r/EntitledParents YOU'RE TOO YOUNG TO BE DISABLED! | (EntitledPeople Reddit Stories)

r/EntitledParents & r/EntitledPeople, today we have a whole bunch of reddit stories from both the EntitledParents subreddit and the EntitledPeople subreddit. A Karen who things an OP is too young to be disabled. These EntitledParents are the worst.
Watch next - 👪 r/Entitledparents - ALL THE EPISODES:
• r/Entitledparents "YOU...
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[@MarkNarrations]

Get involved on Discord: discord.gg/2uMxCfn?

[@HowlingEclipse]

I'll be honest the disabled one got me the most, but all were great! Especially because i'm told on a daily I don't look autistic and it doesn't look like I need a service dog. Or i'm just doing this for attention... Feel bad for the Op... because that was an extreme situation

[@bluechord2928]

I am 18 and have moderate hearing loss. I have been losing my hearing slowly since I was 7 so I don't sound deaf. I genuinely got yelled at by one of my mum's friends because I didn't respond or turn around when they called my name. The friend came up and tapped me on the shoulder to get my attention. As soon as I realised what happened I apologized and we tried to start talking but this mum immediately started having a go at me for being rude and bullying her daughter by ignoring her. I apologized again and explained that I have hearing loss and wear hearing aids for it. She then had a go at me for lying to an adult because I didn't sound deaf and I was too young to loose my hearing naturally. Well I could have explained the build up of scar tissue on my ear drums but instead I just left...I had only recently been officially diagnosed (my hearing loss kinda snuck up on me) and I had only been wearing my hearing aids for a few weeks so I was very self conscious about the whole thing

[@MarkNarrations]

Sorry you're going through that Blue, so are you going to totally lose your hearing? Sorry if that's a bit personal, just curious.

[@bluechord2928]

@@MarkNarrations I don't know to be honest. I have severe scarring on my ear drums and in a cognitive sense I never developed proper listening skills so, while it is likely that I will go deaf earlier than many people as I already have below average hearing, unless something severe happens to my hearing (like another perforated ear drum or standing near something that would deafen most people) I will most likely not completely loose my hearing so that's good :)

[@raggarbergman]

Wow... would she say the same thing to a young person who need glasses to that they are to young? Hearing impaired myself after my first meningits at just a few weeks old.

[@dnprime1737]

"young people can't be disabled!"-karen me: i'm offended by that statement!

[@littledikkins2]

My disabilities are invisible too... unless things are so bad I'm limping which I try like hell not to do. I've had problems and I am FAR from being a young person.

[@dnprime1737]

@@littledikkins2 my disability is invisible and in my head, but my diagnosis was in dutch elementary school, so i have been living with a disability all my childhood. I know how bad it must be for people with visible disabilities and those with a physical disability on the inside of their bodies, so those "people" who either think young people can't be disabled or that they can just be downright rude or abusive to disabled people can jump off a cliff as far as i'm concerned.

[@MarkNarrations]

I'm offended too!

[@dnprime1737]

@@MarkNarrations disabled people, UNITE!

[@user-mama_thomas]

@@littledikkins2 I also have a invisible disability and it really sucks when even doctors don't believe you and say you are just trying to get drugs. I wish I didn't have chronic pain and the fact that I will for the rest of my life. It started when i was in my early 20's and my doctors have done everything they could through surgeries. (Almost 20 surgeries between the ages of 21 and 35. Including a full hysterectomy at age 30) I was also told that I would most likely get cancer from all of the x-rays and CT scans that I've had. Fun. That part really sucks since cancer runs in my family.

