Cargando…

Exploring COVID‐19 experiences for persons with multiple sclerosis and carers: An Australian qualitative study

OBJECTIVE: The COVID‐19 pandemic continues to impact communities around the world. In this study, we explored the COVID‐19 experiences of persons with multiple sclerosis (MS) and carers. METHODS: Using a qualitative approach, interviews were undertaken with 27 participants residing in Australia (10...

Descripción completa

Detalles Bibliográficos
Autores principales:	Correia, Helen, Martin‐Lynch, Pamela, Finlayson, Marcia, Learmonth, Yvonne C.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2023
Materias:	Original Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10010087/ https://www.ncbi.nlm.nih.gov/pubmed/36639883 http://dx.doi.org/10.1111/hex.13704

Ejemplares similares

Multiple sclerosis patients need and want information on exercise promotion from healthcare providers: a qualitative study
por: Learmonth, Yvonne C., et al.
Publicado: (2016)

Identifying preferred format and source of exercise information in persons with multiple sclerosis that can be delivered by health‐care providers
por: Learmonth, Yvonne C., et al.
Publicado: (2017)

Is it worth it?: The experiences of persons with multiple sclerosis as they access health care to manage their condition
por: Pétrin, Julie, et al.
Publicado: (2020)

Patient violence towards their family carers: A qualitative exploration of carers’ experiences in psychosis
por: Wildman, E., et al.
Publicado: (2022)

Clinical Importance of Steps Taken per Day among Persons with Multiple Sclerosis
por: Motl, Robert W., et al.
Publicado: (2013)

Important considerations for feasibility studies in physical activity research involving persons with multiple sclerosis: a scoping systematic review and case study
por: Learmonth, Yvonne C., et al.
Publicado: (2017)

Personal identity and the role of ‘carer’ among relatives and friends of people with multiple sclerosis()
por: Hughes, Nic, et al.
Publicado: (2013)

The Lived Experience of Multiple Sclerosis Relapse: How Adults with Multiple Sclerosis Processed Their Relapse Experience and Evaluated Their Need for Postrelapse Care
por: Asano, Miho, et al.
Publicado: (2015)

Validation of patient determined disease steps (PDDS) scale scores in persons with multiple sclerosis
por: Learmonth, Yvonne C, et al.
Publicado: (2013)

‘You are just left to get on with it’: qualitative study of patient and carer experiences of the transition to secondary progressive multiple sclerosis
por: Davies, F, et al.
Publicado: (2015)

Social connectedness of carers: An Australian national survey of carers
por: Poon, Abner Weng Cheong, et al.
Publicado: (2022)

The effect of the Australian bushfires and the COVID-19 pandemic on health behaviours in people with multiple sclerosis
por: Marck, CH, et al.
Publicado: (2021)

A Qualitative Study Exploring the Experiences of Carers of Service Users With Complex Mental Health Needs
por: Saini, Pooja, et al.
Publicado: (2022)

Exercise Training for Multiple Sclerosis: A Narrative Review of History, Benefits, Safety, Guidelines, and Promotion
por: Learmonth, Yvonne Charlotte, et al.
Publicado: (2021)

Experiences of persons with multiple sclerosis with rehabilitation—a qualitative interview study
por: Ghaidar, Donya, et al.
Publicado: (2022)

Lived experience of persons with multiple sclerosis: A qualitative interview study
por: Persson, Sofia, et al.
Publicado: (2023)

Carers’ experiences of involvement in care planning: a qualitative exploration of the facilitators and barriers to engagement with mental health services
por: Cree, Lindsey, et al.
Publicado: (2015)

Personal experiences of home haemodialysis: patients’ and carers’ experiences
por: Maguire, Nick
Publicado: (2011)

Unmet Needs of People with Severe Multiple Sclerosis and Their Carers: Qualitative Findings for a Home-Based Intervention
por: Borreani, Claudia, et al.
Publicado: (2014)

Hidden caring, hidden carers? Exploring the experience of carers for people with long‐term conditions
por: Knowles, Sarah, et al.
Publicado: (2015)

The MoXFo Initiative: Using consensus methodology to move forward towards internationally shared vocabulary in multiple sclerosis exercise research
por: Mansoubi, Maedeh, et al.
Publicado: (2023)

Experiences of persons with Multiple Sclerosis with lifestyle adjustment–A qualitative interview study
por: Elkhalii-Wilhelm, Saskia, et al.
Publicado: (2022)

Family carers’ experiences of attending a multicomponent psychosocial intervention program for carers and persons with dementia
por: Johannessen, Aud, et al.
Publicado: (2015)

Accuracy of StepWatch™ and ActiGraph Accelerometers for Measuring Steps Taken among Persons with Multiple Sclerosis
por: Sandroff, Brian M., et al.
Publicado: (2014)

Social determinants of health in multiple sclerosis
por: Dobson, Ruth, et al.
Publicado: (2022)

Exploring the experiences and psychosocial support needs of informal carers of men with breast cancer: a qualitative study
por: Herring, Beth, et al.
Publicado: (2022)

Exploring the experience of reablement: A systematic review and qualitative evidence synthesis of older people's and carers' views
por: Mulquiny, Lachlan, et al.
Publicado: (2022)

A multi-site, randomized controlled trial of MS INFoRm, a fatigue self-management website for persons with multiple sclerosis: rationale and study protocol
por: Finlayson, Marcia, et al.
Publicado: (2019)

Experiences of persons with multiple sclerosis of a collaborative care programme: A qualitative study
por: Payamani, Firuzeh, et al.
Publicado: (2023)

Carers Create: Carer perspectives of a creative programme for people with dementia and their carers on the relationship within the (carer and cared-for) dyad
por: Skingley, Ann, et al.
Publicado: (2020)

Exploring the Views and Dietary Practices of Older People at Risk of Malnutrition and Their Carers: A Qualitative Study
por: Avgerinou, Christina, et al.
Publicado: (2019)

Qualitative investigation of patient and carer experiences of everyday legal needs towards end of life
por: Close, Helen, et al.
Publicado: (2021)

Financial, opportunity and psychosocial costs of spinal muscular atrophy: an exploratory qualitative analysis of Australian carer perspectives
por: Farrar, Michelle A, et al.
Publicado: (2018)

Advance care planning in amyotrophic lateral sclerosis (ALS): study protocol for a qualitative longitudinal study with persons with ALS and their family carers
por: Vandenbogaerde, Isabel, et al.
Publicado: (2022)

A qualitative exploration of the physical and psychological wellbeing of family carers of veterans in Australia
por: Post, Dannielle, et al.
Publicado: (2022)

Dealing with Chronic Illness: Experiences of Iranian Families of Persons with Multiple Sclerosis—A Qualitative Study
por: Ebrahimi, Hossein, et al.
Publicado: (2017)

A Qualitative Study to Explore the Employment Experiences and Perspectives of Women Living with Multiple Sclerosis in the UK
por: Railton, Cathie, et al.
Publicado: (2022)

Exploring a collaborative approach to the involvement of patients, carers and the public in the initial education and training of healthcare professionals: A qualitative study of patient experiences
por: Scott, Lesley, et al.
Publicado: (2021)

REFRESH protocol: a non-inferiority randomised clinical trial comparing internet and teleconference to in-person ‘Managing Fatigue’ interventions on the impact of fatigue among persons with multiple sclerosis
por: Plow, Matthew, et al.
Publicado: (2020)

Meta-Analysis of Three Different Types of Fatigue Management Interventions for People with Multiple Sclerosis: Exercise, Education, and Medication
por: Asano, Miho, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_l7igsc3i6pjkm3fri625e0lq68