Interesting bit about endometriosis on Radio 4 this morning - saying huge percentage of women suffer this and can take years to get a diagnosis. There was a women being interviewed about the agony she had gone though for years and how hit and miss the diagnosis had been for her. Also talking about a cancer drug that is being tested now. I can't a find a link to this mornings item. But this from oct:
MPs to launch inquiry into endometriosis care
My thought is if it is so common why are doctors not more aware of it? Various sites say it takes on average
8 years to diagnose. Why?
Why does it take 8 years to diagnose endometriosis?
This rings very true
My grrlf had such severe pain every month that when she had peritonitis from a burst bowel she thought it was period pain. Despite all kinds of intrusive tests they never did find the cause of her gynae pain, nothing wrong with her I think they said, but did offer to remove her uterus, which is not a solution that many women in their 30s would find acceptible. I think they take her pain more seriously more quickly now - only because she can now say
'on a scale of one to peritonitis - it's 11'