Affecting the lungs and digestive system, Cystic Fibrosis (CF) is the most common life-threatening recessive genetic condition in Australia. Children born with CF live with a daily regimen of physical therapy and around 40 enzyme tablets to aid digestion. Whilst there is no cure as yet, average life expectancy has doubled in the last 20 years and is now into the late thirties. CFNSW provides a range of support services and funds vital research through the Australian Cystic Fibrosis Research Trust.
Your support will help CFNSW continue in its mission to improve the quality of life for those with CF and their carers, through the provision of important services including counselling, education, financial assistance, respite and practical support in dealing with the day to day challenges of living with CF.
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Phone: 02 9878 2075
Fax: 02 9878 4890
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