That last drop is the worse. I wish you could have went a little slower. Hang in there and keep us posted.
List Your Symtpoms
#722
Posted 09 October 2017 - 12:28 AM
I knew the 0 would be hard! It will be hard no matter when I start. It felt so good not to add those pills to my pillbox this week!
Still feeling:
Brain zaps
Swooshing brain (like living life swiping through my phone when I move my head—bizarre)
Restlessness
Anxiety
Buzzing in my legs
Trying to stay away from stress in all forms including people who cause me stress.
Thx
LM
#724
Posted 10 October 2017 - 09:33 PM
By mid morning all the brain zaps etc start again. They are really bad at night!
10 days on 0 now! Feel like this could take a REALLY long time.
- JKLJ likes this
#726
Posted 12 October 2017 - 07:34 AM
#727
Posted 12 October 2017 - 08:25 AM
Time for a new dr. The FDA warns of the dangers of quitting cold turkey. I understand the cold turkey as Stevens-Johnson syndrome can be very serious but he should have given you something to lighten the symptoms. I hope all goes well for you but it could be a long ride. Keep us posted on your progress and maybe you will be one of the lucky ones that will have a minimal withdrawal.
#728
Posted 16 October 2017 - 11:57 AM
I feel very unhappy about that because I am getting into arguments I would have stayed out of before. Now I remember why I had such a hard time trying to get off this demon pill before!
More yoga and meditation. And NO news!
—The only real control I have is the choice of my own thoughts, my own words, and my own actions—
- siggyd17 likes this
#729
Posted 16 October 2017 - 02:00 PM
Try to remove as much stress in your life as possible. Anything that bothers you (like noise, talking, telephone ringing, TV, music, etc.) try and avoid it as much as possible. I am sure I mentioned this before but are you willing to try some hydroxyzine or clonidine to help you get through this?
- siggyd17 likes this
#730
Posted 17 October 2017 - 12:36 PM
There are many different posts about symptoms and side effects of Cymbalta and Cymbalta Withdrawal. I wanted to begin a thread to compile a thorough list of effects and symptoms that are related to Cymbalta. (Pleae list symptoms/effects that are confirmed to be related to Cymbalta via your doctor or you just suspect them to be). Also, break your symptoms/effects into two categories: Side Effects (while taking Cymbalta) and Withdrawal Symptoms (while coming off Cymbalta). Also, please note "Dr" by a symptom that was confirmed by a doctor. I'll start by listing mine.
Side Effects:
Depression worsened
Lethargy
Irritability
Trouble sleeping
Nightmares
Withdrew from friends and family
Rage
Agitation
Spending/shopping out of control
Overall health declined: sick frequently
Weight gain
Suicidal ideation
Memory problems
Concentration problems
Vision problems
Withdrawal Symtpoms:
Nausea
Diarrhea
Headaches
Brain “zaps”
Dizziness
Numb fingers
Flu-like symptoms
Sinus pain
Runny nose
Hot flashes
Rage
Mood Swings
Crying
Suicidal ideation
Cold chills: Shivering accompanied by chest and abdominal muscle tightening
Memory problems
Concentration problems
Nightmares
Hey, I've had a LOT of these. In fact, I know it's because of withdrawal and I was never told about the withdrawal symptoms. I personally have had issues with concentration at times, ringing in ears really REALY loudly, off balance, the want/need to cry for no reason (no PMS or anything of that sorts either), hot and cold flashes at all times of the day/night, shivering uncontrollably when I don't feel cold or in weather that normally I'm ok with (like this morning it was about 55 degrees F, and I was shivering as if it was 40), sometimes I have an appetite, PAIN when I don't take it all in my muslces in my back. It feels like it is trying to twitch or something and then the pain just radiates and stays. I also have really bad dreams when I don't take the other meds (prazosin and trazadone). I've always had migraine/headache issues, in fact I'm pretty use to that pain, however the cymbalta migraine is a bit different. I haven't really ever felt something like this before. It's almost like the 'zapping' that people describe, except mine stays, almost like an electrical current that got stuck in the on position. I've only had it happen twice since I've been weaning, but It puts me down for a while. I get so sick as well.
