Learn why this rare disease, Hereditary angioedema (HAE) may be impacting patients' lives more than they realize.
Living with a rare disease means navigating a world that often does not understand your condition. Hereditary angioedema (HAE) is a rare genetic disorder that causes painful, recurrent swelling episodes. This segment of The Balancing Act on Lifetime brings expert medical insight and patient perspective together.
HAE is caused by a deficiency of C1 inhibitor protein, leading to severe swelling in the hands, feet, face, abdomen, and airway. It affects approximately 1 in 50,000 people, though many experts believe the number is higher due to frequent misdiagnosis.
Dr. Daniel Sotores, MPH, MD explains the underlying mechanisms of HAE and the importance of early detection. When properly diagnosed, effective treatments can significantly reduce attack frequency and severity.
Jessica shares her personal experience navigating the unpredictable nature of HAE. Her story illustrates the emotional and practical toll of living with a disease that can strike without warning.
Anyone experiencing recurrent episodes of unexplained swelling should discuss the possibility of HAE with their healthcare provider. A family history of similar symptoms is an important diagnostic clue.
Tune in to The Balancing Act on Lifetime for essential information about HAE and how awareness, early diagnosis, and modern treatment are changing patient lives.
