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, [email protected]

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

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