Fiona Juliet Rosalind Eccles

University of Lancaster

United Kingdom

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Articles (20)

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2025

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2025

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2022

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2021

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2021

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2021

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2021

Collaborators (12)

Jane Simpson

University of Lancaster

UNITED KINGDOM

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Guillermo Perez Algorta

University of Lancaster

UNITED KINGDOM

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Sofia Triliva

GREECE

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Ian Fletcher

University of Lancaster

UNITED KINGDOM

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Craig Murray

University of Lancaster

UNITED KINGDOM

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Fiadhnait O'Keeffe

Senior Lecturer and Principal Specialist Neuropsychologist

University College Cork

IRELAND

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Calum Marr

The Queen's University Belfast

UNITED KINGDOM

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Antonina Luca

Professore Associato

Università degli Studi di Enna Kore

ITALY

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Sandra Varey

University of Lancaster

UNITED KINGDOM

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Sarah Gunn

Lecturer in Clinical Psychology

University of Leicester

UNITED KINGDOM

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Nicolò Zarotti

University of Lancaster

UNITED KINGDOM

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Carol Holland

University of Lancaster

UNITED KINGDOM

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Fiona Juliet Rosalind Eccles

Research Interests

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Articles (20)

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’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

Collaborators (12)

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

Make your next move.

Fiona Juliet Rosalind Eccles

Research Interests

Explore related searches

Contact this professor

Articles (20)

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

Collaborators (12)

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

Make your next move.

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