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My Breathe Team Story

Fadela Macdonald

Fundraising for BMW Berlin Marathon

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Fadela MacDonald



On November 16, 2023, I lost my greatest supporter — my father — to Pulmonary Fibrosis, a progressive and incurable lung disease that slowly takes away the ability to breathe.

Grieving his loss has been incredibly difficult, but running was  my way of healing. My dad always encouraged me to run a marathon. He believed in me, even when I didn’t believe in myself.

One year later, on November 16, 2024, I honored his memory by running my very first marathon — for him. Every race since has been a tribute to his strength, his love, and his unshakable belief in me.

Today, I proudly run as part of  Breathe Team, raising awareness and funds for Cystic Fibrosis. While it’s a different disease than what took my father, both are life-limiting conditions that rob people of their breath and their futures. That connection is deeply personal to me.

I run to remember.
I run to raise awareness.
I run so that one day, no one will lose a loved one to these devastating lung diseases.

If you can, please support my journey. Every step I take is for my dad, and for everyone still fighting to breathe.

There is currently no cure for cystic fibrosis and too many people with CF die young. I’m running to help change that reality.

CF is a genetic, life-shortening disease that devastates the lungs, pancreas, and other vital organs. CF makes it difficult to breathe and fight life-threatening infections, often leading to extensive lung damage and respiratory failure.  

Every person born with cystic fibrosis is on a unique journey and experiences this challenging disease differently. While progress has been made, a long road lies ahead for far too many people fighting this terrible disease. We need a cure so that everyone with CF has a better chance to live a long, healthy life.

Will you help us end cystic fibrosis?

By donating to my fundraising goal, you have the power to advance the research and science needed to drive our shared dream forward – a cure for everyone with CF.

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$1,355
raised of $4,000 goal
 

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The CF Foundation is committed to providing a safe, inclusive, and healthy experience for individuals attending Foundation Events. Individuals attending CF Foundation events must abide by the Foundation's Attendance Policy and accompanying guidelines, which include guidance for event attendee's living with cystic fibrosis.