Dharma Breathes
My name is Dharma Bredell
I am 23 years old and just before my fifth birthday, I was diagnosed with Cystic Fibrosis.
My normal day consists of two nebulisations with chest physiotherapy in between twice a day, in the morning and evening.
I take a handful of supplements and medication to keep me going and I have a port-o-cath to make IV access a little bit easier when I am admitted to the hospital.
My normal might be different from yours, but I wouldn’t change my life one bit. I have a saying, “I have Cystic Fibrosis, Cystic Fibrosis doesn’t have me” and I live by that.
I am currently a Honours Psychology student, working towards becoming a registered counsellor in South Africa. I have a passion for counselling, motivational speaking and spreading awareness for CF!
I am fundraising and raising awareness for a life-saving treatment called Trikafta. When I was younger, and the hospital stays got a little too long and the nebulisations and medications became too much, I told my parents I wished there was a simple treatment in the form of a pill.
Now there is, but without your help, I and many others like myself will not be able to access this treatment.
Let’s show Dharma our support by ordering some really awesome and breathtaking Merchendise from her online store!
Meet More CF Warriors
Baby Juvan’s story
Baby Juvan has had 5 major surgeries and needs continued treatment for Cystic Fibrosis.
Amazing Myrnalise
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.
Memory Makers raising funds for Cystic Fibrosis
We make small pieces of mixed media art and sell them as gift tags.
Battle to breathe: The Olivier Siblings
Joshua (18) and his sister Mia (15) were both born with Cystic Fibrosis.
Ruach: Life-giving breath of God
Ruach’s name means Life-giving breath of God
Richard’s story of hope
I am Richard Burger and I have a genetic lung disease called Cystic Fibrosis.






