Guest guest Posted January 2, 2007 Report Share Posted January 2, 2007 I've been asked to explain what I said about cortisol being a problem in SSRI withdrawal, and how I can tell when mine is high. I'm so used to dealing with it, I forgot that people here might not understand what I was talking about. There's a lot of medical knowledge at the other Yahoo group I belong to, and a lot of people who have come through withdrawal and have been helping others do it for a long time. One common feature of withdrawal, particularly if you do it very fast or cold turkey, is a dysfunctional cortisol response. It's part of the damage that gets inflicted on the body during rapid withdrawal from the psychotropic drug on which it is dependant. The way it was described to me was it's like a light switch that has been broken. Cortisol is part of the " fight or flight " response that also includes adrenaline. The cortisol is supposed to subside rapidly after the stimulus is gone; but after rapid drug withdrawal, it may not. By the way, other things like long-term stress can cause cortisol problems too. If your cortisol is high then you are exahusted a lot of the time, jittery, often tearful, anxious, you have trouble sleeping, and you may feel depressed. I believe there's a saliva test you can have done if you really want to. I personally have decided that doctors have done more harm than good in my life, they're the ones who gave me these drugs telling me they'd help me, and they probably wouldn't believe me if I told them about the withdrawal symptoms I've had. What I've been told about cortisol, and researched on my own, fits well enough with what I've been experiencing. My cortisol went sky-high when I worked in a school for 6 weeks recently. I am a trained teacher but I took a teaching assistant job, as a less stressful way of re-entering the school environment (I've been raising my daughter at home for 4 years). However, the ringing bells, the crowds, the noisy drama and music classes where teachers weren't in control; trying to cycle, then fighting rush hour traffic in the car; working 4 full day a week -- they all left me with the symptoms I described above, plus 100% genital numbness. Cortisol actually robs chemicals out of the sexual hormone system in order to be created and function. I've more or less recovered from that experience, and I've been assured that the cortisol problems will mostly or completely subside over time. In the meantime I have to relax as much as possible, and avoid things that overstimulate my system. The list seems endless, but I've been learning over the past several months how to cope. After all, you don't heal a bruise by repeatedly irritating it. There are times when the cortisol isn't quite so high, but the genital numbness persists, so I don't think there's a simple relationship between the two. What I try to do is remember that the sexual problems aren't the end of my life, that there are other things to enjoy and be thankful for. At least, I'm OK with that attitude until I have another fight with my husband. It's taking him a long time to accept what's happened to me, but I'm hopeful we'll be able to work something out. I'd be interested to hear about what other people here have done when this has happened to them in the middle of a relationship. . Quote Link to comment Share on other sites More sharing options...
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