Solving Rare.
A podcast about the people rebuilding rare disease therapy from scratch.
— Shorts
Short takes from the show
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It’s not impossible. A mom rebuilding rare disease from scratch. #shorts
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No family should have to do this alone. #shorts #raredisease
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Why patient advocacy groups won’t share data and how to fix it. #shorts
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The #1 gap holding back rare disease cures #shorts #biotech
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The real reason biotech founders write grants #shorts
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The Right Type of Capital in Biotech #shorts
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How this parent found Nome after her son’s diagnosis #shorts
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The science works. So why aren’t we curing anything? #shorts #biotech
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Investor told her: stop using “rare disease” #shorts #biotech
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Disability Is a Group Anyone Can Join #shorts
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How Soon Can You Send Me Your Data? #shorts #rarediseases
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Rare is Common. Why we’re all one diagnosis away. #shorts #rarediseaseawareness
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Jul 22, 2026
Amy Krystosic: "Rare Is Common" — The Case for Precision Medicine's Future
What does it actually take to build a foundation, a biotech company, and a clinical trial pathway for one of the rarest diseases in the world — while raising a child who lives with that same disease? In this episode of Solving Rare, Stevie Ringel sits down with Amy Krystosic — e
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Jun 8, 2026
David Apple: The Dad Who Built His Own Biotech to Treat His Son
What does it actually take to build your own biotech company when your child is diagnosed with a rare disease and no treatment exists? In this episode of Solving Rare, Stevie Ringel sits down with David Apple — former tech founder, employee 15 at Typeform, employee 13 at Notion,
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May 26, 2026
Diagnosed at 17. Now I'm Building My Own Gene Therapy. | Welcome to Solving Rare
At 17, I was diagnosed with a rare disease. When my younger sister was diagnosed with the same, I refused to accept that there was nothing we could do. So I went on a decade-long journey to figure out what was possible. I'm Stevie Ringel — a rare disease patient turned biotech b
