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☼ Cymbaltawithdrawal5600: Introduction


cymbaltawithdrawal5600

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Hello Cymbalta,

 

I'm stopping by to wish you a peaceful week. 

 

Be kind to yourself.

 

Tilly x

1999 - 2004 Paroxetine 20mg  -> 2004 - 2007 Citalopram 20mg -> 2007 -  short term Trazedone use (insomnia) -> 2007 - 2009 Fluoxetine 20mg  ->

2009 - Jan 2012 Citalopram 20mg  (Spring / Summer 2012 protracted withdrawal & related agoraphobia) -> 2012 - September Restarted Citalopram - unbearable start up effects. Discontinued in under 1 week -> Oct 12 -   October 2014 Escitalopram - 10mg prescribed. Started on 5mg and worked up to 10mg in 2.5mg increments  -> Oct 2014  - 5mg; 30/03/15 2.5mg; 15/04/15 3.5mg; 20/05/15 2.9mg;  19/09/15 2.8mg; 30/10/15 2.7mg; 13/11/15 2.6mg. Holding until March.

Diet:  mostly pescatarianl & lots of veg. Weekly offal for b vitamins.  Turmeric, nigella seeds, avocados, apple cider vinegar, coconut products daily. Lots of fluids: water, lemon juice, coconut water, herbal & green tea (decaffeinated).

Supplements: vitamin C 4000mg, Omega 3 fish oil - high DPA & EHA, vitamin E 400iu, vitamin D3 5000mg (Winter only - from sun in Spring / Summer), probiotics.

Current Symptoms: chronic fatigue, erratic sleep, extreme photophobia, eye floaters, noise sensitivity, tinnitus, cognitive & speech difficulties, dizziness, irregular gait, poor co ordination, severe facial and upper body muscle tension, head and neck pressure.

Coping Strategies: good nutrition, cooking, gardening & growing my own food, cycling, dancing, yoga, photography, sewing & creative pursuits, self massage, pampering, meditation, journalling, nature, cuddling cats & humans, laughter & humour, gratitude, self care, aromatherapy, audio books, word games & believing in myself, my potential and my future.

 

"Everything I need is within me" - Shakti Gawain

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I agree with what Tilly said. Be kind to you. Be as gentle to you as you have been to me, and I know many others would say the same. It is ok to be where you are at. Maybe don't fight it so hard. Maybe let it happen. Maybe you could just be still and let it pass because we all know that it will. Your umph will come. In the meantime, you are in my thoughts and prayers. (((hug)))

Current:

Lorazapam2mg: 4/9/152mg - 1.5mg: already sick/nothing noticed. No changes in sleep noted after illness.  

Lamictal: 7/27/13 - 8/6/13: 400mg - 500mg(dr order) mouth sores, headache, cognitive/balance, heart palp...8/7/13 - 8/23/13: 500mg - 400mg; symptoms↓...10/10/13: 350mg; fever/flu-like <2-weeks...12/30/13: 325mg; fever/flu-like symptoms <1-week...2/10/17: 300mg; no significant changes noted. 

 

Discontinued:

Omeprazole: 09/2103 40mg...5/1/14: 20mg... 8/21/14 = 0

Wellbutrin: 11/22/13: 300mg – 225mg...12/6/13 delayed reaction- mood swings, weight↓, heart palp/chest pain, alerting...12/14/13: 187mg; physical symptoms↓, neuro emotions ↑, weight stable...12/20/13: 225mg; physical symptoms return, emotions stable <1-week, weight↓...4/21/14: 187mg; weight↑...5/17/14 (neurologist ordered discontinue asap):168mg; headache, mood swings, ↑weight, sleep flux...5/24/14: 150mg; headache, mood swings, ↓cognitive/balance...6/2/14: 112mg; see above, weight stable, <3-weeks... 6/28/14: 100mg; moody...7/25/14: 87.5mg; family troubles... 8/4/14: 75mg; headaches; moody... 8/9/1450mg headaches... 8/12/14: 37.5mg; 8/17/14: 25mg...8/26/14 = 0

Hydroxyzine; 10mg: 5/20/15 *prn 4/5 times then dc'd. Mood changes/rage 

Buspirone: 7.5mg: 5/20/15 *prn 4/5 times then dc'd. No changes.

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MM and Tilly,

 

Thanks for the good wishes and by the way, MM. You said this:

 

 

Maybe don't fight it so hard. Maybe let it happen. Maybe you could just be still and let it pass because we all know that it will

 

Easier to say than to put into practice, sometimes.

 

I have been helping out at the flower shop nearly every day. For a person of my varied talents, there is always something to do and to learn and the owner really can use the help. So that part is going well and is getting me out of the house during the day which is what I so desperately needed. I am able to learn new tasks and there is only one area of my thinking that is broken. I used to be able to visualize the map of a city that has numbered streets both N & S, E & W and figure out where I should be heading. That part is missing in action and I am not sure if it will come back as I have taken to using the GPS and Maps on my phone to find delivery addresses. Just speak the addy into my phone and the route is all laid out and all I have to do is look at my phone for directions.

 

Something interesting has come to light and it is of the "you don't know it till you know it" variety. I remember back around the first of the year, when I lost the one volunteer job, that I was also trying to lose weight. I had been going to the gym and also riding my bike and I was frustrated because I was not losing an ounce. It was so bad that my thoughts turned depressive and suicidal, I was angry that my body would not cooperate and there was nothing I could do.

 

(Talk about the brain working, the power just went off and my brain registered it but my fingers kept typing to a black screen as I have to look at the keys to type. TG for autosaved content!)

 

Have reluctantly been going back to gym but not every day. Happened to see a friend and told her why I stopped going. She told me about a phone app she uses and she has been able to maintain her weight with it for over a year. So I loaded it and got quite a shock. What I thought was "not eating very much" was actually enough for me to gain weight when I stopped exercising and just sat in the house and contemplated dying. For instance, 30 almonds (and I could go through a bag in a few days) is a whopping 207 calories! The app tells me how many calories I am allowed for the day and if I exercise, I get to eat more.

 

So the mystery of not losing any weight was solved. No metabolic problem, just not knowing the proper calorie counts and how much to calculate for the exercise. It will take me a year to lose all of the weight I have put back on: all of my antidepressant weight is back, all 46 pounds of it. The app will keep track for me, all I have to do is log everything properly.

 

The other thing I have noticed is that every joint in my body hurts. I am not sure if some of it might be due to the extra weight, my spine is really stiff and I can hardly bend down anymore. The cymbalta has definitely left my body, I feel every ache now. I wonder if its use for chronic pain numbed my body and allowed me to perform activities that were actually hurting it. All the carrying heavy loads I did, all the grooming and dog washing. I feel every bit of it. I'll have to wait until the weight is off to see if there is any change. Even the bottoms of my feet hurt. Am I going to get to have any kind of life before everything falls apart I wonder?

 

Been making a lot more earrings, it seems to be a more productive use of my time than spending it on the computer. Thank goodness. But the computer stuff kept me going and kept me distracted enough to avoid thinking about suicide too much. Thoughts still flit through my head but not nearly as often and they don't have the 'charge' they did a couple of months ago. I am also crying less frequently.

What happened and how I arrived here: http://survivingantidepressants.org/index.php?/topic/4243-cymbaltawithdrawal5600-introduction/#entry50878

 

July 2016 I have decided to leave my story here at SA unfinished. I have left my contact information in my profile for anyone who wishes to talk to me. I have a posting history spanning nearly 4 years and 3000+ posts all over the site.

 

Thank you to all who participated in my recovery. I'll miss talking to you but know that I'll be cheering you on from the sidelines, suffering and rejoicing with you in spirit, as you go on in your journey.

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Hi CW

 

It was so good to read your post and see that you are getting out of the house to the flower shop.

 

You must have been brilliant to be able to visualise a map of a city! I have never had any sense of direction even when I had lived in my own home town for over 40 years!!

 

Yes, the weight thing is a problem for me too since A.D's. Like you say, it's all the little things like nuts that add up. You can still have them but in moderation. Are you on your feet alot in the flower shop - if so maybe that isn't helping the aches and pains.

 

You must put on some more pictures of the jewellery. I really admire it.

 

Nice to hear that you are doing better than a few weeks ago.

 

As for me I have not been so good but know I have been overdoing things. Have been forced to rest up for a few days and think I am feeling a little brighter today.

 

Best Wishes.

 

Flowers xxx

15 yrs on 20 to 30 mgs CITALOPRAM.  MAY 2014 Increased to 40 mgs per day.SEPT/NOV 2014 tapered in 6 weeks down to 10 mgs as per Dr instructions due to violent nightmares/palpitations.Given Noctamid (lormetazepam) to help with anxiety. On average took 2mg per day for 8 weeks.No taper was advised.DEC 2014 WD severe. Nervous tic in eyes and limbs, muscle pain,fluct  temp, weakness, dep and anxiety, nausea, giddy, unstable when walking. Different Dr suggested taking 20mgs CIT. BROMAZEPAM 3mgs up to 3 x daily for anxiety.DEC 9 2014 Updose CIT to 30mgs. Only taking BROMAZEPAM in emergency.DEC 31 2014 Settling at 30mg CIT - helping with depression. No Brom for 2wks.Found SA.APR 2015 Trying to stabilise on 30mgs CIT.  JAN 2016 Started Cit Taper reducing by 5% per month.  28.5 mgs 
FEB  Taper held bereavement. APR Taper resumed 27mgs . MAY 25.50 mgs .  JUNE 24 mgs .  JULY I stupidly mixed up my BP meds with CIT. Consequently took no CIT for 3 days and doubled my BP meds. Waiting for the fallout....Holding for a while until any chance of repercussions have abated. SEPT taper resumed to  22.5 mgs . OCT 21 mgs .NOV 19.95 mgs DEC crashed. 2017: FEB 3rd updose to 20.5 mgs to try to stabilise.FEB.switched over to 75mgs of Venlafaxine XR for 3 weeks.Too stimulating so switching back to Cit. 12 March 37.5 Ven and 20 Cit. 21 March 18mg Ven 20mg Cit. 4 April 9mg Ven 20mg Cit. Xanax .50mg when needed.  13 April 0 mgs Ven, 20mg Citalopram. Xanax .50 mg per day. 5 May reinstated a small amount of Ven to stabilize  1 mg twice a day. 20 mg Citalopram at night. Xanax .25 mg twice per day.Other Meds: Losartan (BP)Started 1993 at  50 mgs at night.  Seretide (Asthma) Started 1996 at 1 puff twice a day. Jan 2019 Antibiotic Ceclor 500mgs twice a day for bronchitis and  Atrovent 2ml capsules twice a day for asthma. Finished the course of both Jan 17. 

