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Showing posts from 2016

WHO - Vote of No Confidence

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The Land of the Blind

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Once you become severely electrosensitive, and your life is turned upside down, you look at the world in a completely different way. Most of us may not be scientific or medical experts - I'm certainly not - but even so, we reach a deeper understanding of what is going on around us; why we are treated as mere collateral damage in a much bigger game, and why our suffering is diminished - based on no reliable evidence - to the level of a psychological delusion. No matter the thousands of scientific studies showing that this radiation is harmful, and that it is harming everybody, and every living thing, on the planet. When we try to warn people that it is not just us who are being slowly destroyed by the microwaves from wireless technologies, most of them look at us as if we're completely insane, cross their arms, and refuse to listen. They continue giving their children wireless gadgets, and sending

EUROPE - Call for EHS feedback!

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Want a ready-made EHS "White Zone"?

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A previous auction to sell Sugar Grove Station, a 123 acre town within the National Radio Quiet Zone in West Virginia where the use of wireless technologies is severely restricted, fell through when both the winner and the runner-up defaulted on their bids. The town is back on the auction block, and while it would seem to offer a ready-made solution for a consortium of (admittedly wealthy) electrosensitive buyers, it's definitely a case of caveat emptor, due to: Extremely high annual running costs Asbestos being present in some of the buildings A likely rival bid from at least one organisation The risk that the National Radio Quiet Zone may be done away with, if the telescope is no longer required Still, perhaps where there&

EHS Trial - call for expert involvement

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Brett West is the co-founder of Wireless Education, an organisation dedicated to providing balanced education about the biological effects of Wireless Technology. He would like to establish an EHS trial, to discover whether a supplementation protocol may be able to mitigate, or perhaps even eliminate, the symptoms experienced by sufferers, which can often be incapacitating and life-changing. Brett is looking for skilled health practitioners, or clinical groups, to assist him in developing appropriate research protocols and to facilitate the undertaking of such a study. His initial proposal is below, along with his contact details. If you would be interested in being involved, or if you know of someone who might be, please let him know. EHS Trial - Proposal Background: Anecdotal and research evidence points to the existence of food supplements which interrupt, or provide a protective effect, with reference to the complex bio-effe

Finding medical therapy for EHS

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(This image is from: http://sunrise.maplogs.com/wilsons_promontory_national_park_wilsons_promontory_vic_australia.4298.html ) I was contacted by Audrey Aspeling about including her story on the blog. She has already written a full account on the EMR Australia website, and so I've included a link to that below, as well as her recent communications with me. As a retired nurse, and after campaigning to politicians and other prominent people for the past 8 years without much success, I am now concentrating on helping to find a diagnostic test and a legitimate treatment for EHS sufferers by trialling things on myself with the help of my GP, and as I do mention what I have so far found in this regard in my story, others may be interested in my progress so far.  Of course the treatment I am trialling is pharmaceutical in nature because I have already done the shielding

About EHS

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Name: Norm Ryder Location: Currently in Victoria British Columbia, Canada How long have you been electrosensitive? My EHS story started in 1972 Your story: The start of the EHS experience Okanagan Area (near Kelowna) of British Columbia. In 1972 I received a large dose of microwave radiation while working for the provincial government. A first operation was done to remove an acoustic neuroma from the same side of the head that received the radiation in 2001, and second operation to remove a regrowth was carried out in 2010, and a slow awakening to the fact that I was EHS happened later in the same year. I was 20 at the time.

Comments from Professor Olle Johansson

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Have your say by September 30th

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Derailed by Microwaves

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As people are drowning, the FCC is Creating Tsunamis

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We Are The Evidence

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We Are The Evidence website This new initiative has been founded by Dafna Tachover, the attorney and EMF/EHS advocate. She is currently in Washington DC with Kevin Mottus, and they are lobbying Congress against 5G and wireless technologies, and working to raise awareness of electrosensitivity. I think that they are in DC for the whole of September. At the time of writing, the website is still "work in progress", but Dafna is keen for people to submit their own electrosensitivity and wireless harm stories, so that these can be raised with the decision makers. If you'd like to submit your testimonial, please complete the "I Am The Evidence" form - link below. I said in my previous post words to the effect that we need to make our voices heard. This is an excellen

Electrosensitive...and proud!

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I made a throwaway comment on Facebook recently, about how I think that we, the electrosensitive community, need to speak out and assert our fundamental human rights, through something that resembles the Gay Pride movement. While LGBT individuals are making great strides around the world in the quest for an end to the stigma, prejudice and discrimination which has faced them in the past, we - by the very nature of our condition perhaps - are collectively much less vocal, and even when we do manage to get our voices heard, we then usually have to endure the barrage of "tinfoil hat" gags, and patronising, ignorant, and/or downright offensive comments. Here's a recent example of the latter, possibly well-meaning (but who knows?), left underneath a Humans of New York photo and comment from an electrosensitive lady: "It seems the hardest thing for people without mental illness to understand

My comment to the FCC

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My comment to the FCC - Dave Ashton Following on from yesterday's post about submitting EHS-related comments to the FCC regarding their plans for 5G in the US, involving the installation of "millions" of small cells, I've submitted mine today, which I've copied below. I had real problems submitting a file containing my comments - I tried a number of different file types, but the only one that worked for me was a .txt file. I don't know if other people have experienced this, but if you do, a .txt file should work. Also, there are some instructions below which hopefully simplify the process if you have a text file that you want to submit (rather than typing a comment on their website). To add a file with your comments Use the link below: https://www.fcc.gov/ecfs/filings Proceedings - enter number, and select the relevant proceeding from the list (the numbers are 14-177, 15-256, RM-11664, 10-112, 97-95) Na

EHS-related comments to the FCC

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Life Behind a Closed Door

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Ann Hardwick - Life Behind a Closed Door I've never met Ann in person, and due to her condition (and my own), it seems likely that I never will. I've written one or two letters to her, and I received a very nice card from her a while back. Ann has severe multiple chemical sensitivity (MCS) and electromagnetic hypersensitivity (EHS), and she has been made housebound by her condition. She cannot have people in her house, and keeps the windows tightly closed, to keep the toxins outside from getting in. People who visit her, including her son, and her helper, Mel, have to communicate with her from outside, through the window. Mel posts online, as Ann is unable to do this herself. At one time, the NHS did pay for her to have treatment from Breakspeak Medical. This helped her to have a near-normal life, but when the funding was revoked after 3 years, she was forced to stop the treatment, and her condition worsened again. Ann then