What’s the hardest part of having PANS or autoimmune encephalitis as a teen/adult?
I’m not thinking in terms of symptoms, but in terms of how symptoms or your experience of illness in general affects your life.
If you’re a teen or adult with PANS or autoimmune encephalitis, I’d love if you filled out the form below to share your thoughts on this month’s question. When I get enough responses, I’ll publish them one after the other in a post.
This is the first of an ongoing series. My goal is to bring awareness to the unique challenges of being a teen or adult with PANS/AE.
NOTE: By submitting this form, you agree that your comments may be used, edited (slightly), and/or shared on The Dreaming Panda and/or social media. Your email address will not be shared with anyone, and your name will only appear as you have specified in this form.
