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Brian Wallach (born October 9, 1980) is an American businessman, lawyer, and amyotrophic lateral sclerosis (ALS) research and patient advocate. He became known for his activism after being diagnosed with ALS in 2017. [1] Since then, Wallach has founded a nonprofit, I AM ALS, and a telemedicine company, Synapticure.
ALS can strike at any age, but its likelihood increases with age. [64] Most people who develop ALS are between the ages of 40 and 70, with an average age of 55 at the time of diagnosis. [65] ALS is 20% more common in men than women, [65] but this difference in sex distribution is no longer present in patients with onset after age 70. [64]
He was awarded the Congressional Gold Medal for his contributions to ALS awareness. Activist Brian Wallach's advocacy through his foundation I AM ALS saw the Accelerating Access to Critical Therapies for ALS Act signed into law by President Joe Biden in 2021. Jason Becker (born 1969), American musician, songwriter and composer. [1]
Articles relating to amyotrophic lateral sclerosis (ALS), also known as motor neurone disease (MND) or Lou Gehrig's disease. It is a specific disease which causes the death of neurons controlling voluntary muscles. ALS is characterized by stiff muscles, muscle twitching, and gradually worsening weakness due to muscles decreasing in size.
Familial ALS is the most studied; however, a new technique that was recently introduced is the use of induced pluripotent stem cells (iPSC). [2] In this study the researcher can isolate skin fibroblast from a patient with familial or sporadic ALS and reprogram them into motor neuron to study ALS. [ 2 ]
I AM BREATHING reminds us what it is to be alive - a tale of fun and laughs with a smattering of upset and devastation. Within a year, Neil Platt goes from being a healthy 30-something British bloke with a great sense of humor to becoming completely paralyzed from the neck down, thanks to the devastating illness he has inherited - known as ALS, MND, or Lou Gehrig's disease.
Project ALS is a non-profit organization whose mission is to identify and support leading scientific research toward the first effective treatments and a cure for ALS. Founded in 1998 by Jenifer Estess , Valerie Estess, Meredith Estess, and Julianne Hoffenberg, Project ALS recruits scientists and doctors to work together toward a better ...
The ALS Association is an American nonprofit organization that funds global amyotrophic lateral sclerosis (ALS) research, provides care services and programs to people affected by ALS through its nationwide network of clinical care centers, and works with ALS advocates around the country for state and federal policies that serve people living with amyotrophic lateral sclerosis (ALS), also ...