I Have Endometriosis... | My Story, Symptoms, What I've Gone Through | Lauren Norris

[@maryelizabethpendergrass2562]

Coming from a girl who was told she was "making up" and "being dramatic" about having a blood clot, only to be determined later that she did have a blood clot and could've died, I feel you. As women, we are constantly ignored by healthcare professionals and it's something we NEED to talk about. Thanks for sharing your story, let's keep this conversation going.

[@TheLaurenNorris]

Thank you and so happy you’re safe💖

[@roselee1974]

I feel for you. I had over four surgeries for this disease. 20 plus years back, they didn't know much. I was always sick or in and out of the E.R. All this happened after I had my Daughter. I get the Endo stomach alot. I am glad you finally got someone to listen to you.

[@920roxy]

Lauren u got this gril your awsome stay strong😊

[@brbwlk]

I am a 61 year old African-American woman. At 53, I was finally diagnosed with an autoimmune disease after a life time of illnesses and hospitalizations caused by the autoimmune disease. When I was 22 I needed surgery. A doctor told me I was just anxious and take OTC medicine to calm me down. Six months and several doctors later I had the surgery. Women are often told we are being dramatic, attention seeking, et cetera. So very, very glad you finally got a diagnosis. God be with you always.

[@hannahmaldonado3665]

So many women, including myself, have endured medical gaslighting. The best healthcare I've ever received is from my university. During the short time I had private insurance, the healthcare wasn't great either. Medi-Cal and healthcare systems in general need to do better. Thank you for sharing!

[@wearethelarosas6395]

Oh, Lauren! I’m so sorry you went through this but I’m happy to hear you have the answers you deserve! 🤗 I have found that female doctors can be some of the worst, from my own experience, if they haven’t had the same issues and they have trouble empathizing. Get Well Soon! ❤️‍🩹

[@damoab1909]

This is crazy. The healthcare system is damaged.

[@VanessaWhatever_]

Ugh this is so frustrating! I’m so sorry this happened. The healthcare system is broken. 😞

[@jessicadeimar6992]

This is so sad that so many women get disregarded for our very true symptoms. For 10 years I felt unbearable pain every cycle and I had multiple doctors refuse to do more exams. One doctor told me I might be a hypochondriac and another said it’s just period cramps take a midol. Well recently I switched to yet another doctor and they found endometriosis, a large fibroid and multiple polyps. This new doctor said the pain level with the amount of endometriosis found and the masses would be equivalent to birth pains. It only took 10 years to be heard. We know our body’s and we know when something is wrong.

[@sadohljones3724]

As someone who ignored for over 20 years and finally diagnosed in my 40s. No one will ever know the pain of this disease unless you have it. I’m glad you are getting help. Prayers for you.

[@OceanBlue-l1u]

41 and was diagnosed 6 months ago with endo. But even though I am diagnosed I got no help so far so it really dosen't matter because with endo there's not much a doc can do. Yes, there's the surgery but that's not the answer because it comes back so yeah.

[@lovesgucci1]

@ I’ve had two surgeries & my pain isn’t worse than it’s ever been. After my first surgery, I was great for over a year. The second surgery didn’t even work! I literally felt the endo pain through the morphine after surgery & they tried to tell me it was just the surgery pain - as if I couldn’t tell the difference! Norethindrone (5mg) has helped a lot. Also, use an ice pack, not a heating pad for your pains!! I got lucky when I diagnosed because my gynecologist’s daughter had it & recognized the symptoms. The downside was that no one ever heard of it before & my girlfriends thought I was just being dramatic. My boyfriend was a lot more understanding, mood swings and all 😂

[@AmeliaPascoe]

As a nurse watching this its brought me to tears, I'm so sorry you had so many horrible experiences. You should be so so proud you kept on fighting for your health. All the love Lauren love you x

[@TheJemimabean]

Lauren, this really struck home for me. I'm 53 and I have suffered these symptoms for so many years. The pain is indescribable. You literally can't do anything, and nothing helps. Endo belly is horrible. You feel alien in your own body. My doctors never listened either. "It's normal". When I finally got approved for a hysterectomy (after doing everything they asked for FOUR years), I had fibroid tumors in my uterus the size of a 7 month pregnancy. They were benign (noncancerous), thank the Lord. I had a deformed ovary with multiple cysts and a very large cyst on my right fallopian tube. That's the side that has always given me the most pain. I was in surgery over 6 hours while they worked to get all of it out. The endo lesions were everywhere. I'm pain free for the first time in twenty plus years.

[@sallyjane8274]

I'm so happy to hear you are pain free! My right side is my problem side too.

[@jovialambience5638]

My right side is my problem as well.

[@aseygirl9295]

It breaks my heart that you would rather feel extreme intense pain than go to the ER and deal with a medical staff that doesn’t believe you 💔 That should NEVER happen… EVER. It’s happened to me and it’s a horrible feeling and like you, I figured out myself what was going on and it turned out I was right. You are so, so stong and brave, amazing job at being your own advocate until you got answers!

