How Does A Priority Setting Partnership Work?
First of all, we asked everyone affected by psoriasis - individuals who live with it, their families and friends, and the healthcare professionals who treat them - to give us three 'questions' about psoriasis and its treatment that they feel need to be researched.
We are now sorting through the responses to the survey, and producing a list of the questions submitted to us. After this, we will ask people to take part in a second survey to go through the list of nominated questions unanswered by research, to tell us which they think are the most important. It is up to you whether you would like to take part in the second survey. You can tell us on the first survey if you are happy for us to contact you again.
After we have gathered the information from the second survey, we will invite people with psoriasis, their families and health professionals, to a workshop to discuss and prioritise the top ten questions. This top ten will then be published,