My Battle So Far
#1
Posted 21 October 2012 - 12:20 PM
Alternate 60mg/30mg for a week. Week 2 take the 30mg. Week 3 take the 30mg every other day. Week 4 stop.
Hilarious! I knew that by the wds I had from before and how long I have been on this drug there was no way I could do it in that short of time. So I thought OK I will two weeks of each step. I did fine with the alternating 60/30 no issues at all. Then tried to do just 30 and hell began. I thought OK time to research what others have done, look up side effects etc. So that is how I am here now.
I saw someone said they subtracted 7 beads each day. OK cool gave it a try but once I reached 42-49 beads I was so sick I couldn't deal with it. SO I thought OK go back to alternating days for a while. Nope couldn't at this point. So I went back to my regular 60mg for a couple of days and then took out ten beads for two nights and last night I took a 30mg. Tonight I will try taking out 20 beads from the 60mg for a couple of days then take a 30mg. I will see how it goes. I am sure the more I mess around with it doesn't really help but really need to find some way.
Now for the side effects I have had on this drug I see many mention as they taper off which I find interesting.
On the cymbalta:
vivid, crazy dreams
extreme teeth grinding/jaw clenching (bought a bite splint and chewed through it in less than two months)
horrible headaches/migraines (never had any migraines before)
night sweats
chronic sinus infections (which I had no clue could be a side effect of the med until the other day)
fatigue/no energy could nap every day
high cholesterol (which may or may not be related but is a listed side effect)
higher blood pressure (mine always ran on the lower side but I kept linking it to my pain-now I am not so sure)
bouts of anger and still had depressive moments
horrible memory
eye blurriness
raging PMS (never had that before)
sexual dysfunctions ( extreme lack of libido and none or rare orgasm)
-I will add more as I remember or think of them.
Now to mention the whole vitamin thing. I take several because osteo runs in the family and also because I don't eat like I should. However I just realized with the fish oil I wasn't taking near enough. It is about the amounts of DHA and EPA so I greatly increased both that and the fiber. The reason I mention these two is because people have complained of being bloated and upset stomach when tapering and also I notice some have chronic pain as well. So for those who suffer chronic pain please look it up and see how much you really should be taking. It's not the mg of fish oil it's like I said about the DHA and EPA. For myself I need to intake at least 3800mg so for my fish oil supplements I have to take 8 a day. So I began taking 4 in the morning and 4 at night with my magnesium.
Tapering off the med I get the brain zaps, extreme headache, nausea, had upset stomach/bloated feeling until I increased the fiber, dizziness, flu like symptoms, extreme fatigue days though at first I felt great and my energy was up, sleeping much more than usual, shakes or jitters. Of course these are all normal symptoms of withdrawals but would like to avoid as much as possible if I can. And I am sure there will be more as I go as well.
So that is my story so far. Long and boring and like I said even if no one reads it at least I will have it for myself to keep track. I don't feel I have the support I need so writing it all out seemed to help. My hope is to be free of this med, find ME again, get that energy back and find out if the pain is related to the drug or not.
- Jnine, LAnnLanglois, lady2882Nancy and 1 other like this
#2
Posted 22 October 2012 - 07:44 AM
#3
Posted 22 October 2012 - 07:08 PM
I would love to hear how you are doing today/tonight? I have had nausea, been light headed, slight headache, tired (but didn't sleep very well at all last night), have been hot then freezing cold and seeing stars. No brain zaps though!
#4
Posted 23 October 2012 - 07:31 AM
#5
Posted 24 October 2012 - 07:18 AM
#6
Posted 24 October 2012 - 07:50 AM
#7
Posted 24 October 2012 - 07:23 PM
#8
Posted 25 October 2012 - 12:37 AM
#9
Posted 25 October 2012 - 12:47 PM
#10
Posted 25 October 2012 - 11:30 PM
- Jnine likes this
#11
Posted 26 October 2012 - 12:13 PM
- Jnine likes this
#12
Posted 26 October 2012 - 08:45 PM
#13
Posted 26 October 2012 - 11:19 PM
OMG thank you for posting I am new to all this. I injured my back almost two years ago and have all these pills pushed on me becuase the doctors cant/wob=nt find an answeer to my pain. I was forced back to work by WSIB in Feb 2012 and strange as it may sound it might have been the best thing for me as I started looking at my meds and how I had changeNot just from the pain but from the meds. Like you I became disassociated at times,, lost of memory & forcus (ha just tried to spell another word and couldnt). Anger & sadness to the point of "who am I and what happened to who I was". This and the weight gain has got me to where I am today tryong to fight these drugs. I can deal with pain but I cant deal with losing myself in the process if that makes sense to you. I have struggled for the last few months looking for support like yours. Once again THANK YOU for letting me know that I am not alone. My other half works long hours and I am alone most nights so it can get scary at times going thur this alone so it is nice to know that others like you are out there.