[@paranoiarpincess]

I've had so much crap from the "young people can't be disabled" bs throughout my life. It's even worse when it's an invisible disease and you develop insanely high pain tolerance, alongside your doctors training you to try to fit in, in society. So you try to suppress that there is anything wrong with you, meanwhile becoming a social chameleon. You don't "look like" you're in pain. You don't "look" old enough to be disabled, and you have learned to keep quiet about your pain, disease, and to be as unassuming as possible. All of this, only to have people treat you like crap during the times where you really need to rely on their sympathy. Like being on a form of public transit, and being asked to get up. Or always having to be the one to ask others to get up for you. I totally understand that people don't automatically know I'm disabled, but it really sucks having to ask. *Especially* when EMs and honestly, EP in general, give you a hard time, or worse, full on ignore you.

[@MarkNarrations]

Don't take their crap Paranoia!

[@kiarastardust]

i toyally get it. i'm legally disabled due ti autisim and seveare anxiety. If I get sensory overload then my anxiety spikes, which leads to me shutting down compleatly and in serious cases having violent reactions that are compleatly out of my control. Though those reactions are rare now, it was more common when i was a kid. When i went to disney with my family when i was 10 we got to use the disabled entrance for the rides. My family got yelled at multiple times for cutting the line. And a surprising majority of those people refused to believe i was disabled because i was't in a wheelchair. I may not have had a disability that hindered my movement, but due to my sensory issues being in large crowds and around loud sounds where big issues and many lines at disney where long and had no way for my parents to remove me from them. i looked an acted compleatly normal as i was high functioning and alot of the affects of my autisim centered around communication and sensory issues. The cast members on the other hand where amazing and backed up my parents when it came to disability. During the haunted mansion ride they where taking us through the disabled entrance and I got scared so badly that i turned and ran out the door. The cast member leading us apparently learned from my parents about my sensory seeking behavior towards soft things because i was given a lady plush with soft ears that they let me keep

[@paranoiarpincess]

@@kiarastardust Im I'm sorry you have to deal with that. The cast member who gave you the lady plush is a genuinely good person, I'm glad you had them in your life. I hope you have a great day.

[@OZARKMOON1960]

The OP who mentioned not having any happy memories from childhood really hit home with me in regards to my own mom. Dad was always fun and enjoy every kind of holiday, but mom...that woman woke up spitting fire and ruined many a holiday. I'm glad he is getting therapy and dealing with things. I wish him every happiness.

[@thehaveninthehand]

Same. My parents divorced before I was 3, and shared custody. I only got to see my dad and that side of the family every second weekend. That was the only time I got to be an ordinary kid, and that's saying something, since my cousin (whose parents were also divorced, same custody agreement as me) had paranoid schizophrenia, and we had to be careful around her. My dad was my super hero, and he's the reason I'm so well adjusted today.

[@mayle2010]

Ugg it's 2020 people should know that anyone can have a disability. I wish op pressed charges, since Karen was such a plonker.

[@MarkNarrations]

Haha good use of plonker there, A+

[@Mew_Mokuba_Akari]

Yeah its not worth Googling that word

[@xosammy4301]

I've been off KZbin for along time (been in hospital) and I return and you're now Mark Narrations!? Bloody mind blown

[@MarkNarrations]

Welcome back Sammy, I hope your doing well and hospital wasn't nothing too serious!

[@xosammy4301]

@@MarkNarrations awe thanks mate, this made my day. Yeah I'm getting there. Your videos really helped in the road to recovery, thanks☺️

[@tiaraa.k.at-money]

The story about the entitled parent saying someone is too young to be disabled makes me annoyed because I am disabled and I have been since birth people can be disabled at any age.

[@MarkNarrations]

Karens are a strange beast, best to ignore them when possible.

[@tiaraa.k.at-money]

@@MarkNarrations I agree they are definitely strange but they are pretty much everywhere so they are difficult to ignore at least I've only encountered one so far but I have a friend and that's encountered at least two and my bf's mom encountered at least two

[@louellacharlton4425]

It's even worse when you have a hidden disability. They come out of the woodwork to destroy you. Geez

[@tiaraa.k.at-money]

@@louellacharlton4425 yeah you never know when you'll run into one

[@teconnyspearow]

i’ve been since i was 1 1/2 (diabetes) when i was 4 i got diagnosed with Dyslexia and Adhd

[@Emilyweasel2023]

I am from the U.K. and have Ehlers Danlos syndrome, among other diagnosis’s. I have a blue badge too and the amount of dirty looks I get parking in disabled spaces. It doesn’t lessen when I pull my badge out. Funnily enough most look away when I pull my crutch(es) our the car and limp away.

