Resources

• News & Events
  • Events
  • Newsletters
• Patient Empowerment Program
• Media Library
• Physician Letter
• School Resources
• Patient ID Card
• HAEA 2010 Yearbook
• HAE Medical Glossary
• Bibliography
• CME Courses
• HAE International

Resources

The US HAEA is dedicated to improving the diagnosis, treatment and quality of life of persons with Hereditary Angioedema through research, advocacy, compassion and empowerment.

We provide these resources (listed on the left) to help you achieve lifelong health.