Michael DeSabato isn’t new to fundraising. Monroeville’s Bella Capelli Academy cosmetology school, owned by his parents, actively supports Jeremiah’s Place – Pittsburgh’s only free, crisis nursery ...

Tony Arenas, who has cystic fibrosis and received a double lung transplant, was recently diagnosed with stage 4 colon cancer. Despite a lifetime of medical challenges, Arenas maintains a determined ...

This Friday, October 3rd, the Cystic Fibrosis Foundation will host its Little Rock Finest event at 6:30 p.m. in Argenta Plaza, bringing together the best of the city’s food and drink—all for one cause ...

The Seattle Mariners’ season has come to an end after losing 3-4 to the Toronto Blue Jays in Game 7 of the ALCS. In a ruling Monday afternoon, the U.S. Court of Appeals for the Ninth Circuit said ...

The work of Dr. Michael J. Welsh and his fellow researchers has improved the quality of life and life expectancy for people with cystic fibrosis. Michael J. Welsh has won the Lasker Award and the 2025 ...

LITTLE ROCK, AR (KATV) — The Cystic Fibrosis Foundation is hosting an event in Arkansas with the ambitious goal of raising between $250,000 and $350,000 to support research and care for those affected ...

Harry L. Thompson III, a Bell Atlantic Telephone manager and advocate for cystic fibrosis awareness and care, died of heart failure Sept. 3 at the Pickersgill Retirement Community. He was 90. Born in ...

David Dent was spiraling. The swim coach knew something was wrong, but he couldn’t pinpoint it, and it wouldn’t stop affecting him. Eventually, the West Virginia assistant coach was diagnosed with ...

Those who are battling cystic fibrosis may be one step closer to having less invasive care thanks to research being conducted at Colorado State University in Fort Collins. Students and staff are ...

A pair of San Diego scientists who helped develop a treatment for cystic fibrosis, a life-threatening genetic disorder that damages people’s organs, have been named recipients of a 2025 Lasker Award, ...

Their research led to the development of a drug that nearly doubles the life expectancy for adult cystic fibrosis patients Three scientists who revolutionized the treatment of cystic fibrosis and ...

The scientific imperative to identify drugs that could repair mutant CFTR presented a formidable challenge. Small molecules that specifically bound and repaired a defective CFTR peptide fold were ...