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ALS Ice Bucket Challenge Progress

Gala 2021 Hero

Join us on October 30 for the Together for ALS Gala live streamed event benefiting the local ALS community and research.

Join us on October 30 for the Together for ALS Gala live streamed event benefiting the local ALS community and research.

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The Oregon and SW Washington Chapter of The ALS Association provides support and resources for people living with ALS, their families, and caregivers living in the State of Oregon and the six counties of Southwest Washington.
Coronavirus Statement -  9/22/2021
With the developing news regarding COVID-19, we want to take a moment to share how The ALS Association is addressing the concern about our programs and events.

  • We have moved our chapter office in Portland. Our new address is 825 NE Multnomah St., Suite 940, Portland, OR 97232. Please update your records and let us know if you have any questions or concerns at info@alsoregon.org.

  • Please be assured that the work of The ALS Association will continue. The first priority is the safety and well-being of people with ALS, their families and caregivers, and our staff.

  • We have created a COVID-19 Vaccine Information hub to capture breaking news and resources to inform your conversations with physicians about the vaccines, their safety and efficacy, and availability.

  • Chapter staff will be working remotely and are still available to our constituents daily via phone, email, or video chat.

  • All in-person Support Groups have been cancelled. All groups have transitioned to Virtual Support Groups.

  • You can find the latest updates about our activities on our Facebook page.

 

For the most recent information about coronavirus (COVID-19), The ALS Association recommends that you reference the websites for the Centers for Disease Control (CDC), the World Health Organization (WHO), and state and local health authorities. The ALS Association has also made available a fact sheet about COVID-19 and its impact on people with ALS.

For specific information about symptoms you may be experiencing or questions about personal exposure as someone living wth ALS or as a caregiver, please contact your physician directly.

Thank you for your patience as we manage this rapidy shifting situation.

 

Our Mission
To discover treatments and a cure for ALS, and to serve, advocate for, and empower people affected by ALS to live their lives to the fullest.
Get Involved With Us
Help create a world without ALS by getting involved in the way that best suits YOU! When you fundraise with friends and family you take us closer to discovering a cure.

Volunteer with us

Volunteer with us

Our volunteers provide invaluable assistance in the office, help coordinate our chapter events, advocate at The ALS Association's National ALS Advocacy Day and Public Policy Conference, and devote their time and energy so that we are able to provide essential care services.  

Learn more here.  

Remembering Our Loved Ones

Remembering Our Loved Ones

This campaign gives our chapter a meaningful way to remember the remarkable people we provided care and support for during their time living with ALS. These banners are shared at our events such as the Walk to Defeat ALS®. 

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Discover More Ways to Help Fight ALS
How Do You Talk to Children About ALS?
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Resources

Whether you’re newly diagnosed, navigating your journey with the disease, caring for a person with ALS, or researching the cure, there are resources to support you.

Let us help you and your family cope with the day-to-day challenges of living with ALS.

For People with ALS

Learn about our grant program, upcoming scientific meetings, and opportunities to collaborate.

For Researchers

Caring for someone with ALS is hard work. We offer resources and support to help you.

For Caregivers
Stay Connected With Us

Sign up to receive the latest news in ALS and learn how you can continue making a difference in the search to treat and cure this disease.

You Can Help Create A World Without ALS

Your gift will help The ALS Association support research to find a cure for ALS and provide much-needed services to patients and their families. By becoming a part of The ALS Association family and making your gift today, you will help sustain hope in thousands of people affected by ALS.

Our Chapter Year Round Partners

VC Fund   Fortis Construction Logo Numotion Providence Brain and Spine Institute   The Standard

Our Chapter Year Round Partners

VC Fund

Fortis Construction Logo

Numotion

Providence Brain and Spine Institute

The Standard