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Watch these helpful videos to hear stories from people with hereditary angioedema (HAE) and learn from their personal experiences.
Watch these helpful videos to hear stories from people with hereditary angioedema (HAE) and learn from their personal experiences.
Watch these helpful videos to hear stories from people with hereditary angioedema (HAE) and learn from their personal experiences.
Liz is a wife, mother, sister and daughter with HAE. Before her diagnosis, she spent years searching for something to explain her mysterious symptoms.
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 was diagnosed with HAE along with 10 other members of her family. See her story and learn from her personal experiences.
Hear why Shire events are important to Lesa.
Hear why Marsha shares her story at Shire events.
Liz and her older sister both have HAE. Hear how their shared symptoms shaped their lives and strengthened their bond.
Marsha explains why testing for family members has been an important part of her personal experience.
