





The Heart of the Philip Barton Foundation
We are dedicated to bringing compassion to every journey, offering unwavering support to individuals and families, and leading bold advocacy efforts for those affected by Pulmonary Fibrosis, all to create lasting, positive change.
Our Mission
At the Philip Barton Foundation, our mission is simple: to offer compassionate support and essential resources to those living with Pulmonary Fibrosis and to help guide their families through the arduous journey that comes with it. We're here to raise awareness, push for innovative treatments, and fund crucial clinical trials that can make a real difference in patients' lives.
While we focus on South Africa, we stand in solidarity with patients and families everywhere, advocating for awareness, dignity, and care for all within the Pulmonary Fibrosis community.
Philip Barton:
A Legacy of Strength
Philip Barton was more than a brilliant mind—a devoted father, a loyal friend, and a man of unwavering resilience. Known for his wisdom, generosity, and unshakable spirit, he left a lasting impact on all who knew him.
Beyond his intellect, Philip found joy in life's simple pleasures. He cherished time with his family, enjoyed long walks along the beachfront promenade, and deeply loved reading. In his younger years, he was an avid horse rider, and before his diagnosis, he found freedom in running and golfing.
In late 2020 to early 2021, Philip was diagnosed with Pulmonary Fibrosis following a battle with Covid-19. A man who had always valued an active lifestyle faced the devastating reality of losing his ability to do what once came so easily. Simple tasks became battles. The disease stripped away his quality of life. Yet, through it all, he fought with immense courage, never losing sight of who he was. He passed away on 12 March 2023 after a valiant battle with the disease.
Philip lived by the words: "Fear knocked on the door, courage opened, but when he looked around, there was nothing there." This philosophy guided him through life's challenges and continues to inspire those who carry his legacy forward.
The Philip Barton Foundation exists to honour his strength, resilience, and belief in standing up for what you believe in. As his daughter, Mila, beautifully puts it:
"My father was courageous, proud of who he was, and my biggest inspiration."
Philip's legacy lives on through the work of this foundation, ensuring that no one facing Pulmonary Fibrosis has to navigate the journey alone.


Mila Barton:
A Vision for Change
Her journey is one of resilience, empathy, and an unwavering commitment to her father's legacy as she works tirelessly to empower patients and families affected by this disease.
"This foundation is a way for me to carry my dad's strength forward. Every person we support, every story we hear, and every bit of progress we make means his legacy is still doing good in the world." - Mila Barton
The Heartbeat of Our Foundation
A visionary leader dedicated to advancing care for Pulmonary Fibrosis patients and their families.

Mila Barton
Mila Barton founded the Philip Barton Foundation to honour her father’s legacy and support families facing Pulmonary Fib

Catherine Young
Catherine Young supports the Philip Barton Foundation as an Impact Mentor, guiding efforts to scale Pulmonary Fibrosis impact.

Ashley Harper
Ashley Harper supports the Philip Barton Foundation’s outreach as Marketing Assistant, helping share its mission and impact.
Our Commitment to Impact
From small beginnings, our dedication to supporting Pulmonary Fibrosis patients and their families is unwavering. As we grow, we aim to make a measurable difference through advocacy, research funding, and patient support.
Support for Patients and Families
We provide trusted information, emotional support, and a welcoming community to help individuals and their loved ones navigate Pulmonary Fibrosis with dignity.
Advancing Research and Innovation
Through funding and advocacy, we drive clinical trials and groundbreaking research to improve treatment options and enhance quality of life.
Raising Awareness and Advocating for Change
Pulmonary Fibrosis is often overlooked, especially in Africa. We amplify patient voices, educate communities, and push for better care and access to treatment.
Join Us in Making a Difference
If you're passionate about supporting those affected by Pulmonary Fibrosis and want to be part of a mission-driven team, we'd love to hear from you. Whether you're interested in working with us or collaborating on our projects, we can help create real change for patients and their families.
