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Hair Loss PSP questions in review stage

In November 2014, the Hair loss PSP, funded by Alopecia UK and initiated by the British Hair and Nail Society, closed its initial on-line survey. We had 912 survey responders – 81 percent were completed by patients, or carers, and 12.6 percent by healthcare professionals or organisations.

Published: 14 October 2015

Latest news from Priority Setting Partnerships shared learning group

In 2014, we completed our JLA PSP, which set out to identify the top 10 research priorities for Parkinson’s. The process itself was a fairly daunting task but the real challenge has been how to take these priorities forward within the funding and research world.

Published: 08 October 2015