Hi Lela;
You may be on something similar to my wife--guessing here. Abilify, (her current med) is a 'better' version of Olanzapine. I am making broad assumptions here.
Here is what wiki says about Olanzapine;
Olanzapine is believed to work by blocking, or antagonizing, the dopamine D2 receptorwhich is an action it shares with most antipsychotics.[7] Like most other atypical antipsychotics olanzapine also strongly antagonizes the 5-HT2A receptor, which may partially underpin its reduced propensity for causing movement disorders.[7] Despite its close structural relation to traditional benzodiazepine anxiety-relieving medications, it possesses no affinity for the GABAA receptor, its anxiety-relieving effect is mediated through its effect on dopamine and 5-HT receptors.
So, again, I am assuming that Abilify is related to 'benzos', somehow.
Please, anyone reading, my assumptions must be researched properly. What I'm getting at is; my wife also tried to ween off of Abilify (unsuccessfully). You mentioned "cold turkey" and weening together, but I thought the former means stopping abruptly? (which we know is generally not a good idea).
She 'weened' off Abilify, over the course of a year. I noticed some psychotic symptoms returning, but I hoped this was attributed to withdrawal effects, rather than a general, continued necessity for he drug.
After a particularly bad episode, long story short, she is back on a monthly 400 mg Abilify injection.
At the moment, my hope is to get a referral to a Doctor, specializing in menopause, if they exist in (Ontario) Canada. Even if we are lucky enough to find one, treatment etc., will be clouded by her current prescription.
I have to investigate "SERMs" further. IIRC, they are hormones that affect the brain, without the (breast) cancer risks of traditional HRT.
Has anyone had experience with these?
Thanks, Lela and all. Regards, Peter