How I Transfer During a Paralysis Episode 🧡 #awareness #disability #paralysis

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#neurologicaldisorder #wheelchairuser #paralysis #wheelchair #chronicillnesswarrior

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✰ FAQs ✰
1.What conditions do I have?
‣ I have Tourette's Syndrome, FND and dysautonomia along with being autistic and queer! I also advocate for mental health.
2. What is FND? 🧠
3. What is Tourette's?
4. What do I use to edit videos? 🖥️
‣ Final Cut Pro X
5. What filming equipment do I use? 📸

(*af links mean i make a small cut from any purchases, but this doesn't cost or affect you! 💕)

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✰ About Me ✰
My name is Zara Beth (zeezee25 on tiktok) and I post videos about disability, neurodiversity and living with Tourette's Syndrome, Functional Neurological Disorder (FND) and Dysautonomia. Tourette's syndrome is a neurological condition causing involuntary movements called tics.
I use my social media (TikTok, YouTube & Instagram) to advocate and raise awareness for my conditions and share what it's like living as a neurodivergent and disabled person. I am autistic, sharing my sensory struggles along with my experiences with mental health disorders.
I share the accommodations I use to help my daily life, and I'm an ambulatory wheelchair user documenting my life using mobility aids and how chronic illness symptoms vary from day to day!
I'm a musician with a song called "She's Mine" available on all streaming platforms, and I'm an artist with a small business and website selling my artwork, disability merch. I also love reading, writing, and I'm currently writing a novel and a book/memoir about my life!

[mariahmendenhall]

You’re the first person I’ve seen talk about the temporary paralysis!! I have FND and I get paralysis episodes too, it always feels weird to explain because I’ve never known anyone else with the same issue. Thank you for sharing this stuff, it really helps.

[chocochipbananasplit]

Thank you so much for showing us how bad days can look i would have never imagined and rhis has opened my eyes to the invisible struggles disabilities may present, which a lot of us might ignore and/or bot think about. You are a baddie ❤ your strength is admiring

[whatsthetemma]

It looks so exhausting. I always appreciate you sharing all of this people dont understand.

[Rey-juic]

I've got ME with a bunch of complications, the days when my body just refuses to work scare me the most... It's so hard when you can't even lift your own head off the bed, thank you for just being you and showing people what it's like to live this reality ❤

[freakzoid__]

thank you for talking about this <3
due to my anxiety, i sometimes get episodes where my legs get paralyzed, sometimes causing people to have to carry me or help me walk, like human crutches, lmao
its incredibly validating to see somebody else showing their struggles as well, even if its not for the same reasons
thank you <3

[PickleRick-mfi]

Thanks for posting this. I really have wondered about this a lot! These videos help me understand people with rarer conditions around me, especially at my daughters SEND school.

[MrEd-rikh]

Aww, I'm so sorry... I teared up when I saw you struggle. You're in my thoughts. You still make me smile. 🎉

[complimentsofanna]

I’m currently undergoing testing to figure out if I have FND, and my brother was just diagnosed with autism in his 20’s. Seeing your videos has been so helpful for us to understand more about each other and our journeys. You’ve also given me so much hope for future mobility! Thank you for having the strength to share your life and struggles. ❤

[Borrisssa]

This looks like it takes so much resilience. I hope you're ok❤

[jazzybair]

I have FND and I don't hear very many people talk about this very much and I have these a bit frequently and it's very difficult to go threw the day but watching your videos make me feel better about myself and make me less embarrassed about my condition❤️❤️

[whimsyelf]

I have FND too and whenever I watch your videos I am astounded by how similar our conditions are. You struggling to sit up looks just like me when I am having a hard time. Thank you so much for sharing and spreading awareness about FND, it is very brave of you. If you haven't yet, would you consider doing a video about things you have found that trigger worse episodes for you? I find illness, stress, heat, fatigue, periods, and overexertion are big triggers for me.

[Whzja]

Oh dear ❤love youre amazing i feel a very subtle symptoms of this sometimes but youre so strong

[maaikebouwman]

Interesting! Thank you that you keep showing these things. It's so good to learn from it. (as long as you can/want to:)) Hope you're ok:)

[Looonymoony]

Aaa I feel for you Zara ❤️ stay strong 💪 !!

[Aethryx]

I appreciate you sharing this so much, as much as it sucks hell I feel seen for when I have these episodes/flares 💙

[ethankendig]

I’m so sorry honey! I have non epileptic seizures as well and have paralytic attacks but mine mostly happen to my whole body all at once and usually connect with my seizures. It is extremely scary and isolating so thank you for sharing your experiences and making space for us to find comfort in each other❤️ Much love queen💗

[Nature_girl]

I hope you are ok now. Keep on being an awesome person.❤

[Eden]

I don't have this, but it feels relatable. I know I'm able bodied but thanks for the content that normalizes just any struggles people go through, big or small.

[RivDio]

I cant Imagine what it’s like to have neurological things like ticks and stuff. Just remember that you are strong and that you are amazing and I hope you keep having lots of positive thoughts and lots of happiness and no negativity in your life ❤

[masongraffice]

This looks exhausting to live with I am sorry that you are going through this this