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Dear Billy and others, I also, went through a period of trying to hide symptoms and avoiding telling anyone of my problem. We probably all do. Since then, I have come to the conclusion that by trying to stay invisible I am hindering the progress towards public awareness, more funding and a possible early cure. I realise that there may be reasons why an open approach with one's employer may not be advisable, but other than that or similar circumstances, I would urge all people with PD to take opportunities to inform the public. I am not suggesting we stand shaking on sreet corners with a notice around our necks. However, if we struggle at the checkout or at the bank, a quick, "Sorry, I have Parkinsons and it affects my movement and co-ordination", will not hurt. Under the right circumstances, a futher few words such as, "Still, can't complain, some people with PD are confined to bed and wheelchair", are easy. Said with a smile and perhaps a joke about the handwriting, there are many instances where one more member of the public can be made aware in only a minute or so that: a. PD is nasty and progressive. b. It does not only affect old people. c. The people like me they meet, are only the tip of the iceberg. After all, why have a Parkinsons awareness week once a year and then go back to hiding for another 51 weeks? I will be adding Ropinerole to my three daily dosages of Sinemet CR 200/50 this week. Will let you know how I get on. Ernie. Age 54. diag 3.4 yrs. Ernie Peters <[log in to unmask]>