[@MarkNarrations]

You should really rub it in their faces!

[@SkylighWillo]

I very much understand the first story because I have costochondritis, the nightmare of a name to pronounce for inflammation of rib cage cartilage. I also have a few other conditions that cause me mobility issues (CFS, Fibro, CRPS) so I'm either using some sort of walking aid or I'm in a wheelchair, I'm 26 but often mistaken for younger and I've noticed that the worst people are often old people. They can be so nasty, I've been pushed into shelves, ignored (they talk to whoever is with me) because they think a wheelchair means I can't talk for myself, told I'm faking it. It's never a dull moment that's for sure!

[@raggarbergman]

As someone with ankylosing spondylitis I understand. And understand OP to as even if not that severe, there are times you hate breathing and a cough is a real bastard.

[@lesliezin2627]

That first story was shocking! I mean I always think people here in England are so nice. Guess I was wrong in thinking that... Entitled people are EVERYWHERE! Also to clarify I'm an American living in England. I don't drive either mainly because I know I would be a menace on the road. I would slip into automatic pilot, start driving on the right side of the road and be completely lost at a round-about. So I take the buses but absolutely AVOID the priority seats. I got legs and intend to use them. It's back of the bus or if it's a double-decker bus I like the upstairs view. The only time I will consider sitting towards the front is if I only have one or two stops to go or the bus is packed, but if I see someone that needs it more then me I move faster than someone could say "Entitled people." Furthermore, I never question it, if someone sits in the priority seats I accept that they may have some kind of medical issue or be pregnant (A woman on the pregnant part). My motto is Never 'Assume' I don't want to make an ass out of myself.

[@MarkNarrations]

And a great motto to live by, the world would be a much better place if no one assumed :)

[@ettinakitten5047]

From what I've heard from British disabled folks, England is actually really bad like that. Awhile back some politician decided to run on a campaign of making up bullshit about how many people were scamming government services and benefits and how he'd cut down on that and reduce taxes. I don't know the details, but apparently a lot of disabled people in England noticed a significant uptick in rude nasty public encounters after that campaign.

[@ettinakitten5047]

5:15 It's not an exaggeration to say she attacked you, OP. She touched you with aggressive intent, and caused you harm as a result, that's an attack.

[@Echo-hk9xo]

I developed CRPS from a car accident when I was 15 and subsequently other disabilities, and people like the Karen in the first story piss me off. I avoid any disabled parking or seating and always have just to avoid this junk (I would 100% beat someones ass if they touched me). I still have people pull the "You're too young to be disabled" and "It's all in your head" cards. Right, Karen, because I love pain 24/7 that's incurable. People can be so rude and ignorant.

[@gina928]

Favorite story is the chocolate bar one. That Karen was a plonker!

[@MarkNarrations]

Karen is indeed a plonker

[@digitalharmony26]

Gotta love people that don’t understand invisible disabilities. I have a few, they’re debilitating but I don’t walk around with a sign saying I’m disabled.

[@bye6651]

I'd say about 10 years ago, me and my buddy got bitched at by some idjit woman for parking in a handicap spot. Mind you, we're both disabled veterans, and he had the DV on his license plate. He has major back issues, and I have a bum knee. He had some choice words for her. He's Russian, and I'm pretty sure than lends to him having less of a filter than even I do. She huffed off, and gave us the evil eye while passing us in the store, but kept her mouth shut.