XANAX  Jan 27  - Feb 3 2019 Failed Valium Crossover.   Feb 14 2019  Updosed Xanax by .0625  Feb 17 2019 Decreased Xanax by .0625. Back to .50mg daily.  Update Xanax 28.2.20 tapered to .1250 mg 8am .25 mg midnight. Update Xanax 11.8.21 tapered to .25 mg at night. 

Current Meds 28.2.19: CITALOPRAM  20mg  taken at midnight. VENLAFAXINE  .9 mg twice a day at 8am and 10pm.  XANAX .50 mg split into 4 doses per day. 10am .0625mg / 2pm .1250mg/ 6pm .0625mg / midnight .25mg.Update 10.8.22 .25 mg at night.  LOSARTAN 50 mgs taken at midnight.  SERETIDE 1 puff taken at 8am and 10pm.   7.7.19 VENLAFAXINE UPDATE: Started tapering 10% every 4 weeks. Currently .4 mg twice a day at 8am and 10 pm.  2.9.19 .36 mg x 2. 1.10.19  .32 mg x 2. 26.11.19 .29 mg x2. 26.12.19 .26 mg  x 2. 23.1.20  .23 mg x 2.  20.2.20 .21 mg x2.20.3.20  .19 mg x 2. 21.4.20 .17 mg x 2. 19.5.20 .13 mg x 2.  18.6.20 .11mg  x 2 .18.7.20.10 mg x 2.1.9.20.09 mg x 2. 30.9. 20 .08 mg x 2. 1.11.20 .07 mg x 2.  2.12.20 .06 mg x 2.  8.1.21 .05 mg x 2.  4.2.21 .04 mg x 2. 9.3.21 .03 mgx2.  7.4.21  .02 mg x 2.  9.5.21 .01 mg x 2.  21.6.21 .01 mg x 1.  11.8.21 ZERO!

 

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MM and Tilly,

 

Thanks for the good wishes and by the way, MM. You said this:

 

 

Maybe don't fight it so hard. Maybe let it happen. Maybe you could just be still and let it pass because we all know that it will

 

Easier to say than to put into practice, sometimes.

 

I have been helping out at the flower shop nearly every day. For a person of my varied talents, there is always something to do and to learn and the owner really can use the help. So that part is going well and is getting me out of the house during the day which is what I so desperately needed. I am able to learn new tasks and there is only one area of my thinking that is broken. I used to be able to visualize the map of a city that has numbered streets both N & S, E & W and figure out where I should be heading. That part is missing in action and I am not sure if it will come back as I have taken to using the GPS and Maps on my phone to find delivery addresses. Just speak the addy into my phone and the route is all laid out and all I have to do is look at my phone for directions.

 

Something interesting has come to light and it is of the "you don't know it till you know it" variety. I remember back around the first of the year, when I lost the one volunteer job, that I was also trying to lose weight. I had been going to the gym and also riding my bike and I was frustrated because I was not losing an ounce. It was so bad that my thoughts turned depressive and suicidal, I was angry that my body would not cooperate and there was nothing I could do.

 

(Talk about the brain working, the power just went off and my brain registered it but my fingers kept typing to a black screen as I have to look at the keys to type. TG for autosaved content!)

 

Have reluctantly been going back to gym but not every day. Happened to see a friend and told her why I stopped going. She told me about a phone app she uses and she has been able to maintain her weight with it for over a year. So I loaded it and got quite a shock. What I thought was "not eating very much" was actually enough for me to gain weight when I stopped exercising and just sat in the house and contemplated dying. For instance, 30 almonds (and I could go through a bag in a few days) is a whopping 207 calories! The app tells me how many calories I am allowed for the day and if I exercise, I get to eat more.

 

So the mystery of not losing any weight was solved. No metabolic problem, just not knowing the proper calorie counts and how much to calculate for the exercise. It will take me a year to lose all of the weight I have put back on: all of my antidepressant weight is back, all 46 pounds of it. The app will keep track for me, all I have to do is log everything properly.

 

The other thing I have noticed is that every joint in my body hurts. I am not sure if some of it might be due to the extra weight, my spine is really stiff and I can hardly bend down anymore. The cymbalta has definitely left my body, I feel every ache now. I wonder if its use for chronic pain numbed my body and allowed me to perform activities that were actually hurting it. All the carrying heavy loads I did, all the grooming and dog washing. I feel every bit of it. I'll have to wait until the weight is off to see if there is any change. Even the bottoms of my feet hurt. Am I going to get to have any kind of life before everything falls apart I wonder?

 

Been making a lot more earrings, it seems to be a more productive use of my time than spending it on the computer. Thank goodness. But the computer stuff kept me going and kept me distracted enough to avoid thinking about suicide too much. Thoughts still flit through my head but not nearly as often and they don't have the 'charge' they did a couple of months ago. I am also crying less frequently.

This post is full of positive change. It reminded me of a Maya Angelou quote:

 

"When you know better, you do better"

 

Your world / life is transforming, slowly but surely, Cymbalta.

 

I hope that the coming week is both peaceful and kind to you.

 

Hugs,

 

Tilly x

1999 - 2004 Paroxetine 20mg  -> 2004 - 2007 Citalopram 20mg -> 2007 -  short term Trazedone use (insomnia) -> 2007 - 2009 Fluoxetine 20mg  ->

2009 - Jan 2012 Citalopram 20mg  (Spring / Summer 2012 protracted withdrawal & related agoraphobia) -> 2012 - September Restarted Citalopram - unbearable start up effects. Discontinued in under 1 week -> Oct 12 -   October 2014 Escitalopram - 10mg prescribed. Started on 5mg and worked up to 10mg in 2.5mg increments  -> Oct 2014  - 5mg; 30/03/15 2.5mg; 15/04/15 3.5mg; 20/05/15 2.9mg;  19/09/15 2.8mg; 30/10/15 2.7mg; 13/11/15 2.6mg. Holding until March.

Diet:  mostly pescatarianl & lots of veg. Weekly offal for b vitamins.  Turmeric, nigella seeds, avocados, apple cider vinegar, coconut products daily. Lots of fluids: water, lemon juice, coconut water, herbal & green tea (decaffeinated).

Supplements: vitamin C 4000mg, Omega 3 fish oil - high DPA & EHA, vitamin E 400iu, vitamin D3 5000mg (Winter only - from sun in Spring / Summer), probiotics.

Current Symptoms: chronic fatigue, erratic sleep, extreme photophobia, eye floaters, noise sensitivity, tinnitus, cognitive & speech difficulties, dizziness, irregular gait, poor co ordination, severe facial and upper body muscle tension, head and neck pressure.

Coping Strategies: good nutrition, cooking, gardening & growing my own food, cycling, dancing, yoga, photography, sewing & creative pursuits, self massage, pampering, meditation, journalling, nature, cuddling cats & humans, laughter & humour, gratitude, self care, aromatherapy, audio books, word games & believing in myself, my potential and my future.

 

"Everything I need is within me" - Shakti Gawain

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Ah, thank you Tilly and Flowers.

 

Tilly, I hope you start to feel better and you too, Flowers. I had read your thread about too much exercise and I remember thinking that I should have said something but I didn't. Sometimes people have to learn for themselves. Too much exercise was one of the triggers ffor wd syndrome for me, I had been off the drugs for a whole year up to that time. But I decided to start jogging and painting the house and that's how it triggered. Nothing more than gentle walking for one half hour a day is recommended.

 

I have found most people are not very receptive to advice while they are in the throes of wd so I have stopped giving it.

 

I love my diet app! Lost 3.5 lbs in the first week!

 

And now for a rant: to plural most words in the English language simply add an S. Stop adding an apostrophe with the S. It is incorrect. Period.

What happened and how I arrived here: http://survivingantidepressants.org/index.php?/topic/4243-cymbaltawithdrawal5600-introduction/#entry50878

 

July 2016 I have decided to leave my story here at SA unfinished. I have left my contact information in my profile for anyone who wishes to talk to me. I have a posting history spanning nearly 4 years and 3000+ posts all over the site.

 

Thank you to all who participated in my recovery. I'll miss talking to you but know that I'll be cheering you on from the sidelines, suffering and rejoicing with you in spirit, as you go on in your journey.

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What a great update! Would you be comfortable sharing the name of your app? I think I need it too! I eat very healthy food, but not losing.

1st round Prozac 1989/90, clear depression symptoms. 2nd round Prozac started 1999 when admitted to dr. I was tired. Prozac pooped out, switch to Cymbalta 3/2006. Diagnosed with bipolar disorder due to mania 6/2006--then I was taken abruptly off Cymbalta and didn't know I had SSRI withdrawal. Lots of meds for my intractable "bipolar" symptoms.

Zyprexa started about 9/06, mostly 5mg. Tapered 4/12 through12/29/12

Wellbutrin. XL 300 mg started 1/07, tapered 1/18/13 through 7/8/13

Oxazepam mostly continuously since 6/06, 30mg since 12/12, tapered 1.17.14 through 8.26.15

11/06 Lithium 600mg twice daily, 2.2.14 400mg TID DIY liquid, 2.12.14 1150mg, 3.2.14 1100mg, 3.18.14 1075mg, 4/14 updose to 1100mg, 6.1.14 900 mg capsules 7.8.14 810mg, 8.17.14 725mg, 8.24.24 700mg...10.22.14 487.5mg, 3.9.15 475mg, 4.1.15 462.5mg 4.21.15 450mg 8.11.15 375mg, 11.28.15 362.5mg, back to 375mg four days later, 3.4.16 updose to 475 (too much going on to risk trouble)

9/4/13 Toprol-XL 25mg daily for sudden hypertension, tapered 11.12.13 through 5.3.14, last 10 days or so switched to atenolol

7.4.14 Started Walsh Protocol

56 years old

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Congrats on the weight loss CW. 

