What alternative treatments worked for you
I have me/cfs and it’s been gradually getting worse for about a year but I’ve been ignoring it because I was still able to function except now I really can’t function!
I’ve seen some people take electrolytes and I was wondering what other things along the same lines has worked for people
I’m willing to try anything really as long as I can access it in the uk without a prescription.
Symptoms include.
Severe fatigue and PEM
Headaches (not sure if they’ve got to the point they would be classed as migraines)
Randomly going really hot especially if I’ve exerted myself
Brain fog
Leg weakness
Some dizziness when I stand
Give me your most unhinged chronic illness hacks!