[@MarkNarrations]

WHat choice words? :)

[@PeacheIIe]

The poor mum in the second story, she should never be ashamed of herself for being poor and struggling and I wish I could give her a hug

[@aindrilaroy4464]

I have had that kind of rib pain. It is excruciating. It hurts beyond belief. Sometimes, it hurt to even breathe or to even shower because the water hitting the swollen ribs HURT.

[@estherdenenga5227]

I get frustrated when they don’t call the police and/or press charges. There was physical abuse, Karen should be held accountable dammit P.S. thanks for the long episode. I really enjoyed all the stories. Great work Also Karen is a plonker lol

[@raggarbergman]

Sadly in cases like these, it is more trouble than it is worth as it rarerly get any punishments dealt.

[@TheMadHatterx]

I was declared a selective mute due to my ADHD a few years back. I experienced shit like the 1st story. I'm pissed. Edit: I am not anymore. I still do have episodes, though.

[@Mew_Mokuba_Akari]

Ok the Walmart story is r/thathappened. I'm not a cashier but I am friends with a lot of them. A. You don't keep your belongings like your purse at the register. You can get into trouble if you try [I know a lady that did try to keep hers with her and was told several times to keep it in her locker in the back.] Plus after your break/lunch you rarely go back to the same register, so you would always have to remember to take it. The reason your not allowed is obviously because the temptation to steal would be higher. B. There us no such button on the register to secretly call for a manager or CSM [Customer Service Manager]. I can't tell you the number of times a cashier has asked me if I've seen a CSM or can go get one or tell them they need them. If they need a CSM they turn the light on their register to flash and hope a CSM sees it and responds.

[@fhuber7507]

1... I feel for OP. 100% NTA. I am SEVERELY disappointed Karen was not hauled off in handcuffs. I had a type of benign bone tumor I described as causing it to feel like my knee was being held by a vice and a 900 lb gorilla was wrenching on my ankle with a 5 ft pipe wrench. Never a positive diagnosis of what the tumor was. 6 of them removed. Finally had them just chop the leg off. Best decision ever.

[@TheNormExperience]

“You’re too young to be disabled!” Funny. That’s exactly what I keep saying! Dang body just refuses to listen though. But that’s nothing compared to your hardships in life Karen - I mean, how dare I not spend every waking minute of my life worrying about how hard MY disability must be for YOU. /s 😒🙄🤬

[@qanile]

The first story sounds like costochronditis. It is really painful.

[@MarkNarrations]

Reading the comments on these kind of stories teach me so much about disabilities I know nothing about. Thank you.

[@eloraandkhan3288]

On story 1, I have a similar problem its caused by EDS - Ehler Danlos Syndrome. What helped me recover, funny enough, was wearing actual metal boned corsets. It held the ribs in place so they weren't able to shift (where it hurts) that allowed the problem to heal, when accompanied by a diet change (I needed more nutrients, and to stop trying to do fad diets as it was literally killing me). People with EDS have "extreme" relationships with salt, from what I've seen... Either they need to go low-sodium, or they need to go high-sodium in their diets. That could be a factor for them.

[@vCoralSandsv]

Note to self: Karen is a plonker...ignore her 😂🤣😂

[@MarkNarrations]

Haha good use of plonker :)

[@meralb7929]

30 MINUTES?? 🥺🥺 you're amazing man

[@MarkNarrations]

Thank you mer alb, hope you enjoy

[@raggarbergman]

You are to young to be disabled. Me when I was younger (I am 36 today) "Well sorry that my arthritis and meningitis forgot to check my ID before attacking."

[@alicerosetrevormusic]

I'm a wheelchair user. 23 yo. It took me over a year to get my blue badge because THE COUNCIL said I wasn't old enough to be disabled.

