This #GivingTuesday, your donation to benefit people affected by ALS and ALS research will have twice the impact, thanks to a matching gift from the Condon family!
- 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.
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- Researcher Spotlight: Caroline McHutchison
November 16, 2021 - Loving and Caregiving for Someone Living with ALS and FTD
November 12, 2021 - Finding Critical Resources for ALS Caregivers
November 9, 2021 - Patty Letters: Advice from a Caregiver
November 5, 2021 - GREAT NEWS! House Subcommittee Unanimously Approves ACT for ALS
November 4, 2021
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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
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Our Chapter Year Round Partners