Re: Re: University doing EMF study; any feedback for her?

[Guest guest]

Could you private message me ( necessejamais@....)  w/ the names of the

naturopaths & practitioners who've helped you w/ your ES? My MCS started to

improve when I saw 1 of the best classical homeopaths in the country, but all

the improvement stopped & my health took a nosedive after a 4-day Smart Meter

exposure in March, & now my constitutional homeopathic remedy, Morphinum, seems

to hurt more than help. 

-E. Drew

From: joshfinley1985 <josh416@...>

Subject: Re: University doing EMF study; any feedback for her?

Date: Tuesday, June 14, 2011, 5:45 PM

 

I can't comment on the " refugee " communities, except the one that was widely

reported in the media as existing in an undeveloped low-RF area in France. I

know that the organization " Next Up " would have more to say about this topic.

See slideshow at the beginning of this video:

http://videos.next-up.org/BBCWorld/Les_refugies_des_micro_ondes/01_11_2009.html

As for support from the medical community in the United States, it's there if

you know where to look for it. I have helped tremendously in my battle with ES

by naturopaths that are familiar with ES and have had success treating it. I

have, however, been lucky; these people are by no stretch of the imagination

common; I doubt they exist outside of cities with large progressive/liberal

populations (I live in Seattle). And among MDs in the U.S., knowledge about ES

is almost nonexistent (this is not the case in some countries; in Germany, for

instance, thousands of mainstream physicians long ago signed the " Freiburger

Appeal " . See: http://www.starweave.com/freiburger/).

So yeah, I'd say that while it has been largely up to my family and I to figure

out how to deal with ES, I have gotten some important help from the alternative

medical community. Also, the psychologist I saw about the issue when I was

first trying to figure out what was going on didn't just tell me I was crazy and

needed years of talk therapy and/or drugs; he didn't have any experience with

the condition and couldn't help me, but he was at least decent and humble enough

to say so, which meant that I didn't waste time and money trying to treat a

physiological response to an environmental stimulus as if it were a

psychological problem. I do think that ES has a lot of ramifications for

psychological and neurological processes, however, which contributes to the

deluded belief that it's a psychosomatic phenomenon. If I had not been able to

escape-to a degree-the microwaves and to treat the problem successfully, I'm

sure I ultimately would have been

diagnosed, quite fairly, as having psychological and/or neurological problems.

Microwave-based communications technologies undermine people's wellbeing and

healthy mental and physical functioning; this is simply the nature of the

monster we have created, and thus the fact that many ES people are not in a very

good psychological state is utterly unsurprising.

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> Below is part of a recent email sent from University student doing research on

EMF sensitivity!

> She has some questions about differences in countries related to treatment of

this impairment!

> Any feedback I can send to her would be appreciated!  Loni

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> I'm beginning to start to work on all the interviews i've collected from EMF

sufferers and wanted to ask you a question. I've heard about EMF " refugee "

communities? Would you know if these are these real communities living together

or just the communal feeling of being a refugee from technology? Do you ever

feel like a refugee? or abandoned?

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> Also, I was wondering what you might think of my conclusions about the state

of EMF sufferers in the US compared to other nations. It seems like in the US,

EHS people, especially in the United States, have been essentially abandoned by

the biomedical and scientific community, branded psychosomatic, and expected to

create their own new forms of treatment. Is there a different type of attitude

in the UK? It seems like scientists in the us are more stuck in trying to

disprove your illness rather than actually looking for some kind of biomedical

or genetic predisposition of your suffering. Does this seem accurate?

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