Exploring Sources of Emotional Distress among People Living with Scleroderma: A Focus Group Study

• Published in: PloS one Vol. 11; no. 3; p. e0152419
• Main Authors: Gumuchian, Stephanie T, Peláez, Sandra, Delisle, Vanessa C, Carrier, Marie-Eve, Jewett, Lisa R, El-Baalbaki, Ghassan, Fortune, Catherine, Hudson, Marie, Impens, Ann, Körner, Annett, Persmann, Jennifer, Kwakkenbos, Linda, Bartlett, Susan J, Thombs, Brett D
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 23.03.2016; Public Library of Science (PLoS)
• Subjects: Anxiety; Biology and Life Sciences; Connective tissues; Content analysis; Cost of Illness; Counseling psychology; Disease control; Emotions; Employment - psychology; Family - psychology; Female; Focus Groups; Health aspects; Health care; Hospitals; Humans; Interviews; Male; Medical research; Medicine and Health Sciences; Middle Aged; Nursing; Patients; People and Places; Psychiatry; Psychological aspects; Psychology; Qualitative research; Risk factors; Scleroderma; Scleroderma (Disease); Scleroderma, Systemic - psychology; Self image; Skin; Social factors; Social interactions; Social Sciences; Stress (Psychology); Stress, Psychological - etiology; Stress, Psychological - psychology; Systemic sclerosis; United Kingdom > UK; Canada
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0152419

Systemic sclerosis, or scleroderma, is a chronic and rare connective tissue disease with negative physical and psychological implications. Sources of emotional distress and the impact they have on the lives of people with scleroderma are not well understood. To gain an in-depth understanding of the emotional experiences and sources of emotional distress for women and men living with scleroderma through focus group discussions. Three semi-structured focus group discussions were conducted (two in English, one in French) with a total of 22 people with scleroderma recruited through the Scleroderma Society of Ontario in Hamilton, Ontario and a scleroderma clinic in Montreal, Canada. Interviews were recorded, transcribed, and then coded for emerging themes using thematic inductive analysis. Core themes representing sources of emotional distress were identified, including: (a) facing a new reality; (b) the daily struggle of living with scleroderma; (c) handling work, employment and general financial burden; (d) changing family roles; (e) social interactions; and (f) navigating the health care system. Collectively, these themes refer to the stressful journey of living with scleroderma including the obstacles faced and the emotional experiences beginning prior to receiving a diagnosis and continuing throughout the participants' lives. Scleroderma was portrayed as being an unpredictable and overwhelming disease, resulting in many individuals experiencing multiple sources of emotional distress. Interventions and supportive resources need to be developed to help individuals with scleroderma and people close to them manage and cope with the emotional aspects of the disease.