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488d
Hi! I'm Erin, I'm 23 and from the UK. I was (finally) diagnosed with general FND and severe PPPD in January 2022. I have been through a lot and continue to go through a lot. I would love to meet people with the same conditions as me (especially PPPD as I know it can be different for everyone and I would love to relate to others) and also others who have different illnesses! Hope we can connect :)
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Disorders of The Nervous System
Depression
Persistent postural perceptual dizziness
Migraine
Anxiety (Including GAD)
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281d
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
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308d
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
459d
I was 21 when I first started getting symptoms and I’m 28 now
462d
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
478d
Happy to connect
Hi I also have fnd and I also have Tourettes syndrom
485d
Hi!! I also have FND, 10nyears now. Happy to connect :)
☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision
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