Update on my health:
I finally got a neurology letter, I FOUGHT MY ASS OFF GUYS I was not going to allow anyone not to listen to me, I got a letter stating that everything I am struggling with is indeed because of M.E including not being able to mobilise and needing a wheelchair, and this is a big fuck you to everyone (including doctors) that made me feel like a failure and like I wasn’t “trying” to get better.
If anyone needs advice on how to get more support with this illness (especially in the UK) please message me❤️









