Welcome. It's currently FND aka functional neurological awareness month and I thought it's time I talk about how this condition affects me and others. Not a lot of people know about it yet. I'm hoping that I can help others by talking about symptoms. I know that others may be suffering in silence after being invalidated. You're not alone. If you'd like to talk with Lola, Visionette.Laila@gmail.com If anyone recognises symptoms in themselves, ask to see a neurologist through your GP and keep a diary of symptoms. Much love to you warriors, you're amazing, keep fighting xox