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No, I don't think the concept here is even remotely akin to Carsville or a quarantine of Aids victims. It just is a more comfortable option for care or help particularily for those people where loners like Mary Yost can be caregivers for each other. There is a young man in our support group with rather advanced PD whose wife couldn't cope so she left him and took their young children and moved so her parents could help look after the children whilst she worked. He can't afford an apartment near his medical help so lives in a nearby town with no transportation. His world fell apart when his family left and again when he recently had to stop driving his car. A nursing home for him seems to loom on the horizon. Wouldn't Pee Dee Village help his situation? Maybe our Ca computer friend would still be alive with special support from other victims of PD. My cowboy friend fears his next step is a nursing home as it is harder and harder to cope at the ranch in the wilds. Wouldn't they all be happier in a "colony" specifically set up to making PD easier to cope with. The healthiest of us teaching patients and caregivers to be independent. Housing with no stairs. Big doorways. Lots of strategically placed grab bars. Large stall showers with seats, and lever type door handles and water tap handles, and a trapeze over the bed to help turn over or arise. Nearby accessible medical care by knowledgable professionals. Social and recreational facilities. It would not be utopia but it would be more comfortable and safer and maybe less lonely for a lot of people. Less caregiver burnout too. Think about it. I received a message from a man who said he had heard that thirty or forty years ago a woman from New York sought to establish a Parkinson's "village" to better care for people with PD. She put together a community in Florida and the idea later evolved into the National Parkinson's Foundation. This man doesn't have any specifics, but thinks it would be interesting to verify this and see how the concept developed. Interestingly I lived in Miami many years ago and there was an apartment building on the 79th Street Causeway which was used as a PD clinic and I believe a residence for patients coming to be evaluated and treated. Probably some patients lived there after the big NPF state of the art headquarters was built near Jackson Memorial Hospital. Anne Rutherford (Newfoundland) - the UK PD village I read about is either in Walsall or Birmingham. Simon Coles father, Derek Coles was a member of the Executive Committee and Chairman/Trustee of PDS at that time - l992. The opening of their specialized housing project for people with PD was planned for l994 the 25 anniversary of the Society. I hope you can get an update. Yes Anne, we need a dedicated mover and shaker with ability to tap the business and finance end of a project like this. Are you out there grant writer or philanthropist or interested talented business person with energy? Canadian, American - both. Barbara Yacos