I just wondered what type of support, information etc. you have received from your GP since diagnosis?
I got diagnosed January 2017 and wasn’t given any information at all about PCOS and they just suggested I take the pill to help with hormones (could only put me on mini pill at the time as I suffered from migraines and smoked) but that just made me bleed all the time.
So I’m currently not taking anything to help with the symptoms and neither doctor or nurse have really discussed this any further with me. Love the NHS and all they do, this isn’t a dig!
Is it because PCOS isn’t deemed to be that big of a deal? Not enough real information about it? Just curious how other people have got on since diagnosis. I’m new here so if this isn’t the type of thing that usually goes on in the forum apologies!