AI summary & topic connections

The commenter reports EHS, neurological and heart symptoms after local 5G testing, perceived changes in plants and insects, forced relocation and difficulty obtaining support for a disabling condition.

  • Electromagnetic sensitivity: “I live in Denmark. I developed electro-hypersensitivity (EHS) in 2020, when new frequencies were introduced in the country. Th”
  • Neurological symptoms & sleep: “ served as a test site for 5G. I experienced headaches, tremors throughout my body, and a sensation of heat on my skin. My eyes ”
  • Heart symptoms & implanted devices: “ a critical point one night when I developed heart problems. I received no help, as I was not believed when I spoke about Wi”
  • Environmental effects: “in the middle of summer. Simultaneously, the insects disappeared from my garden; the air became completely empty. My symptoms reached a critical”
  • Housing, work & access barriers: “ed when I spoke about Wi-Fi and masts. I was forced to move away from that municipality and had to purchase clothing and hats to ”
  • Towers & siting: “so reacting to these new frequencies; leaves near the masts and wireless equipment took on autumn colors—turning red, yellow”

Matched review of original text; attachments excluded. Review provenance

ORIGINAL COMMENT · UNEDITED TEXT
I live in Denmark. I developed electro-hypersensitivity (EHS) in 2020, when new frequencies were introduced in the country. The municipality where I lived served as a test site for 5G. I experienced headaches, tremors throughout my body, and a sensation of heat on my skin. My eyes would hurt whenever I looked toward a mast, and I felt these adverse effects whenever I drew near one. At the same time, I observed that nature was also reacting to these new frequencies; leaves near the masts and wireless equipment took on autumn colors—turning red, yellow, and brown—in the middle of summer. Simultaneously, the insects disappeared from my garden; the air became completely empty. My symptoms reached a critical point one night when I developed heart problems. I received no help, as I was not believed when I spoke about Wi-Fi and masts. I was forced to move away from that municipality and had to purchase clothing and hats to protect myself. I am now disabled, yet I cannot access any assistance regarding employment or other support, as this disability is not officially recognized in this country. Doctors acknowledge my condition but dare not speak out, fearing repercussions. Since then, I have met many others who share my experience— people living highly isolated lives, unable to obtain any help. A young, exceptionally talented musician who developed this disability died by suicide a few years ago; he could find no support, and his family never acknowledged his condition. He ended his life while staying at a nursing home for the elderly. It is deeply tragic.