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-- hypermobility
hypermobility
anyone here has it?
Yes, in my fingers, elbows, shoulders, knees.
Why?
Just wondering if there anyone else who's as poorly put together as me 
Have you recieved medical treatment of any kind for your problems? And what about pain?
I have it pretty much throughout my body. Especially my spine, so I pretty much wake up several times every fucking night drenched in sweat because of muscle spasms. Oh and my right knee is totally fucked, I can 'detach' my calf from the knee joint, any direction i want.
Last couple of years it's been getting more and more painful, and now I've been sent to a specialist to see if I have Ehlers-Danlos Syndrome type 3/hypermobility type, so that's always fun.
No medical treatment for HM specifically. The rheumatologist I saw said that I had EDS Type III. Had a couple cardiac ultrasounds to check for heart issues. I have high blood pressure, but that is probably unrelated (my dad has it, too, with no hypermobility).
I'm very fortunate as far as pain. I did something to my knee a while ago and I don't think it ever healed properly -- I no longer run because of it, and it hurts sometimes. And my back "goes out" occasionally and feels stiff many mornings (don't know if this is related to hypermobility or not). But other than that I have been pretty much fine my whole life. Which I guess is kind of unusual for someone with hypermobility all over the place. Hope it stays that way!
Oh, also neither of my parents have hypermobility, nor my brother or any of my relatives. I guess I'm just the weird mutant. 
Oh a fellow EDS'er... Do you get mad awesome scars too? Like they're wider than normal but skin is thinner than on regular ppl. I've got a pretty bad ass one about the size of my thumb on my wrist.
The back going out is most definitely the hypermobility. On me it's just a matter of not paying enough attention when turning over in bed etc. It suuuuuuucks.
How old are you by the way? I know most people with EDS3 it doesnt really kick in until late twenties. Started getting BAD at 25-26 for me. But I think I havent noticed too much of the pain, being a wake&bake kinda guy, so it's taken me until now to seek professional help.
And that's really weird, I don't have any hypermobile relatives either.
Maybe we're adopted?

I will be 28 soon. I get scars somewhat frequently, but they don't look unusual. I believe odd scarring is supposed to be more common in EDS I and II than in Type III.
I really doubt that I am adopted, since my face is practically a copy of my dad's. 
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| Originally posted by Vector A I will be 28 soon. I get scars somewhat frequently, but they don't look unusual. I believe odd scarring is supposed to be more common in EDS I and II than in Type III. |
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I really doubt that I am adopted, since my face is practically a copy of my dad's. |
They need to stop naming diseases/conditions that sound shitty with names that make them sound awesome. Hypermobility makes it sound like you guys are able to teleport or some shit like that. 
Head shoulders knees and toes
Knees and toes
For the shoulder people; How often does you shoulder subluxate? And how much force is needed?
For me it's eough to carry like shopping bags for them to pop out. Also after I've started working out I can do it just by using the shoulder/arm muscles, I don't know what they're called, but it looks freaky. 
is there not a more derogative term for this condition ? hypermobility sounds like something i want.
Gimpitis Majora.
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| Originally posted by dj_alfi For the shoulder people; How often does you shoulder subluxate? And how much force is needed? |
this smells of restless leg syndrome.
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| Originally posted by Looney4Clooney this smells of restless leg syndrome. |


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| Originally posted by Vector A I'm not sure if it is actually even subluxing; all I know is that I can pop it out and then back in, in a way I've never seen anyone else do. Also, it almost never pops out involuntarily, and doesn't cause any pain. |
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Some of the fairly common symptoms of EDS, like frequent involuntary dislocations and chronic pain, have never happened to me yet. But I have all the crazy joint flexibility, so I got tagged with it. I read on an NIH site that some men live with the disorder until late in their lives without having those problems, so I hope I'm one of those dudes. |
caps lol
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| Originally posted by Vector A looool How about now? ![]() ![]() |
you seemed to have some sort of but device in the photo on the floor.
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| Originally posted by Vector A looool How about now? [pic] [pic] |
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| Originally posted by Looney4Clooney you seemed to have some sort of but device in the photo on the floor. |
Haha, I thought somebody might comment on that. It's actually my dog's chew toy: http://i.imgur.com/L8nZw.png
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| Originally posted by Vector A |
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| Originally posted by dj_alfi damn boi. ive never had that bendy fingers. they pull out, but not as far back. i think theyre getting arthritic (word?) though, so soon i wont have to worry about them moving about at all |
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| Originally posted by Vector A That sucks. Mine have never bothered me, even if I bend them back like that. It's supposed to be bad for the joints, though, so I don't normally go around showing people. |
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