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Disability and Rehabilitation Volume 42, 2020 - Issue 11
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Letters to the Editor

Living with systemic sclerosis: exploring its impact on caregivers

M. Rita SchriemerNVLE, Dutch patient organization for systemic sclerosis, SLE, APS and MCTD, Utrecht, The Netherlands; ;Department of Rheumatology, Radboud University Medical Center, Nijmegen, The Netherlands; View further author information
,
Julia SpieringsDepartment of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht, The Netherlands; Correspondence[email protected]
View further author information
,
Jeska K. De Vries-BouwstraDepartment of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands; View further author information
,
Lian A. J. de PundertDepartment of Physical therapy, Haga Ziekenhuis, The Hague, The Netherlands; View further author information
,
Cornelia H. van den EndeDepartment of Rheumatology, Radboud University Medical Center, Nijmegen, The Netherlands; ;Department of Rheumatology, Sint Maartenskliniek, Nijmegen, The NetherlandsView further author information
&
Madelon C. VonkDepartment of Rheumatology, Radboud University Medical Center, Nijmegen, The Netherlands; View further author information
Pages 1632-1633 | Received 04 Apr 2019, Accepted 12 Apr 2019, Published online: 30 Apr 2019

References

  • Milette K, Thombs BD, Dewez S, et al. Scleroderma patient perspectives on social support from close social relationships. Disabil Rehab. 2019;14:1–11.
  • Nakayama A, Tunnicliffe DJ, Thakkar V, et al. Patients' perspectives and experiences living with systemic sclerosis: a systematic review and thematic synthesis of qualitative studies. J Rheumatol. 2016;43:1363–1375.

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