Thank you so much.
I thought I was going crazy with the brain zaps becuase when I was explaining them to my neurologist, she said she never heard of such a thing.
Like short electro shock in the head.
I went from 90 to 60 week by week, for example- Monday I take 60 and then the rest of the week 90, next week Mon and Tue 60mg and the rest of the week 90mg, and so on until I get to 60 every day of the week...but it was so hard, I wasn't able to function because of brain zaps.
And now I take 60 mg and have medium brain zaps every day.
The funny thing is, is that you learn how not to move your head and blink hard - so you minimize the brain zaps .
List Your Symtpoms
#451
Posted 04 January 2014 - 10:13 AM
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#452
Posted 04 January 2014 - 11:14 AM
Lele
Your withdrawal from 90 to 60 was done in abrupt steps, and that brings on withdrawal pretty fast. We advocate a linear reduction of the dosage rather than one that is stepped- hence the bead counting method. Cymbalta has a short half-life of 12 hours, so withdrawal symptoms are never far away.
If you restore some medication (say to 75 mg), the brain zaps will probably go away.
#454
Posted 08 January 2014 - 11:04 PM
Welcome Lele. You are in good hands already with fishinghat and thismoment. They are mentors to many around here. I have learned to listen closely to their advice - it has never failed me.
If you are about to take exams, have you considered delaying the start of this process until after the exams? While this slow tapering certainly makes this experience tolerable, it isn't without its effects. I still feel like my brain is operating at about 40% of its capacity. Of course, it's up to you, but I would want to be "certain" about my body chemistry during exams. This journey can be a bumpy one - you don't always knows how you are going to "feel" or "think" from one day to the next.
I don't want to discourage you...I am just being practical. You will get through this eventually. I think you are going to be amazed at the wonderful support you are going to find here. :-)
#458
Posted 13 January 2014 - 10:16 AM
#459
Posted 13 January 2014 - 10:45 AM
#460
Posted 13 January 2014 - 10:47 AM
Hi Vtybee- that's a steep drop- almost cold turkey- and it sounds like you're in full-blown withdrawal at the moment.
You've certainly had your share of suffering! Oh dear, that's been a struggle. And the rage is not uncommon in withdrawal, and it may turn to tears before too long. Hang on! If you stay cold turkey, this could be tough for a month or more before it lets up.
What to do. Your withdrawal symptoms would ease a lot if you tapered off the drug. Therefore you could consider re-instating on the drug until you stabilize, then organize a tapering plan from a position of strength. Right now with the buzzing, brain fog, and rage- confusion reigns.
Aside from the possibility of injuring yourself, you may further alienate those you will need for support as you go through this. If you can bring your medical contacts into the loop, so much the better.
With your medical people advised, consider re-instating to your last dosage of 30 mg until you feel level and stable enough to take on a tapered withdrawal.
Please let us how you are doing and what you plan.
#461
Posted 13 January 2014 - 07:41 PM
I've had multiple side effects since starting cymbalta. Daily headaches, blurred vision, weight gain, spending out of control, isolating myself, irritable, overly emotional etc....Ive only been on Cymbalta for 2.5 months. Was taking Cipralex before that and celexa before that. I tolerated Celexa quite well but had no energy and of course the weight gain (which I think are a part of all anti depressents) I have some Celexa and would like to stop taking the cymbalta and go back to celexa. I am on 40 mg of cymbalta, 20 mg twice a day and 10 mg of cipralex with the secong dose of cymbalta.... does anyone think it would be wise to take 20 mg of celexa twice a day to get off cymbalta? I know that cymbalta is an SNRI and Celexa is a SSRI. My physician put me on Cymbalta because I can't seem to find energy. I still don't have energy and am suffering from all the side effects...... so why stay on?
#462
Posted 13 January 2014 - 08:34 PM
#463
Posted 14 January 2014 - 12:19 AM
Welcome aboard. Switching to Celexa shouldn't be difficult, and it's standard procedure to allow a period of overlap. But even so, taper the Cymbalta slowly, while introducing the other medication.
Tell your physician what you wish to do, and he or she will be in the loop and advise on the logistics.
Best wishes!
