Being Electrosensitive (in a microwaved world)

About 40 years ago I noticed that close proximity to neon tubes made me feel ill, but my life wasn't badly impacted as they were easy to avoid. Then, while working as a graphic designer in the 90's, the industry went Apple Mac mad, and I had to use one or become unemployable (and they certainly made previously laborious tasks quick and easy). However, I soon developed headaches and mild nausea if I used the computer for long periods, so I took frequent breaks. In about 2005 I started working in publishing as a sub-editor, which necessitated spending ages online, in proximity to Wi-Fi, and I acquired a cellphone, despite being wary of them. And then the poo really hit the fan... Headaches, poor concentration, insomnia, brain fog and poor memory were just the start, followed by sore glands in the throat and M.E. However, I didn't join the dots and relate these odd symptoms to radiation until about three years ago, when very frequent shingles attacks started ...

On 6th April 2018, La Croix reported that the former French Environment Minister, Corinne Lepage, is calling on the current French Environment Minister and the Health Minister to suspend the roll-out of 'Linky' smart meters, as many people have claimed that these meters are adversely affecting their health. The Connexion France reported that: '...She (Corinne Lepage) has called for scientific studies "to assess the health effects of these meters". "If the government does not react within two months, we will launch a class action against the State in the tribunal administratif on behalf of the mayors and citizens opposed to Linky," Ms Lepage told Le Parisien. The threat of legal action comes on top of another court case. A lawyer is due to file a summary judgment on June 5 with 11 regional courts on behalf of 3,000 householders who want the meter withdrawn or who refuse to have one fitted at their homes. Meanwhile, an email calling ...

Name: Stephanie Dickerson Location: Georgia, USA How long have you been electrosensitive (and how long did it take you to make the link to EMFs?) My symptoms started in 2005, and I realised that I was electrosensitive in 2012. Your story: Since I discovered I am EHS, in 2012, I have had to accept loss; loss of my career, loss of my income, family, friends and so much more. It seems every time I feel like I get used to my “new” restricted life, I must face yet another loss. As more places implement wifi, my world shrinks even more, until there is literally no where I can go comfortably. It is impossible for non-ehs people to even comprehend the huge burden and the isolation that this condition creates, and the grief one experiences daily for all that has been taken away. Around 2005 I started having debilitating insomnia and feelings of agitation; I could not relax. I tried everything to keep healthy, and considered many different reasons...