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Janet's question about John Argue comes as I was about to post this brief "review" I wrote about his book, a copy of which was sent to me by Kasey Pfaff. Perhaps it will be helpful? Date: Sun, 20 Aug 2000 07:06:57 -0400 From: janet paterson <<[log in to unmask]> Subject: john argue hi all has anyone attended movement and/or voice classes with john argue in california? any opinions? janet # # # # # # PalatinoComments about Parkinson's Disease & the Art of Moving This is not your typical "exercise book" by any means. John Argue obviously knows his subjects--PD and exercise-- in great depth, and conveys this to the reader by means of text and photos. His unique approach is philosophic---as when he tells us that we must "shift to an artful action--one that is graceful, mindful, and complete, " in order to cope with PD symptoms ---to "speak and move consciously". He also gives practical advice, reminding us that it is truly a case of "use it or lose it" in terms of mobility for PWPs, but also that even one who is in a later stage of PD can participate within her/his own limits in the program he describes. While the program can be followed individually, it seems obvious that the greatest benefit is in following it with a group. That program is a detailed, graduated approach to maintaining and improving mobility of body and quality of speech. The excellent photos which accompany the text of the exercise portion are clear and easy to follow, while the text is readable, interesting, and persuasive. For a PWP who is motivated to make the sustained effort required, and has a positive attitude toward exercise of any kind, this would be a very valuable resource. Unfortunately, not all PWPs are blessed with such motivation, and the very completeness of the program may for them be "off-putting". There is a useful appendix, with resources, additional reading, and a note about the importance of political advocacy. Argue wisely reminds us that PWPs must plan to keep exercising "for the rest of your life".....adding, "Always be beginning". Camilla Hewson Flintermann, co-owner of the CARE list for Caregivers of People With Parkinsons disease. 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