I don't know one in Australia, but the Pulmonary Fibrosis Foundation has many services, including on-line support group and if anyone could hook he up, I suspect they could.

I am not sure about a ''Special'' Group but we have a few with it plus a good friend of mine in the US is pretty clued up on the disease..........Anyway if your friend wants to join us, she is more than welcome to come over. Besides we can provide answers to her questions, as best we can....I can approve her if i see her among the requests so it would help with a name or part of the country.....otherwise just apply..

https://www.facebook.com/groups/1631814360423043/

I will look into the site again Every time I go into the sites I start to think there must ne an easier way to get all the information being in a country area makes it a little slower to catch on with new releases I some times think the sheep must think faster than out politicians have a great day

I don't know if I answered you or not Stretch but I get the the Lung Foundations Lungnet each month good info there and the even have seminars to go to to find out more imformation about your illness. the site is www.lungfoundation.com.au hope this helps yoour friend..xx

many thanks I will pass on the message have a great day