
Nevada Law Firm Leads The Way In Fight Against Cystic Fibrosis
Holley Driggs receives award from Cystic Fibrosis Foundation
LAS VEGAS, February 15, 2022 – Nevada-based law firm Holley Driggs has been awarded Nevada’s 2021 Corporate Team Sponsor by the Cystic Fibrosis Foundation (CF).
Championing progress in the fight against cystic fibrosis, Holley Driggs has been nationally recognized for their sponsorship and fundraising efforts.
“We are honored to receive this award,” said Holley Driggs Attorney, Frank A. Ellis III. “However, more importantly, I am blessed to have the support of [my firm] to be a part of this nationwide effort to help fight this disease and provide hope.”
According to the CF website, there are about 30,000 people in the U.S. who have cystic fibrosis, a rare genetic disease that affects the lungs, pancreas, and other organs.
Holley Driggs’ Las Vegas and Reno offices are a part of the 70 chapters and offices across the country that work diligently to raise funds and support our community in the search for a cure.
To learn more about cystic fibrosis or ways to get involved head to Cystic Fibrosis Foundation.
About Holley Driggs
Holley Driggs is proud to be a Nevada-based law firm focused on making positive contributions to their local and regional communities through the dedicated leadership of its team of more than thirty experienced attorneys. With offices in Las Vegas and Reno, the general practice business law firm represents national and international clients on a wide spectrum of business and corporate practice areas including commercial litigation, real estate, natural resources, eminent domain, employment law, bankruptcy, construction, gaming, and technology and intellectual property. The Firm’s shareholders also have broad experience in administrative law, estate planning, probate, and tax law. For more information, please visit www.nevadafirm.com or call (702) 791-0308 for the southern Nevada location or (775) 851-8700 for the northern Nevada location.
About Cystic Fibrosis Foundation
The mission of the Cystic Fibrosis Foundation is to cure cystic fibrosis and to provide all people with CF the opportunity to lead long, fulfilling lives by funding research and drug development, partnering with the CF community, and advancing high-quality, specialized care. We are fueled by a dedicated group of scientists, caregivers, donors, volunteers, and people with CF and their families who are united by a common goal: to find a cure for this devastating disease and help those with CF live longer, healthier lives. We are driven by a dream that one day, not one person will lose a life, child, sibling, parent, or friend to cystic fibrosis, and we are determined to succeed.