Posted by
evie15422 on
URL: https://www.es-forum.com/inquiry-re-MCS-EMF-resources-tp1554844p1554853.html
Hi, Jason,
I had a question.... I have never heard of an ES person having problems with ES from batteries (not that I am doubting your wife; I am justtrying to clarify). The problem that SOME Essers have with batteriesis draining the batteries when they touch them or change them, not with ESsymptoms from them. Also, I have heard of some who have ES from particular items powered by the batteries: particular digital electronics/appliances, wifi electronics.... Are you saying that she has problems fromjust the batteries themselves? Are these symptoms exactly the same as ES symptoms, or are they due to MCS? Just curious. It helps others to know what they are reacting to (and how) and since this was novel, I thought I'd ask.
My best wishes to you and Nicole,
Diane
--- On Sat, 7/24/10, cocopollyphenol <
[hidden email]> wrote:
From: cocopollyphenol <
[hidden email]>
Subject: [eSens] Re: inquiry re: MCS/EMF resources
To:
[hidden email]
Date: Saturday, July 24, 2010, 10:40 PM
There is an interview on planet thrive (planetthrive.com, I think that's the URL) with a woman who, with her partner, is living in a remote stone cabin in Arizona. They're renovating it, she was in a tent for a long time. Shecan't be around EMF either. I think there is some kind of trombe wall to retain heat in winter, and a wood burning stove. Trombe walls are interesting. You could also consider a good yurt, made of wool. One can put wood burning stoves in those and they stay warm. The Mongolians still use them. Thatmight well allow you to stay in Vermont this winter. Perhaps you can rent a house on some acreage where you can put the yurt far enough away from theelectricity and still have access to the house to cook, shower, etc.
--- In
[hidden email], Jason McGill <jasonmcgill@...> wrote:
>
> Hello all, I haven't written in to the group in a long time. I am currently
> taking care of my wife, Nicole, who suffers from severe MCS and EMF
> sensitivity, as well as severe CFIDS. So, not only does she have very
> little energy (and can barely walk a few feet), we are forced to live
> outside in a tent, because she cannot be around any electricity
> whatsoever...even batteries. We are in the process of having an Airstream
> renovated, but we are most likely going to have to relocate once this winter
> hits (we currently live in Vermont). We are attempting to find contacts in
> the southwest, as we barely know anyone in that region. Any and all
> resources in more temperate climates would be an absolute blessing. This is
> a truly intense situation, and we need all the help we can get in order to
> make it through this!
>
> Nicole has always been mildly EMF-sensitive, but after a hospital stay last
> summer, it has just gotten stronger and stronger, to the point where no
> amount of shielding does the trick. She cannot be in a house with any
> electricity, flashlights, furnace, heater, ANYTHING, without having severe
> symptoms.
>
> sincerely,
> Jason McGill
>
>
> [Non-text portions of this message have been removed]
>
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