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Amanda,

Perfectly put; we share the same thoughts. I also recently bought a book on
the 'Brain'. I have always had an interest in biology and I am blessed with
a logical, analytical and inquisitive mind [ which the author of my book
refers to as - the control centre of a living machine; the mind not me
(LOL)], I don't trust any of the Doctors, Neuro's etc. that I've met so far
[dxd 4/03] - my GP told the Triage Nurse '.. he is argumentative and
stuuborn...', he said this because I ask [too many] difficult questions. I
certainly don't trust the Pharmaceutical industry - it's almost 200 yrs
since Dr. James Parkinson wrote his ' Essay on the Shaking Palsy' and
there's still no cure and many of the drug therapies [that only manage the
symptoms] cause serious side-effects and the benefits are short-lived. It
doesn't make one hopeful when one hears the UK's leading Prof,-. of
<Neurology say, " we're not sure whether it[l-dopa] is responsible for the
acceleration of PD or PD its self".

This group has many others who also share our thoughts; we have the combined
intelligence and the desire to find a real cure; we have the time; we have
the technology; we can collect, analyse and present data, which will force
through the most significant chages in the diagnosis, treatment annd therapy
of PD, in the last 150yrs. Collectively we can 'tip the balance' to force
change.

I live in Ruislip and you live in NW London; we're sort of neighbours and I
would really like to meet you and your family and invite you to my home for
coffee/tea/brunch/lunch/dinner - I'm not a bad cook (LOL)- whenever you have
the time and/or maybe passing by.

regards,

Marco

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