Seizures in a College Class
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- čas přidán 19. 06. 2023
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⭐️ FAQs ▹
1.What conditions do I have?
‣ I have Tourette's Syndrome, FND and suspected POTS
2. How old are you?
‣ 17
3. What is FND?
‣ fndhope.org/fnd-guide/
4. What is Tourette's?
‣ www.cdc.gov/ncbddd/tourette/f...
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Tourette's syndrome is a neurological condition and disability which causes involuntary movements called tics. I use my platforms on social media such as TikTok, CZcams and Instagram to advocate and raise awareness for the condition and show what it is like living with a disability as a teen in school.
My name is Zara Beth (zeezee25 on tiktok) and I post videos about tics, tic disorders and what its like to be a teen living with Tourette's syndrome, Functional Neurological Disorder (FND) and a seizure disorder (NEAD/NES).
I show what its like having tics and Tourettes in class and in school and college, vlog, and I also bake, do other challenges and answer all your questions in Q and A videos.
I am also an ambulatory wheelchair user so I show what life looks like using various mobility aids and how needs change from day to day!
I am also a musician! My newest release is my first single (original song) called "She's Mine" which is now available on all streaming services - I sing and play piano, guitar, ukulele and I write, produce, mix and master all my own songs and content myself!
When you can predict seizures so you record them instead of laying down
I hate how people say she’s faking it. It’s very hard for people with conditions like these, nobody seems to get it or understand what we’re going through. My brother is deaf and so I have to be with him to help him translate things, people always say he’s faking it for attention. It breaks my heart to see how people always treat them. 😔
As a child of a mom with seizures, ur seizures look very different from my moms! And that’s normal. It depends what causes the siezure usually. My mom has a scar on her brain which causes them and it’s in a emotional part of her brain which makes her cry.
I passed out and started shaking on the first day of my psych class, and the professor was super kind about it and even checked on me multiple times after class. Just a reminder that good people are still out there.
Zara no matter what u go through u need to know that there are so many people out there who care about u and other people with tics and stuff. Keep fighting! I love u guys!❤
Gay tag on your card holder…. Really?
My friend has epilepsy, and she usually has absence seizures where she spaces out and slightly wobbles (although shes recently had a couple grand mal which is unusual and bad), so seeing more people bring awareness is amazing!
Drama queen
This makes me feel so much normal and I feel like I understand my small seizures even more when it comes to twitching ect
Bless your heart sweetheart, I’m sorry you have to go through this. God bless you and your family.
I have epilepsy but have been "sober" of them for about 12 years now. I constantly suffered from tonic-clonic seizures. My heart stopped and I almost died in front of my parents. Seizures are a real thing! No joke about it.❤
I live with a very similar condition and I absolutely HATE fainting or having absence seizures in public. Especially when I’m not with my friends. Mostly because it’s so scary to be alone and unconscious or not conscious enough to be able to act normally, protect myself, etc.
Just wanted to say for those of you who arent fully aware of absense seizures!!
Had absent seizures when I was younger, they went away right before high school. They’d happen frequently throughout the day, it’s so draining and frustrating, remember to take care of yourself.
It's scary reading the comments and realizing people are even offended by disabled people. Are any group safe from the mindless mob of hateful people?
One of my high-school teachers had a medical condition of some sort that would cause her to have seizures. One of the first classes of hers I was in she used it to educate everyone on seizures and what to do if one happened.
I got in trouble all thru school for "day dreaming" I'm 59 and was only recently diagnosed. My children would get mad at me bc I'd not answer them right away. It's tough unless the people around you understand.
What’s so scary is how subtle these seizures can look. Thank you for making videos like these so that I can be more aware of the signs in my friends/work colleagues
Thank you for showing the signs of what seizures look like. It's scary to finally see what my husband see when I'm seizing but it's good to know. Every job I have applied for recently, I have always mentioned that I am epileptic and the ones that truly care always ask what to do in these situations. Please talk, sweet girl. Which I'm sure you do, but you're never alone. I wish we could be cured, we just have to stay strong through all the bullshit that we go through.
Wow! I never knew this type of seizure existed. My brother has had epilepsy for 14 years and his seizures are violent. He falls to the ground, thrashing about and most of the time becoming sick while still laying on the floor. I had nightmares for a month when I barely heard a noise and saw him in his room tangled up in his headphone wires and hanging by his neck/arm from his desk. It's the only type of seizure I've known about for 14 years. Stay safe!