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DOI 10.3109/09638288.2013.833301

Медицинская библиотека · Disability and rehabilitation · 2013

Life on hold: the experience of living with neuromyelitis optica.

Mutch Kerry, Methley Abigail, Moore Phil, Jacob Anu

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

PURPOSE: Neuromyelitis optica (NMO) is a rare autoimmune condition characterised by acute relapses of optic neuritis and extensive transverse myelitis. The aim of this qualitative study was to develop an improved understanding of the experiences of people living with NMO.

METHOD: Fifteen participants completed a semi-structured interview and data were interpreted using a constant comparative method. Participants were recruited from the Northern UK NMO Service.

RESULTS

Five major themes were identified: diagnosis and treatment, symptoms, adjustment, identity and support.

CONCLUSION

Results suggest NMO is a difficult condition to live with due to the unpredictability of relapses and accrued disability of visual or spinal symptoms occurring with each relapse. Poor vision, reduced mobility, bladder dysfunction and pain affected participants' independence and experience of living with NMO. Participants reported that during relapse and recovery they would "put their life on hold". They identified the importance of periods of stability to enable them to adjust to their condition and therefore aim for "normality" of life that they believed was comparable to their peers. Implications for Rehabilitation Disability due to NMO has a major impact on an individual's life, abilities and identity. Timely treatment of relapse is essential to reduce or prevent disability. Health care professionals need to coordinate care locally and nationally. Multi-disciplinary work is vital to promote adjustment, coping strategies and support for people living with NMO.

Для цитирования: Mutch Kerry, Methley Abigail, Moore Phil, Jacob Anu. Life on hold: the experience of living with neuromyelitis optica.. Disability and rehabilitation. 2013. DOI: 10.3109/09638288.2013.833301.

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