National Psoriasis Foundation Advocacy

The National Psoriasis Foundation works to shape the laws and policies that affect people with psoriasis and psoriatic arthritis.

Harnessing the collective efforts of tens of thousands of advocates, the Psoriasis Foundation aims to:

  • Make insurance fair and affordable and improve coverage for people with psoriatic disease
  • Set public health policy for psoriasis and psoriatic arthritis through the findings from data collection at the Centers for Disease Control (CDC)
  • Improve the safety and affordability of psoriasis and psoriatic arthritis treatments
  • Increase federal funding for psoriasis and psoriatic arthritis research in order to find better treatments and a cure.

Advocacy Priorities

Public policy prioritiesLearn about our policy priorities at the federal and state level that break down barriers to care for people with psoriasis and psoriatic arthritis and advance us toward better treatments and a cure for psoriatic disease.

Take Action

Get involvedRead more about NPF's grassroots advocacy efforts including Hill Day at Home. Sign up for advocacy alerts and participate in advocacy activities like Town Hall meetings, letter writing and phone-in campaigns.

Advocacy Toolkit

Tools for psoriasis and psoriatic arthritis advocatesA wealth of resources to help individuals advocate effectively with elected officials and decision-makers.

Policy Overview

Materials for policymakers Links to our issue briefs and white papers, federal policy priorities and positions, and patient profiles. Read more »