Hi! I was diagnosed with PCOS last Nov. after having super inconsistent, heavy periods, some hair growth, oily skin, acne - basically all the symptoms the NHS website tells you to look out for - super helpful, for once. I was prepared to be diagnosed, honestly, I felt quite relieved that it had happened quickly and my GP listened, the ultrasound was pretty weird and uncomfortable (especially being told to drink a million litres of water and thinking my bladder was gonna burst there and then) and within a week my GP called and said it was quite a 'severe' case of PCOS - which definitely didn't sit well with me.
Told my parents, only for my dad to say ' so you can't have kids then?' and my mum to say 'it's super common, you're fine', two verrry different responses. I instantly felt like it didn't matter - my diagnosis was common, can live with it, not a big deal, so who cares? Suddenly, as if over night, my friends became experts in the field and told me 'oh you just need to exercise more' or 'you'll have kids just fine, this woman said she fell pregnant straight away!'. As much as I appreciated their intentions, all it did was invalidate me for a minute. I don't want pity, I think most women on here can agree that doesn't solve anything, but I'd like for someone to just listen to my worries without them being invalidated by people who don't live with this condition, who don't feel insecure about the hair that grows (literally) everywhere, who don't worry about the fact they are more likely to develop diabetes and potentially struggling to conceive.
I'm really not dramatic, I was very much accepting of the diagnosis, honestly, felt good to know I'm not insane from thinking I had it. I'd just maybe like to not be told how MY body will react to something someone else DOES NOT have - I'd never try to inform/correct someone on their own illnesses, etc., so it feels sorta disheartening that others do - has anyone felt like this? I'm not sure if it's my age (I'm 20) that people still feel the need to treat me with kid gloves sometimes but it would be nice to meet people who are in a similar boat to me, so it doesn't feel like such a lonely diagnosis.
Hope everyone's well in these trying times!