#464
Posted 27 January 2014 - 10:31 PM
#465
Posted 28 January 2014 - 12:55 AM
ThI have had so many of these symptoms:( I can't get off it no matter what I do. I stopped last Wednesday and today is Monday and I just couldn't do it so I took the pill:( I feel like a failure......my worst symptom is prob the brain zaps and the horrible sadness, I also expierience rage and anger that I've never felt in my life, vomiting, shaking, major mood swings and thoughts racing thru my mind I feel like I'm going to loose everyone around me. If I'm on it they say get off it because Im not ME:( and to try to get off it no one understand what it does to u unless u expierence it.....I feel like I will never be me again
Thiar..don't you dare feel like a failure. None of this is your fault. Trust yourself enough to know you had the strength to try and stop. It's just that you may need a different approach in trying to get off this horrible drug. Read through the forums here and learn how others used differ methods, which they could tolerate, which are helping them..Everyone is different therefore everyone uses a different planned out method. I'm sure you will find one here and also sure other members will chime in and offer their feeling on your post along with suggestions they will offer..The members are so caring here and will make you feel safe and comforted..Good luck..keep posting and you will get lots of feedback. Good luck. .keep us all posted on your progress!I have had so many of these symptoms:( I can't get off it no matter what I do. I stopped last Wednesday and today is Monday and I just couldn't do it so I took the pill:( I feel like a failure......my worst symptom is prob the brain zaps and the horrible sadness, I also expierience rage and anger that I've never felt in my life, vomiting, shaking, major mood swings and thoughts racing thru my mind I feel like I'm going to loose everyone around me. If I'm on it they say get off it because Im not ME:( and to try to get off it no one understand what it does to u unless u expierence it.....I feel like I will never be me again
#466
Posted 28 January 2014 - 11:18 AM
I have had so many of these symptoms:( I can't get off it no matter what I do. I stopped last Wednesday and today is Monday and I just couldn't do it so I took the pill:( I feel like a failure......my worst symptom is prob the brain zaps and the horrible sadness, I also expierience rage and anger that I've never felt in my life, vomiting, shaking, major mood swings and thoughts racing thru my mind I feel like I'm going to loose everyone around me. If I'm on it they say get off it because Im not ME:( and to try to get off it no one understand what it does to u unless u expierence it.....I feel like I will never be me again
Yes, you can ... And WILL ... Get off cymbalta..... I went off cold turkey and wouldn't recommend that approach even to Lucifer himself... But I'm dumb, and stubborn, and once I realized what I'd done, I just blundered through it .... However, the better approach is to just slow down, follow the bead counting technique that others here far wiser than me have used and can explain to you....
You are already YOU, it's just that this drug masks everything....most of all our true self....all the things, thoughts, feelings, pains that you describe feeling are what I, and most of us here, have had...do still have....you've just got 'em all colliding inside you simultaneously..... That's why slowing down, focusing on just "this moment" (one of our wonderful members goes by that name!) ....and reducing your dose bead by bead.....do NOT let anyone else, friend, family, or medical professional, dictate how. Why or when to do this....this is all yours to determine, and we are here to help.....
My worst symptom was also the brain zaps....and then, when those faded, every day, late afternoon or evening, I'd get "red hot pokers" driven into my eyeballs and optic nerves, and sometimes my ears and whatever those nerves are called.... For hours on end...
I discovered that self induced "brain freezes" helped tremendously.....I covered my eyes, sides of my head, back of my neck...basically my whole damn skull...with those refreezeable ice packs....the pea bag sorta thingies .... The cold hurt like hell, but it took my mind off the red hot pokers, and gradually, as the ice bags warmed up it seems like the hot pokers cooled down....
The other trick I learned was to put gentle pressure on the lymph nodes just under my eyebrows...sort of massage gently...in fact, I could feel that some of them were really swollen and almost "stiff".....if you've got someone who can do that for you, it's heaven.....I asked my cats, but they were too busy with personal grooming....so I massaged myself. ;-)
Keep checking in and letting us know how you're doing!
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#467
Posted 28 January 2014 - 05:53 PM
After 6 months of using this miraculous drug, my primary care physician told me he suspects the Cymbalta has been the cause of my significant weight gain. The psych said I could reduce from 60 to 30 within a week and then be off the drug to confirm whether or not my primary doc is right. After a week off Cymbalta (still on Wellbutrin and Buspar), I'm having many bouts of vertigo and I suspect the new sensations are "brain zaps". I am awaiting a response from the psych for suggestions of how to deal with this. (though I doubt he will have any solutions) I loved that Cymbalta gave me the capacity to experience happiness and less pain from fibromyalgia, so I have been looking for alternatives. I'm trying 5 HTP but maybe I need a combination of something else with it. The psych laughed that there is no proof anything like that would work, so my research has led me here.
On Cymbalta, I only experienced side effects of weight gain and excessive sweating. The sweating went away when I cut back from 90 to 60 mg.
Off Cymbalta, I am having vertigo and "brain zaps". I also have very vivid dreams...not nightmares but intense enough to confuse me when I wake up. We are in the middle of a polar vortex, but I sweat all night long.
Anyone have an estimate how long this will last? Anyone have cures to help me get through this phase?
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#469
Posted 28 January 2014 - 07:52 PM
Check out the nutritional supplements area of the site...also, a couple of us have been posting on a thread today about what's helped us...I'm tired and can't remember who started it...but it's listed I think on the right side column of the main page....
