Naples, Florida-based complementary and alternative medicine center helps patient restore mobility, confidence and return to daily living.

This is the new fantasy creature from the Phantasticals campaign that Ferrer has relaunched, coinciding with Global Amyotrophic Lateral Sclerosis (ALS) Awareness Day, on June 21. The aim is to raise public awareness of this rare, neurodegenerative, progressive disease that affects the motor neurons in the brain. Ferrer is leading the ADORE Phase III clinical trial to evaluate the safety and efficacy of the investigational drug FNP122 in the treatment of ALS.

Financial Assistance From The Assistance Fund Now Available for Eligible People Living With Amyotrophic Lateral Sclerosis (ALS).

A new set of rich Answer ALS project data is now available through the Answer ALS Data Portal

Administered by Kaggle, the End ALS Challenge asked participants to help identify solutions to the disease.

Administered by Kaggle, the End ALS Challange asks participants to help identify solutions to the disease

The Answer ALS Data Portal seeks to empower researchers around the globe with the data needed to finally answer ALS

Using AI to Increase Access to Communications for All with ALS

Set to debut on May 28, 2020, Gleason explores our human purpose with his guests

A new set of rich Answer ALS project data is now available through the Answer ALS Data Portal

Keegan-Michael Key, Weezer, Leon Bridges, Cynthia Erivo, Jon Dorenbos, and St. Paul and the Broken Bones come together to support Steve Gleason's Team Gleason and Answer ALS

WSU alum Steve Gleason and UW alum Phil Green challenge each other and their alma maters to raise the most funds in the first annual event

Samera Entertainment is proud to announce the Indiegogo campaign for the harrowing new short LAYERS from Angry Bee Films.

Simplesa, a nutrition company established in 2013 has expanded its products for the Deanna Protocol with the addition of LunaCell™.

Radicava is the first ALS treatment option approved in more than 20 years.

Stops in Philadelphia, Wilmington, Delaware, and a pregame ceremony prior to the Phillies-Mariners game at Citizen Bank Park on Tuesday

Leading a 10 Day, 233 Mile Journey by Wheelchair from Yankee Stadium to Washington DC, Determined To Strike Out ALS, May 5-15, 2017

Treatment options for Amyotrophic lateral sclerosis from ARS Therapeutics

ARS Therapeutics, Inc. Could Provide Immediate Help For ALS Patients

The Deanna Protocol is an all-natural metabolic program developed by Dr. Vincent Tedone which is continuing to improve the quality of life for people with ALS.

Simplesa® Reaches New Milestones in Customer Satisfaction

An ALS diagnosis is considered terminal but Simplesa examines why the Deanna Protocol can assist in easing symptoms and improving quality of life in some patients.

Simplesa ® is sponsoring a digital video project to help their clients leave a legacy.

Simplesa's dedication to making the Deanna Protocol simple and less costly for ALS Patients has led to the addition of more choices and lower costs for consumers.

Simplesa is working together with the Florida Chapter and supporting the Walk to Defeat ALS® in Florida by sponsoring several different area events in 2016.

Simplesa ® starts its "Share your Simplesa Story" holiday contest to raise awareness and thank its customers this holiday season.

The introduction of these two new dietary and nutritional supplements assists those facing challenges in weight management and/or bone management and loss.

A Group of ALS Patients and Families have been invited to the BBT Center on November 19th for an evening of Hockey

101 Mobility to have dog wash, hot dog sale to benefit Muscular Dystrophy Association.

101 Mobility of North Georgia is slated to hold an exhibition at this year's statewide ALS Educational Symposium.

New Product (ChillaVino) launching on Kickstarter.com on May 18th with contributions going to two ALS charities - The Angel Fund for ALS Research and Compassionate Care ALS.

Cycling for a cause. Fitness fanatics unite in order to help a fallen comrade raise money for a cure.

Award-winning limo company seeks to perpetuate past five years of growth and exceptional achievement

Award-winning Limo Company now offers exceptional line of executive motor coach buses

ALS Ontario, in conjunction with Bombardier Aerospace and The Marketing Store, will be running the second annual Plane Pull, a fun competition involving teams of 10 people, running as fast as they can in tthey can in 100-metre dash pulling a plane

19Events brought out supporters, sports figures, and celebrities alike, to raise money for individuals battling ALS (Amytrophic Lateral Sclerosis) during the Chargers vs Jaguars MNF Game at Gordon Biersch in Burbank, CA.

Day Tours Tampa Bay Introduces All-Inclusive Experience to Ybor City's Historic Ybor

Limo Company Reaches Elite Measure Despite Launching in the Midst of Struggling Economy

Carl Eller, President of the Retired Players Association, will be presenting at the American Academy of Professional Ringside Physicians Conference in Manila, Philippines

ALS Ontario is Paralyzing Poverty, the same way ALS, a fatal, rapidly progressive neuromuscular disease, paralyzes those afflicted.
ALS, also known as Lou Gehrig's disease, has no known cause, cure or effective treatment.