The ALS Association | LinkedIn
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The ALS Association | LinkedIn
The ALS Association | 27,917 followers on LinkedIn. Fighting ALS on every front through research, care services, and advocacy. | Established in 1985, The ALS Association is the only national non-profit organization fighting ALS on every front. By leading the way in global research, providing assistance for people with ALS through a nationwide ...
Mar 10, 2011
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#ALS Association ALS Ice Bucket Challenge
The ALS Ice Bucket Challenge, founded by Pat Quinn, Pete Frates, and Anthony Senerchia Jr., changed the future of ALS research. Their idea inspired millions, raised critical funds which led to the discovery of new genes, new potential treatments, and more care services around the country for people living with ALS. | The ALS Association
The ALS Ice Bucket Challenge, founded by Pat Quinn, Pete Frates, and Anthony Senerchia Jr., changed the future of ALS research. Their idea inspired millions, raised critical funds which led to the discovery of new genes, new potential treatments, and more care services around the country for people living with ALS. | The ALS Association
Facebook6 months ago
The ALS Ice Bucket Challenge may have started 10 years ago, but we won't stop until there is a cure! Join us by taking the Ice Bucket Challenge and let's see a world without ALS! #IceBucket10 #ALS | The ALS Association
The ALS Ice Bucket Challenge may have started 10 years ago, but we won't stop until there is a cure! Join us by taking the Ice Bucket Challenge and let's see a world without ALS! #IceBucket10 #ALS | The ALS Association
FacebookAug 25, 2024
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Help change the future of ALS. Join our community committed in the fight to treat, cure and care for people with ALS. | The ALS Association
0:16
Help change the future of ALS. Join our community committed in the fight to treat, cure and care for people with ALS. | The ALS Association
FacebookThe ALS Association
17.1K viewsJul 17, 2020
Your gift will help lead the fight to treat, cure and care for people with ALS - Donate Today! | The ALS Association
0:31
Your gift will help lead the fight to treat, cure and care for people with ALS - Donate Today! | The ALS Association
FacebookThe ALS Association
79.5K viewsJul 17, 2020
ALS is 100% fatal and there is no cure…yet. People living with living ALS need your help now—for care, for research, for hope. Give today to help make ALS livable for everyone, everywhere, until there is a cure. | The ALS Association
0:26
ALS is 100% fatal and there is no cure…yet. People living with living ALS need your help now—for care, for research, for hope. Give today to help make ALS livable for everyone, everywhere, until there is a cure. | The ALS Association
FacebookThe ALS Association
55.4K views7 months ago
ALS Association ALS Research Progress
Amid progress in fight against ALS, there's plenty of work ahead
Amid progress in fight against ALS, there's plenty of work ahead
suntimes.com
1 month ago
Vanderbilt ALS Research Center promotes research, funding for cure
Vanderbilt ALS Research Center promotes research, funding for cure
wkrn.com
2 months ago
ALS research
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ALS research
MSNWGRZ-TV Buffalo
2 months ago
Help change the future of ALS. Join our community committed in the fight to treat, cure and care for people with ALS. | The ALS Association
0:16
Help change the future of ALS. Join our community committed in the fight to treat, cure and care for people with ALS. | The ALS Association
17.1K viewsJul 17, 2020
FacebookThe ALS Association
Your gift will help lead the fight to treat, cure and care for people with ALS - Donate Today! | The ALS Association
0:31
Your gift will help lead the fight to treat, cure and care for people with ALS - Donate Today! | The ALS Association
79.5K viewsJul 17, 2020
FacebookThe ALS Association
ALS is 100% fatal and there is no cure…yet. People living with living ALS need your help now—for care, for research, for hope. Give today to help make ALS livable for everyone, everywhere, until there is a cure. | The ALS Association
0:26
ALS is 100% fatal and there is no cure…yet. People living with living ALS need your help now—for care, for research, for hope. Give today to help make ALS livable for everyone, everywhere, until there is a cure. | The ALS Association
55.4K views7 months ago
FacebookThe ALS Association
We’re on a mission to not only discover treatments and a cure for ALS, but also to advocate for and empower people affected by ALS. Join us on our mission to help those living with ALS and their families - give now to make a direct impact. | The ALS Association
0:12
We’re on a mission to not only discover treatments and a cure for ALS, but also to advocate for and empower people affected by ALS. Join us on our mission to help those living with ALS and their families - give now to make a direct impact. | The ALS Association
4.7K viewsJul 31, 2024
FacebookThe ALS Association
This year, walk your way! Register for the Walk to Defeat ALS and support research, care services and advocacy for those living with ALS. Register yourself or start a team. | The ALS Association
