Hi all, I have been recently diagnosed with FND I will be honestly. I never heard of it.
I am looking to meet others and chat etc..
It's all new to me tbh
Hope you all are in good form and well ❤️
Hi all, I have been recently diagnosed with FND I will be honestly. I never heard of it.
I am looking to meet others and chat etc..
It's all new to me tbh
Hope you all are in good form and well ❤️
Hi Welcome, your not alone
Can I ask, now that you have been diagnosed, can I ask if that was by a GP and what sort of help they offered you. Also what symptoms have you been experiencing?
You will find useful links here from other members and search for the "FND Podcasts" here from another member, where the specialists try to explain it to the neurologists, other specialists, GP's (how to deliver a diagnosis) etc.
I am a mother of a teenager who was diagnosed with Regional Chronic Pain Syndrome (June 22) and FND (although didn't quite explain the 'N' bit originally (Nov 22) and its been a bit of emotional journey.
Hello, hope you're keeping well? I've noticed you're from Ireland, we have brilliant FND hope Ireland group on Facebook and WhatsApp, you can look it up and join us anytime, we welcome new members.