PsA Action Month

This is PsA: PsA Action Month 2025 - Rachel lives with PsA

About 1 in 3 people with psoriasis develop psoriatic arthritis.

In a perfect world, we wouldn’t need PsA Action Month. We’d have cures or, at the very least, everyone would have access to effective treatments at affordable prices. If you live with PsA – the pain, fatigue, and for some, the permanent damage – it’s all incredibly unfair. 

Luckily, we do have each other, and anyone with psoriatic disease has NPF. Psoriatic disease can be very isolating, but PsA Action Month is one of our annual reminders that this vibrant, inclusive community is here to make sure you are not alone. 

From the Community – #ThisIsPsA

Your experience with PsA is unique to you, and your story is a powerful tool that helps others navigate this challenging disease. Share your story or see the stories of others on Instagram with the hashtag #ThisIsPsA.

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This program is supported by the Centers for Disease Control and Prevention of the U.S. Department of Health and Human Services (HHS) as part of a financial assistance award totaling $351,404, with 2 percentage funded by CDC/HHS and $14.3 million amount and 98 percentage funded by non-government source(s). The contents are those of the author(s) and do not necessarily represent the official views of, nor an endorsement, by CDC/HHS, or the U.S. Government.

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