 

I am feeling much better now I am not exhausting myself overexercising!  Interesting that it made you worse too! Great i now have an excuse not to go to the gym. lol!!

 

Thanks for the grammar lesson - never was my strong point!!

 

Take care.

 

Flowers xxx

15 yrs on 20 to 30 mgs CITALOPRAM.  MAY 2014 Increased to 40 mgs per day.SEPT/NOV 2014 tapered in 6 weeks down to 10 mgs as per Dr instructions due to violent nightmares/palpitations.Given Noctamid (lormetazepam) to help with anxiety. On average took 2mg per day for 8 weeks.No taper was advised.DEC 2014 WD severe. Nervous tic in eyes and limbs, muscle pain,fluct  temp, weakness, dep and anxiety, nausea, giddy, unstable when walking. Different Dr suggested taking 20mgs CIT. BROMAZEPAM 3mgs up to 3 x daily for anxiety.DEC 9 2014 Updose CIT to 30mgs. Only taking BROMAZEPAM in emergency.DEC 31 2014 Settling at 30mg CIT - helping with depression. No Brom for 2wks.Found SA.APR 2015 Trying to stabilise on 30mgs CIT.  JAN 2016 Started Cit Taper reducing by 5% per month.  28.5 mgs 
FEB  Taper held bereavement. APR Taper resumed 27mgs . MAY 25.50 mgs .  JUNE 24 mgs .  JULY I stupidly mixed up my BP meds with CIT. Consequently took no CIT for 3 days and doubled my BP meds. Waiting for the fallout....Holding for a while until any chance of repercussions have abated. SEPT taper resumed to  22.5 mgs . OCT 21 mgs .NOV 19.95 mgs DEC crashed. 2017: FEB 3rd updose to 20.5 mgs to try to stabilise.FEB.switched over to 75mgs of Venlafaxine XR for 3 weeks.Too stimulating so switching back to Cit. 12 March 37.5 Ven and 20 Cit. 21 March 18mg Ven 20mg Cit. 4 April 9mg Ven 20mg Cit. Xanax .50mg when needed.  13 April 0 mgs Ven, 20mg Citalopram. Xanax .50 mg per day. 5 May reinstated a small amount of Ven to stabilize  1 mg twice a day. 20 mg Citalopram at night. Xanax .25 mg twice per day.Other Meds: Losartan (BP)Started 1993 at  50 mgs at night.  Seretide (Asthma) Started 1996 at 1 puff twice a day. Jan 2019 Antibiotic Ceclor 500mgs twice a day for bronchitis and  Atrovent 2ml capsules twice a day for asthma. Finished the course of both Jan 17. 

XANAX  Jan 27  - Feb 3 2019 Failed Valium Crossover.   Feb 14 2019  Updosed Xanax by .0625  Feb 17 2019 Decreased Xanax by .0625. Back to .50mg daily.  Update Xanax 28.2.20 tapered to .1250 mg 8am .25 mg midnight. Update Xanax 11.8.21 tapered to .25 mg at night. 

Current Meds 28.2.19: CITALOPRAM  20mg  taken at midnight. VENLAFAXINE  .9 mg twice a day at 8am and 10pm.  XANAX .50 mg split into 4 doses per day. 10am .0625mg / 2pm .1250mg/ 6pm .0625mg / midnight .25mg.Update 10.8.22 .25 mg at night.  LOSARTAN 50 mgs taken at midnight.  SERETIDE 1 puff taken at 8am and 10pm.   7.7.19 VENLAFAXINE UPDATE: Started tapering 10% every 4 weeks. Currently .4 mg twice a day at 8am and 10 pm.  2.9.19 .36 mg x 2. 1.10.19  .32 mg x 2. 26.11.19 .29 mg x2. 26.12.19 .26 mg  x 2. 23.1.20  .23 mg x 2.  20.2.20 .21 mg x2.20.3.20  .19 mg x 2. 21.4.20 .17 mg x 2. 19.5.20 .13 mg x 2.  18.6.20 .11mg  x 2 .18.7.20.10 mg x 2.1.9.20.09 mg x 2. 30.9. 20 .08 mg x 2. 1.11.20 .07 mg x 2.  2.12.20 .06 mg x 2.  8.1.21 .05 mg x 2.  4.2.21 .04 mg x 2. 9.3.21 .03 mgx2.  7.4.21  .02 mg x 2.  9.5.21 .01 mg x 2.  21.6.21 .01 mg x 1.  11.8.21 ZERO!

 

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Meimei,

 

The app is Lose It! I have the android version. What is totally neat about it is that it has an integrated barcode scanner so all you have to do is scan the code and the calorie content for most foods comes right up, you just pick the portions. I was completely shocked at how much I was overeating. Now I have totally cut out snacking only because of being to lazy to log what I want to eat into the phone. Successfully passed up some Whitman's Sampler candies when I read they were avg. 170 calories per piece. I have to be careful tho, some days I have been under my calorie limit and even though I am not hungry I make myself eat something. Women should not eat less than 1200 cal/day, too low a calorie count causes us to retain our weight. You'd have to look that one up for the physiology behind as I have forgotten it.

 

Flowers, the grammar rant was not directed at you, I hope you did not think so. There are probably some here who need a brush up though. That is why I haven't been reading here much lately. A lot of stuff really hurts to read in more ways than one.

 

I have a lot of experiential knowledge in my 32 page thread. Too bad no one wants to read it. There are far too many who come to the board and start topics in Symptoms wanting people to give them information instead of them going to find it for themselves. I found out so many things because I read so many things, it all came in handy at some point.

What happened and how I arrived here: http://survivingantidepressants.org/index.php?/topic/4243-cymbaltawithdrawal5600-introduction/#entry50878

 

July 2016 I have decided to leave my story here at SA unfinished. I have left my contact information in my profile for anyone who wishes to talk to me. I have a posting history spanning nearly 4 years and 3000+ posts all over the site.

 

Thank you to all who participated in my recovery. I'll miss talking to you but know that I'll be cheering you on from the sidelines, suffering and rejoicing with you in spirit, as you go on in your journey.

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Hey I read it.  And it helped me.

 

I was using the Lose It app before I got sick, and it similarly helped me.  I had gotten into the habit of using it every day and was pretty good about logging every thing I ate.  As I settled into the delayed withdrawal, the Lose It app helped me notice how severely my appetite was weakened. 

 

I've never in my life had low appetite.  When I was in the worst of depression decades ago, I would crave and eat lots of junk food and gain weight.  That was one of the clues that the delayed withdrawal was not a 'relapse of depression'; because my appetite had vanished.

1983-1995: On and off several tricyclic ADs
1995: Quit alcohol, started Prozac
2003: Stopped Prozac; 2004: Started Effexor XR 225
2014: Tried and failed three rapid tapers; stopped cold turkey March 11, 2014, eight days of Prozac as a bridge.
March 19, 2014: SSRI/SSNI free; four weeks acute withdrawal, then five month window of minimal symptoms.

Sept 2014-June 2015: Delayed, prolonged severe withdrawal from Effexor. Roller coaster, way up and way down.  Symptoms swing widely. Clear improvement in Mar-Apr, but still much hell. In May symptoms shifted to insomnia and depression, less HA, tinnitus and brain fog.

July-Sept 2015: After two weeks of using CES device, tremendous relief of insomnia, depression and other symptoms. Feeling much better, finally! Symptoms still come and go, good and bad days.Sneaking up on return to good health.  Alto gave me a 'Here Comes the Sun'!!!  ☼

Oct 2015-Feb 2016: Difficult several months, some good days but the bad days felt like I'm moving backwards.  Struggling after steady improvement, but hanging tough.

 

Current supplements:  Mg-Threonate; glutathione; krill oil; borage oil; phosphatidyl choline; multivite, vit B12, vit C, vit D vit E; OTC meds pseudoephedrine in the AM and benadryl at bedtime.  Clonidine 0.2 bid for high blood pressure.

Filled with hope, courage and self-appreciation.

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I should say that I don't encourage people to read my thread, the first several pages (up till protracted wd started in earnest in Nov 2013) are the ravings of a lunatic whose brain was still under the influence of the drugs. Kudos to you, OE, for reading it.

 

Had I known about Lose It during my year in protracted wd, I would have been able to see the effects of high cortisol on my system and appetite. I had to force myself to eat and I lost a lot of weight. My clothes were falling off me. The same pants that I can barely button and zip now I was able to take them off without unbuttoning or unzipping them. That is why I gained so much weight. When the cortisol levels had fallen (beginning of this year), I was used to eating a certain amount and it piled the weight on me (inactivitydue to depression, anhedonia, apathy and SI did not help my cause either).

 

You were pretty smart to figure that out, OE, that the drugs were doing it. they really mess a lot of things up, not just neurotransmitters.

 

I have had to switch to using another computer, one that I have had in a box since 2012. I am letting the flower shop use mine for the mother's (<--- proper use of an apostrophe) day rush. For some reason this version of firefox (which is the newest one) is not giving me the red snakes for misspelled words. Maybe I will be able to figure out why and then I can try to find out who else was having this problem. I have already had to troubleshoot it not wanting to save the login creds for this site, PITA to type them in everytime I want to post something.....

What happened and how I arrived here: http://survivingantidepressants.org/index.php?/topic/4243-cymbaltawithdrawal5600-introduction/#entry50878

 

July 2016 I have decided to leave my story here at SA unfinished. I have left my contact information in my profile for anyone who wishes to talk to me. I have a posting history spanning nearly 4 years and 3000+ posts all over the site.

 

Thank you to all who participated in my recovery. I'll miss talking to you but know that I'll be cheering you on from the sidelines, suffering and rejoicing with you in spirit, as you go on in your journey.

