Dr Suzanne Nevin

Post-doctoral researcher / Lecturer

UNSW Sydney

Australia

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About

Dr. Suzanne Nevin is a Post-doctoral researcher and Lecturer at UNSW Sydney, Australia. Her research primarily focuses on the psychosocial aspects of healthcare, particularly related to children with dementia, cancer, and neurological impairments. She has contributed to various studies examining caregiver quality of life, psychosocial oncology, and the impact of digital health on childhood cancer survivors.

Articles (17)

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2025

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2025

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2024

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2024

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2024

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2024

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2024

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2022

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2022

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2022

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2022

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2022

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2022

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2022

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2022

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2022

Collaborators (3)

Kate Hetherington

UNSW Sydney

AUSTRALIA

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Deepak Gill

Clinical Senior lecturer

University of Sydney

AUSTRALIA

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Richard Cohn

Professor

UNSW Sydney

AUSTRALIA

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Dr Suzanne Nevin

Research Interests

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About

Articles (17)

Bridging the Gap: Embedding Psychosocial Oncology Research into Comprehensive Cancer Care for Children and Young People

'Fighting every day': Exploring caregiver quality of life and perspectives on healthcare services for children with dementia - A cross-sectional, mixed-methods study

Psychosocial experiences of clinicians providing care for children with severe neurological impairment

Neurodevelopmental outcomes in a cohort of Australian families with self-limited familial epilepsy of neonatal/infantile onset

Exploring childhood cancer survivor, parent, healthcare and community professionals’ experiences of, and priorities for, using digital health to engage in physical activity: a mixed methods study

Family planning and preimplantation testing: family experiences in congenital adrenal hyperplasia

Social Anxiety Symptoms in Adolescents and Young Adults Recently Diagnosed with Cancer

The psychosocial impact of childhood dementia on children and their parents: a systematic review

Hearing parents' voices: A priority-setting workshop to inform a suite of psychological resources for parents of children with rare genetic epilepsies

Acceptability and feasibility of an online information linker service for caregivers who have a child with genetic epilepsy: a mixed-method pilot study protocol

Hope in the uncertainties and certainty for parents of children with rare neurological disorders. Part I (of 3): Uncertainty

Hope in the uncertainties and certainty for parents of children with rare neurological disorders: Part 2 (of 3): Certainty

Hope in the uncertainties and certainty for parents of children with rare neurological disorders: Part 3 (of 3): Hope

Genetic Testing in the Pediatric Nephrology Clinic: Understanding Families' Experiences

Piloting positive psychology resources for caregivers of a child with a genetic developmental and epileptic encephalopathy

The opinions and experiences of people with intellectual disability regarding genetic testing and genetic medicine: A systematic review

Psychosocial impact of genetic testing on parents of children with developmental and epileptic encephalopathy

Collaborators (3)

Kate Hetherington

Deepak Gill

Richard Cohn

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