I rate this video 47/46

What’s necks on your agenda

Had my first in November,been on keppra for 6 months.No seizures but dizzy spells and butterflies in stomach feeling always.Pins and needles sensation in body at suoermarket,thought i was gonna have another seizure,luckily no.Seem to be no improvement.

I only have seizures when I awake from my sleep so in my case it's like waking up and feeling this sudden feeling of dread and anxiety, then it slowly builds up to panic until finally my vision starts to blur and I fall into my bed unable to control my body. It's a very scary and annoying experience since all I can do is listen to the commotion around me and think what am I am gonna say when I finally am in control again. (Been 2 years since I have discovered this and still holding to hope that it will end one day)

"well, there goes your sex life"

Cringe

My Rigga just get over it💀

😂😂😂 oh my fucking god

I've only just discovered this man, Dave Hingsburger, and I understand he has just passed away recently. RIP. In this particular circumstance, he's spot on. And it's not just lying and leaving, about misrepresenting who they are to people with disability. It's also about paid support workers getting an inflated sense of importance and consequence in the lives of people with a disability and, either consciously or unconsciously, competing with, rejecting, even isolating parents, families, and other unpaid carers; people who actually love people with disability, who've been through the traps for years, decades, blood sweat and tears. Assigning inappropriate roles to paid support workers manifests to undermine those critically important family relationships and to take people with disability away from lifelong and dedicated supports. Individualised budgets have been disastrous in this resoect. Such budgets, introduced in recent years via national disability insurance schemes in the UK, Australia, and.others, provide perverse incentives to the entire disability sector, to commodify or commercialise people with disability, who sre now lifelong disability slaves, to be captured, isolated and endlessly exploited by the very sector obscenely funded to protect and care for them. The NDIS in Australia is just overt corruption. Hiding in plain sight. It is literally a criminal conspiracy, from the top down, that has defrauded the Australian public of hundreds of billions of dollars, and will continue to do so. It is the enslavement of people with a disability, fully endorsed and fully funded by the federal government, all the state governments, NGOs, peak disability bodies, etc. They are all in on it. They are all on the tale. They are all criminals. Things don't happen by accident. It's a disaster for people with disability and their families.

My blood boils. My young adult son with ID goes out dancing all night long. Walks home at 5am. He wants to be where the young people are, especially the young ladies!! Haha! 🤣

the monster under my bed

Ureer gurrensurrrr ajdsdidididi altrroouuuuu quote from one of them

Bro why did he put up 2 fingers😭

I just had my first seizure I collapsed and started jerking and couldn’t get up was like was dreaming though when I got up I felt like I was dead and a ghost could never describe it

I can't think of a better word to describe this video than "Retarded"

2 words... impending doom... thats how it feels... (at least for me)

Hello. I am wondering if there has been a change at all since this video was posted that you have experienced? I work in the field and am curious to see what's going on around the globe regarding this. Thanks!