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Hi CW

 

No offence taken. I am reading through people's threads as much as I can. It is quite time consuming and I haven't got to yours yet! 

  Reading through the members threads who have been here a while can help so much with what us newbies are going through. It gives me reassurance and hope to see that  so many have improved albeit over a long time.

 

Keep up the good work weight watching! I am trying to eat heathily - lots of veg and fruit. If i can't force myself to eat a proper meal I make healthy soups. The tomatoes are so full of flavour here and make a great base for a lot of recipes.

15 yrs on 20 to 30 mgs CITALOPRAM.  MAY 2014 Increased to 40 mgs per day.SEPT/NOV 2014 tapered in 6 weeks down to 10 mgs as per Dr instructions due to violent nightmares/palpitations.Given Noctamid (lormetazepam) to help with anxiety. On average took 2mg per day for 8 weeks.No taper was advised.DEC 2014 WD severe. Nervous tic in eyes and limbs, muscle pain,fluct  temp, weakness, dep and anxiety, nausea, giddy, unstable when walking. Different Dr suggested taking 20mgs CIT. BROMAZEPAM 3mgs up to 3 x daily for anxiety.DEC 9 2014 Updose CIT to 30mgs. Only taking BROMAZEPAM in emergency.DEC 31 2014 Settling at 30mg CIT - helping with depression. No Brom for 2wks.Found SA.APR 2015 Trying to stabilise on 30mgs CIT.  JAN 2016 Started Cit Taper reducing by 5% per month.  28.5 mgs 
FEB  Taper held bereavement. APR Taper resumed 27mgs . MAY 25.50 mgs .  JUNE 24 mgs .  JULY I stupidly mixed up my BP meds with CIT. Consequently took no CIT for 3 days and doubled my BP meds. Waiting for the fallout....Holding for a while until any chance of repercussions have abated. SEPT taper resumed to  22.5 mgs . OCT 21 mgs .NOV 19.95 mgs DEC crashed. 2017: FEB 3rd updose to 20.5 mgs to try to stabilise.FEB.switched over to 75mgs of Venlafaxine XR for 3 weeks.Too stimulating so switching back to Cit. 12 March 37.5 Ven and 20 Cit. 21 March 18mg Ven 20mg Cit. 4 April 9mg Ven 20mg Cit. Xanax .50mg when needed.  13 April 0 mgs Ven, 20mg Citalopram. Xanax .50 mg per day. 5 May reinstated a small amount of Ven to stabilize  1 mg twice a day. 20 mg Citalopram at night. Xanax .25 mg twice per day.Other Meds: Losartan (BP)Started 1993 at  50 mgs at night.  Seretide (Asthma) Started 1996 at 1 puff twice a day. Jan 2019 Antibiotic Ceclor 500mgs twice a day for bronchitis and  Atrovent 2ml capsules twice a day for asthma. Finished the course of both Jan 17. 

XANAX  Jan 27  - Feb 3 2019 Failed Valium Crossover.   Feb 14 2019  Updosed Xanax by .0625  Feb 17 2019 Decreased Xanax by .0625. Back to .50mg daily.  Update Xanax 28.2.20 tapered to .1250 mg 8am .25 mg midnight. Update Xanax 11.8.21 tapered to .25 mg at night. 

Current Meds 28.2.19: CITALOPRAM  20mg  taken at midnight. VENLAFAXINE  .9 mg twice a day at 8am and 10pm.  XANAX .50 mg split into 4 doses per day. 10am .0625mg / 2pm .1250mg/ 6pm .0625mg / midnight .25mg.Update 10.8.22 .25 mg at night.  LOSARTAN 50 mgs taken at midnight.  SERETIDE 1 puff taken at 8am and 10pm.   7.7.19 VENLAFAXINE UPDATE: Started tapering 10% every 4 weeks. Currently .4 mg twice a day at 8am and 10 pm.  2.9.19 .36 mg x 2. 1.10.19  .32 mg x 2. 26.11.19 .29 mg x2. 26.12.19 .26 mg  x 2. 23.1.20  .23 mg x 2.  20.2.20 .21 mg x2.20.3.20  .19 mg x 2. 21.4.20 .17 mg x 2. 19.5.20 .13 mg x 2.  18.6.20 .11mg  x 2 .18.7.20.10 mg x 2.1.9.20.09 mg x 2. 30.9. 20 .08 mg x 2. 1.11.20 .07 mg x 2.  2.12.20 .06 mg x 2.  8.1.21 .05 mg x 2.  4.2.21 .04 mg x 2. 9.3.21 .03 mgx2.  7.4.21  .02 mg x 2.  9.5.21 .01 mg x 2.  21.6.21 .01 mg x 1.  11.8.21 ZERO!

 

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The tomatoes are so full of flavour here

 

Hmmm. British (Canadian?) spelling for flavor, but living in Spain? Must be a good story there. I'll bet it is in your thread, which I have not read yet (so many people, so little time.....)

 

The reason for the great flavor is probably because Spain has old, noble dirt, high in heritage (as opposed to the chemically treated, newer and profane dirt of America). That is my guess, anyway.

What happened and how I arrived here: http://survivingantidepressants.org/index.php?/topic/4243-cymbaltawithdrawal5600-introduction/#entry50878

 

July 2016 I have decided to leave my story here at SA unfinished. I have left my contact information in my profile for anyone who wishes to talk to me. I have a posting history spanning nearly 4 years and 3000+ posts all over the site.

 

Thank you to all who participated in my recovery. I'll miss talking to you but know that I'll be cheering you on from the sidelines, suffering and rejoicing with you in spirit, as you go on in your journey.

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Hi CW - I caught up on your thread. And as you know, I read it from the beginning too, even though you warned me. So glad to read your update, that's great about the flower shop work. I know I could benefit from being involved in something away from the homestead, but not there yet. Baby steps, and I'm starting to waddle without falling down so slow and steady goes my race.

 

I had similar weight fluctuations to what you described. I recently dropped off a couple bags of my smaller sized clothing to the thrift shop, it was depressing me to see them sitting there in the tote. I thought I'd lose this excess by now. I put on about 25 pounds. So maybe I'll check into that app too. My husband got me an iphone and I am slowly learning how to use it. Some days I get very frustrated. I had only ever used a flip phone until the end of December, never even sent a text. So big learning curve for me. He said he ordered a user's manual for me, so I'm looking forward to getting that.

 

Have a nice evening!  -- Chia

Read my intro here: http://survivingantidepressants.org/index.php?/topic/7569-chia1214-tapering-lamotrigine-maybe-clonazapam-later/#entry110043

1975 Hospitalized and first exposure to psych. drugs age 13-15 Haldol, Tofranil, Cogentin, Thorazine. On and off numerous AD’s & AP’s no records until 2000

2000 Celexa, Clonazepam 1mg – never exceeded 1 mg except occasional emergency use

2004 Lamictal (Lamotrigine), Effexor, recall add-on trials of Lexapro, Prozac, Wellbutrin during this time also

2007 Lithium added, switch Effexor to Pristiq, still on Lamictal (Lamotrigine) Clonazepam. Some cold turkey quits of everything over the years. No knowledge of WD

2011 Lithuim Gabapentin Lunestra, Lamictal (Lamotrigine), Clonazepam

2012 Taken off all but Lamictal (Lamotrigine), Clonazepam, began Zyprexa

2013 Abilify replaced Zyprexa (high lipids) added Wellbutrin, Prozac, Adderall

2014 Discontinued Abilify, Wellbutrin, Prozac, Adderall, added Latuda, Quetiapine, then stopped those.

December 2014 Found SA Began slow taper of the only remaining two drugs I'm taking

Clonazepam 0 mg Benzo free as of May 30, 2017

Lamotrigine 0 mg as of Jan 7, 2018   

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Just catching up with your life CW glad things have worked out in so many different ways.  I used that lose it on the computer for a time it helped me a lot too bit of a pain when I am not in a mood to log stuff.  I gave up on it sometime I don't recall when but I liked it too for awhile. 

Flavour is spelled that way in Canada I have given up and with trying to correct the world :) and just go with flavor... why fight it?

 

Just wanted you to know I was here see how you are doing and say hello. Hope things keep going well. :)

peace

WARNING THIS WILL BE LONG
Had a car accident in 85
Codeine was the pain med when I was release from hosp continuous use till 89
Given PROZAC by a specialist to help with nerve pain in my leg 89-90 not sure which year
Was not told a thing about it being a psych med thought it was a pain killer no info about psych side effects I went nuts had hallucinations. As I had a head injury and was diagnosed with a concussion in 85 I was sent to a head injury clinic in 1990 five years after the accident. I don't think they knew I had been on prozac I did not think it a big deal and never did finish the bottle of pills. I had tests of course lots of them. Was put into a pain clinic and given amitriptyline which stopped the withdrawal but had many side effects. But I could sleep something I had not done in a very long time the pain lessened. My mother got cancer in 94 they switched my meds to Zoloft to help deal with this pressure as I was her main care giver she died in 96. I stopped zoloft in 96 had withdrawal was put on paxil went nutty quit it ct put on resperidol quit it ct had withdrawal was put on Effexor... 2years later celexa was added 20mg then increased to 40mg huge personality change went wild. Did too fast taper off Celexa 05 as I felt unwell for a long time prior... quit Effexor 150mg ct 07 found ****** 8 months into withdrawal learned some things was banned from there in 08 have kept learning since. there is really not enough room here to put my history but I have a lot of opinions about a lot of things especially any of the drugs mentioned above.
One thing I would like to add here is this tidbit ALL OPIATES INCREASE SEROTONIN it is not a huge jump to being in chronic pain to being put on an ssri/snri and opiates will affect your antidepressants and your thinking.

