1 00:00:04,000 --> 00:00:07,000 ALS research counts on you. 2 00:00:08,000 --> 00:00:11,000 For progress in ALS research, we need your help. 3 00:00:12,000 --> 00:00:16,000 You can help by sharing your data with the National ALS Registry. 4 00:00:17,000 --> 00:00:21,000 The National ALS Registry is the only research project of its kind. 5 00:00:22,000 --> 00:00:27,000 Data from the Registry will be used to help us better understand risk factors for ALS. 6 00:00:28,000 --> 00:00:32,000 If more people with ALS join the Registry, we can add to that knowledge. 7 00:00:34,000 --> 00:00:39,000 We are gathering information to help us learn what may cause ALS. 8 00:00:40,000 --> 00:00:44,000 Your data will be used to identify people in the U.S. with ALS, 9 00:00:45,000 --> 00:00:48,000 learn more about the characteristics of those with ALS, 10 00:00:49,000 --> 00:00:51,000 and better understand risk factors for ALS. 11 00:00:52,000 --> 00:00:54,000 How can you make a difference? 12 00:00:55,000 --> 00:00:58,000 You can take part by safely and securely sharing your information, 13 00:00:59,000 --> 00:01:01,000 and taking the risk factor surveys. 14 00:01:02,000 --> 00:01:06,000 Finding out what may increase the risk of getting ALS could help guide 15 00:01:06,000 --> 00:01:09,000 research into the treatment and prevention of ALS. 16 00:01:10,000 --> 00:01:14,000 Patients can also use the Registry to connect to other research studies and clinical trials. 17 00:01:15,000 --> 00:01:19,000 Turn ALS research into ALS progress. 18 00:01:20,000 --> 00:01:24,000 Learning more about people with ALS is critical to defeating it. 19 00:01:25,000 --> 00:01:27,000 Learn more about the National ALS Registry. 20 00:01:28,000 --> 00:01:33,000 Visit cdc.gov/als for more information. 国产精品久久久久久一级毛片