Good Morning, I have received a diagnosis of FND after being passed from pillar to post since 2017. It wasn't until my eyesight was so poor, double vision and loss of peripheral vision which the optamologist couldn't find a reason for and referred me to a neurologist that I got my answer. I had been diagnosed with fibromyalgia and chronic fatigue in 2018 and then trigeminal neuralgia in 2020. Most people who ask what's wrong with me give me the "attention seeker" or "yeah yeah" look smile politely and say "aww it must be awful. 😐. Yes it has been awful and so far continues to be. All I have been is a website to look at and a bunch of referrals. I have read across sites the longer a misdiagnosis the harder it is to resolve the issues. I am generally a positive person with a nothing I can't push through attitude but it's hard not to feel irratated when you feel you are having to defend your symptoms and explain your condition even to your GP.
As a newly diagnosed member I would really appreciate seeing some positive stories 💗 it's already brought me comfort reading through some of the posts on here. It's reassuring to see I'm not on my own.