National Scandal Exposed

Many thanks to Cindee Rice <cmarie3@cox.net>,
who drew my attention to this important broadcast

ME/CFS - A Hidden National Scandal Exposed
~~~~~~~~~~~~~~~~~~~~~~~~~~~~

This moving broadcast by Meridian TV (Meridian
Tonight) is a MUST for physicians, parliamentarians,
newspapers, tv stations, charities, lawyers,
teachers, patients, their family, friends, etc., etc.

It can be found at:
http://hk.youtube.com/watch?v=hkGq0BH6AHw


By opening *luminescentfeeling* on the right site,
you can find this excellent article:

Dr Kerr & the 'cure' that never was.
~~~~~~~~~~~~~~~~~~~~~~

Dr Kerr & the 'cure' that never was. No cure had been
made available. Not due to Dr Kerr - but due to the
blocking of funds to continue his work. (As has
happened to Dr Gow) - another genetic expert from
Scotland who is also finding things in this illness
that people don't want to hear. I wonder why? Not
that they have anything to hide or anything, no......

This is an edited (for time) clip of a Meridian TV
news item that appeared on our screens over here in
England,UK in 2005.

Meridian TV should be applauded for having the
bravery to broadcast this - it was NOT broadcasted
nationally to protect the Government from shame
and being asked questions - obviously.
Consequently, only a few people saw it.

Even after this ground breaking genetic discovery
was broadcast the UK Government still continue to
block funding for research and a diagnostic test for
ME/CFS.

In 2008, not one ME/CFS clinic exists in the UK. All
money is still going to psychiatry and the 'Wessely
School' - despite M.E being recognised as a
neurological illness by the World Health Organisation
(W.H.O) since 1969.

This flow of money is blocked by the MRC (Medical
Research Council) who are influenced by the insurance
industry - who have too much to loose to open the
flood gates with 100,000's of thousands of patients
making disability claims. The truth on ME/CFS is thus
kept tightly shut. Doctors, civil servants and the
general public -still have no idea that ME can be
fatal.

All we hear about is 'recovered' CFS patients in the
newspaper - who 'recover' by taking anti-depressants
and deciding they weren't actually ill after all. As you
may know, the 'recovery' rate for ME is around 2%.
Meaning 98% of people do not recover. Despite this,
the british media rarely print articles on the severely
chronically sick and instead focus on the mentally ill.

These mentally ill people are 'volunteered' towards
the media by bogus CFS charities. These charities
are funded by the national lottery (Lotto) and extra
government funding - to push a psychiatric agenda.
The UK Government, and the BMA (British Medical
Association) are thus a disgrace - as are bogus CFS
patients, bogus CFS charities and the corrupt and
evil Psychiatrits who prey on desperately ill patients.

The NHS website in the UK claims 'most' people get
better, and that this illness may 'last for months'.
This is surely immoral? Promising people with viraly
induced brain stem/ cardiac damage/DNA damage a
cure with CBT/GE - graded exercise and behavioural
therapy!

For the TRUTH on what ME does to people, go to:
http://www.meresearch.org.uk/
http://www.investinme.org
http://www.cfsrf.com/
http://www.investinme.org
http://www.ahummingbirdsguide.com
http://phoenix-cfs.org
http://www.ahmf.org  (??)

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Many other *ME/CFS-YouTube's* can be found at the
same address as above; some examples:
ME/CFS - Shortens lifespan by 25 years.
ME/CFS - Doctors disbelief kills young woman
Chronic Fatigue Syndrome CFS
ME/CFS - Doctors trained to neglect (part 2 of 4)
ME/CFS - The Possible Consequences Of Medical
Neglect
Why 'CFS' is a wastebasket diagnosis
ME/CFS - Doctors trained to neglect (part 1 of 4)
CFS 2006 awaresnes Campaign CDC
Sleepydust - About M.E. / Chronic Fatigue Syndrome
Missing my Life -deutsche Version-
A symptom list: Myalgic Encephalomyelitis
The Psychiatry Scandal
Japanese CFs
'CFS' harms everyone, not just M.E. sufferers
Problems with 'our' M.E. (and CFIDS, ME/CFS)
advocacy groups
Wessely wants "Chronic Fatigue Syndrome" - ITN
Gupta Programme for ME, CFS & Fibromyalgia
M.E. and Incapacity Benefit
A short CFS documentary
WHO's right? M.E. is neurological not psychiatric

~jvr