I was just wondering if anyone tried Transcranial Pulse Stimulation( TPS ) for FND symptoms? 3 years ago I tried Transcranial Magnetic Stimulation( TMS ). Actually it was Intermittent Theta Burst Stimulation( ITBS ), new version of TMS. No luck. I was told before the session that I had roughly 50% chances to improve. Improvement usually means coming back to normal, but it didn't go well for me.
TPS just as TMS is really expensive and before I take another loan, I just wanted to check if anyone of you tried this non-invasive brain stimulation therapy for FND.
Many thanks in advance
SS
Feeling lost 
Cycling and FND
Amitriptiline 
What was it like leading up to your diagnosis? Did you feel that you were taken seriously?
WARNING: If you have FND and live in UK
