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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 – and those who care for them.
To assist and encourage support groups to organize and spread knowledge about EDS in their local communities
To help EDSers 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 held twice a month.
Providing free tools and mentoring to help start 100+ EDS Local Support Groups world-wide… and growing
Host 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.
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.