National Psoriasis Foundation

Not sure what type of psoriasis you have or how to treat it given where it may be?

Join psoriasis patient, Kaleigh Welch and dermatologist, Dr. Ronald Prussick in this pre recorded webinar as they discuss the five types of psoriasis, their symptoms, and treatment options. 🔗https://ow.ly/JWfo50T72mq

Psoriasis can affect anyone at any age, but there are unique challenge for anyone under 18. So we created Our Spot, the meeting place for families and kids living with .

Head to our website to find stories, resources, and more.
🔗 psoriasis.org/our-spot/

Mark your calendars for a night of community, celebration, and unforgettable memories! 🎉

Join us in New York City on June 18 to celebrate the work and accomplishments of Joel M. Gelfand, M.D., Carol Ostrow, and Jose U. Scher, M.D. at the 2025 Commit to Cure Gala. We are thrilled to honor these three incredible individuals for their tremendous contributions to advancing the mission of curing psoriatic disease and improving the lives of those affected.

For more information or to reserve your seat, visit 🔗 www.psoriasis.org/committocure

No one should have to stop their treatment due to cost—but for many with psoriatic disease, this is the harsh reality.

The time to act is now. The psoriatic disease community needs better care and resources today. Your gift can make an immediate difference, breaking down barriers and ensuring that millions can treat their disease without delay.

on give the gift of hope: https://ow.ly/bSIA50T3nZ0

For some, Labor Day serves as an unofficial end to summer, but for those still a long way away from fall weather, check out our tips for taking care of your skin in the heat.

Learn how the season can impact your symptoms and what to do to minimize flares: https://ow.ly/bMLf50PEwT4

How does the weather impact your psoriasis?

Taking Care of Your Skin in Summer Learn how the season can impact your psoriasis and psoriatic arthritis symptoms and what to do to minimize flares.

The start of a new school year may stir up emotions: fear of what others might say, or feeling self-conscious, lonely, or depressed. We can help.

First take a deep breath, then head to our website to find all the tools you need to help prepare for the upcoming year.

4 Back-to-School Tips for Kids With Psoriatic Disease Here are some tips for you and your kids with psoriasis or psoriatic arthritis to be their best in school.

Over 8 million people in the U.S and 125 million worldwide live with psoriasis, each with their own unique story.

August may be ending but our efforts to raise awareness around what psoriasis looks and feels like isn’t.

Join the movement today! Use the hashtag and show us your unique definition of psoriasis, then head to our website to find all the tools you need to best manage your disease.
🔗 psoriasis.org

Thank you to CeraVe Skincare for sponsoring .

Whether it's stress, new lotion, or just because—don't let your next psoriasis flare take you by surprise.

Head to our website to learn more about what might be causing your psoriasis to flare 🔗psoriasis.org/causes/

Austin Tolchin took all the “right” actions, but he still faced barriers in treating his psoriatic disease. His story is a reminder: treating psoriasis must be a priority now.

At NPF we are committed to breaking down the barriers that stand in the way of effective treatment for millions living with psoriatic disease. But we can’t do it alone.

Your gift today fuels our mission to optimize health now—because waiting is not an option. Give the gift of relief today. https://ow.ly/ERAm50T3k4J

Knowledge is power, and understanding the other health conditions you're at risk for can help you manage, and possibly prevent them.

Visit our website to learn more about psoriatic disease comorbidities: psoriasis.org/advance/psoriatic-disease-affects-more-than-skin-and-joints/

What does your psoriasis look like?

People of all skin tones, races and ethnicities can be affected by psoriasis. But that doesn't mean it looks the same on everyone.

That's why we created our Skin of Color Resource Center—to share stories, resources, and information on psoriasis on skin of color 🔗psoriasis.org/skin-of-color-resource-center/

Kim's story

My name is Kim Benner and I was diagnosed with psoriasis at age 14 and was always self-conscious as a teenager. I remember my lesions got really bad when I was in college and the lesions on my forehead were growing down close to my eyes. I had bangs for most of my adulthood because I was so self-conscious.

I was on and off creams and topical treatment for years ( have you ever tried using coal tar shampoo and or putting creams on your scalp before bedtime and then sleeping in those pillowcases covered in medicine?!) but after the birth of my second son my psoriasis flared over my elbows and knees I had to take more action.

My physician started me on a biologic. I even enrolled in a study that followed me for 5 years since at that time TNF alpha inhibitors were new to the market and as a pharmacist I thought being in a drug study was cool! I teach the therapy of psoriasis in my pharmacy program so I knew all about the risks and benefits.

Years later I came off the study and tried 2 different biologic agents (due to insurance) and am stable on one to this day. (I learned so much about patient assistance programs for myself that it helped me navigate PAPs when helping my own patients now!)
I was diagnosed with skin melanoma a few years ago so I see my dermatologist every 6 months for skin checks and biopsies. That does limit which psoriasis therapy I can be on.

I have noticed my lesions are very weather and seasonal dependent so I am pretty clear in the summer and have to be diligent about using regular moisturizers.

A tip I would share with others living with psoriasis is use lots of moisturizer and try to stay in humid environments - not hard for Birmingham Alabama!! My other tips are trying variations in diets and any other (safe) herbal products in conjunction with medications and consulting your health care provider.

Mostly, I have gotten used to living with psoriasis. Due to my BSA coverage I fall into the moderate category but I try not to let it affect my quality of life. I am used to folks throughout my entire life asking me "what happened to you" when pointing at my lesions. I usually answer "That is how God made me" 😉 but I explain that I have psoriasis.

