EHS isn't always invisible...
My comment: In addition to Diana's post here, Towards Better Health has published an article about her containing links to interviews and press coverage. There's a link to this below. Edited 4th October 2016: Links to Diana's YouTube videos added Name: Diana Boughton Location: UK How long have you been electrosensitive? Over 15 years Your story: Discriminated against, ridiculed, disbelieved, humiliated, misunderstood, isolated – these are some of the ‘symptoms’ of electrohypersensitivity (EHS), from which I have suffered for over 15 years. I noticed a problem when my parents gave me a computer for my new home, which connected to the internet via dial-up. It was the first piece of technology I’d had during my adult life and within a few days of regular use I noticed that my ears were ringing whenever the computer was switched on. ...