Select Region: North America | Germany | Japan  
 
 
Healthcare Professionals
HOME HAE AND YOU CLINICAL TRIALS ASK AN EXPERT FAMILY TREE JOURNAL
UNDERSTANDING HAE LIVING BETTER WITH HAE TREATING HAE FINDING MORE RESOURCES CONNECTING WITH HAE COMMUNITY

 
Email:
Password:
Forgot Password?



This website is accredited by Health On the Net Foundation. Click to verify. We comply with the HONcode standard for trustworthy health
information:
verify here.

PERSONAL STORY

Melissa Hopes Study Will Provide Cure

At any moment and as often as once a week, Melissa Savor, 43, of Rowlett is stricken by attacks of hereditary angioedema (HAE).

The rare blood disorder can lead to painful attacks of edema, or swelling, of the face, airway, abdomen, and extremities.

"Often there is no warning," Savor said. "Everyone is different in the severity of the disease. Mine seems to have manifested to a weekly spell. It is usually as I wake up and there it has started."

The challenge for those afflicted with HAE is in treatment. The Federal Drug Administration has not approved C1-INH concentrate, a treatment which is being used in Europe to treat those living with HAE.

Read Melissa's Story

Share your story


Document Published: 12/21/2006 3:44 PM
Last Updated: 2/23/2007 11:05 AM

CSL Behring Biotherapies for Life
All About HAE

© 2010 CSL Behring | Home | Patients Site Map
Healthcare Professionals Site Map | Privacy | Terms of Use
About AllAboutHAE.com | HAEA.org | Contact Us