In this video, five people with hypermobile EhlersDanlos Syndrome run through the hEDS diagnostic criteria from 2017! Hypermobile EDS is a painful genetic connective tissue disorder that makes connective tissues abnormally weak, fragile, and stretchy, leading to chronic joint and muscle pain, joint instability and dislocations, dysautonomia, fatigue, and GI tract dysmotility, among so many other symptoms. While the diagnostic criteria help to diagnose, it barely scratches the surface of the impact of this disease.
The views expressed in this video are my own and do not reflect the views of Mount Sinai Hospital.

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HEDS DIAGNOSTIC CRITERIA 2017: https://ehlersdanlos.com/wpcontent/...

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The views expressed in this video are my own and do not reflect the views of Mount Sinai Hospital.
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WHAT’S EHLERSDANLOS SYNDROME?
The EhlersDanlos Syndromes (EDS) are a group of more than 13 genetic connective tissue disorders that affect the joints and ligaments, blood vessels, gastrointestinal tract, and autonomic nervous system, among others. The most common type of EDS is hypermobile EDS (hEDS), which used to be known at type III. Some of the most common symptoms and comorbidities of hEDS include chronic joint pain, joint instability and dislocations, dysautonomia, and GI tract dysmotility.

MORE INFO ABOUT EDS:
https://www.ehlersdanlos.com/edstypes/
https://bit.ly/2N95xTE
MORE INFO ABOUT POTS:
https://www.potsuk.org/what_is_pots2
❤ https://cle.clinic/2p1lByR
MORE INFO ABOUT GASTROPARESIS:
https://mayocl.in/2BRQTuR
MORE INFO ABOUT MUSCLE TENSION DYSPHONIA:
https://bit.ly/2MLUYXI

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#eds #ehlersdanlos #hypermobileeds