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Jester2005
But if you haven't had paxil in 6 months and STILL have electric shocks, I would book an appointment with your DR RIGHT AWAY if you have one. If not, call your pharmacist... if you'd like, I can call mine tonight :)
I have been off paxil for over 5 years and I still get them "the zaps", usually more often in the afternoon after I've had a busy day. I was put on Prozac after my first spine surgery 4 years ago and a year ago my doctors added cymbalta too. But till this day I still get them and I know of many others too that still suffer with this. Out of the blue I will get zapped, feelings of electricity shoots out of my head, tip of my tongue, thru the spine and around my ankles. It use to be with almost all quick movements, but maybe because I'm on the other SSRI's they have dulled some of the feeling. When you Google zaps you will find out many sufferers have to take smaller amounts to much smaller amounts to much much smaller amounts,,,,,, and you can see what I'm saying, until you can finally get off of it.
With you being a dancer I can't imagine what you're feeling along with the other W/Ds that go with it. If you have any questions write me back. I am so sorry you have been going through this. elaine
mtgoat911: They are a bit less frequent, and only with extreme movement, but as a dancer I do that quite a lot. thursday I had it maybe about 10 times in a 4 hour rehearsal, but today none at all. Today I also didn't dance.
Thanks again it just helps to know there is support out there :)
mtgoat911 thanks for the tip. Great website.
Well, I go back to rehearsal tomorrow we'll see how it goes. Too bad this choreographer really likes headbanging movemnts