As I do not update much I will put my quit date Nov. 17 2007 I quit Effexor cold turkey. 

http://survivingantidepressants.org/index.php?/topic/1096-introducing-myself-btdt/

There is a crack in everything ..That's how the light gets in :)

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I have lost 9 pounds since April 21 when I started the LoseIt tracker on my phone. I have it set to lose 1 lb a week but I see I have been losing more, probably because I am active at the job and I don't account for that. So straight calorie restriction works well for weight loss. My daily calorie allotment started out at 1344 (I am 5'3" and age 65) and somewhere along the line it decreased itself to the high 1200's, in response to my lighter body I am sure. If I go over on a certain day it notifies me, if I am under it does that too. I can go by the average for the week and it will tell me if I am trending over/under and I can eat a few more calories if I want. It is the weekly week numbers that are important. I have noticed that my weight varies by as much as 4 pounds day to day. I do morning weight when I first get up, after I pee, and with my light housecoat on. When it first drops a half pound I record that and then I do not record any decreases until they occur again. Because of the daily variance I don't want to have a wiggly graph, I prefer a straight downward slope. Yeah!

 

The best days are when I am not really hungry and maybe because of work, I don't eat lunch or just have a light snack. I will come home with 500 or so calories left to be eaten and some days, instead of eating one of my frozen meals (I am not in the cooking recovery stage yet) I'll just snack the rest: ice cream, nuts, chips. I can eat anything I want (and I do), it is simple calorie counting. When I have eaten at least 1200 cals for the day I stop eating till the next day. I mentioned before that women are cautioned not to go below 1200 cals/day.

 

I found out something interesting: I have always hated eating breakfast because it causes me to get ravenously faintingly stomach growlingly hungry way before lunch. Always. So I have been experimenting with those frozen breakfast sammiches (I do the turkey meat kind as I don't do beef or pork). The ones with just a whipped egg patty (either white or with yolk) and cheese slice do not cut it. I tried the healthy choice turkey sausage/egg/cheese concoction and yea! that did the trick. It is that turkey patty that prolongs digestion and is the key to preventing those hunger pangs. I learned in wd that I absolutely have to eat breakfast so that was the reason for the experiment.

 

All this is elementary nutrition anyway. But my personality (and some of yours I am sure) detests extra weight and wants it gone NOW. My wd ravaged body doesn't deserve to be subjected to severe calorie restrictions and I sure don't want to risk protracted wd rearing its very ugly head again. So slow it is and I just avoid looking in the mirror or glass windows and doors so I don't get discouraged. One of these days I am going to start adding in some exercise. I wanted to see if calorie restricion actually worked first.

 

I love LoseIt!

 

(the link is upthread somewhere, I am too lazy to link it today as I am on a tablet).

What happened and how I arrived here: http://survivingantidepressants.org/index.php?/topic/4243-cymbaltawithdrawal5600-introduction/#entry50878

 

July 2016 I have decided to leave my story here at SA unfinished. I have left my contact information in my profile for anyone who wishes to talk to me. I have a posting history spanning nearly 4 years and 3000+ posts all over the site.

 

Thank you to all who participated in my recovery. I'll miss talking to you but know that I'll be cheering you on from the sidelines, suffering and rejoicing with you in spirit, as you go on in your journey.

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Eggs are also a source of choline which is very important to healing your liver and or detoxing it.  If my memory is correct there are few sources. 

I LOVE lose it too!

 

Though I am not doing it now and have not used it in a long time.. I did use it for a time. Lost a lot of weight but was also following the fatty liver diet to improve liver health.  I felt a lot better then. I won't get into my resistance to start over not here. 

 

One thing I noticed about the Lose It system is it tracked my food and kept an eye on what I was eating... when I fell off the diet I still put in what I was eating... they sent me a note saying a large amount of my calories were coming from diary.  So left to my own devices and cravings I eat too much diary.  I have read a lot of books about weight the 4 hour body .. wheat belly... and others getting something from then all.  One thing I see over and over is often the foods we are craving eating on our own are the ones we are actually allergic too and we keep eating them to stop the wd type reactions to the affect they have on our bodies.  

 

Just an interesting tidbit. 

 

Congratulations on great success CW WAY TO GO!!!!!!!!

WARNING THIS WILL BE LONG
Had a car accident in 85
Codeine was the pain med when I was release from hosp continuous use till 89
Given PROZAC by a specialist to help with nerve pain in my leg 89-90 not sure which year
Was not told a thing about it being a psych med thought it was a pain killer no info about psych side effects I went nuts had hallucinations. As I had a head injury and was diagnosed with a concussion in 85 I was sent to a head injury clinic in 1990 five years after the accident. I don't think they knew I had been on prozac I did not think it a big deal and never did finish the bottle of pills. I had tests of course lots of them. Was put into a pain clinic and given amitriptyline which stopped the withdrawal but had many side effects. But I could sleep something I had not done in a very long time the pain lessened. My mother got cancer in 94 they switched my meds to Zoloft to help deal with this pressure as I was her main care giver she died in 96. I stopped zoloft in 96 had withdrawal was put on paxil went nutty quit it ct put on resperidol quit it ct had withdrawal was put on Effexor... 2years later celexa was added 20mg then increased to 40mg huge personality change went wild. Did too fast taper off Celexa 05 as I felt unwell for a long time prior... quit Effexor 150mg ct 07 found ****** 8 months into withdrawal learned some things was banned from there in 08 have kept learning since. there is really not enough room here to put my history but I have a lot of opinions about a lot of things especially any of the drugs mentioned above.
One thing I would like to add here is this tidbit ALL OPIATES INCREASE SEROTONIN it is not a huge jump to being in chronic pain to being put on an ssri/snri and opiates will affect your antidepressants and your thinking.

As I do not update much I will put my quit date Nov. 17 2007 I quit Effexor cold turkey. 

http://survivingantidepressants.org/index.php?/topic/1096-introducing-myself-btdt/

There is a crack in everything ..That's how the light gets in :)

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CW... You sound great. I've not much energy to say much more, but I am following you and happy for you.

*I'm not a doctor and don't give medical advice, just personal experience
**Off all meds since Nov. 2014. Mentally & emotionally recovered; physically not
-Dual cold turkeys off TCA & Ativan in Oct 2014. Prescribed from 2011-2014

-All meds were Rxed off-label for an autoimmune illness.  It was a MISDIAGNOSIS, but I did not find out until AFTER meds caused damage.  All med tapers/cold turkeys directed by doctors 

-Nortriptyline May 2012 - Dec 2013. Cold turkey off nortrip & cold switched to desipramine

-Desipramine Jan 2014 - Oct. 29, 2014 (rapid taper/cold turkey)

-Lorazepam 1 mg per night during 2011
-Lorazepam 1 mg per month in 2012 (or less)

-Lorazepam on & off, Dec 2013 through Aug 2014. Didn't exceed 3x a week

-Lorazepam again in Oct. 2014 to help get off of desipramine. Last dose lzpam was 1 mg, Nov. 2, 2014. Immediate paradoxical reactions to benzos after stopping TCAs 

-First muscle/dystonia side effects started on nortriptyline, but docs too stupid to figure it out. On desipramine, muscle tremors & rigidity worsened

-Two weeks after I got off all meds, I developed full-blown TD.  Tardive dystonia, dyskinesia, myoclonic jerks ALL over body, ribcage wiggles, facial tics, twitching tongue & fingers, tremors/twitches of arms, legs, cognitive impairment, throat muscles semi-paralyzed & unable to swallow solid food, brain zaps, ears ring, dizzy, everything looks too far away, insomnia, numbness & electric shocks everywhere when I try to fall asleep, jerk awake from sleep with big, gasping breaths, wake with terrors & tremors, severely depressed.  NO HISTORY OF DEPRESSION, EVER. Meds CREATED it.

-Month 7: hair falling out; no vision improvement; still tardive dystonia; facial & tongue tics returned
-Month 8: back to acute, incl. Grand Mal seizure-like episodes. New mental torment, PGAD, worse insomnia
-Month 9: tardive dystonia worse, dyskinesia returned. Unable to breathe well due to dystonia in stomach, chest, throat
-Month 13: Back to acute, brain zaps back, developed eczema & stomach problems. Left leg no longer works right due to dystonia, meaning both legs now damaged
-7 years off: Huge improvements, incl. improved dystonia

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Thanks for commenting B and Wig. I am not there yet, far from it. But getting there as are we all.

 

Today is 31 years alcohol free. How time flies when you are having fun.....

What happened and how I arrived here: http://survivingantidepressants.org/index.php?/topic/4243-cymbaltawithdrawal5600-introduction/#entry50878

 

July 2016 I have decided to leave my story here at SA unfinished. I have left my contact information in my profile for anyone who wishes to talk to me. I have a posting history spanning nearly 4 years and 3000+ posts all over the site.

 

Thank you to all who participated in my recovery. I'll miss talking to you but know that I'll be cheering you on from the sidelines, suffering and rejoicing with you in spirit, as you go on in your journey.

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todayis 31 yrs. alcohol free

that's wonderful! congratulations!

 

and good to hear you've been able to lose weight-that's what always bothered me most about ADs-the weight gain-I'd go off start to lose then back on & just blow up! I've lost over 15 lbs. since being off paxil-keep up the good work!

 

also wanted to say how much better you're sounding lately! so happy for you!

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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Hi CW

 

It's good to read how well you are doing and losing weight too. You deserve a pat on the back for putting in the effort to lose weight when you have everything else to contend with too. It's so easy in withdrawal not to eat properly and just grab anything to ease hunger pangs or nausea.

 

I really admire you for going out to work, losing weight and getting your life back on track during difficult times.

 

It's so good to read some happy news - good wishes to you.

