NPF Community

NPF Community Welcome to The National Psoriasis Foundation's page made for the psoriatic disease community!

Kinda chic to hop on this bandwagon in support of Inside Psoriatic Disease ✨Coming this November:📍 New York📍 Washington,...
08/14/2026

Kinda chic to hop on this bandwagon in support of Inside Psoriatic Disease ✨

Coming this November:
📍 New York
📍 Washington, D.c.
📍 San Francisco

Stay tuned for dates, details, and opportunities to connect with leading psoriatic disease experts on new research and care initiatives.

✨ Philadelphia Soirée Tickets & Tables Are Nearly Sold Out! ✨Join us on October 15th at the Fitler Club for the Philadel...
08/12/2026

✨ Philadelphia Soirée Tickets & Tables Are Nearly Sold Out! ✨

Join us on October 15th at the Fitler Club for the Philadelphia Soirée! Tickets and tables are nearly sold out, so if you’re interested in attending, purchase yours soon to make sure you don’t miss this special event.

🎟️ Get your tickets or table here: www.psoriasis.org/phillysoiree

Have questions about the event? Please reach out to Julia Hamel at [email protected].

We hope to see you there!

08/11/2026

👀 Come on, come on… NEW EVENTS ARE COMING!

We’ve got some exciting things on the horizon, and trust us- you’re going to want to be there 💙

🎟️ Save the dates, grab your tickets, and get ready to make an impact with us!

Check out what’s coming up in the link in our bio ✨

✨ Looking for a meaningful way to make a difference in the psoriatic disease community?Whether you're passionate about s...
07/14/2026

✨ Looking for a meaningful way to make a difference in the psoriatic disease community?

Whether you're passionate about supporting others, sharing your story, volunteering at events, advocating for change, or simply want to learn more about ways to get involved—we'd love to connect with you! 💙

Complete our interest form to let us know how you'd like to make an impact during the August meetings. There are opportunities for every interest, every schedule, and every experience level.

Together, we can educate, advocate, and empower our community. 💪

🔗 https://qr.psoriasis.org/a5f2150f to complete the interest form!

Today, we’re celebrating all the dads, grandfathers, and father figures in our psoriatic disease community. Wishing you ...
06/21/2026

Today, we’re celebrating all the dads, grandfathers, and father figures in our psoriatic disease community. Wishing you a Father’s Day filled with love, appreciation, and moments that make you smile. 💙

  Jonathan’s Story:It’s been 7 years since I first got diagnosed with psoriasis. For 26 years of my life, I had no idea ...
06/18/2026

Jonathan’s Story:

It’s been 7 years since I first got diagnosed with psoriasis. For 26 years of my life, I had no idea what an immune mediated disease was.
 
For years, psoriasis made me feel like I had to hide parts of myself. Not just my skin, but my confidence too. It was never just about the flakes, the redness, or the itching. It was the planning before leaving the house. The clothes I chose to cover up. The moments I avoided because I didn’t want people staring, asking questions, or thinking I was contagious.
 
There were times I felt embarrassed, frustrated, and just tired. So exhausted from trying different treatments. Tired of explaining myself to everyone I met. Tired of acting like it didn’t affect me when, deep down, it did. But over time, specifically this year, after one of the worst flares I’ve ever had, I realized something: psoriasis may be part of my story, but it will never get to define me.
 
I also want to take a moment to say how grateful I am for my girlfriend. Through every flare, setback, and difficult day, she has always been there for me. Always cheering me on, encouraging me, and reminding me to keep going. Having someone by your side through the highs and lows of a chronic disease is something I never take for granted.
 
Sharing my journey has helped me find strength in the very thing I used to hide. It reminded me that there are so many of us going through this quietly, trying to look okay on the outside while carrying so much inside.
 
That’s why I started speaking up. For awareness. For the people who feel alone. For the men who were taught to stay quiet and ‘just deal with it.’ And for my younger self, who needed to know that having a visible disease doesn’t make you any less worthy of being seen.

I’m grateful to have found the NPF Community. Knowing that I’m not alone in this journey has brought me comfort I never knew I desperately needed. It has also given me a greater push to be proud of sharing my story with others, in the hope of providing support to the rest of our psoriasis community. Know that you are not alone. ❤️

This is psoriasis. This is my story.

And I’m still learning to show up as myself.

✨ What a way to close out NPF’s 2026 spring event season! ✨Our inaugural San Francisco Soirée held on May 30 brought tog...
06/08/2026

✨ What a way to close out NPF’s 2026 spring event season! ✨

Our inaugural San Francisco Soirée held on May 30 brought together patients, healthcare providers, researchers, industry partners, and advocates for an inspiring evening focused on advancing the future of psoriatic disease care.

A special congratulations to our 2026 honorees:
Dr. Lianne Gensler
Dr. Wilson Liao
Dr. Melissa Leeolou

Through their leadership, innovation, and dedication to improving the lives of those living with psoriatic disease, each honoree embodies the spirit of our mission and the progress we continue to make together.

We are also deeply grateful to our event sponsors whose partnership helped make the evening possible:

Cures Sponsor: Johnson & Johnson⁠

Reception Sponsor: Alumis⁠

Promise Sponsors:
• AbbVie⁠
• Amgen⁠
• DermGPT⁠
• Novartis⁠
• Sun Pharma⁠
• Dynergy Dermatology⁠
• UCB⁠

Because of the generosity and commitment of our community, we exceeded our fundraising goal and expanded our ability to fund research, provide patient support, and advocate for improved access to care.

Thank you to everyone who joined us, supported us, and helped make this inaugural event such a success. Together, we are moving closer to a future free from the burdens of psoriatic disease.

As we look ahead to fall, we are excited to continue building connections, celebrating leadership, and advancing our mission—together.

06/05/2026

Taking our logo on a little springtime adventure 🌷✨
We’ve been so many places this season, and we’re so excited to share a little glimpse of the journey 💙

It’s hard to believe it’s already been three months since our IMPACT Volunteer Summit! 💙What better time to hear from IM...
06/02/2026

It’s hard to believe it’s already been three months since our IMPACT Volunteer Summit! 💙

What better time to hear from IMPACT Ambassador Izz about his experience at this incredible community event? Check out Izz’s blog to read his reflections in his own words 🥰

https://qr.psoriasis.org/IzzIMPACT

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