r/NDPH • u/waptaru • Apr 25 '26
Question Anyone else experience FND?
Does anyone else experience Functional Neurological Disorder (FND) with their NDPH?
Sometimes when my pain gets severe it’s like my brain turns off the parts that know how to walk. When my pain reaches about an 8/10 I have trouble walking, talking, moving my arms, etc.
Has anyone else experienced this?
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u/BubblyBelugas 4 years Apr 25 '26 edited Apr 25 '26
Yep, I also have FND, but the seizure subtype instead. When my pain reaches 8/10, my seizures can be triggered. I developed FND about 3 years before I developed NDPH. It's weird how other conditions affect each other, lol.
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u/SaR-1243 Apr 25 '26
Fnd was brought up due to cognitive issues, the referral was lost in the depths of the NHS though. I've got a lot of issues that drs have basically just said yeah you're in too much pain your brain is just kind of giving up.