Streetschool
Join Us on an Incredible Journey to Support Cystic Fibrosis Patients!
This amazing team from streetschool embarked on a monumental expedition to Everest Basecamp, symbolizing the resilience and strength of those battling Cystic Fibrosis.
Imagine the breathtaking moments and challenges they’ll face along the way – pushing through when the going gets tough, just like individuals living with CF.
Climbing to Everest Basecamp isn’t just a physical feat; it’s a testament to the daily battle of individuals with CF. It’s about pushing past limitations, embracing the journey, and creating unforgettable moments.
This journey reflects the unseen efforts, sacrifices, and support that involve the whole CF community.
Join us in this extraordinary fundraiser as we climb towards our goal of raising awareness and support for those affected by Cystic Fibrosis.
Together, let’s show that with perseverance and unity, anything is possible. Let’s conquer this challenge and make every step count!
All funds raised will go towards providing access to life-saving medication.
To donate:
Use our bank details with Reference ” Streetschool “
Meet More CF Warriors
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.
O2 For Beth Too
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.