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Patients and Caregivers

Being a patient or the caregiver of a patient with hereditary angioedema (HAE), you know that HAE is never NOT a big deal.
 

Whether it’s missing an important day at work or school due to an attack, or a ruined family celebration or business trip, or even just feeling tired, unable to sleep at night and in a bad mood – HAE always has an impact.

Patients - Articles

Patients

What is HAE?

Learn about HAE, including symptoms and triggers, types of HAE, and how HAE attacks happen.

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Patients

How does HAE impact your life?

Learn about the impact and burden of HAE, as well as stories from patients with HAE.

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Patients

Management of HAE

Find out about HAE management, including treatment goals and current treatment options.

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Patients

Living with HAE

Discover more details on how to monitor HAE symptoms, what to discuss with your doctor, and how to manage HAE while travelling.

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Patients

Advice for parents of children with HAE

Learn about HAE in children, including symptoms and triggers, treatment options, and the importance of individualised treatment plans.

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This website is intended for users in Europe. The website has been developed by CSL Behring in accordance with industry and legal standards. CSL Behring makes every reasonable effort to include accurate and current information. However, the information provided on the website is not exhaustive and should not be used in place of a consultation with or the advice of your doctor or other healthcare professional.

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EUR-OTH-0307/EUR-OTH-0308 August 2024