Rare Community Profiles: Could It Be HCM? A Mother-Daughter Duo Raise Hypertrophic Cardiomyopathy Awareness
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Rare Community Profiles: Could It Be HCM? A Mother-Daughter Duo Raise Hypertrophic Cardiomyopathy Awareness

  Rare Community Profiles is a Patient Worthy article series of long-form interviews featuring various stakeholders in the rare disease community, such as patients, their families, advocates, scientists, and more.…

Continue Reading Rare Community Profiles: Could It Be HCM? A Mother-Daughter Duo Raise Hypertrophic Cardiomyopathy Awareness
How Wendy Borsari Translated Her Hypertrophic Cardiomyopathy Diagnosis into Impact (Pt. 2)
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How Wendy Borsari Translated Her Hypertrophic Cardiomyopathy Diagnosis into Impact (Pt. 2)

Before you read on, don't forget to check out Part 1 of our interview. In Part 1, Wendy discusses what hypertrophic cardiomyopathy (HCM) is, her rare variant, the diagnostic journey, and her…

Continue Reading How Wendy Borsari Translated Her Hypertrophic Cardiomyopathy Diagnosis into Impact (Pt. 2)
How Wendy Borsari Translated Her Hypertrophic Cardiomyopathy Diagnosis into Impact (Pt. 1)
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How Wendy Borsari Translated Her Hypertrophic Cardiomyopathy Diagnosis into Impact (Pt. 1)

Wendy Borsari is not just a patient living with hypertrophic cardiomyopathy (HCM); she is also a mother, a fierce advocate, and part of the patient advocacy team at Tenaya Therapeutics,…

Continue Reading How Wendy Borsari Translated Her Hypertrophic Cardiomyopathy Diagnosis into Impact (Pt. 1)