idk what these chromosomes lovers are on about😭🙏

kzbin.info/www/bejne/lX22YpmmmZKGaZY

My sister had that exact same disability as a boy and she passed away suddenly because she had a disability with cancer and all her hair fell off. She was super sad. She would stay with school and try and try her best. She actually got diagnosed with a disability which is called that the ammonia pia and I don’t think no one‘s heard that before but if you guys think it’s not a disability, it is a disability because I know people might think that disability like anxiety. I have an anxiety and it’s a disability People think it’s not in, but I think it is because you know having disability you don’t have disability you know because you never know what could happen always person because you never know what they can be going to do and just love yourself but yourself and never let no one stop you because since I go to school, I still get bullied me and my sister would always be. My sister would be tired and that, there was this Monday exact same that when she got disability well she was already born like that boy but she the exact same day Monday when she got diagnosed that when she went to sleep well she went to sleep because her parents picked us up at three at school 330 she was wasn’t feeling good and so picked us all up so we could go home and they wouldn’t have to go for me again back to school just like pick us up at once and then my sister she went to go to sleep and my parents, are you sure you wanna go to sleep and she was like yes so she did go to sleep and we were Like so nervous because of her cause she only had five days and it was it was the fourth day that she would be alive but she would be dead for the 50 in the night. We didn’t know she was gonna try the fourth there only.4 so she went to sleep and then the next so then when she went to sleep, we never she always wakes up like when she has naps. She always gets up around like eight and that’s normal for someone that wasn’t normal for her because she wouldn’t wake up and then, she had a heart attack and we took her to hospital and then she woke up when she woke up to the home actually and that was her last time and you know we don’t have memories of her. It’s been three days since she died. I’m super sorry if anything happens like I have a channel if you can church it up anytime if you guys pass through a video of me, I don’t honestly I don’t have. I don’t care but just like please comment and give you some advice. I have no memories of her, but the doctors gonna give us a port of her and I cup of her and her fingerprints. Hopefully that helps us more and have her as a memory we have we’re gonna have a teddy bear that has her voice and her heartbeat like if he was a real person and then so yeah so she had that and we we panic so much because the doctors said that’s the only time she would be able to be with us and we just didn’t know when so that night when she went to sleep she never woke up so yeah I was very sad and cried everybody cried at her funeral not a single person stayed wide up. It was just like oh my gosh how why did this happen? She was supposed to die the second day and we were just like oh my gosh why why why so I just like panic and my heart starts stopped my heart stopped and they took me to hospital on an airplane and I was just super scary that time I wasn’t being able to be there at her funeral hours and I just don’t want to with any of my family members so just be yourself and love yourself. Hope you guys have an amazing time. Always love your family and just never give up on them and you know you know like they even though they say they’re gonna die it doesn’t matter know they might have another chance of life. Just pray to God just pray to God because God always amazing lives and he just created us and we were just like oh my gosh how did this happen? So yeah thank you guys for all your support goodbye.😢

I am going straight to hell ngl

Most horrible pain I’ve ever experienced waking up and seeing paramedics. It’s taken me 3 wks to get back to feeling normal after not remembering anything and it’s still some thing I have forgotten. My personality feels different and so does my feelings about life. This is weird and so embarrassing.

I'm just looping the clip and can't stop laughing my ass off!! These girls and guys are awesome....Congratufuckinglations!!

I have FND causeing me to have 98.9% non epileptic seizures I’m very foggy can’t speak normally for almost 1 hr after my seizures hard to move sometimes can be cranky for almost a week and weakness and headaches are quite common sometimes for me it almost takes a full week for me to fully recover and I always have cluster seizures but am semi conscious during them including I can hear so I listen to my calming comforting music during my seizures and yes I do use valtaco during the seizures

He was so right. I miss his words of wisdom.

Just add to that sing un

Epilepsy seizure recovery explained that you have mentioned 😮 thank you

I toth e was going to eat me

ah, the wire hanger missed you

it's like waking up from the dead. i feel nothing, see nothing, and when i come back i get horrible migraines for about 2-3 hours after

This is not how the situation whould have gone

This is brilliant! I am an autistic adult and I may have taken a lot longer to figure things out, I realized I had the same desires as other people but the problem was, no one treated it like that. Even more important, everyone needs sexual education and I find often that people with disabilities do not get that education and it can make things dangerous. Thank you for making a great video and a very important one at that.

😂😂😂

Because I have severe epilepsy I can have Grandma seizures petite seizures all of them

Well I know when I wake up from a seizure I feel like I'm drunk

😂😂😂🤣🤣🤣

“Be happyyy” got me rollin

He dance wayyyyyyy better than me

Get in the car grjerrr

Bruh stop disrespecting this dude… ya’ll are wild for this bruh 💀💀 love to this dude though.

Womp womp

You have no balls if you don’t post this to instagram

I woke up during a seizure and I thought I was being electrocuted.. anyone else?

Tard

"499 out of 500 babies suffer from lack of down syndrome" Bro wants EVERY SINGLE ONE here suffer from down syndrome

I got diagnosed with epilepsy just about 5 months ago. I’ll never forget my first seizure, i was getting ready for school (I’m 17 btw) and started feeling very unwell and then it just happened, i seriously thought i was dying and it was so confusing and scary. I’m still not entirely used to having seizures and it’s so scary and frustrating every time, especially when they happen at school. I hope things get easier over time.

Are they restarded?

This made me so happy this morning. God bless them all

dud you look like a nomal person

💯💯💯💯