[@paranoiarpincess]

Hey, I take offense to that! I'm Canadian and I'm equally as ignorant about Brittish slang as any American ;P

[@MarkNarrations]

Haha ok, Canadians included! :)

[@canadaiantenten]

I'm both Canadian and American, does that make me double ignorant? Lol

[@jessicawelch7755]

I know For A Fact that disabilities Don't have an age limit, (being that I've had multiple disabilities Since Birth!) Any1 who says otherwise Needs To Have Their Head Examined!

[@unclegpa707]

I would usually just type the line you ask us to but I actually have a short story this time. I am in the process of getting over cancer. I do not like to consider myself disabled and I'm sort of old school, meaning I like to work for what I want so being told I could not wasn't very fun haha, but having people treat me like the woman in the first story just makes it all the more enjoyable, oh the fun we have 😊. Anyways enough depressing stuff Pip pip, cheerio mate! Was that offen... erhm... BRITISH yeah British enough for yah?

[@jaimejones3177]

Sounds like OP has a severe case of costochondritis. I have it as well... took them almost 30 yrs to diagnose me. It's actually a lot more common than I realized. I get flare ups a couple times a year that leave me feeling like my ribs are broken on one side or the other. Breathing is excruciating. It'll last for a month or 2 then subside. The rest of the time I feel it around my xyphoid process... feels like a terrible stomach ache right under the front of my ribs. Hopefully they've sorted her out by now.

[@tailsnick]

I am American and don't know what a plonker is, but hopefully my sentence will be amusing to you all in the UK. Imatating the Crocodile Hunter: "Crikey! Look at the size of that plonker!"

[@SergioPerez-vm8zw]

Shygirlturnedsassy:*exists * Every Karen in the vicinity wants to know your location

[@MarkNarrations]

Haha, she certainly gets about :)

[@MegaGinia]

I am usually unable to choose a “favorite” story, but I can absolutely wholeheartedly call Karen a plonker and tell her to go pound sand! Sending my love and wishing you and your family all my best.

[@Timecavachon]

Today I encountered a Karen, who was quite the plonker, tried to make us move, when we were boxed in.

[@aprilrichards762]

Bloody hell! You didn't tell me Karen has a plonker!?!

[@MarkNarrations]

lol!

[@gelibeanzcantrell7192]

Karen is a plonker 🤣 idk what it means, but it sounds funny 😜

[@MarkNarrations]

I'm glad you used it :)

[@Tammohawk1]

Hey! I bloody well love English slang. One of my favs is gobsmacked.

[@MarkNarrations]

Haha didn't even realise it was English slang :)

[@somanyhumanssolittlecommon6947]

In another video that included the chocolate story, some dimwit in the comments was actually siding with the psycho mom and putting down OP! As if pushing out a crotch goblin that you don't teach basic manners gives anyone the right to tell total strangers what they can and can't do!!! 🤦

[@MarkNarrations]

Really?! Siding with the EM? wow....

[@somanyhumanssolittlecommon6947]

Hey, Mark! Yep, it blew my mind when I read that! They actually claimed that OP was being unfair...it makes you wonder just how many times they were dropped on their head as a baby, doesn't it? LOL

[@Buff_Helpy]

The brothers psycho wife story was so abrupt and badly written. Buff Helpy is displeased.

[@MarkNarrations]

I'm sorry buff helpy!

[@Buff_Helpy]

@@MarkNarrations you are forgiven, my child.

[@apackofquackers6008]

Karen is a ‘Plonker’!! 🤣🤣

[@glosaint-aime16]

Loved this episode.... loved the opening music and the stories. Need more. I related to alot of the stories

[@9999plato]

I was expecting the packages that Karen Mom brought by and was so insistent about she needed to be brought up and into the home to be loaded with roaches or something like that.

