TRX Electronics and Pachas Restaurant donate R400 000

We want Janco to live and breathe freely and we want you to be a part of his journey. Read his story here.

Ceasar’s liver and kidney functions need to be monitored regularly. For this reason he needs to be on a different medical aid plan – to cover extra medical costs.

Zea’s family did not know what was wrong with her until she was diagnosed at the age of 13. Getting access to Trixacar has been a life-changing experience.

Marnus extremely sick from birth. In 2009 at the age of 14 years drastic actions had to be taken. A feeding tube and Port were his only hope.

Scarlet has endured so much already and this medication could make a life-changing difference to her health in such a way that she can live a life with easier breathing and less hospitalizations.

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.