Bonnie Schneider leads the IGA Nephropathy Foundation and has been on a long journey advocating for this condition for 21 years since her 13-year-old son was diagnosed.

Bonnie shares how she transformed a mother's determination into a global movement that's helped bring the first specific treatments for IGA nephropathy to market after decades of relying only on steroids. We explore the challenges patients face, the breakthrough treatments now available, and why this is such an exciting time for the IGA nephropathy community.

Amy Dixon is a remarkable patient advocate in ophthalmology and USA Paralympian. Amy shares her powerful journey living with glaucoma and uveitis, having undergone 42 surgeries to save her remaining 2% vision. She discusses the critical importance of early diagnosis, treatment compliance, and establishing a partnership with your healthcare providers. Amy also reveals her passion for patient advocacy and her mission to ensure better support for those diagnosed with eye conditions. Join us for this fascinating conversation about living with vision loss while maintaining an extraordinary life.

Stephanie George is a patient advocate and peer mentor for the Sickle Cell Society. Stephanie shares her powerful personal journey living with sickle cell disorder, from childhood experiences to her work supporting young people with the condition. She discusses the unpredictable nature of sickle cell pain, treatment challenges, healthcare disparities, and the importance of awareness and community support. Join us for this illuminating conversation about a condition that impacts thousands of lives worldwide.

In this episode Scott McLean from the Haemophilia Society shares his personal journey living with severe haemophilia A, from childhood challenges to the transformative treatments available today. We explore the evolution of care, the psychological impact of the condition, and how modern therapies are allowing people with haemophilia to live fuller lives than ever before.

Gabrielle Davis is a patient advocate living with and championing awareness about lupus. Gabrielle shares her deeply personal journey—how she turned a life-altering diagnosis into a mission to educate, inspire, and build community for others living with chronic illness.

We talk in detail about experiences navigating the healthcare system, balancing mental health, and finding hope in the toughest moments.

This episode brings you a personal, unfiltered look at what it means to face a chronic condition head-on. Andy Collinson, isn’t just a patient—he’s a passionate advocate who’s transformed his lifelong battle with atopic dermatitis into a powerful mission for change. He shares the highs and lows of navigating a healthcare system that often underestimates the severity of skin conditions, and he reveals how emerging treatments are bringing hope to those in the thick of it.

So, whether you’re living with a chronic condition, supporting someone who is, or simply curious about the human side of health innovation, this episode is packed with insights.

In this episode we speak with Heather Russell-Kay, a dedicated advocate for individuals living with multiple sclerosis. Heather shares her deeply personal journey—from navigating the complex path to diagnosis to advocating for better understanding and support for MS patients. This conversation highlights why patient voices must guide how we approach treatment, care, and research into new drugs.

This episode features Kirstin Spencer, a patient advocate with MetUp UK and a patient expert for NICE and SMC. After her own challenging journey with breast cancer, Kirstin has dedicated her life to closing the gaps in care between primary and secondary diagnoses. From raising awareness about metastatic breast cancer to addressing systemic challenges in treatment, Kirstin brings a wealth of knowledge and an unyielding commitment to empowering others.