News

The ALS Association is urging Congress to pass legislation that would waive the Social Security Disability Insurance (SSDI) five-month waiting period for patients with amyotrophic lateral sclerosis (ALS). Under the ALS Disability Insurance Access Act of 2017, people with ALS could immediately begin receiving SSDI, which in turn qualifies patients to get…

The journal Neural Regeneration Research has published a review detailing the latest findings in the use of cannabis-derived compounds to treat amyotrophic lateral sclerosis (ALS). The review, “Can cannabinoids be a potential therapeutic tool in amyotrophic lateral sclerosis?,” notes that to date, the only available therapy for ALS patients is riluzole, which…

An eight-week mindfulness-based meditation program improved the quality of life and psychological well-being of patients with amyotrophic lateral sclerosis (ALS), a study reported. The randomized, open-label, controlled clinical trial covered 100 patients recruited between November 2012 and December 2014. All were diagnosed with ALS at least 18 months before the…

Researchers at Flinders University in Australia identified a new potential biomarkers in the urine of patients with amyloid lateral sclerosis (ALS).

Researchers in the U.S. showed that thanks to a computer-brain interface device that they developed people with different forms of paralysis, including amyloid lateral sclerosis (ALS), can type using direct brain controls faster than was previously possible.

People who eat fish and seafood containing high concentrations of mercury may be more likely to develop amyotrophic lateral sclerosis (ALS), a new preliminary study suggests. Researchers will present their study’s findings at the American Academy of Neurology’s 69th Annual Meeting, set for April 22-28 in Boston. The question isn’t whether people should…

People who have amyotrophic lateral sclerosis (ALS) know how hard it can be to communicate, but a new app developed by Microsoft researchers, called GazeSpeak, may make speaking with the eyes a reality. GazeSpeak, to be unveiled in May at the Conference on Human Factors in Computing…

Researchers have developed a method to measure the effectiveness of a process of RNA destruction that clears abnormal molecules from cells. Since abnormally high production of junk RNA has been thought to contribute to amyotrophic lateral sclerosis (ALS), the method can be used to screen for drugs that may boost…

The fitness franchise Orangetheory Fitness has partnered with Augie’s Quest to raise $1 million over the next two weeks for amyotrophic lateral sclerosis (ALS) research. During the campaign (#IBurnForALS) — which lasts from February 20 to March 5 — more than 570 Orangetheory studios nationwide will encourage their members…

If parents pass on mutations in the C9orf72 gene, their children not only develop amyotrophic lateral sclerosis (ALS) or frontotemporal dementia but do so at an earlier age due to an expansion of the mutation. This finding makes it easier for physicians to determine when to start monitoring an individual carrying a C9orf72…