Posted by angela england on
URL: https://www.es-forum.com/Magnetic-Therapy-tp1550371p1550471.html

COULD YOU PLEASE SPECIFY WHAT IS REKI AND Q GONG?   ALSO, WHERE DO YOU FIND A KEYBOARD EXTENSION AND TV PROJECTOR?  THANKS,  MIKE

--- On Fri, 9/18/09, Christina Steils <[hidden email]> wrote:


From: Christina Steils <[hidden email]>
Subject: Re: [eSens] Husbands Anonymous
To: [hidden email]
Date: Friday, September 18, 2009, 10:46 AM


 



I recognized that I had ES last year, when my body crashed and i ended up in AE. Over the year I realized i had to detox from wifi mobile phones, mostimportantly clear the bedroom of Electrical devises, phone etc.
Reki helped in the early days, then Q Gong this is really a must! As it makes you understand and take control with what your body is doing under the stress of wifi and mobile phones and life.
Rose quartz under the  pillow really helped me sleep, amazing!! I hadnt slept for so long.Waking up at 4.30am each morning for months. Pins and needles, sweating dizzy etc
Make sure you arent sleeping on a  GS /  Geopathic stress, this is veryimportant. We were! Not good.
I feel much better now, dealing with  wifi and mobile masts.Mostly Just atickle/ pressure from from the phone masts at the top of the nose and brow. No more coughing when on the motorway as i go past a mast.
I still dont get to close to mobiles TV , and the computer due to EMF but have worked how to us the Mac all day, just with a ext key board. I use a projector for a TV great cinema.

Good Luck.
GilesUK

--- On Fri, 18/9/09, Jennie Wassenaar <ad-in@ameritech. net> wrote:

From: Jennie Wassenaar <ad-in@ameritech. net>
Subject: Re: [eSens] Husbands Anonymous
To: eSens@yahoogroups. com
Date: Friday, 18 September, 2009, 5:11 PM

 

Ian,

That sounds like a great idea. This is such a strange condition, who can myhusband talk to about it? We personally do not know anyone else who struggles with EMS.

I do not have the opportunity to read all the groups posts, I only open theones whos subject line catches my eye. The irony is that I learn more about EMS on line but because I have EMS the amount of time I can spend on lineis limited. But I do save all the posts to a file in hopes that one day ifone of my family members is willing they can go through the saved post andgarner some helpful information for me. That might be a helpful hint for asupport person.

Good Luck,

Jennie

I wonder sometimes if I should set up a group called "Husbands (or

Spouses/Partners) Anonymous" to help the partners of ES people and, hence,

ES'sers themselves! Having been through it myself I can see how tough it is

for someone when their partner starts experiencing symptoms which seem to

defy all normal experience and "common sense". It would be good to help

relationships by reassuring people that neither they nor their partner is

suffering delusions, nor is it psychosomatic, and that there are other

people around who have gone through this too.

I feel I was fortunate in that I had already gone through the "disbelief

phase" when Sue developed MCS and started reacting to perfumes, household

chemicals, weedkiller and traffic fumes. We then agreed together to try a

new doctor and we were both there when he used a machine which caused her to

start developing ES symptoms within an hour. I'd been a bit surprised at the

time that 3 Ghz microwave radiation was being used unshielded, and I knew

that neither Sue or I had ever heard of ES, so there was no danger that we

were "imagining she'd got something we'd seen on the internet". Even with

this knowledge, I still found it hard to cope over the following months as

Sue gradually became sensitive to mobile phones, computers, TV's, household

electricity and even the earpieces of normal phones, and her associated fear

as the environment around her became "unsafe". We had a complete range of

reactions from our friends, who varied from the highly supportive to the

totally incredulous, and sadly we have lost some long-standing friendships

as a result. On the other hand some casual friendships became deeper - for

example with my boss whose daughter had dust mite allergy and other mild MCS

symptoms.

Would be interested in others' views on this! Mostly it is sceptical

husbands who seem to be mentioned - not sure if wives are usually more ready

to believe, or that more women than men get ES (or both factors together).

_____

From: eSens@yahoogroups. com [mailto:eSens@ yahoogroups. com] On Behalf Of

Jennie Wassenaar

Sent: 11 September 2009 18:07

To: eSens@yahoogroups. com

Subject: Re: [eSens] Magnetic Therapy

That is incredible that you have to go to the park and sleep! I had never

thought of that option, I am hoping that some of the adjustments I am making

will help. I have talked to my husband about turning off the breaker at

night but unfortunately he is not willing to make that inconvenience to help

me. Thanks for the suggestions, if you think of anything else let me know.

Have a great day,

Jennie

____________ _________ _________ __

From: Loni <loni326@yahoo. <mailto:loni326% 40yahoo.com> com>

To: eSens@yahoogroups. <mailto:eSens% 40yahoogroups. com> com

Sent: Friday, September 11, 2009 11:41:29 AM

Subject: Re: [eSens] Magnetic Therapy

Are you turning all the electric off at the breaker at night? I have to go

to the park & sleep (camp) due to the masts here. Loni

--- On Thu, 9/10/09, Jennie Wassenaar <ad-in@ameritech. net> wrote:

From: Jennie Wassenaar <ad-in@ameritech. net>

Subject: [eSens] Magnetic Therapy

To: "EMS" <eSens@yahoogroups. com>

Date: Thursday, September 10, 2009, 8:46 PM

Does anyone have any information or experience with magnetic therapy?

I had sent an e-mail a few months back regarding my inability to get a good

night's sleep after they upgraded a mast near our home (1/2 mile). It's been

4 months and I still have not had a good nights sleep but it has improved by

taking Melatonin and doing some magnetic therapy. I'd like to hear some feed

back on long term/on going magnetic therapy.

Thanks,

Jennie

PS we will be taking delivery of a sleep number mattress soon (air chambers

with no metal springs) and I'm crossing my fingers that it will help me get

a good nights sleep.

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