With a goal of raising expanded public awareness of ALS, Team Gleason provides and documents extraordinary life Adventures for individuals with ALS. Team Gleason has been grateful to send families on unique Adventures they would otherwise have never dreamed possible after their diagnosis. 💛 Your support empowered 88 individuals living with ALS to go on 54 Adventures throughout 2024. We're looking forward to another amazing year of helping families make important memories - thank you, thank you,
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With a goal of raising expanded public awareness of ALS, Team Gl…
3.1K viewsJan 3, 2025
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Kaitlin Gonzales has been living with ALS for 9 years—and recently joined Her ALS Story and ALS TDI during our ALS Town Hall series to shed light on the lesser-known symptoms of ALS that often go unspoken. From acid tears to chronic pain that’s too often overlooked, Kaitlin bravely shared how these symptoms have shaped her experience—and why open conversations like this matter so much. This powerful discussion is part of our ongoing Town Hall series, hosted by Her ALS Story and ALS TDI, aimed at
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Kaitlin Gonzales has been living with ALS for 9 years—and recentl…
34.3K views8 months ago
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ALS is physically, emotionally, and financially devastating. People living with ALS need your help now—for access to care, for the next research breakthrough, for more time with their families. Give today to ensure no family is left waiting for the care, treatments, or hope they so desperately need. | The ALS Association
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ALS is physically, emotionally, and financially devastating. People livi…
55.4K views6 months ago
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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
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We’re on a mission to not only discover treatments and a cure fo…
4.6K viewsJul 31, 2024
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ALS doesn’t stop when the credits roll…and neither will we! Join us in making ALS livable and finding a cure! #MakeALSHistory | The ALS Association
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ALS doesn’t stop when the credits roll…and neither will we! Join us i…
21.8K views4 months ago
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Teens can get ALS too. Help us find out why. Project ALS met with 7 mothers nationwide who lost their teenage daughters to ALS. Watch their stories. Support crucial ALS genetics research now so we can end this disease - forever. Give now: https://fundraise.projectals.org/give/211906/#!/donation/checkout | Project ALS
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Teens can get ALS too. Help us find out why. Project ALS met with 7 m…
6.5K viewsDec 11, 2018
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It’s Walk to Defeat ALS season! We want to see you and your teammates back for another year of helping make ALS a livable disease. ✅ Sign up and activate your team 👥 Recruit past and new members ❤️ Fundraise for those living with ALS 🚶Walk together at an event in your community | The ALS Association
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It’s Walk to Defeat ALS season! We want to see you and your teammat…
1.4K viewsAug 9, 2023
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The Walk to Defeat #ALS is the largest annual fundraiser that sup…
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Kaitlin Gonzales has been living with ALS for 9 years—and recentl…
57.6K views8 months ago
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ALS takes away so much but it can’t take away our love. | The ALS Ass…
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In 1985 we became the first organization to fight ALS through …
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The Walk to Defeat ALS is our largest annual awareness and fun…
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How does your support help people with ALS? Watch this video to fin…
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Join us for episode 9 of ALS Matters tomorrow night at 8 p.m. EST. Cor…
13.3K views8 months ago
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Collaboration drives progress. The ALS Roundtable brings researche…
592 views2 months ago
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Members of Her ALS Story have found support, advice and optimis…
626 viewsJan 15, 2023
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“The ALS Association makes me feel heard! They don't pity me. The…
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In the summer of 2014, the world came together to support the figh…
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At 29, Lee is planning for her future while facing the harsh reality of A…
153K viewsFeb 15, 2025
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Kelly Kay – Mother and daughter posing together? Deal! | HDPornP…
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