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The CF in Africa Research Network exists to advance equitable diagnosis, care, and research so that every person living with cystic fibrosis in Africa is seen, supported, and included.

Doctor Examining Child

Vision

A future in which cystic fibrosis is recognized, accurately diagnosed, and sustainably managed within African health systems, with patients, families, and local leaders at the center.

Doctor Examining Child
Child's Health Checkup

Mission

We aim to advance equitable diagnosis, care, and research for people living with cystic fibrosis across Africa through collaboration, locally led research, and shared learning. Our vision is a continent where cystic fibrosis is recognized, accurately diagnosed, and managed within sustainable health systems that center patients, families, and African clinical and research leadership.

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Coordinating Circle:

Dr. Marco Zampoli- Director, Network Registry, Advocacy and Clinical Collaboration



Dr. Hugues Abriel, Director, Network Research Coordination




Dr. Leah Ratner, Director of Network Integration



Muriel Helmers - Director, Pan-African CF Registry



Dr. Seyram Wordui- Associate Director, Advocacy and Clinical Collaboration




Dr. Sheila Agyeiwaa Owusu- Associate Director of Data and Evidence 





Co-leads, Clinical Collaboration
                Dr. Areej Dakshi and Dr Abate Yeshidinber  Weldetsadik

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