ALS is a progressive neurodegenerative disease and we need your help to find a cure.
ALS is a progressive neurodegenerative disease and we need your help to find a cure.Learn More
2018 Bite Nite Phoenix
Phoenix Bite Nite will be on Saturday, June 2nd at The Westin Kierland Resort & Spa. Click on the button below to purchase your tickets today! For more information give us a call at 602-297-3800.
Become an ALS Research Ambassador!
Want to become even more active in the effort to find a cure for ALS? The ALS Clinical Research Learning Institute (CRLI) educates attendees on clinical research and therapy development, and empowers people to become advocates for ALS research. This free training, hosted by The Arizona Chapter, will take place on July 14 & 15, 2018. People with ALS, Caregivers, and surviving spouses are encouraged to apply. Click the button below to download an application! Hurry, applications are due by May 15th!
Celebrate a Loved One with ALS
Pay tribute to a friend or loved one affected by ALS. Each tribute is a personalized online fund designed to honor or memorialize someone special. Your Community of Hope fund creates a lasting legacy.Learn More
Whether you’re newly diagnosed, navigating your journey with the disease, caring for a person with ALS, or researching the cure, there are resources to support you.
Let us help you and your family cope with the day-to-day challenges of living with ALS.For People with ALS
Learn about our grant program, upcoming scientific meetings, and opportunities to collaborate.For Researchers
Caring for someone with ALS is hard work. We offer resources and support to help you.For Caregivers
Sign up to receive the latest news in ALS and learn how you can continue making a difference in the search to treat and cure this disease.
Your gift will help The ALS Association support research to find a cure for ALS and provide much-needed services to patients and their families. By becoming a part of The ALS Association family and making your gift today, you will help sustain hope in thousands of people affected by ALS.