Guess My Disability | Lineup | Cut 

olive ik🥺 and the lady was like “aw sweetie”

So sad

how , a lot of the time it can be a mental disorder

Lamar alharbi# don’t be so mean ._.

jeez this generations full of pussies 😂

Rest assured they already did put her in a video very often

I LOVED her!!

Eww no! Her foul mouth is just overkill!

@@JamieSuzanne69 According to you. Good thing your opinion isn't the only one that matters.

@Yadira Arnold I really don't get it. This seems like a plot hole because that means if criminals like pedos and rapists get to go to heaven simply if they believe Jesus is gods son

Alyssa Novella why? Because he’s a dating coach?

Oh yea. With the girl in the wheelchair. Oh yea. They’d be super cute too

but he's cute though

Moon Boi right though?? It’d be adorable

12:32

Does anyone know her social media info? I'd love to follow her.

@@small_chickens1026 her name is raine but that's all ik

"you be fuckin?"

“that black lady”. She has a name. She said it in the video.

@@SnailHatan Damn bruh, I really don't care.😐 I forgot overly sensitive people watch these videos.

I never even thought of my BPD as a disability, but when thinking about my daily life I can see how it has done a lot of damage. I'm also very glad to see it being represented in this video along with other disabilities that aren't seen on the surface.

Same!!!!

I dated a girl with BPD. It was a roller coaster and a half, but jesus it was a lot of fun too. She was extremely open about, saying that she would end up hurting me sooner or later, and I accepted that. Even though she hurt me pretty badly (cheating and texting me about it), I was prepared for it, so it didnt hurt as much. That said, it doesnt defend her actions, but I respect that she was open about it to me. We are still friends :)

Ikr

As soon as she said that she had that I screamed ‘YES QUEEN, THANK YOU!!!!!’ I have it too

Was that the girl with the bun?

Tara she’s the black one in all black

ajah224 oh I loved her as well

And she's so damn funny, made my day 😆

Nah son. She was lucky people didn't try to give her shit. Tip toeing is what a lot of disabled people ask for because of the current culture we have

Ya like jazz?

@@adudeandhisdog23 Absolutely love it.

Karl MacKinnon bro fr. his flirting had me blushing and smiling through the screen

Karl MacKinnon yA lIkE jAzZ

I beg to differ

Fucking same!!!! My nanna, my mom and I have endometriosis. It is awful and I hate when people just respond with that bullshit. Unless you were diagnosed with a condition like endometriosis or pcos I have a hard time believing the bad period thing.

I absolutely agree that people that don't have the diagnosis in question shouldn't say that they can relate to it, and to say "I have bad periods too" is a bad answer. But! People can have real bad period pains without them. My mom used to more or less drop to the ground because her cramps were so severe. They probably don't compare to the pain you're going through, but they shouldn't be dismissed, either.

I personally don't have endometriosis, but I my cousin does and from what she's told and from what I've witnessed, anyone who suffers with it, you are some of the strongest people on this fucking planet and I'm so proud of you for not letting it get in the way of your life and not letting it define you

Alexandra McHaffie I have bad periods and all of my female family members have had it on my moms side, and I learned from my mom that if you’re family has had it you have a higher chance of having it. Is that true

