Most people think HAE is something to be afraid of.
I see it as a way to be different.
I created something where you can say how you feel about HAE, what you do for it and how you advocate for yourself.
Emma Parker, USA
Most people think HAE is something to be afraid of.
I see it as a way to be different.
I created something where you can say how you feel about HAE, what you do for it and how you advocate for yourself.
Emma Parker, USA
HAEi Youngsters is a part of HAE International (HAEi) – a global non-profit network of patient associations dedicated to raising awareness of hereditary angioedema (HAE) around the world and improving the lives of people with HAE.
Operations: Vejlevej 16, 1. • DK-8700 Horsens • Denmark • info@haei.org
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