emma
Region: US
Monday 10 February 2025 22:35:48 GMT
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hannahfayem :
you make me feel like maybe I’m not actually crazy 😭
2025-02-10 22:47:40
71
Ally :
NO GIRL you make us feel less crazy. This was the first account I ever saw where I felt like I was watching MY LIFE play out in front of me ❤️❤️❤️😭
2025-02-13 06:40:00
17
Emm :
I love watching your videos! They help me so much don’t stop!!
2025-08-23 00:57:28
0
MamaMia 🇨🇦 :
Diagnosed over 20 years ago. Considered a top painful disease. Women’s health is so undermined and understudied!
2025-03-24 21:38:06
4
Vero💛☀️ :
I myself have the same condition. I didn’t notice till late. I know how it feels and I still struggle with treatment
2025-07-01 00:16:37
0
sayla 🖤 :
honestly thanking you for spreading awareness love 🩷 I've been dealing with endo symptoms for years & doctors never want to listen to me or take my concerns seriously
2025-03-18 03:26:26
0
just_breath24 :
I think that's me 😭 abdominal pelvic CT scan with contrast soon. I get called crazy too 😭
2025-08-13 14:05:32
0
Claudialykke77 :
SO TRUE!! ❤❤ Same situation in Denmark 😔
2025-02-11 08:05:44
1
the_queen_of_queens_1 :
Thank you . Currently on a horrible flare up of endometriosis and adenomyosis and it feels pretty lonely and frustrating . It affects your work and personal life so much
2025-07-14 15:41:14
1
Katie McG :
A friend once told me they call it practicing medicine because they’re ✨just practicing✨ 😩
2025-02-10 22:49:54
28
mkm13 :
you have helped me SO much, so thank you for being vulnerable and posting these moments💛
2025-02-28 15:37:47
0
Karissa ✨ :
Yup to everything you said 💯
2025-04-04 17:13:41
0
Tamuna :
🥺so familiar, i still dont understand (for me 3 years) how nobody thought about endo with my symptoms, thnx for your videos
2025-02-10 22:49:08
6
StregaSavy :
BECAUSE YOU HELP VALIDATE MY SYMPTOMS AND MAKE ME FEEL LIKE IM LESS INSANE, THATS WHY
2025-02-11 14:20:22
19
User648282637 :
I’m 19 and my parents act like my endo does not exist. Currently in bed having a flare up. Your content helps so much 🩷ily✨
2025-02-24 23:16:06
0
emilysarahcohen :
People that get it, get it
2025-03-02 20:01:27
0
j :
i’m diagnosed and your content is still validating to see. daily i say or thing “no one in my life truly gets it.” they think ill be better tomorrow, but it’s chronic. so thx for sharing w us
2025-02-11 06:36:17
2
syd :
you just described my life. I love your videos, you make me feel seen. I follow you on insta and you introduced me to myobi and somedays. THANK YOU ❤️
2025-02-13 22:36:26
0
Crystal Steers :
30 years, it took me 30 years & by the time my specialist did surgery I lost part of my bowel part of my stomach, I have permanent hip &nerve damage, the list goes on. People who get it get it 💕💕💕
2025-02-24 19:38:37
0
Carolina ♡ :
only us know what it's like to live with it and I think we deserve to talk about it because it's so hard! this is real and this type of content makes me feel that I'm not alone 🙏🏻
2025-02-13 19:05:29
0
spicycheesetaco :
Thank you for your service, Queen❤️
2025-02-10 23:34:22
1
Paul :
I appreciate you 🙏🙏
2025-03-04 12:50:05
0
kileigh_jordan🐟 :
How were you diagnosed what testing was done? I feel defeated :( gave up on doctors.
2025-02-11 04:44:04
1
Jessica Rae :
bc we need you . finally diagnosed after 8 years !
2025-02-12 20:05:36
1
ccs1988 :
12 years undiagnosed me is grateful for the other girls you're helping
2025-03-01 22:51:28
0
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