Ehlers Danlos Syndrome Explained Clearly

Ehlers Danlos Syndrome (EDS) explained, including subtypes such as Hypermobile EDS and Vascular EDS. We look at the hypermobility criteria (including Beighton score), as well as Ehlers Danlos Syndrome treatment.
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Video Timestamps:
0:00 What is Ehlers Danlos Syndrome?
0:25 Ehlers Danlos Syndrome Pathophysiology
1:17 Ehlers Danlos Syndrome Causes
1:50 Ehlers Danlos Syndrome Symptoms and Signs
4:17 Ehlers Danlos Syndrome Diagnosis
6:15 Ehlers Danlos Syndrome Treatment
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Please remember this video and all content from Rhesus Medicine is meant for educational purposes only and should not be used as a guide to diagnose or to treat. Please consult a healthcare professional for medical advice.
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[@missillicity]

There are no doctors with availability around me 4 plus hours out. my mom is diagnosed. i have all the symptoms. yet no doctor will diagnose me, and im in limbo and im in so much pain everyday. i had a big surgery 2 years ago and my life flipped and i havent been the same.

[@Emily7778]

Its so difficult. I finally found a doctor who will see me and my appointment was scheduled 8 months out 🙃

[@GizmoGremlinDog]

I asked my GP about EDS as myself, my daughter and son have symptoms. She asked "what's that?" So I'm pretty much screwed if this is what we have

[@ascargot]

Same with me. I live in Ontario and apparently the only ones that can diagnose are the doctor of the Ehlers-Danlos Clinic i Toronto, with a wait list of 2.5 years.

[@shannongreenwell1278]

Awesome job on explaining EDS! Keep up the great work! I have Classical EDS and not many physicians have an inkling of a clue what it is! Which means going to hospital for a EDS patient is very difficult and scary! Luckily my Neurologist’s office is very familiar with EDS and POTS, which I have. I have GERD AND PCOS. Along with Migraines and CCI( I sleep with a CCollar on at night). I could do these things as a child and young adult and a teenager, but due to a fatal car accident that killed my mother and mangled me I am unable to do much of anything at the moment. I am still very hyper mobile however! Especially in my arms and knees and the tops of my feet’s. .

[@faree38green]

Excellent presentation re Ehlers Danlos

[@RhesusMedicine]

Thank you!

[@JS_bioclasses12]

Nicely explained

[@RhesusMedicine]

Thanks 🙂

[@waelfadlallah8939]

Thank you 😊

[@RhesusMedicine]

You're welcome 😊

[@tessaelisabeth7393]

I was diagnosed with EDS recently. It impacts my entire body. Does anyone have severe tummy problems from it? I am looking for another doctor bc they think I have something else (POTS)

[@shannongreenwell1278]

I have GERD due to my EDS and I have POTS, too. I have cEDS.

[@liliumdahlia]

I have irritable bowl syndrome and a prolapsed pelvic floor

[@anntunaley9974]

U most likely have gastroparesis. Most of us with EDS do.

[@ngocquynhnhuhuynh3227]

Luckily, I have only hypermobility (up to now), so I can’t run

[@happyhenryxii1956]