Jump to Navigation
MDA | Muscular Dystrophy Association
  • About MDA
  • Advocacy
  • Publications
  • Media
Give Now.
Give online Give by mail Give by phone

Main menu

  • Home
  • Learn About Muscle Diseases
  • Help Through Services
  • Hope Through Research
  • Ways to Help MDA

Search form

Milestones in ALS Research

April 2012

Download a printable PDF of this entire booklet PDF Document

MDA’s ALS Research Mission

ALS (amyotrophic lateral sclerosis, or Lou Gehrig’s disease) is a multisystem neurodegenerative disorder that primarily affects motor neurons, the nerve cells that control voluntary muscle movement. The loss of motor neurons causes the muscles they control to become weak and then paralyzed. Death, often within five years of diagnosis, usually is due to respiratory complications caused by paralysis of the muscles used in breathing.

MDA is the world’s leading nongovernmental funder of ALS research. Its worldwide program supports research efforts ranging from basic (early-stage) science, to preclinical testing and therapy development, to human clinical trials. Since its inception, MDA has dedicated more than $307 million to ALS research, services, education and advocacy programs.

Current MDA-supported ALS research is focusing on several areas, including:

  • ALS-associated genes SOD1, TDP43, FUS, UBQLN2 and C9ORF72;
  • potentially toxic protein clumps called aggregates;
  • oxidative stress
  • facts that cause support cells to attack motor neurons instead of nourishing and protecting them;
  • disruption of the cellular waste-disposal system
  • the role of the immune system in ALS;
  • ways to nourish and protect motor neurons;
  • mitochondrial energy production;
  • stem cell therapy; and
  • drug discovery and development.

Other critical MDA-funded ALS research contributions include:

  • establishment of an MDA/ALS Clinical Research Network to streamline and support tests of experimental treatments, with locations at Methodist Hospital (Houston), Massachusetts General Hospital (Boston), Columbia University (New York City), Emory University (Atlanta), and California Pacific Medical Center (San Francisco); and
  • sponsorship and hosting of national and international scientific meetings on ALS research.

MDA continues to be inspired by the words of the late Michael E. DeBakey, world-renowned heart surgeon and an MDA national vice president, who said, “There are no incurable diseases. There are only diseases for which no treatment has yet been developed.”

View the Timeline

Publications

  • Magazines
    • Advertise
    • Subscribe to Quest
  • Guidebooks
  • Daily Living
  • "Facts About" Booklets
  • MDA Programs
  • Frequently Asked Questions

Milestones in ALS Research

  • ALS Milestones Timeline
MDA in Your Community
Stay informed. Stay involved.
SIGN UP FOR RESEARCH NEWS

Quick Links

  • Tell Us About Your MDA Clinic
  • Become an MDA Advocate
  • Be a Summer Camp Volunteer
  • Sign Up for MDA News Updates
  • MDA's Muscle Shop
Give Now.

Ways To Help

  • Advocacy
  • Become a Volunteer
  • Donor Login
  • Legacy Gifts
  • MDA Programs
  • Matching Gifts

About MDA

  • Art Collection
  • Contact MDA
  • Become a Volunteer
  • Careers
  • FAQ
  • Media
  • What is MDA?

MDA.org

  • Find Support
  • Get Involved
  • Publications
  • Site Map
  • Muscle Shop

Connect with MDA

  • Facebook Twitter YouTube  

Muscular Dystrophy Association — USA
National Headquarters
3300 E. Sunrise Drive
Tucson, AZ 85718
(800) 572-1717

Privacy Policy | Terms of Use

©2013, Muscular Dystrophy Association Inc. All rights reserved.
 

Advertise