TRX Electronics and Pachas Restaurant donate R400 000

We deeply appreciate the support from companies like TRX Electronics and Pachas Restaurant – Maroelana Pretoria who are instrumental in advancing our mission to improve the lives of those impacted by Cystic Fibrosis.
We believe that everyone should have access to this life-saving treatment for improved quality of life and extended life expectancy.
Meet More CF Warriors
Help JC breathe
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.
There is always hope
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.
My Battle with CF
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.
Family Schaper Shout-Out
Family Schaper Shout-OutAbout the projectThank you to family Schaper who entrusted Breathtaking Fundraising Npc to collect the medication on their behalf from the pharmacy in Argentina and a big shoutout to Esthe Smith (esthe leather shoes) for donating to this cause....
Bea’s story of hope with Cystic Fibrosis
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.
Kayla
Caring for Kayla is an initiative that was started by Kerry, mom to Kayla.
Chantelle’s Story
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’s Journey
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.
Let’s do this for Janco
We want Janco to live and breathe freely and we want you to be a part of his journey. Read his story here.
Cesare’s Story of Cystic Fibrosis
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.