Cari-- good points you make--#5 would be true at our house :-( Please poist those sites to the list when you are ready,so others may check them too. Thanks! >Mary - >there are so many options, yet so many considerations - > >1. is hearing an issue with the PWP? >2. will they have the timer or will someone else? >3. male or female >4. where will the timer be kept? >5. where will the meds be kept? >6. are there any problems with concentration, forgetfulness - so that even >after hearing the timer - getting to the meds - getting liquid to take them >with - they've forgotten what they started out doing? > > >All this may seem overly concerned, but it isn't - it's truly important as >i've found out with my dad! > >please advise on above when you can and i can also refer you to some great >web sites to check out for yourself. . . > >my best - > > >Cari > daughter of Dempsey-PWP (71/16+) > & Jo Ann-CGiver Camilla Flintermann, CG for Peter 82/70/55 Oxford, Ohio <[log in to unmask]> on PDWebring at http://members.tripod.lycos.nl/genugten/flinterm.htm "Ask me about the CARE list for Caregivers of Parkinsonians ! " And visit the CARE webring at http://www.crosswinds.net/~caregivers/index.html