@lehuulong74688: Uncovering the Link Between POTS and Pelvic Venous Disorders! 🩺✨ #POTS #EDS #HealthAwareness #VascularHealth #fyp #ehlersdanlossyndrome

lehuuqinr94
lehuuqinr94
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Wednesday 07 October 2026 21:48:00 GMT
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33.luna.33
🌙Luna✨ :
can these disorders be found with an MRI with or without contrast?
2026-10-08 06:46:34
39
overlydramaticdare
Overly Dramatic Dare 😱 :
I have POTS and pelvic congestion syndrome both.
2026-10-07 22:02:25
61
sevolyentruoc1110
courtneylovesitso :
You guys watch the actual page this is a fake
2026-10-11 22:01:49
0
migibingus
ScoopOBingus :
This explains why I have a huge ivc and my uterus has tons of vascularity :/ I found this out because I was an ultrasound student, I also found a lot of my veins throughout my body were very large, and my thyroid was very vascular as well compared to all the other student’s anatomy
2026-10-12 22:36:13
0
jessicalee81
Jessica :
Would u see a vascular doctor for this? I got an ultrasound done on my legs but they didn’t see anything
2026-10-12 03:06:42
0
babymtuk
Melissa :
I have hypermobility and pots and I was told I had big veins in my pelvis but at the time I didn't follow it up and now I can't find the proof that existed.
2026-10-12 15:11:57
1
ratbag_jewellery
✯ Ratbag Jewellery ✯ :
This would explain my aching hips right???
2026-10-10 08:49:35
3
kalynnejensen
Kalynne :
My first diagnosis was Pelvic Congestion Syndrome. I had a vein embolized and all of my symptoms got so much worse.
2026-10-08 07:12:27
32
kthomas2016
Kimber Emerson :
What’s the testing needed?
2026-10-08 03:40:56
4
noharmminifarm
Catalina :
how is this diagnosed? (the compression)
2026-10-08 04:16:17
12
juleslarsen
Jules Larsen :
Would this explain why one side of my body goes numb randomly but not the other?
2026-10-09 04:57:50
7
katslaysandplays
KatSlaysAndPlays :
Diagnosed orthostatic intolerance. What doctor do I go see for the pelvis? When I asked the urologist what to do about the pain they said just keep doing what you’re doing.
2026-10-11 01:21:12
0
__a.rose
a.rose :
Weird question for people reading the comments; does anyone with POTS, OH or EDS get extremely cold with chills rather than the normal sensation of a full bladder? Especially in the middle of the night.
2026-10-08 05:29:45
8
kikiscreativelife
Kiki's Creative Life :
stop telling us the patience and go tell your colleagues doctors don't listen to us anyway
2026-10-10 07:23:48
11
newdawnblue54
YesINeedAllTheseCatsFU :
Only a 3-6 month improvement?
2026-10-08 03:38:44
6
katttbass
Kat Basman :
So what doctor can determine this or who am I supposed to see for this
2026-10-09 04:17:05
1
meatispartvegetable_2
B👁️tch :
I needed this video thank you. I’ve been having such pelvic issues. It’s miserable
2026-10-11 20:45:57
1
wrennables
jen :
this is so interesting because I have a lot of sacroiliac problems and I get blood pooling in my abdomen (and some urinary symptoms) but when I asked if there could be anything going on in the joint that was affecting blood flow they literally laughed at me and said muscles and joints are different to blood vessels.
2026-10-08 16:14:50
23
maiden2mother321
Lacy :
I have all the above, thanks to EDS
2026-10-09 13:52:45
5
nadinefoyster
Nadine Foyster :
im in the uk, who would we see to look into this , cardiology wont see me for pots symptoms, rheumatologist completely disregards my eds/heds symptoms, then dermatology was sending me for immunology/genetics for mcas , but they've also refused me and sent me back to my gp without even seeing me.
2026-10-11 16:48:46
0
sycamore_susie
Sycamore_Susie :
How do you even go about being tested/ diagnosed with this? I have severe vestibular migraine, PPPD, dysautonomia, pelvic/SI joint dysfunction, wide spread pain (I believe EDS or hEDS), BAV... and I can't really get anywhere with treatments that have been undertaken/ suggested. I just want answers and want to feel better, so I can get my life back!!!
2026-10-08 13:46:19
2
htedz
htedz :
possibly crazy coincidence, but could early term miscarriages cause this?
2026-10-08 03:34:01
4
4000rds
4000RDS :
My pelvic is not functional in the lady area…had endometriosis and PCOS got all that taken out…had precancer. So it all went bye bye
2026-10-08 17:25:25
2
highnoondragonfly
Gigi or Aunt Hoey :
I was diagnosed with SMAS and admitted for “emergency surgery “ . Surgery never happened. Suspected of more. The more constipated I am the worse the symptoms. In a yucky circle of WTF- it’s the SMAS is causing me to be unable to poop on my own. can’t find a doctor to treat it. I’m so tired of this game
2026-10-08 22:46:31
3
juliette.kranyez.artist
juliette.kranyez.artist :
Can it feel like a shooting pain when you stand up, in the hip/ groin?
2026-10-10 20:44:17
1
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