[@Gulfcoastgirl22Kelli]

I am one of your older followers at 54 years old. I had endometriosis as well. Unless you have it, there is no way to really explain it because there are so many different symptoms. But I want you to know you were heard and you are validated! I’ve been through so many things in the course of my years. After having my children, I opted for hysterectomy which may be controversial. Regardless of what you choose to do with your body, I want you to know that you have a huge following of supporters myself included. I am so very sorry you’ve had to endure this, especially in private. I will say you’re one of the few people that will share things online in hopes of helping other people whether it was Elle’s sickness or now your own. I will be praying for your path. You are strong you are beautiful and you are amazing. God made you and you are perfect!💕

[@indierad]

I’m turning 50 next week. The way she was dismissed was awful.

[@angelabeatty6538]

🙋‍♀️56 over here😎 I am horrified by how this sweet woman has been treated!!!😡🤯❤️‍🩹

[@jennharman2396]

I am so happy to see that there are other “older followers” of Lauren! I have raised 2 boys and I love them dearly, but if I had been blessed with a daughter, I would have loved a daughter like Lauren. So happy to see other older women following her!!

[@TheLaurenNorris]

Thank you so much for sharing your story!💖 I am so sorry you had to go through that. Thank you for all your encouragement and support🥹💖

[@snowygirl131]

​@jennharman2396 🙋‍♀️ A 60-yr-old here! Exactly; a daughter like her would make anyone proud! It makes me happy to see the next generation enjoy the benefits of progress we fought so hard to make happen.

[@heyyyitsnat]

I cannot FATHOM how health professionals can push their notions of “you’re making it up” on us. I feel such rage too when I think about people not thinking Endometriosis is not important enough to do more research on.. I’m so so sorry you had to go through that, sending you all my hugs Lauren😭💓 .. To all the women who are going through endometriosis, please please PLEASE consider going to Penang! I just got endometrial surgery myself, and multiple friends have recommended me go there to do this since they experienced a successful surgery themselves. The doctors were quick to diagnose, and they told me sooo many women go through endo! for me, in total with all the checkups, I think would total up to around 28000 Ringgit or less, incl all surgery fee, hospital room fee, food in the wards, medicine when you’re a patient (which would be: arnd 6000 dollars I think) I had my own long journey w Endometriosis so I thought I’d share in case this can help someone, anyone. I’m truly looking forward to be healthy❤sending love to all women struggling with menstrual pains/ any reproductive pains! Thanks for the video Lauren! Stay healthy and happy recovery!

[@LJHolly]

As someone with PCOS, I've had countless awful OBGYN experiences. I am so deeply sorry for what you've been through. Women, people of color, people in larger bodies, etc. are constantly gaslit and dismissed by health professionals, which is deplorable. Medicine was never designed to ensure that EVERYONE got the care they need, and we need to advocate for change. The field of medicine needs to DO BETTER. This is a great example of how the patriarchy, how fatphobia, how racism shows up in such deep embedded ways in our society. Thank you so much for sharing your story.

[@TheBiafashion]

Lauren, I am so sorry you went through all that with health care professionals. It is sickening how women are consistently ignored and mistreated, and the conditions that affect us are under researched. I wish you all the best and hope you have better experiences from now on!

[@Amanda20248]

💛🎗️🎗️🎗️🎗️🎗️

[@thefroggy_664]

Sweet girl, I'm so sorry that our healthcare system failed you so many times. But I so greatly admire your courage in sharing your story. I watched your college vlogs while I was in college and your joy was always a great comfort and inspiration to me in the hard times that come with being a college student. I don't have endo, but I've always struggled with horribly painful periods. Having your pain belittled and dismissed is one of the most humiliating and dehumanizing experiences that anyone can go through, and unfortunately so many of us women have experienced it at one point or another. I went to the student health center for a UTI once and the doctor told me that the only thing he could do for me was prescribe birth control... No recognition of my horrible pain (I was weeping) & no bothering to really look into the issue (which in my case was easily identifiable and treatable). I'm so proud of you for advocating for yourself, even when you felt like you couldn't. I'm so glad to see that you're finally getting some answers. Keep smiling & keep being your beautiful self

[@graceclennon8513]

People that don’t have chronic pain have no idea the emotions that overflow when you’re validated by a physician! I’m in the process of my diagnosis for Endo too after being diagnosed with PCOS. Your video gives me hope that I’ll eventually get diagnosed! You’re a role model and I appreciate your sharing this story. Thank you so much. Currently crying😂 congratulations on your diagnosis.

[@MicarahTewers]

Oh my goodness, I wanted to hug you so bad at so many points during this. 🥺 what a nightmare. So glad you finally got the help you deserve!

[@jennharman2396]

Please report the OBGYN that told you that endometriosis isn’t real to the medical board. They need to be held accountable for providing false information that could lead to other medical concerns for patients. As a psychotherapist, I have had women in my office who were treated like you were. They developed anxiety, depression, and a clinical mistrust of the medical community. These doctors caused them to develop mental health disorders bc they were told they were liars, dramatic, immature, and sometimes pill seeking addicts! It’s horrible what you went through. Thank you for bei my so transparent for the young women who are your peers and those who look up to you as a mentor & someone to aspire to be. I pray that the remainder of your endometriosis journey is a better one and that the doctors that made you feel less than, see your story and they apologize for causing you 13 years of unnecessary trauma and pain.

