Citations (30)
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Erin Beneteau, Heather Feldner & Wanda Pratt. (2023) “I miss work:” employment experiences and attitudes of adults with acquired disabilities who use assistive technologies. Disability and Rehabilitation: Assistive Technology 0:0, pages 1-10.
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Elliottnell Perez, Paul B. Perrin, Sarah K. Lageman, Teresita Villaseñor & Joseph M. Dzierzewski. (2022) Sleep, caregiver burden, and life satisfaction in Parkinson’s disease caregivers: a multinational investigation. Disability and Rehabilitation 44:10, pages 1939-1945.
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Christie L. Stilwell, Susan L. Hutchinson & Brad A. Meisner. (2019) ‘I’ve got Parkinson’s and that makes a difference’: Understanding health and leisure through a Parkinson’s disease diagnosis. Loisir et Société / Society and Leisure 42:1, pages 43-55.
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Amanda Frier, Fiona Barnett, Sue Devine & Ruth Barker. (2018) Understanding disability and the ‘social determinants of health’: how does disability affect peoples’ social determinants of health?. Disability and Rehabilitation 40:5, pages 538-547.
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Amanda Pavey, Narelle Warren & Jacquelyn Allen-Collinson. (2015) “It Gives Me My Freedom”: Technology and Responding to Bodily Limitations in Motor Neuron Disease. Medical Anthropology 34:5, pages 442-455.
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Shahla Abolhassani, Ahmadreza Yazdannik, Fariba Taleghani & Ahmadreza Zamani. (2015) Social aspects of multiple sclerosis for Iranian individuals. Disability and Rehabilitation 37:4, pages 319-326.
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Gerda Drutyte, Maria João Forjaz, Carmen Rodriguez-Blazquez, Pablo Martinez-Martin & Kieran C. Breen. (2014) What impacts on the stress symptoms of Parkinson’s carers? Results from the Parkinson’s UK Members’ Survey. Disability and Rehabilitation 36:3, pages 199-204.
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Joanna Sweetland, Eimi Howse & E. Diane Playford. (2012) A systematic review of research undertaken in vocational rehabilitation for people with multiple sclerosis. Disability and Rehabilitation 34:24, pages 2031-2038.
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Nick Miller, Jill Taylor, Chloe Howe & Jennifer Read. (2011) Living with foreign accent syndrome: Insider perspectives. Aphasiology 25:9, pages 1053-1068.
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Josephine Anne Spring, Mark Baker, Loreane Dauya, Ivie Ewemade, Nicola Marsh, Prina Patel, Adrienne Scott, Nicholas Stoy, Hannah Turner, Marc Viera & Diana Will. (2011) Gardening with Huntington's disease clients – creating a programme of winter activities. Disability and Rehabilitation 33:2, pages 159-164.
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Articles from other publishers (20)
Kasper F. van der Zwaan, Marit D.C. Mentink, Milou Jacobs, Raymund A.C. Roos & Susanne T. de Bot. (2022) Huntington's disease influences employment before and during clinical manifestation: A systematic review. Parkinsonism & Related Disorders 96, pages 100-108.
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Siok-Bee Tan, Allison F. Williams, Eng-King Tan, Richard B. Clark & Meg E. Morris. (2020) Parkinson's Disease Caregiver Strain in Singapore. Frontiers in Neurology 11.
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Christopher Vincent. (2019) Illness, Couples and Couple Psychotherapy. British Journal of Psychotherapy 35:4, pages 628-641.
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David Morley, Sarah Dummett, Laura Kelly, Ray Fitzpatrick & Crispin Jenkinson. (2018) Predictors of activity and participation across neurodegenerative conditions: a comparison of people with motor neurone disease, multiple sclerosis and Parkinson’s disease. BMC Neurology 18:1.
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Nadine LacroixM. serv. sM. serv. s, Normand BoucherPh.D.Ph.D. & Patrick VilleneuvePh.D.Ph.D.. (2016) Participation sociale et sclérose en plaques : Réalité particulière. Service social 62:2, pages 94.
