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Hi... My name is Bob Matherly, I too have PD (Diagnosed 3 Yrs., symptoms for 6 Yr), I am also currently taking sinamet and eldyprl, I am now 35 yrs. old. I am writing because my wife (Kuan, Li-Yung) is from Taiwan (Taichung (not sure of the spelling)). I would like to offer my assistance in relaying any information I may come across about PD to you. Are you a subscriber to this list? It is a great source of information. Let me know how I can help you gather the information you want and I will do my best to accomadate you. Bob Matherly [log in to unmask] >Hello, all: >I live in Kaohsiung, Taiwan (the other China). I was diagnosed with PD five >years ago when I was 36. I started to take Sinemat last year, first 50mg a day, >now I am taking 100mg a day first thing in the morning. I have been on Jumexal >for four years. >My neurologist suggested that I take 2.5mg of Parlodel every night to enhance >the effect of l-dopa. I have some reservation though because of the recent >controversy over the side effect of Parlodel. Can someone share the thought >with me? >There is very few information concering PD available in Chinese in Taiwan. I >feel strongly for the PD suffers in my country. I wonder if I can be on some >sort of list so I can receive the most update info on PD and pass them out in >Chinese. For ex., the recent flame on pallidotomy could be a very interesting >topic to discuss with my fellow patients and doctors here. >I am also interested in learning more about Pacemaker for PD. >We pray everyday for those who suffer from PD and the doctors to come up with a >real cure. > >Liangshiu Lee, [log in to unmask] > > >Liangshiu Lee ([log in to unmask]) > >