Summer Advocacy Volunteer Hub

Welcome to your portal for this summer's local advocacy. We are very happy to have you join our community of patients, doctors, and advocates who have given their time to improving care for those living with psoriatic disease.

In August, members of Congress will return to their home districts and states for an extended in-district work period. This is a great opportunity to advocate locally and continue to build relationships with your legislators by requesting a legislative meeting or attending a town hall or coffee in your area. We are happy you are joining NPF for local summer advocacy this year!

Get Involved

If you’d like to participate this summer, please let us know by signing up!

Sign up today

Key Resources

Below are links to help you schedule and participate in a local meeting or event with your legislator. If you need assistance, you can email Will Hubbert, Grassroots and Advocacy Manager, at advocacy@psoriasis.org.

Prepare your Asks

We recommend selecting one of the topics below to discuss with your legislator. The three documents below are designed to provide background information, questions that are frequently asked by members of Congress and their staff (plus the answers!), and ideas to help you connect your experience to the policy issue. Once you sign up to participate, an NPF advocacy team member will be in touch with information about which issue could benefit the most from your lawmaker’s attention.

Following Up on Your Meeting or Event

Follow up is key to ensuring your legislators take the action you requested. Use the resources below to find out how!

Questions About NPF Advocacy?

Your answers are just a click away. Email Will Hubbert, Grassroots and Advocacy Manager, at advocacy@psoriasis.org for further information.

Stay in the Know

Expert tips, can’t-miss events, and the latest news, straight to your inbox.

National Health Council Standards of ExcellenceCharity Navigator

Copyright © 1996-2025 National Psoriasis Foundation/USA


The National Psoriasis Foundation is a qualified 501(c)(3) EIN 93-0571472.


Duplication, rebroadcast, republication, or other use of content appearing on this website is prohibited without written permission of the National Psoriasis Foundation (NPF).


NPF does not endorse or accept any responsibility for the content of external websites.


NPF does not endorse any specific treatments or medications for psoriasis and psoriatic arthritis.

We use cookies to offer you a better experience and analyze our site traffic. By continuing to use this website, you consent to the use of cookies in accordance with our Privacy Policy.