get to the medical facility right away. When I responded to my symptoms very quickly, the doctors kept me in the waiting room until the repair could be done, which took less than an hour. They told me I did the right thing to get to them immediately. If you wait, you are more likely to be admitted to the hospital for a more radical procedure to save your eye. Or they may not be able to save it.

When I was heading into the worst period of WD last summer, my wife and I flew to Japan, where I gave a keynote speech at a conference, then traveled around Japan in 95 degree heat and high humidity for several days. If I had been further into the WD, I would have been sorely tempted to cancel the trip. "I can't do this!" But I did it, and though it never felt like an enjoyable vacation, I got through it and saw sights I had always wanted to see. And when I came back, I was having heavy anxiety and derealization all day. But I did not get a lot worse, having made that trip. And gradually, gradually, I started to get better. I'm still in WD, though the anxiety has much receded. Now it's weird derealization, blurry vision, sore eyes, and fatigue. That's all!!🥴

Fluoxetine 1997-2014, 2015, 10-40 mg. GAD and DR symptoms returned  April 2013.

Bupropion 2013-14, 4 mos; Lexapro 2014; Cymbalta 2014. Gabapentin 2014; Mirtazapene 2014. Buspirone 2015.

Venlafaxine Dec. 2015 – May 2019, 150 mg, tapered to 0 in 3 weeks, May-June 2019

Bupropion Mar 2017 – July 2019 300 mg, tapered to 0 in 3 weeks, July 2019

Fluoxetine/Prozac May 2019 – present, tapered from 20 mg started Jan 2020, linear 10% every 4 wks.; tapered 6 to 4 mg June, 2, 2020; 4 to 1.8 mg Aug. 26, 2020; updose from 1.8 mg to 2.0 Nov. 16, 2020. Holding at 2.0 mg as of Mar 14,2021. April 14, 2021 updosed to 2.5 mg.

D3 2,000 mg; Omega 3 360 EPA/240 DHA; Magnesium Chelate 250 mg; Inositol powder started Nov 12, 2020; Theanine 400 mg; cranial electrotherapy stimulation device, self-treatments started Mar 14, 2021.

 

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In short, you will survive the retina repair and continue your recovery. I recommend that you get to the doctors tomorrow!

Fluoxetine 1997-2014, 2015, 10-40 mg. GAD and DR symptoms returned  April 2013.

Bupropion 2013-14, 4 mos; Lexapro 2014; Cymbalta 2014. Gabapentin 2014; Mirtazapene 2014. Buspirone 2015.

Venlafaxine Dec. 2015 – May 2019, 150 mg, tapered to 0 in 3 weeks, May-June 2019

Bupropion Mar 2017 – July 2019 300 mg, tapered to 0 in 3 weeks, July 2019

Fluoxetine/Prozac May 2019 – present, tapered from 20 mg started Jan 2020, linear 10% every 4 wks.; tapered 6 to 4 mg June, 2, 2020; 4 to 1.8 mg Aug. 26, 2020; updose from 1.8 mg to 2.0 Nov. 16, 2020. Holding at 2.0 mg as of Mar 14,2021. April 14, 2021 updosed to 2.5 mg.

D3 2,000 mg; Omega 3 360 EPA/240 DHA; Magnesium Chelate 250 mg; Inositol powder started Nov 12, 2020; Theanine 400 mg; cranial electrotherapy stimulation device, self-treatments started Mar 14, 2021.

 

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