Guys,
As some of you know I’m from the UK and live in the north east of England. When discussing all of this shit (PFS) one of them asked if fellow sufferers ever meet up to talk through it all,eg symptoms, impact, ideas F2F. While I recognise we all have our own lives I don’t think it would be a bad idea. As PFS is a lonely disease and those in our lives can’t relate! Just putting it out there to what you think. I’m not knocking the forum as it’s provided me with lots of info from guys in the same boat. Cheers