Do you have Ehlers-Danlos Syndrome?

Ehlers-Danlos Syndrome is a connective-tissue disorder and is often undiagnosed. These r some of the symptoms of the disorder. See if you or anyone else has it because you could save someone from suffering from this disease without the proper treatment. I will make another video soon.

Category:

People & Blogs

Tags:

• ehlers
• danlos
• syndrome
• hypermobility
• streachy
• skin
• joints
• double
• jointed
• flexible

[Zamester]

hi, im gonna get tested soon for this disorder and was just wondering what your opinion was about my issues. First off i can do all of the finger tricks that you do like extending them really far. I can almost bend my hands almost parallel to my wrists. The last possible indicator is that my wrists, shoulders, and knees always pop out unexpectedly. Please Reply,

Zamester

[BuddyBoy091994]

@Zamester theres a chance you have it or something related but only a doctor or in many cases doctors can properly diagnose it. It deffinently worth getting checked out

[mybieber95]

I FRIKKEN LOVE YU YU WIERDOO !

[BuddyBoy091994]

@mybieber95 i miss you! :(

[SenoraFabregas]

hey,

I'm just curious, my fingers are REALLY stretchy and i can do the thumb and finger thing but that's about it. does this mean i have it????

thanks

[BuddyBoy091994]

@SenoraFabregas no not EDS. people with EDS have stretchy joints everywhere not just a certain few. alot of people are just hypermobile in a few joints but that doesnt mean they have it

[spoonsonrice101]

thank you for posting this video i just got diagnosed (sorry for the bad spelling) and it nice to see that i'm not the only one going through this!!!! thanks!!!:)

[sarahdionna]

Thank you for posting this!

[planetrock23]

@rodentrose how were you diagnosed?

[planetrock23]

@rodentrose what was the process by which you were diagnosed, i am 90% sure i have EDS but can't seem to find a doctor who knows anything about it. Where did you go to get diagnosed and what did they do?

[luckiebabe88]

I've been doing some research on EDS and I think I might have it. My joints are all flexible like yours, my skins not quite as stretchy but I also bruise a lot. My joints are always popping out, but I can always pop them back in. .. I know there's no cure for EDS... so I'm debating on if its even worth dealing with....I get a lot of joint pain, but I don't like the idea of taking pain meds... I'm also afraid my doc will have no idea what I'm talking about if I ask about it.... is it worth it?

[rodentrose]

i was video-surfing ahwhile ago and saw your video on EDS, and i was like i can do that and my skin is even stretchier. And started researching more about it, and all the blocks started to fall together; my joint pains, my easily bruised and damaged and soft skin. So i got an appointment and was diagnosed with it. Thank you :)

[AskariWaryaa]

Ehlers-danlos can also give you a marfanoid body habitus, so it's always good to not get the two conditions confused.