Cystic Fibrosis Queensland
Field of Interest
- Health/wellbeing and medical research
- Individual/family services and support
Target Population
- People with a disability, illness or disease
- People experiencing socio-economic disadvantage or vulnerability
Cystic Fibrosis Queensland is the peak NFP charity dedicated to supporting individuals and families affected by cystic fibrosis across QLD, the NT, the ACT and northern NSW.
Our charity seeks to alleviate the financial, emotional, and physical burden of the disease experienced by sufferers and their immediate family.
Despite people with cystic fibrosis living longer lives than ever before, there remains no cure. The chronic disease remains life limiting and while it is no longer just a lung disease, many of our members will die of a myriad of comorbidities. We fund research, advocate at a State and Federal level, and provide a range of practical support and service programs to our members and their families.
Our Values are:
– To be relevant to our community
– To work collaboratively and advocate for our community
– To be effective in the work we do for our community
– To be respectful of our community, our stakeholders and each other.
Our Strategic Priorities are:
– To continue to proactively drive the agenda by being a leading voice for our community
– To be relentless in our pursuit of programs which increase our members’ overall well-being and mental health
– To be a strong advocate for our community, increasing the access and equity to medication, disability, service and support programs
– To ensure our charity remains financial.
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