yovodo
Region: US
Tuesday 03 February 2026 23:30:33 GMT
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Aster :
I gave myself bilateral carpal tunnel sewing masks in 2020, I wish I could tell every hypermobile crafty person to wear ones like this now so they don't have to wear the ones with big hunks of metal in them that I needed to recover 😭
2026-02-05 01:31:38
1000
🌲Of the forest🌲 :
it is a good idea to know what kind of hypermobility you have as you may need to take even further precautions
2026-06-14 22:31:10
477
bonanza.jellybeans :
building strength also helps protect the joints
2026-02-07 19:34:15
364
🦇Calem🦇 :
I have hEDS and was "fine" until 27 and I gotta say - get a pt who knows how to deal with hypermobility asap. I put off diagnosis and tried to diy treament for years. there WILL come a time when this crashes. it's not worth it. get on a routine before you have to fight for one. I cannot stress this enough. you have to relearn how to hold yourself and do everything, and having hands-on guidance cannot be replicated with research.
2026-02-18 02:45:28
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Ameen :
I gave up on a formal diagnosis when I, a) saw the price for seeing a geneticist 🙂, and b) understood that knowing doesn't provide a cure, its just a thing you live with and can only alleviate by strength building. but being told by my ortho doctor that im likely hypermobile was pretty validating after feeling all these problems all my life
2026-07-06 08:56:53
36
Adore :
pro tip: restrictive braces with metal in them are bad for hEDS unless you are actively healing an injury. You weaken the only thing holding your wrists in place (your muscles) and increase your chances of injury.
2026-02-28 18:06:03
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Sarah B :
As a hypermobile lab scientist, BE CAREFUL WITH YOUR NECK! Constantly looking down caused problems for me over time 😅
2026-03-04 17:45:28
97
Seren :
It fitting under nitrile gloves is PEAK I might need to try these
2026-02-05 02:50:33
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Emry (xe/xem or they/them) :
I relate a lot to this with how I felt a few years ago. I kept saying my “benign” joint hypermobility probably wasn’t full-blown EDS (and thought I may not get the hEDS diagnosis due to preexisting diagnosis of Sjogren’s) until my shoulders started going out in my sleep… I was already getting the same PT I would get for EDS, so I didn’t think I needed to seek the diagnosis until it started becoming debilitating which prompted me to get more serious about using the diagnosis to get insurance to cover prophylaxis or earlier interventions for related issues (this does take some persistence and doctors’ cooperation to appeal a lot of the time). The other argument for getting a diagnosis would be that if you were to need emergency surgery, the surgeon could use suture techniques that are less likely to tear out of hypermobile tissue, but you can also ask your providers to note that you may have fragile stretchy tissue in your chart to help guard against potential complications without seeking diagnosis at this time
2026-02-05 02:20:55
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Brady Bones :
After struggling with chronic joint pain my whole life with no answers, it took a new physical therapist one look at me to tell me that I’m hypermobile 😭 I’m a crocheter so this seems perfect for me! Thanks for sharing and I love your fits!
2026-02-04 20:09:06
271
floatawhile :
If and when you’re able I would recommend seeking a diagnosis. If you develop other health issues because of the hypermobility it can really speed up the diagnostic process. 💗
2026-06-13 19:18:12
5
Sunny :
You look so cool omg
2026-02-06 19:20:42
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momma.spooky.bunny :
Just a warning. You may want to try to figure out what it is and soon. The reason is because it could be the reason you get sick as often as you do because some hypermobility issues are immunocompromisations on top of it. Be safe hun, and good luck.
2026-02-23 17:28:25
9
vampirepeepaw :
unrelated but the way your lipstick matches your shirt??? stunning
2026-02-07 03:49:46
9
weewoo :
YOU HAVE THE COOLEST STYLE like edna mode would LOVE love you xx
2026-02-11 19:06:00
0
The Eternal Forest System :
As someone with hEDS, if you are able please get your hypermobility checked out by a doctor. EDS effects the whole body, can change how you react to medications, can change how surgeons operate on you, and with some subtype can have deadly complications. Use braces/compression garments on your own in the meantime if you want but get checked by a geneticist to make sure it's just your joints that are effected. 🦓❤️
2026-02-10 21:17:07
10
Sunnycutt Art :
yess as an illustrator with a family history of arthritis everyone take care of your hands! take breaks and stretch my loves. in fact I do need to replace my own wrist bands ❤️❤️❤️
2026-02-04 21:46:23
17
Krystal :
i was literally looking at one yesterday, and was wondering how helpful it was, thank you
2026-02-07 11:11:53
6
jojo 🇵🇸 :
also hypermobile and going into lab work soon! ive always used my hands a lot for art and while i havent had many problems with them, i wanna keep it that way!! will definitely be looking into these 🙂↕️
2026-02-06 19:22:04
6
ItchyPu$$y :
Why wouldn’t you seek a formal diagnosis?
2026-07-22 16:16:51
2
Megan :
As someone who went without diagnosis for YEARS and recently got diagnosed, I HIGHLY recommend physical therapy if possible. Assistive garments help, but it’s nowhere close to the affects of PT imo
2026-03-15 17:01:39
4
kat of the week :
my shoulders are hypermobile and ive had to just completely stop wearing bras or tight tops
2026-07-02 15:37:49
4
Sherry Zhang :
Wait I can’t see the link ;-; what’s the brand? Or can someone copy and paste the link pl
2026-02-25 18:54:47
1
roe :
fun thing about hypermobility it affects your blood and lymph vessels. highly suggest trying mld massage therapy
2026-03-10 06:44:37
4
bubbles :
I bought them from your link cause you look cool, and I already have carpal tunnel
2026-07-05 04:33:55
2
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