Rare Bleeding Disorders in Tennessee and Finding Answers (with interview)

Oct 25, 2021 at 03:44 pm by WGNS



 

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.

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