El año pasado, a Brian Davis le diagnosticaron ELA a los 35 años. Esta temporada navideña, él y su esposa, Katy McNeil, quieren compartir cómo la enfermedad ha cambiado sus vidas y lo mucho que el apoyo a la Les …
2023 Gift Guide for People Living With ALS
On Black Friday, Cyber Monday, or any day this holiday gift season, it’s never too early to start looking for the perfect present. If your holiday shopping list includes someone who is living with ALS or a caregiver, we’ve compiled …
November 2023 Foundation eNews
ALS Better Care Act Makes Its Way to the Senate Exciting news from Capitol Hill: the ALS Better Care Act has been introduced in the U.S. Senate, a crucial step towards improving access to multidisciplinary care for those battling ALS. …
Studies Identify Novel Underpinnings of Genetic ALS
A pair of recent studies from the laboratory of Evangelos Kiskinis, PhD, associate professor in the Ken and Ruth Davee Department of Neurology’s Division of Neuromuscular Disease and of Neuroscience and a member of the Les Turner ALS Center at Northwestern Medicine, have uncovered novel …
Letter to the Editor: Support veterans with ALS
This letter was published in the Chicago Tribune on Saturday, Nov. 11, 2023 For many people, baseball is the first thing that comes to mind when they think of amyotrophic lateral sclerosis, or ALS, thanks to New York Yankees player …