[@samanthabixler8568]

💛it is frustrating as women that we are told to "wait and see" or "this is normal" about all things pertaining to our reproductive health. Thank you for sharing and setting an example to be an advocate for your own health. I hope your recovery is smooth. I am 26 and seeking proper help for my own set of feminine health issues. You are NOT alone!

[@kristentucker1049]

I was diagnosed with stage 2 Endometriosis in 2020 when I had my laparoscopy surgery. It’s so sad but I remember feeling happy when they told me they found it. Years of my life spent feeling crazy because I had pain that no one could see or understand. Unfortunately I am one of the unlucky who has infertility because of this condition. If I could go back in time, I would freeze my eggs. We’ve done fertility treatments with no success yet. I will say, the surgery helped my pain a ton but recently my symptoms are coming back which isn’t uncommon as there is no cure. I wish you the very best in your recovery! Thank you for being open with your story! Endometriosis isn’t talked about enough so I appreciate you using your platform to speak on it.🎗️

[@suhanishah3073]

I am suffering through the similar situation. Let me know if you are willing to connect. This way we can help each other.

[@laurielee7520]

💛 Lauren, I am an RN and mom to 4 girls. I’m so sorry that you have been ignored for years. Now you live in a city with some of the best doctors in the world. So thankful that you kept pushing for answers and good medical care. You deserve that.

[@KiaraMadisen]

I’m so sorry you’ve had to experience such a runaround with the messed up healthcare system. So frustrating and I’m so proud of you for advocating for yourself and fighting for the answers you deserve. Your story is going to help so many others ❤

[@JoleneH756]

I’m 29 years old, found out 2 months ago that I have Endo. It’s really heartbreaking to me, especially because I’ve been told my entire life that it’s all normal and I’m just overly dramatic. I’ve already had one emergency surgery with my one fallopian tube (which unfortunately I no longer have) and was told after I demanded more test be done that “there’s slight damage on my other tube, but I’m super healthy and nothing is wrong and I don’t need to be concerned” - so finding out that I have Endo and there are major infertility connections to it has finally given me some answers to why my one tube was removed and the other one is damaged and also that all of this wasn’t me being dramatic and that it’s a very real pain and issues I’ve been having. Thank you for sharing this video 💗 honestly, without the internet and being able to connect with people all around the world, I probably would have still believed that “it’s just normal” - all of this really gives me hope that living with this pain and being intense pain killers doesn’t need to part of my future forever and that I can actually do something to heal it 💗

[@hopesmith1471]

I am only 27 years old just had a hysterectomy and my ovaries removed because of endometriosis had 3 surgeries in the last year because of how severe my endometriosis was.. I feel so sorry for anyone dealing with endometriosis. Praying for your recovery 🙏

[@jennacaswell4467]

This is exactly my experience! The gaslighting, the years of vomiting and passing out during periods, the doctors telling me it's all in my head, the YEARS of infertility with no answers. Finally, a doctor believed me and did the surgery to diagnose and treat. Afterward, he told me that I had one of the worst cases he had ever seen and that he couldn't even burn off all the lesions as some had fused my internal organs in places he wasn't comfortable ablating. It has been 4 years since my surgery and my symptoms have improved so much. I don't experience endo belly as often and my periods are so much more bearable now. It didn't cure my infertility but I am so thankful someone finally listened after all that time!

[@the.aspycat]

this story makes me sad to be a girl. i’m so sorry that you had to suffer for so long lauren. praying for a speedy recovery and (hopefully!) less pain 🫶🏻

[@nicole3876]

I was shocked to see this title under one of your videos Lauren. I originally found your channel because I was insecure about starting college a little bit older and stumbled upon your videos. I was happy to be able to relate to someone who was the same age I was when starting at a university and have been a subscriber since, your videos made me feel a lot better. Saddened to know we relate on more than just that now, I actually flew to New York City for the first time this past Christmas to have my first Endometriosis surgery after suffering and being gaslit since I was 12, I'm 24 now. I wish you nothing but the best and hope your surgery brings you peace and healing. Prayers and love from Arizona.

[@jessicawise7486]

This is the prime example that you can never see what people are going through. I am so happy to hear that you finally got some relief Lauren. Hopefully from this point on you wouldn't have to struggle as much as you have. 💛🎗

[@maddiekaetterhenry6373]

I’m an OR nurse and we do these surgeries regularly! There are only a handful of surgeons in the country who do this type of surgery and I’m so glad you were able to have this done! I’m proud of you for speaking up!❤

[@vrodriguez214]

Will you share any you might know of in Texas or direct me to a website I could search for one?

[@rachealfaucher4520]

Please can you share if there are any doctors in California I’m in so much pain

[@quabrewton]

I know that feeling of thinking it is all in your head.. NO. Continue to advocate for yourself. Sending hugs, and prayers ❤❤

[@kayleehalterman5349]

I appreciate you telling your story! I also wasn’t taken seriously by healthcare professionals and took me 5 different ob/gyn’s until I finally had someone take my pain seriously and diagnosed me! I’m forever thankful for my dr💛

[@kayleehalterman5349]

Thankful it took me 7 years and not 13 to get answers but it still shouldn’t have taken that long!

