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Fiona Juliet Rosalind Eccles

University of Lancaster

United Kingdom

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Research Interests

Psychiatry

40%

Clinical Psychology

60%

Covid-19

40%

Parkinson's Disease

40%

Mental Illness

30%

Health Psychology

30%

Major Depressive Disorder

30%

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Articles20

Predictors of Informal Caregiver Burden in Parkinson’s

Article Link

Year:

2025

Navigating the social world with neck dystonia

Article Link

Year:

2025

“A young person in an old person’s body”

Article Link

Year:

2025

The association between body image and psychological outcomes in multiple sclerosis

Article Link

Year:

2025

Stigma, coping strategies, distress and wellbeing in individuals with cervical dystonia: a cross-sectional study

Article Link

Year:

2024

A systematic review of the factors associated with the psychological wellbeing of people with Parkinson’s in the COVID-19 pandemic

Article Link

Year:

2024

Maintaining psychological well‐being when living at risk of Huntington's disease: An interpretative phenomenological analysis

Article Link

Year:

2024

Alexithymia and illness perceptions in persons with multiple sclerosis and their partners

Article Link

Year:

2024

Living with functional movement disorders: a tale of three battles.

Article Link

Year:

2024

Coping with Tourette’s syndrome: a meta-ethnography of individual and family perspectives

Article Link

Year:

2024

“I Feel Like I Work Full-Time for Parkinson’s”: A Longitudinal Interpretative Phenomenological Analysis of the Experiences of Parkinson’s Informal Caregivers during COVID-19 in England

Article Link

Year:

2023

Stigma, self-compassion, and psychological distress among people with Parkinson’s

Article Link

Year:

2023

‘It's a double whammy’: A qualitative study of illness uncertainty in individuals with Parkinson's disease in the context of COVID-19

Article Link

Year:

2022

Using a Clinical Formulation to Understand Psychological Distress in People Affected by Huntington’s Disease: A Descriptive, Evidence-Based Model

Article Link

Year:

2022

More than Just a Brain Disorder: A Five-Point Manifesto for Psychological Care for People with Huntington’s Disease

Article Link

Year:

2022

Healthcare professionals’ involvement in breaking bad news to newly diagnosed patients with motor neurodegenerative conditions

Article Link

Year:

2021

Impacts of COVID-19 lockdowns on frailty and wellbeing in older people and those living with long-term conditions

Article Link

Year:

2021

Adjusting to living with Parkinson’s disease; a meta-ethnography of qualitative research

Article Link

Year:

2021

Psychological interventions for people with Parkinson’s disease in the early 2020s

Article Link

Year:

2021

Factors predicting first appointment attendance at a Traumatic Brain Injury clinical neuropsychology outpatient clinic

Article Link

Year:

2021

Collaborators12

Jane Simpson

University of Lancaster

UNITED KINGDOM

Guillermo Perez Algorta

University of Lancaster

UNITED KINGDOM

Sofia Triliva

GREECE

Ian Fletcher

University of Lancaster

UNITED KINGDOM

Craig Murray

University of Lancaster

UNITED KINGDOM

Fiadhnait O'Keeffe

Senior Lecturer and Principal Specialist Neuropsychologist

University College Cork

IRELAND

Calum Marr

The Queen's University Belfast

UNITED KINGDOM

Antonina Luca

Professore Associato

Università degli Studi di Enna Kore

ITALY

Sandra Varey

University of Lancaster

UNITED KINGDOM

Sarah Gunn

Lecturer in Clinical Psychology

University of Leicester

UNITED KINGDOM

Nicolò Zarotti

University of Lancaster

UNITED KINGDOM

Carol Holland

University of Lancaster

UNITED KINGDOM

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Fiona Juliet Rosalind Eccles

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Research Interests

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Articles20

Predictors of Informal Caregiver Burden in Parkinson’s

Navigating the social world with neck dystonia

“A young person in an old person’s body”

The association between body image and psychological outcomes in multiple sclerosis

Stigma, coping strategies, distress and wellbeing in individuals with cervical dystonia: a cross-sectional study

A systematic review of the factors associated with the psychological wellbeing of people with Parkinson’s in the COVID-19 pandemic

Maintaining psychological well‐being when living at risk of Huntington's disease: An interpretative phenomenological analysis

Alexithymia and illness perceptions in persons with multiple sclerosis and their partners

Living with functional movement disorders: a tale of three battles.

Coping with Tourette’s syndrome: a meta-ethnography of individual and family perspectives

“I Feel Like I Work Full-Time for Parkinson’s”: A Longitudinal Interpretative Phenomenological Analysis of the Experiences of Parkinson’s Informal Caregivers during COVID-19 in England

Stigma, self-compassion, and psychological distress among people with Parkinson’s

‘It's a double whammy’: A qualitative study of illness uncertainty in individuals with Parkinson's disease in the context of COVID-19

Using a Clinical Formulation to Understand Psychological Distress in People Affected by Huntington’s Disease: A Descriptive, Evidence-Based Model

More than Just a Brain Disorder: A Five-Point Manifesto for Psychological Care for People with Huntington&rsquo;s Disease

Healthcare professionals’ involvement in breaking bad news to newly diagnosed patients with motor neurodegenerative conditions

Impacts of COVID-19 lockdowns on frailty and wellbeing in older people and those living with long-term conditions

Adjusting to living with Parkinson’s disease; a meta-ethnography of qualitative research

Psychological interventions for people with Parkinson’s disease in the early 2020s

Factors predicting first appointment attendance at a Traumatic Brain Injury clinical neuropsychology outpatient clinic

Collaborators12

Jane Simpson

Guillermo Perez Algorta

Sofia Triliva

Ian Fletcher

Craig Murray

Fiadhnait O'Keeffe

Calum Marr

Antonina Luca

Sandra Varey

Sarah Gunn

Nicolò Zarotti

Carol Holland

How do I reach out?

More than Just a Brain Disorder: A Five-Point Manifesto for Psychological Care for People with Huntington’s Disease