The Walk to Defeat ALS is the #1 way to unite and fundraise for those living with ALS. Join us to fund vital research and help make ALS livable for everyone. Find your local walk today! ❤️ | The ALS Association
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FacebookThe ALS Association
The Walk to Defeat ALS is the #1 way to unite and fundraise for those living with ALS. Join us to fund vital research and help make ALS livable for everyone. Find your local walk
The ALS Association. . The Walk to Defeat ALS is the #1 way to unite and fundraise for those living with ALS. Join us to fund vital research and help make ALS livable for everyone. Find your local walk today! ️
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Understanding ALS: Symptoms, Causes, and Living with the Disease
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YouTubeApr 11, 2025
ALS EXPLAINED SIMPLY! What is Amyotrophic Lateral Sclerosis? Causes, Signs, Symptoms & Progression!
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YouTubeMay 11, 2025
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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
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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
55.5K views10 months ago
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
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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
FacebookThe ALS Association
2.1K views7 months ago
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
0:14
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
FacebookThe ALS Association
76.4K views10 months ago
ALS Association ALS Research Progress
ALS EARLY SYMPTOMS & FIRST SIGNS | Patients Muscle Twitching Stages & Body Progression Explained!
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ALS EARLY SYMPTOMS & FIRST SIGNS | Patients Muscle Twitching Stages & Body Progression Explained!
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LIVING with ALS EXPLAINED! How Patients Cope with Muscle Twitching Fasciculations & Atrophy Symptoms
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ALS PAIN EXPLAINED by AI ✨ ALS Journey Progression Video of Early Signs, Stages & Muscle Symptoms
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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 Association55.5K views10 months ago
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
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
FacebookThe ALS Association2.1K views7 months ago
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
0:14
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
FacebookThe ALS Association76.4K views10 months ago
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
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
FacebookThe ALS Association76.9K viewsDec 19, 2024
No matter where you live you can make a difference by becoming an advocate for ALS! Become an advocate today by visiting https://www.als.org/advocacy | The ALS Association
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No matter where you live you can make a difference by becoming an advocate for ALS! Become an advocate today by visiting https://www.als.org/advocacy | The ALS Association
FacebookThe ALS Association521 views5 months ago
For families affected by ALS, Lou Gehrig Day is a chance to unite as a community, raising awareness and critical funds for ALS research. Help us make ALS a livable disease - join our Lou Gehrig Day team and fundraise with us by asking friends and family for support. Or make a donation to help find a cure for ALS. Let’s strikeout ALS - together! | The ALS Association
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For families affected by ALS, Lou Gehrig Day is a chance to unite as a community, raising awareness and critical funds for ALS research. Help us make ALS a livable disease - join our Lou Gehrig Day team and fundraise with us by asking friends and family for support. Or make a donation to help find a cure for ALS. Let’s strikeout ALS - together! | The ALS Association
FacebookThe ALS Association60.7K viewsMay 30, 2025
Make your donation today by visiting als.org/givingtuesday | The ALS Association
2:06
Make your donation today by visiting als.org/givingtuesday | The ALS Association
FacebookThe ALS Association30.2K views7 months ago
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Our goal is by 2030, ALS will be a livable disease. Help us make that goal a reality for people living with ALS and their families. | The ALS Association
FacebookThe ALS Association4.5K viewsMar 17, 2025
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We love our work! And we love when our friends and allies in the ALS community love their work! | The ALS Association
FacebookThe ALS Association3K views7 months ago
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It’s the 25th anniversary of Walk to Defeat ALS! Join us at a 2025 event near you as we walk and fundraise to discover treatments and a cure for ALS. Sign up today to support people living with ALS. | The ALS Association
FacebookThe ALS Association436.5K views8 months ago
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Veterans are more likely to be diagnosed with ALS, but the people who served our country with honor shouldn’t have to fight for fairness. Last week we had a chance to speak to offices on Capitol Hill about the Justice for ALS Veterans Act. Ask your lawmakers to cosponsor: https://als.quorum.us/campaign/Justice-for-ALS-Veterans-Act/ Thank you to the House and Senate original sponsors for their support: Sen. Lisa Murkowski, U.S. Senator Chris Coons, U.S. Senator Mike Rounds, Senator Sheldon Whiteh
FacebookThe ALS Association5.2K views9 months ago
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Help Find a Cure for ALS
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My orthotist’s favorite patient. And I’m considered a slow progressor! #ALS #endALS #findacure #wheelchair #mobilityaid #afo #braces #rollator #walking #neurodegenerative #orthotist #orthotics #oneyear
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There is no cure for ALS, but researchers are working to change that. Find out how you can join the fight at ALS.org #als #findingacure #helpingothers #lougehrigsdisease #nonprofitsoftiktok
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