*Disclaimer: This video is for educational and entertainment purposes only. Please consult with your medical provider before making any changes to your health plan.
In today's video, I am joined by Dr. Sophie Rees to discuss her research on missed opportunities in the diagnosis, care, and education of people with lichen sclerosus.
Sophie Rees is a medical sociologist and applied health researcher whose main research interests are vulval disease, especially LS, based at the University of Bristol in the UK. She was Chief Investigator of a mixed methods study called ‘Living with Lichen Sclerosus’ that explored the experience of people with LS using interviews, focus groups, and a survey. She produced a short film based on the interview findings, which is aimed at healthcare professionals to help them understand what it is like to live with LS.
Follow Dr. Rees on Instagram and Twitter as @drsophierees
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Time Stamps:
0:00 - Introduction
2:20 - What motivated Sophie to work in vulvar health and what drives her to continue in this field
6:00 - What is qualitative research
10:20 - What motivated the study
13:00 - Who was included
18:21 - Missed opportunities and lichen sclerosus
34:50 - Living a secret life with lichen sclerosus
45:34 - Living with a chronic condition affecting the vulva
54:18 - Clinical implications of missed opportunities and lichen sclerosus
58:30 - Study limitations
1:00:55 - Summary and outro
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Негізгі бет Missed Opportunities in Lichen Sclerosus Diagnosis, Care, and Education. Feat. Dr. Sophie Rees
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