It hasn’t been studied because it only happens to women
2025-10-18 06:14:57
24205
petuniamaye :
Raise your hand if you have endometriosis & a doctor has told you to “just get pregnant” to help it 🙋♀️raise your hand if you were 20 when they told you this 🙋♀️🤦🏼♀
2025-10-18 06:36:24
3758
poznajumepotebi :
No one of the hardest things about endometriosis is people caring more about women ability to reproduce rather than their health and wellbeing!
2025-10-18 00:41:15
6583
Aria’s journey :
No doctor believes how painful it is
2025-10-18 06:54:31
3492
Jaz :
My grandfather dedicated his life to trying to find a better way to diagnose endometriosis. He’s nearly 90 now and had to retire but made incredible breakfthroughs. His name is Fred Wong from Sydney University ❤
2025-10-20 12:29:32
1476
CVT.11741 :
Endometriosis has literally ruined my life
2025-10-18 11:43:48
2722
sami.k.77💜🦋 :
It’s basically cancer
2025-10-19 00:06:47
969
lala_moons :
The best thing I ever saw was “if not cancer..then why cancer shape?”
2025-10-18 11:35:46
959
mzabfab :
Even after removal of endometriosis women still have chronic pain. It does not end with surgery unfortunately and more surgery means more adhesions.
2025-10-17 23:41:50
3750
mosaicmind01 :
I am suddenly seeing all this media attention towards endo and adeno. Hope it converts to more research being done on it and not just talk. Whereas all these years we women have been dismissed by docs, friends and relatives where no one really understands how painful and taxing this condition is on the overall wellbeing.
2025-10-17 20:38:10
1546
articulatechaos :
I cried watching this. I’m so tired. So so tired. Nobody takes it seriously. Nobody sees it as the epidemic that it is.
2025-10-18 00:51:35
508
lifewithluchiax :
So good to see endo being spoken about accurately and honestly on a big platform
2025-10-18 00:15:10
451
ShadySipsWithK 🤍👑🐩 :
Endometriosis has ruined my life for 20 years now
2025-10-18 04:55:29
618
Billybob :
That’s so horrible and I don’t get why no one is researching it.
2025-10-18 02:10:43
899
beckgracediaries :
This was needed 🩷 lets raise awareness for endo
2025-10-17 20:28:53
711
Paige🆘🇺🇸 :
male pattern baldness is more studied than endo… think about that
2025-12-17 04:20:20
21
Tami_Studio_Grabski💪🤓 :
I was watching someone else and also a doctor saying why isn’t endometriosis classed as cancer! It destroys the tissues and affects hormones and fertility. Yeah sounds like cancer to me, more research please, more funding please, we need a cure please.
2025-10-18 08:19:16
277
NatCee :
When I had my laparoscopy, my surgeon was fascinated because it appeared my body had an autoimmune response and was literally fighting the endometriosis. She sent my results all over the world, no one had seen anything like it. She asked if I'd consent to having my details shared so it could be studied and I said yes, perhaps it would help advance finding a cure. That was 4 years ago and I haven't heard anything since. I assume it's because there is little to no research or funding in finding a cure, when my body could have shared some answers.
2025-10-18 12:19:22
550
Soychantelle :
I suffered for years even after surgery 💔 it’s exhausting and the pain unbearbale
2025-10-18 03:58:56
136
Aria’s journey :
Birth control made it worse for me
2025-10-18 06:55:12
128
EndoInk :
This is why I do free endometriosis tattoos and all I ask for is donation of any size all money goes to endometriosis research 💛 giving this illness some visibility and making money for much needed research 💛
2025-10-18 05:34:58
363
Georgia • Naturopath :
I have stage 4 and fell pregnant naturally just for anyone watching that got upset at that stat
2025-10-20 06:21:24
30
AmyBarry.xo :
i recently found of my endometrioma has over double in size to 11.5cm in less than a year and i have surgery in a few weeks. it’s really terrifying that this illness isn’t studied more.
2025-10-17 22:34:23
96
To see more videos from user @steven, please go to the Tikwm
homepage.