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