The Middle East CF Association is a nonprofit organization registered in Massachusets, USA. MECFA is governed by a Board of Trustees who manage the day to day operations working to support the MECFA Medical and Scientific Committee. The MECFA Medical and Scientific Committee is a community of clinical professionals committed to improving the survival and quality of life for people born with cystic fibrosis in the Middle East.
MECFA plays an important role in developing a network between CF health professionals, patients, and other groups affiliated with a rare disease. Our members engage in high-quality medical practice treating cystic fibrosis patients, they guide research, newborn screening, and data collection and work towards implementing EU and NA CF standards of care in the Middle East.
MECFA offers opportunities that help translate scientific and medical progress into the efficient delivery of effective medical care. MECFA works to develop resources that guide our members in advancing CF care in the region.
The MECFA mission is to improve the health outcomes of cystic fibrosis patients in the Middle East.
All patients born with cystic fibrosis living in the Middle East and surrounding countries are diagnosed early and have access to quality care, medication, and equipment that extends their life expectancy and quality of life.
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