ECTRIMS launch for new patient-centred initiative
Today at ECTRIMS, the European Charcot Foundation together with the MS International Federation and Italian MS Society launched a new global initiative to put the patient experience at the heart of research and healthcare for MS. The Italian MS Society will act as the lead agency for, and on behalf of the Global MSIF Movement.
The Patient Reported Outcomes Initiative for MS (PROMS) will bring together the global MS community, people with and affected by MS, healthcare workers and researchers, healthcare industry and many more- to enable science with and of patient input in research, clinical trials of new therapies, and the design of healthcare systems.
Read the full Press Release for further information – Global initiative to integrate patient input in MS research and care
The NZ Multiple Sclerosis Research Trust looks forward to following the development of this and the beneficial outcomes for people with MS.