Lupus Foundation of America - Pacific Northwest Regional Office

Lupus Foundation of America - Pacific Northwest Regional Office The LFA, PNW Region ( WA, OR, MT, AK, WY and ID) is dedicated to solving the mystery of lupus.

Join Team Captains from across California, Oregon, Arizona, Washington and Idaho, for this hour-long virtual call. Durin...
08/10/2026

Join Team Captains from across California, Oregon, Arizona, Washington and Idaho, for this hour-long virtual call.

During this call, you'll learn how to:
• Recruit a strong team of friends, family, coworkers, and supporters.
• Hit your fundraising goals with simple, effective fundraising strategies and resources.
• Engage your workplace and unlock new opportunities for corporate support, matching gifts, volunteer participation, and more.

You'll also connect with fellow Team Captains, exchange ideas, and leave feeling motivated and ready for an incredible 2026 Walk season.

Have you registered for Walk to End Lupus Now yet?Join us as we come together to raise awareness, support those living w...
08/07/2026

Have you registered for Walk to End Lupus Now yet?

Join us as we come together to raise awareness, support those living with lupus, and fund critical research. Whether you walk as an individual or with a team, every step makes a difference.

Register today through the link in our bio. 💜

07/29/2026

🔬💜 Lupus starts today! This week, we're taking you From Lab to Life: sharing the science changing how is understood, diagnosed, and treated, and introducing you to the researchers and lupus warriors making it possible.

Follow along all week as we highlight groundbreaking research and the people whose stories drive it forward.

Every gift made during Research Week is matched dollar for dollar, up to $25,000. Make your gift today: https://buff.ly/RiAaXyy

Lupus shows up in different ways for different people. Learning about the four types is an important step in understandi...
07/06/2026

Lupus shows up in different ways for different people. Learning about the four types is an important step in understanding just how varied and complex this disease can be.
lupus.org

We're looking for volunteers to help make our 2026 Walk to End Lupus Now events a success!If you can help with setup, as...
06/29/2026

We're looking for volunteers to help make our 2026 Walk to End Lupus Now events a success!

If you can help with setup, assist during the event, stay for teardown, or volunteer all morning, we'd love to have you on our team. Volunteers will receive a free event T-shirt as a thank you for their support.

Interested? Sign up to volunteer on the Walk to End Lupus Now registration page. We can't do it without you! 💜

Registration for Walk to End Lupus Now 2026 is officially open for all West Region Walks!Join us in the movement to end ...
06/26/2026

Registration for Walk to End Lupus Now 2026 is officially open for all West Region Walks!
Join us in the movement to end lupus. Sign up, start a team, and begin fundraising today to help advance critical research, expand education programs, and support those living with lupus. Whether you walk as an individual, create a team with friends and family, or join an existing group, every step and every dollar makes a difference. Register and fundraise $500 by June 30th and you’ll receive a customizable Walk to End Lupus jersey!
http://walktoendlupusnow.org/

This year, Cynthia is celebrating 20 years living with lupus!Her team is made up of an incredible circle of support incl...
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

People with lupus are often sensitive to UV light, which can trigger flares like rashes, fatigue, joint pain, and more. ...
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.

June is Men's Health Month.While lupus is often thought of as a disease that only affects women, 1 in 10 people living w...
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.

Steve is currently the  #1 fundraiser in our Men on a Mission campaign!Men on a Mission is a platform for fathers, sons,...
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!

Address

1417 NW 54th Street, Suite 476
Seattle, WA
98107

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