HAEi is the international umbrella organization for the world’s Hereditary Angioedema (HAE) patient groups.
HAEi is dedicated to raising awareness of C1-inhibitor deficiencies around the world. We strive to improve time to diagnosis and facilitate access to and reimbursement of life saving HAE therapies, which will enable lifelong health for all patients – no matter where they live.
Suffering from HAE? You are not alone!
Members of the HAEi family
Meet your HAEi Regional Patient Advocate
Check out HAEi events around the world
Sheraton Brussels Hotel
Nov 15, 2016 - Nov 17, 2016 at All Day
>> See list of all events here
Be the first to know about HAE news, treatments, events and related topics
HAEi on social media
You can follow HAEi on a number of social media platforms where we will keep you updated on the latest news regarding HAE.
Find HAE “Points of Interest” relevant to you
Missed opportunities due to HAE
It’s important to get the right treatment to get the most out of life
Patients report that HAE has hindered their education and work opportunities.
Getting the right treatment will allow you to live a normal life without missing out on education and job opportunities.
Read the stories of HAE patients from around the world
HAE patients from all corners of the world share their stories, inspiring other patients and proving that it is in fact possible to lead a close to normal life with HAE.
Reach out to HAEi
At HAEi we are constantly focusing on how to improve the awareness of HAE, and how to create a better environment for timely diagnosis and access to therapies.
Your experience and your story can help us. Reach out to us!
Your personal story, an invitation to your community’s event, local or national news, feedback, questions …
All that and much more is always welcome in HAEi’s mailbox.
So please, send us a message, if you have anything you want to share with us.
Fill in the form to reach us