WEBHome - The Ehlers Danlos Society. I am an... Individual. …looking for advice and information on EDS or HSD, support groups, and the helpline. Explore. I am a... Health Pro. …looking to increase my knowledge of EDS, HSD, and research to better assist my patients. Explore. May Is EDS and HSD Awareness Month.
WEBOur Mission. The Ehlers-Danlos Society is a global organization dedicated to advancing and accelerating research and education in Ehlers-Danlos syndromes (EDS) and hypermobility spectrum disorders (HSD). We support the development of effective and equitable EDS and HSD therapies and work collaboratively to improve the lives of …
WEBThe Ehlers-Danlos syndromes (EDS) are a group of 13 heritable connective tissue disorders. The conditions are caused by genetic changes that affect connective tissue. Each type of EDS has its own set of features with distinct diagnostic criteria.
WEBThe Ehlers-Danlos syndromes (EDS) are currently classified into a system of thirteen types. Each EDS type has a set of clinical criteria that help guide diagnosis; a patient’s physical signs and symptoms will be matched up to the major and minor criteria to identify the type that is the most complete fit.
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Hypermobile EDS and hypermobility spectrum disorders - Ehlers-Danlos
WEBHypermobile Ehlers-Danlos syndrome (hEDS), which used to be known as the hypermobility type or type 3, is thought to be the most common genetic connective tissue disorder. There is no up-to-date research to tell us exactly how frequently it occurs.
WEBThe Ehlers–Danlos Society is an international nonprofit organization dedicated to patient support, scientific research, advocacy, and increasing awareness for the Ehlers–Danlos syndromes (EDS) and hypermobility spectrum disorder (HSD).
WEBThe Ehlers-Danlos syndromes (EDS) are a group of thirteen individual genetic conditions, all of which affect the body’s connective tissue. The Ehlers-Danlos Support UK is the only UK charity to support anybody touched by the Ehlers-Danlos syndromes
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Healthcare Professional Directory Archive - The Ehlers Danlos Society
WEBThe Ehlers-Danlos Society acknowledges how hard it is to find healthcare professionals who are knowledgeable about EDS and HSD. To improve access to care, we have a directory of healthcare professionals from around the world who are committed to helping people with EDS and HSD.
WEBAug 25, 2022 · Luna Coming to Life. Expertise and rankings. Because Ehlers-Danlos syndrome is a rare condition, it may be difficult to find a doctor with experience diagnosing and treating the disorder. Mayo Clinic doctors care for hundreds of adults and children with Ehlers-Danlos syndrome each year.