Subject: Mobile phone use and the blood-brain-barrier (Maisch)
Date: Thu, 23 Sep 1999 170200 -0500 (CDT)
From: "Roy L. Beavers"
To: emfguru
--------------------------------------------------
Good work, Don!!
I should have reminded folks about the recent blood-brain-barrier
research -- which could be "a factor" with Marilyn's problems.....
We still need to know ** why ** the Drs. out there in New Mexico
are telling her this condition is EMF related??
(For our contact in Sweden: We don't want to miss info about the
publication -- or peer review -- of that BBB research.....)
Cheerio.....
Roy Beavers (EMFguru)......
rbeavers@llion.org.......
.....It is better to light a single candle than to curse the darkness.....
EMF-L web-site can be found at:
EMF-L archives can be found at:
..................PEOPLE ARE MORE IMPORTANT THAN PROFITS..................
---------- Forwarded message ----------
Date: Fri, 24 Sep 1999 06:49:27 +1000
From: Don Maisch
To: CHINAGRVE@aol.com
Cc: rbeavers@mail.llion.org
Subject: Mobile phone use and the blood-brain-barrier
Dear Marilyn
I just read your message on the Roy Beavers discussion group and would
like to add that recent research in Sweden indicates that use of a mobile
phone may open up the blood-brain barrier and allow toxic chemicals into
the brain.
The possibility exists that if you were exposed to pesticides and also
using a mobile phone this may have allowed chemical entry into the brain
causing a number of effects, possibly MCS? This is all surmising but do
you use a mobile, and if so, for how long daily?
Sincerely
Don Maisch
>---------- Forwarded message ----------
>Date: Thu, 23 Sep 1999 03:50:28 EDT
>From: CHINAGRVE@aol.com
>To: rbeavers@llion.org
>Subject: Re: Query on EMFs (Marilyn)....
>
>Roy,
>
> I had two doctors diagnose me with MCS. One was a pulmonary specialist
>with Lovelace. He told me he was diagnosing me with MCS even though his
>supervisor didn't believe it existed because he saw too many patients with
>the same symptoms. He told me Lovelace in Alb. had no one who could treat
>this and gave me the name of an environmental doctor in Los Alamos who is now
>my current doctor. She diagnosed me with MCS from pesticide poisoning. When
>I first became ill, I was salivating (foaming at the mouth,) my jaw would
>not stop moving back and forth and I was having much difficulty breathing
>and swallowing which she said were classic symptoms of pesticide poisoning. I
>was so sensitive to everything back then I could not take a shower , wash my
>hair, hug my boyfriend, go outside ,etc. without having serious breathing
>problems. I have improved about 75% since then but still have many lingering
>symptoms.
>
> I'm a photographer, and I became sensitive to all the darkroom chemicals
>so I believed that to be the cause,.but my doctor was adament that it was the
>malathion because of the foaming at the mouth. When the city accidently
>sprayed my neighborhood with malathion again (about the l6th time in four
>years), I reacted so badly that I knew she was right.
>
> Anyway, I was on a electrical sensitivity site recently that claimed
>pesticides were one cause of electrical problems..
>
> Medical treatment - detox baths, sauna, nutrient therapy,
>immunotherapy, eat only organic food, no additives or drugs and avoid
>polluted air and chemicals. A very simple house with no rugs, only cotton
>washable curtains and rugs, no toxic cleaning products, no leather. Many
>people only improve after they move to the country to cleaner air which is
>what I'm doing. One environmental doctor summed it up -
>If you are not getting better, you are still being exposed to toxic chemicals
>- lessen your load and you will improve.
>
> Marilyn
>
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Reprinted with permission of Roy Beavers, http://www.emfguru.com