Distribute Registry materials like fact sheets and guides at support group meetings, clinic visits or other events and gatherings where you may see people living with ALS, caregivers, family members or others from the ALS community. You can request these materials from the CDC for free – click here.
Share information about the Registry through social media and in any ALS online forums where you participate. An easy way to do this is to follow/like us by clicking on the social media icons at the bottom of this page and then sharing our posts about the Registry.
Include information about the Registry in your email signature.
Become an ALS Advocate and help educate state and federal government representatives about the importance of the Registry. Click here to learn more.