My name is John Ferman. I am the president of Chronic Pain Partners, a non-profit 501(c)(3) organization. My daughter Deanna and I created the Ehlers Danlos Awareness program in 2011 to help support those with a genetic disorder called Ehlers-Danlos Syndrome (EDS.)
The vision of Chronic Pain Partners is to bring chronic pain support groups and Ehlers danlos support groups to people in need.