Long story short, I have MH issues (undiagnosed but GP prescribed me citalopram a few months ago and I do think it's taking the edge off). Have also tackled with various stints in therapy over the years.
DH has very negative opinion of MH issues after being in an abusive relationship in his early 20s with a woman who used her MH issues as an excuse to abuse him/blame him for everything.
I went through a total breakdown 3 years ago and had to dig myself out, eventually did swearing to myself I'd not do that again and sought help/pills. However still 'ashamed' and haven't insisted DH uses his work insurance to get me the psych appt I was given a referral for months ago. Own fault etc.
Part of not chasing it up was we are moving to the USA and I wasn't sure how a UK diagnosis (if any), would 'stand' or if I had time to get a diagnosis in the timeframe. Decided would approach MH issues when in the US. Decided to make an appointment with my GP to discuss whether she can give me extra pills (not sure if this is possible), to cover the adjustment period. Mentioned this to DH.
He said that as medications are very expensive in the US he had hoped I'd stop taking the anti-ds as 'we're not sure if they're making a difference anyway' (true). Then a load of guilt-tripping about money etc.
I said 'but what about the side-effects, I can't just stop!', and he said 'yeah but that's only a few days versus thousands of dollars for pills you might not even need'.
I have been up for hours brooding over it. I feel really shocked and... horrified really. Feel really diminished and shit. I CAN insist on seeing a psych, getting medication and whatever else in the USA but I really would rather be facing it all with his support. AIBU to think he is a wanker?