Has anybody with hppd ever tried electroconvulsive therapy????
after 16 years of hppd and i tried every drug, that only worked for a few days/weeks, i'm thinking serious about trying a
electroconvulsive therapy. i had read a ton about the effects of a ect.
for me that will be the last chapter in fighting hppd after beeing a drug test pilot for the last 16 years.
here' the very short wiki link for the people, who don't know about.
http://en.wikipedia.org/wiki/Electroconvulsive_therapy
Problem: in germany it is not common to get an ECT like in sweden.
i'm thinking about 5 years for a try....and i'm sure: you cannot damage more, than hppd did.
question: has anybody information about doctors, or hospitals in europe, that will practice ECT??