Abstract
To explore the experience of living with parkinsonism, a survey form was sent to the members of a patients’ association; 1,256 forms were analysed. The mean age was 65.75 ± 9.29 years; 64.4% males. A family history was reported by 19.2%. Basic abilities were preserved in 75% of the responders; the ability to do indoor and outdoor activities was preserved in 42 and 28%, respectively. 70% of the responders liked to meet other people and about 50% liked discussing their condition. 80.3% of the responders lived with partner, while 7.8% did not live with family. Of the patients’ partners, 38.9% took drugs, and 9.4% themselves needed assistance. Care programmes for parkinsonians should take into account the disease duration, the degree of disability, the presence of caregiver/s, and the level of caregiver burden; but it should also be appreciated that social habits, need of help, and severity of symptoms influence disability.
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We are grateful to the Italian Parkinson’s Disease Association (AIP) for distributing the survey forms together with copies of its journal.
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Martignoni, E., Citterio, A., Zangaglia, R. et al. How parkinsonism influences life: the patients’ point of view. Neurol Sci 32, 125–131 (2011). https://doi.org/10.1007/s10072-010-0435-x
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DOI: https://doi.org/10.1007/s10072-010-0435-x