National Psoriasis Foundation

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

National Psoriasis Foundation page Guidelines

The National Psoriasis Foundation (NPF) page is a open, supportive environment for people affected by psoriasis and/or psoriatic arthritis. It provides opportunity for people to connect, exchange information, find understanding and build friendships. We are committed to providing a safe, welcoming community. We encourage your commen

ts, photos, videos, questions and links. Posts on the NPF page are for educational purposes only and not for the purpose of rendering medical advice. The information presented should not replace the counsel of your health care provider. NPF does not endorse any medications, products, equipment or treatments. Guidelines

The NPF page is monitored by Foundation staff. We reserve the right to remove posts that violate the community and our guidelines. No abusive behavior or conversations. We will remove comments that are harassing, threatening, harmful, obscene, racially offensive or otherwise inappropriate. This page is for personal use only. Posts that advertise, promote products or services, or distribute unsolicited information for financial gain will be removed. We'll ban users who repeatedly try to sell their products or services.

What looks like a blister could be the beginning of something much more serious. For Janene, a rapidly spreading GPP fla...
08/19/2026

What looks like a blister could be the beginning of something much more serious.

For Janene, a rapidly spreading GPP flare left her in excruciating pain and searching for answers. Her first trip to the ER ended with a diagnosis of athlete’s foot. It wasn’t until she saw her dermatologist days later that she learned she had Generalized Pustular Psoriasis.

Because it’s rare, GPP can be difficult to recognize and diagnose. That’s why awareness matters.

Your generosity can help NPF raise awareness of GPP and give people facing this rare disease a better path to answers and care. Will you donate today? https://giving.psoriasis.org/page/FY27SUMdgS

How do you manage your psoriatic disease symptoms? 🌿Managing pain is an important part of living with psoriatic disease....
08/19/2026

How do you manage your psoriatic disease symptoms? 🌿

Managing pain is an important part of living with psoriatic disease. Find out what we know about cannabis, how it may affect psoriatic disease, and what the research says.

Head to our website to get the facts.➡️psoriasis.org/advance/cannabis-marijuana-pot-or-weed/

The NPF Seal of Recognition highlights and recognizes products created or intended to be non-irritating and safe for tho...
08/16/2026

The NPF Seal of Recognition highlights and recognizes products created or intended to be non-irritating and safe for those living with psoriatic disease.

From skincare and clothing products, to scalp serums and supplements, our seal highlights options that are safe, gentle & backed by science.

Explore trusted brands like CrescelSkin, Phoilex, and Sphagnum Botanicals on our product directory🔗 psoriasis.org/seal-of-recognition

"I have psoriasis on my nails.... is that a thing??"Nail changes can be one of the signs of psoriatic disease, and nail ...
08/15/2026

"I have psoriasis on my nails.... is that a thing??"

Nail changes can be one of the signs of psoriatic disease, and nail psoriasis affects more than 50% of people living with psoriatic disease. 💅 Not sure what to look for? Head to our website for the signs, treatment options and everyday care tips for nail https://ow.ly/ZZa750ZA1JX

  .... not eczema While psoriasis and eczema might look similar, deep down, they are quite different. Get all the facts ...
08/14/2026

.... not eczema

While psoriasis and eczema might look similar, deep down, they are quite different. Get all the facts about the similarities and differences on our website. 🔗psoriasis.org/advance/psoriasis-or-eczema-atopic-dermatitis/

Have you ever been told your psoriasis was something else?

Can you relate? 🙋Living with GPP can affect so much more than your skin. If you’re living with GPP, you’re not alone. Vi...
08/14/2026

Can you relate? 🙋

Living with GPP can affect so much more than your skin. If you’re living with GPP, you’re not alone. Visit our GPP Resource Center to hear stories from others in the community, find helpful resources and learn more about this rare and serious form of psoriasis.

What’s one thing that helps you take care of yourself while living with psoriasis? 🧡Today is GPP Awareness Day, and Jord...
08/13/2026

What’s one thing that helps you take care of yourself while living with psoriasis? 🧡

Today is GPP Awareness Day, and Jordan is sharing the tips that help her care for both her mental and physical health while living with generalized pustular psoriasis.

Read Jordan’s story 👉 https://www.psoriasis.org/advance/how-jordan-got-her-groove-back-gpp/ and share your own tips in the comments!

08/13/2026

: Janene’s Story

"I always thought I had a pretty good handle on my psoriasis. I’d lived with plaque psoriasis for years, managed it with topicals, and just got used to the ups and downs. But nothing prepared me for what happened that summer day in Utica, New York.

It started with a blister on my foot. I noticed it while volunteering at a charity golf event. It didn’t hurt, didn’t seem like much. I figured maybe it was from my flip-flops. But then I started feeling dizzy, nauseous, and feverish. More blisters showed up. I drove home, thinking rest would help. It didn’t.

By that evening, I could barely stand. My skin was swelling, and I felt like I was burning from the inside out. I was trying to hide it from my kids. I looked like an alien or something, and I didn’t know why. I didn’t want to scare them. Finally we went to the ER, where I was told it might be athlete’s foot, but I knew it wasn’t. By the next day, the pustules had spread to both feet. The pain was unbearable. I couldn’t walk. I couldn’t function. But it wasn’t until I saw a local doctor on that I finally got answers.

He took one look and said, “This is serious. This is pustular psoriasis.” Specifically, GPP [generalized pustular psoriasis]. I had never even heard of it.

The following weeks were some of the hardest of my life. My husband and I became my care team. We changed dressings, cleaned wounds, managed pain. My skin peeled away. My nails fell off. The blisters moved to my hands. I spent weeks unable to walk, relying on a bedpan next to my bed. The physical pain was excruciating, but so was the fear.

Eventually, I started treatment with a biologic, and that’s what helped turn things around. I can tell when it’s time for my medication toward the end of the month, I can feel it in my feet. Slowly, I regained some strength and mobility. My skin began to heal. But GPP left its mark on me physically, emotionally, and mentally.

It changed how I see myself, how I move through the world. I had to stop working. I had to learn to ask for help. But I also learned what it means to keep going when everything feels like it’s falling apart."

Thank You to Our GPP Resource Center sponsor, LEO Pharma

Today is Generalized Pustular Psoriasis (GPP) Awareness Day!GPP is rare, serious, and can appear without warning. Today ...
08/13/2026

Today is Generalized Pustular Psoriasis (GPP) Awareness Day!

GPP is rare, serious, and can appear without warning. Today take a moment to learn what GPP can look like and how it can impact those living with it.

Learn the signs, hear real stories, and find resources to better understand and support those living with this disease on our GPP Resource Center.➡️ psoriasis.org/gpp-resource-center

Thank You to Our GPP Resource Center sponsor, LEO Pharma

📣Tomorrow is GPP Awareness Day!📣Generalized pustular psoriasis (GPP) is a rare, painful, and potentially life-threatenin...
08/12/2026

📣Tomorrow is GPP Awareness Day!📣
Generalized pustular psoriasis (GPP) is a rare, painful, and potentially life-threatening type of psoriasis. Together, we can raise awareness, build understanding, and support those living with this serious condition.

Join us tomorrow for patient stories, resources, and more! Head to our resource center for all the ways you can get involved👉 psoriasis.org/gpp-resource-center

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