The National Psoriasis Foundation’s Government Relations and Advocacy team has decades of experience driving policy change to improve patient health outcomes for those living with psoriatic disease – but we can’t do it alone! Every day, we work with passionate volunteers and patients living with the disease who write letters, share information on social media, advocate in front of legislators and contribute financially to help support NPF’s many programs, including advocacy work. Join us today and help us stimulate research into psoriatic disease and advance legislation that improves access to treatments and health care providers! Read more about NPF Advocacy »
Here are the ways YOU can help move our work forward:
1. Sign up to receive NPF Advocacy email notifications.
2. Learn about our team of volunteers who advocate for reforms in your community.
3. Share your journey with psoriatic disease that we can use as a testimonial in our advocacy efforts.
4. View upcoming events in your area.
John Latella | From Psoriasis to Service
John Latella has been “through the wringer” in dealing with psoriasis. Now, he says, he’s come out “clean” and eager to help the world understand what it means to live with a severe case of the disease.