The help you need to best manage your psoriasis or psoriatic arthritis.

Alisha lives with psoriatic disease.

The mission of the National Psoriasis Foundation is to drive efforts to cure psoriatic disease and improve the lives of those affected.

Over 8 million people in the U.S. have psoriasis. Nearly a third of them will develop psoriatic arthritis. A world without psoriatic disease and the related burdens is possible. We won't stop until you have the cure you deserve. 

Your Solution is Waiting

Everyone has a unique experience with psoriasis, and how you manage your disease should reflect that. Your solution is waiting.

Find your solution
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What's New at NPF

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How to Catch Zs

There is no easy fix, but better sleep is possible.

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NPF Monkeypox Q&A

The NPF Medical Board addresses key questions about monkeypox for people living with psoriatic disease.

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Free Resource

Did you know that psoriasis increases your risk of developing other diseases, known as comorbidities? Learn more about comorbidities, your risks, and steps you can take to improve your overall health, including your mental health, with our free resources.

Request your resource

New CEO Announcement

NPF selects Leah M. Howard, J.D. as President and CEO, moving boldly and bravely into a new chapter.

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Leah lives with psoriatic disease.

Information to Stay Healthy

Advance Online

Get the latest news and inspiring stories from experts, advocates, and people like you.

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COVID-19 Resource Center

Stay healthy even during these trying times. Here's your home for updates on COVID-19 and psoriatic disease.

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A Virtual Community for You

Share and connect with others living with psoriasis on Twill Care, our official community partner. Twill Care offers digital tools, including a daily stress tracker, symptom diary, guided meditations, and more.

Join Twill Care now

Join Us, Wherever You Are

Upcoming Events
Tue10/04
9:00 a.m. PT | 12:00 p.m. ET

Advancing Psoriatic Disease Research

As part of our community, you are invited to join us for the NPF Congressional Briefing on Advancing Psoriatic Disease Research! The briefing will discuss federally funded medical research and public health activities that help those living with psoriatic disease. Speakers include Leah Howard, J.D., CEO, NPF, Dr. Craig Thomas, Director, Division of Population Health, CDC, Dr. Lindsey Criswell, Director, NIAMS, NIH, Representative Debbie Wasserman Schultz (D-FL-23), and Representative John Joyce, M.D. (R-PA-13). All attendees that join the briefing will receive an NPF advocacy sticker! Take action and register today!

Learn More About This Event
Wed10/05
4:00 p.m. PT | 7:00 p.m. ET

Upcoming Webinar: SpA and PsA Treatment Update

Please join rheumatologists Dr. Atul Deodhar from Oregon Health & Science University and Dr. Anand Kumthekar from Albert Einstein College of Medicine for a discussion of the latest treatment updates for spondyloarthritis (SpA) and psoriatic arthritis (PsA).

Learn More About This Event
Thu10/06
6:00 p.m.10:00 p.m. ETIndianapolis, IN

Pstamp Out Psoriatic Disease Indianapolis

Join NPF for a memorable evening as we play bingo and hold a silent auction to fund education, advocacy, and research efforts. Ticket purchase includes dinner, two drink tickets, and eight games of bingo.

Learn More About This Event

NPF hosts live and virtual events to connect the community, spread awareness, and raise funds for a cure.

Find an event near you

Stay in the Know.

Expert tips, can’t-miss events and the latest news, straight to your inbox.

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