Hannah’s Story - Living with hATTR Amyloidosis

This video was created for U.S. audiences.
Hannah talks about being diagnosed with hereditary ATTR (hATTR) amyloidosis and shares her experience with others interested in learning more about this condition.
hATTR amyloidosis is a rare, inherited disease caused by a genetic variant, or change, in the transthyretin (TTR) gene. This change in the TTR gene may also be referred to as a mutation. hATTR amyloidosis affects approximately 50,000 people worldwide. Many people remain undiagnosed or misdiagnosed. Learn more at hattrbridge.com/.
TTR-USA-00074