Join the Hike to Defeat ALS on September 18 and wander through the lush trails of Silver Falls State Park to raise awareness and funds for the ALS community!
- 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- Meet Kaiden Anderson, One of This Year’s Recipients of The Jane Calmes ALS Scholarship Fund
September 17, 2021 - Case of AMX0035 Proves Advocacy from ALS Community Can Impact Drug Development
September 15, 2021 - ALS Association Applauds Amylyx's AMX0035 Announcement, Urges Swift FDA Approval
September 15, 2021 - Meet Emma Thompson, One of This Year’s Recipients of The Jane Calmes ALS Scholarship Fund
September 10, 2021 - Researcher Spotlight: Yichen Li, Ph.D.
September 7, 2021
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.
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
 |
 |
 |
 |
 |
 |
|
Our Chapter Year Round Partners