My aim for this event is simply to raise awareness and some funds for Cystic Fibrosis (CF) and CF Ireland (CFI) through holding an evening of entertainment and showmanship where people can sing/rap/dance for cystic fibrosis as a means of fundraising.
CF is an inherited chronic disease that affe...
My aim for this event is simply to raise awareness and some funds for Cystic Fibrosis (CF) and CF Ireland (CFI) through holding an evening of entertainment and showmanship where people can sing/rap/dance for cystic fibrosis as a means of fundraising.
CF is an inherited chronic disease that affects the lungs and digestive system of about 1200 children and adults in Ireland. Ireland has some of the most severe strains of CF and the highest incidence of CF in the world.
CFI is a great support to CF sufferers and their families. They have been instrumental in providing essential tools to people with CF in order to maintain health as best as possible and in the developments of new generation drugs which correct the underlying genetic defect and cause of CF. These drugs have been life changing for many sufferers. Although not a cure, they are a significant step in the right direction.
As CF is a degenerative, lifelong condition, we can only hope that research into the development of these drugs will continue only become more effective so that, one day, CF is completely cured. Until that day, CFI will be needed and can assist in pushing for this research. Any donation- none too little- is greatly appreciated.
Open Mic Night for Cystic Fibrosis For Cystic Fibrosis Ireland
Words of support
Sorry I missed it! Well done on all your hard work! x
You are a rockstar, sorry i missed the night
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Donation summary
Total raised:
€1,225
Offline donations
€375
Online donations
€850
About the Cause
Cystic Fibrosis Ireland
Cystic Fibrosis Ireland (CFI) is a voluntary organisation set up by parents in 1963 to improve the treatment and facilities for people with cystic fibrosis in Ireland.
CFI are supported by fundraising and voluntary contributions and are solely concerned with the well-being of people with Cystic Fibrosis.
Cystic Fibrosis Ireland aspires to be a leading advocacy group in Ireland that professionally represents its membership with empathy while achieving results by improving t