The flags above represent the countries with a national HAE organization.
Contact our regional contact and let us help you get organized.
Fernanda de Oliveira Martins
Regional Patient Advocate – South America and Mexico
Helping to change the lives of patients with hereditary angioedema (HAE) with a medication access program
Magazine with timely information on the issues, activities, and events that are relevant to the global HAE community
Free, secure online membership database and communications platform for HAEi’s member organizations
Constantly strive to improve the situation for HAE friends all over the world – no matter how they are organized
BE THE FIRST TO KNOW ABOUT HAE NEWS, TREATMENTS, EVENTS AND RELATED TOPICS
This 4th HAE conference was record breaking: A total of 736 patients and care givers participated from no less than 57 countries
Hosting of your national website or help for you to create a new website – naturally all in your native language