Video library

Chaeli
Diagnosed with
HAE in 1997

Watch helpful videos of people with hereditary angioedema (HAE)

These HAE patients share their stories about everything from their search for an accurate HAE diagnosis, to what it’s like to have family members with HAE and more.

  • Meet Liz, a Takeda Patient Ambassador.

    Meet Liz, a Takeda Patient Ambassador

    Liz is a wife, mother, sister and daughter with HAE. Before her diagnosis, she spent years searching for something to explain her mysterious symptoms.

  • Meet Lesa, a Takeda Patient Ambassador.

    Meet Lesa, a Takeda Patient Ambassador

    Lesa was diagnosed with HAE along with 10 other members of her family. See her story and learn from her personal experiences.

  • Meet Alex, a Takeda Patient Ambassador.

    Meet Alex, a Takeda Patient Ambassador

    Alex and his twin brother both suffered with undiagnosed HAE symptoms for years before discovering the truth.

  • Liz and her older sister both have HAE.

    HAE and sisterhood

    Liz and her older sister both have HAE. Hear how their shared symptoms shaped their lives and strengthened their bond.

  • Several people in Chaeli's family have HAE, including her mother.

    Inheriting HAE

    Several people in Chaeli’s family have HAE, including her mother. Growing up watching her mom live with HAE made a lasting impact. See how.

  • Alex gives his take on talking about HAE

    Talking about HAE

    How do people respond when you tell them about your condition? What kinds of questions do you get? Alex gives his take.

  • Learn more about the HAE community from Chaeli

    HAE and community

    Chaeli says that meeting people outside of her family who also have HAE has been life-changing for her. Find out why.

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