Finding a cure for Cystic Fibrosis by the 2022 World Cup


He plays for the ?BlueBottles? in Sydney?s Mosman division and is one of the competitions leading goal scorers.
He?s a mad Manchester United supporter to his father?s eternal regret.
He?s a passionate supporter of Sydney FC.
He?s a little Aussie Football tragic.
He?s a future Socceroo and he?s living with Cystic Fibrosis.
Imagine always being short of breath, always being congested, and only being able to breathe in enough air that you could suck through a straw.
That?s what it can be like living with Cystic Fibrosis.
Angus is on a daily cocktail of pills, nebulizers, chest physiotherapy and coughing exercises.
For Angus, his game starts before he gets onto the field.
Help Angus get to the 2022 World Cup by donating to the Cystic Fibrosis Association of NSW for medical research to find a cure for Cystic Fibrosis.
Angus will do his bit to play for Australia in the 2022 World Cup.
Do your bit to help him get there. Be part of the team in finding the cure for Cystic Fibrosis by 2022.
All donations can be made at:
Thank you for your support.