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Disability and Rehabilitation Volume 37, 2015 - Issue 10
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Research Papers

Participation in life situations by persons with systemic sclerosis

Janet L. PooleOccupational Therapy Graduate Program, School of Medicine, University of New Mexico, Albuquerque, NM, USA, Correspondence[email protected]
,
Annandhi ChandrasekaranHealthSouth Rehabilitation Center, Albuquerque, NM, USA,
,
Kristal HildebrandSaint Anthony Home Health Care, Rockford, IL, USA, and
&
Betty SkipperDepartment of Family and Community Medicine, School of Medicine, University of New Mexico, Albuquerque, NM, USA
Pages 842-845 | Received 17 Feb 2014, Accepted 10 Jul 2014, Published online: 23 Jul 2014

Citations (12)

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Read on this site (2)

Janet L. Poole, Kristin Forno, Ashley Prokopiak & Betty Skipper. (2023) Importance and difficulty with valued life activities for people with systemic sclerosis. Disability and Rehabilitation 45:2, pages 220-225.
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Janet L. Poole, Donna Haygood & Cindy Mendelson. (2018) “I'm still dad”: The Impact of Scleroderma on being a Father. Occupational Therapy In Health Care 32:1, pages 1-13.
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Articles from other publishers (10)

Janet L. Poole, Jessica Greaves & Cyd Mendelson. (2023) ‘It's just not the same… I am just a spectator’: A qualitative study on changes in leisure participation experienced by people with scleroderma. Musculoskeletal Care 21:3, pages 733-740.
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Janet L Poole, Monica Baldonado, Aubrie Powell & Virginia Stofer Hukill. (2023) Strategies used by people with systemic sclerosis to perform valued occupations. British Journal of Occupational Therapy.
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Julianne G. Clina, Cassandra Herman, Christine C. Ferguson & James H. Rimmer. (2023) Adapting an evidence-based physical activity questionnaire for people with physical disabilities: A methodological process. Disability and Health Journal 16:3, pages 101447.
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Susan L. Murphy, Janet L. Poole, Yen T. Chen, Alain Lescoat & Dinesh Khanna. (2021) Rehabilitation Interventions in Systemic Sclerosis: A Systematic Review and Future Directions. Arthritis Care & Research 74:1, pages 59-69.
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Susan L Murphy, Daniel Whibley, Anna L Kratz, Janet L Poole & Dinesh Khanna. (2020) Fatigue predicts future reduced social participation, not reduced physical function or quality of life in people with systemic sclerosis. Journal of Scleroderma and Related Disorders 6:2, pages 187-193.
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Susan L. Murphy, Anna L. Kratz, Daniel Whibley, Janet L. Poole & Dinesh Khanna. (2021) Fatigue and Its Association With Social Participation, Functioning, and Quality of Life in Systemic Sclerosis. Arthritis Care & Research 73:3, pages 415-422.
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Seher Arat, Jessica Rassart, Philip Moons, Koen Luyckx, Joris Vandenberghe & René Westhovens. (2018) Prospective associations between illness perceptions and health outcomes in patients with systemic sclerosis and systemic lupus erythematosus: a cross-lagged analysis. Rheumatology Advances in Practice 2:1.
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Seher Arat, Jan L Lenaerts, Ellen De Langhe, Patrick Verschueren, Philip Moons, Joris Vandenberghe, Veerle Taelman & Rene Westhovens. (2017) Illness representations of systemic lupus erythematosus and systemic sclerosis: a comparison of patients, their rheumatologists and their general practitioners. Lupus Science & Medicine 4:1, pages e000232.
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Natalie McCormick, Carlo A. Marra & J. Antonio Aviña-Zubieta. (2017) Productivity Losses and Costs in the Less-Common Systemic Autoimmune Rheumatic Diseases. Current Rheumatology Reports 19:11.
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Ayano Nakayama, David J. Tunnicliffe, Vivek Thakkar, Davinder Singh-Grewal, Sean O’Neill, Jonathan C. Craig & Allison Tong. (2016) Patients’ Perspectives and Experiences Living with Systemic Sclerosis: A Systematic Review and Thematic Synthesis of Qualitative Studies. The Journal of Rheumatology 43:7, pages 1363-1375.
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