Quiz Night – 28 Aug 2020 8PM

The Central Region Cystic Fibrosis Association invite you to join our online quiz night fund raiser to help make a difference to those with CF. Cash prizes for the winners Invite your friends and come have some fun while supporting a great cause. BUY YOUR TICKETS...

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A first chance at life after transplant- Fawn Rogers

A first chance at life after transplant- Fawn Rogers

Hello, I’m Fawn, Cystic Fibrosis owner, double lung transplant recipient and lover of life.    I was born in Zimbabwe but I was the only CF patient in the country and had to travel often to see specialists and get my meds from SA. I eventually...

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CrossFit changed my life! – Louise Coney’s CF story

CrossFit changed my life! – Louise Coney’s CF story

Where my story began I was diagnosed with Cystic Fibrosis at birth when I was born with a meconium Ileus, with the delta F508 mutation. My parents were told I would live till I was 7 years old….both being Engineers, and determined individuals, they decided to...

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Nutrition in CF- Maintaining weight and diet tips for CFRD

Nutrition in CF- Maintaining weight and diet tips for CFRD

Eating well, and maintaining a healthy body weight are vital for individuals with Cystic Fibrosis (CF). A good nutritional status has been directly linked to improved lung function, reduced chest infections and ultimately, improved survival rates. However, as many CF...

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