Rare Bleeding Disorders in Tennessee and Finding Answers (with interview)
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 lear ...
Source: wgnsradio.com