[@ElviraStorm13]

As a healthcare professional and a girl with PCOS, I am so sorry you're journey went down the path it did. But I am SO proud of you for never giving up. You are an inspiration and sharing your story makes other women feel seen and for that...thank you ❤️ 🎗

[@Jogigames2024]

I also have endometriosis and PCOS, and trying to get a healthcare worker to understand the pain that you were in without them physically, seeing it is incredibly difficult. We have a lot in common when it comes to how we were treated by doctors. Having that surgery and recovering from it was the best for my cycles. I am almost 2 years after the surgery and I am still having way less pain bloating and heavy flows. good job for always advocating for yourself, and finding the help that you needed! That heating pad is going to be your best friend for the next few weeks ❤

[@heyMommaToni]

that look at the beginning of your story, I remember that feeling. I felt every part of your video. I'm 55. Suspected endo at 19, laparoscopy at 21 confirmed it. I spent so much of my life dealing with endo and the IBS it created. It affected my college years, my career, relationships, everything. I was told at 25 that I couldn't conceive kids naturally because endo closed up my fallopian tubes. I ended up conceiving and having 2 kids, at 27 and 35 with no issues (much to my dr's surprise). I was told at 37 by my ob/gyn that she didn't believe in endo so I lost a great dr there. I took so much Tylenol that if affected my intestines. It's so hard dealing with something that you just don't know how to deal with. But you have a great community out there of fellow Endo survivors. They helped me so much in just listening. After my last baby, I tried to get a total hysterectomy but no dr would touch me. So when I went into perimenopause in my early 40's, it was a welcomed thing. Menopause is the only thing that "cured" my endo. Big hugs to you and know that you have a supporter in me.

[@1115TinaM]

Bless your sweet heart!! I am 45, and I have had a lifetime of absolute nonsense from our American healthcare system. If I can give any advice it is NEVER stop advocating for your health because nobody else will. I have dealt with endometriosis,PCOS, ovarian cysts, and thyroid problems. Nobody listened to me and I finally found a specialist that took me seriously. I went through a thyroid cancer scare last year on top of everything else. And endometriosis is not rare. I have it, my daughters have it, and my mom has it. My mom hemorrhaged when she was in her early 30’s and it could have easily taken her from us. Never stop fighting for your health! 🩷🩷🩷

[@brittanypittman5714]

Thank you for sharing your story. It’s infuriating that you were not taken seriously and that you were just dismissed for what you were feeling. I’m so glad that you found someone who took you seriously and helped you. I’m praying for a speedy and easy recovery.

[@emilymcgowan3119]

Lauren, you are truly one of the sweetest people and knowing how you been treated and feel breaks my heart. I was gaslit for many years over my PCOS. While it’s not exactly the same healthcare professionals need to understand if we say something is wrong something is wrong! We will pray for you on your journey!

[@mollywilliams7658]

I hate that you had such a bad first experience with the OBGYN I absolutely love mine but I know that’s not the case for most people hoping you found a way better care team now 💗 I’m so happy that you found people that listen to you and I hope you have a speedy recovery no one should be told their pain isn’t real 💗

[@l.a.c.e.]

When you’ve shared little bits on prior videos, I thought that it sounded like you may have endo. I have severe endometriosis, myself. I finally had a full hysterectomy at 25, after THIRTEEN surgeries for it. I am glad you’re getting answers. It is intense. I know that the right doctors have made a world of difference for me. Huge hugs to you! ❤

[@AnnaMazingFusion]

This made me tear up 😢 You are soooo sweet and don’t deserve the treatment you received 💔😭 I have experienced medical gaslighting too unfortunately. Women’s pain isn’t taken seriously 😡 I’m sending you so much love. Thank you for sharing your story 💜 I wish you all the best!!! You deserve the world!!!

[@theashleybclay]

As a fellow Endometriosis sister ;) something you may want to talk to your doctor about is if you possibly have IBS as well. I have Endometriosis, IBS and Interstitial Cystitis. A lot of women have those three diagnosis because they tend to come together. Your IBS and Endometriosis could be exacerbating each other. Wishing you all the best and hoping you feel so much relief after your surgery. 💗💗

[@TheLaurenNorris]

I will for sure write this down to ask my Dr at my follow up appointment next week, thank you!💛🎗️

[@rosemarie4394]

Endo can also come with pelvic floor issues and bladder issues. I’ve been reading a book this month called Beating Endo which has been so helpful talking about treating all these endo-related issues together. I’m diagnosed w pelvic floor dysfunction but never really heard of endo before this month actually so have been looking into it.

[@jenica9705]

I have all 3 of these diagnosis(endo just suspected until lapo) and now being tested for crohns. The thing is no doctor has ever told me they are related which is really frustrating. I just finally got told I probably have endo after 20 yrs of constant issues. It’s crazy they aren’t making the connection because everything I have been reading says most women that am have endo have these other issues. Its frustrating

[@theashleybclay]

@@jenica9705 I'm so sorry to hear you have suffered for so long. My hope for the future generations is that they won't have to wait as long as we did. It really takes finding a good doctor who will be focused on the root problem and not just throwing medication at symptoms. I used to have women be the most unsupportive before I was diagnosed. They would tell me every woman has a period and I must be making a bigger deal than it really was when my endometriosis ended up being one of the most aggressive my doctor had seen. With the new diagnosis being done now, I'm considered stage 4. I wish you all the best in your healing and hopefully feeling better.

