13/03/2026
Great to be asked to be involved in this blog from the European Committee for Treatment & Research in Multiple Sclerosis team!
Follow the link to read what Register lead Dr Rod Middleton has to say about patient registries and their importance in real-world research.
Patient registries may sound technical, but they are actually one of the easiest ways people living with a long-term condition can get involved in research. By sharing their own experiences of everyday life, either directly or via their healthcare team, they can help researchers find answers to ques...