I was diagnosed with FND after brain surgery that went wrong 5 years ago. My recovery has been very slow, with not much help. It is a year’s wait to see a neurologist with FND experience.
I am having non-epileptic seizures daily, still lots of nerve pain, long-term and short-term memory loss, poor cognition, and fatigue.
Walking and speech have greatly improved. With speech, I had three fantastic speech therapists who helped me talk again. Still not perfect, but to come back from nothing is great. Walking was mostly down to one OT who gave great advice, mostly about not giving up. I am proud of the work I have done.
Any and all tips or advice are welcome, and if you are going through the same thing, it can improve, even if it feels like a struggle every day.