Cycling for a purpose
Raised: R90 000
Donation amount is adjustable.
For direct donations please use reference “CTCT 2026” to donate towards this campaign
Bank details:
Bank: FNB
Account Holder: Breathtaking Fundraising NPC
Account Type: Gold Business Account
Account Number: 63029888287
Branch Code: 250655
SWIFT code: FIRNZAJJ
Feedback about CTCT 2025:
This year we will be partnering with CTCT to raise awareness and vital funds for Cystic Fibrosis.
Our BREATHTAKING TEAM consists out of 31 cyclists and they will be looking BREATHTAKING FOR CF.
Date: 8 March 2026
Cape Town Green Point Stadium
Smiley & Dirk Smit
Dr Jaqui Batt
Casper Badenhorst
Burger Coetzee
Neal de Graaf
Vredendal team
Erna van Zyl.
Esthé Erasmus
PC Blom
CALL TO ACTION:
Please support our efforts to raise funds for CF by donating. All funds raised will be going towards medical equipment like nebulizers and oxygen machines for people with CF who do not have access to modulator therapy yet.
Meet our CF Warriors
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.
Zea found new hope and energy
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’ story: Living with Cystic Fibrosis
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’s story: Living with CF and new 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.
Aspiring Abi’s Story of hope
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.
Super Samuel and Cystic Fibrosis
Samuel is 6 years old, and at the young age of 10 months, Samuel was diagnosed with Cystic Fibrosis.