{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,21]],"date-time":"2026-08-21T11:53:59Z","timestamp":1787313239520,"version":"build-2736575974"},"reference-count":57,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2020,10,15]],"date-time":"2020-10-15T00:00:00Z","timestamp":1602720000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["bpspsychub.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["British J Health Psychol"],"published-print":{"date-parts":[[2021,5]]},"abstract":"<jats:sec>\n                    <jats:title>Objectives<\/jats:title>\n                    <jats:p>With few empirically supported treatments, functional movement disorders (FMD) can be challenging to manage. To enable service providers to better support people with FMD, this study sought to understand the lived experience of FMD: to gain insight into how individuals make sense of their experience from symptom onset through medical evaluation and diagnosis to post\u2010diagnostic adaptation.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Design<\/jats:title>\n                    <jats:p>An interpretative phenomenological analysis (IPA) of patient accounts of living with FMD.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>Eight participants were recruited from a UK teaching hospital adult neurology service: seven females, varying in age (20s\u201070s), FMD symptom type (tremor, dystonia, and tics), and time to diagnosis (10 \u2010 192\u00a0months). Semi\u2010structured interviews facilitated participant accounts of key events. Interviews lasted 75\u2010125\u00a0minutes and were transcribed verbatim.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>Three super\u2010ordinate themes were apparent. The first covered the experiences of onset (\u2018Something is wrong with me\u2019), including loss of control \u2010 with the affected body part often described as a separate entity \u2010 threats to identity and disturbance in relationships. \u2018At last! What now?\u2019 outlined the bittersweet experience of diagnosis and of treatments. Third, \u2018Living my life with it\u2019 incorporated ongoing experiences of coping with symptoms. While some continued to struggle with the emotional impact of symptoms, others developed a compassionate relationship with their self and maintained satisfying activities.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>FMD has a significant impact on patients\u2019 relationships with themselves and others, which in turn affects well\u2010being. These findings suggest some nuanced additions to interventions (diagnosis, psychotherapy, physiotherapy, public education.)<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/bjhp.12478","type":"journal-article","created":{"date-parts":[[2020,10,15]],"date-time":"2020-10-15T11:35:54Z","timestamp":1602761754000},"page":"325-342","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":29,"title":["What is it like to live with a functional movement disorder? 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