Dr. David Traster explains clinical neurology, shares how his own delayed diagnosis shaped his approach to patient care, and explores how neuroplasticity and targeted rehabilitation can support brain recovery.

Drew Motiv shares his journey through addiction, suicide survival, and the hard road to recovery, healing, and purpose.

From a sudden loss of movement to an inspiring story of recovery, Ra-Jon James shares his journey of surviving Guillain-Barré Syndrome and the grueling, triumphant process of relearning how to stand and walk again.

Patient experience expert Meredith Mangold shares how to build a sustainable support system that honors the invisible journey.

Yale-trained scientist and autism parent, Dr. Teresa Lyons demystifies the autism spectrum, offering families a clear roadmap from identifying early red flags and debunking common myths to implementing evidence-based, personalized support strategies.

Exploring reproductive acupuncture, emotional wellness, and new technology shaping fertility care.

One woman’s story of autoimmune disease, emergency diagnosis, and life after vision loss.

Carolyn Routh, of the band Nu-Blu, opens up about health, resilience, and returning to the stage after life-altering medical events.

One woman’s journey through devastating chronic pain—and the personalized care that helped her reclaim her life.

Genetic Counselor Amy Patterson shares about genetic screening and testing available for rare disease including her speciality of skeletal dysplasia.

Genetic Counselor, and our podcast co-producer, Kira Dineen shares her insight on when to pursue genetic counseling and how genetic counselors can help people in the rare disease community.

At 16 years old, Leanna Scaglione was diagnosed with NF2-Related Schwannomatosis, having to leave her dreams of becoming a ballerina behind, she altered her athletic journey becoming a multi-marathon runner.

Dr. Fumihiko Urano shares his world renowned expertise from leading the clinical, translational, and interventional studies of Wolfram syndrome and related disorders.

From misdiagnosis to empowerment, Rachel Hyman and Cathy Gildenhorn share their real stories of being diagnosed with a rare disease, Wolfram Syndrome, in adulthood.

Nikki McIntosh, a rare disease advocate, shares how her family has navigated her son’s diagnosis of Spinal Muscular Atrophy (SMA).

Kenny Kasnett, a seasoned executive and entrepreneur whose life took an unexpected turn with a diagnosis of interstitial lung disease (ILD) leading to a choice, should he get a lung transplant?

Pruitt was born with ornithine transcarbamylase (OTC) deficiency, hear from his mother Jordan Kruse and geneticist Dr. Susan Berry about the condition and how healthcare can do better.

Discover how Latin America offers new opportunities for clinical trials and how Julio G. Martinez-Clark is leading the way in advancing medical device innovation in emerging markets.

Elizabeth Ansell, founder of #NotJustFatigue, joins the show to share about living with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and the advocacy she does through her non-profit.

Sally Pirie opens up about the condition that has plagued her family for decades: Hereditary Angioedema Type III (HAE-3).