While we're hard at work in the lab, there are thousands of ALS Community members working just as hard to help us put an end to ALS. They're running events, creating fundraising campaigns and taking time out of their lives to help other pALS and their families deal with the ups and downs of living with the disease.
Go ahead, have fun. It's for a good cause!Fundraising events raise money for ALS research.
Every 90 minutes someone else is diagnosed with ALS. It isn't just our fathers and mothers, but an alarming number of our sons and daughters as well. This campaign is designed to create grea...
During the event at Boston's historic Fairmont Copley Hotel, US Congressman Michael Capuano will be awarded the first ever "ALS TDI Lou Gehrig Award" while chairman of the board Augie Nieto ...
An open discussion between ALS patients and ALS researchers hosted by the world's leading translational ALS research center. The ALS TDI Leadership Summit is a two-day event aimed at providi...
Events run by ALS Community members fund our work, too.
The Harlem Wizards take on the ALS All Stars at Siena College on February 9th. This is an event that combines aspects of big time production with hometown community flair. A fundraiser, wher...
On February 11th, family and friends of Pete Zucker will attend the Frank Sinatra Gala in Danville CA, to support the Pete Zucker Fund with ALS TDI. Get your dancing shoes ready and enjoy a ...
Meet the people that inspire our work and find out how you can help them beat ALS.
Diagnosed at age 20, Corey has led a crusade to end ALS. He's raised $2 million with the ... More >
The South Bend community once again showed its support for ALS (Lou Gehrig’s disease) rese... More >
Sean was president of the ALS Therapy Development Institute and died in 2009 at the age of... More >
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