The Bullous Pemphigoid patient journey output from the ePAGS (European Patient Advocacy Groups) is now available.
This journey includes and reflects the experiences of patients throughout the UK & Europe and is the result of a collaborative work between BP patients, their carers and health care professionals, mainly our doctors.
These journeys are used by doctors so that they can be informed of what patients really experience about the disease and its treatments, and know how to inform in return their own patients in regards to their of quality of life. Click here
A shorter version as well as a visual one should be available soon.