Chronic Pain Partners Educational Series -Free Ehlers-Danlos Educational Programs
Now that most of us are asked to stay in our home this is a perfect
time to increase our knowledge about Ehlers Danlos Syndromes.
Learn more through these Free educational video programs about
Ehlers-Danlos Syndromes presented by over 60 experts covering
50 EDS related topics.
Ehlers Danlos Syndromes is a genetic condition that is NOT “Rare” but “Rarely Diagnosed”
Patients & healthcare providers can attend all programs
90 EDS Educational Webinars listing with patient Q & A
Select by presenter’s name, topic, specialty and location.
https://www.
chronicpainpartners.com/ webinars/ EDS Physician CME Educational Program
https://ehlers-danlos-cme.org/
Newly launched this year EDS Nursing Educational Program.
https://ehlers-danlos-nursing-
edu.org/ EDS Support Group Leaders’ Educational Program with Mandy Harvey
120 world wide EDS support Groups listing
https://www.
chronicpainpartners.com/ Kind Regards,
John Ferman – President Chronic Pain Partners 501(c)(3)
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Non-profit organization which empowers the gluten-free community through consumer support, advocacy, and education. Initiatives include provision of community support through local Branches, provision of extensive educational materials and programs, and certification of gluten-free food products. Dedicated to improving the quality of life and quality of care for individuals and families affected by Hidradenitis Suppurativa (HS). Founded for the sole purpose of funding efforts to discover the molecular and cellular causes of HS, to aid in the development and delivery of more effective therapy to patients with this common, debilitating, and eminently chronic disease.