why is it that PCOS is so poorly treated in the healthcare sector❓
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1 in 10 people who menstruate have PCOS, so why is it that doctors are leaving patients feeling so isolated and helpless after communications? negative experiences with healthcare providers and GPs often have a lasting impact on the mental heath and wellbeing of those living with pcos.
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according to research by Professor Ogden, those who had felt uncomfortable with the consultation process were "more likely to report poorer body esteem, reduced quality of life and greater concerns about health in later life.”
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Professor Ogden continues, “Over a quarter of those surveyed were dissatisfied with how doctors managed their distress and were unhappy with the lack of rapport they had with their practitioners”
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in light of this research, we thought we would share some of our favourite creators shining a light of life with PCOS. these inspirations are supporting fellow pcos sufferers with pain relief tips, wellness hacks and an understanding ear. let's stick together and fight for the kind, beneficial treatment we deserve 🚀
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this research was published in the British Journal of General Practice. University of Surrey Ogden, J & Bridge, L., (2022) How communicating a diagnosis of polycystic ovarian syndrome (PCOS) impacts wellbeing: a retrospective community survey. 📸 @harnaamkaur @thatgirlsare @imogenfkingivy @lookgoodinpcos