About Us

About the Chronic Pain Partners non-profit 501(c)(3)

Who is Chronic Pain Partners?

The mission of Chronic Pain Partners and its EDS Awareness programs is to ensure greater understanding of Ehlers-Danlos Syndromes (EDS) by patients, the general public and within the medical community, in order to improve the quality of life for those affected by EDS.

To assist and encourage support groups to organize and spread knowledge about EDS in their local communities

To help those affected by EDS locate valuable information, continue to learn, and to share awareness materials with their EDS peers

To educate patients, healthcare providers and the public about EDS through live webinars conducted by EDS experts.

Contributions and Achievements

Providing free tools and mentoring to help start 100+ EDS Local Support Groups world-wide… and growing

Hosting free EDS educational webinars typically each month since 2013

Recordings of these patient directed webinars are available at our EDS Awareness website

You can learn more about Chronic Pain Partners on our website.

How can I work with your organization?

Please use the contact form at Chronic Pain Partners to get in touch with us about working to raise awareness. May is our EDS Awareness month, and people the world over hold events to help us raise awareness. Contact us about our EDS Support Groups and their EDS Awareness activities.

Can I make a donation?

The Chronic Pain Partners is a registered 501(c)(3) and your donations are tax deductible in the US. 

Click here to donate