Lupus Foundation of America - Pacific Northwest Regional Office

06/17/2026

This year, Cynthia is celebrating 20 years living with lupus!

Her team is made up of an incredible circle of support including family, friends, and coworkers who show up for her year after year.

As Cynthia shares, “Every year that I walk, my Walk To End Lupus Team gets bigger and bigger -- a great testament of the community I am so fortunate to have around me. I'm looking forward to walking again at this year's Walk To End Lupus with a trail of loved ones walking beside me.

Inspired by Cynthia’s story? Start your own Walk to End Lupus Now team today and bring your community together in support of those living with lupus. https://www.lupus.org/california/events-13

06/15/2026

People with lupus are often sensitive to UV light, which can trigger flares like rashes, fatigue, joint pain, and more. Protecting yourself from UV exposure (through sunscreen, protective clothing, limiting sun exposure, and even reducing indoor UV sources) can make a meaningful difference in managing symptoms day to day.

06/12/2026

June is Men's Health Month.

While lupus is often thought of as a disease that only affects women, 1 in 10 people living with lupus is a man. Men are often diagnosed later and can experience more severe complications, making awareness and access to care especially important.

This month, we recognize the men in our lupus community and encourage open conversations about health, support, and seeking care. No one should have to navigate lupus alone.

06/09/2026

Steve is currently the #1 fundraiser in our Men on a Mission campaign!

Men on a Mission is a platform for fathers, sons, brothers, and partners to champion their loved ones and help improve the future for everyone living with lupus.

Steve is participating in honor of his daughter, Kristina, who lives with lupus. Through his fundraising efforts, Steve is helping advance research, education, and support programs while raising awareness for the millions of people affected by lupus.

Thank you, Steve, for leading the way and showing what it means to be a Man on a Mission. We're grateful for your dedication to the lupus community!

06/05/2026

For years, Jean lived with symptoms that were dismissed or misunderstood before finally receiving a lupus diagnosis. By turning her passion into action, she organized the very first Walk to End Lupus Now in Star, Idaho last year.

What started as one person wanting to make sure no one else felt alone turned into a day full of lupus warriors, families, friends, and support from the community. Together, the event raised over $10,000 for lupus research and programs!

Jean knows what it feels like to go through lupus feeling alone. That’s one reason why she walks (and why we think you should too).

Join us at your local Walk to End Lupus Now. https://www.lupus.org/walk-to-end-lupus-now

06/01/2026

Looking for ways to get involved in lupus research? The Lupus Foundation of America’s RAY® Registry allows people living with lupus to share their experiences through confidential surveys that help researchers better understand the disease.

To participate, create a new account through the RAY® patient portal and complete the registration and survey process at your own pace. If you already have an account, you can log in through the secure portal to access your information.

05/30/2026

We hope you enjoyed the first Team Week Challenge! 💜 We’re excited to announce the final challenge of our first Walk to End Lupus Now Team Week of 2026.

For this final challenge, you have TWO DAYS to focus on fundraising. Your goal is to receive the highest NUMBER of donations by midnight on Sunday, May 31st.

The winner will be determined by number of donations received (not total dollars raised). Click the link in bio to register today and start fundraising. You must be registered to be eligible to win!

Winners will be announced after Team Week concludes.

05/29/2026

We’re excited to kick off the first Walk to End Lupus Now Team Week Challenge of 2026! From today through Sunday, we’ll be sending out daily challenges and tasks. Complete them for a chance to win a $25 Amazon gift card!

Today’s challenge is simple:

1. Register for your local Walk to End Lupus Now (link in bio)
2. Make a $25 self-donation
3. Complete both by midnight tonight

Already registered? Great! Just make a $25 self-donation and you’ll automatically be entered to win. Good luck!

05/20/2026

Today, the LFA is hosting a free virtual webinar on Phase III clinical trials and FDA Fast Track therapies. We are breaking down what participation actually looks like, featuring real patient stories, and opening the floor to your questions during a live Q&A. Register at

This webinar connects people living with lupus, their care partners, and the broader community directly to Phase III clinical trials and investigational therapies with FDA Fast Track designation. Through clear, accessible information and real patient stories, attendees will learn what clinical trial...

05/18/2026

This past Friday, the Seattle hosted Lupus Awareness Night at the ballpark! ⚾💜 Over 100 lupus warriors, family members, friends, and supporters joined us for a fun evening of baseball, hot dogs, community, and of course, the salmon run.

Thank you to everyone who came out to support lupus awareness and spend the night with us. We loved seeing our community together and hope to continue this special tradition for years to come!