Looking for Support and Connection with Chronic Illness

I'm 39 & in the UK. I was diagnosed with FND which causes partial & complete paralysis which is usually triggered by migraines. I also have Ehlers-Danlos which I've recently found out is linked to FND

Hi, I'm in Australia, and I have been suffering from PPPD for nearly 5 years now. When I first had symptoms, they were quite severe, and I had to give up working. Initially, i went to a neurologist and was diagnosed. I was sent to a neurological physiotherapist, and whilst it did help somewhat, I still have varying symptoms but am never entirely free of them. Just recently, I went for a review at a second neurologist, and he has since commenced me on a medication called Luvox. I can not confirm whether this is helpful as yet as my symptoms have previously varied in severity, but I am feeling hopeful

I was 21 when I first started getting symptoms and I’m 28 now

Hi Erin, I'm also in the UK, and I, too, have FND. Please feel free to contact me on my Facebook. My name is Kim spamer. Xx

Happy to connect

Hi I also have fnd and I also have Tourettes syndrom

Hi!! I also have FND, 10nyears now. Happy to connect :)