Projects

JC need Trikafta urgently to be able to breathe normally, however he is at the start of a 24 month waiting period before his medical aid will cover it. Read his story here.

The road was rocky and scary at times but today 34 years later I am as healthy as can be. Living life to my fullest with my life partner and 7 year old twins.

I have lost many friends and 2 family members to this disease, and I am planning to continue fighting not only for the fallen ones but the family that I have in my life.

This is not to say that the journey was not tough and exhausting at times.
It was a journey of faith, and it still is.

Caring for Kayla is an initiative that was started by Kerry, mom to Kayla.

My name is Chantelle van Wyk and I have cystic fibrosis. I have a 7yr old son. It was extremely hard coping with being “less” of a mom than what I would like to have been for him.

Jaco used all of his savings and borrowed the money to pay for life-saving medication.
He is doing better already and coughing much less but he urgently needs your support to repay the loan and use the money towards his next batch of medication.

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.

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.