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diop how do you all work right now? Don't you get really bad symptoms?
It has been awful for the past year and a half. I go home torn and I start in the morning pretty much in the same condition. My productivity has become very low in spite of all my efforts. I thought of changing job, but not understanding what causes my issues, and the sensitivity I developed to modern lighting in addition to electronic devices make me hesitate. I am completely lost. I have not received any real support nor inspiration from any of the medical doctors and practitioners I visited. Recently I have been spending a fortune on massages of various type and acupuncture to release neck and face tension, but if there is any relief it is only temporary. Exposure to a bad device restore the bad symptoms within few minutes. The worst is probably eyelids and facial spasms.
I have not been yet to an orthoptics specialist, because here that science is considered "folk remedy". I will try my luck in Europe during the Christmas break. That is my last option.
My problems date before 2012. I used my ThinkPad T60 on XP from 2010 to 2017 day and night no problem, but from 2007 to 2010 I kept it in a drawer thinking it was unusable. What made the difference was changing the display resolution from native to 1024x768. Same hardware, same software. Not a matter of font size, because I ran that test too. At native resolution my eyes fried, at lower resolution I could work for hours without a break.
My eyes or brain are not able to cope with external optical impulses the vast majority of people are fine with. That is my only conclusion.
With regard to making our discomfort more public, maybe one option is to support already existing campaigns, e.g., https://lightaware.org/about/individual-stories/.
That is what one of the ambassador wrote me months ago: "We are collecting case studies of the way that lighting affects different people to show how many people are affected and how it impacts on their daily lives. The idea is that if we can collect hundreds of similar stories then we can show medics and researchers that this is a problem which is affecting a diverse range of people, and also potentially provide case studies for researchers."
In my opinion there are many people affected. We are not just a few hundreds. We should try to have sufferers converge on one or few platforms rather than spreading them out?