I know exactly what you mean. It makes me sad and angry feeling like I have lost ten years of my life and didn't even realize it! I emailed a friend of mine today and told her what ppl don't understand is this isn't like having surgery or giving birth. It won't be all finished within hours or healed with a few days or even weeks. Heck of a way to compare but it gets the point across. There are going to be highs and lows and feeling ill for a long period of time. We just have to keep focus on the light at the end of the tunnel. It will get better with time. I am not sure how long you have been on it but what scares me the most is what damage it has done mentally and if I will ever be the real me again. From what I can tell as well is that most doctors don't truly acknowledge the fact there are withdrawals from these types of meds. It is considered non narcotic so they don't look at it as a drug that someone is hooked on. What I don't understand is why they don't when they know it messes with the brain chemicals. Then when ppl mention their withdrawal symptoms they just tell them it's depression coming back so they need to go back on the med. BS!!! Ive heard ppl compare getting off cymbalta to getting off heroine. My husband tries ( I think) to be supportive in this ordeal. I guess in a way I just don't feel it's the right support. Don't ask me what's wrong when you already know and asking if I'm OK is fine but it's not really helpful. I wish he would research like I told him to do. My mom lectured me when I went through withdrawals a few months ago about how I should get off this drug and think of what its doing to me then the other day lectures me that I should wait until I'm working as she thinks I am just sitting around thinking about it and that won't help anything, etc. Drives me crazy. It's not what I need to be told. I feel for anyone trying to work and get off this drug because I think when your body tells you to rest and if you can sleep through most of it you should. Not too mention the emotional roller coaster that it is. Thankfully I haven't truly hit that part yet this time around. It's awful to be in that state. Ive tried some herbal supplements that ppl on here have mentioned to help ease things but for me they made it worse and you have to be so careful what you take with cymbalta. I did pick up some alpha lipoic acid today because I read that some antidepressants can deplete certain nutrients and also that the alpha helps boost the B and C vitamins so hoping that will help my fatigue problem. I guess it's also good for preventing pain, burning or tingling and helping muscle. I have muscle atrophy in my leg from the RSD. I will keep updating daily as I go. Today truly was a much better day for me. The fog is slowly lifting! Thinking I will give my body a few more days of the 30 mg then split those in half for a few. We will see.
#14
Posted 27 October 2012 - 10:06 AM
#15
Posted 27 October 2012 - 01:24 PM
#16
Posted 27 October 2012 - 03:43 PM
My breakfast basically lol.....
Multivitamin
Super B complex
Vit C
D3
Vit A
Calcium
Potassium
Fish oil ( only taking 3 now)
ALA (as of today)
Was taking a probiotic, Co-Q10 and also a fiber supplement but have ran out of them and figure I can wait on those for now.
Then at night I take 2 Magnesium
Some say to take with meals and some say to take 3 times a day etc. Each I listed I just take one except the fish oil and magnesium. Can't say much about the ALA yet. Although I did notice my muscle cramps aren't near as bad today but it could just be one of those days too. Going to be a long process but I keep saying to myself that I'm half way there now. Each day is a step closer to being free. I will check in again tonight.
#17
Posted 27 October 2012 - 05:19 PM
#18
Posted 28 October 2012 - 01:19 AM
#19
Posted 28 October 2012 - 04:34 PM
I have been on cymbalta since January 2012 for depression and anxiety. Feb 18th 2013 will mark the 2nd year of my being on disability. I was given ciprolex at first and that was nat managing my anxiety so I was switched to cymbalta when I was during an outpatient program. It seemed to work at first, and over the summer I actually had some great days/weeks. I thought I had turned the corner and remember telling my therapist as such. That I was considering going back to work part time and things were looking up. The very next day I work up miserable and the following day i didn't get out of bed.. well except that I had to go see my MD (fortunately his office is across the street from where I live). I went back to bed as soon as I got home. I was so frustrated.... How can i go from being on top of the world one day, to being unable to get out of bed the next? My Dr decided it was time to try a different med. The drug of choice is now Wellbutrin, but of course I first have to come off Cymbalta.
