Phi Delta Theta Fights ALS

About Us
The Florida Delta Chapter of Phi Delta Theta at the University of Miami is raising money to benefit research for ALS, which may be better known as Lou Gehrig’s Disease. Phi Delta Theta’s international philanthropy, the ALS Association, is a non-profit organization that funds ALS research and assists those with ALS to fight the illness. On the 75th Anniversary of Lou Gehrig’s farewell speech to baseball we ask that you please help our cause and join the fight against ALS.

About ALS Association
Established in 1985, The ALS Association is the only national non-profit organization fighting Lou Gehrig’s Disease on every front. By leading the way in global research, providing assistance for people with ALS through a nationwide network of chapters, coordinating multidisciplinary care through certified clinical care centers, and fostering government partnerships, The Association builds hope and enhances quality of life while aggressively searching for new treatments and a cure.

As the preeminent ALS organization, The Association leads the way in research, care services, public education, and public policy — giving help and hope to those facing the disease. The Association’s nationwide network of chapters provides comprehensive patient services and support to the ALS community. The mission of The ALS Association is to lead the fight to treat and cure ALS through global research and nationwide advocacy, while also empowering people with Lou Gehrig’s Disease and their families to live fuller lives by providing them with compassionate care and support.

Just what is ALS?
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Motor neurons reach from the brain to the spinal cord and from the spinal cord to the muscles throughout the body. The progressive degeneration of the motor neurons in ALS eventually leads to their death. When the motor neurons die, the ability of the brain to initiate and control muscle movement is lost. With voluntary muscle action progressively affected, patients in the later stages of the disease may become totally paralyzed.

ALS was first described in 1869 by French neurologist Jean-Martin Charcot, but it wasn’t until 1939 that Lou Gehrig brought national and international attention to the disease when he abruptly retired from baseball after being diagnosed with ALS. Most commonly, the disease strikes people between the ages of 40 and 70, and as many as 30,000 Americans have the disease at any given time. ALS has cut short the lives of other such notable and courageous individuals as Hall of Fame pitcher Jim “Catfish” Hunter, Senator Jacob Javits, actors Michael Zaslow and David Niven, creator of Sesame Street Jon Stone, television producer Scott Brazil, boxing champion Ezzard Charles, NBA Hall of Fame basketball player George Yardley, pro football player Glenn Montgomery, golfer Jeff Julian, golf caddie Bruce Edwards, British soccer player Jimmy Johnstone, musician Lead Belly (Huddie Ledbetter), photographer Eddie Adams, entertainer Dennis Day, jazz musician Charles Mingus, composer Dimitri Shostakovich, former vice president of the United States Henry A. Wallace and U.S. Army General Maxwell Taylor. Additional information about ALS and the ALS Association can be found at

How you can help
Please help us by sharing our campaign on Twitter and Facebook or by donating directly via this GoFundMe campaign page. Thank you for all of your support so far and continue to share our mission!
  • Chris Mullins 
    • $25 
    • 82 mos
  • Elissa and Marty Cascio 
    • $50 
    • 82 mos
  • Warren and Lisa Marcus 
    • $100 
    • 82 mos
  • Adam jakubowitz 
    • $26 
    • 82 mos
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    • $25 
    • 82 mos
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Brandon Butera 
Miami, FL
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