by c4cfadmin | Oct 11, 2020 | Get Active Events
Our Cure4CF Army is already 30 strong! Be surrounded by thousands of runners from around the world in Australia’s largest and most prestigious Half Marathon event. The iconic course takes participants past the beautiful sights of Sydney’s harbour side and is open to...
by c4cfadmin | Oct 11, 2020 | Get Active Events
Join the Cure4CF Army in this year’s virtual City 2 Bay Fun Run! Led by CF Warrior and Cure4CF ambassador Emmah Money aka CF Mummy. Put on your war stripes and head into battle with us! This is a virtual event so register, pick your distance and complete your run or...
by c4cfadmin | Oct 11, 2020 | News
Ambassador Update – Mae Our Youth Ambassador, Mae has kindly given us an update on how school has been for her this year as she completes year 12 and on going to her school formal. School as a CF patient has been crazy this year. It has been much more...
by c4cfadmin | Oct 7, 2020 | News
Fundraising Ideas Facebook Fundraiser – Create a fundraiser for Cure4 Cystic Fibrosis on Facebook. Set a goal and encourage your friends to support a great cause. Quiz Night – Organise a quiz night. Invite friends and family and organise a fun night with a quiz,...
by Amy Hourigan | Jul 1, 2020 | News
Jonathan Despinidic Takes Over Cure4CF Jonathan Despinidic Jonathan Despinidic, or JD, was looking at a very short life expectancy after being diagnosed with cystic fibrosis at the age of 13. Now at 33 years old, he is one of only 653 adults living with CF over the...
by Amy Hourigan | Jun 22, 2020 | News
Kristy Thomas Takes Over Cure4CF Kristy Thomas Kristy Thomas is a communications specialist and a Mum to a little boy with cystic fibrosis. She knows all too well the impact cystic fibrosis has on sufferers and their loved ones. Sharing her story through social media...
by Amy Hourigan | Jun 22, 2020 | News
Emmah Money Takes Over Cure4CF Emmah Money Emmah Money lives with the life-threatening lung disease Cystic Fibrosis and knows firsthand the challenges that come with this debilitating, invisible disease. With a life expectancy of just 37, she was given up for adoption...
by Amy Hourigan | Jun 2, 2020 | News
Jen, James and Aveline Kozlowski Take Over Cure4CF Jen, James and Aveline CF Mum Jen, her brother and Cure4CF Ambassador for NSW – James and cute as a button CF Warrior Aveline are taking over for the week! James is the school principal at Endeavour Sports...
by Amy Hourigan | Jun 2, 2020 | News
Ben Mudge Takes Over Cure4CF Ben Mudge Ben Mudge is originally from Belfast, Northern Ireland. He was born with cystic fibrosis, a genetic disease that affected his lungs, pancreas, and other organs. Growing up, Ben was a sporty child who loved to play around with...
by Amy Hourigan | May 20, 2020 | News
Mae Johnson Takes Over Cure4CF Mae Johnson My name is Mae Johnson, I am 16 years old. I was diagnosed with cystic fibrosis when I was born and even though it makes my life more challenging I am determined to live life to the fullest and achieve all of my dreams. I...
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