[@Adrianaaaa365]

Lauren, i am so proud of you for demanding help & answers! My mom (54) had endometriosis her whole life. She suffered horrible symptoms & never was able to receive any real diagnosis. When she was about 40 years old, she went into surgery to remove a cyst that the doctor found on an ultrasound & once they cut her open they found endometriosis so severe that tissue was growing around most of her organs in her lower abdomen, including her colon. Nobody was aware that she had endometriosis at all because they could never see it. Since it was so severe, they had to remove her uterus & reroute her colon for a few months while her organs healed from the tissue that was removed. I was 10 years old at the time & I remember the doctor explaining to my dad that she almost died because she lost so much blood since it was an unexpected surgery. You are so lucky to be aware of your condition & to be receiving help this young. Thank you for spreading awareness to women around the world.

[@parib8995]

We love you Lauren and we appreciate you being vulnerable to us ❤. Many women go through this, so please know you are not alone :)

[@SimsTherapy]

I am so sorry you went through this. I had a grapefruit size tumor on y uterus and had to have an hysterectomy. My situation was different but please know you are not alone

[@EverythingGirlyXoxo]

I don't have endo, but I've had chronic heath issues that doctors have not been able to figure out or provide me any relief. This made me feel less alone and I'm motivated to find a specialist and other options for treatment!! I never would've known you were dealing with this unless you had shared. Thank you for sharing this💜

[@Hollymodz]

wishing you a speedy and healthy recovery 💗💗🎗

[@TheLaurenNorris]

Thank you Holly🎗️💖

[@camt8237]

Lauren, I'm so sorry you've been dealing with this! Been following you since your sorority days, and it's crazy to think of how long you've been dealing with that pain. It never showed in your videos considering how you're always so fun and bubbly. It's horrible to think of how many women get their lives screwed over by the health system, and I'm so grateful you've finally gotten the closure and help you needed. I'm wrestling with similar medical gaslighting (albeit not on this level) with possible PCOS/hormonal imbalances, so to see someone get a diagnosis and surgery is wonderful. hope your recovery goes well 💞

[@KellyDinsmore-vx9ql]

Oh Lauren, I am so sorry you had to go through all of that. As a fellow chronic illness girly, I feel your pain of not being believed. But you, and only you, know your body best. Your struggles are real and valid, and I am SO glad you finally got the care you needed and deserved. I'm so proud of you for being an advocate for yourself, that's so hard. But you did it! 💓Wishing you a speedy recovery, the best of luck with moving forward with your care management, and stable health overall moving forward. You got this! We're here for you 💖

[@tpolly480]

My sister has endo and just had her first baby. She has had such bad pain and just hearing your story makes me feel for both of you. God bless!

[@AshleyNicoleFlow]

This is so disheartening.. So proud of you for advocating for yourself. I’m so sorry you experienced this, you did not deserve it. You are not crazy you know your body. I’m so glad you pursued this.

[@daniboulware7766]

Oh Lauren, 🥺 Thank you so much for sharing your story and for being vulnerable! I can’t imagine how hard all of this must be! I’m so sorry that you were mistreated, felt unheard, invalidated, etc. As a healthcare professional I really try to make all my patients feel seen and cared for. It can be so hard to find that these days. What you went through should not happen, and I’m so sorry that it did. I’m proud of you for taking going back, facing your fears, and taking steps to get better and get answers. I’m praying for you!

[@julieveras2839]

I luckilu have not had any issues like this personally but I cannot express how important this video is! It is sooo important that woman share these experiences!

[@mariacromwell3822]

It is absolutely okay and valid to cry. as someone who has gone through something similar and having heart problems and being treated as just a number is not okay. I am so sorry you had to deal with this for so long. Just know that you have people that love and support you. Praying for you and your recovery.

[@TheLaurenNorris]

Thank you so much for your comment and for listening to me💖 I hope you are doing better now!

[@Darklink7884]

My heart goes out to you, your family, and Will. Wishing you a speedy and healthy recovery. 🙏 I almost started crying when I saw your Instagram post.

[@mckullataylor]

I love your vulnerability and honesty in this video, Lauren. It’s a shame you were treated the way you were by those who are supposed to be helping treat your health. While I don’t have endo, I was diagnosed with PCOS last October, so I always enjoy women talking about these specific health conditions because it’s not talked about nearly enough. Love you and hope you continue to heal both physically and mentally from your surgery and previous endometriosis experiences! ❤️

[@hannahmaharrey1490]

I'm 41, and was only officially diagnosed with PCOS at 36 and finally started receiving actual treatment for it. There were years of absolutely torturous periods and pain that I will never get back because my previous healthcare providers didn't care about my quality of life and blamed all my issues on my weight. They were too busy fat shaming me to even diagnose me with the chronic metabolic disorder that was affecting my weight. Thanks for sharing your story, we need to be more open and honest about women's health issues and this is a great example to set for younger women!

