My life with EHS
November 15, 2025
Today I’m privileged to share this personal story by one of our readers. It may resonate with you, too.
Living with Electromagnetic Hypersensitivity (EHS) has been one of the most challenging experiences of my life – physically, emotionally, and socially.
My symptoms are real, not imagined. They’re triggered by everyday EMR exposures that most people never think twice about when I’m exposed in the vicinity of powerlines, appliances, mobile phones and wireless devices.
Sometimes I experience a rush of blood to my head and pressure on my temples and inside my ears. I also experience headaches – sometimes severe - restlessness, concentration problems, tingling sensations, fatigue, memory problems, depression, and ringing in my ears.
When I move away from the triggers, my symptoms improve slightly but it takes days or weeks from exposure to recover completely.
I approached government bodies and health authorities, hoping for recognition, compassion, and action. Armed with a background in psychology, I spent years researching EMR’s biological effects, referencing medical and military studies to back my case. But instead, I encountered indifference, denial, and clear conflicts of interest - especially as 5G rolled out rapidly during the pandemic.
Isolation became my reality - both socially and geographically - as I sought refuge from the constant bombardment of EMR. The emotional toll was immense, amplified by a lack of understanding from even those closest to me.
Yet, in the darkest moments, I found a lifeline: Lyn McLean of EMR Australia. Her advocacy and her tireless support helped restore my strength and hope. She gave me – and many others – what the system would not: validation, respect and a voice!
To anyone living with EHS: you are not alone. There are ways to cope: reducing exposure, detoxing, EMR shielding (with professional guidance) and nature connection all help. Most importantly, stay connected to those who understand. EMR Australia is an incredible resource and ally!
I continue to fight for EHS to be recognised as a functional disability. We deserve protection, dignity and a safe space in this increasingly wireless world.
To Lyn: thank you for helping me be seen.
To my fellow EHS sufferers: keep going. The truth is on our side.
To reproduce this article for your network, please include the following text: Article reproduced with permission from EMR Australia, www.emraustralia.com.au
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