Thank you but need more signatures

We’ve gotten 100 signers but need much more momentum to grab the attention of those who can help change the game for PNES/PNEA research and public awareness!

Please share, spread the word. Better treatment may be right around the corner. We deserve to know more about our disorder and better access to specialists who treat it!

Last research found was from 2016!!! People have known about this since the late 1980’s with barely any progression in research and treatment.  

6 month waiting lists are not acceptable to those having seizures daily like myself, but there is little resources out there.

Thanks for your support on this matter,

NURSE MARI

PNEA/PNES ADVOCATE FOR CHANGE