I have Violets permission to post this...I have set up a Facebook page (with two other ladies) for Pudendal Neuralgia pain for ladies and men who live in the UK. We have been going just over two months and it is proving very successful. It does not replace this page, obviously, but it does allow to discuss on UK time and we can discuss what specialists the UK has to offer.
If anyone is interested, please private message me as there are three who have contacted me as it would be great if you wanted to join. If anyone has emailed me to 'Bertie' then please email me again in case i didn't receive it. The group is secret so it's a very safe place for us to openly discuss anything we need too...