My Dr's withdrawal plan was as follows:
1) drop from 90mg to 60mg for 1-2 weeks
2) then drop from 60 to 30 for 1-2 weeks
3) then 5 days of nothing
4) start taking Wellbutrin
I am currently on step 3, and my 4th day of taking nothing at all. and I've been going through hell just like everyone else on here. The brain zaps won't stop. I have no energy for anything, and I don't care about anything either. I am fortunate that I am not working right now. I don't have kids either, so it's just my Husband and I and he works and has a very busy schedule so i am at home alone a lot which i am quite fine with. So I can just indulge my desire to do absolutely nothing if that's what I want to do. Another part of me thinks (or perhaps it's because I've been told it's not healthy to be alone all the time) it would be better for me if I did have kids or work to motivate me to leave the house... to get showered and dressed.
I have to say I related to so much of what you have written: not having an interest in things you normally would, wanting to "just be alone" all the time. Heck, I even smiled when you wrote about wishing your husband would stop asking if you are ok. Mine does that too. He has been a great husband.. works all day and the comes home and makes dinner. These past two weeks I have barely left the house. Only when it's absolutely required.. like Dr's appt etc. I feel hot then cold. I sweat more than I used to - especially around my neck - and swear I have hot flashes, if I'm with people they laugh and tell me I'm too young (i'm 38) to be having hot flashes.
I am also at a point where I am questioning whether I should stay on meds or try to find alternate solutions. I have had periods in my life where I was working out at a gym regularly eating normally - i.e., mostly healthy with the odd dessert here and there, and just felt happy and alive. It's been a long long time since I felt that way. and I'm not sure if starting Wellbutrin will help with that goal or not.
Yesterday and today I have just slept and slept and watched TV and cried at the ending of all the TV shows. I feel defeated and not sure I'll ever come out of the gloom. I feel like my husband deserves so much more.
Anyway, just wanted to thank you again for writing about your experience. It has given me a lot of insight into my own experience.
#20
Posted 28 October 2012 - 06:47 PM
I too sweat like crazy Bunny515 and just around my neck and head. I can wake up in the middle of the night totally soaked many times. So much for a full night's sleep as I havent had one of those for 2yrs now.
I hope the two of you are getting some much needed rest and can sleep peacefully tonight. I need to go back and stare at my closet still trying to figure out what to wear to work tomorrow.....urgh WORK~~~ ((hugs)) Thanks for being here & sharing your stories it helps so much as most people have not idea!!!!
#21
Posted 29 October 2012 - 08:56 AM
thank you truckprincess for posting your info. And I'm thankful for this site. Here's a bit of my story;
I have been on cymbalta since January 2012 for depression and anxiety. Feb 18th 2013 will mark the 2nd year of my being on disability. I was given ciprolex at first and that was nat managing my anxiety so I was switched to cymbalta when I was during an outpatient program. It seemed to work at first, and over the summer I actually had some great days/weeks. I thought I had turned the corner and remember telling my therapist as such. That I was considering going back to work part time and things were looking up. The very next day I work up miserable and the following day i didn't get out of bed.. well except that I had to go see my MD (fortunately his office is across the street from where I live). I went back to bed as soon as I got home. I was so frustrated.... How can i go from being on top of the world one day, to being unable to get out of bed the next? My Dr decided it was time to try a different med. The drug of choice is now Wellbutrin, but of course I first have to come off Cymbalta.
My Dr's withdrawal plan was as follows:
1) drop from 90mg to 60mg for 1-2 weeks
2) then drop from 60 to 30 for 1-2 weeks
3) then 5 days of nothing
4) start taking Wellbutrin
I am currently on step 3, and my 4th day of taking nothing at all. and I've been going through hell just like everyone else on here. The brain zaps won't stop. I have no energy for anything, and I don't care about anything either. I am fortunate that I am not working right now. I don't have kids either, so it's just my Husband and I and he works and has a very busy schedule so i am at home alone a lot which i am quite fine with. So I can just indulge my desire to do absolutely nothing if that's what I want to do. Another part of me thinks (or perhaps it's because I've been told it's not healthy to be alone all the time) it would be better for me if I did have kids or work to motivate me to leave the house... to get showered and dressed.
I have to say I related to so much of what you have written: not having an interest in things you normally would, wanting to "just be alone" all the time. Heck, I even smiled when you wrote about wishing your husband would stop asking if you are ok. Mine does that too. He has been a great husband.. works all day and the comes home and makes dinner. These past two weeks I have barely left the house. Only when it's absolutely required.. like Dr's appt etc. I feel hot then cold. I sweat more than I used to - especially around my neck - and swear I have hot flashes, if I'm with people they laugh and tell me I'm too young (i'm 38) to be having hot flashes.
