Views : 536,881
Genre: Education
Date of upload: Mar 2, 2022 ^^
Rating : 4.981 (167/35,310 LTDR)
RYD date created : 2022-04-09T13:53:07.709363Z
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Top Comments of this video!! :3
As a male I had no idea that this condition even existed. Iâm so glad Anthony and his team can create content that can educate people like myself on the severity and inter workings of people. I feel like periods, abdomen pain, and endometriosis shouldnât be taboo to talk about as theyâre important for womenâs health
2.6K |
Had it since I was 15, (almost 27 now) and was doubled over sweating, vomiting, shaking, crying, feeling like I was being ripped from the inside out. My mom used to joke with her friends that I was so naive about my first period that "she thought she had cancer" and I actually went to the ER. They all just laughed and said I just wasn't used to periods yet, and then over the next 2 years the jokes stretched on about me being "overdramatic" or "just needing to suck it up like everyone else," and "Its just a heavy period, it wont kill you." Curled up in bed unable to move I remember hearing my mom yell at me to get out of bed because "no woman ever let a period stop her," so I needed to do my chores and go to school but I remember my fucking vision blurring due to the waves of pain. Tylenol, Advil, Aleve, none of it worked. The pain burned right through it... so I started secretly buying more of it to take more instead of asking my mom for hers... I was up to taking 5 Advil at once and STILL feeling the pain... but all I ever heard was the same shit "You'll never hold down a proper job if you spend the whole day in the bathroom! Get over it!" Even other women would berate me "you're too young to be complaining," "wait until you're my age, then you can talk," and I felt so damn defeated... Finally prayed and God put it on my heart to get my tubes removed right before I turned 26... they said they found it EVERYWHERE... my intestines, my ovaries, my liver, my bladder, EVERYWHERE. Luckily none of my organs aside from my fallopian tubes needed removal, and the damage is healing... I used to spend my first day of my period clinging to a toilet or passed out on the bathroom floor (sometimes I slept in the tub), and then I would bleed for 10-15 days after that, and they were random as hell... sometimes I'd get two periods a month or one long one that lasted almost a month... it was exhausting. My cycles were between 15 and 48 days, meanwhile I'm fighting ADHD, BPD/Bipolar disorder type 2, Anxiety, Depression, Interstitial Cystitis (sensitive bladder syndrome), and undiagnosed Fibromyalgia. When they called my parents and left a voicemail saying they got rid of the scar tissue and all the confirmed endometriosis they found, that they had tested it due to the size of the lumps but found no cancer, my mom broke down in tears and apologized profusely while my dad just sat in shock... it was insane... now my periods are 2-6 days long, my cycles are somewhat regular (between 25 and 33 days now), and I'm finally able to have sex without pain and vomiting too! I'm so blessed!
1.6K |
I have had doctors literally tell me âpeople my age donât get cancerâ multiple times between the ages of 15-25 and refuse me investigatory health care. This is after laying out my enormous family history of multiple types of cancer (many hormone related). Heath care systems needs to do better by women, non binary and ftm trans people when it comes to their bodies, especially surrounding our reproductive systems.
2.2K |
The idea that a doctor with an oath to treat the sick and injured to the best of their ability and to do no harm would not only dismiss the pain of this disease, but would also value a woman's fertility over her quality of life is just messed up. Women don't just exist to give birth. We're not incubators with legs. To value a life that doesn't even exist over a life sitting right in front of you asking for help and pretty much turning them away is just disgusting.
607 |
When my mum told her doctor she'd investigated her symptoms and thought she had endo, the Dr looked down her nose at her and said 'oh, and you're a Dr now, are you?' Years later when she was trying for a baby, a lesion ripped and she ended up having an emergency hysterectomy and nearly passed from bleeding. Her bowel was stuck to her spine with endo.
165 |
people never talk about endometriosis thank you anthony, Iâve have many people (even period havers) deny my experiences with endometriosis. I started developing horrible symptoms when I was 12 (3 years after my first period) and many told me that I was too young to be experiencing the pain that I was and I was likely dramatic. EVEN THOUGH MY MOM HAD THE EXACT SAME EXPERIENCE and had to get her uterus out as a result.
2.2K |
My girlfriend has endometriosis. She hasn't been believed by her mother or father, and has been passed off as normal pain. I've been in the ER multiple times with her because of it, and it's heartbreaking to see her in so much pain. I didn't know of it before I met her, and turns out it's super common. People need to believe women when they voice their pain!
140 |
This also makes me think of Polycystic Ovarian Syndrome (PCOS), another widely misunderstood condition. Up to 1 in 10 people in possession of a female reproductive system are estimated to have it and more than half of them don't even know it. It is the leading cause of infertility in women and so little is known about it. I'm so glad that invisible illnesses like chronic pain and endometrosis are being covered by this show and I hope one day maybe this one will be as well.
657 |
my mom didnât have endometriosis, she had endoSALPINGIosis, itâs very similar, except the tissue growing on the organs is fallopian tube-like epithelium. itâs extremely rare and it spread to her bowels. she would cry and shake on the floor while sweating like crazy when she had cramps. no one believed her pain, she suffered for years. sheâd have blood in her stool but only right before and on her period. luckily, one wonderful nurse practitioner suggested she might have bowel endometriosis, and referred her to gynecology. but even in gynecology, it took them way too long to suggest exploratory surgery. that surgery became a hysterectomy, appendectomy (there was a ton of endosalpingiosis on her appendix), and literally scraping all of the endosalpingiosis off of her bowels. it was a rough 3 month long recovery but sheâs finally free from it. thank you so much for making this video, anthony. so many people with this condition, and other similar ones, are often unheard and misunderstood.
667 |
That one woman who spoke about having symptoms when she was 6 is making me click on my own situation. I had symptoms like this when I was 8 and one doctor I saw thought I was pregnant.l, another say it was no biggie, just a stomach ache. Hearing someone else share going through a similar situation is validating af
487 |
Here I am, almost dying from pain from suspected endo, crying about statics of women in stem and how long ago the cure could have been invented if men didnât only care about themselves. Can you believe that there was research to find out whether women with endo are more attractive than those without it INSTEAD of looking for the cure from crippling pain? and you come out with a video about it. Thank you
750 |
@AnthonyPadilla
2 years ago
next week we rest. but come back in two weeks for I spent a day with people w/ DOWN SYNDROME UNCENSORED ON SPOTIFY ⸠open.spotify.com/show/5aOLuPenneHbhLh05fmkeu UNCENSORED ON APPLE ⸠podcasts.apple.com/us/podcast/i-spent-a-day-with/iâŚ
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