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Advocacy

Spearheading global change

IFPA unites the global psoriatic disease community to fight for progress. Together, we speak up for people living with psoriatic disease. From the national to the global level, the time to act is now.

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IFPA COALITION logo ON PURPLE RGB

IFPA Coalition

What is the IFPA Coalition?

NOW ACT 01

Our needs, our demands

NOW ACT

More than promises, the psoriatic disease community demands progress. Read our petition!

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IFPA's most significant policy breakthrough

WHO Resolution on Psoriasis

In 2014 the Resolution on Psoriasis was unanimously approved by all United Nations. It declared psoriasis a chronic, painful, disfiguring and disabling non-communicable disease, without a cure.

Report

Shine a spotlight on the public health impact of psoriatic disease

WHO Global Report on Psoriasis

As a result of the Resolution, in 2016 the World Health Organization published a Global Report on Psoriasis. The Report explores the challenges of psoriatic disease in depth, and provides direction to meet the unmet needs.

We demand a change in perspective: psoriatic disease is a serious non-communicable disease.

We combat for equal access to affordable, safe, effective, and quality treatments.

We insist on holistic, person-centered care.

We fight stigma.

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Advocacy Resources & Tools

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GPP Charter

IFPA Forum 2022 Briefing Book

Visit the Briefing Book

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Printable Stickers: Speak Up for Psoriatic Disease!

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Briefing Book: IFPA Forum 2022

NCD Alliance's Practical Guide to Strategic Advocacy Planning

Check out the guide (EN, ESP, FR)

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Digital Transformation and Telemedicine

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Involving patients and their organizations in decision-making processes

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Health Workforce and Psoriatic Disease

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Access to Care

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Psoriatic Disease, Mental Health, Stigma, and Quality of Life

The World Health Assembly adopts global targets for diabetes

Read the press release

Brain Skin Axis

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Inside Psoriatic Disease: Mental Health

Mental health: the best investment the world has never made

Read the article

Diverse hands

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Participate in the WHO’s informal consultation with people living with noncommunicable diseases and mental health conditions!

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Social media toolkit on psoriatic disease and mental health

Rare Disease Day Type 1 Moment

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Chiara Shares Her Story with Erythrodermic Psoriasis

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Whistleblower Policy