Join us online to make a difference in the fight against ALS. Our online auction and make a difference donations help people with ALS in our local community and support research for finding treatments and a cure for ALS.
- At face-to-face meetings and events, our Chapter will follow the State of Oregon and State of Washington guidance for Covid-19 precautions. As of March 2022, the recommendations do not require masking.
- Our chapter will also follow the policy of the facility or buildings where we meet for masking or social distancing, so if a facility requires masking, we will always comply with their direction and will ask you to do the same.
- As we all transition through this change, we ask that everyone respect one another’s space and comfort level. We should all be proactive to ask what the other person is comfortable with. We want to keep in mind that each person is autonomous in their own decisions around masking and social distancing. Whether a person has ALS or not, being cautious around Covid is important. Each person may decide to wear a mask or maintain social distancing and each person’s decision is fully valid and should be respected.
- Some people may not be comfortable attending live events at this time. We understand. Our team is here to listen and discuss any concerns you may have.
- Visit our Covid-19 Vaccine Information hub for updates and to learn more about vaccines, their safety and efficacy, and availability.
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.
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.
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®.Learn More
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
The Three of Us, Telling Stories Through Music
September 27, 2022
Meet Ashley Wong, One of This Year’s Recipients of The Jane Calmes ALS Scholarship Fund
September 23, 2022
Adapting and Adjusting—Strategies for Combating Malnutrition for People with ALS
September 20, 2022
Meet Liam Rudin, One of This Year’s Recipients of The Jane Calmes ALS Scholarship Fund
September 16, 2022
Public Comments Filed in Push for Medicare Coverage of Seat Elevation
September 15, 2022
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Our Chapter Year Round Partners
Our Chapter Year Round Partners