On May 18, 2022, several guests joined ALS Texas for a special virtual ALS advocacy event. During this insightful...

On May 18, 2022, several guests joined ALS Texas for a special virtual ALS advocacy event. During this insightful...
On December 23, 2021, we reached a groundbreaking milestone for the ALS community. President Joe Biden has just signed...
One month ago on May 25, 2021, representatives from the FDA joined a We Can’t Wait Action Meeting. During this...
The average life expectancy for someone after an ALS diagnosis is only 2 – 5 years. However, the process of...
In a huge win for the ALS community, the Centers for Medicare & Medicaid Services (CMS) expanded telehealth...
Fort Worth local Colin Hadley is an ALS Hero and inspiring PALS who advocates for the rights of those living with ALS....
On June 9th-11th fourteen ALS advocates from Texas, along with our Executive Director and Sr. Director of Mission...
Last week the ALS Disability Insurance Act was reintroduced in the 116th Congress. The bill (S.578) aims to eliminate...
On December 4th, 2018 ALS Advocate Sunny Erasmus joined scientists, health care professionals, and other fellow PALS...
Since being diagnosed with ALS in 2015, right before her 28th birthday, Sunny Erasmus has become a warrior for others...
More than 570 ALS advocates from across the country joined together for the 2018 National ALS Advocacy Conference in...
We had the privilege of awarding the first Harrison Brown Volunteer of the Year award to Whitney Sadler at the 2017...