Everything is a Miracle Quote

ALS Quote: Albert Einstein You are a miracle. Choose how you live. Albert Einstein once said, “There are two ways to live your life. One is as though nothing is a miracle. The other is as though everything is a miracle.” Use this quote to stay motivated when the daily…

Cytokinetics has enrolled the first patient in the VIGOR-ALS extension trial (NCT02936635), which will assess the effects of tirasemtiv in patients with amyotrophic lateral sclerosis (ALS) who participated in the Phase 3 VITALITY-ALS (NCT02496767) study. Tirasemtiv is a novel skeletal muscle activator that triggers the muscle troponin complex, increasing…

In this short film from Project ALS (a research-based non-profit organization founded by Jenifer Estes), the role motor neurons play in amyotrophic lateral sclerosis (ALS) is discussed. Study validates the use of social cognitive measure in ALS patients. Read more here. The computer-generated graphics explains what happens…

Amyotrophic lateral sclerosis (ALS) is a disease that progressively shuts down your muscles by attacking certain cells in the brain and spinal cord that are needed to keep muscles moving. Eventually, patients will lose their mobility, have trouble moving, walking, swallowing and even breathing. But what exactly is ALS?…

The U.S. Food and Drug Administration (FDA) has designated  MediciNova’s Ibudilast (MN-166) an orphan drug as a potential treatment for amyotrophic lateral sclerosis (ALS). Ibudilast is a first-in-class, orally bioavailable small molecule phosphodiesterase (PDE)-4 and -10 inhibitor and a macrophage migration inhibitory factor (MIF) inhibitor that suppresses pro-inflammatory cytokines and promotes neurotrophic factors.

In this Houston Methodist video, we get to meet Kevin Kinchen. Kevin was diagnosed with amyotrophic lateral sclerosis (ALS) six years ago, but he hasn’t let that stop him from getting on with his life.  Nanci is a much-loved Hollywood publicist who was diagnosed with amyotrophic lateral sclerosis (ALS)…

Patients with amyotrophic lateral sclerosis (ALS) experience a gradual loss of the ability to walk, swallow and even breathe, and there’s no cure. It’s incredibly important that patients seek specialized treatment to address the different aspects of the disease. Find out seven ways to diagnose ALS. In this…

An analysis of previously published data suggests that neurofilaments in the blood and spinal fluid of people with amyotrophic lateral sclerosis (ALS) may be used to assess disease progression and neurodegeneration in general. Levels of the factor also were higher in ALS patients than in patients with diseases mimicking ALS,…

Augie’s Quest announced the 11th annual ‘Tradition of Hope’ gala event will be held Oct. 15 at the Beverly Hilton Hotel to raise funds for amyotrophic lateral sclerosis (ALS) research. Augie’s Quest is a cure-driven nonprofit effort dedicated to finding treatments and a cure for ALS. The effort…