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Target ALS

A New York based ALS research organization that's leading the fight for a cure.

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ALS Awareness Month

What is ALS Awareness Month?

In May 1992, a resolution was passed by the United States Senate to appoint May as National ALS Awareness Month, when ALS organizations and communities can unite to spread awareness regarding the disease, also called amyotrophic lateral sclerosis. At Target ALS, we recognize this time as an opportunity to share educational and inspirational content to not only the ALS community but those who are not yet familiar with ALS.

Statistics You Should Know 

$250k

The estimated cost of care
for a person with ALS.

15,000

The estimated amount of U.S. ALS patients at any given time.

55-75

The average age at diagnosis is between 55 and 75 years old.

5%  – 10%

Only 5% -10% of ALS cases are based on genetics.

69%

By 2040, ALS incidence rate will increase worldwide by 69%.

3 to 5 years

ALS patients typically survive 3-5 years after diagnosis.

Getting Involved in ALS Awareness Month

Join Our #WriteaNewFuture Campaign on Social Media

We’re optimistic now more than ever about achieving the innovative breakthroughs needed to end ALS, and for this year’s ALS Awareness Month, we want to inspire others to share optimism they have for their own future – whether they are a member of the ALS community, or not. Join us on Instagram Stories or Facebook Stories by downloading the background below on your phone, visiting our profile, and sharing how you’d like to #WriteaNewFuture for your personal journey. Don’t forget to tag our social handle, @targetals, in your Stories so we can follow along!
Click here to download the Stories background.

Annual Meeting

We foster ongoing networking and communication within our Target ALS Innovation Ecosystem, and are proud to host the premier ALS research meeting in the world, every year in Cambridge, Massachusetts. Nearly 350 academic and industry scientists, venture capitalists, and other investors, foundations and thought leaders attend. Learn more about this annual event, here.

Impact Takes Courage

We are proud to introduce the Target ALS Rebecca Luker Courage Award winners, presented by Mitsubishi Tanabe Pharma America, which recognizes the men and women making a difference in the fight against Amyotrophic Lateral Sclerosis (ALS).

Meet the winners

More ALS Resource

  • How to Help Someone with ALS: Tips for Friends, Family Members and Caregivers
  • How ALS Research Studies Work
  • The Stages of ALS: Framing the Progression of a Nonlinear Disease
  • Top 4 Things You Need to Know About ALS
  • False Positives and False Negatives: How ALS Can be MisdiagnosedS

ALS patients need your help.

With your support, we can and we will achieve breakthrough results. Finding effective treatments would finally bring new hope to patients and change the future for anyone who faces this disease. It will push us that much closer to realizing our mission: discovering a world where no one dies of ALS.

Donate Today

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We are a 501(c)(3) public charity (EIN: 81-0756743), eligible to receive tax-deductible contributions that directly support our mission to break down barriers to ALS research to find effective treatments.

The Target ALS (TALS) website is intended for informational purposes only. Opinions expressed may not be that of TALS or its employees. For more information about our digital policies, click here.

© 2023 Target ALS Foundation, Inc.
Target ALS Foundation
244 Madison Avenue #1025
New York, NY 10016
(332) 333-4140
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Join us this ALS Awareness Month to discover the people, stories, and science accelerating progress in ALS research.

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