Humans of ME/CFS
Doctors aren't sure if I have ME/CFS from glandular fever, but all I know is that it's debilitating and life changing.
It's hard for people to understand that I'm in constant pain and I'm tired. I have no energy. Talk about life changing. I've had to leave my dream job, I can't do grocery shopping, or do other things that I used to do. I have been a swimming instructor and lifeguard. I wouldn't be able to do any of these activities now. I'm very limited in what I do, and I'm mentally and physically exhausted.
I don't feel like there is enough support and information on this horrible illness, and I pray doctors find a cure soon.