Chronic Pain Partners/EDS Awareness, a US-based non-profit 501(c)(3) organization, was created in 2011 to support people with Ehlers-Danlos syndromes. It is an online resource for the Ehlers-Danlos Syndrome community, their caregivers, medical professionals, and everyone interested in learning more about the genetic connective tissue disorder.

Chronic Pain Partners helps create independent, local EDS Support groups, hosts live webinars to help educate our members, caregivers and healthcare providers, and launched a CME program for physicians and another one for nurses, and lately, we have developed towards becoming a multimedia online magazine for people with varying chronic pain conditions, producing high-quality video content and documentary films as well as a monthly newsletter with original content only found on our website!

Website: www.chronicpainpartners.com