Proudly supporting Cystic Fibrosis Australia
65 Shows in 65 Minutes

65 Shows in 65 Minutes 

Supporting Cystic Fibrosis Australia
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About 65 Shows in 65 Minutes

Hi everyone! I am a musician and cystic fibrosis carrier. To honour and help those in my family, and beyond, who live with CF I am using my skills to create a super exciting, immersive and fun night! The challenge to performers - to present your favourite musical in 50 secs. I am accepting submissions and we will choose 65 of the best! 65 shows in 65 minutes...there will be mayhem! The selected performers will perform on the night alongside local musicians and you have to see if you can guess each show. There will be prizes for the highest level of correct guesses! For more information about the event head to I am doing this to raise much-needed funds for Cystic Fibrosis Australia. You can donate here or purchase a ticket to the event through All profits from the event will be added to the total donated here! This work is really important, and I want to do what I can to help. But there is only so much I can do on my own. You can help too, by donating to my page. Any amount you can give makes a difference! You can also support me by encouraging others to get involved too. Please email the link to my page to your friends and family, or share it on social media. Thank you for your generosity and support -- it means a lot to me. Together we can help Cystic Fibrosis Australia create the world we want to see. Emma

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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