ALS research counts on you.
For progress in ALS research, we need your help.
You can help by sharing your data with the National ALS Registry.
The National ALS Registry is the only research project of its kind.
Data from the Registry will be used to help us better understand risk factors for ALS.
If more people with ALS join the Registry, we can add to that knowledge.
We are gathering information to help us learn what may cause ALS.
Your data will be used to identify people in the U.S. with ALS,
learn more about the characteristics of those with ALS,
and better understand risk factors for ALS.
How can you make a difference?
You can take part by safely and securely sharing your information,
and taking the risk factor surveys.
Finding out what may increase the risk of getting ALS could help guide
research into the treatment and prevention of ALS.
Patients can also use the Registry to connect to other research studies and clinical trials.
Turn ALS research into ALS progress.
Learning more about people with ALS is critical to defeating it.
Learn more about the National ALS Registry.
Visit cdc.gov/als for more information.