High Definition Standard Definition Theater
Video id : 0aJ9wFUaSUM
ImmersiveAmbientModecolor: #d5a8a3 (color 1)
Video Format : 22 (720p) openh264 ( https://github.com/cisco/openh264) mp4a.40.2 | 44100Hz
Audio Format: Opus - Normalized audio
PokeTubeEncryptID: b5988e03990aaa0a05afcdd8ba6b2f6221d06e5784f8c1d596545b6b5d4c4924cc954213d889694900e1d1c9a8eb4084
Proxy : eu-proxy.poketube.fun - refresh the page to change the proxy location
Date : 1715795004699 - unknown on Apple WebKit
Mystery text : MGFKOXdGVWFTVU0gaSAgbG92ICB1IGV1LXByb3h5LnBva2V0dWJlLmZ1bg==
143 : true
I spent a day with people w/ ENDOMETRIOSIS
Jump to Connections
536,881 Views • Mar 2, 2022 • Click to toggle off description
I spent a day with people w/ Endometriosis to learn the truth about the struggles this disorder poses. Sponsors ▸Go to betterhelp.com/padilla to get 10% off your first month! ▸Visit joinhoney.com/PADILLA to get Honey for FREE.

🎙THE PODCAST (UNCENSORED)
Spotify ▸ open.spotify.com/show/5aOLuPenneHbhLh05fmkeu
Apple ▸ podcasts.apple.com/us/podcast/i-spent-a-day-with/i…

💥NEW YOUTOOZ FIGURE: youtooz.com/products/anthony-padilla (Every cent will be reinvested into improving this series.)

🧨HUGE thank you to:
▸ Jenneh - instagram.com/lifeabove_illness/?hl=en & jennehrishe.com/
▸ Kate - Squeaky Bicycle Productions can be found at: squeakybicycleproductions.com/about-us And @squeakybicycle on all social media platforms
▸ Morgahna- instagram.com/morgahnagodwin & morgahnagodwin.com/

🗯MORE EPISODES…
▸ CHRONIC PAIN SUFFERERS -    • I spent a day with CHRONIC PAIN SUFFE...  
▸ PTSD -    • I spent a day with people w/ PTSD  
▸ NARCOLEPTICS -    • She can’t stop falling asleep - I spe...  



🎥Crew
▸ Creator, Director, Writer, etc. - Anthony Padilla
▸ Executive Producer - Alessandra Catanese
▸ Producer, Co-writer & Research - Elise Felber
▸ Director of Photography/Gaffer - Kathy Sue Holtorf
▸ Social Media Manager - Mallory Myers
▸ Editor - Mike Criscimagna AKA Mork Crispy
▸ Assistant Editor - Patrick Horba
▸ Assistant Editor - Ash Duckworth
▸ Sound Editor - Gareth Hird
▸ Post PA - Levi Villalpando

🎵Theme Music Composer - Matt Good AKA The King of Emo
🖼Portrait painted by: Rhianna Robles - instagram.com/zerogattsu
🦥Slade mascot built by: The Pastel Prince -    / @theepastelprince  
📺3D animations by: Jacob Dalton - twitter.com/jacobdaltonvfx

📢BE ON THE SHOW
▸ If you are part of an underrepresented subculture or live a lifestyle you feel is not widely understood and would like to be interviewed by me, email inquiry[at]pressalike.com with your subculture in the title of the email.

❗️You dug this deep into the description. You owe it to yourself to subscribe ▶ youtube.com/subscription_center?add_user=AnthonyPa… or get more at instagram.com/anthonypadilla & twitter.com/anthonypadilla
Metadata And Engagement

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
See in json
Tags
Connections

YouTube Comments - 2,180 Comments

Top Comments of this video!! :3

@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/i…

911 |

@moodymay1423

2 years ago

My own father didn’t believe I had endo until my surgeon showed him pictures post op. The physical pain is horrible but the emotional pain of not being believed is far worse.

4K |

@kpk1171

2 years ago

As a male I had no idea that this condition even existed. I’m 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 shouldn’t be taboo to talk about as they’re important for women’s health

2.6K |

@shadowykitty5588

2 years ago

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 |

@cyclical_

2 years ago

This video really opened my eyes on how sexist medicine actually is, i had no idea. It really sucks that the world is still based on sexist opinions and people act like it’s not. So much love to anybody that suffers from this disease<3

1.9K |

@maryamsheikh7597

2 years ago

I struggle with endometriosis personally and let me tell you that it’s such a relief to hear others stories and how they dealt with it. Thanks Anthony for making such inclusive videos ❤️

4.6K |

@littlecat4415

2 years ago

I have had doctors literally tell me “people my age don’t get cancer” 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 |

@torycatherine2044

2 years ago

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 |

@rosiebronte

2 years ago

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 |

@DonovanHerleyman

2 years ago

people never talk about endometriosis thank you anthony, I’ve 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 |

@ButeraMelina

2 years ago

Having this disorder seems so awful. As someone who stuggles with ither disorders / illnesses I'm sending much love to anyone who suffers from that or any other disorder <3

917 |

@therareguyshow6018

1 year ago

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 |

@kynsleestewart1319

2 years ago

my mom suffers from this and it’s like she’s dying every single month. it rly sucks what these people have to go through. so glad anthony is bringing awareness to this because this is so serious.

894 |

@spiker2178

2 years ago

\male\ didn’t know this was a disease and it made me upset to know it’s just as common as asthma. Thanks for spreading information!

400 |

@hedera1332

2 years ago

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 |

@trashcan2926

2 years ago

my mom didn’t have endometriosis, she had endoSALPINGIosis, it’s very similar, except the tissue growing on the organs is fallopian tube-like epithelium. it’s 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. she’d 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 she’s 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 |

@lynxwarden1774

2 years ago

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 |

@IdoGindes

2 years ago

I’m a medical student, and we’ve learned about endometriosis as early as the first year of med school. Glad to see this phenomenon has more recognition in the medical community!

199 |

@ladyfoxwf1075

2 years ago

I've been to the doctors sooo many times about my period pains, once I bought up Endometriosis, and they said to me "yeah it's possible you have it but there's no point checking because even if you have it there's nothing we can do. There's an operation but it would just grow back".

134 |

@holycas2949

2 years ago

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 didn’t 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 |

Go To Top