PELVIC ORGAN PROLAPSE
There. In big letters. Affects so many of us (there are some really supportive threads on MN) but it needs awareness raising.
I belong to APOPS-
www.pelvicorganprolapsesupport.org/pelvic-organ-prolapse-the-silent-epidemic-3
A really informative and helpful site. There is also a FB site that again, is extremely informative and supportive.
The founder has recently embarked on a large campaign to highlight awareness. I enquired if she had approached Mumsnet (as it seems obvious) and she informs me that yes, she had approached MN but sadly had no response?
Is this something that can be rectified revisited? It's such a huge, invisible and relatively unknown condition that I'm sure MN would be a great advocate. Perhaps MN could invite the founder to a Webchat?
I, for one, have suffered, am still suffering in fact. I considered myself to be quite well informed and I'd never heard of it! I actually though it was predominantly a "male" thing, then realised I was muddling it up with prostate 
Anyhow, would anyone like to badger suggest a Webchat about it? The founder has said she is more than happy to send the book and I'm quite sure she's also jump at the chance to use MN's worldwide platform to raise awareness.
Thanks in advance