Information about you

If you have NMO, your clinical team will pass information about you on to the National Congenital Anomaly and Rare Diseases Registration Service (NCARDRS).

This helps scientists look for better ways to prevent and treat this condition. You can opt out of the register at any time.

Find out more about the register .



Content supplied by the NHS Website

Medically Reviewed by a doctor on 21 Dec 2018