Connect. Collaborate. Change the Future of ALS.

ALS Nexus conference header graphic

More than a Conference

ALS Nexus is more than a conference – it’s an opportunity to spark new ideas and accelerate progress towards our goal of making ALS a livable disease until we can cure it.

By attending ALS Nexus, researchers, health care professionals, advocates, and members of our ALS community will gain:   

  • Meaningful connections with peers, insight into the needs of the ALS community, updates on cutting-edge research and clinical advancements, and inspiration to guide future efforts.   
  • Strategies to effectively advocate for more funding for ALS research, clinical care, and patient-centric legislation to ensure people impacted by ALS receive the benefits they deserve.   
  • The opportunity to influence future research, advocacy initiatives, and patient care. 

Register and Learn More

Changing the Future of ALS Together

We invite you to join leaders in the ALS community as we connect, collaborate, and change the future of ALS.

Read the 2024 recap

 

Frequently Asked Questions

Why Should I Attend ALS Nexus?

We are the only national nonprofit organization fighting ALS on every front. By leading the way in global research, providing assistance for people with ALS, coordinating multidisciplinary care through certified clinical care centers, and fostering government partnerships, we build hope and work to enhance quality of life while urgently searching for new treatments and cures.   

Our conference, ALS Nexus, provides a unique opportunity to gather the best and brightest minds across the full spectrum of the community where they can come together, ask questions, learn from one another, and use that experience to propel our mission further, faster.   

I’m not a medical professional. Can I still register for ALS Nexus? 

Yes! Our entire ALS community is welcome to attend. 

I am interested in becoming a sponsor, but I have questions. Who should I contact? 

Please email [email protected] and we will get back to you right away! 

I have another question that is not listed here. Who should I contact? 

Please email us at [email protected].

 

Image
ALS Association Logo


About the ALS Association

The ALS Association is the world’s leading ALS organization. We fund global research, provide on-the-ground care services, and advocate for people living with ALS. We are committed to making ALS a livable disease for everyone, everywhere, until we can cure it. 

Print Friendly and PDF