Tag Archives: Lou Gehrig
Volunteers Needed for 2024 I AM ALS Flag Event on the National Mall
We are seeking Phi Delta Theta and Live Like Lou volunteers in the DC/MD/VA area to take photographs of a meaningful flag display at the National Mall for people living with and affected by ALS (Amyotrophic Lateral Sclerosis), also known as Lou Gehrig’s Disease.
Make a real difference for people and their families living with ALS by coming out to the National Mall on Wednesday, May 29 from 1 PM to 6 PM (or until the project is completed) to help take pictures of 6,000 flags that symbolize the number of people diagnosed with ALS this year. Flags are personalized for people living with and lost to ALS as well as ALS gene carriers. Photographs will be downloaded and shared all over the country.
Volunteers should meet at the National Mall between Washington Monument and 14th St NW. Metro stops near the installation are Smithsonian and Archives/Navy Memorial/Penn Quarter.
Volunteer Registration
https://forms.office.com/r/w424hwujPf
Questions? Please email Deb Paust, Community Organizing Associate at I AM ALS, at deb@iamals.org or Emily Johnson, Communications and Operations Associate, at emily@iamals.org.
Phi Delta Theta and Live Like Lou are proud to partner with I AM ALS in support of their DC ALS Awareness Event 2024.
About Live Like Lou
Named in honor of MLB Hall of Famer Lou Gehrig, a member of Phi Delta Theta Fraternity, Live Like Lou supports ALS families, funds emerging researchers seeking meaningful treatments and cures for ALS, and helps generate awareness of Lou Gehrig’s disease. Learn more at https://www.livelikelou.org.
Phi Delt DC Walks to Defeat ALS
Amyotrophic lateral sclerosis (ALS) is more commonly known as Lou Gehrig’s Disease. Lou Gehrig was not only a legendary New York Yankee, he was also a Brother in the Bond of Phi Delta Theta.
To honor Brother Gehrig’s memory and to help fight this horrible disease and provide resources to those currently affected by it, the Phi Delta Theta Washington, DC Alumni Club formed a team to participate in the annual “Walk to Defeat ALS” consisting of undergraduates, alumni and other supporters.
On Saturday, October 14, 2017, members of our team walked three miles around the Washington Monument Grounds in Washington, DC. Walkers included Phi Delt alumni and members of the DC Alpha Colony of Phi Delta Theta located at George Washington University.
Support the DC Alumni Club team “Phi Delta Theta DC” by visiting:
http://web.alsa.org/goto/phideltdc17
Whether or not you were able to walk with us, please consider joining our fight. Let’s do it for Brother Lou!
ALS Ride For Life
Christopher Pendergast was diagnosed with ALS twenty-four years ago. A former teacher for over thirty years, he chose to fight.
In an effort to build ALS awareness and raise financial support in search of a cure, Chris founded a non-profit, volunteer-run organization called ALS Ride For Life. For the past 20 years, Chris has traveled in his motorized wheelchair, along with other patients, families, and friends from Lou Gehrig’s memorial in Yankee Stadium either to Washington, DC or across Long Island.
To date, he has raised over $7M for research, patient care, education and awareness of the horrific disease that took the life of New York Yankee legend, and our own Phi Delta Theta brother, Lou Gehrig. Chris has made this ride for a cure his second career. He is on a ventilator now but soldiers on. He is one amazing man!
On Sunday, May 4, 2017 Chris and his team started their journey to Washington, DC. They made stops at the University of Maryland in College Park and George Washington University in Washington, DC en route to the United States Capitol.
While at GWU, Chris was welcomed to the Nation’s Capital on Sunday, May 14 and members of the DC Alpha Colony of Phi Delta Theta greeted him and showed their support in the fight against ALS. For more information, please contact Ride For Life’s Dick Iannuzzi, (631) 352-8998 or Dennis Constanza, DC Alpha Colony of Phi Delta Theta.
Ryan Zimmerman honored for his charitable work with the Lou Gehrig Memorial Award
By James Wagner, The Washington Post
Posted at 02:45 PM ET, 06/25/2012
Ryan Zimmerman before the 3rd Annual “A Night at the Park” at the Nationals Park on June 14. (Ilya S. Savenok – GETTY IMAGES FOR ZIMS FOUNDATION)
Zimmerman was honored for his charitable work, notably his ziMS Foundation, which he founded to raise money for a cure for multiple sclerosis, the disease his mother Cheryl suffers from. Zimmerman will be presented with the award before the Nationals game in Colorado on Friday. (Note: The award will be presented during Phi Delt Night at Nationals Ballpark on the evening of Friday, July 6th.)
Soon after being drafted in 2005, Zimmerman started his foundation, and created a golf tournament and a yearly event at Nationals Park. Zimmerman’s contract stipulated that he be given full use of the stadium one day a year for an event, Night at the Park, that raises money for his charity. In 2011, the event raised more than $300,000.
The award is given by the Phi Delta Theta Fraternity at Columbia University, Gehrig’s college fraternity. Zimmerman is the first National or Expo to be honored. Yankees shortstop Derek Jeter was honored last year, and Angels first baseman Albert Pujols and Phillies center fielder Shane Victorino the previous two years.
RELATED
Ryan Zimmerman of the Washington Nationals to Receive Lou Gehrig Memorial Award at Washington, DC Convention (Phi Delta Theta, 5/22/12)
Lou Gehrig Memorial Award at the Baseball Hall of Fame (Phi Delta Theta)
