Top 36 alternative sites to ehlers-danlos.org
The HMSA | The Hypermobility Syndromes Association
The hypermobility syndromes association (HMSA) provides support and information for everyone with a hypermobility syndrome as well as health and social care professionals who support them.
The Ehlers-Danlos Society
The Ehlers-Danlos Society is a global community of patients, caregivers, health care professionals, and supporters, dedicated to saving and improving the lives of those affected by the Ehlers-Danlos syndromes, hypermobility spectrum disorders, and related conditions.
Ehlers-Danlos Support Groups and EDS education
Ehlers-Danlos Support Groups and EDS education
Home - NORD (National Organization for Rare Disorders)
NORD, a 501(c)(3) organization, is the leading patient advocacy organization dedicated to improving the lives of individuals and families living with rare diseases.
Ehlers-Danlos News Home - Ehlers-Danlos News
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Weill Cornell Brain and Spine Center |
The BMJ: Leading Medical Research, News, Education, Opinion
High impact medical journal. Champion of better research, clinical practice & healthcare policy since 1840. For GPs, hospital doctors, educators, policymakers.
More Than Tired™ | Narcolepsy Information and Resources
Narcolepsy can potentially have an impact on overall health. Find resources and take a screener to find out if you or your child may have symptoms.
Oregon EDS Home Page
Oregon EDS Group Home Page - learn about Ehlers-Danlos Syndrome Support in Oregon
CEDSA Home
CEDSA helps patients and families who are diagnosed with Ehlers-Danlos Syndrome by providing advocacy, medical resources, and additional help.
Long Island – EDS Group
Local Support Group (Long Island, NY) for patients with Ehlers-Danlos Syndrome (EDS) or benign hypermobility syndrome
Vascular EDS is a life limiting rare genetic disorder
UK registered charity supporting patients & families touched by Vascular Ehlers-Danlos syndrome. Vascular EDS is a rare genetic disorder and is life limiting.
Waterloo Wellington Myalgic Encephalomyelitis Association
The WWMEA provides support group meetings and information for those affected by CFS (chronic fatigue syndrome), M.E. (myalgic encephalomyelitis), CFIDS (chronic fatigue and immune dysfunction syndrome)
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Home - The Migraine Trust
The Migraine Trust is dedicated to helping people affected by migraine. We are the only UK migraine charity providing information and support, campaigning for awarenessand change, and funding and promoting research.
Endometriosis UK | the leading UK charity that supports women living with endometriosis
Find out more about endometriosis from the leading UK charity dedicated to providing information and support to those with endometriosis.
Homepage - OCD Action
THE UK'S LARGEST OCD CHARITY. We provide support and information to anybody affected by OCD, work to raise awareness of the disorder amongst the public and front-line healthcare workers, and strive to secure a better deal for people with OCD.
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