15 yrs on 20 to 30 mgs CITALOPRAM.  MAY 2014 Increased to 40 mgs per day.SEPT/NOV 2014 tapered in 6 weeks down to 10 mgs as per Dr instructions due to violent nightmares/palpitations.Given Noctamid (lormetazepam) to help with anxiety. On average took 2mg per day for 8 weeks.No taper was advised.DEC 2014 WD severe. Nervous tic in eyes and limbs, muscle pain,fluct  temp, weakness, dep and anxiety, nausea, giddy, unstable when walking. Different Dr suggested taking 20mgs CIT. BROMAZEPAM 3mgs up to 3 x daily for anxiety.DEC 9 2014 Updose CIT to 30mgs. Only taking BROMAZEPAM in emergency.DEC 31 2014 Settling at 30mg CIT - helping with depression. No Brom for 2wks.Found SA.APR 2015 Trying to stabilise on 30mgs CIT.  JAN 2016 Started Cit Taper reducing by 5% per month.  28.5 mgs 
FEB  Taper held bereavement. APR Taper resumed 27mgs . MAY 25.50 mgs .  JUNE 24 mgs .  JULY I stupidly mixed up my BP meds with CIT. Consequently took no CIT for 3 days and doubled my BP meds. Waiting for the fallout....Holding for a while until any chance of repercussions have abated. SEPT taper resumed to  22.5 mgs . OCT 21 mgs .NOV 19.95 mgs DEC crashed. 2017: FEB 3rd updose to 20.5 mgs to try to stabilise.FEB.switched over to 75mgs of Venlafaxine XR for 3 weeks.Too stimulating so switching back to Cit. 12 March 37.5 Ven and 20 Cit. 21 March 18mg Ven 20mg Cit. 4 April 9mg Ven 20mg Cit. Xanax .50mg when needed.  13 April 0 mgs Ven, 20mg Citalopram. Xanax .50 mg per day. 5 May reinstated a small amount of Ven to stabilize  1 mg twice a day. 20 mg Citalopram at night. Xanax .25 mg twice per day.Other Meds: Losartan (BP)Started 1993 at  50 mgs at night.  Seretide (Asthma) Started 1996 at 1 puff twice a day. Jan 2019 Antibiotic Ceclor 500mgs twice a day for bronchitis and  Atrovent 2ml capsules twice a day for asthma. Finished the course of both Jan 17. 

XANAX  Jan 27  - Feb 3 2019 Failed Valium Crossover.   Feb 14 2019  Updosed Xanax by .0625  Feb 17 2019 Decreased Xanax by .0625. Back to .50mg daily.  Update Xanax 28.2.20 tapered to .1250 mg 8am .25 mg midnight. Update Xanax 11.8.21 tapered to .25 mg at night. 

Current Meds 28.2.19: CITALOPRAM  20mg  taken at midnight. VENLAFAXINE  .9 mg twice a day at 8am and 10pm.  XANAX .50 mg split into 4 doses per day. 10am .0625mg / 2pm .1250mg/ 6pm .0625mg / midnight .25mg.Update 10.8.22 .25 mg at night.  LOSARTAN 50 mgs taken at midnight.  SERETIDE 1 puff taken at 8am and 10pm.   7.7.19 VENLAFAXINE UPDATE: Started tapering 10% every 4 weeks. Currently .4 mg twice a day at 8am and 10 pm.  2.9.19 .36 mg x 2. 1.10.19  .32 mg x 2. 26.11.19 .29 mg x2. 26.12.19 .26 mg  x 2. 23.1.20  .23 mg x 2.  20.2.20 .21 mg x2.20.3.20  .19 mg x 2. 21.4.20 .17 mg x 2. 19.5.20 .13 mg x 2.  18.6.20 .11mg  x 2 .18.7.20.10 mg x 2.1.9.20.09 mg x 2. 30.9. 20 .08 mg x 2. 1.11.20 .07 mg x 2.  2.12.20 .06 mg x 2.  8.1.21 .05 mg x 2.  4.2.21 .04 mg x 2. 9.3.21 .03 mgx2.  7.4.21  .02 mg x 2.  9.5.21 .01 mg x 2.  21.6.21 .01 mg x 1.  11.8.21 ZERO!

 

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Johnson, Dire and Flowers: I love it when I get comments from all of you! I do wish I could call myself a recovery story and I actually thought about it again recently but the time is not yet. I have a pretty nasty paresthesia in my thigh as a result of the period of physical inactivity brought on by the wd syndrome of the past and my goal in weight reduction is to see if that is the reason (in addition to the fact that the extra weight was making me feel much worse).

 

I logged on this morning to paste a copy of something I found on a website after I did a search for a cryptic comment made to me by some numnutz on the dating site. Has no relation to anything but I want to remember to explore it when I have more time.

 

 

Auric Attacks
These are attacks on the auras of people as in the cases of possession, but the attacks are much less serious and the predator does not inhabit the victim. The most common type of an auric attack is when a relative goes and visits a patient in a hospital or attends a funeral wake. The places are identical to those enumerated above for possession, as these locations are loaded with ghostly predators. So after an attack, when the victim comes home he experiences symptoms of 'influenza', but there is no temperature present. He gets weaker and weaker by the day, even though he feeds himself voraciously. He puts on weight, but he gets more and more debilitated. This continues until he reaches a state in which he cannot even get out of his bed. Of course, the doctor has no idea what is going on, even after numerous tests have been carried out. Finally, the attack may wear off on its own, but it may take months or years. Basking in the sun and an overseas trip may help to clear the condition. However, a healer can put the patient back to health in one or two sessions of healing. These auric attacks are quite common, and very few people realise it. They are often misdiagnosed as chronic fatigue syndrome.

 

Misdiagnosed as CFS? Weird..... I am sure the person who wrote this has never had any exposure to withdrawal syndrome. I am thinking of the fact that the aftermath of the really acute phase (and its prolonged recovery period) has been likened by some to be 'like CFS'. So that is why the above writer's description intrigues me.

 

I also want to make note of the fact that I survived some criticism at work which in the past would have prompted me to leave the job. 2 people complained that I was 'bossing' them. I want to get to the point where this does not cause me such extreme anguish because I am starting to see that after 65 years of being who I am this is going to be an immutable fact of my personality and that instead of me worrying excessively about it and trying to change, people need to learn to 'get over' me. I have decided to make it their problem instead of mine.

What happened and how I arrived here: http://survivingantidepressants.org/index.php?/topic/4243-cymbaltawithdrawal5600-introduction/#entry50878

 

July 2016 I have decided to leave my story here at SA unfinished. I have left my contact information in my profile for anyone who wishes to talk to me. I have a posting history spanning nearly 4 years and 3000+ posts all over the site.

 

Thank you to all who participated in my recovery. I'll miss talking to you but know that I'll be cheering you on from the sidelines, suffering and rejoicing with you in spirit, as you go on in your journey.

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Yeah way to go CW. Hey i think that is a sign of some healing....when you brace yourself knowing that you have triggered a cognitive implosion and then the wave/ tsunami of mental carpet bombing doesnt occur. Its a pleasant surprise.

 

The world needs more of us and less of them!!!

 

Well done on losing weight.

nz11

Thought for the day: Lets stand up, and let’s speak out , together. G Olsen

We have until the 14th. Feb 2018. 

URGENT REQUEST Please consider submitting  for the petition on Prescribed Drug Dependence and Withdrawal currently awaiting its third consideration at the Scottish Parliament. You don't even have to be from Scotland. By clicking on the link below you can read some of the previous submissions but be warned many of them are quite harrowing.

http://www.parliament.scot/GettingInvolved/Petitions/PE01651   

Please tell them about your problems taking and withdrawing from antidepressants and/or benzos.

Send by email to petitions@parliament.scot and quote PE01651 in the subject heading. Keep to a maximum of 3 sides of A4 and you can't name for legal reasons any doctor you have consulted. Tell them if you wish to remain anonymous. We need the numbers to help convince the committee members we are not isolated cases. You have until mid February. Thank you

Recovering paxil addict

None of the published articles shed light on what ssri's ... actually do or what their hazards might be. Healy 2013. 

This is so true, with anything you get on these drugs, dependance, tapering, withdrawal symptoms, side effects, just silent. And if there is something mentioned then their is a serious disconnect between what is said and reality! 

  "Every time I read of a multi-person shooting, I always presume that person had just started a SSRI or had just stopped."  Dr Mosher. Me too! 

Over two decades later, the number of antidepressant prescriptions a year is slightly more than the number of people in the Western world. Most (nine out of 10) prescriptions are for patients who faced difficulties on stopping, equating to about a tenth of the population. These patients are often advised to continue treatment because their difficulties indicate they need ongoing treatment, just as a person with diabetes needs insulin. Healy 2015

I believe the ssri era will soon stand as one of the most shameful in the history of medicine. Healy 2015

Let people help people ... in a natural, kind, non-addictive (and non-big pharma) way. J Broadley 2017

 

 

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nz11,

 

I love your way with words....

 

Mental carpet bombing indeed!

 

So glad you stopped by. (I read all of your posts, btw)

What happened and how I arrived here: http://survivingantidepressants.org/index.php?/topic/4243-cymbaltawithdrawal5600-introduction/#entry50878

 

July 2016 I have decided to leave my story here at SA unfinished. I have left my contact information in my profile for anyone who wishes to talk to me. I have a posting history spanning nearly 4 years and 3000+ posts all over the site.

 

Thank you to all who participated in my recovery. I'll miss talking to you but know that I'll be cheering you on from the sidelines, suffering and rejoicing with you in spirit, as you go on in your journey.

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oh shucks i feel some false humility coming on.

 

i'm jealous ...wish i could loose weight. (jusr wish you americans would go metric ).

Go well.

Was wondering how on earth i had accumulated over 3000 views!

Mind you i know of some people out there  who have over 15,450!! views ..Holy Eketahuna...Oh boy!!

Thought for the day: Lets stand up, and let’s speak out , together. G Olsen

We have until the 14th. Feb 2018. 

URGENT REQUEST Please consider submitting  for the petition on Prescribed Drug Dependence and Withdrawal currently awaiting its third consideration at the Scottish Parliament. You don't even have to be from Scotland. By clicking on the link below you can read some of the previous submissions but be warned many of them are quite harrowing.

http://www.parliament.scot/GettingInvolved/Petitions/PE01651   

Please tell them about your problems taking and withdrawing from antidepressants and/or benzos.

Send by email to petitions@parliament.scot and quote PE01651 in the subject heading. Keep to a maximum of 3 sides of A4 and you can't name for legal reasons any doctor you have consulted. Tell them if you wish to remain anonymous. We need the numbers to help convince the committee members we are not isolated cases. You have until mid February. Thank you

Recovering paxil addict

None of the published articles shed light on what ssri's ... actually do or what their hazards might be. Healy 2013. 

