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

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.

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

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

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!

I have it too but the doctors don’t want to freaking do me a right diagnose me for it! It’s very painful I always feel pulse on my lower back and when I start my cycle I crying for 15 30 mins I’m only 26 I’m not planning on having kids either so I don’t know what to do anymore

Ikkkkkkkkk

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

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.

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

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

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...?

Samee

oof too accurate

Yessss me tooooooo

She’s wonderful

Same tho

literally her comments had me dying

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

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 !!!

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.

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

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 💛😭

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.

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.

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 KZfaq. Hello queen!

Hey Molly, you always talk about how you're always watching KZfaq 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😭

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.

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

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!!

I couldn't stop laughing when she said that

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

😆

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´´

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

Me too!

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?

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 😭

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 💕💕

fatpanda101 such a good idea 💡

fatpanda101 that’s a really good idea

Good idea!

OH YEEEEES

so glad this comment is getting recognition 💓

Pots squad ❤️ that made me so happy!

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.

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

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.

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

She’s got the strength to live with it, she’s currently without your praise or pity living the hell out of her life, as are all disabled people.

@@codename495 sure...why bring in that snark about my praise and pity. Chill out

@@codename495 Not true, my life sucks because of my disability, and I appreciate the sympathy and kindness even if it doesn't fix anything.

Theres a difference between pitying someone and having empathy and understanding.. also gotta keep in mind that not everyone _wants_ a cure for their disabillities

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.

Most people think we’re stupid . We’re not and most determined to stop that by trying to be independent I’m in middle school with Cerebral palsy this hit me in the feels. Thanks you so much for spreading the word😊

C-E-R-E-B-R-A-L P-A-L-S-Y

@@vogelvogeltje Thanks lol, It’s funny that the name of a condition that can sometimes cause speech difficulty is hard to pronounce!

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 😂😂

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.

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)

“Woke” 😬

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

Sadly not true anymore

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 😗

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.

💕💕💕

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

You should check out Jessica Kellgren Fozard!

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

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

Kate 42 omg this is actually genius

+

Kate 42 Thats such a good idea!!

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!

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

It’s much more common than people think and it sucks that so many doctors have no idea what it is. It’s also hard to explain to people sometimes I have no idea where to start

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

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.

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!

Maria Hernandez that chick is fucking awesome!