#731
Posted 21 October 2017 - 10:28 AM
But I don’t believe the side effects and the potential long term damage of the drug are worth it. I feel like my brain needs time to recover and get back some normal functioning after having been on cymbalta for so long.
Stress has a lot to do with the way I feel. Trying really hard to get away from that. If I could leave for about six months to avoid the people and major stresses in my life it would be great!
Ha!
On another note I saw my pain management doc yesterday and she had so much praise for my getting off all the drugs but of course she had no idea about the withdrawal. She just said some people have trouble and others report nothing.
Whatever.
- fishinghat and siggyd17 like this
#732
Posted 02 November 2017 - 09:26 AM
So, I felt the bran zaps for the first time a couple of weeks ago. I've been stuck at 4 beads once to twice a week now...which is fine...but as this has progressed, the zaps became more of like a stop and go thing. It didn't hurt, but I could feel it..almost like my brain was restarting. I'm praying these side effects go away soon. I feel so sick and tired today..mainly bummed and just want to go cry. I will not, however, allow this med to bring me to the breaking point, suicidal. NEVER again! I am in control not the meds. I'm so happy this group is here to talk to or else I would probably feel so alone. I hope everyone is doing well. If you feel suicidal and wanna talk, please reach out. It isn't worth it to take your life on something like this. This too will pass, but in the mean time, people like me are here with you to support you and talk you through it. Thank God for y'all!
- fishinghat and TryinginFL like this
#733
Posted 02 November 2017 - 02:00 PM
Her answer was they may never completely go away. Didn’t like that answer. Anyone else ever get an answer like that? She suggested waiting a few months and then either going to a very low dose again or Zoloft or something similar. This is not my plan because my use of cymbalta was not for depression it was for pain and now I have issues that are caused from being on cymbalta. So I may never be rid of an antidepressant?
Gonna stick it out until after the new year at least. I am better than a month ago.
- siggyd17 likes this
#734
Posted 02 November 2017 - 02:04 PM
Stick it out is right. The majority of our long term members that have come back say they pretty much returned to normal in 6 to 9 months. Some (maybe 10%?) said 1 to 2 years and we have had 3 members that I know of that took 3 to 5 years to really stabilize. If you don't need the Zoloft for psychiatric treatment then stay off it and just be patient. It does take nerves a long time to recover.
#735
Posted 03 November 2017 - 01:01 PM
#736
Posted 06 November 2017 - 09:35 AM
#738
Posted 06 November 2017 - 10:53 AM
Just wondering if you can get something for your pain. I mean that there must be something out there to make you feel better, as you were given cymbalta for pain. It must be replaced by a pain reliever, so I think.
An opiate perhaps low dosage? As for being addictive, I found it quite easy to wean from 150mg to none. Had to get back on them as the pain resurfaced. (Big surgery on my back). But now 5 mg once a day is enough. Gets rid of depression at the same time. I'm nicer too. Lol!
- TryinginFL likes this
#739
Posted 08 November 2017 - 02:37 PM
As of today, I am 9 days without any cymbalta. Still a little nauseous but the worse for me right now is the pain my back, neck, and shoulders. I am also having some zaps, but not as bad as I had before. I have been making sure I eat a little more proteins than normal, as well as some fruits and a little veggies. I also take a multi-vitamin just in case my body isn't getting or able to soak up some of the nutrients. I also have been trying to eat one of the protein bars in the morning to get going instead of coffee. So far, I'm feeling great. (Other than the pain) The pain though is from my accident.
I will not give up. Cymbalta is a great answer for a little bit, but I wouldn't recommend it for long term use. It's also expensive, and the withdrawals are not good, especially if you don't have the money to always get your meds. I will be talking with my doctor in December, and hopefully she will have some more answers that could help out. If so, I will make sure to pass them along.
- Jillybeans likes this
#740
Posted 08 November 2017 - 04:46 PM
I did forum-wide searches on "erectile dysfunction" and "libido" and surprisingly, for such an extensive and long-term site as this, there was very little return on the searches. Perhaps, people don't like to discuss their sexual issues related to Cymbalta and other SSRI's? Or, maybe I may have missed the topics?
