>
>
> 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]<csteils%40yahoo.co.uk>>
> wrote:
>
> From: Christina Steils <[hidden email] <csteils%40yahoo.co.uk>>
>
> Subject: Re: [eSens] Husbands Anonymous
> To: [hidden email] <eSens%40yahoogroups.com>
> 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, most
> importantly 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 very
> important. We were! Not good.
> I feel much better now, dealing with wifi and mobile masts.Mostly Just a
> tickle/ 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 my
> husband 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 the
> ones 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 line is
> limited. But I do save all the posts to a file in hopes that one day if one
> of my family members is willing they can go through the saved post and
> garner some helpful information for me. That might be a helpful hint for a
> support 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% <loni326%25> 40yahoo.com> com>
>
> To: eSens@yahoogroups. <mailto:eSens% <eSens%25> 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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>
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>
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>
>