· Norway · Europe
On this page we have pulled together presently available information relevant for HAE patients and caregivers in Norway.
HAE online in Norway
News and events
The latest news from HAEi
HAE Emergency Cards in local languages
The HAE Emergency Card contains clear and simple information about HAE and treatment required during an attack. It also contains space for patients to add personal information such as emergency contact details and their specialist treatment center.
The Emergency Card has been translated into a number of languages and can help you to quickly and effectively let healthcare professionals know that you have a diagnosis of HAE and what treatment should be considered.
HAE related topics that might interest you
Global Access Program
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
HAEi Connect Member database
Free, secure online membership database and communications platform for HAEi’s member organizations
Regional Patient Advocates
Constantly strive to improve the situation for HAE friends all over the world – no matter how they are organized
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HAE Global Conference 2018
This 4th HAE conference was record breaking: A total of 736 patients and care givers participated from no less than 57 countries