▲ 1 r/FND
Questions about your experiences
Hi there,
I'm writing a novella where the main character has FND. I think it's nice when stories have representation but don't revolve around someone's illness/disability. What I've read from papers/research differs from what I read on forums. I'd like her story to reflect lived experiences. I'd appreciate if you could answer some or most of these questions!
What has been your experience getting a diagnosis?
If you have a family doctor/GP, what is your relationship with them like?
What are your primary symptoms?
How does FND affect your daily life?
What mobility aids have you used? Are your friends, family, and/or doctor supportive of you using mobility aids?
How has your life changed before vs after getting sick?
Thanks in advance!
u/sunofseas — 3 days ago