I blame over a decade's use of first Paxil then Cymbalta on my low libido and recent episodes of erectile dysfunction. I'm convinced that my SSRI uses significantly contributed to the end of my marriage. Unfortunately, I have only just recently come to realize these side effects and to associate them with SSRI use. Honestly, I thought it was just that I was getting older (I'm 62) and that it was normal, and especially having spent nearly 4 decades with the same woman who is now my ex (she left me due to my lack of desire and love for her). And now that I have found a new partner who I'm madly in love with, I want so badly to have a healthy sexual relationship with her, I barely can...
I was hoping to find some success stories of men recovering their libido and sexual function after stopping SSRI's. Not to be selfish, but I'd like some real-life experiences that will reassure me that I can look forward to a normal sex life again...
#741
Posted 08 November 2017 - 06:04 PM
You need to do a search for PSSD. That stands for Post SSRI Sexual Dysfunction. As you mentioned during the course of taking ssri or snri sexual performance and ability to reach orgasm is very limited (male or female). When you are totally off the ssri/snri everyone goes through an adjustment period. Typically there is a 4 or 5 day period about 1 week after coming off the med where sexual arousal and performance surges. Now that is also the time where many are suffering bad withdrawal so they may not notice this. Shortly after that the testosterone levels drop like a rock and sexual desire and performance completely tanks. Then over the next 3 months, if you stay off antidepressants, the sexual issues slowly improve and by the end of the 3rd month things should return to pretty much normal for your age and condition. This 3 month period is called PSSD. For some the symptoms never totally fade. There are a few that are left with, no periods, no erections, penus anaesthia (lack of feeling), no ejaculation, no orgasms, no libido. It is all gone. I am one of 4 from this site who have been left with this condition. I have seen many specialists and there is NO treatment for it. I came off Cymbalta in 2013 and have had the full set of symptoms since. I have been told I will never have intercourse again. I am an old goat so while it matters less it is still very disturbing. One of the other members was a 32 year old woman. Luckily for you this is very rare. I thought this would give you some idea what to expect during your recovery. By 3 months you should be seeing a return to 'normal'.
- JohnnyZ likes this
#742
Posted 09 November 2017 - 08:53 AM
You need to do a search for PSSD. That stands for Post SSRI Sexual Dysfunction. As you mentioned during the course of taking ssri or snri sexual performance and ability to reach orgasm is very limited (male or female). When you are totally off the ssri/snri everyone goes through an adjustment period. Typically there is a 4 or 5 day period about 1 week after coming off the med where sexual arousal and performance surges. Now that is also the time where many are suffering bad withdrawal so they may not notice this. Shortly after that the testosterone levels drop like a rock and sexual desire and performance completely tanks. Then over the next 3 months, if you stay off antidepressants, the sexual issues slowly improve and by the end of the 3rd month things should return to pretty much normal for your age and condition. This 3 month period is called PSSD. For some the symptoms never totally fade. There are a few that are left with, no periods, no erections, penus anaesthia (lack of feeling), no ejaculation, no orgasms, no libido. It is all gone. I am one of 4 from this site who have been left with this condition. I have seen many specialists and there is NO treatment for it. I came off Cymbalta in 2013 and have had the full set of symptoms since. I have been told I will never have intercourse again. I am an old goat so while it matters less it is still very disturbing. One of the other members was a 32 year old woman. Luckily for you this is very rare. I thought this would give you some idea what to expect during your recovery. By 3 months you should be seeing a return to 'normal'.
Thank you for a great post and the reassurance that I may return to a normal sex life eventually. May I ask what is your age?
#744
Posted 09 November 2017 - 11:01 AM
Side Effects on Cymbalta:
Profuse sweating
Hot flashes
Anxiety
Hair Loss
Poor appetite
Severe constipation
Sleeping problems
Irritability
Weight gain
Depression
Vision problems
Anger
Digestion problem
Withdrawal Effects:
Dizziness
Sleeping problem
Weight loss
Confusion
Brain zaps
Out of body feeling
Sensitive to lights, sounds and some smells
Hearing loss?
