THEREFORME
Publishing and promoting evidence-based information about Myalgic Encephalomyelitis (ME), related health & social care policy, and lived experience of the conditionRaising awareness among the public, media, healthcare professionals & decision-makersCampaigning for patient safety, biomedical research and improvements in the provision of health, education & social care for people living with ME
Objects
THE OBJECTS OF THE CIO ARE, FOR THE PUBLIC BENEFIT, TO ADVANCE HEALTH AND RELIEVE SICKNESS AND DISABILITY AMONG PERSONS LIVING WITH MYALGIC ENCEPHALOMYELITIS (ME) AND RELATED OR CO-MORBID CONDITIONS; AND THE RELIEF OF THOSE IN NEED WHO ARE LIVING WITH, OR AFFECTED BY, ME AND RELATED OR CO-MORBID CONDITIONS, INCLUDING THEIR FAMILIES AND CARERS; IN PARTICULAR BUT NOT EXCLUSIVELY BY: (A) PUBLISHING AND PROMOTING EVIDENCE-BASED INFORMATION ABOUT ME, RELATED HEALTH AND SOCIAL CARE POLICY, AND LIVED EXPERIENCE OF THE CONDITION;(B) RAISING AWARENESS AMONG THE PUBLIC, MEDIA, HEALTHCARE PROFESSIONALS AND DECISION-MAKERS; AND (C) CAMPAIGNING FOR PATIENT SAFETY, BIOMEDICAL RESEARCH AND IMPROVEMENTS IN THE PROVISION OF HEALTH, EDUCATION AND SOCIAL CARE FOR PEOPLE LIVING WITH ME.
Trustees
- Karen Hargravechair
- Emma Gore-Lloyd
- Jonathan Scorer
- Kimberly Brown
- Melanie Archer
- Nigel Taylor
- Rosie May Barrett
- Suzanne Russell
- Veronique Marie Clemence Barbelet