#vEDS
Sense halpe! Imb as tha veds! Flerkin 🐾
November 28, 2025 at 3:59 PM
Vascular Ehlers-Danlos syndrome (vEDS) is a heritable connective tissue disorder that makes the connective tissue very fragile, particularly in the blood vessels and hollow organs. vEDS can cause life-threatening complications. Learn more about #vEDS: www.ehlers-danlos.com/veds/

#VascularEDS
July 7, 2026 at 10:44 AM
April 10, 2025 at 10:30 PM
"It is a suicidal attitude."

The Pope, on conservatives:

www.youtube.com/watch?v=VEdS...
POPE
www.youtube.com
May 19, 2024 at 11:52 PM
❤️Help us raise awareness of vEDS today - Comment below with where in the world you're joining in from and share your photos!

Learn more about vEDS here www.ehlers-danlos.com/veds/

#vEDS #VascularEDS #Vascular #VascularEhlersDanlosSyndrome #EhlersDanlosSyndrome #MyEDSChallenge #EDSawarenessmonth
vEDS - The Ehlers Danlos Society
Learn about Vascular Ehlers-Danlos Syndrome (vEDS) and it's signs and symptoms. Navigate the body map to learn more about the condition.
www.ehlers-danlos.com
May 16, 2025 at 5:26 AM
With awareness, we can ensure earlier diagnosis and monitoring to improve and save lives.

With awareness, we can increase the number of research studies into vEDS, working towards treatments and therapies to improve and save lives.
vEDS - The Ehlers Danlos Society
Learn about Vascular Ehlers-Danlos Syndrome (vEDS) and it's signs and symptoms. Navigate the body map to learn more about the condition.
www.ehlers-danlos.com
May 16, 2025 at 5:26 AM
Vascular Ehlers-Danlos syndrome ( vEDS ) is a rare type, maybe 1/100,000 and can be genetically tested looking for the COL3AI gene mutation but here are some key markers
#vEDS
Do you know the red flags for vascular #EhlersDanlos syndrome? Our clinical pathway outlines red flags, diagnostic steps, and essential follow-up for patients with vEDS.

Learn more 👉 bit.ly/4hEn7en

#RareDiseases #vEDS #PatientPathway #vascularhealth
April 15, 2025 at 5:49 AM
When I was diagnosed with vEDS I was crushed. I was angry it took over 3 decades to figure out because of the harm that had been done to me

My solace was that nieces & nephews would have the benefit of my knowledge

Some are in the US & won’t consider preventative care before MAHA kicks in. Tips?
February 14, 2025 at 9:24 PM
Arterial Fragility is a real thing: vEDS is the subtype more likely to suffer from arterial rupture, but it can happen to any subtype due to collagen abnormalities. EDS is FAR more than being bendy 🩵🦓🩵

#ehlersdanlossyndrome #ehlersdanlos #EDS #vEDS #chronicillness #raredisease
November 11, 2025 at 8:32 PM
Oh, you mean my mother who decided she has vEDS (she doesn’t, we both have plain ole hEDS) and then when she did genetic testing and the geneticist and my EDS provider both told her she has plain ole hEDS, not life threatening vEDS, got Claude to assure her she was right and she has vEDS? 😭
May 17, 2026 at 11:05 PM
Thoracic aortic enlargement is only present in less than 10% of people with COL3A1 deficiency, ie you can’t screen for vEDS with an echocardiogram, please don’t try this at home consult a professional
July 29, 2025 at 9:20 PM
🌟 Did you know there are many types of #EhlersDanlossyndrome (EDS) and #hypermobilityspectrumdisorder (HSD), each with their own distinct signs and symptoms?
May 9, 2025 at 3:40 PM
Arterial vs Aortic Events in #HeritableThoracicAorticDisease
N=1790
#VascularEhlersDanlosSyndrome
#LoeysDietzSyndrome
#MarfanSyndrome

Risk by 40 y/o
Arterial
♂️vEDS>LDS~MFS
♀️vEDS~LDS>MFS

Aortic
TGFBR2>FBN1>TGFBR1~TGFB2>COL3A1~SMAD3

#AortaEd
#JACC 2025
www.sciencedirect.com/science/arti...
June 25, 2025 at 7:23 PM
I remember seeing somebody on Vent who was dying from vEDS and one day they just suddenly stopped posting. I still think about them. I hope that they've found peace, wherever they are
March 19, 2025 at 4:25 PM
“Two years of daily irbesartan, a long-acting oral blood pressure medication, reduced the risk of severe arterial events by 50% in adults with vascular Ehlers-Danlos syndrome (vEDS).”

