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Thank you for this video. I can totally relate to everything you are saying. I was diagnosed with FND four years ago but it took me eight years to get that! Getting stressed out is a major trigger for my NEAD and it is truly terrifying. I wish you all the very best.

🤔25th of march?🤨☝️#IDC.🤷‍♀️I'll keep you all in my 🙏prayers💖.#Every Day.😉⚡👍😎-me.

Was the statement "treatment is always available" one of the myths? It's near non existent. Also it's wierd that a video on FND has such hideous and constant background noise capable of triggering a reaction for those with FND!

My 'follow up care plan' was being directed to a website for information. So basically put, we are on our own!

I have Fibromyalgia and FND and I totally get this video. Thanks for helping to raise awareness.

Thank you for sharing your story and helping to raise awareness.

Thanks for this video and excellent description of what exactly neuropsychiatry involves. Here in Ontario, Canada it is appalling from my experience as an FND patient how neurologists have no interest in FND and simply don't want to follow us. I will say I've had conversations by email with Dr. Sarah Lidstone from University Health Network in Toronto who has an interest in this condition and is making inroads getting the message out to neurologists and psychiatrists and medical students to take more of an interest in this condition in Canada and particularly in the province of Ontario.

Excellent information and thanks for sharing your experience Sarah. I have some of your symptoms and others and have been diagnosed with FND but as you say, it's a heterogenous condition and presentation and yes, with more research hopefully more answers will be the result.