@chloemarie1992: This is Functional Neurological Disorder🧡 In this moment during my flare up in January my speech disappeared. I knew exactly what I wanted to say but no matter how hard I tried, the words wouldn’t come… My brain wasn’t able to send the signals it needed to. I knew why. I’d already pushed through so much that day. I’d ignored the warning signs cos I wanted to keep going, to keep showing up, to keep trying. But FND has a way of reminding u that ur body always has the final say. This was my nervous system sayin “Enough. U need to stop.” So many of us have spent years pushing through pain, fatigue & symptoms cos we’re scared of letting people down or being seen as lazy. But with FND, pushing through isn’t always strength. Sometimes it’s the very thing that causes our symptoms to become more severe. For me that day, it meant losing my speech. That’s what FND does. It can steal ur voice, ur movement, ur balance, ur independence & ur confidence. One minute u can seem fine & the next ur fighting to do things most people never have to think about. I’ve had to learn my triggers, find my patterns, ease my body back to feelin safe again & reset my nervous system to get to where I am. Its an ongoing daily routine, keeping a tight eye on what my bodies telling me🧡 We spend so much energy hiding our worst moments to make other people comfortable but hiding them also hides the truth. FND is a real neurological condition. It deserves the same understanding, respect & compassion as any other neurological disorder. We shouldn’t have to prove we’re ill just because our disability doesn’t always look the same. So before u tell someone they’re “too young” “don’t look sick” or that they “don’t look disabled”… remember this video. This is what trying as hard as u possibly can, can look like. We shouldn’t have to fight our own nervous system AND fight to be believed!💪🏼🔥 Until every person with FND is believed, respected & given the care they deserve, I’ll keep using my voice. Even on the days FND tries to take it away. #fnd #myjourney #awareness #truth #fyp
chloemarie1992
Region: GB
Tuesday 21 July 2026 18:02:59 GMT
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Michael Charlton :
a love this girls fight👊🥰
2026-08-22 17:57:31
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Darren :
Not being funny but have tried slowly singing your words out?
it might help! apologies but I'm not being rude xx 💕
2026-08-18 21:17:44
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Mohsin - GMK Media🎥 :
hey I've got FND but mine looks very different. could you share how you got into remission? also you're journey is inspiring 👏
2026-07-21 21:05:35
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owenmullen32 :
This breaks my heart. Big hugs Chloe darling. Hope your doing well ❤️❤️❤️❤️❤️
2026-07-21 18:26:41
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just_scrolling_3 :
Do you still get flares that affect your speech ?
2026-07-21 21:40:23
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RW :
Have you ever experienced strange behaviour, like acting like you’re not yourself during a flare up?
2026-07-22 17:45:23
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Fitz :
It’s amazing to see how far you’ve come in the span of 7 mths! 🫶🏽🫶🏽
2026-07-21 22:53:13
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Gillian Mayo :
your so strong and brave keep going sweetheart xxx
2026-07-21 21:07:26
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Natalie💕🍀🏴 :
i followed you so i can try help my wee dad, he was diagnosed in december last yr and he is struggling with it but he knows of your account so i'm going to make sure he follows and i am defo taking notes! thank you for bringing awareness x
2026-07-21 18:49:25
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The Gamer Dad 🎮 :
Have to say this and the paralysis are the worst…so frustrating! I’ve found distractions help a bit but obviously won’t help for everyone
2026-07-22 11:49:21
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Becca 🤪 :
awww chloe 😭 hope your OK beautiful cxxx
2026-07-22 12:26:40
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carol :
your so strong and beautiful ❤️❤️
2026-07-21 19:01:32
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Abraham :
Don't forget to dance and exercise. This long process should be done for a year or two. You may forget to exercise and dance to control your tremors. You know better than to continue exercising and dancing. God bless 🙏🙏🙏
2026-07-21 18:15:09
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Peter Oliphant :
Your an inspiration, keep battling you Bonny brunette beauty
2026-07-26 20:42:32
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kingggdo :
Forever proud of you x
2026-07-22 07:26:25
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Mellissa Pert :
your amazing person keep shining bright. your one of my top fnd hero's on tiktok. thank you for making me realise it does not define me as a person.❤️❤️❤️
2026-07-22 22:40:43
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shez :
ur amazing
2026-07-22 20:07:04
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Makai ZSolt :
🤗
2026-07-22 19:35:56
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Blu3 Crush :
Thank you for being people's voices when you also struggle with your words. I wish I can explain my situation to my brother who just mocks me.
2026-07-22 09:34:28
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Shannon 🤎TSY🤎 :
Stay strong lovely ♥️
2026-07-21 18:32:52
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cin.82.dy :
I live in the Netherlands one of my dearest friends has FND she is fighting this for the past 6 months.. one day is good next day is shit.. maybe we can get in touch?
2026-07-21 18:57:07
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Megs Arunachalam :
I follow you from the small island of mauritius.. all love, prayers and good wishes for you. God bless, keep fighting and raising awareness.
2026-07-21 19:43:01
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ste.. 😘😘😘 :
Take your time and try not get frustrated. I also have a speech impediment because I got brain damage… it can be very frustrating sometimes but people understand well Welsh people.. You’re doing fantastic be proud..xx
2026-07-23 14:06:20
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