Proudly supporting Cystic Fibrosis Australia
Newcastle Ball

Newcastle Ball 

Supporting Cystic Fibrosis Australia
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About Newcastle Ball

BRINGING BACK A LITTLE MYSTERY. On behalf of Cystic Fibrosis Australia and John Hunter Hospital Cystic Fibrosis Service, we are set to combine the history of yesteryear with the glamour of Hollywood. A premier black-tie charity ball at the historical City Hall, Newcastle will showcase fine wine and dining, with an amazing array of entertainment.

It's time to unmask the disease and find a cure. And the inaugural CF Masquerade Ball is the event, like no other to unveil your support and recognition to raise awareness and funds for research and services for families living with the daily challenges of Cystic Fibrosis.

Date: Saturday 7 October
Time: 6pm drinks on arrival. Seated at 6.30pm.
Venue: Newcastle City Hall
Dress: Black Tie, with a touch of masked mystery.

Disclosure: There may be patients with Cystic Fibrosis at the event some may carry harmful bacteria that may be dangerous to other CF patients. The organisers take no responsibility and recommend general hygeine principles are followed. Wash Hands frequently, Cover mouth and nose when coughing and sneezing. By purchasing a ticket you accept these terms and enter at own risk.

About Cystic Fibrosis Australia

Cystic Fibrosis (CF) primarily affects the lungs and digestive system because of a malfunction in the exocrine system, responsible for producing saliva, sweat, tears and mucus.

There is currently no cure. People with CF develop an abnormal amount of excessively thick and sticky mucus within the lungs, airways and the digestive system. The mucus causes impairment of the digestive functions of the pancreas and traps bacteria in the lungs resulting in recurrent infections which lead to irreversible damage. Lung failure is the major cause of death for someone with CF.

We advocate on behalf of our members to gain better access to services, obtain information or resources. On a larger scale we have been involved in several national campaigns to increase the rights of all people with cystic fibrosis.

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