I am also at a point where I am questioning whether I should stay on meds or try to find alternate solutions. I have had periods in my life where I was working out at a gym regularly eating normally - i.e., mostly healthy with the odd dessert here and there, and just felt happy and alive. It's been a long long time since I felt that way. and I'm not sure if starting Wellbutrin will help with that goal or not.
Yesterday and today I have just slept and slept and watched TV and cried at the ending of all the TV shows. I feel defeated and not sure I'll ever come out of the gloom. I feel like my husband deserves so much more.
Anyway, just wanted to thank you again for writing about your experience. It has given me a lot of insight into my own experience.
Hi Bunny, I hope this finds you feeling better today. I can't understand why your doctor decided to have you go 5 days of nothing before starting the wellbutrin. I was on wellbutrin for a while, I didn't think it was too bad to get off of but again everyone is different. You might want to research it to check any side effects and what not. I do think it's one of the lesser evil of drugs. Though they told me it would also help me quit smoking which it never did lol but I don't think I was on a very high dose either. Your story really touched me, I feel for you. I know I really miss working, I was a nurse aid for years and enjoyed my job, my co-workers, friends, went out and did things, had more energy and was in really good shape, I had a life. Since my accident I don't really have any friends other than a couple that I email but I don't see anyone, I don't go out. I am sure part of that is my fault as I know I have changed. When you chronic pain you don't really feel like going out and living it up. Then after so long of being at home it makes you lazy in truth and I have never been one who did well being a homebody all the time. It's never bothered me being alone and I do like it for the most part but also blame a lot on the cymbalta. It's hard to face facts and realize the person you have become on this med. I used to talk with my mom and friends all the time on the phone too and for the past few years the only one I talk to is my mom and that's when she stalks me lol. Then she complains I never call and we never do anything together any more. I feel bad and yet part of me doesn't. You made me LOL about the hot flashes and sweating. I remember telling my doctor years ago that I sweat so bad in my sleep I can't stand it and he told me I was too young for that. Yeah no kidding when you are in your twenties and dealing with that. Ive gotten used to it but lately with tapering I'm either freezing or hotter than hell. I keep turning the heat down and my husband cranks it up. I have been on a few different ads the last ten years (Im now 38 as well) but the cymbalta for at least 7yrs. Please don't feel defeated, it will get better in time. I know it feels like forever though. There were a few times I said I can't do this, I can't get off this stuff but I kept pushing anyway. Just know that you are not alone in this. I try to check in here a few times each day. Though yesterday I was wrapped up in trying to figure out how I'm going to taper from 30mg so I was side tracked and kind of zoned out just watching tv. Any way thank you for sharing your story as well and feel free to vent, scream (well type it loudly lol) whatever you need to do on here. I am happy to help support anyone in anyway that I can as I go through this too.
#22
Posted 29 October 2012 - 09:05 AM
Just a quick check in tonight. I had a preety good day and managed to do a few things around the house (making up for yesterday). I made a nice lasanga dinner & home made apple pie for desert but not I am done. Overwhelmed just thinking about work tomorrow. The weather here is nasty rainy & cold and is suppose to be like this all week. I have managed to keep the sappers at bay today and I think it is the clarition that is helping. The headache from hell is still here and seems to spike ever so often. Bunny515, it is a balancing act between wanting to be alone and needing the motivation of having people around. It;s a rollercaoster ride for sure as right now my guy is annoying the hell out of me for absolutely no reason yet I have wanted him here all week when he was at work....lol. Oh I should state that if I misspell anything or things are disjointed at times I can thank the lyrica for that as it has affected not only my short term memory but my ability to remember how to spell words at times.
I too sweat like crazy Bunny515 and just around my neck and head. I can wake up in the middle of the night totally soaked many times. So much for a full night's sleep as I havent had one of those for 2yrs now.
I hope the two of you are getting some much needed rest and can sleep peacefully tonight. I need to go back and stare at my closet still trying to figure out what to wear to work tomorrow.....urgh WORK~~~ ((hugs)) Thanks for being here & sharing your stories it helps so much as most people have not idea!!!!
Hi Jnine! I am so glad you had a better day yesterday Also glad to hear the clariton is helping. You had me cracking up about your guy wanting and not wanting him around I was LMAO! All I could think of was I was so glad to know I am not the only one who wishes he would stop talking or better yet don't breathe my air. Just go sit in the other room or something LOL. Oh it's horrible. I don't like Lyrica at all. For one it didn't do crap for me and for another when I was working we had a lady who was on it and gained 90pds in 6mo being on that stuff. NO thank you! I hope you have a good day at work today and that all goes well for you. I will check in later and see how things are.
