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Murder by the Bureaucracy

Tue Apr 29, 2008 9:39 am (PDT)

*The reason -- in spite of the fact that there are already a number of established biological markers -- they are trying to turn ME (Myalgic Encephalomyelitis) into a psychological problem (the same way they are trying to do with ES [electrosensitivity]) is that they don't want to admit for one what really causes this problem, and two they don't want to spend
money on it. It's another big lie being propagated in the name greed and stupidity. Here is another story of murder by the sickos running the sick bureaucratic system of which many of us are being forced to live in and deal with.

Paul*

Subject: Fwd: Message from Criona Wilson, Sophia's Mother

May be reposted

Today, 9am, sees the launch of a website I have created in memory of my beautiful daughter who died of Myalgic Encephalomyelitis. It deliberately coincides with a conference being held by the Royal Society of Medicine on the subject of ME/CFS to which many psychiatrists and psychologists have been invited to speak. ME is a physical illness but the problem facing most ME patients is that a psychological causation of their symptoms is part of the dogma that has been foisted on them by a very small but highly influential group of psychiatrists who have established a niche market in what is a controversial but highly debilitating illness.

In June 2003 a warrant was granted through Brighton Magistrates Court that resulted in the sectioning of my daughter, Sophia Mirza, because she would not accept psychiatric treatment for her physical condition, Myalgic Encephalomyelitis (ME).

Despite our Solicitor being confident that there were no grounds for a warrant to be issued, a warrant was granted and my very ill daughter was sectioned against her will until a Tribunal sanctioned her release almost two weeks later.

My daughter never recovered from the shock of this incarceration and died in November 2005. The coroner's verdict recorded that she died of CFS/ME.

Six doctors and a social worker were among the people who were involved in Sophia's case.

I have tried, without success, to gain justice from the GMC and Social Services over the dreadful treatment my daughter received, but to no avail. I have written to two Attorney Generals, numerous MPs and solicitors - again with no result. It seems that ordinary people like me and my daughter can be treated in the most appalling way and no-one is accountable.

I have therefore decided to publish all letters and communications appertaining to my daughter's ordeal at the hands of the authorities, in an effort to ensure that this should never happen again to someone suffering from ME.

I hope that the doctors and social workers involved in my daughter's care will now reflect on what they did and learn from their mistakes and intransigence. I hope that other professionals will also learn lessons from what I have published and that no other person with ME will be treated so callously.

For more information see
http://www.sophiaandme.org.uk/

Criona Wilson 28th April 2008

--

Paul Raymond Doyon
Yunnan Normal University (China)
Lecturer - English and Japanese
MAT (TESOL), School for International Training
MA Advanced Japanese Studies, University of Sheffield
BA Psychology, University of California

[ http://omega.twoday.net/search?q=Myalgic+Encephalomyelitis

http://omega.twoday.net/search?q= electrosensitivity ]

Posted by: Paul Doyon
Wed Apr 30, 2008 1:37 pm (PDT)

*This is exactly what I had: ME (Myalgic Encephalomyelitis) / CFS
(Chronic Fatigue Syndrome). It is a very serious disease! Very few
people recover -- and most usually die of one of three causes: (1)
Suicide, (2) Heart Failure, or (3) Cancer.

When I removed myself completely from an electrosmog environment, 50%
of my symptoms disappeared in the first 24 hours. It took another two
months of living in this log house up in the mountains of Saga
Prefecture, Japan (where there was no TV or cell-phone reception)
before I was able to get off the sleeping pills. (The only
pharmaceuticals I ever took were antibiotics for about two months and
sleeping pills for about three months -- although the doctor I went to
wanted to give me anti-depressants, I refused.) After about four
months I would say I was about 90% recovered -- but by that time I had
become extremely electrosensitive! Why? Because my body knew very well
exactly what it was making it sick.

ME/CFS is certainly not a psychological disease -- though we can say
without a doubt that "yes the microwaves and other EMR affect the
hormones in the brain." However, the cure is certainly not going to
see some psychologist or psychiatrist who obviously doesn't have a
clue and is probably frying his or her own brain with some cell phone.
There are multiple biological markers which the "people in charge"
refuse to accept for only one reason -- they are working in collusion
with the insurance companies which do not want to pay out to the
massive amount of people with this disease now! Otherwise, they would
certainly go broke!

And now they (those bought and paid for by the cell-phone industry)
are trying to say that electrosensitivity is psychosomatic. However,
these are the people who should be thrown into a psychiatric hospital
with the key thrown away -- these are the executives of the cell phone
companies and anyone working in collusion with them! They are the ones
making us sick! They are the criminals who should be put in jail for
"premeditated murder" and "crimes against humanity!"

How many more people like Sophia will have to die before the truth is
known?

paul