My Functional Neurological Story / Q&A | Chronically Emily

Hey guys! Today I am sharing my personal story with FND, I know I do not cover absolutely everything in this video because if I did it would probably be 2-3 hours long. If you have ANY questions feel free to leave a comment or you can DM me on Instagram, whichever you prefer. Until next time I hope you are well.
xo Emily
More Information on Functional Neurological Disorder
rarediseases.org/rare-disease...
fndhope.org/
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[@anadjuric5360]

Did providers get played for the wrong diagnosis?

[@Horchatalover22]

I was diagnosed with FND a couple months ago and tbh my parents just don’t really understand how everything is fine and at the same time I have non epileptic seizures. I’m honestly just trying to slow down in life at this point and trying to survive high school. Any tips would really help. Also I saw that you had a funtional stroke hope you’re better ❤️

[@Emily-hy4yf]

I totally feel you. FND is hard. Just understand your parents are worried and scared for you because they don’t understand. I didn’t go through high school with this so I don’t have a bunch of tips but my biggest one is allow your body and mind to rest when you need to, this is not being lazy, it’s medicine. If you ever want to chat, DM me on Instagram ❤️ also yes I am feeling better thanks