Research

FibroIreland has supported several research projects and hopes to see the development of a patient registry. A patient registry is a collection (for one or more purposes) of standardised information about a group of patients who share a condition or experience. One of the current blocks to more research on fibromyalgia happening, is that there is no patient registry.

WE AIM TO:

  • Develop a patient registry
  • Find better treatment options for FM
  • Support researchers who take an interest FM