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 the fight against 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, patient care, and advocacy, providing hope and support to those affected by this devastating condition.

Our Mission

The mission of the ALS Association is to lead the way in global research, provide comprehensive support for patients and families, and advocate for public policies that benefit those living with ALS. With a commitment to improving the quality of life for individuals diagnosed with ALS, the Association works tirelessly to fund innovative research and provide essential resources to patients and caregivers.

Impact of the ALS Association

Since its inception, the ALS Association has made significant strides in the fight against ALS. Through funding groundbreaking research, the Association has contributed to the development of new treatments and therapies that have the potential to change the lives of those living with ALS. In addition to research, the ALS Association offers a variety of programs and services designed to support patients and their families.

Research Funding

The ALS Association has invested millions of dollars in research initiatives aimed at understanding the causes of ALS and developing effective treatments. This funding has led to numerous breakthroughs, including advancements in gene therapy and drug development.

Patient and Family Support

Understanding the challenges faced by those living with ALS, the Association provides a range of support services, including care consultations, support groups, and educational resources. These services are designed to empower patients and families, helping them navigate the complexities of the disease.

Advocacy Efforts

The ALS Association is a strong advocate for policies that support ALS research and improve access to care. By working with lawmakers and stakeholders, the Association strives to ensure that the voices of those affected by ALS are heard and that necessary resources are allocated to combat this disease.

Why Donate to the ALS Association?

Your generous donations, whether in cryptocurrency or cash, play a crucial role in advancing the mission of the ALS Association. Every contribution helps fund vital research, support programs, and advocacy efforts that directly impact the lives of individuals and families affected by ALS.

Make a Difference

By donating to the ALS Association, you are joining a community of supporters dedicated to making a difference. Your contribution can help fund innovative research projects, provide essential resources to patients, and advocate for policies that improve the quality of life for those living with ALS.

Support Research and Care

With your help, the ALS Association can continue to support groundbreaking research and provide critical care services to those in need. Every dollar counts, and your support can lead to significant advancements in the fight against ALS.

Join the Fight Against ALS

Donate today to support the ALS Association's mission and help create a world without ALS. Your contribution, whether in cryptocurrency or cash, can make a lasting impact on the lives of those affected by this disease.