Living with chronic WHO

If anyone happens to know more about chronic WHO, I’d love it if you could share...
What kind of symptoms should I look out for, what does treatment involve, and is it actually possible to get better?
Any bit of info would be so incredibly helpful 😉

tell me exactly what's on your mind? feel free to shoot me a DM too
"symptoms" is such a vague term when you're dealing with chronic WHO, it hits everything from your skin and liver to your GI tract...