#23
Posted 29 October 2012 - 09:48 AM
#24
Posted 29 October 2012 - 05:04 PM
#25
Posted 29 October 2012 - 07:58 PM
#26
Posted 29 October 2012 - 09:14 PM
Today I slept most of the day, got up around 4pm and then been watching tv since. Last night had the worst nausea! took 2 gravol and went to bed, Gotta love Gravol! Not only does it make me have a deep sleep, it also helps prevent the nightmares.
I am supposed to start taking wellbutrin tomorrow and I have to say I'm a little scared. My husband says I should take it, he took it to help him quit smoking too. LOL He did quit but I don't think it was because of the drugs. He's just a very stubborn person so when he decides to do something, nothing stops him He said he felt great on wellbutrin. I could certainly use an uplift
Perhaps I should start another thread and journal my day to day experience of the transition.
#27
Posted 30 October 2012 - 07:05 AM
Hey truckprincess and Jnine, thanks for the encouraging words.
Today I slept most of the day, got up around 4pm and then been watching tv since. Last night had the worst nausea! took 2 gravol and went to bed, Gotta love Gravol! Not only does it make me have a deep sleep, it also helps prevent the nightmares.
I am supposed to start taking wellbutrin tomorrow and I have to say I'm a little scared. My husband says I should take it, he took it to help him quit smoking too. LOL He did quit but I don't think it was because of the drugs. He's just a very stubborn person so when he decides to do something, nothing stops him He said he felt great on wellbutrin. I could certainly use an uplift
Perhaps I should start another thread and journal my day to day experience of the transition.
Hi Bunny, Glad to hear from you! Oh I am happy to hear you got some really good deep sleep. Gravol is a motion sickness med right? Is that prescribed or over the counter? I know it's amazing how much that stuff really helps with a lot of the withdrawal symptoms! I took mine first thing this morning with my allergy med and some advil. Not waiting for symptoms to arrive figure I might as well just stay on top of it.
You could start another thread if you wish or you are more than welcome to just add to mine as you go. I started mine originally to keep track of what was going on and to help others so they know they aren't alone. I just think it really helps for me to write it all out and might help give others some ideas to try or not try lol. I know I tend to ramble on so I understand if you want your own thread. I just have no other outlet at the moment. It's nice to have someone else to talk to and check up on too to see how they are doing.
Well I agree if you feel you need "something" then take the Wellbutrin for a while. You can see how it works for you and always decide later on if you want to get off that or stick with it. I give you a lot of credit for sure, I don't know how managed to make it tapering the way the doctor had you do it. I know I couldn't do it the way my doctor told me. Sometimes I think they just do that fully knowing you will relapse and go back on it. Which is so sad to me. If it wasn't for me trying the motion sickness med finally I don't think I'd be as far as I am now. I hope you got some good rest again and feel better today!
#28
Posted 30 October 2012 - 09:16 AM
I will check back later on
#29
Posted 30 October 2012 - 02:28 PM
#30
Posted 30 October 2012 - 03:24 PM
Thanks Truckprincess,if you don't mind then I will just post my entries in this thread. Sorry you've having a bad day Jnine!
So I am in Toronto Canada, so I guess some of the meds I reference are local. Gravol is an OTC med to help with nausea and dizziness. I does help with the nausea but it also makes me sleepy so I can't imagine taking it during the day on a regular basis. I slept until 11am today. I had wanted to get up earlier but 11am is better than 4pm. I have been watching CNN, my heart goes out to anyone dealing with the storm. We were just in NYC this past summer, can't imagine the city deserted with no subways running.
Tprincess, I now what you mean about showering. I haven't showered since Friday... I know it's gross isn't it... but the thought of standing up in the shower is just too much. i think i'll just take a bath tonight and ask my hubby to help me wash my hair.
So I talk my first dose of Wellbutrin this morning. So we'll see what happens. I still feel really spacey. Brain zaps still happening.. not as much, but still happening. Feel dizzy and nauseas when I stand up so I'm reclining on a chair most of the day, or in bed. My emotions are all over the place. I can cry at the drop of the hat... watching all the storm coverage isn't helping My eyes feel really strained, didn't want to even put contacts in so I've been wearing glasses. I have no energy and no desire to do anything either.
Just going to take it day by day!
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