Thanks to Camille Schrier (aka Miss America) for sharing her experience with EDS! Check out Camille's Instagram here:   / camilleschrier  
Please consider donating to the Norris Lab or passing this info along in order to support the research for genetic causes and possible treatments and tests for hEDS.
DONATE TO MUSC NORRIS LAB (EDS research in regenerative medicine): https://connect2.musc.edu/com
If you want to learn more about how you can be involved in research, email [email protected]
SUBSCRIBE TO MY CHANNEL ▶ http://bit.ly/2M4Ko0c
📸 Instagram ▶   / izzy.kornblau  
⏰ TikTok ▶   / izzyk_dna  

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 EHLERS-DANLOS SYNDROME?
The Ehlers-Danlos 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 co-morbidities of hEDS include chronic joint pain, joint instability and dislocations, dysautonomia, and GI tract dysmotility.

MORE INFO ABOUT EDS:
🧬 https://www.ehlers-danlos.com/eds-types/
🧬 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 #missamerica #camilleschrier