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hi all

At 11:23 1999/04/18 EDT, marie wrote, in part:
>Hi All! I've been watching the replies to  the agonist survey
>and the only real problems I see - endured by all PWP's - is
>the variable WAYS the DR. are approaching the situation  of
>prescribing for the symptoms.  True, each individual is a
>variable themselves, but the medical community should be a main
>source for tabulating the variables and finding some common
>answers - but they haven't...

they 'should' but they haven't

part of that may be due to us folks with pd [present and past]
wanting to hide the symptoms away in shame and anger
[which i hope is a downward trend]

not to say we've caused the ignorance which is pretty widespread out there
but it surely hasn't helped to dispel any either

i have pd
i tell everyone i meet for longer than half an hour that i have it
which usually results in a conversation that feels good on both sides

we have to be our own best advocates

pd visibility = pd awareness = pd knowledge = pd power


janet

janet paterson - 52 now /41 dx /37 onset - [log in to unmask]
613/256/8340 - po box 171/almonte/ontario/k0a 1a0/canada

Scan some of My Past Posts at:
     http://www.newcountry.nu/pd/members/janet/index.htm
Mine the PD List Archives at:
     http://james.parkinsons.org.uk/
Cull Nine Million Pub-Med Medical Studies at:
     http://www.ncbi.nlm.nih.gov/PubMed/
Comb the 'People With Parkinson's' Web-Ring at:
     http://www.webring.org/cgi-bin/webring?ring=parkie;list