[@c_mann6558]

Thank you so much for telling your story. As a women with chronic pain, I can relate to professionals and family/friends/peers not understanding or invalidating pain. All it takes is that one person who says I believe you to bring some kind of relief. I hope that you continue to feel relief from the surgery and other treatments. Thank you for being vulnerable and know that we stand with you ❤

[@Abbrexoxo]

I was diagnosed with pcos at 17. We get no answers or no help. We’re left to figure things out on our own. Hundreds of dollars on supplements and trying to figure out what diets work. I feel like I’ll always be in this battle. Thank you for opening up with us, it helps so much to know I’m not alone 💓 prayers sent to you and every woman in these comments going through these things 💓

[@annjames1837]

Watch Dr. Ken Berry's KZbin channel on PCOS 😊

[@AbbyMCDuplessis]

That’s currently what I’m going through. I was diagnosed with endo and pcos at 16 and I’m 23 now still trying to find answers

[@luluocampo1523]

Best management would be birth controll pills as long as you are not trying to get pregnant, and, as I understand the US just released an OTC FDA aproved pill so you could give it a shot?

[@luluocampo1523]

Also, theres surgical management if you are trying to get pregnant where they basically pop each od the cysts

[@hn6810]

How you were treated by those doctors and what you've gone through is absolutely horrible. You are so strong, Lauren. Truly wishing you all the best and better health ahead

[@jessiadamcurran6281]

As a fellow endo sufferer also i just wanna say im so happy for you to finally have answers! Being gaslit for so long is something we shouldn’t have to go through but i take my hat off to you for being persistent and knowing your body ❤ you are so so strong and please don’t forget it! The endo community is a amazing supportive one so know we are all supporting you and sending you love for a speedy recovery 🎗️

[@misserikaleighx3]

14:00 and I’m crying. I relate to this so hard. I’m so proud of you for being so venerable with this. It is so hard for people who don’t have this; both men and women, to understand what this struggle is like. Thank you so much for validating yourself, me, and every other woman in the world who is on this tragic journey. I love you girl!!

[@michelledemers350]

I am sending so much love your way. My heart hurts hearing how doctors have treated you in the past, you deserved to be heard at 13 years old just like you were heard this month. Thank you for being vulnerable and sharing ❤

[@nikkidodd6445]

Thank you for bringing attention to this. So many women are shamed and ignored in healthcare, and yet we are conditioned not to talk about it with each other. By using your platform to share your story, you could make a real difference. Let's keep talking about these issues.

[@elisabethz0710]

This is so inspiring🩷.. I found out after my miscarriage that I have PCOS. It’s been hard for us to get pregnant. I’m trying to change my lifestyle and going gluten free to try to help it. I completely understand the irregular periods, makes things really difficult. Thank you for sharing your story 😊

[@adrionapride1590]

I am also gluten free and it has helped with flair ups so much!!

[@nobodycares10300]

thank you for being so open and encouraging to us, it gives me as a teen, the feeling of empowerment and encouragment to speak out. Sending hugs and hope you heal soon!❤❤

[@TheLaurenNorris]

You are so welcome! I’m glad this gave you some encouragement💖🙌🏼🪽

[@amielawson8344]

Moving to New York led to this healing. I am so thankful that you finally got answers and treatment.

[@TheLaurenNorris]

I didn’t even think about that😭🥺 it truly did. This move has helped me in so many ways.

[@diamondwalker9188]

I know this wasn’t easy to talk about but thank you. I have chronic pain and hormonal issues that have gone unaddressed for years. I had no idea I was having migraines because I had no choice but to push through and go to work. It’s caused so much stress on my body. And now I am trying to address problems with cysts. Women, let’s stick together and constantly remind each other to keep going, keep calling, keep advocating. No doctor should say you are making anything up. Lauren, so much love to you.

[@ansleyhaynie7551]

As someone who deals with chronic pain, my heart goes out to you. I’m so sorry that medical professionals have treated you so poorly, but I’m thankful you got answers. You have the best support system and all of us are in your corner cheering you on! Love and hugs! 🥰

[@Brynn_Pratt]

Lauren crying made me cry 😭 I’m so sorry that this has happened to you and anyone who assumes someone is pregnant when they haven’t said anything about it is absolutely cruel! I. So sorry that you got gas lit and got told that you did it for attention! Just remember, God is with you and god loves you Lauren!

[@aCloudspov]

sending pure love and magical blessings your way, sweet soul 🌷

[@TheLaurenNorris]

Thank you so much angel💖🎗️

[@cynthiabutler3363]

Lauren do you know how many women you have helped with this video? So many women go to the doctor with pain and they tell them the samething. Be proud of yourself for fighting for the right to know what was going on with your body. Thank you for being brave enough to bring this journey you are going thru to us. Please know we are here for you and we love and care about you and we support you. Stay strong

[@velvetstonebraker9874]

This is INFURIATING. Women are constantly disregarded and our concerns about our health are thrown back at us as being dramatic or over exaggerated. I’m so sorry that you were treated this way by licensed medical professionals.

