Hey everybody

[Theskylarsthelimit]

Hiii new here! Just found out about this forum as I was looking up headway. My name's Skylar and I have been battling with encephalopathy since I was four, I haven't found people like me to relate to and be understanding really.. hoping this community will help make me feel less on my own

[cat3]

Hi Skylar and welcome. I was drawn to your post initially by your profile photo ; foxes have figured in my daily life for many years. I'm privileged to have them living close by and coming when I call.. 🦊🦊🦊

I'm here owing to a brain haemorrhage 12 years ago and have found great support and friendship along the way. I hope you'll find as much reassurance and comfort from others here as I have.

Maybe you could tell us more of how the encephalitis impacts on your daily life, and your methods of coping day to day. I'll keep an eye out for you. . . Cat x

[BaronC]

Hello there and welcome. My name is Andy and I'm a thirty year veteran of brain injury.

Writer, raconteur, father, idiot.

As soon as you feel more comfortable here do tell us more...

Andy

[Lulu_Lollipop]

Lovely to have you here, Skylar 😁 I'm here because I had a big brain aneurysm operated on and these people are helpful and lovely. I've also had a stroke, which apparently was nothing to do with the aneurysm xx

[Alibongo60]

Hi Skylar, welcome, my names Alice I had a brain haemorrhage seven years ago due to a aneurysm, we are all survivors here and will help and support each other in any way we can, keep popping back when you can even just to say hello love Alice xx

[AntiNMDAWarriorWife]

hi Skylar!

I’m the wife and carer of someone dealing with the aftermath of 2 different types of encephalitis. He spent the majority of last year in hospital but is home now I’d never even heard of it prior to his diagnoses.