If you have lichen sclerosus, or care for or treat someone who does, this survey is for you.
The James Lind Alliance Lichen Sclerosus Priority Setting Partnership (PSP) has been set up to identify and prioritise research questions that are important to people who have lichen sclerosus, the people who care for them, and the health professionals who treat them.
The project is funded by the British Society for the Study of Vulval Disease (BSSVD) and co‐ordinated through the Centre of Evidence Based Dermatology.
Researchers are asking people with experience of lichen sclerosus, as a patient, parent, carer, partner or health professional, to complete the survey.
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