@melrobbins: 1 and 10 women struggle with endometriosis. In this episode of The Mel Robbins Podcast, Dr. Sharon Malone, one of the most trusted medical experts in women’s health, explains why severe period pain should not be ignored, what it may be signaling, and why so many women spend years having their symptoms dismissed. Dr. Sharon Malone has been in clinical practice for nearly 40 years. She explains what every woman needs to know about endometriosis, and why it can take years for women to get properly diagnosed. Stay tuned - this episode drops Thursday July 23rd! 🎧 “The Women’s Hormone Health Episode for Every Age: Take Control of Your Body & Feel Amazing”
The biggest tragedy isn’t endometriosis… it’s how long we’re taught to suffer before someone finally listens. 💛
2026-07-26 10:57:45
162
LadyGrady :
Stage 4. All over my uterus, ovaries, one ovary stuck to the top of my uterus & one ovary stuck to my bowels, on my bladder, inside of the bladder (my bladder was adhered to my uterus), gall bladder (removed), all of these organs were stuck together in a big ball. Had excision surgery, surgeon found it in my bladder while I was on the operating table. 2 months later went back in to have surgery on the inside of my bladder, the endometriosis covered my bladder wall. Fun times 🥲. So many doctors failed me.
2026-07-24 12:54:19
19
Lisa Donnelly makeup and nails :
Definitely have had it since starting cycles age 11. Attended gp office many many times and always told its just your body's way. Finally diagnosed 2017 after years of fighting. Horrendous condition. 🥺
2026-09-15 22:03:42
4
Robyn Prevost :
I’m one in 10 🤚… I don’t wish it upon my worst enemy!
2026-07-21 18:38:58
79
The Songbird Sings :
Just officially diagnosed after years of debilitating pain 💔
2026-09-16 17:12:02
0
Katie Martz :
31 and scheduled for a hysterectomy for Endometriosis, Adenomyosis and PCOS this month. Sadly I finally got answers this year. It truly is over looked or misdiagnosed. 💛 Prayers to anyone dealing with this. 🫶🏼
2026-08-03 06:04:53
33
noone05 :
I was diagnosed with endometriosis on my first ultrasound. The doctor used a gynecologic Doppler scan, which helped detect it.
2026-08-02 08:26:27
9
emma.m :
Stage 4 here! Had surgery to remove it at 22 but months later still struggling. It truly affects my everyday life. For so long I was told my symptoms were normal.
2026-08-31 13:58:20
5
lovebeatxz :
False! It’s it not the endometrium. It is similar to it. It is a mutation. I have suffered from endo for over 20 years and there is waaayy to much misinformation out there. It’s not about the uterus anymore it’s about there entire body being affected! Thank you for the awareness either way. 💕
2026-09-02 20:57:51
2
Grace D'O-A🦋🐞🤘 :
I'm 1 in 10, unexplained infertility.
2026-07-21 18:44:38
10
Coach Dallas :
Just want to friendly mention to those who are unaware of endometriosis, that for countless women the extreme pain is daily, debilitating, and life altering. Suicide rate is significantly higher in women with endo. Many woman know they have it and spend a decade convincing doctors to do something or believe their symptoms. It’s also been found in men so it’s much more than endometrial tissue growing outside of the uterus. Not at all to say that what was said here is wrong. I just want to put out there that it is SO MUCH MORE than this short video could express.
2026-07-21 20:48:45
5
ygnj :
what stressful for me is its so unpredictable, this month it can be easily handle with my usual painkiller, next time it wreck havoc, nothing works and I felt like dying.
2026-07-22 09:41:45
7
Savannah Regensburger, MS, MBA :
Extremely happy to see endometriosis being spoken about! This disease truly changed my life.
2026-08-06 15:01:58
10
Telli :
1 in 10 is only the statistics for women who’ve been diagnosed. 😞 So many women are under treated or misdiagnosed.
2026-07-23 03:22:18
11
Dogmom1979 :
I had severe cramps and fatigue my whole life and no doctor ever mentioned endo. I was finally diagnosed with stage 4 at 38yo. Now everything is basically fused together. Never was able to get pregnant. There needs to be alot more awareness.
2026-08-01 20:23:54
7
alisha :
I’m so happy that endo and PCOS are finally getting the attention they deserve, but can we also start talking about PMDD and other women’s health issues that are so understudied, even drs are unable to discuss 😭😭
2026-07-24 22:50:44
6
Versace70 :
I had this hell since I was a teenager . Suffering for more then 40 yrs! no dockors gave me any help ! they just said that it was normal!
2026-08-29 07:46:28
4
♥️ :
It’s excruciating 😖! I’d rather give birth once a month than have to deal with the pain of endometriosis!
2026-07-22 02:25:27
5
Kelli134 :
It robbed me of my life , im still thankful for what i do have but i have so much pain and bladder pain
2026-09-06 13:21:50
2
h_d_ouellette :
I had endometriosis and had three surgeries last year to remove where it had grown. It grew into my chest cavity, diaphragm, bladder, bowel, ovaries, pelvis. It completely cemented my organs together creating a frozen pelvis. It’s not talked about enough nor have enough education or funding.
2026-09-09 19:14:25
2
redlipsrevival_26 :
Thank you Mel for bringing this guest and raising awareness about endometriosis 🙏🏻🍀
2026-07-22 02:43:41
4
HumanLove :
So IBS can be endometriosis?! I cannot leave the home after eating anything.
2026-07-28 04:27:10
3
BellaGibson91054 :
Stage 4 here. Took 14 years to get diagnosed. Thank you so much for bringing awareness Mel! I have follow you for a long time you have helped me through so much! Thanks again!
2026-09-01 14:33:34
2
Annie :
Me watching this with extreme cramps right now , looking forward to watching this episode 💓
2026-07-21 21:38:18
3
Shadow Lily 🥀 :
I went for years & years with every symptom of endometriosis & was specifically asking & saying I felt this is what it was. I was dismissed repeatedly. Told “if you had it, you would know. You wouldn’t be able to get out of bed” etc. I’m like that’s why I’m here.. was accused to pill seeking bc of stressing the amount of pain I m in despite saying I didn’t want pills I wanted help. A tech even saw it on an ultrasound & the obgyn said she’s not qualified to diagnose you don’t have it … finally years later, end up in ER severe pain & have a huge endometrioma cyst on my ovary and was finally diagnosed after an internal ultrasound. Surgery is upcoming & I cannot wait to finally not be in pain every day of my life. It’s not once a month, it’s daily pain for me now. It’s exhausts me. Affected every aspect of my life. Dozens of doctors… all failed me.
2026-09-14 09:13:19
1
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