[@OneToxicPixel]

Karen is a... what? Plonker? Yeah whatever. My little add on friend who tells me how to type says this is a word that exists, so I'll take it. The story that is infuriating me the most is the last one. Two of my closer friends went through something like that, had kids with their respective girlfriends, then Mommy dearest just wouldn't let them near their kids and it destroyed them. I lost contact with one of them unfortunately (he was never really one to keep in touch with someone), the other one is still trying everything he can to see his little boy as often as possible. Recently his ex has stopped responding to his messages again and it really upsets me. My friend is a hard working, kind and funny guy, he would never hurt any of them, yet he gets cut off like he is a bad guy. Our government won't even help him because well, he is the father so who cares right? I just hope OP gets to see his son as often as possible so he can be a good influence on the boy and see him grow up.

[@bethyadamec7057]

Another winner Mark!

[@livewellwitheds6885]

I was born with a genetic progressive disability. most symptoms aren't visible, neither is what I need to manage my illness [implanted medical devices, medication, braces under clothing] unless I am in my wheelchair also what OP had sounds like costichondritis, which I have. it's literally the inflammation of the cartilage in your chest.

[@pearldragon6508]

I wonder how 'old' Karen would think ppl need to be for disabled if she had a 'precious baby' who suddenly contracted a non-visible disability like the OP has or lupus or something like that She wouldn't give a single s*** about the age then. I think buses should come with a 'Karen' section that only has 2 seats in it, and watch them try to out-entitle each other for them. Oh, and all Karens need to carry a Karen ID with them, with either bronze, silver, gold, or platinum class Karen. They can wave them in each other's faces and 'REEEEEE!'. The rest of the bus gets complimentary ear-plugs in the colour of their choice:p

[@scousemouse9566]

First story for me too and Karen is a plonker

[@ch33se857]

I have: autism adhd ocd trichotillomania developmental co ordination disorder low mental age insomnia epilepsy Tourette’s Anemia Intermittent explosive disorder Pica Asthma Depression Scoliosis Incontinence Dyslexia Bipolar disorder Depression Anxiety Enlos danlos syndrome Hyper mobility Hoarding Sensory overload Panic attacks and Schizophrenia The amount of Karens who tell me I don’t “look” disabled. Seriously.....?! Not all disabilities are visible I have 20+ medical conditions (as you can see⬆️) and I really DO need that priority seat. And that Caroline cart (shopping trolley with the big blue seat.) And the disabled toilet. I’m sorry I don’t look disabled but I really am...

[@missluciddreams3472]

I liked the first one as well...i have had accusations thrown in my face in the past about being disabled...well, i may b disabled but Karen is a plonker... Edit: I know what a plonker is...lol 😂

[@loturzelrestaurant]

If your Pro-Mobbing wheres your Drive to Action?

[@ljh5141]

Karen is a plonker (not American🤣)! My fave...The therapist one, I can identify with that one. 👍👍👍👍👍😊❤

[@AmyMichelleMosier]

I was born with Hirschsprung’s disease (at a time when doctors believed only boys got it) but it wasn’t so bad when I was small. It’s progressive and people have commented about how a person can be born with a colon condition. They think only old people have those kinds of things.

[@canadaiantenten]

The fist one was good, but I want updates on the last one lol Mark what in the world is a plonker (if that's how it's spelt)??

[@MarkNarrations]

Basically a fool haha

[@canadaiantenten]

@@MarkNarrations lol okay then 😆 I like it, I'm gonna start using that

[@earndoggy]

Interesting that Karen on the bus is almost word for word the same as another Karen on the bus and a person with a bad knee. r/thathappened

[@miyawedaplayer1237]

Karens thinking young people can’t get into debilitating accidents or be born with defects or illnesses

[@laurabaumgartner3085]

Karen is not only a plonker, but a wanker too, lol!! There you go, Mark. An American using two British terms, lol!! 👍😂👍 At least I hope I used it right. If not, I apologize!!

[@HowlingEclipse]

Karen is a plonker

[@MarkNarrations]

Indeed Howling, indeed!

[@beccilouise404]

Did op ever give an update for the last story?? Karen is a plonker

[@bethotoole6569]

Love it Daddy-O!😎

[@artitrash7052]

Gosh had it really been a year that I’ve been listening to you?

