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Sharon Manship

Sharon Manship

Public health researcher at the University of Kent, co-founder of the Inclusive Women's Health Research Group, and lay member on the NICE PMOS guideline committee

Jul 29, 2026

GeorgieHOST
2:45
Can you tell us a little bit about your experience of having PMOS, how it affected you? Yeah,
2:54
sure.
2:55
So I guess for me, it's been going on for over 30 years.
2:58
I had symptoms from my teens and I'm now in my mid 40s.
3:03
My symptoms included an irregular cycle, often having very painful periods, issues with my weight and also my mental health.
3:12
And in my teens, it was a case of things were probably settled down or this is normal for a teenager, but when it continued, in my 20s I tried seeking support but the GP that I saw at the time unfortunately fobbed me off and told me it's just part of being a woman it's something we have to put up with and also that there wasn't any point in doing blood tests as they're not accurate for women's hormones so for a long time after that I believed it was something I just had to put up with although I did research into it myself and I had an inkling that it was PCOS as it was called at the time.
3:45
And then finally it was in my mid thirties that I saw a new GP and they organised an ultrasound to investigate my symptoms and then I got my diagnosis of PMOS.
GeorgieHOST
4:42
How do you think that might make a difference?

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