Cycling for a purpose

Abi dreams of opening a coffee and bubble tea café where people can relax, enjoy a good cup of coffee. She wants to use the proceeds from the shop to fund medication for people with Cystic Fibrosis.

Samuel is 6 years old, and at the young age of 10 months, Samuel was diagnosed with Cystic Fibrosis.

Elizabeth was only 2 years old when we came to learn that monthly visits to specialists and regular extended hospital stays would become the norm, nutritious food would never be enough on its own and each breath she would ever take, would be a battle.

Ella, a remarkable 10-year-old battling Cystic Fibrosis, has to fight for each and every breath she takes. 

Vanna, was diagnosed with Cystic Fibrosis (CF) at the age of 3 months.

Baby Juvan has had 5 major surgeries and needs continued treatment for Cystic Fibrosis.

Myrnalise’s journey from a determined child to an aspiring lawyer is a testament to the power of perseverance and the unwavering commitment to making a difference in the lives of others.

Joshua (18) and his sister Mia (15) were both born with Cystic Fibrosis.

Ruach’s name means Life-giving breath of God

I am Richard Burger and I have a genetic lung disease called Cystic Fibrosis.