Whatever It Takes
ALS Awareness Month: It Takes All of Us
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ALS is a progressive neurodegenerative disease. People with ALS lose the ability to move, eat, speak, and eventually, to breathe. There is no cure for ALS. Yet.

Every May, the ALS community bands together for ALS Awareness Month. Through community events, volunteerism, advocacy work, and donations, we’re doing Whatever It Takes to create a world without ALS. We’ve already seen amazing progress through our collective efforts. But we’re not done yet.

Celebrity hairdresser and beauty expert, Ken Paves, talks about the impact of ALS on families.

Ken and his mom

Learn how you can help us spread awareness, share stories, and accelerate our pace of discovery

Advocate

Advocate

You can lead us closer to a world without ALS by joining the dedicated network of ALS advocates nation-wide. Help change the laws and policies that affect those living with ALS. Our advocacy efforts have helped pass the ACT for ALS, pushed the FDA to fast-track a promising new ALS treatment, and more.

Become an advocate

Participate

Participate

When you fundraise with friends and family you take us closer to discovering a cure. We host a variety of community events and offer volunteer opportunities. Get involved in the way that best suits you!

Get Involved

Donate

Donate

Your gift will support research to find a cure for ALS, provide urgently needed services to people with ALS and their families, and increase our advocacy efforts.

Make a Donation

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Get the latest ALS news, be inspired to take action, and learn more about how you can create a world without ALS.

Follow Us

Stay in touch! You can find us on Facebook, Instagram, Twitter & YouTube. Share our facts and stories with your networks to help spread ALS awareness.

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