Exploring the Life Experiences of Bell’s Palsy Patients: A Qualitative Study
Year 2025,
Volume: 35 Issue: 2, 95 - 102, 11.06.2025
İlknur Özkan
,
Murat Kar
,
Seçil Taylan
Abstract
Objective: Bell’s palsy is the most common type of peripheral facial paralysis. The sudden onset and unknown cause of Bell’s palsy lead to significant psychological distress and social disabilities in patients, which can severely impact their quality of life. This study aimed to explore the experiences of patients with Bell’s palsy using a qualitative approach to gain a better understanding of the outcomes from the patient’s perspectives.
Material and Methods: This study was conducted as a qualitative research employing a hermeneutic phenomenological framework. Inductive thematic analysis was used for data analysis
Results: The study included a total of 11 participants (six females and five males) from different phases of Bell’s palsy. Because of the inductive thematic analysis, the experiences of patients with Bell’s palsy were categorised into six main themes: “First Confrontation with Bell’s Palsy,” “Treatment and Self-Management Experiences”, “Physical Challenges Experienced”, “Psychological Effects”, “Social Effects”, and “Impact of Bell’s Palsy on Today”
Conclusion: Bell’s palsy is understood to be a traumatic experience that affects the physiological, psycho logical, and social aspects of patients’ lives, thereby significantly impacting their quality of life. Although patients receive medical treatment for Bell’s palsy, they often face the physiological and psychological challenges alone. Therefore, treatment should not be solely prescription-based; it must address the physiological, psychological, and social challenges through an interdisciplinary approach, including the involvement of nurses.
Ethical Statement
The ethics board approval for the study was collected from a University Clinical Research Ethics Board (protocol no: KAEK-39). Participants’ written and oral consent was collected after informing them.
Supporting Institution
This research received no specific grant from funding agencies in the public, commercial or not-for-profit sectors.
Thanks
We express our gratitude to the patients who participated in the completion of this study.
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Year 2025,
Volume: 35 Issue: 2, 95 - 102, 11.06.2025
İlknur Özkan
,
Murat Kar
,
Seçil Taylan
References
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- Muhammad Kassim N, Abdullahi A, Usman JS. Relationship Between Psychological Symptoms, Age, Severity of Symptoms, and Societal Integration in Patients With Facial Nerve Paralysis. Iranian Rehabilitation Journal 2019;17(3):235-40. google scholar
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- Silva MFF, Cunha MC, Lazarini PR, Fouquet ML. Psychological contents and social effects associated to peripheral facial paralysis: a speech-language approach. Int Arch Otorhinolaryngol 2011;15(4):450-60. google scholar
- Mooney T. Diagnosis and management of patients with Bell's palsy. Nurs Stand 2013;28(14):44-9. google scholar
- Sarhan F, Saif A, Saif D. Bell's palsy: an overview. British J Neuroscience Nursing 2012;8(4):163-8. google scholar
- Walker DT, Hallam MJ, Ni Mhurchadha S, McCabe P, Nduka C. The psychosocial impact of facial palsy: our experience in one hundred and twenty six patients. Clin Otolaryngol 2012;37(6):474-7. google scholar
- Newell R, Marks I. Phobic nature of social difficulty in facially disfigured people. Br J Psychiatry 2000;176(2):177-81. google scholar
- Kim JH, Fisher LM, Reder L, Hapner ER, Pepper JP. Speech and communicative participation in patients with facial paralysis. JAMA Otolaryngol Head Neck Surg 2018;144(8):686-93. google scholar