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
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.
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.