@lululemonlover76: #awareness #heds #disability #pov #fyp

Casey Jones
Casey Jones
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Region: US
Wednesday 29 April 2026 04:18:19 GMT
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dp_db_
NDHD :
Or general hypermobility, I went through all the testing and whatnot and I don’t have Ed’s but pretty much everything that goes with it (not stretchy skin)
2026-05-23 21:15:43
12
misktisk
femboy_luver :
I finally know whats wrong with me oh my god
2026-05-16 05:29:50
175
alex_d._shannon
Shannon D. Alex :
I was so mad when I found out I couldn’t donate plasma because of it
2026-06-22 04:35:47
1
i_love_my_man143
Ruby🖊️ :
The doctor thought I had it, but it turns out I’m just hyper mobile still sucks though
2026-06-14 06:01:36
10
nosehair.com
👩🏻‍❤️‍💋‍👩🏻 :
Like all joints hurt and it’s making me mad plus I have plantar fasciitis so my feet hurt up to my cankles
2026-05-21 11:28:50
26
_emery_164
Emerydayimshuffling :
Hey so I experience ALL of this but like ion have eds sooo…
2026-05-22 23:40:55
7
lazy_orca9595
Sunset9595 :
I have EDS along with celiac. if you dont know what celiac is. It's an Autoimmune disease that makes it so your gut doesnt getvthe nutrients you normally get from gluten. There are 200 known symptoms of celiacs and there could be more. if you have questions about celiac add me and ill do my best to answer all✨️✨️
2026-05-23 13:39:12
18
pokapotfox
⋆˚࿔pokapotfox⋆˚࿔⋆ :
the second picture is exactly how i feel all the time
2026-05-21 21:32:34
2
_soultosqueeze
ฅ^•ﻌ•^ฅ :
Literally constantly in pain. Take pain relievers everyday before work and some nights before bed. I use pain relievers patches and ice packs and heating pads. I’m 22, I’m so scared for when I get older
2026-05-22 12:26:52
10
arizonas_sunshine04
🪷𝒦𝒶𝒾🪷 :
The flare ups feel like your body is made out of Legos. They feel like they’re gonna break at any moment. 😭 It’s so painful. I work in a warehouse and it’s so bad during those said flare ups
2026-05-23 20:39:28
4
um.hi.16
Annalise :
Feel so seen rn omg🥹
2026-05-19 22:21:25
4
sourrat01
Sourrat01 :
I can do a lot of the things in EDS but I feel like I’m not in much pain to have it so I’m so confused why my body can move like this
2026-05-22 21:23:00
1
izbz1077
☆izzy☆ :
im getting tested for it right now! my pt says probably not eds but definitely hypermobile but we have genetic testing next
2026-05-23 16:09:36
1
ajwanawad16
Jojo🎀ྀིྀི :
I thought this was about Anna
2026-06-19 19:41:21
1
yourflower18
Ophelia🦭 :
I feel seen
2026-05-22 02:19:05
2
daydreamer_dreaming
daydreamer_dreaming :
😢 😭
2026-06-02 02:26:18
0
spiciestcookie
destroyer :
what
2026-05-24 23:20:12
1
masked_artist
Ashton🏳️‍⚧️🦴(he/it) :
me
2026-05-20 23:58:54
0
_silver_boi_
Sliver Stream :
no bc my bones are genuinely hurt all the night and it took me years to realize that's not normal. I was 12 complaining about back pain, I had untreated scoliosis.
2026-06-19 20:56:30
1
xbemylittlewitch69x1
🔮🖤Xbemylittlewitch69X🖤🔮 :
Hey so how do I go about getting my doctor to check for this? I knew since I was little something was wrong I’m constantly in pain! Super flat feet , my knees bend in backwards worse than the pictures showing it , I can’t walk for long my feet and legs swell. I’m just in constant pain all the time . And I can do everything on the Brighton test
2026-05-25 18:49:13
0
thebadestbitch17
La-Loyd? :
It's ture and I have it unfortunately
2026-06-20 21:38:29
0
flv511
Flv :
2026-05-21 16:21:42
6
theyfwstein
theyfwstein :
Everything kinda hurts
2026-05-22 20:49:26
2
t0x1c_b741n_zlvdg3
Toby :
oh hey..
2026-05-18 14:02:56
1
its.gay.meag
Meag :
Wait one darn diddly minute! This is why I can’t breathe?!? It’s not just allergies and a deviated septum 😱
2026-05-27 13:25:57
0
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