Because you will have access to de-identified information in the Registry, you can learn more about DM, how it's experienced by other community members, and what the broader community looks like. This includes:

• Information regarding clinical trials and studies for which you or members of your family may be eligible
• Where Registry participants are located
• What symptoms are most and least prevalent
• How other community members manage living with DM
• How DM has impacted other families living with this disease