Episode 558 - Anton Morkin episode artwork

EPISODE · Feb 3, 2026 · 17 MIN

Episode 558 - Anton Morkin

from I'm Aware That I'm Rare: the phaware® podcast · host phaware global association

One Dad's Mission to Cure His Son's Genetic Disease When Anton Morkin's son was diagnosed with "idiopathic" pulmonary hypertension, he refused to accept "no known cause" as an answer. What followed was a crash course in genetics, the discovery of a rare mutation, and the formation of a worldwide coalition, TBX4Life. Learn more about pulmonary hypertension trials at www.phaware.global/clinicaltrials. Follow us on social @phaware Engage for a cure: www.phaware.global/donate #phaware Share your story: [email protected] Like, Subscribe and Follow us: www.phawarepodcast.com. @TBX4_Life

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Episode 558 - Anton Morkin

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This episode is 17 minutes long.

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This episode was published on February 3, 2026.

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One Dad's Mission to Cure His Son's Genetic Disease When Anton Morkin's son was diagnosed with "idiopathic" pulmonary hypertension, he refused to accept "no known cause" as an answer. What followed was a crash course in genetics, the discovery of a...

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