This is so true, with anything you get on these drugs, dependance, tapering, withdrawal symptoms, side effects, just silent. And if there is something mentioned then their is a serious disconnect between what is said and reality! 

  "Every time I read of a multi-person shooting, I always presume that person had just started a SSRI or had just stopped."  Dr Mosher. Me too! 

Over two decades later, the number of antidepressant prescriptions a year is slightly more than the number of people in the Western world. Most (nine out of 10) prescriptions are for patients who faced difficulties on stopping, equating to about a tenth of the population. These patients are often advised to continue treatment because their difficulties indicate they need ongoing treatment, just as a person with diabetes needs insulin. Healy 2015

I believe the ssri era will soon stand as one of the most shameful in the history of medicine. Healy 2015

Let people help people ... in a natural, kind, non-addictive (and non-big pharma) way. J Broadley 2017

 

 

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Mind you i know of some people out there  who have over 15,450!! views

 

12 more views since 2 o'clock? Must be a slow news day....

 

Some people can't help but stare when they are passing the scene of an accident......

 

Hey! I am proving to myself that just plain old daily calorie reduction will do the trick. I am hoping to lose the weight slowly enough that I don't get all hangy dangy with my skin. A pound a week has been very doable and I can eat anything I want, just not over what my daily allotment for the day is (a little less than 1250 cals right now). I am finding I am able to tolerate a slight amount of hunger between meals and this is a good thing. But I am still too heavy, all of my joints still ache just not as bad as 9 pounds ago.

What happened and how I arrived here: http://survivingantidepressants.org/index.php?/topic/4243-cymbaltawithdrawal5600-introduction/#entry50878

 

July 2016 I have decided to leave my story here at SA unfinished. I have left my contact information in my profile for anyone who wishes to talk to me. I have a posting history spanning nearly 4 years and 3000+ posts all over the site.

 

Thank you to all who participated in my recovery. I'll miss talking to you but know that I'll be cheering you on from the sidelines, suffering and rejoicing with you in spirit, as you go on in your journey.

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What happened and how I arrived here: http://survivingantidepressants.org/index.php?/topic/4243-cymbaltawithdrawal5600-introduction/#entry50878

 

July 2016 I have decided to leave my story here at SA unfinished. I have left my contact information in my profile for anyone who wishes to talk to me. I have a posting history spanning nearly 4 years and 3000+ posts all over the site.

 

Thank you to all who participated in my recovery. I'll miss talking to you but know that I'll be cheering you on from the sidelines, suffering and rejoicing with you in spirit, as you go on in your journey.

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I also want to make note of the fact that I survived some criticism at work which in the past would have prompted me to leave the job. 2 people complained that I was 'bossing' them. I want to get to the point where this does not cause me such extreme anguish because I am starting to see that after 65 years of being who I am this is going to be an immutable fact of my personality and that instead of me worrying excessively about it and trying to change, people need to learn to 'get over' me. I have decided to make it their problem instead of mine.

This IS very significant! I can't imagine it was easy. Yay for you, CW!

 

Working, weightloss, shrugging critism; All great stuff!!! (though being bossy isn't really a critism in my book. That kind of critism has to do more with the person criticizing than the one "bossing.")

1988-2012: Prozac @ 60mg (with a few stops and starts)

Fall 2012: Returned to 40mg after discontinuing and horrid withdrawal 

Fall 2013: 40mg Fluoxetine, added 150mg Wellbutrin to treat fatigue 

Winter 2014: Attempting to taper both (too fast)

April 2014: 9mg Fluoxetine + 37.5 Wellbutrin 

Summer 2014: 8 mg Fluoxetine + 0 Wellbutrin (way too fast a drop)

Late summer/Early Fall 2014: Debilitating Withdrawal symptoms 

Fall 2014 - Wellbutrin successfully kicked to the curb but…

Oct- Dec 2014: Panicked reinstatement of Fluoxetine ->30mg - held for 5yrs

Jan 2021: taper to 20mg Fluoxetine  then tapering by 1mg every 2-3 months

Fall 2022 - held at 10mg->December 2022: 9mg->Feb 2023: 8mg ->March 2023: brassmonkey slide begins: 7.8mg -> 7.6 -> 7.4->2 week hold (April)->7.2->7mg->6.8->2 week hold->6.6-> 1-month hold ->(June)-6.5->4-week hold-> (July)-6.4 (discontinued brassmonkey slide and slowed taper)-> (Aug)-6.2->(Sept)-6.0->(Oct)-5.9->(Nov)-5.8->(Dec)-5.7->wave!->(Jan)-5.8->(Feb)-6mg and holding.

 

My 2014 withdrawal experience: https://rxisk.org/antidepressant-withdrawal-a-prozac-story/

 

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That is what I thought too, when I analyzed it.

 

Why did these people feel the need to tell the boss those things? And why did she feel she needed to tell me? I did not command (use a forceful tone) nor word anything in such a way as to make it seem I needed to be obeyed as a 'boss' but I have gotten that stuff all my life. I am still blind to my effect on others, it seems. And maybe my tone was bossy, idk.

 

I am a cultivatedly assertive person, of that there is no doubt. I understand most people have a problem with that especially since I have avoided positions of authority my whole life.

 

I am just tired of feeling guilty for being the way I am and I told the boss if those people want me to leave then I will. I have my self confidence back now and I am pretty sure I can make my way by myself, I don't need the flower shop (but I love it like crazy!)

What happened and how I arrived here: http://survivingantidepressants.org/index.php?/topic/4243-cymbaltawithdrawal5600-introduction/#entry50878

 

July 2016 I have decided to leave my story here at SA unfinished. I have left my contact information in my profile for anyone who wishes to talk to me. I have a posting history spanning nearly 4 years and 3000+ posts all over the site.

 

Thank you to all who participated in my recovery. I'll miss talking to you but know that I'll be cheering you on from the sidelines, suffering and rejoicing with you in spirit, as you go on in your journey.

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Pasting in IE now works as follows: can 'CTRL+V' or choose 'paste' from the browser edit menu but the paste function in the right click menu is still greyed out.

 

That is what I thought too, when I analyzed it.

 

Why did these people feel the need to tell the boss those things? And why did she feel she needed to tell me? I did not command (use a forceful tone) nor word anything in such a way as to make it seem I needed to be obeyed as a 'boss' but I have gotten that stuff all my life. I am still blind to my effect on others, it seems. And maybe my tone was bossy, idk.

 

I am a cultivatedly assertive person, of that there is no doubt. I understand most people have a problem with that especially since I have avoided positions of authority my whole life.

 

I am just tired of feeling guilty for being the way I am and I told the boss if those people want me to leave then I will. I have my self confidence back now and I am pretty sure I can make my way by myself, I don't need the flower shop (but I love it like crazy!)

 

Quoting now works, I thought I remembered that being broken so that is a win for IE (no more of that 'quote' and 'timestamp' stuff, hopefully).

 

An update while I am here: went to the water park today and it was delightful. Even went down the big slide and though my suit was jammed up my wazoo, it was as much thrilling and fun as I remembered it being before the ugliness of wd. Yay!

What happened and how I arrived here: http://survivingantidepressants.org/index.php?/topic/4243-cymbaltawithdrawal5600-introduction/#entry50878

 

July 2016 I have decided to leave my story here at SA unfinished. I have left my contact information in my profile for anyone who wishes to talk to me. I have a posting history spanning nearly 4 years and 3000+ posts all over the site.

 

Thank you to all who participated in my recovery. I'll miss talking to you but know that I'll be cheering you on from the sidelines, suffering and rejoicing with you in spirit, as you go on in your journey.

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((((HUG)))

Current:

Lorazapam2mg: 4/9/152mg - 1.5mg: already sick/nothing noticed. No changes in sleep noted after illness.  

Lamictal: 7/27/13 - 8/6/13: 400mg - 500mg(dr order) mouth sores, headache, cognitive/balance, heart palp...8/7/13 - 8/23/13: 500mg - 400mg; symptoms↓...10/10/13: 350mg; fever/flu-like <2-weeks...12/30/13: 325mg; fever/flu-like symptoms <1-week...2/10/17: 300mg; no significant changes noted. 

 

Discontinued:

Omeprazole: 09/2103 40mg...5/1/14: 20mg... 8/21/14 = 0

Wellbutrin: 11/22/13: 300mg – 225mg...12/6/13 delayed reaction- mood swings, weight↓, heart palp/chest pain, alerting...12/14/13: 187mg; physical symptoms↓, neuro emotions ↑, weight stable...12/20/13: 225mg; physical symptoms return, emotions stable <1-week, weight↓...4/21/14: 187mg; weight↑...5/17/14 (neurologist ordered discontinue asap):168mg; headache, mood swings, ↑weight, sleep flux...5/24/14: 150mg; headache, mood swings, ↓cognitive/balance...6/2/14: 112mg; see above, weight stable, <3-weeks... 6/28/14: 100mg; moody...7/25/14: 87.5mg; family troubles... 8/4/14: 75mg; headaches; moody... 8/9/1450mg headaches... 8/12/14: 37.5mg; 8/17/14: 25mg...8/26/14 = 0

Hydroxyzine; 10mg: 5/20/15 *prn 4/5 times then dc'd. Mood changes/rage 

Buspirone: 7.5mg: 5/20/15 *prn 4/5 times then dc'd. No changes.

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Oh how I love boredpanda.com! Watched this vid over and over and over again and each time 29 weeks came up, I couldn't stop laughing! (I also loved the 'outtake' at the end).

 

 

The boss says I am 'growing on' my co-workers. That's good, right?

 

Have lost 15 pounds in a hair over 60 days, woo hoo!

What happened and how I arrived here: http://survivingantidepressants.org/index.php?/topic/4243-cymbaltawithdrawal5600-introduction/#entry50878

 

July 2016 I have decided to leave my story here at SA unfinished. I have left my contact information in my profile for anyone who wishes to talk to me. I have a posting history spanning nearly 4 years and 3000+ posts all over the site.

