An organization in Tennessee is educating others on a rare blood disorder that impacts 20 to 30-thousand Americans...

That was Janet Patterson who serves as the Board President of The Tennessee Hemophilia & Bleeding Disorders Foundation, based in Murfreesboro.

WGNS' Scott Walker spoke to Patterson, who further highlighted how rare Hemophilia is across the country...



The Tennessee Hemophilia & Bleeding Disorders Foundation is a non-profit organization that was founded in 1970.

To learn more, hear our interview (above this story) on WGNSradio.com or visit THBDF.org.