I am wondering if anyone else has had Bell's Palsy? I have not been to a doctor yet because of COVID-19. But my psoriasis is off the charts, it's all over my scalp and behind ears my ears in my nose, my scalp is so bad I am picking because I am so stressed out about the Bell's Palsy.
I can't get a neurologist to call me back so that I can have a CT scan. As the ER said I should do the next day and its been over a month. I feel like this monster has changed my life. I can't get anyone to listen to me. I feel like I used to be pretty and now I'm just a monster. Does anyone else feel like this has ruined there lives???