[@kaireadamczyk1124]

When i was younger i had something similar like in the first story but my parents never took me to the doctors and it went away after a few years

[@dianeessex300]

Karen is the best part of a man?!?!?

[@lovelywolv]

Que me getting excited Everytime there is a long episode

[@user-mama_thomas]

What in the world is a plonker? Hell i don't even know if I spelled that right or not lol

[@rachelfox8108]

You spelt it right -- a plonker is an idiot (in the sense of someone who chooses to be ignorant, who is an idiot and likes it that way).

[@MarkNarrations]

Haha and this is why I love US folks using the British slang. YES!!

[@user-mama_thomas]

@@rachelfox8108 oh ok thank you

[@user-mama_thomas]

@@MarkNarrations the bad thing is i am mostly British. Like 64% and never knew that my family even had a little British in us. I was always told that we were Irish, German, Black Dutch and 2 types of Native Americans. We do have the German and Irish but none of the others. I would suggest to anyone who has thought about trying the DNA tests to do it because you never know if what your family has told you is the truth or not. I do wish that I had the money to go and see where my family came from.

[@MarkNarrations]

@@user-mama_thomas Yeah I always wanted to try ancestry or something like that. I may just do it :)

[@hilarywitt]

So what about people who are born with a disability? 🤦‍♀️

[@dr.health1688]

Hmmm, late night Mark binge.

[@globalwarming5243]

... The world is confusing

[@MarkNarrations]

It is indeed Global.

[@OneMoreWord1]

Heyyyyyyy Daddy....

[@MarkNarrations]

Hey Chaos, I hope you're doing good!

[@clrtwallace0116]

That karen in the first story, i would love to slap her in the face for being such a freakin plonker. And yes, i had to look that up. Edit to add, i think if i had an invisible disability, i would bring a cane with me everywhere i went. It wouldnt satisfy ALL of the karens, but it could be an inexpensive way to possibly deter a few. 🤷🏼‍♀️

[@fudgeroll3255]

I like the new challenge Daddy Cringe

[@TrishaSmith]

Yay!!

[@MarkNarrations]

Yay to you too Trisha :)

[@itjustmemanning8441]

Why doesn't OP( in the first story ) have a wheelchair?! She shouldn't go out by herself. Karen should have been arrested. 😏⚘

[@littledikkins2]

From the sound of it her condition would be like having chronic broken ribs times about 3, I doubt if a chair would help her much unless it was electric as there is a lot of exertion to using a manual wheelchair.

[@velvety2006]

@@littledikkins2 also possible that health insurance is being a jerk since it is not really diagnosed

[@MarkNarrations]

Karen should defo be sorted out!

[@rachelfox8108]

The nature of the NHS is that while treatments are free, some accessible devices can still cost money, and doctors won't recommend anything they don't think is necessary. (For example, I have bad stomach cramps after ingesting gluten, which would suggest I have a gluten intolerance, but because the test for it can be iffy and throw up false positives or negatives, they won't put me forward for it -- even though testing positive could mean assistance in buying gluten free food (which can be very expensive, all added up)). If they don't think she will need every benefit of an electric wheelchair, they won't offer one.

[@TheGRavist]

I made it to the bottom of the list woo

[@gracemckinnon1102]

whats the name of the into music

[@Tammohawk1]

When our boys were little, we used to tease them that we were going to "beat them like an ugly stepchild," or "beat them so bad that they would bleed all over the floor." Well, when my oldest was in his early 20's he tried to convince me that one time I had beat him so bad that he wasn't able to sit for three days. I about died laughing. My response? "First off son, if I had of ever beat you that bad, your father would have beat me and thrown me out of the house. Secondly, that's something we used to tease you about!" Too funny.

[@christineeverett2043]

first story fake as hell

[@Fiery_Latina_Goatchan_GF_681]

YA e,e i aint buying that ribs story x.x