#470
Posted 30 January 2014 - 11:52 PM
I started Cymbalta in 2009 and for years it seemed to work well. However, in recent months I have been feeling increasingly numb, except about my weight gain and inability to lose weight despite exercise and diet. I was on 90 mg and went down to 60 mg with no problems but stopping from 60 has been difficult. I have terrible brain zaps, and feel in a fog as though I have been drinking even though I haven't. I have shakes as though I'm cold even when wrapped in blankets, and every time I eat I find myself in the bathroom right after. Yesterday I slept for over 12 hours. I tear up at the most ridiculous things (most recently about the history of Spartan women), but other than that I don't feel much psychologically different. I feel like the withdrawal effects are mostly physical and my psychological state might be getting a little better. I don't want to discourage anyone from seeking pharmaceutical help if they need it but by god be prepared for the consequences.
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#471
Posted 31 January 2014 - 03:05 AM
We'll you will be receiving much support from this site..Wonderful members from all over the world are here to give you whst the can from a tender word, share their experiences, sharing their support, and love...
They will be chiming in on your post..Post us daily concerning you questions, options, and progress..good luck
#472
Posted 31 January 2014 - 05:15 AM
And Carleeta ... You're in my DC time zone .... What in the world are you doing up and posting at 3:05 a.m.? Is this your usual rising time, or are you having trouble sleeping? That's my reason for being here ... After my great day yesterday, I spaced out on how much 5-htp I took at bedtime ... I think I took my usual two 50 mg capsules Twice .... Meaning 200 mg total ... and put myself into "lucid dreaming la-la-land" .... Wild wild stuff, on the nightmare side of dreaming ... I had to get up and walk around and shake it off ... Googled the side effects of the stuff, and yep, sure enuf, some folks report vivid dreams ... I went beyond vivid into "get me the hell out of here" .... So, I just had some peanut butter toast and read a bit, including comments here on 5-htp ... And will now put myself back to bed for another try at plain ole' vanilla flavored sleep ..... Note to self- make a supplement dose checklist to prevent further unintended consequences .... :-$
G'night / g'morning y'all .....
#473
Posted 31 January 2014 - 02:04 PM
#477
Posted 04 February 2014 - 11:55 PM
Eous.i am worried about the nausr|>inue to be nausEous.i am worried about nause
vtybee..considering has wonderful nutritional advice. If I may add to this, if you do get nauseous always keep saltine (they have some without salt on top) keep a fan on you, and there are otc meds for nausea..If you feel extremely sick you can also lay down on a cool floor..Iff you can try and not think it will happen as to keep your stress level to a minimum. .Take care and keep us posted..Eous.i am worried about the nausr|>inue to be nausEous.i am worried about nause
#478
Posted 07 February 2014 - 09:22 PM
Miss the mark completely). I was on 60 mg a day. He weaned me off of it over 3 weeks. First week 60 30 60 30. Second week 30 everyday. Third week 30 0 30 0. I started having problems the first week with vertigo,massive 24/7 headache, horrible nightmares & some rage. Well, by the time I got to the last dose I had real issues. All of the above had intensified, felt kind foggy in my head @ times, felt like bugs were crawling on me, twitching, itching, numb heels & palms, serious irritability & blood boiling rage. Suicidal thoughts all the time. I am trying really hard to hang onto my sobriety(261 days). I am a self injurer and this crap has brought that back. Hot & cold you name it this poison has given it to me. After the 3 weeks I called my Psych. Dr and he said "I wen off of it to fast" I had found this site rite before that. Doc wanted me to go back on it. I asked him for how long? He said " I dunno a few weeks or so". I told him no way that I would probably never get off of it & he had no idea when I would either. So, here I am today is 6 days without that poison, and I weaned off of it for 3 weeks prior to that. And I am still in hell. I still feel like I am going crazy. Chasing my family away, acting like a lunatic on the road, racing mind then hard to put things together, struggling ever so hard to stay sober & all the other side effects listed above. I can only hope that there will be an end to this madness; however, it needs to come real soon for me for I am holding on by a thread. This is a horrible drug. I have been I every psych drug out there in my 24 years and I have never had any side effects that I recall. This crap needs to be pulled from the market, just bad medicine period. Anyways I am grateful for this site exist and all of you on it. I will
never put that poison back in my body. I will ride this wave out(hope it is a short one) & I survive. Thank u very much for letting me write my book. And bless all of you for your sharing & caring. And not making me b alone through this hellish nightmare of withdraw.
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#479
Posted 07 February 2014 - 10:22 PM
spread the word to all on this site. To go to the FDA site & there is a form you can fill out regarding your problem/s with a medicine for it really needs to be looked into & re evaluated. I know I am for I don't want others to have to suffer like I had to if at all possible. I find this horribly addicting(2 say the least) & I for One would like it investigated further if not pulled from the market. If you already know about the site & have done so, awesome. If not, I strongly encourage you too. Take care of yourselves.
#480
Posted 07 February 2014 - 11:46 PM
Thank you for the reminder about the FDA site ... I knew, but got so caught up in my struggle that I forgot ... I will make a visit and report tomorrow, after I get some sleep ....
Hang in there, and keep us posted...welcome to the group!
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