National ALS Registry

The United States National ALS Registry opened this month. There is an introductory page on the ALSA website, and a recorded webinar outlining the Registry can be replayed by clicking here. I believe it is the duty of each PALS to register so that finally accurate numbers can be known of the toll of ALS in the US. The oft-quoted "30,000" is a very rough estimate and in all likelihood much too few. This is an important tool too long missing from researchers' kits. I registered yesterday. How about you?