Hypermobility - Skin & Joints
Uploader Comments (moblifex)
All Comments (74)
-
for sure you have EDS! my daughter has it also. I have so much research on this syndrome that I would say an absolute yes
-
I didn't get diagnosed 'till I was 27. I got my first dislocation when I was 7 months pregnant and you can dislocate when you're pregnant anyway. I did gymnastics in high school and other sports growing up. It is genetic, my sister has it too, we believe we got it from our father, but he hasn't been diagnosed. They have both had several dislocations. For me, it's not a big deal, it just sucked when I was pregnant.
-
@moblifex Not every hypermobile person has dislocations or pain, your best bet is to do light weighttraining just to strenghen your muscles and i bet your hypermobility wont give you problems later.
-
PLEASE DONT READ THIS ,YES I HATE THIS BUT THIS IS TRUE.KELSEY BRIGGS IS A GIRL THAT DIED PEOPLE DONT KNOW HOW BUT IM SURE YOU WILL FIND OUT ON GOOGLE,WELL LOTS OF PEOPLE SAID THEY HAVE FOUND HER IN THEIR BEDROOM ,WHEN YOU SEE HER THE 4TH TIME SHE WILL KILL YOU AND YOUR FAMILY FORGETS ABOUT YOU ITS REALY SAD THE ONLY WAY TO PREVENT THIS DEATH IS TO COPY THIS ON 3 OTHER VIDEOS!!!I AM REALY SORRY I HATE PEOPLE WHO WRITE THIS!AND THIS IS TRUE SEARCH IT UP ON GOOGLE!START NOW
-
From vid I'd say good chance but you would know about dislocations if your anything like me how about hips? What's your left shoulder feeling like? Twist ankles now or when you where younger? All these things really mean nothing there are so many cross overs it's hard to tell.
-
I have EDS... I'm one of the those who gets frequent dislocations, but I've heard not everyone with EDS gets so easily dislocated...my point is, just because you don't get dislocated, doesn't necessarily mean you don't have EDS...my advice is to get a genetic test...
-
i can do this thing with the finger on 0:24
-
just need a soul dude
-
super duper eds..I have the same thing. If you are in alot of pain I would say yes. They have genetic testing. I have mixed eds which is both hypermobile and vascular. Just had heart surgery to fix the supra ventricular Tachycardia and it didnt work which leaves the only explanation of dysautonomia-vascular eds. sucks but I adapt ...accept and move on...learn to live with it. Its the only way to be happy.
not neccessarily. How many Joints are Hypermobile?
stretchy skin does not confirm EDS?
how do your scars look?
is your skin transparrent-like on your trunk?
do you have arthritis?
chondramalacia?
loads of pain every second of the day?
MCRdarkfaerie 1 year ago
@MCRdarkfaerie 6 fingers, both thumbs.
moblifex 1 year ago
Easy dude, i have the same thing, strechy skin but never had a dislocted joint or any of that...I only realised the other week and im 29 now...never had any problems and do loads of sport...if u r worried go and see the doctor but I im sure its nothing to worry about...looking on the internet makes anyone paranoid =0)
antjmi 2 years ago
Thanks.
moblifex 2 years ago
have you ever dislocated a joint?
if so it is very possible
cartercool90 2 years ago
@cartercool90 Yeah, when I was a baby my arm used to come out of socket a lot. This school year I also dislocated my pinky. Other than that nothing though.
moblifex 1 year ago