Same! I'll tell someone how bad my cramps used to be (on birthcontrol now so I don't have my period at all) and they'll be like "oh yeah, I have bad cramps too". You know, I dont doubt that it feels bad, I really don't - but there is a difference between endometriosis period cramps and normal period cramps. When I was in school and had my period, the first 1-2 days I almost always stayed at home because he cramps where so bad i could barely stand up. A few years ago it even got so bad that I threw up because of the pain. (It was also really hot outside so that could have somehing to do with it too, most likely a combination of pain and being really warm). I've had friends tell me "yeah, I have bad cramps too but then I take naproxen (painkiller for period cramps) and then I'm fine". They don't work for me. I would always take it during my period out of desperation because nothing else worked, and they did work a tiiiny bit but still not enough for me to walk normally. And yes ofc anyone is allowed to complain about their pain or their anxiety etc. I don't blame people for complaining about shit that is really hard, but there is a different betwen "I'm so sick of -----" and comparing two different levels of pain and essentialy be like "oh its the same". I have also had friends respond with "I wish I could stay at home too" when I told them I wasnt able to get up to go to school because of my depression. Nowadays I cant go to school or work because of fibromyalgia, and I have had several people tell me that they'd love to stay home and watch netflix/tv all day too and not having to do things, or even some who'll say "yeah I have a hard time getting up in the morning too but I just force myself". That's great for yu that you're able to do that, but when you entire body hurts you cant just force yourself to go to school pr work. And it is anything but fun to stay at home all day. I have nevernliked school, but I still miss it- I miss having somehing to go to every day. It is not fun being forced (by your own body) to not do anything but sleep and watch tv. I cant take showers because I cant stand for that long, I cant even stand for 2 minutes while brushing me teeth. I take baths because the hot water helps a little bit wih the pain. I wash ny hair about once a werk because I get so exhausted from it and holding my srms above my head to wash it really hurts. I barely see or talk with friends (they kinda stopped talking with me after the pain got this bad). I can't travel by myself, I can't go to concerts or other events anymore. I can't even be in the same room as someone who is esting because of noise sensitivity. I cant go on walks with my grandma's dog anymore. I cant go ANYWHERE by myself because i cant walk much, I have a wheelchair but I'm not strong enough to wheel myself outside (both because its super hard to do it on asphalt and because I cant even get out of the street where i live without going up a hill (yay for living in Norway where there are hills everywhere) and the pain in my arms get worse when using the wheelchair) I get tired from everything. I can literally lie in bed or on the couch all day and atill need a nap after a few hours because I get exhausted from it. I can sleep for 11 hours and still be more exhausted when waking up than I was when going to bed. Yes, of course people who don't have it that bad can complain if they struggle. I'm always there for my frienda if they need to talk about something or if they just need to complain for a while. I get it. But don't compare your struggles to other people's struggles. I have had many friends who will do the whole "oh I have it worde than you" thing. Don't. Just don't. And don't tell anyone who is forced to stay home all day that you wish you could do the same. Trust me, you don't want this. You don't want an invisible illness that cant be cured. My chronic pain might not be life threatening in any way, but it is life changing. I both wish people would experience this just for a day to know what its like, but I also wouldn't wish this on anyone.

You should check out the Andy Cutler protocol, it has helped so so many people, start with the success stories. Wish you the very best.

Lo Lo it sure is

Yeah like my mom She has diabetes and she has a pump (idk if that’s what it’s called I’m not English) but like she kinda hides it

Ayla Stinks I’m type one diabetic as well. You spelt it right :).

Lo Lo I have Aspergers and apparently I’m disabled...?

I’m happy for you having your gf, hopefully you’re still together. I’m sad you get looked at badly as a couple and as a person outside. It’s so awful people can’t just be who they are in the world and not be judged.

I'm so happy for you two! Just subbed😊

Shane and Hannah have the best channel!!! Brightens my day every time they post something :)

KIMBAP BE KIDDING they’re engaged! :)

AHHHH i love yall's videos so much !!!

Ikkkkkkkkk

kaytse kt Thanks!

kaytse kt as a girl with endometriosis I can confirm it is hell to have period in your stomach

I have polycystic ovarian syndrome

Random myths ... and then they find out it doesn’t always help...

endometriosis is such a horrible disease to live with, trust me 💛😭

Me too!! Mostly because that would be exactly me in that situation! This actually made me realize that when I get choked up and start crying in a not necessarily sad situation that its actually anxiety. I know I have anxiety but I never understood why I’d cry in very stressful situations and now I realize its a nervous reaction. As much as Im not glad she had so much anxiety Im glad it helped me learn about me and feel more normal. Other people experience this too its not just me :)

please stop ik🥺

angelique jasmine what

@@eshalsiddiqi3054 I think she was replying to the person saying I Know Right

Me too damn

I flipped out bc I have borderline personality disorder and when I saw her I felt a connection and I was like does she have borderline and when she was describing it I was like am I overthinking Bc she more seems depressed then she said borderline I jumped up and was like "HOLY SHIT I WAS RIGHT"

I wish her the best. Her response broke my heart.

Jackie Koochembere Same girl. I knew it the second she came out.

Jackie Koochembere I also think the girl at the end he was crying who thinks she has anxiety probably has BPD.

@@chelseygarrett4221 oh true. But I mean she could be right about it being her anxiety tho. I'm not entirely sure I just was diagnosed with bpd in May so I actually mixed up a lot of my anxiety with my bpd so I can never tell anymore.

Hang in there, beautiful! 💪🏻💛

Stay strong darling

you are so strong girl hope you're doing great!

