webor.alsa.org Open in urlscan Pro
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3 forms found in the DOM

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http://web.alsa.org/site/Survey

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Text Content

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ALS Ice Bucket Challenge Progress
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Oregon and
SW Washington
Chapter

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 * About ALS
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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!
Learn More

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!

Learn More


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.

Find Services

Take Action

Raise Awareness

Latest Research

Find Services
Take Action
Raise Awareness
Latest Research

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

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

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

Discover More Ways to Help Fight ALS

How Do You Talk to Children About ALS?
Read More

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

In The News
 * 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

Read More News Here

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.

Join Us
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.

Give Now
Learn About Other Ways to Give





OUR CHAPTER YEAR ROUND PARTNERS

   


OUR CHAPTER YEAR ROUND PARTNERS














 
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The ALS Association Oregon and SW Washington Chapter

825 NE Multnomah St. - #940 - Portland, OR 97232

503-238-5559




All content and works posted on this website are owned and copyrighted by The
ALS Association. ©2021

Lou Gehrig® used with permission of the Rip Van Winkle Foundation /
www.LouGehrig.com



     


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