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Anyone have experience with PSP (Progressive Supranuclear Palsey)? It's becoming quite clear that this is what my mother inlaw is dealing with. She's in a near-coma, on life support and NOBODY'S DOING ANYTHING to help. They're concerned about a lung infection and that's the sole focus of the doctor's help. I'm watching this from long-distance, and feel helpless to do anything. I've searched the web for PSP info, and have gotten some helpful stuff. I'd love to hear of personal experiences or ideas. Thanks, friends. Maggie long-distance advocate for Bernydette, 77/1