I have endo too and my life was put on hold because of it. Sad how the medical field looks at it like that too. Stay strong hun, I know you can get through this and kick that endo in the ass!

@@PoppyUr I have had lower abdomen pain basically every day since my period started, no joke, but any doctor even ever brought up endometriosis as an option.... They just say it might be IBS and hemorroids and that I have to live with it.....I study medicine so I'm quite aware of things going on in the body, I'm not saying it's endometriosis for sure, but I feel like this disease is being ignored by many.... I hope I can become a doctor and help people like us.

Sarah Wallace ikr

I think she thought that guy was totally hitting on her but damn his voice is so soothing i think he's just naturally smooth

Belinda S He's definitely very attractive.

Who?

I think it’s funny that you didn’t name names and we still all knew who you meant

Hi Molly ❤️❤️❤️

Hahaha it’s always fun to find people that you’re subbed to in the comment section of other channels’ videos.

Just scrolling through the comments and see the one person I actually religiously follow on RU-vid. Hello queen!

Hey Molly, you always talk about how you're always watching RU-vid so it isn't shocking to see your comment but it's cool to see we watch the same things

♥Molly!!!! ♥

THIS COMMENT 💖💖💖 yes!! I suffer with numerous invisible chronic illnesses and chronic pain and it means so very much to me to hear that!! Thank you for saying this😭

It can't come out the hoo haa

💀💀💀deceased

R.I.P 💀

That's how my friend reacted! She literally goes "YOU BLEED IN YOUR FUCKING STOMACH" and I just go, yea

@@introvertedbandnerd3289 WAIT WHAT

Lying to people often makes them feel better about themselves.

colormesarge She didn't lie. Her smile was beautiful even when she started crying.

I hope I’m a pretty crier (I’m not) because a lot of people have seen me cry

Wait, when was it said?

@@c-man6114 15:00

I couldn't stop laughing when she said that

ikr! lmaoo. but she is so beautiful

I love it 😂

And that fit -

She is like mama Krone from The promised Neverland

@@4vr1l57 no no no 😭

Samee

oof too accurate

Yessss me tooooooo

She’s wonderful

Same tho

Kayla Hurd As someone who also struggles with those, I completely agree!

I agree

I also suffer from anxiety, depression, PTSD, and some learning disabilities that effect my social ability and most people don't understand but seeing people be so supportive fills my heart

Kayla Hurd I’m autistic which means I learn social cues differently ( basically if people from 18-35 my age group go to a party I’m the last invitee IF I EVEN GO AT ALL )

I have anxiety, depression, and OCD, and I really appreciated them adding someone with PTSD and BPD

Yes! She didn't treat them like different people. She remained herself and funny (:

YES! She’s such a sweetheart❤️

She is a dominatrix. So, mentally she has to be strong.

she's dirty too, and very confident.

still the only Person in the Video who used bad language i mean is it that hard to not use ´´bitches´´

That's why he's professional Dating Coach 😏😂

He's throwing all the game at her...

He definitely wasn't hitting on her? Just because they're both in wheelchairs doesn't mean they're supposed to be together, becky

@@charleswow9552 or you instantly feel camaraderie with another person that goes through the same struggles as you do?

AwesomeKitCat You should see the "Kids meet" she was in. I think it was uploaded yesterday. It was awesome!

I have TS!! The second she walked out I knew it lmaoo

I would love to see you trying so hard to hold back tics 90% of your waking hours

Pizza most of us can... I have severe TS and I am able to surpress them a lot of the day. No one knew I had TS until I got up and told them. I just hold them back when I need to and get up and walk away to let them out. Many people can do that

SkyHigh_ I know, I have TS myself. Just pointing out how - for most people - going around holding impulses back all the time is not fine at all.

Summer Hendrix dude when she asked me, that just came out my mouth without thinking LOL

Me!! Not in physically but mentally😂

Lani Nguyen I have Borderline Personality Disorder as well but it is not a disability for me because medication and therapy work so that I am able to go through with daily activities. Yet I can totally relate to you. Even though I am able to go through with my daily activities, if I'm not at work I still want to be alone. I have had symptoms of BPD since I was 10 or 11 and I was not properly diagnosed until I was 20. I only hope for the best for you 💕💕

Invisible disabilities are real. I have an invisible disability but you would of never of known unless I had told you

Jamie Brower I did horribly. They just edited me nicely lol

Rayne E. Daze This is going to sound weird but are you on Instagram? Cos you're cool!