So in summary, I am very much an advocate for the disease, understanding it and finding a cure.
No one should have to live embarrassed by their skin so I try to embrace it and do all I can to increase understanding and support.

Have you tried cannabis to manage psoriasis symptoms?

Head to our website to find out how and why cannabis affects psoriatic disease. ➡️psoriasis.org/advance/cannabis-marijuana-pot-or-weed/

This , dive deep into the realities of psoriatic disease and discover tips to identify your triggers and control your symptoms.

Request your free e-kit today: psoriasis.org/psoriasis-action-month-e-kit

For Hannah, psoriasis was never going to hold her back from living life—and getting her tattoos. While tattooing psoriasis-affected skin comes with some risks, it’s not stopping people from expressing themselves.

Hear our community’s experiences with getting inked while living with psoriatic disease.➡️https://www.psoriasis.org/advance/women-with-ink-tattoo-psoriasis/

Do you have psoriasis and tattoos?

Planning for pregnancy while living with psoriatic disease? Whether you're navigating treatment changes or have concerns about breastfeeding, we've got you covered.

Head to our website to discover what to expect when you're expecting ➡️https://ow.ly/WvAb50SXa9M

Psoriasis affects more than 8 million people in the U.S. and yet the experience is different for everyone.

Join us as we share your stories during Psoriasis Action Month. Get more psoriasis facts at 🔗 psoriasis.org/psoriasis-action-month/

Psoriasis affects over 7.5 million adults in the U.S., yet misconceptions and stigma persist.

National Psoriasis Foundation and Amgen are collaborating to shed light on the lives of those living with psoriatic disease.

Through , we’re highlighting the journeys of four individuals who refuse to let their visible symptoms define them.

Stay tuned to hear their stories and see how they’re challenging perceptions.

Nail psoriasis affects more than 50% of people living with psoriatic disease 💅

Head to our website to learn about the signs, treatment, and daily care for nail psoriasis. psoriasis.org/hands-feet-nails/

We get it. You are not alone.

Living with a chronic disease can take a huge toll on your mental health. Visit our website psoriasis.org/psoriasis-action-month and contact our free Patient Navigation Center either by phone (800-723-9166) or by email ([email protected]) to find support and resources to care for your psoriatic disease and your mental health.

Remember to be kind to yourself, you're doing the best you can.🧡💜

.... 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/

Ava's story ✨

Hi my name is Ava and I first developed psoriasis when I was around the age of eight. I have struggled throughout my life with my psoriasis; it has always been a source of insecurity when it comes to my appearance. Since then, I have been diagnosed with other autoimmune and chronic illnesses. Although psoriasis will always be special to me, it initially interested me in health care.

From the time I was a kid, I knew that I wanted to help people, and in my senior year of high school, I was tasked with one final project, which was to be started in May of my junior year and continue until April of my senior year. I chose to do my project on autoimmune diseases, which led to finding the National Psoriasis Foundation, which I later became involved in. Through this, I had the opportunity to teach at local middle schools about what autoimmune diseases were to raise awareness about them starting from a young age. Doing this process made me realize I wanted to go to college to pursue a degree in nursing.

I am currently in my second year of nursing school, and after graduation, I plan to pursue a master's degree in nursing to become a nurse practitioner. A nurse practitioner is who first diagnosed me with psoriasis, so I would like to be able to help other children in a similar way that I was once helped.

""Oh no, did you fall?" "Is that a sunburn?"

Mateo remembers hearing these questions on his very first day of kindergarten when his psoriasis plaques first appeared. Instead of dreading the "classic" questions, he's learned to turn them into opportunities to raise awareness.

Discover Mateo's journey with psoriasis and his advice for the newly diagnosed ➡️https://ow.ly/rCBi50STi95

What is your least favorite "question" about psoriasis?

Psoriasis affects more than just the people living with it. When Mary's 7 year old daughter developed severe plaque psoriasis she knew she needed to find support not just for her daughter, but for herself.

Read more of Mary and her daughter's journey with psoriatic disease 🔗psoriasis.org/volunteer-spotlight/

Stress 🤝 chronic disease

Did you know there might be a link to your stress and your psoriasis?

Managing stress with a chronic disease is easier said than done, but we're here to help. Head to our website for tips on how to tackle stress at home and comment below ways you manage your stress with psoriatic disease ⬇️psoriasis.org/life-with-psoriasis/

📢Roll call 📢

there are 5 types of psoriasis, and it's possible to have more than one at a time?

What type (or types) of psoriasis are you living with? Let us know in the comments then head to our website to read about the 5 types and their differences. 🔗psoriasis.org/locations-and-types/

Kayla's story ✨

My name is Kayla Bolton. I was diagnosed with psoriasis when I was 8 years old, and I am currently 33 years old. I suffered a great deal throughout my teenage years, trying various ointments, pills, and injections. Some worked for a while, and my skin was clear for many years thanks to biologics. Since then, I have tried a couple more medications but eventually wanted to give my body a rest. I have been off injections and all medications since 2021, and my body has only broken out in small patches on my stomach, elbows, and knees. I’ve been able to manage it by making some lifestyle changes, but nothing too drastic.

If I could give any advice to someone dealing with psoriasis, it would be not to let it dictate your life. Continue to live your life, and don’t shy away just because of your skin’s appearance. While working through my insecurities with my skin, I continued to push myself out of my comfort zone and was able to achieve my dream job as a media manager in the off-road (motocross) racing industry.

psoriasis.org/psoriasis-action-month