@shanecooke12: 😱 SHOCKING TRUTH: For 30 Years HEDS Patients Were Told 'Just Connective Tissue' – New Study EXPOSES Blood Proteins Causing IMMUNE CHAOS, Not Collagen! 80% Linked to Inflammation & Clotting – Your Symptoms Are REAL 💥 #hEDS #EhlersDanlos #ChronicIllness #MedicalGaslighting

June Court
June Court
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Region: US
Saturday 15 August 2026 13:01:04 GMT
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vintagegemini82
VintageGemini :
I have HEDs, MCAS, POTS, I’m rh-, have double clotting MTHFR, I’m allergic to everything, past menopause as well. I feel like I’m drying daily. Daily migraines too.
2026-08-17 18:02:30
11
sdp83467
SDP83467 :
We all know it’s an inflammation issue someone needs to find the treatment
2026-08-15 18:33:26
97
manicpixiecabgirl
Manic Pixie Cab Girl :
In a flare & I feel.like all my bones are breaking 😭
2026-08-17 22:59:57
4
thenirvanamama
lindsey • fort worth creator :
As someone with HEDS, we’re exhausted
2026-08-16 14:53:14
27
nanettekeepsherheadup
Nanette :
i have all the other problems, but i have deds. i think every ctd causes auto immune shit😅
2026-08-17 06:43:28
0
stratohaline
Amanda :
idk if it is a chicken or an egg situation, but hopefully this will lead to a blood test
2026-08-17 03:45:00
2
georgianavear
georgianavear :
And this is why i have now developed rheumatoid arthritis
2026-08-16 14:28:18
18
nyralunellauthor
Nyra Lunell 📚|Aspiring Author :
MCAS is insane and I hate it 😩
2026-08-16 16:18:39
7
mmmm393911111
mmmm393911111 :
Literally had a cardiologist tell me it's just a flexible jointbissue and has NOTHING TO DO WITH THE HEART
2026-08-16 06:10:38
19
manthedann
user7569212720953 :
Blood is a connective tissue.
2026-08-16 07:55:27
20
anonymous555555555555555
user686271751687 :
Is this why there is angiodema ??
2026-08-16 14:54:02
1
amberstarrrn
amberstarrRN :
This is what happened to me, after two bad viral episodes over two years, my system has gone haywire and I am still trying to get it sorted out! 😭😭😭
2026-08-15 13:21:29
11
chocotaco888
ChocoTaco :
I suspect it affects the interstitium too
2026-08-16 14:16:37
3
.bruja.athena
Brujã.Athena :
this is what kicks my ass every day.
2026-08-15 14:18:01
4
dollfacetosomeone
dollfacetosomeone :
I have type 3. I tell doctors that I have type 3 so they don't automatically write me off as seeking because I couldn't possibly have the symptoms I say I have when they think "hypermobile" just means I'm more flexible.
2026-08-16 22:32:03
1
blyssbybalance
Loving life! :
https://www.musc.edu/content-hub/News/2025/12/29/rethinking-heds
2026-08-16 05:18:04
4
nancycollinsphotography
Nancy :
What’s the study called!
2026-08-16 08:00:58
2
bb1234holla
1234ideclareathumbwar09 :
Yup. We know this and we want a fix. I’m 44. Showed symptoms since a very small child. It’s always something. Currently I’m battling parvob19 chronic. My immune system cannot clear it.
2026-08-16 00:53:04
6
zebrawarrior
Zebrawarrior :
Rubbish study doesn’t solely compare hEDS, how can they make claims when they’ve compared it to anyone on the hypermobility spectrum? IMO the studies from Norris Labs are being pressured to align with EDS societies goals since they fund them
2026-08-16 15:03:34
3
isabella.thomas68
Isabella Thomas :
So is it autoimmune because I have two autoimmune conditions and lipodema and hds and they can’t see any connection
2026-08-16 23:00:34
0
12345sld
Stevie1111 :
Huh
2026-08-16 01:12:12
0
xnamelessowl
poupy 🦉 :
so that would explain why i became symptomatic (and dramatically disabled) after covid...?
2026-08-16 15:09:00
2
george35813
Lester :
Coagulation? Maybe that explains the DVTs
2026-08-16 10:00:20
0
tallnewyorker8
TallNewYorker :
❤️
2026-08-17 03:31:34
0
_sunny_sig
☀️sunny☀️ :
@ThirstiiKirsty
2026-08-17 12:28:48
0
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