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This filing was submitted as an attachment. Open the document below to read the comment.

This filing was submitted as an attachment. Open the document below to read the comment.

This filing was submitted as an attachment. Open the document below to read the comment.

This filing was submitted as an attachment. Open the document below to read the comment.

This filing was submitted as an attachment. Open the document below to read the comment.

This filing was submitted as an attachment. Open the document below to read the comment.

This filing was submitted as an attachment. Open the document below to read the comment.

Hello, I'm living in Belgium and I know I'm electrohypersensitif since 4 years, but I'm suffering from electrohypersensitivity since 28 years. I had a lot of symptoms since all these years, tinnitus, headaches, visual problems and burning eyes, fatigue, sleeping problems, burning sensations in the head, balance problems, nervousness, agitation, just feeling horrible... I live since these 28 years near to an antenna and little by little my symptoms became worse, particulary after the installation of 4G and 4G+. I can't live in my house anymore and have to go sleeping outside in my van, summer and winter. I'm still searching for a white zone, but i't's really hard to find, since antennas are installed everywhere. I've asked for help at the local authorities, but they don't want to take away the antenne or change the orientation of the antenna, even if other neighbours have symptoms as well. I lost my job as a welder, and can't even follow another formation to learn another job, because there is wif-fi and phones everywhere. My health is suffering a lot from the wireless technology. During this 4 years, I met so many other people who are suffering from electrohypersensitivity. It's terrible for the young generation too, who are themselves impacted, sometimes without knowing why. I want to thank you that you give us the opportunity to alert around this question. There was a local tv that made a news report about our situation. Here is the link: https://www.notele.be/it505-media162960-le-plus-de-l-info-l-electro-hypersensibilite-comment-vivre-avec-ce-calvaire.html. I'm part of one of the 2 belgian organisations (AREHS and VEHS) of people suffering from ehs, there are more 1000 people in the both, but we can observe that a lot of more people have become ehs and are not yet membres.

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