Gender-aware Parkinson’s care: a design-based study of patient perspectives on gender norms and gender-sensitive care

Göttgens, Irene; Modderkolk, Linda; Vermuë, Paula; Darweesh, Sirwan K.L.; Bloem, Bastiaan R.; Oertelt-Prigione, Sabine

doi:10.1016/j.eclinm.2023.102285

Cited by 2 publications

(1 citation statement)

References 54 publications

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“…All were White, English speaking and educated, with over half retired/medically retired. The promotion of an intersectional approach that emphasises the intersectionality of PD with other contextual aspects such as ethnicity and socioeconomic status [ 79 , 80 ] and disease characteristics (stages of disease progression [ 81 ], age at PD onset [ 82 ]) could offer additional insights into the impact of NMS. Moreover, those who took part likely had a general interest in NMS, compared to other persons with PD.…”

Section: Discussionmentioning

confidence: 99%

Experiences of Living With the Nonmotor Symptoms of Parkinson's Disease: A Photovoice Study

Smith,

Callis,

Bridger‐Smart

et al. 2024

Health Expectations

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BackgroundNonmotor symptoms (NMSs) are frequently experienced by people with Parkinson's disease (PD) and are often perceived as their most bothersome symptoms. However, these remain poorly understood with suboptimal clinical management. These unmet needs are an important determinant of health‐related quality of life (QoL) in PD.ObjectiveThe aim of this study was to gain insights into the experience of living with the NMS of PD in real‐time using participatory action methodology.MethodUsing the photovoice method, 14 people with PD took photographs to document their experiences of living with the NMS of PD. They composed corresponding written narratives to capture the impact of NMS on their daily activities and QoL. In total, 152 photographs and corresponding narratives were analysed using thematic analysis with an inductive approach.ResultsFour interrelated themes were identified. Emotional well‐being and sense of self encompassed a process of adjustment to living with PD. Engaging in valued activities, adopting a positive mindset and utilising coping strategies were thought to enhance confidence and self‐esteem. Social support and societal awareness highlighted the importance of supportive relationships and socialising to aid participation and avoid isolation. Barriers to social engagement included the unpredictability of NMS and nonvisible NMS being neglected or misunderstood.ConclusionFindings demonstrated the far‐reaching impact of nonmotor aspects of PD on emotional, occupational and social dimensions. These needs could be addressed through person‐centred and comprehensive approaches to care.Patient or Public ContributionThis study utilised a participatory research approach allowing participants to choose the subjects that mattered to them and how to present their results. Additionally, a group workshop was held with people with PD, their family members and healthcare professionals to guide theme development.

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