What the CF!
Contact Us & Donate
Contact Us
To learn more about how you can get involved and help spread the question, What the CF?, drop us a line at Cystic Fibrosis Queensland.
Email: admin@cfqld.org.au or fundraising@cfqld.org.au
Freecall: 1800 670 990 (outside Brisbane)
Phone: 07 3359 8000
Post: Cystic Fibrosis Queensland, PO Box 2245 Chermside Centre, Q 4032
Follow us on Facebook: http://www.facebook.com/people/Cystic-Fibrosis/701953896
Follow us on Twitter:http://twitter.com/CysticFibrosis_
Donate to CFQ
Cystic Fibrosis Queensland receives only 46c per client per day from the government, when what we really need is $3.74. Donations are essential to helping us provide support services to families directly affected by CF.
Your tax-deductible donation will help to provide real assistance to these families across Queensland, Northern New South Wales and the Northern Territory.
"CF is such an isolating and debilitating disease, so any support we have is precious," says Merylene Osborne - Mum of Amy. "We're talking about supporting kids who are really sick - I know that the CF community all sees it the same way."
Make a donation now!
Regular Giving options
Leave a Bequest in your will 
Workplace Giving
Donate your shares
To learn more about how you can get involved and help spread the question, What the CF?, drop us a line at Cystic Fibrosis Queensland.
Email: admin@cfqld.org.au or fundraising@cfqld.org.au
Freecall: 1800 670 990 (outside Brisbane)
Phone: 07 3359 8000
Post: Cystic Fibrosis Queensland, PO Box 2245 Chermside Centre, Q 4032
Follow us on Facebook: http://www.facebook.com/people/Cystic-Fibrosis/701953896
Follow us on Twitter:http://twitter.com/CysticFibrosis_
Donate to CFQ
Cystic Fibrosis Queensland receives only 46c per client per day from the government, when what we really need is $3.74. Donations are essential to helping us provide support services to families directly affected by CF.
Your tax-deductible donation will help to provide real assistance to these families across Queensland, Northern New South Wales and the Northern Territory.
"CF is such an isolating and debilitating disease, so any support we have is precious," says Merylene Osborne - Mum of Amy. "We're talking about supporting kids who are really sick - I know that the CF community all sees it the same way."
