Video Library

Watch these helpful videos to hear stories from people with hereditary angioedema (HAE) and learn from their personal experiences.

Alex — Diagnosed with HAE in 2014

Discover helpful videos

Watch these helpful videos to hear stories from people with hereditary angioedema (HAE) and learn from their personal experiences.

  • Liz talks about her HAE diagnosis

    Meet Liz, a Shire 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.

  • Marsha finally met the doctor who diagnosed her with HAE

    Meet Marsha, a Shire Patient Ambassador

    When Marsha finally met the doctor who would diagnose her HAE, she was starting to lose hope that she would ever discover the cause of her symptoms.

  • Lesa has 10 family members with HAE too

    Meet Lesa, a Shire Patient Ambassador

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

  • Lesa is thankful that she attended a Shire event

    Why attend an event?

    Hear why Shire events are important to Lesa.

  • Marsha was able to meet other people with HAE at a Shire event

    Why attend an event?

    Hear why Marsha shares her story at Shire events.

  • 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.

  • Marsha emphasizes the importance of getting family members tested for HAE

    HAE and family

    Marsha explains why testing for family members has been an important part of her personal experience.

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