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