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Living the journey to school: Conceptual asymmetry between parents and planners on the journey to school

Social science & medicine (1982), 2021-09, Vol.284, p.114237-114237, Article 114237

2021

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Exploring illness identity among children and youth living with cancer: A narrative review

Pediatric blood & cancer, 2021-11, Vol.68 (11), p.e29251-n/a

2021

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Contemplating art and identity during a research study: Reflections on working with a youth with cancer

Pediatric blood & cancer, 2021-08, Vol.68 (8), p.e29059-n/a

2021

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The Unspeakable Nature of Death & Dying During Childhood: A Silenced Phenomenon in Pediatric Care

Omega: Journal of Death and Dying, 2024-05, Vol.89 (1), p.88-107

2024

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Therapeutic endings: Reflections on the termination of counselling-based research relationships among patients with cystic fibrosis and their caregivers

Time & society, 2019-02, Vol.28 (1), p.358-374

Moola, Fiona J

2019

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Illness conversations: Self-disclosure among children and youth with chronic illnesses

Chronic Illness, 2023-09, Vol.19 (3), p.475-494

2023

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Anything but simple: the disclosure practices of children with cancer in residential camp and non-camp settings

Children's health care, 2023-04, Vol.52 (2), p.151-172

2023

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Using photo-elicitation to explore health promotion concepts with children and adolescents with disabilities: a rapid scoping review

Disability and rehabilitation, 2022-09, Vol.44 (19), p.5708-5718

2022

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Moving beyond narrative archetypes among children with cancer

Children & society, 2022-11, Vol.36 (6), p.1262-1279

2022

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What's "quickest and easiest?": parental decision making about school trip mode

The international journal of behavioral nutrition and physical activity, 2010-08, Vol.7 (1), p.62-62

2010

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Ensuring long‐term benefits of camp for children with chronic illnesses?

Developmental medicine and child neurology, 2019-12, Vol.61 (12), p.1355-1355

2019

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“A place to call our own”: The impact of camp experiences on the psychosocial wellbeing of children and youth affected by cancer – A narrative review

Complementary therapies in clinical practice, 2019-08, Vol.36, p.18-28

2019

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This is the Best Fatal Illness That You Can Have: Contrasting and Comparing the Experiences of Parenting Youth With Cystic Fibrosis and Congenital Heart Disease

Qualitative health research, 2012-02, Vol.22 (2), p.212-225

Moola, Fiona J.

2012

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The weight of (the) matter: A new material feminist account of thin and fat oppressions

Health (London, England : 1997), 2019-09, Vol.23 (5), p.497-515

2019

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Listening to the Margins: Reflecting on Lessons Learned From a National Conference Focused on Establishing a Qualitative Research Platform for Childhood Disability and Race

International journal of qualitative methods, 2023-01, Vol.22, p.160940692311513

2023

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On judgement day: Anorexic and obese women’s phenomenological experience of the body, food and eating

Feminism & psychology, 2017-08, Vol.27 (3), p.259-279

2017

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The Road to the Ivory Tower: The Learning Experiences of Students with Disabilities at the University of Manitoba

Qualitative research in education, 2015-02, Vol.4 (1), p.45-70

Moola, Fiona J.

2015

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A Therapeutic Recreation Camp for Children with Congenital Heart Disease: Examining Impact on the Psychosocial Well-Being of Parents

Journal of child and family studies, 2016-10, Vol.25 (10), p.3034-3043

2016

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Telling My Tale: Reflections on the Process of Visual Storytelling for Children and Youth Living With Cystic Fibrosis and Muscular Dystrophy in Canada

International journal of qualitative methods, 2020, Vol.19, p.160940691989891

2020

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Speaking on behalf of the body and activity: Investigating the activity experiences of Canadian women living with anorexia nervosa

Mental health and physical activity, 2015-03, Vol.8, p.44-55

2015

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Portraits of Resistance: Exploring Intra-personal, Social, and Institutional Resistances through the Use of Arts-Based Research among Racialized Parents of Autistic Children and Youth

Studies in social justice, 2024-02, Vol.18 (1), p.103-124

2024

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Exercise in the care of patients with anorexia nervosa: A systematic review of the literature

Mental health and physical activity, 2013-06, Vol.6 (2), p.59-68

2013

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Physical Activity Counseling for Children With Cystic Fibrosis

Respiratory care, 2017-11, Vol.62 (11), p.1466-1473

2017

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The complexities of contagion: The experience of social isolation among children and youth living with cystic fibrosis in Canada

Journal of child health care, 2018-12, Vol.22 (4), p.631-645

Moola, Fiona

2018

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"No Time to Play": Perceptions toward Physical Activity in Youth with Cystic Fibrosis

Adapted physical activity quarterly, 2012-01, Vol.29 (1), p.44

2012

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Living the journey to school: Conceptual asymmetry between parents and planners on the journey to school

Exploring illness identity among children and youth living with cancer: A narrative review

Contemplating art and identity during a research study: Reflections on working with a youth with cancer

The Unspeakable Nature of Death & Dying During Childhood: A Silenced Phenomenon in Pediatric Care

Therapeutic endings: Reflections on the termination of counselling-based research relationships among patients with cystic fibrosis and their caregivers

Illness conversations: Self-disclosure among children and youth with chronic illnesses

Anything but simple: the disclosure practices of children with cancer in residential camp and non-camp settings

Using photo-elicitation to explore health promotion concepts with children and adolescents with disabilities: a rapid scoping review

Moving beyond narrative archetypes among children with cancer

What's "quickest and easiest?": parental decision making about school trip mode

Ensuring long‐term benefits of camp for children with chronic illnesses?

“A place to call our own”: The impact of camp experiences on the psychosocial wellbeing of children and youth affected by cancer – A narrative review

This is the Best Fatal Illness That You Can Have: Contrasting and Comparing the Experiences of Parenting Youth With Cystic Fibrosis and Congenital Heart Disease

The weight of (the) matter: A new material feminist account of thin and fat oppressions

Listening to the Margins: Reflecting on Lessons Learned From a National Conference Focused on Establishing a Qualitative Research Platform for Childhood Disability and Race

On judgement day: Anorexic and obese women’s phenomenological experience of the body, food and eating

The Road to the Ivory Tower: The Learning Experiences of Students with Disabilities at the University of Manitoba

A Therapeutic Recreation Camp for Children with Congenital Heart Disease: Examining Impact on the Psychosocial Well-Being of Parents

Telling My Tale: Reflections on the Process of Visual Storytelling for Children and Youth Living With Cystic Fibrosis and Muscular Dystrophy in Canada

Speaking on behalf of the body and activity: Investigating the activity experiences of Canadian women living with anorexia nervosa

Portraits of Resistance: Exploring Intra-personal, Social, and Institutional Resistances through the Use of Arts-Based Research among Racialized Parents of Autistic Children and Youth

Exercise in the care of patients with anorexia nervosa: A systematic review of the literature

Physical Activity Counseling for Children With Cystic Fibrosis

The complexities of contagion: The experience of social isolation among children and youth living with cystic fibrosis in Canada

"No Time to Play": Perceptions toward Physical Activity in Youth with Cystic Fibrosis

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