You should check out the Andy Cutler protocol, it has helped so so many people, start with the success stories. Wish you the very best.

Love your profile pic! Bi Pride!!

literally her comments had me dying

Take my word it is horrible. 30mg uterus.Ugh. Be glad you're a guy.

fatpanda101 such a good idea 💡

fatpanda101 that’s a really good idea

Good idea!

OH YEEEEES

so glad this comment is getting recognition 💓

Melissa Reynolds This. Yes.

As someone with severe anxiety and vertigo with a brother who has spina bifida I needed to read this.

I know the people above me kinda already said this first but I also REALLY-REALLY needed to hear this!! I’m always the person that feels others pain (emotional & physical), so extremely that I completely ignored my own feelings to the extreme. Well, cut to now & I’m at the point that I myself can barely function any longer because I’ve run myself so ragged for so many years now. I’m actually now beyond panic attacks & anxiety & depression and have pseudo-seizures constantly. It just really helped me to hear what you had written. Thank you for writing what you did!! You truly must be an incredibly amazing person💕!! Thank you...just remember that YOU deserve everything as well, love!!!

Thank you💕

Thank you so much. I wish you all the best. 💚

it is literally a pain in the butt.This is why I back up Planned Parenthood.

Flo Russo RIGHT😂😂

Or when someone says their head hurts or something I’m coming up with diagnosis and stuff😂

I just laughed out loud. Literally in he middle of the night.

Flo Russo fr💀💀

ME TOO 😂😂

marcopolo208 I did hug them and they are wonderful!

Ray Audrey You are from the vid right?😁

Panic!AtTheCrybabyies Fan yep! Such an incredible experience with the most beautiful and kind people I have ever met.

You didn’t wanna hug the guy too? Was it because of his disability? You sick fuck

Josh Castro Hahah nothing to do with the disability. But now it would be weird to hug him too just because he has a disability😉 Sounds like a pity hug then.

I understand even though I dont have depression. There was a week I was really hurt in and the whole time trying to forget or ignore what I was annoyed by, but couldnt. It was painful to hold back my tears every minute I remember it. This is absolutely nothing compared to what you or people with depression feel like, but it definitely makes me understand that you are probably experiencing the same thing but have it tougher and more excessive. Stay strong

I get it! Sometimes people will only acknowledge the physical disabilities, but having ADD and anxiety (myself) are just as much a disability. I would say that a disability is something that hinders your daily functioning, so whether it’s physical or mental.

Blair Underwood my mum has it and doctors thoughts I had it cause I had severe period pains but thankfully I don’t have it👌

Some doctors dont care enough to check properly, and i know that as much as anyone Sad but true eh

I was recently diagnosed. It sucks sm. They only diagnosed me post laparoscopy and it sucks. But I'm gonna be okay

I was fortunate my doctor listened to my and I got it diagnosed quickly. Unfortunately this is not the case for a lot of women. If you feel like your doctor is not listening to you, you know your body better than anyone else. Switch doctors until you get answers!

It took me almost two decades to get diagnosed. I have suffered so so so much. It is really debilitating. My diagnosis came after a small bowel obstruction and a open exploratory surgery found a mass blocking my intestines. Everybody thought it was cancer, but the pathology came back saying "endometrium like tissue". After this first surgery I already had two more, a hysterectomy and another resection of my bowel. I really hope that my life will be better now. But these two decades of excruciating pain have had messed up with my body and mind. I have been diagnosed with migraine and I am also depression.

I guess you missed that he is a dating coach.

haminda ojo we were saying the same thing on set. He was smooth as hell lol. He changed the entire dynamic of the guessers. It went from awkward to just a couple of friends catching up

haminda ojo He's a dating coach after all.

Baby use that Colgate baby keep your teeth straight

DVS GAMING shut the fuck up man

she needs her own series tbh she's great haha!

You be fucking? Lol

Qveen Crimson idk if funny is the right word tho

*I S T H A T R A C I S M I S M E L L* *sarcasm sign*

ikr I am dying

where? i heard 1 person

Joel Miller you can also hear a different person say " you're a pretty crier,How do you manage that?"

Kritika Shenoy I cried

except for the music in the back, kind of ruined what could've been a touching moment for me at least.

