Tools and Resources for Patients

CSL Behring offers numerous tools and other resources to help you as well as your patients living with hereditary angioedema (HAE).

Working with your doctor Resources

Two-way communication between HAE families and their physicians helps to build trust and solidify patient-doctor relationships. This “contract” suggests responsibilities for both parties.

Tools and resources Resources

Use these tools and resources to help your patients get the latest news on HAE, explore their family trees, and find the meanings of term used to explain the causes, symptoms, and treatment of HAE.

Understanding HAE: a video Resources

Hear the latest thinking on hereditary angioedema, see why it is often misunderstood and misdiagnosed, and explore new approaches to therapy.

Registration

Register for updated information on HAE disease management.

Professional resources

Use these tools and resources to get the latest news about HAE, download diagnostic tools, and read related clinical articles. Find out about professional resources

US Hereditary Angioedema Association (HAEA)

Learn about the HAEA, a non-profit organization that provides a wide range of services, including clinical trial placement, physician referrals, education, and individualized patient case management. Visit HAEA.org