Do you still have voices on meds?

Amisulpride was the first AP I ever tried, 9 years ago.

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It’s a very strong med. Highly effective. I used it 3rd, after Aripiprazole and Risperidone.

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I have used all of these and more.

Nothing stopped symptoms completely

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Nothing ever will. Only a small percentage of us will be completely free of symptoms. The rest will have some/a little/a lot of relief. And then some of us will not respond at all. Its sad for us.

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Last year I had visual hallucinations of a limping girl wandering my neighborhood, but usually I don’t hallucinate on meds.

I was pretty sleep deprived back then.

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Oh yeah. The difference is my voices are kind and supportive, or at worse neutral narration. All of the insults and commands go away with medicine. Not sure why that is but you won’t hear me complain too often.

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Nope I’m a normie lols :).

No negative or positive symptoms.

High functioning.

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It’s sad but I think most of my voices are real even though it’s hard to differentiate. They are pretty bad, saying I’m unattractive, that I have no personality, that I’m a wimp, that I’m going to get shot.

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I have a lot of similar things going on

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If they are saying stuff like that, it is likely they are not real. It’s hard to tell the difference without experience.

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