Philip Flynn III Appointed New President and CEO of The ALS Association Florida Chapter

FLORIDA – The ALS Association Florida Chapter, a nonprofit organization dedicated to the fight against ALS, announces the selection of Philip Flynn III as its new President and CEO.  ALS, also known as Lou Gehrig’s Disease, progressively paralyzes its victims, attacking nerve cells and pathways in the brain or spinal cord, taking away their ability to walk, talk, eat and eventually breathe.  ALS has no known cause or cure, but The ALS Association is striving to change that.

“We’re really fortunate to gain a leader with Phil’s experience, talent and vision,” said Sandi Torres, Chairman of the Board for the Florida Chapter.  “The Board and the Leadership Team are confident that Phil is the best person to lead us into the future, while adding value to our chapter, our staff and most importantly to our patients.”

Mr. Flynn is a seasoned and successful executive who has spent over 35 years in fundraising and executive leadership roles in the nonprofit and education sectors.  His vast experience includes work with international medical programs, community and family foundations, higher education, and animal welfare.  With a Bachelor of Science and a Master of Science in Education Administration, Mr. Flynn has played a pivotal role as a leader, excelling in strategic planning, setting organizational direction, collaborating, and building invaluable teamwork to advance each organization’s mission.

“I am truly humbled and excited to join this organization to help fight this horrible disease,” said Mr. Flynn. “My experience with similar organizations gives me the knowledge and confidence to lead this team, to make a positive impact on the ALS community, and ultimately to advance the work to find a treatment and cure.”

The ALS Association Florida Chapter, www.ALSAFL.org, offers care and support to people living with ALS in Florida and funds research to find the cause and cure for ALS.  We are part of a nationwide network of local ALS Association chapters with the same vision – a world without ALS.  Through care, advocacy, research, education and support, we work to empower those with ALS to live fuller lives.  Every year, The ALS Association invests millions of dollars in research conducted by the best and brightest scientists around the world.  As the only national not-for-profit health organization dedicated solely to the fight against ALS, we give help and hope to those facing a devastating disease.  For more information, visit www.ALSAFL.org.