Me and FND- Part 1

[@helendonohoe1575]

Thankyou for doing your video you are very lucky you have not broken bones I have I broke my wrist last year I was I very hard time I believe I've had all my life

[@catherinejackson24]

Hello, My name is Catherine. I'm 27 from Glasgow. My journey with FND started when I was 14/15. I take non- epileptic seizures. They seamed to build up over time to where I am with them now which is everyday, throughout the day. It's been that way for about the last 8 years. My amazing partner is also my carer as the seizures are so unpredictable & can become violent. I'd be lost without him & the close family we have around us. From spending time in a epilepsy centre to seeing Doctors, Neurologists, Phycoligists & mutiple tests. The list is endless 🙈 & still continuing as I try to see anyone or anything that could help. The fight goes on ✊ Of course there are groups & awareness out there that show help & support for this condition but we still need more. Always good to hear other people's stories on how this condition affects their life & realising you are not the only one. Thank you for sharing 😊👏

[@helendonohoe1575]

Well done I do not work either I do lots of art it helps me rest

[@helendonohoe1575]

You can courses on line