About IFPA

Global leader in fighting psoriatic disease

Founded in 1971, IFPA is the international federation of psoriatic disease associations. We are the psoriatic disease community. Our members represent over 60 million people living with psoriatic disease. Together, we advocate for progress.

Vision

A future where all people living with psoriatic disease enjoy good health and wellbeing, free from stigma and preventable disability and comorbidities

Mission

Unite, strengthen and lead the global psoriatic disease community to improve the lives of all people affected by psoriatic disease.
 

62

national member organizations

3

regional organizations


Representing over

60 million

people living with psoriatic disease worldwide

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Global Team

IFPA Members Frankfurt 2014

Meet the international psoriatic disease community

Members

Advocacy 1 01

Fueling international action against psoriatic disease

Our Cause

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Event Calendar

See what is coming up with IFPA and in the psoriatic disease space!

Goals

  1. Ensure global representation: Boost the voices of everyone living with psoriatic disease, everywhere.
  2. Lead global advocacy: Fight for the interests of people affected by psoriatic disease. Demand representation on global health and development agendas.
  3. Strengthen member capacity: Strengthen IFPA members. Raise national support for people living with psoriatic disease.
  4. Share knowledge: Close the gap between knowledge and action. Trigger breakthroughs for people living with psoriatic disease.
  5. Unite stakeholders: Build alliances. Transform global, regional, and national collaboration.


Values

  • Person-centered: Ensure that people living with psoriatic disease are at the heart of everything IFPA does.
  • Collaborative: Work together and openly with members and partners.
  • Accountable: Be responsible for all actions
  • Bold: Have the confidence and courage to lead the global psoriatic disease community.

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