Shakiness
Suicidal thoughts
Depression
Memory problems, forgetful
Concentration
Numbness
Muscle weakness
Skin crawling like, electric shocks
Burning sensation feeling
Vision blurriness
Hot flashes, though I'm sweating less at a time
I'm not sure about hearing loss, but it seemed like I had some hearing loss. Is this part of the withdrawal symptoms? I am on a low dose of 5mgs of Prozac which I had started Wednesday, and to go on increase dosages until I reached 20mgs then let it kick in to combat these withdrawal symptoms. The symptoms I have now is mostly some muscle weakness, vision blurriness, tingly in my hands, feet, anxiety, some depression, hearing loss, sensitive to lights, sounds, feeling some hyperness probably from anxiety. My appetite comes and go, I am making sure I stay hydrated. The sleeping problems persist, only it's not way too severe like before while on Cymbalta and when the withdrawal happened. I do the best as I can to make sure no stress, it's not simple and I also try to stay positive as much as I can.
#746
Posted 09 November 2017 - 02:35 PM
Hello Lisa,
Just wondering if you can get something for your pain. I mean that there must be something out there to make you feel better, as you were given cymbalta for pain. It must be replaced by a pain reliever, so I think.
An opiate perhaps low dosage? As for being addictive, I found it quite easy to wean from 150mg to none. Had to get back on them as the pain resurfaced. (Big surgery on my back). But now 5 mg once a day is enough. Gets rid of depression at the same time. I'm nicer too. Lol!
Hi God-like
Unfortunately I have been on fentanyl,percocet,Vicodin,morphine,muscle relaxers,gabapentin... blah blah blah. I finally realized I was feeling worse after 6 years of adding higher and higher dosages. I started coming off them a year ago. Then just decided since cymbalta was the last one I would try ridding myself if it as well. I know that cymbalta made me able to cope with my pain much better. I don’t know if the pain is worse because of withdrawal or if it was a truly really helping my pain as well. Now when I read my journaling from July I see I was feeling really good before I started to come off cymbalta—as I said I just was on a crusade to rid my body of everything.
I am currently taking a low dose of tramadol 2 times a week when I just need relief. While I do think pain killers provide occasional relief —in the long term and daily they become ineffective and may make pain worse. Took me a long time to realize that!
The jury is still out on the cymbalta for me-if going back to a low dose proves to work for me I am not going to rule it out and I know I can wean from a low dose again. Have been in several conversations with my doctor and family to hopefully make a good decision.
Thanks!
Lisa
- gail, siggyd17 and Jillybeans like this
#747
Posted 09 November 2017 - 04:31 PM
Hearing loss is not a common complaint but tinnitus (ringing in the ear) is. A little hearing loss would not surprise me though.
Yes, I had noticed some ringing of the ears, and hear things loud like. I forgot to mention that sometimes I actually feel the palpitations or thumping like sensations in my ears. Perhaps this makes it feel like I lost some hearing.
- siggyd17 likes this
#749
Posted 10 November 2017 - 10:18 AM
I've been getting the hot flashes..and cold sweats. Today, I'm in a bit of pain..nerve pain I'm guessing? Is there anything that can help the nerve pain that won't harm my body or cause me issues? I don't like to take a lot of advil, excedrin, or tylenol (tylenol does nothing for me), mainly because I don't want the tummy issues. This pain causes my left shoulder (back and front) to become weak, which in turns weakens my left arm. I have dropped a few things the past couple of days. I really want to go back on the cymbalta, as this sucks bad. But Im 11 days free of this med. If anyone has any suggestions, message me. I'll try to be back on throughout the day and weekend, this weekend though is our Friendsgiving. I'm stressed, I know, because I haven't gotten everything done I want to get done. My husband has been cleaning the house, so I'm thankful for that. lol! It's just a lot. I use to be able to do stuff like this, now it just seems a bit difficult, which is depressing in itself.
#750
Posted 10 November 2017 - 12:00 PM
Hey Siggyd
I jusr added a new section to 'and the answer to your question is...). I deals with a lot of over the counter treatments that members have tried. The OTC analgesics you mention do not have a good outcome for most. Believe it or not Bragg's apple cider Vinegar is one of the best. There is even considerable medical research that has been done on that. Good for fibro, arthritis and general body aches and pains. Read through the new post and see what you think,
- siggyd17 and Jillybeans like this
0 user(s) are reading this topic
0 members, 0 guests, 0 anonymous users