Functional Neurological Disorder - FND Hope | HealthUnlocked

I used to be completely debilitated by my FND. I felt isolated and alone. I couldn't drive. Couldn't work. Now I'm FND symptom free. I highly recommend...

Hello I'm interested in anyone who has found any benifit from medication for FND if so what was it ?

Hello everyone! My neuro consultant has recently referred me to the Rosa Burden Centre in Bristol and I wondered if anyone has any experience of going there...

Hi I am looking for anyone who has functional myoclonus, I was recently diagnosed as a consequence of a car accident I suffer from weakness in one hand and...

Hi, I have recently been diagnosed with FND and I'm finding this diagnosis very overwhelming. My GP is very good, specialists etc are good but I just need...

Help. FND seems to be progressing at a very fast rate, symptoms are making very depressed. Hospital are mucking me around and I am out of area for treatment...

Has anyone been told that their FND has now put them under the umbrellas of neurodiversity and/or disability?

Anybody come across any links between FND and Self Harm.

... here: https://virology.ws/.../trial-by-error-questions-about.../

I told my story in my profile. I'm 65. I'm from California. My mom had MS. She spent years trying to get a diagnosis. I have been struggling with "Essential...

I see that a few of you have experienced cluster goosebumps. I am getting them on my one arm with tingling sensation, does anybody know what it is please ? ☺️

Has anyone had any success with nutritional supplements?

hi all, it’s been awhile. I had a bad year with symptoms then things seemed to ease, still got odd bouts of stuff but not as consistent as when it all kicked...

https://tinyurl.com/BackThe1in6 #FND2023 I signed for everyone with migraine, Mal de Debarquement Syndrome and other rare neurological conditions (there are...

I’ve just found some recent posts 🫢