*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 ]