Hereditary angioedema (#HAE) is a rare, inherited disease that frequently presents in childhood. We support the entire HAE community affected by this rare disease, including caregivers, who often put their own needs aside to care for a loved one. Hear from Lisa, as she shares her experience of caring for her granddaughter who lives with HAE. #HereditaryAngioedema | BioCryst Pharma
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Hereditary angioedema (#HAE) is a rare, inherited disease that freque…
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302K views · 167 reactions | Each member of our community has a unique hereditary angioedema (HAE) journey. Learn more about HAE by joining our rare family. | DiscoverHAE | Facebook
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302K views · 167 reactions | Each member of our community has a u…
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Hereditary angioedema (#HAE) is a potentially life-threatening rare disease. Because HAE is so rare, it can take as long as a decade to receive an accurate diagnosis after symptoms are first experienced, and delayed diagnosis is a significant concern. Even the presence of a family history of HAE does not guarantee children will be diagnosed earlier than others. | BioCryst Pharma | Facebook
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Hereditary angioedema (#HAE) is a potentially life-threatening rare dis…
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1M views · 163 reactions | The symptoms of hereditary angioedema (HAE) can include attacks of swelling that can happen anywhere in the body. Some people experience a tingling sensation or a rash before an attack. Learn more about how an HAE attack occurs. | DiscoverHAE | Facebook
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HAE for me
HAE for me
Apr 11, 2022
haei.org
May 16th is hae day :-)! The HAEA invites YOU to TAKE ACTION FOR HAE throughout the entire month of May! Order a newly updated HAE ER Toolkit and receive a FREE limited edition TAKE ACTION FOR HAE t-shirt! Order yours today, and share it with your local first responders, medical emergency rooms, school nurses, dentist, family physician, coaches, and anyone you would like to learn more about HAE. Order your ER Toolkit here: https://fundraise.haea.org/2021-hae-day #haeday #HereditaryAngioedema #HA
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