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Merete Røthing, Kirsti Malterud & Jan C. Frich. (2015) Family caregivers' views on coordination of care in Huntington's disease: a qualitative study. Scandinavian Journal of Caring Sciences 29:4, pages 803-809.
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Tamara McKenzie, Mary Elizabeth Quig, Tuula Tyry, Ruth Ann Marrie, Gary Cutter, Edward Shearin, Kamau Johnson & James Simsarian. (2015) Care Partners and Multiple Sclerosis. International Journal of MS Care 17:6, pages 253-260.
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Merete Røthing, Kirsti Malterud & Jan C. Frich. (2014)
Balancing needs as a family caregiver in
H
untington's disease: a qualitative interview study
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Josephine A. Spring, Marc Viera, Ceri Bowen & Nicola Marsh. (2013) Is gardening a stimulating activity for people with advanced Huntington's disease?. Dementia 13:6, pages 819-833.
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Sally Hartley, Maggie McArthur, Michaela Coenen, Maria Cabello, Venusia Covelli, Joanna Roszczynska-Michta, Tuuli Pitkänen, Jerome Bickenbach & Alarcos Cieza. (2014) Narratives Reflecting the Lived Experiences of People with Brain Disorders: Common Psychosocial Difficulties and Determinants. PLoS ONE 9:5, pages e96890.
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Rozina Bhimani. (2014) Understanding the Burden on Caregivers of People with Parkinson’s: A Scoping Review of the Literature. Rehabilitation Research and Practice 2014, pages 1-8.
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Gabriele Moriello, Christopher Denio, Megan Abraham, Danielle DeFrancesco & Jill Townsley. (2013) Incorporating yoga into an intense physical therapy program in someone with Parkinson's disease: A case report. Journal of Bodywork and Movement Therapies 17:4, pages 408-417.
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Bradley Brossman, Janet K. Williams, Nancy Downing, James A. Mills & Jane S. Paulsen. (2012) Development of the Huntington Disease Work Function Scale. Journal of Occupational & Environmental Medicine 54:10, pages 1300-1308.
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Nancy R. Downing, Janet K. Williams, Anne L. Leserman & Jane S. Paulsen. (2012) Couples’ Coping in Prodromal Huntington Disease: A Mixed Methods Study. Journal of Genetic Counseling 21:5, pages 662-670.
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Marilyn Trail, Nancy J. Petersen, Naomi Nelson & Eugene C. Lai. (2012) An exploratory study of activity in veterans with Parkinson?s disease. Journal of Neurology 259:8, pages 1686-1693.
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Andreas A. Argyriou, Panagiotis Karanasios, Amalia A. Ifanti, Gregoris Iconomou, Konstantinos Assimakopoulos, Alexandra Makridou, Fotini Giannakopoulou & Nicolaos Makris. (2011) Quality of life and emotional burden of primary caregivers: a case–control study of multiple sclerosis patients in Greece. Quality of Life Research 20:10, pages 1663-1668.
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Kori A. LaDonna. (2011) A Literature Review of Studies Using Qualitative Research to Explore Chronic Neuromuscular Disease. Journal of Neuroscience Nursing 43:3, pages 172-182.
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Nancy R. Downing, Janet K. Williams & Jane S. Paulsen. (2010) Couples’ Attributions for Work Function Changes in Prodromal Huntington Disease. Journal of Genetic Counseling 19:4, pages 343-352.
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Marita P. McCabe & Elodie J. O’Connor. (2009) The Economic Impact of Progressive Neurological Illness on Quality of Life in Australia. Journal of Family and Economic Issues 31:1, pages 82-89.
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Marita P. McCabeElodie J. O'Connor. (2009) A longitudinal study of economic pressure among people living with a progressive neurological illness. Chronic Illness 5:3, pages 177-183.
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