[@olivialeigh752]

💛🎗️ lauren im so sorry you’ve been dealing with this for so long. im proud of you for advocating for yourself 💛💛

[@incurablyawesome2024]

Thank you so much for sharing your Endometriosis story. I just shared mine on my channel. Your experience and story are so powerful in helping other people. You are incurably awesome! 💛💛💛

[@mads1864]

💛🎗️ I was gaslight through middle and high school. I went to college, my freshman year they finally did the tests and examinations to find the endometriosis tissue. Much love for you Lauren! Feel better soon ❤

[@EllieM]

You have no idea how much this video has helped. Hearing someone else talk about the symptoms that I've had ignored for years makes me feel so heard and seen and understood. I just got my surgical referral and this video helps me feel so much less anxious. Thank you💙

[@AmeliaJ.R.]

You literally deserve an MD after going through all of this, I'm sorry the system failed you Lauren but I'm so so so happy you've finally gotten answers and praying for a pleasant recovery. It is so incredible you are sharing this and it takes incredible strength to even speak about it after being abused by the medical system for so long. No one should EVER downplay the amount of strength and courage it takes to relive all of this by telling your story. God is with you through all of this 💗🪽🎗 Love and prayers from NH

[@Flow714-w7w]

Hi Lauren! Sending you lots of love and positive energy on your healing journey! I have endometriosis as well and very much empathize with you! All of the very best to you 💜

[@queeniequeen949]

As a fellow endo sufferer myself, I’m sending you so much love and prayers for healing. ❤️‍🩹❤️‍🩹❤️‍🩹❤️‍🩹

[@amyhansen6829]

Thank you for sharing this Lauren. Speaking up about health issues, especially reproductive health issues, is so important. As someone who had never had issues with her period, I had never heard of endometriosis until I was in college and a friend was diagnosed with it. That's why it's so important to share our stories and help others. Education and speaking up for your needs is key. Thank you for your bravery and courage for being public with this. You got this!

[@kalei8568]

i love this video, im so happy you got the help that you needed after all those years💛💛 and for the women that need to know they’re not alone💛🎗️🎗️

[@ashtongray1444]

I was ignored for so many years about my issues and finally I found an amazing doctor who listened and helped me!!! I had horrible endometriosis and had to have a full hysterectomy which is sad but ok cause im healthy and its gone!!! Also I had to have my appendix removed because it also had endo in it and was literally on the verge of bursting because it was infected really bad and deformed. He was amazing and did so good. Im almost 2 weeks in recovery and doing better each day!!

[@TheStormyrules]

Lauren it breaks my heart to see you crying in pain🥲 I’m just glad a professional finally understands your situation and you’re finally able to have surgery. I hope thin gs get better for you and I’m sending all my love and prayers your way 💞💞💛🎗️🎗️

[@Bexinbos]

I’m so sorry you went through all that medical gaslighting! Thank you for your courage to share your story and best wishes for a speedy recovery!!

[@julih1383]

Honestly this video is exactly the little reassurance I needed today, I feel like God just plopped this in my lap. I am dealing with a similar health issue (more urology-related... same thing of "youre too young to have these issues", "you're a healthy person, are you sure it actually hurts" etc. etc.) and am finally getting surgery in about 3 weeks. thank you thank you thank you, seriously.

[@rachelflores1125]

Lauren, I am usually a silent follower but I wanted to say I am so proud of you! You did not give up. You were told it was all in your head for 13 years and grew stronger to be able to put your foot down and get real answers. I don’t have endo, but I understand your pain when it comes to health care. I am a Type 1 Diabetic and have heard from my doctors in the past that it is my fault for my disease and that I should fix it, without giving me the proper tools and guidance to fix it. I finally found a doctor that helps me and got my diabetes in better control but it took standing up for myself and knowing my body. I’m so grateful to shared your story for all of us who suffer and get ignored.

[@happynhealthy5667]

Hi Lauren, I've been watching your videos for a year now and wanted to thank you so much for sharing this. I'm a medical student about to start my clinical rotations tomorrow, and hearing your story really made me understand how important it is for us healthcare providers to listen to our patients and trust that they know they're own bodies better than we ever will and that we should never gaslight our patients about their health. Your videos have helped me get through some of the most stressful times during medical school, and hearing everything you've gone through on your endometriosis journey has really inspired me to be a better clinician as I enter the hospital. I hope you know how much of a positive impact all of your videos have on us viewers, and I really hope you are able to get the care that you deserve.

[@maiajeffs7399]

Hi Lauren, I just want to say a massive THANK YOU. I don't have endometriosis but I have a few friends who have had to deal with endo and I thank you foerbeing so open and sharing your journey. Thank you for being so real, open and honest. I know that so many girls and women who are suffering with pain similar to yours will have so much courage seeing your video and will try and get the help and support that they need. We need more positive influences on the world like you. So from one girl to another thank you so much Xx

[@jasmynelabeau4961]

i am so proud of you for sharing your story and speaking out. we stand beside you- always. health care professionals should NEVER treat anyone this way.

