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The ALS Association, the leading national non-profit organization dedicated to fighting ALS on every front, is excited to announce its inaugural ALS...
"LUKi & The Lights," an animated short film aimed at helping young audiences understand and cope with the complexities of ALS, will make its public...
The ALS Association proudly announces the largest single gift in its history from the estate of the late philanthropist Hugh Hoffman. The $58 million ...
The ALS Association has created a new diagnostic guide, thinkALS, that will help neurologists more quickly diagnose ALS. Earlier diagnoses allow...
Following Amylyx's announcement that it intends to submit a New Drug Application (NDA) for AMX0035, The ALS Association today urges the Food and Drug ...
The ALS Association today announced that California's legislature, in conjunction with the Department of Health has approved $15 million over the...
The ALS Association today announced a goal of making ALS a livable disease by 2030. Currently, there are no cures or significant life-extending...
May is ALS Awareness Month, and people living with the disease are part of a new ALS Association campaign to educate the public about the urgent need ...
Following the lack of action by the FDA to expedite approval of AMX0035, an experimental treatment for ALS, The ALS Association today called on the...
Congress passed a law ending the five-month waiting period for people with ALS to access Social Security Disability Insurance benefits on Tuesday....
Today, in response to the New England Journal of Medicine publication of encouraging clinical trial results showing that Amylyx Pharmaceuticals'...
The ALS Association today announced a $3 million commitment to the first platform trial for ALS, taking place at the Sean M. Healey & AMG Center for...
The ALS Association is partnering with, and will be directly investing in, the ALS Investment Fund II to raise $100 million to accelerate investment...
Hundreds of Bostonians today joined The ALS Association to commemorate the fifth anniversary of the ALS Ice Bucket Challenge with its co-founders,...
An independent research organization reported that donations from the 2014 ALS Ice Bucket Challenge enabled The ALS Association to increase its...
ALS Ice Bucket Challenge co-founders Pete Frates and Pat Quinn, along with The ALS Association, today kicked off the fifth anniversary of the...
Several ALS organizations announced on Wednesday that the first participant was successfully given a dose of AT-1501 in the first in-human trial of...
The ALS Association is providing new funding to allow GNS Healthcare to use artificial intelligence (AI) to create a comprehensive disease model to...
The ALS Association has released a series of public service announcements (PSAs) highlighting what life is like with ALS. Throughout May, which is...
The ALS Association is kicking off ALS Awareness Month by encouraging the public to "Raise Your Voice" in May on behalf of those living with ALS....
The ALS Association today announced the launch of "Project Revoice," an international initiative to help people with ALS [also known as Motor Neurone ...
The family of Carmen Schentrup, who was killed in the February mass shooting at Marjory Stoneman Douglas High School in Parkland, Fla., has...
Researchers have identified a new ALS gene: KIF5A. This important gene discovery, funded by The ALS Association through ALS Ice Bucket Challenge...
The ALS Association today announced that Calaneet Balas has begun her role as President and CEO. Her appointment marks the culmination of an orderly...
Following the devastating effects of Hurricane Harvey, The ALS Association today announced the establishment of a Disaster Relief Fund to ensure that ...
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