Hi,
About 6 months ago I was told by a neurologist that I have FND. Ive been in denial since and didn’t even want to look it up. Tonight I heard an interview on UCB radio about FND Hope.org and decided to take a look. So here I am. Totally new to all this yet relieved also that I’ve found somewhere to come with all my strange and frightening symptoms that vary day to day yet always remain. So I just wanted to say hi everyone and it’s really good to hopefully feel not so alone in my anxiety about the weirdness of the symptoms and it also feels hopeful that I might not be actually dying from a misdiagnosis.....For the first time in over 3 years I feel calmer about my health, so thank you FND Hope.