The National Psoriasis Foundation was created in 1967 by volunteers. For more than 50 years, patients, families, friends, scientists and health care providers have pitched in to help our cause. Volunteering takes many forms, from following us on Facebook to running with Team NPF to sharing your story with the people who represent you at the state and federal levels.
In this series, you’ll meet a crew who, in their own quiet, steady way, have been working hard to help everyone with psoriasis and psoriatic arthritis. Today: Michelle Strangis.
Michelle Strangis is one of those lawyers who decided early on not to practice law. She has instead used her training to reinforce her real calling: diplomacy. Strangis worked for 26 years for the Minnesota Department of Health on state health policies. She spent five of those years writing the first licensure system for occupational therapists.
Around the time she retired in 2018, she received an email from NPF asking if any Minnesota residents had been denied insurance coverage for a physician-prescribed drug. “That’s exactly what happened to me!” says Strangis, who has been coping with psoriasis since she was 35. “I had had a bad experience with step therapy. In that case, I used my skills as a lawyer, calling out the improprieties of the process, to help win my appeal.”
Strangis answered the email and instantly became a volunteer. “It’s always better to change policy as opposed to going to war with insurers, patient by patient,” she says. “I know how effective policy is at addressing large-scale issues. A policy is like a blanket. It’s for everybody.”
Strangis’ two priorities going into retirement were preparing to downsize and traveling, but now she’s added volunteering with NPF as she advocates for her own cause.
Like Michelle Strangis, you can advocate for your own cause
More from our series of community profiles:
Photo: Diana Yepez
Driving discovery, creating community
For more than 50 years, we’ve been driving efforts to cure psoriatic disease and improve the lives of those affected. But there’s still plenty to do! Learn how you can help our advocacy team shape the laws and policies that affect people with psoriasis and psoriatic arthritis – in your state and across the country. Help us raise funds to support research by joining Team NPF, where you can walk, run, cycle, play bingo or create your own fundraising event. If you or someone you love needs free, personalized support for living a healthier life with psoriatic disease, contact our Patient Navigation Center. And keep the National Psoriasis Foundation going strong by making a donation today. Together, we will find a cure.