Yeah, @creative_writer 🙂💜 the future, when it’s things that aren’t yet on the radar, are very uncertain, and imho, not worth too much consideration till the time comes when they become a blip 🙂🌺
Thank you regarding medication.. I hope that for us both too 🫂🌺
I am taking it for a bone marrow disorder 🙂
it’s true that lots isn’t known about medications - particularly in MH, however that’s also the case with some rare disorders..this one here is experimental 😉
And MH medications do come with stigma, I agree.
I think you’ve said it really well: you can’t think yourself out..I feel that with this problem I have which is virtually invisible - people often tell me I ‘look fine’ hehe. And it’s like that with MH… just because it’s not seen with eyes, doesn’t mean that without support things can be overcome 🙂🌺
I hope your afternoon is going ok 🙂🫂