Rare Care Podcast
Rare Care Podcast
Rare Disease Advisor's Rare Care Podcast features exclusive interviews with experts and stakeholders from the rare disease community.
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Rare Care Podcast
Category
Podcast website
Latest episode
Jul 6, 2026
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Episodes
232: An Interview With John MacMahon, CEO of CytoKind, on the Benefits of Artificial Sunlight 06.07.2026 16:20
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews John MacMahon, a New Hampshire-based medical devices company that specializes in phototherapy to treat fatigue in people with multiple sclerosis.
231: An Interview With Dr. Eric Small, Former President of ASCO 29.06.2026 14:58
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Eric Small, MD, who recently stepped down as president of the American Society of Clinical Oncology (ASCO).
230: An Interview With Jessie Dubief, Social Research Director at Eurordis, on Mental Health in Rare Diseases 23.06.2026 13:54
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Jessie Dubief, social research director of Eurordis, about the organization's new survey on the importance of addressing mental health among both patients and caregivers affected by rare diseases.
229: An Interview With Naomi Aziz, Patient Advocacy and Engagement Lead at the Endometrial Cancer Research Foundation 16.06.2026 21:46
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Naomi Aziz, patient advocacy and engagement lead at the Endometrial Cancer Research Foundation. June is Uterine Cancer Awareness Month, and endometrial cancer now ranks as the nation's most common gynecologic cancer.
228: An Interview With Dr. Michelle Ng Gong, New President of the American Thoracic Society 09.06.2026 11:07
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Michelle Ng Gong, MD, president of the American Thoracic Society (ATS). Dr. Gong formally replaced Raed Dweik, MD, at the ATS 2026 conference in Orlando, Florida.
227: An Interview With Dr. Andrew Wilson, Scientific Director of the Alpha-1 Foundation 31.05.2026 7:51
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Andrew Wilson, MD, scientific director of the Alpha-1 Foundation, about the latest therapies to treat alpha-1 antitrypsin deficiency, an incurable genetic disease that causes both lung and liver damage.
226: An Interview With Dr. Vallerie McLoughlin, Director of the University of Michigan's Pulmonary Hypertension Program 26.05.2026 9:17
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Vallerie McLoughlin, MD, director of the Pulmonary Hypertension Program at the University of Michigan-Ann Arbor, about results of a phase 3 trial for ralinepag to treat pulmonary arterial hypertension.
225: An Interview With Craig Martin, Founder and CEO of the Orphan Therapeutics Accelerator 18.05.2026 14:50
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Craig Martin, founder and CEO of the Orphan Therapeutics Accelerator (OTXL) — a nonprofit biotech dedicated to advancing shelved clinical-stage therapies for ultrarare diseases.
224: An Interview With Henriette Farkas, Director of the Hungarian Angioedema Reference Center in Budapest 14.05.2026 13:16
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Henriette Farkas, MD, PhD, director of the Hungarian Angioedema Reference Center in Budapest, and a world expert on the treatment of HAE.
223: An Interview With Dr. Antón Blatnik on the Molecular Mechanisms Driving Neuromuscular Disease 04.05.2026 11:01
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Antón Blatnik, PhD, who recently won a $150,000 grant from Cure SMA to study the molecular mechanisms that drive neuromuscular disease and gene expression.
222: An Interview With SMA Expert and Neurologist Dr. Kathryn Swoboda 27.04.2026 14:32
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Kathryn Swoboda, MD, faculty emerita at Massachusetts General Hospital and a neurologist and rare disease specialist who's been working on SMA for nearly 30 years.
221: An Interview With Dutch Neurologist Ewout Groen of SMA Europe 20.04.2026 8:51
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Dutch neurologist Ewout Groen, PhD, a member of the Scientific Advisory Board of SMA Europe.
220: An Interview With Dr. Jaime Moore on Obesity Medications and Neuromuscular Disease 13.04.2026 14:11
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Jaime Moore, MD, about weight loss drugs—specifically the role of GLP-1 receptor agonists in treating children with neuromuscular diseases and obesity.
219: An Interview With Dr. Natalie Truba on the Psychological Aspects of Gene Therapy 07.04.2026 14:43
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews pediatric psychologist Natalie Truba, PhD, on the psychological aspects of gene therapy in neuromuscular disease.
218: An Interview With Donna Shipp on Her IgG4-RD Patient Journey 31.03.2026 14:26
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Donna Shipp, a Boston-area nurse who was misdiagnosed with cancer, underwent surgery and later realized she had IgG4-RD. She now advocates on behalf of others with this rare disease.
217: An Interview With Abby Bronson of Edgewise Therapeutics About Becker Muscular Dystrophy Awareness 30.03.2026 12:26
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Abby Bronson, vice president of patient advocacy at Edgewise Therapeutics, about a new effort to raise awareness of Becker muscular dystrophy as a disease distinct from Duchenne muscular dystrophy.
216: An Interview With Allison Moore, Founder and CEO of the Hereditary Neuropathy Foundation 23.03.2026 10:05
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Allison Moore, founder and CEO of the Hereditary Neuropathy Foundation. Moore was the winner of the Muscular Dystrophy Association's 2026 Donavon Decker Legacy Award for Community Impact in Research.
215: An Interview With John Crowley, President and CEO of the Biotechnology Innovation Organization 17.03.2026 14:23
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews John Crowley, president and CEO of the Biotechnology Innovation Organization (BIO), founder of Amicus Therapeutics, and father of 2 children with Pompe disease.
214: An Interview With Dr. Hyun Kim, Director of the University of Minnesota's Interstitial Lung Disease Program 02.03.2026 13:01
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Hyun Kim, MD, professor of medicine and director of the University of Minnesota's Interstitial Lung Disease Program, about idiopathic pulmonary fibrosis.
213: An Interview With Andrea Wilson-Woods, Founder of Blue Faery, a Nonprofit That Advocates for Patients With Hepatocellular Carcinoma 24.02.2026 13:21
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Andrea Wilson-Woods, founder of Blue Faery: The Adrienne Wilson Liver Cancer Association—a nonprofit that advocates for patients with hepatocellular carcinoma.
212: An Interview With Dr. Michael Schilsky of the Yale School of Medicine, and an Expert on Wilson Disease 17.02.2026 10:57
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Michael Shilsky, MD, of the Yale School of Medicine, on potential therapies for Wilson disease.
211: An Interview With Yen Chen, PhD, on Brain Fog Among People With Scleroderma 11.02.2026 12:23
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Yen Chen, PhD, of the University of Michigan, on the subject of cognitive dysfunction or "brain fog" among people with scleroderma.
210: An Interview With Dr. Aleksander Krag on Diagnosing and Treating Alpha-1 Disease 02.02.2026 12:20
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Danish hepatologist Aleksander Krag, MD, PhD, on the diagnosis and treatment of alpha-1 antitrypsin deficiency (AATD).
209: An Interview With Vesna Aleksovska, a Rare Disease Patient Advocate in North Macedonia 28.01.2026 19:52
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Vesna Aleksovska, chair of the nonprofit organization Life With Challenges. Aleksovska, who has Gaucher disease, advocates for all rare disease patients in North Macedonia, a former Yugoslav republic.
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