ehlersdanlosnews.com/news/blood-p...
Blood pressure medicine combination cuts vEDS arterial events in...
Two years of daily irbesartan, a long-acting blood pressure medicine, reduced the risk of severe arterial events by 50% in adults with vEDS.
ehlersdanlosnews.com
March 1, 2025 at 4:56 PM
Today is RARE Disease DAY 2025!💜

EDS has 13 types—12 can be genetically tested.
But are we rare or just rarely diagnosed?

🧬Do you have a rare type like Classical (cEDS) or Vascular EDS (VEDS)?

Join the conversation: #RareDiseaseDay
#EDS #HSD #VEDS #CEDS #hEDS
February 28, 2025 at 5:34 PM
Understanding vEDS – A severe form of EDS affecting blood vessels, organs, and skin, with life-threatening risks. Early diagnosis is vital. To learn more check out the resources at UnremarkableMe.com
#vEDS #EhlersDanlos #RareDisease

www.unremarkableme.com/post/veds-ge...
vEDS, Genetics, Biomarkers, and How to Live Life Like a Tissue Paper Superhero
Vascular Ehlers-Danlos Syndrome (vEDS) isn’t your average connective tissue disorder. Nope, it’s the drama queen of Ehlers-Danlos Syndrome (EDS), shaking up your blood vessels, organs, and skin with t...
www.unremarkableme.com
February 20, 2025 at 10:05 AM
The Marfan Foundation just published activity and exercise guidelines for people living with Marfan syndrome, LDS, vEDS and related disorders developed by experts from the professional advisory board
marfan.org/resource-lib...
Physical Activity Resource - Marfan Foundation
Exercise & Physical Activity With the right guidance, children and adults living with Marfan syndrome, Loeys-Dietz syndrome (LDS), or Vascular Ehlers-Danlos syndrome (VEDS) can — and should — safely i...
marfan.org
May 6, 2026 at 2:55 PM
🌎It’s Day 2 of the 2025 International Scientific Symposium here in Toronto, Canada! Today, sessions will cover classical EDS (cEDS), vascular EDS (vEDS), and research into rarer types of EDS.
September 18, 2025 at 8:11 PM
I wish i could help, but even pre MAH(ell)A, vEDS care is limited. I am trying to figure out how to get my 2 vEDS babies out of this country
February 14, 2025 at 9:32 PM
Join the #REDS4VEDS campaign today Friday, May 16, and help to raise awareness of vascular Ehlers-Danlos syndrome (vEDS).⁠ ⁠
⁠
To take part simply:⁠
⁠
🔴Wear something red⁠
⁠
🤳 Post a picture on social media with the hashtag #REDS4VEDS⁠
⁠
May 16, 2025 at 5:26 AM
Dalton has a twin sister now!! Her name is Remy and she has vEDS, unfortunately making hed dad Jik view her as a failure of an experiment. Remy and Dalton both try to keep each other safe from their horrid dad.

[ #ocsky ] [ #shundraws ]
December 26, 2025 at 10:08 PM
Day 16 – Wear Red 4 vEDS ❤️
"Global REDS4VEDS Day! A day dedicated to raising awareness of vascular #EhlersDanlosSyndrome: show support for people living with #vEDS. 👉 Wear red, take a selfie, and post it on social media + #REDS4VEDS
Info: @ehlersdanlos.bsky.social
#VascularEDS #EDS #raredisease
May 16, 2025 at 1:05 PM
#VascularEhlersDanlossyndrome (vEDS) is a heritable connective tissue disorder that makes the connective tissue very fragile, particularly in the blood vessels and hollow organs.

youtu.be/hL2uWv1z7vc?... #Healthcare #HealthProfessionals #Vascular #vEDS
A Doctor’s Guide to Vascular EDS: Recognizing the Signs for Early Diagnosis
YouTube video by Doctor Clair
youtu.be
September 26, 2025 at 1:13 PM