National Amyotrophic Lateral Sclerosis (ALS) Registry
Register in advance for this webinar. After registering, you will receive a confirmation email containing information about joining the webinar.
ALS research counts on you! Be counted and join the fight against ALS.
Tell your story and take the risk factor surveys and help researchers learn more about ALS.
View the clinical trials and studies the Registry has helped to recruit for and how you can be notified.
Donate your blood and saliva at no cost to you and help ALS researchers learn more about this disease.