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Stay informed with the latest breaking news from Calaneet balas on our comprehensive webpage. Get up-to-the-minute updates on local events, politics, business, entertainment, and more. Our dedicated team of journalists delivers timely and reliable news, ensuring you're always in the know. Discover firsthand accounts, expert analysis, and exclusive interviews, all in one convenient destination. Don't miss a beat — visit our webpage for real-time breaking news in Calaneet balas and stay connected to the pulse of your community

Cincinnati millionaire leaves world's largest-ever gift for ALS

Hugh Hoffman passed away from natural causes in March 2023 at the age of 91.

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$58 Million Gift Largest In ALS Association History

$58 Million Gift Largest In ALS Association History
thenonprofittimes.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from thenonprofittimes.com Daily Mail and Mail on Sunday newspapers.

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NuvoAir partners with ALS Association to launch virtual pulmonary care service

The partners will initially launch in two clinics in Texas to provide patients with ALS access to virtual-first specialty care providers, including respiratory therapists.

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South Carolina Commits $500,000 for People Living with ALS

South Carolina General Assembly Designate Grant Towards ALS Patients and Their Families

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South Carolina Commits $500,000 for People Living with ALS

South Carolina Commits $500,000 for People Living with ALS
postandcourier.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from postandcourier.com Daily Mail and Mail on Sunday newspapers.

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South Carolina Commits $500,000 for People Living with ALS

The ALS Association, the country’s largest nonprofit organization devoted to curing and caring for people with Amyotrophic Lateral Sclerosis (ALS), today publicly thanked the South Carolina General Assembly and Rep. Bill Herbkersman, Rep. Leon Stavrinakas, and Sen. Sandy Senn for including $500,000 to support ALS patients and caregivers in the state. “State lawmakers can play […]

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7th annual CEO Soak benefits ALS Association

CEOs don’t wait for things to happen — they make things happen. That’s what more than 50 executives, along with local business and community leaders, did on Thursday at CEO Soak, the seventh annual ALS Association Western Pennsylvania Chapter’s fundraiser to support the fight against the disease. Amyotrophic lateral sclerosis

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May to chair CEO Soak event for ALS research

Tommy May, Arkansas-based businessman, has been named chair of the 2023 Inaugural CEO Soak Arkansas, a program of The ALS Association.

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Drug for rare form of Lou Gehrig's disease OK'd by FDA | Courthouse News Service

Drug for rare form of Lou Gehrig's disease OK'd by FDA | Courthouse News Service
courthousenews.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from courthousenews.com Daily Mail and Mail on Sunday newspapers.

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Drug for Rare Form of Lou Gehrig's Disease OK'd by FDA

Food and Drug Administration regulators on Tuesday approved a first-of-a-kind drug for a rare form of Lou Gehrig’s disease, though they are requiring

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