Hereditary Angioedema (HAE) is a very rare and potentially life-threatening genetic condition that occurs in about 1 in 10,000 to 1 in 50,000 people. HAE symptoms include episodes of edema (swelling) in various body parts including the hands, feet, face and airway.
The US HAEA is a non-profit patient advocacy organization dedicated to serving persons with angioedema. The HAEA has worked for 15 years to support the development of new HAE drugs, therapies, and research for Hereditary Angioedema. We value the continued support of our community and the general public to fulfill the HAEA patient community's mission of improving the quality of lives of those afflicted with HAE and, ultimately, finding a cure.
HAE IN-MOTION® 5K events will be held nationwide and open to the public. Each event promises to be a fantastic opportunity for family, friends, students, co-workers and colleagues to come together in support of a worthy cause. Please come join us at Lake Zorinsky in Omaha on Sunday, June 5th at 8am!