0:23
This year, walk your way! Register for the Walk to Defeat ALS and support research, care services and advocacy for those living with ALS. Register yourself or start a team. | The ALS Association
827.3K viewsJul 8, 2021
FacebookThe ALS Association
An ALS diagnosis is life changing. Steve from Massachusetts is an ALS advocate and is sharing his experience of what it's like to live with the disease. | The ALS Association
0:53
An ALS diagnosis is life changing. Steve from Massachusetts is an ALS advocate and is sharing his experience of what it's like to live with the disease. | The ALS Association
2.2K viewsNov 8, 2023
FacebookThe ALS Association
Bringing the ALS community together like never before. In 2024, the ALS Association launched ALS Nexus, the first conference designed for the entire ALS community, focused solely on making ALS livable and finding a cure. Interested in joining us for ALS Nexus 2026? Visit alsnexus.org to learn more. | The ALS Association
0:36
Bringing the ALS community together like never before. In 2024, the ALS Association launched ALS Nexus, the first conference designed for the entire ALS community, focused solely on making ALS livable and finding a cure. Interested in joining us for ALS Nexus 2026? Visit alsnexus.org to learn more. | The ALS Association
2K views4 months ago
FacebookThe ALS Association
ALS Therapy Development Institute
Aug 29, 2019
als.net
1:23
Navigating health insurance while living with ALS shouldn’t be hard. Denials, delays, and unexpected roadblocks can add stress to an already challenging journey. That’s why the ALS Association created the ALS Insurance Navigator—a free, interactive resource. With step-by-step guidance on managing claim denials, submitting appeals, and securing coverage, people living with ALS can finally get the support they deserve. Check out our blog to learn more and access the ALS Insurance Navigator™ today!
1.5K viewsFeb 21, 2025
FacebookThe ALS Association
0:14
Thanks to your support, since 2014, we've funded over 580 ALS research projects across more than 20 countries, with the goal of finding effective treatments and, ultimately, a cure. Today on Global ALS/MND Awareness Day, the need for progress is as urgent as ever. Every project we fund brings new insight. Every dollar gets us closer to answers. Help us fund the next breakthrough. Donate today to support research that spans borders and changes lives. Donate today: www.facebook.com/donate/19427059
1.2K views10 months ago
FacebookThe ALS Association
1:03
If we are being honest... Your donation helps people living with ALS, funds critical research that can help create a world without ALS, and so much more. Tonight, the host of the ALS Matters podcast, Cory Mosley, sits down with our Director of Individual Giving, Ashley Yoder. Like Cory, Ashley is no stranger to #ALS after witnessing her mother pass from the disease. Together, they talk about their connection to ALS and how you can help make a difference this holiday season. Join us for the full
2.1K views5 months ago
FacebookThe ALS Association
0:07
Every 90 minutes someone is diagnosed with ALS. Help fund treatments and a cure. Donate Today. | The ALS Association
330.7K viewsDec 27, 2023
FacebookThe ALS Association
0:10
Walk to Defeat ALS is the #1 way to unite and fundraise for those living with ALS. Join us for a 2025 event near you - register today! | The ALS Association
450.1K viewsFeb 14, 2025
FacebookThe ALS Association
0:06
The year’s almost over, but there’s still time to make a difference. Donate by Dec. 31 to support ALS research and care that changes lives. | The ALS Association
76.9K viewsDec 19, 2024
FacebookThe ALS Association
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The ALS Association on Reels
3.3K views4 months ago
FacebookThe ALS Association
0:18
Melanie shares that navigating insurance denials for treatments, medications, and equipment is one of the most frustrating challenges for people living with ALS and their caregivers. Denials for critical care, like ventilators, are not just frustrating—they can be life-threatening. It’s time we take back control of our health care. That’s why our care services and advocacy teams have worked together and created the ALS Insurance Navigator—a tool to help guide you through the process of appealing
3.1K viewsFeb 19, 2025
FacebookThe ALS Association
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New Treatment for ALS Gives Hope to Patients and Families
8 months ago
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Make your donation today by visiting als.org/givingtuesday | The ALS Association
20.5K views5 months ago
FacebookThe ALS Association
1:00
Breaking News! The Centers for Medicare and Medicaid Services (CMS) has announced a groundbreaking directive requiring Medicare Advantage plans to approve coverage for Qalsody, a treatment for individuals living with genetic SOD1-ALS. This milestone is a direct result of our collective advocacy for research, approval, and accessibility of life-changing treatments like Qalsody. This decision marks a significant step in accelerating access to ALS treatments, helping to ensure that those living wit
3.2K viewsDec 11, 2024
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