Published with the Parkinson's Disease Society, this book contains highlights of PDS-sponsored welfare research over the last 10 years, with reports of key projects carried out to improve the lives of people with the disease and provide them with better standards of care, both professional and voluntary. Some studies involve quality of life measures; others are concerned with a range of therapies, both old and new, others with symptomatology. This is a unique collection of information for readers at all levels.