I actually did start to cry

Niff That's hell for a girl to go through

Niff oh HELL no

i want someone to say this to me next time i tell them i have endo

Melanie Hollows same😂

My life on the daily #endoprobs

voidz death by snu snu

She is very tall

voidz she is 6ft at the shortest

voidz 6’2” (and from chicago) she mentioned it in an earlier video

Catherine Jones she is way taller then that

Endometriosis isn’t always considered a disability since it’s severity differs case-by-case. Some people with this disease suffer completely debilitating pain, and others who have it might not even know.

Xhoose prerrt sure its tourettes

i have a mild version of tourettes and i cant even imagine how hard it must be to have severe cases bc even the mild one has messed me up

lollyspipoca right! I only have mild tics and they interfere w my life so much I can’t imagine having it vocally also :/ she is a strong woman

I have very severe Tourette’s and I can assure you it’s a tough thing to deal with. I’ve broken bones many times from it too which I can’t stand but it’s more painful mentally and emotionally. People stare and it’s embarrassing. And it’s so uncomfortable to have no control over your brain and body. I cried like a baby when that woman came on and told them.

aside from the physical aspects that affect all of your guys' life that makes it a burden i cannot imagine how often you feel like a burden to others because you are making them uncomfortable and that's super upsetting. when she said along the lines of do i take the pills to make other people uncomfortable or do i not take them and be comfortable really was eye opening.

angelmushahf She's a pro-domme so I'm not surprised. It takes a huge amount of ability to read body language and faces to do that job really well, she's got a really good rep in the community so I'm not surprised she's good at it.

angelmushahf Why are you suprised? Why to put your foot in your mouth inbred.

lol at ppl offended by my comment xD

even she was surprised that she got so many of them right. see how she was celebrating? I'm celebrating with her. no disrespect here :)

Nir Alkalay I KNOW

Sofia A i have it too. And I was super lucky and getting it diagnosed when I was 17. It makes me really upset that when women go to doctors and say “I have extremely painful periods” it’s not viewed as a problem. I was lucky and I had my mom in my corner going “no it’s not just painful periods, this isn’t normal”. I am really happy it was mentioned too, cause I still deal with people telling me I’m being dramatic even though I’ve been diagnosed.

Moriah Maxwell I was diagnosed at 12 and my mom was super helpful also. Most people think it’s not as bad as it is and it really makes me upset, because it’s the worst pain I’ve ever felt

yes!!! My mom didn't struggle with it, but most of my great aunts/aunts do and so do both my grandmothers. My mom just thought "oh its just part of being a woman" until I was vomiting, fainting, and missing weeks of school because I couldn't get out of bed. Like the PELVIC PAIN is something else aswell as the migraines etc etc. I got my period at 14, and by the time I was 15 (I'm almost 18) I was on the pill so my symptoms are not present now because I do extended cycles so I only have a period 2-4 times a year. The pill doesn't alleviate the pain, but it made it shorter from 9 to 4/5 days. Thankfully I did not have to do the surgeries because they caught it very early, after I only had maybe 5 periods (?) because I was so irregular. I honestly did not know it was considered a disability. It's nice seeing other women understand it.

exactly. mine is in a very early stage because I caught it early on and I take steps to keep myself from further developing It because my mom had stage four and was in chronic pain 3 out of 4 weeks each month and it almost developed into cancer. mine was getting to be about 2-3 weeks out of the month with symptoms and during my period I was in such intense pain I was severely suicidal and unable to function but I never hear anyone talk about it in chronic pain discussions

honestly when a doctor finally put me on the pill I could've cried. like my mom is pro natural medicine and kind of anti medicine at times and was hesitant to put me on the pill (even tho she went through the same stuff) but like my birth control is an honest to god life-saver (genuinely I think I may have done something drastic with the direction it was heading in)

Heather Rose 💛

I feel the same way!! I was literally clapping when she told her disability.

I cheered out loud for our EndoSisters everywhere 😀 and you're so right about the disability aspect SMDH! Love you guys 😘

Any suggestions on treatments?

Gia Barrone I have a suggestion against... lol Zoladex or medically induced menopause was something was not right for me. I'm over a year an a half from my last injection and still having SEVERE hot flushes. Just be sure the consultant has given no other viable options. Waiting to start merina coil life..... Not enthusiastic.... lol coukd be worse! But glad to see after so long I and we are really not alone in this 😗

She can’t pronounce her own name smh

Not every Bjork is a Björk and names can be pronounced in any way a person wants. They're not in the dictionary.

