There is one on here if you haven't already seen it. There's also www.pwcf.net
The trouble is, for some reason, CF chat rooms don't tend to be all that busy. There is another website, where there's usually always people online: www.cftrust.org.uk
It's a busy site, so you tend to get responses to things quicker, and reliable information. It is UK based, but I know there's a few people from other countries who visit the site.
Hope this helps!
It's true!: Smile and the whole world smiles with you. Frown and the world turns upside down.
Diagnosed with: Cystic Fibrosis, Asthma, ABPA, Clinical Depression, Mild liver cirrohsis, mild osteopenia. Waiting for final diagnosis on Muscular Dystrophy type symptoms.
Allergies: Any dressing except Mepilex border. Even plasters make my skin blister. Hayfever, Tazocin, Tobromycin, Ibruprofen, Asprin, Codeine, Mirtazapine.
I have a pretty little port-a-cath on left side of chest wall