[@kimj6447]

You are a solider girl ! Last year I got diagnosed with endometriosis as well . Dealing with the most painful period for 2 years. Going to doctors that didn’t know what to do for me treating me like I’m an alien & feeling so defeated leaving the offices. I finally found a doctor who specializes in endo where I live . She’s got to control the painful periods now which I am so grateful for . This is gonna be a fight but we got this ! Praying for you , you’re not alone 💛

[@jamiegarrett4050]

You are a Gorgeous, smart, kind, caring, and phenomenal woman, with such a beautiful and genuine soul … I am so glad you finally got answers … Rest easy & prayers for a healthy & speedy recovery!!❤️‍🩹 💛⭐️🌻🌝🌙🌼🐥🔆👱‍♀️🎗️

[@christinavarozza3791]

Hey Lauren Norris I love you and I’m here for you and I love your videos and your my idol and this video touched my heart and I am praying for a fast recovery and I am so happy for you Sharing.🎗️💛

[@annahunter3632]

Girl... I am so sorry. Finally being diagnosed with Pre-Menstrual Dysphoric Disorder was life changing. I hear you. Your feelings are so valid and I am just happy we are slowly but surely making progress in diagnoses and research.

[@monicahwang2746]

I wish I could give you a hug. Thank you for sharing your story and for releasing some of the emotional pain that you had to endure alongside such physically debilitating effects of your endometriosis. I was recently diagnosed with it, after trying to get help for really painful fibroids. I understand how alienating it is to have to silence your voice and your knowledge of your own body is a misogynistic medical system. Much love to you on your recovery journey ❤

[@JoyfullyJaelene]

Side note: I would love to see a healing journey type of vlog! Documented as like a diary while you continue to heal. Praying for your healing! 💛💝

[@TheLaurenNorris]

I love this idea💖🎗️ thank you so much

[@lauriieee]

I respect you so much. Not that I didn‘t already but the level of vulnerability you‘re showing just to help others get a diagnosis and make them feel less alone is just really incredible. Love you 🫶🏻 I will always be a supporter of you!

[@saramathilde76]

As someone who struggles with mental illness, thank you for speaking up about invisible pain and suffering. I'm sorry you had to go through these horrible experiences. 💖

[@TiffanySchutte]

Ugh I want to give you a hug! Can definitely relate to being told you’re “making up” your pain. I’ve had so many health problems the last two years now. First was my gallbladder and the first time I went to the ER they said I was just “anxious” and that was it. Found out 5 months later I was having hour long gallbladder attacks and was told oh yeah they feel like a heart attack 🙃 now after several tests looking “normal” working with a more holistic NP and found out sooo many issues we are working on and getting fixed and also found out I have fibroids and possibly Endo. Finally started advocating for myself to get everything taken care of! It’s so sad how many women get dismissed and told oh nothing is wrong when we know our bodies better than anyone!

[@madisonhexter4243]

I'm sure this was very difficult to share but thank you for your vulnerability and bravery! I am a physician assistant and one of the things I've learned is people usually know when something is not right with their body, and the best thing a provider can do is listen to that and advocate for them! It makes me so sad and mad to hear of all of the gaslighting.

[@taylorcarr8007]

I’m so glad you had a doctor listen to you! I’ve never had endometriosis, but I was experiencing major side effects from my iud. So much so that it impacted all areas of my life. Emotions, weight, acne, relationships, also an attempt on my life. Thankfully I called my gynecologist and booked an appointment. When I explained my symptoms and why it tools 3 years to realize, she didn’t hesitate and removed it immediately. Since then I feel more like myself, but I can’t use normal contraceptives because all my children were conceived on contraceptives. I decided to remove my tubes. I had full support and encouragement from the doctors! So I’m glad to hear there are other women whose voices are being heard about the crazy and painful things that happen to our bodies!

[@shayseeley]

This video could not have come at a better time. I have been gaslit for years that my debilitating pain is IBS. I finally mustered up the courage to see another gyno after a similar flare up and the doctor finally believed me. This has made me feel seen. It has made me feel that I’m ready to schedule the surgery. Thank you for this 💛.

[@eastmeck011]

I hope you feel better soon. You are such a beautiful spirit and I am glad that you got this taken care of!! 💛💛🎗️🎗️

[@cyndeya]

I am in med shcool, one year away from being a doctor, and currently on my OB/GYN rotation. Thank you for putting this video out there, it is so important to share this perspective, and i really appreciate hearing these stories directly from patients. Endometriosis is real, it is more common than you'd think, and IT IS TREATABLE!

[@biahoppe701]

💛 as someone who wants to work with women’s health, this video was eye-opening. Thank you for sharing your story. I admire your courage.

[@carmendevine5670]

THANK YOU SO MUCH for speaking about this!!! I had cysts on my ovaries when I was in middle school and the pain was so bad I would become physically ill. I had to have one cyst surgically removed from my right fallopian tube because it wasn’t receding and it ended up helping me so much for the next few years but I still had immensely painful cramps. So many people didn’t believe that I was really feeling that pain, and it’s so incredibly frustrating and crushing to experience that, especially from doctors who are supposed to help you. So proud of you and happy to hear that you’ve finally found an answer❤