It depends if she spells it with an umlaut or not

This went in a different direction than intended. I only said that because its the same name of my icon, Björk Guðmundsdóttir. Ps: yes I did copy and paste her last name... I don't have the time.

I laughed way too hard at this because same

“Woke” 😬

Please dont ever use the word "woke" again, its the shittiest word ever

Sadly not true anymore

I don't have endo but as a teen i am so glad to see different chronic illnesses reconized

You are not alone. I didnt know there were support groups. I am happier with having had a hysterectomy.

This is so true, I have PTSD from being kidnapped by my step mother

Yep. I have PTSD from abuse and sexual assault.

Same... from disasters.

I have PTSD from severe bullying in high school where they held a knife to my throat. The amount of time I’ve been told I couldn’t have it because I never went to war is insane. The disease is horrible and being called a liar screws with your head.

Same. I wish people would get that.

I know right!!! I'm a bpd myself, there are even mean websites like don'teverdateagirlwithborderlinepersonalitydisorder.com where guys just bash bpd women by calling them soul sucking women -.-

@@belsrevenge24 wth thats awful!

@@monkeybluecheese i know right!!

@@belsrevenge24 Yay it was removed i think

My sister and I have POTS. You aren’t alone!

Gigi V Stay Strong! You are amazing and you are never alone!

❤️

I have pots and ncs dysautonomia

I have POTS and i was diagnosed with this after MANY, MANY misdiagnosis and when I found this and a few other comments about POTS i was brought to tears bc i was told that POTS is rare and this proves that statement wrong. I am currently going through a trial and error process with medications bc my body won't take to the ones i have tried so far. So i am trying to get people to contact me so we can form some kind of group to talk about it and help others cope with it. So please reply or contact me on my instagram @faithsanchez03 Thank you!

I felt the same way! For me, fatigue has been a debilitating effect of endometriosis. But before I knew what it was, I was basically told I was just depressed and needed to pull myself up by my bootstraps. I think it’s easy to internalize that kind of rhetoric.

Kate 42 omg this is actually genius

+

Kate 42 Thats such a good idea!!

Yeah he was in a different video where he talked to some kids about his condition and I saw him in this and I super excited.

Maria Hernandez that chick is fucking awesome!

Laya yes same I found it really heartwarming

PREACH #potssquad

Yes!! I saw the chair and thought "SHE HAS POTS!!"

same!

Same!!! LOL

Yes!! Same here. It's definitely a hard disability to see from the outside. I tend to push myself too much to keep up because no one ever accommodates me. Its nice to see others making waves in the community though! Get the representation we need!

I relate too much to that. (Mine only a 1 in a thousand have it) You can tell shes used to it too because she had a quick explanation shes clearly used to giving. I have Secondary Adrenal Insufficiency and Growth Hormone Deficiency. I've only had two people actually know mine so far... a med student and a professor. I was absolutely shocked, and then teary when the professor understood and I didn't have to fight for understanding and accomodation for my invisible illness. When I'm throwing up due to pain... School and proffessors judging is the last thing I want to be worrying about!

My little brother has Adams Oliver Syndrome which is so rare that it's prevalence is unknown, I've gotten pretty good at explaining it to people who ask but I get so tired of people asking me whats wrong with my brother in a hushed whisper. First of all he's capable of answering for himself, and second theres nothing wrong with him. third I almost want to get "I HAVE A DISABILITY TOO" tattoo on my forehead so maybe people will stop being assholes to my little brother (who given is taller than I am at this point) and pick on someone their own damn size.

Part of me was like "Wow don't get sassy with him for not knowing" and the other half is like "women's issues aren't taken seriously enough to be known by men. If endro was a man's desease, it would be wide known and probably a lot more research and treatments on it."

l know exactly what that is because I have Primary Adrenal Insufficiency! I never met anyone else with it and always had to explain to even doctors what it is unless they're endocrinologists! However, I'm a nurse now and have actually met a few patients with it! We're just rare unicorns is all

I agree! Endo has been found in some men, as well... I haven't read the studies on it myself. And don't forget trans men.

Emma Still yes!!!! I literally have never met anyone who knows about it.

I also have vasovagal syncope and when I say either people just give me a blank stare

Lexi Burns ikr! Syncope has to do with fainting right? I haven’t fainted yet, but I’m scared I might

Emma Still yeah, I used to faint multiple times a day but now that I’m on fludrocortisone and propranolol I’m okay!

