Take ACTION for Psoriatic Disease 2024

Take ACTION for Psoriatic Disease

Hello everyone! My name is Olivia, and I'm from Scarsdale, NY. Four years ago, I started experiencing a flaky scalp, and plaques gradually formed around my hairline and neck. Two years later, I was diagnosed with psoriatic arthritis in addition to scalp psoriasis. I found myself hiding under my hair, wondering if I could ever play tennis again without pain. Many of us living with psoriasis can relate to how this disease impacts our daily lives. Although I still experience symptoms, I can confidently say that biologic therapy has made managing this disease much easier, and this progress wouldn’t be possible without cutting-edge research. 

 

With 8 million Americans living with psoriasis, this statistic represents not just a number, but a community of individuals bonded by strength and resilience. After attending my first NPF Take Action event in San Francisco last year, I no longer felt alone in my struggle. The National Psoriasis Foundation provides a platform for us to unite through our lived experiences and share invaluable support. Being part of this community has shown me that together, we can face any challenge and inspire one another to keep moving forward.

 

It is a true honor to return as the National Psoriasis Foundation’s Honored Hero at San Francisco’s Take Action Event on Saturday, September 28th, at the San Francisco Zoo. I am excited to meet you and all supporters of the NPF as we raise funds towards a cure for psoriasis. Sign your team up today!