Welcome to IPOPI...

IPOPI is the Association of national patient organisations dedicated to improving awareness, access to early diagnosis and optimal treatments for primary immunodeficiency (PID) patients worldwide

Established in 1992, IPOPI works as the global advocate for the PID patient community in cooperation with its National Member Organisations (NMOs) and key PID stakeholders.

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  • Patients' family camp in Sweden
  • Global Leaders Meeting – London, UK
  • A patients and physicians awareness event in Belgium
  • 2nd PID Forum - EU Parliament
  • Family weekend in Wernigerode Germany
Improving awareness, access to early diagnosis and optimal treatments for PID patients worldwide

News

Jan 19, 2012
The European Commission published its work plan for 2012 for the second programme of Community action in the field of health. The work plan sets out the activities to be co-financed from the work plan
Jan 16, 2012
PLUS, the Plaftorm of Plasma Protein Users, organised its 3rd Stakeholders consensus meeting in Dublin, Ireland on 12-13 January.

Publications

Jan 19, 2012
IPOPI has published three information leaflets comprising helpful information and guidance for patients, their families and schools as well as other interested stakeholders.
Dec 7, 2011
IPOPI’s recently released a co-edited issue of Pharmaceuticals Policy and Law in collaboration with Professor Jose-Luis Valverde (University of Granada, Spain) looking at Health Technology Assessments

IPOPI Global Immunoglobulin list

This list is dedicated to the global PID community! It provides information about the supply of Immunoglobulin in some 100 countries. To let every patient or relative know about the situation in the different areas and countries of the world.

Website Sponsors
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Our NMOs

World PI Week