My Functional Neurological Story / Q&A | Chronically Emily

[@Cryershoney]

I got diagnosed in January this year but have been showing signs for 15 years it’s been hard been told by the doctors I was faking it

[@TheGalwayfan]

Wow! It sounds like non celiac gluten sensitivity. They have no small bowel damage, have negative bloodwork, yet they say gluten makes them sick. I wonder if it's a similar type of problem as FND? 😊

[@Moose185]

I’ve been newly diagnosed but I have to be honest, it just seems like doctors don’t know what it is. How can they prove it? It’s just by exclusion and assumption. I pray that you feel better.

[@lindasmith8771]

Is the "software problem" just a euphemism for soft in the head?

[@julietyler7300]

I'm 63 I have been unwell a year now

[@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

[@LivinLifewithFND]

Just came across you and would love for you to follow me. 🧡💙🧡💙🧡

[@julietyler7300]

This is awful I have a lot of symptoms