 

Thank you to all who participated in my recovery. I'll miss talking to you but know that I'll be cheering you on from the sidelines, suffering and rejoicing with you in spirit, as you go on in your journey.

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Loved the vid! What cuties!

 

Glad that your work colleagues are getting to know you better. Hope they feel rotten for going to the boss about you.

 

You are doing so well - a few weeks ago this would have shattered you!

 

Had to chuckle at the thought of you in your swimsuit tearing down the slide! lol!

 

What is it you say in USA? - way to go CW!!

15 yrs on 20 to 30 mgs CITALOPRAM.  MAY 2014 Increased to 40 mgs per day.SEPT/NOV 2014 tapered in 6 weeks down to 10 mgs as per Dr instructions due to violent nightmares/palpitations.Given Noctamid (lormetazepam) to help with anxiety. On average took 2mg per day for 8 weeks.No taper was advised.DEC 2014 WD severe. Nervous tic in eyes and limbs, muscle pain,fluct  temp, weakness, dep and anxiety, nausea, giddy, unstable when walking. Different Dr suggested taking 20mgs CIT. BROMAZEPAM 3mgs up to 3 x daily for anxiety.DEC 9 2014 Updose CIT to 30mgs. Only taking BROMAZEPAM in emergency.DEC 31 2014 Settling at 30mg CIT - helping with depression. No Brom for 2wks.Found SA.APR 2015 Trying to stabilise on 30mgs CIT.  JAN 2016 Started Cit Taper reducing by 5% per month.  28.5 mgs 
FEB  Taper held bereavement. APR Taper resumed 27mgs . MAY 25.50 mgs .  JUNE 24 mgs .  JULY I stupidly mixed up my BP meds with CIT. Consequently took no CIT for 3 days and doubled my BP meds. Waiting for the fallout....Holding for a while until any chance of repercussions have abated. SEPT taper resumed to  22.5 mgs . OCT 21 mgs .NOV 19.95 mgs DEC crashed. 2017: FEB 3rd updose to 20.5 mgs to try to stabilise.FEB.switched over to 75mgs of Venlafaxine XR for 3 weeks.Too stimulating so switching back to Cit. 12 March 37.5 Ven and 20 Cit. 21 March 18mg Ven 20mg Cit. 4 April 9mg Ven 20mg Cit. Xanax .50mg when needed.  13 April 0 mgs Ven, 20mg Citalopram. Xanax .50 mg per day. 5 May reinstated a small amount of Ven to stabilize  1 mg twice a day. 20 mg Citalopram at night. Xanax .25 mg twice per day.Other Meds: Losartan (BP)Started 1993 at  50 mgs at night.  Seretide (Asthma) Started 1996 at 1 puff twice a day. Jan 2019 Antibiotic Ceclor 500mgs twice a day for bronchitis and  Atrovent 2ml capsules twice a day for asthma. Finished the course of both Jan 17. 

XANAX  Jan 27  - Feb 3 2019 Failed Valium Crossover.   Feb 14 2019  Updosed Xanax by .0625  Feb 17 2019 Decreased Xanax by .0625. Back to .50mg daily.  Update Xanax 28.2.20 tapered to .1250 mg 8am .25 mg midnight. Update Xanax 11.8.21 tapered to .25 mg at night. 

Current Meds 28.2.19: CITALOPRAM  20mg  taken at midnight. VENLAFAXINE  .9 mg twice a day at 8am and 10pm.  XANAX .50 mg split into 4 doses per day. 10am .0625mg / 2pm .1250mg/ 6pm .0625mg / midnight .25mg.Update 10.8.22 .25 mg at night.  LOSARTAN 50 mgs taken at midnight.  SERETIDE 1 puff taken at 8am and 10pm.   7.7.19 VENLAFAXINE UPDATE: Started tapering 10% every 4 weeks. Currently .4 mg twice a day at 8am and 10 pm.  2.9.19 .36 mg x 2. 1.10.19  .32 mg x 2. 26.11.19 .29 mg x2. 26.12.19 .26 mg  x 2. 23.1.20  .23 mg x 2.  20.2.20 .21 mg x2.20.3.20  .19 mg x 2. 21.4.20 .17 mg x 2. 19.5.20 .13 mg x 2.  18.6.20 .11mg  x 2 .18.7.20.10 mg x 2.1.9.20.09 mg x 2. 30.9. 20 .08 mg x 2. 1.11.20 .07 mg x 2.  2.12.20 .06 mg x 2.  8.1.21 .05 mg x 2.  4.2.21 .04 mg x 2. 9.3.21 .03 mgx2.  7.4.21  .02 mg x 2.  9.5.21 .01 mg x 2.  21.6.21 .01 mg x 1.  11.8.21 ZERO!

 

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Thanks for the vote of confidence, Flowers. I thought about going to the water park again over the Fourth but it kinda seemed like old hat and I did not want to spend the day feeling slightly dizzy again. Something about floating down their 'Lazy River' on the provided inner tubes makes me slightly seasick and mars my enjoyment of the day. I refuse to take any pills for it, though.

 

Which brings me to the reason for posting: I am shocked (but not surprised) at how many members, even after reading the information on the site (though I wonder, do people read? There are so many repetitive questions about stuff that has been covered to death in the symptoms forum, for example, but the same questions keep getting asked in new topics anyway) that a lot of members still have a deep belief in the efficacy of psychoactive drugs to 'treat' disturbances of mood and feeling and also the belief that the turds that prescribe the drugs know what they are doing.

 

Stop eating pills, people. Get wise and get off and never look back. The dam things only work to take a functioning organism and turn it into a flat, lifeless, uncaring being who is blind to their effect until they try to get off them and then they are in for more misery than they ever bargained for. Kinda like all the bad stuff is stockpiled only to return with a vengeance once the chemicals are removed.

 

In order to recover any semblance of your 'true' self (whatever that is), is going to take years. The body cannot remake itself overnight and the hell has to be endured until it goes away on its own. No benzos, no Z drugs (I survived without sleep for almost 6 months and lived to tell about it), no magic supplements or magic electrical devices are going to help and they just serve to further delay healing. Find something to keep yourself occupied while the healing is going on, like a permanent subscription to the cat vid channel on YT for instance if you can't sleep. That is far better than visits to a clueless shrink who has no clue what these powerful drugs actually do and would stop prescribing them in a heartbeat if they knew how much people suffer when they try to go off them. Let one of them agonize through months of suicidal 'depression' and see how THEY feel about the drugs afterwards.

 

Why don't we get any recovering psychiatrists on these boards I wonder? Maybe their belief that they 'know better' on how to treat unhappy people (for is that not the reason most of us started these drugs to begin with? Some degree of unhappiness? Or the manifestation of it?) insures they will never consider taking the stuff they so cavalierly dish out?

 

Stop believing the hype, stop believing in 'pills' and start trying to figure out what is wrong in your life and work to change that instead.

 

Dammit! I did not know these things did not (and would not ever) work. I lost 8 years of my life because of them. I did some great stuff but somewhere along the line my ability to plan for the future got disrupted and now I am pretty much screwed. It is hot as Hades right now in Florida and the AC seems like it is running all of the time. I had been keeping the thermostat at 81o but lowered it to 80o because mom is now using the oxygen generating machine 24 hours a day and it generates a lot of heat in her room. That one degree of change bumped the electric bill up about 30 bucks. So out of the 600 odd dollars I am getting for social security now that they started making me pay for medicare, the rent (which includes the elec and water) was $530. When mom dies, how far is that monthly allotment going to stretch to cover food, transportation, sundries? It won't. I am not looking forward to spending my later years sweating in 95o hear in the summer with no AC but what am I going to do? No pill will ever fix what I did to my life.

 

I am screwed. And it is my own fault. I was the one who went to the doctor because I could not stop crying and asked for pills. A child of the baby boom years, constantly bombarded with TV ads touting pills for everything. It is ten (no hundreds) of times worse now, all the advertising for that crap. And the people who come here are as indoctrinated as I ever was and the only difference is most of them cannot see their own secret bias in favor of psychiatry and pill taking.

 

You'll never beat this if you keep relying on pills. No pill will ever fix what I did to my life and it is not going to fix yours either. I am positive of that.

What happened and how I arrived here: http://survivingantidepressants.org/index.php?/topic/4243-cymbaltawithdrawal5600-introduction/#entry50878

 

July 2016 I have decided to leave my story here at SA unfinished. I have left my contact information in my profile for anyone who wishes to talk to me. I have a posting history spanning nearly 4 years and 3000+ posts all over the site.

 

Thank you to all who participated in my recovery. I'll miss talking to you but know that I'll be cheering you on from the sidelines, suffering and rejoicing with you in spirit, as you go on in your journey.

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  • 3 weeks later...
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This is going to be a rant, I am hurting and I need to let some of the pain out. I have no one to talk to if not for this screen, so if you are in a bad place, go read someone else's thread.

 

 

Stop believing the hype, stop believing in 'pills' and start trying to figure out what is wrong in your life and work to change that instead.

 

Oh such fine words from an arrogant ass. I wrote that some time ago after reading post after post here of people wanting to take this drug or that supplement to 'fix' themselves. What if you know what is wrong in your life and it happens to be 'you'? What do you do then?

 

The problem is me, I have known it for years but I cannot figure for the life of me how to change who I am. I am unemployable, permanently so it seems and I don't know what to do. But I do know that I don't want to try anymore. I hate myself, I hate life and I don't want to be here anymore. And there is not a pill in the world that can fix that. How much longer do I have to wait until I just die?

What happened and how I arrived here: http://survivingantidepressants.org/index.php?/topic/4243-cymbaltawithdrawal5600-introduction/#entry50878

 

July 2016 I have decided to leave my story here at SA unfinished. I have left my contact information in my profile for anyone who wishes to talk to me. I have a posting history spanning nearly 4 years and 3000+ posts all over the site.

 

Thank you to all who participated in my recovery. I'll miss talking to you but know that I'll be cheering you on from the sidelines, suffering and rejoicing with you in spirit, as you go on in your journey.

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