What is Fabry's disease?
Fabry disease is a rare genetic disorder that causes a lack of or decreased amount of alpha-galactosidase-A, an enzyme that is needed for the body to break down a specific type of fat. As a result, this fat can accumulate throughout the body which can lead to complications with many organs.
How do members experience Fabry's disease?
*Reports may be affected by other conditions and/or medication side effects. We ask about general symptoms (anxious mood, depressed mood, fatigue, pain, and stress) regardless of condition.