The Hair Loss Priority Setting Partnership (PSP) Survey opens from today and is available until 31 October.
The PSP is a chance for people with alopecia to influence the priorities for research into treatments for the condition. The PSP survey is an opportunity for people affected by hair loss and people involved in treating hair loss to have their say on existing treatments and what improvements they’d like to see in research.
The PSP is an initiative steered by leading UK clinicians, patients, Alopecia UK, the British Hair & Nail Society and The James Lind Alliance.
You can find further information about the PSP on our website, which details of who is part of the steering group, the PSP partners and other useful information, including a Q&A page.
This is a fantastic opportunity for those with alopecia to make their voice heard and their opinion count. Please ‘get involved’ and complete the survey. Opportunities like this are rare, so please don’t miss your chance to have your say!
Click here to take you directly to the survey.