Lexi Burns good! I take fludrocortisone too. I also take atenolol and midodrine.

Me too!

He is short

@@user-pp9df6ml6i He may be a little short. But Raine (is that the womans name?) is also tall.

Hes buff and his Pants are baggy so he looks short in comparison

@@ashlynnheller8400 her name is rayne, I just saw her comment on a reply under the comment section:)

@@desireandfire Okay. So my spelling was just off.

Jamie Maybe i have autism

same

If they did that with a lineup of fortnite players it would be all too easy.

I'm also on the spectrum and it be nice to see them showcase people on different ends of the spectrum from the "normal looking ones" to the ones we see more classically in movies.

peter panda It takes one to know one. I'm autistic and I don't play Fortnite.

Pots squad ❤️ that made me so happy!

YES

Grace Jersey Why? I have it And i have never seen it as a disability

I think Endo is one of those things that can be a disability for some people and not for others. She said she was in pain at that moment, do you often finds things difficult to do because you are in so much pain? I have a chronic illness so I know how much symptoms can vary between suffers. At one point I was in so much pain I could not leave my apartment. I could not walk to classes. I could not sit through a lecture. I couldn't go grocery shopping. I thought I would never get to walk my dog again. I couldn't have sex with my spouse. My mom with the same illness lives a nearly normal life.

Is it actually considered a disability? Can a person get therapies and ssi with it?

(Just my personal feelings) I have endometriosis too and it's been quite miserable but I've always thought of it as a condition and not a disability. I have multiple sclerosis too but don't think of it as a disability either. Disabled is a frame is mind that I refuse to allow myself to embrace. I'm fearful that when I do then my body will follow my mind.

I went several years undiagnosed with endo and it nearly killed me. I ruptured my spleen and waited several hours before going to the hospital because the pain from the rupture wasn't half as bad as the daily endometriosis pain. By the time I got to the hospital I was unconscious from blood loss. That was the first time a doctor took my endometriosis pain seriously.

Wasn’t funny.

Brittany Stewart they cut out so much amazing content to make the video shorter. We filmed for over 9 hours! Rain was hilarious the entire time

I love her, funny & she's so warm & down to earth too

ikr she's my favorite

Yay, Rayne's back!

"I like helpin' people find new jobs." I laughed for years after she said that LOL

meeee lmao

Yeh me too

I love that she followed that statement immediately with the right answer. She was so shocked.

same

SHE WAS DEAD ON IT TOO LMAOOO

Imogen Rogers yes. This idea is great!

Imogen Rogers omg yessss

Belive me u are not alone❤ (i have anemia to)

Cloud King me too because I have it

I thought PCOS too because my close friend has it

I have PCOS too and I have been admitted into hospital way too many times because of the chronic pains I get. One of my friends also has PCOS and it barely affects her life, it affects everyone differently I guess.

happy ghost yeah mine is awful periods and massive gain weight when I’m eating healthy.

PCOS and Endometriosis are often linked. It is not uncommon for someone who has one to have the other.

I don't want to offend but can you explain what you mean when you said resting your knee on a chair keeps you awake a bit longer?

PhantomAmber I can not imagine how it must be to live with such a disability / illness(please do say if you prefer another umbrella term for it). I have a classmate with narcolepsy who often kind of falls asleep for a second or so in class and a teacher kind of called her out, obviously not knowing about it and she just shyly said "I'm not doing it on purpose". A lot of people know about epilepsy and take it seriously, but narcolepsy isn't as well known.

Rachel I think?

Its interesting you say that because for me it immediately gave away the MECFS and POTS (i have both) I mostly use a cane and wheelchair but on good days I use this technique a lot.

My hearts the same we actually had to get it tested it was so bad. I went from laying to sitting and my heart was like 134 beats per minute. I need to drink a lot of water because of it and I get headaches quickly.

Daphne Stier same, but I don’t have Tourette’s, I just could kind of tell.

same! i’m so glad they knew what it was

I have Tourette’s too Btw: I think I have seen this Woman on Kids Meet

I have tourettes too, people around me sense that I'm different, but can't tell until I don't hold back. It's often really invisible. I could realate so much, when she said, that it kinda hurts to hold the tics back, 'cause it's really uncomfortable to opress the urge to tic.

same I also have tourette's and I was glad that people could at least recognize it

😆