Video about HAE Day – Aiming "to raise awareness of hereditary angioedema (HAE) – a potentially life threatening disease – across the world, to ensure each and every patient receives faster diagnosis and the care they deserve to enable them to lead a healthy life."
The world of HAEi – 2016 trailer
"HAEi is the international umbrella organization for the world’s Hereditary Angioedema (HAE) patient groups."
Joy of life
Benedikte Hellevik tells her personal story about life with HAE.
HAE day :-) keep smiling
Share a smile on HAE day.
The world of HAEi
A video about the global and unconditional support that HAEi offers.
(Source: HAEi – International Patient Organization for C1 Inhibitor Deficiencies, 2016)