Amyotrophic Lateral Sclerosis Association

About the ALS Association

The Amyotrophic Lateral Sclerosis Association, commonly known as the ALS Association, is a leading organization dedicated to fighting ALS, a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Founded in 1985, the ALS Association has been at the forefront of research, advocacy, and support for individuals and families impacted by this devastating disease. With a mission to discover treatments and a cure for ALS, the organization also provides essential services to improve the quality of life for those living with the disease.

Our Impact

Through innovative research funding, the ALS Association has played a pivotal role in advancing scientific understanding of ALS. The organization has invested millions of dollars into research initiatives that have led to significant breakthroughs in treatment options and care strategies. Additionally, the ALS Association offers a range of support services, including care consultations, support groups, and educational resources, ensuring that patients and their families have access to the information and assistance they need.

Why Donate?

Your contributions, whether in cryptocurrency or cash, are vital to the ALS Association's mission. Donations directly support groundbreaking research, advocacy efforts, and essential services for those affected by ALS. By donating, you are not only helping to fund critical research that could lead to a cure but also providing immediate support to families navigating the challenges of this disease. Every dollar counts and can make a significant difference in the lives of those impacted by ALS.

Join the Fight Against ALS

Make a difference today by donating to the ALS Association. Your support is crucial in the fight against ALS, and together, we can work towards a future without this disease.