Cure for ALS

Mission Statement:
Cure for ALS is a nonprofit organization whose mission is to host fundraising events, and support advocacy
and awareness for Amyotrophic Lateral Sclerosis (ALS), to advance medical research that will discover a cure.

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We need your help to STOP ALS

Amyotrophic Lateral Sclerosis (ALS) is a disease that attacks the motor neurons, or nerve cells, in the brain and spinal cord. It is more commonly known as Lou Gehrig’s Disease. ALS can strike anyone. Without warning it happens to 15 people each day in the United States. The average life expectancy is only two to five years from the time of diagnosis. ALS slowly takes away the ability to move, speak, swallow, and ultimately breathe. There is no cure so there are no survivors to tell their stories.

Every 90 minutes someone is diagnosed with ALS while another person with ALS dies. There are currently 30,000 Americans living with ALS. Without raising awareness and funding ALS will not receive the research necessary to find a cure. It will continue to strike down every person who is diagnosed.




2012 Events & Fundraisers:

  • Ongoing

  • T.E.A.M. Cure ALS Foundation
    handcafted jewelry sale
    Click Here for more info...



  • January 29th, 2012

  • "Season of a Lifetime" movie screening
    Cumming, GA
    Click Here for more info...






    Magnets are in. Download the order form and help in the fight to find a "Cure For ALS".
    Click Here





    Research, News,
    ALS Testimonials


  • The Promise and the Reality of Stem-Cell Therapies for Neurodegenerative Diseases



  • New work highlights axon sickness



  • Mike Winston- "How are you really doing?


  • A letter from Professor Gey.  It is wonderfully written and a great visual of ALS and it's progression.
            Steven G. Gey,
            Constitutional Law Professor,
            Florida State University College of Law


  • On Borrowed Time



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