It's also called neuromyelitis optica spectrum disorder (NMOSD) or Devic's disease.
Symptoms of neuromyelitis optica (NMO) vary between people, and can be mild or severe.
The symptoms can include:
You may have symptoms only affecting your eyes (called optic neuritis), or only affecting your spinal cord (called transverse myelitis).
Symptoms start over a few hours or days. They usually last a few days or weeks, before gradually improving. Some people recover well with treatment, while others have longer lasting problems.
It's common for symptoms to come back, known as relapses. This can happen after a few weeks, months or years. In some people, relapses lead to permanent problems such as sight loss or mobility problems.
You can call 111 or get help from 111 online.
If a GP thinks you could have neuromyelitis optica (NMO) they'll refer you to a specialist in nerve conditions (neurologist) for tests and treatment.
NMO can be hard to diagnose because the symptoms vary and are similar to other conditions, such as multiple sclerosis.
You may have tests such as:
If you're diagnosed with neuromyelitis optica (NMO) you'll need treatment to stop the inflammation in your nerves and reduce the risk of relapses.
When your symptoms first start or if you're having a relapse, where symptoms come back, the main treatments are:
You'll usually also need to take medicines long term that reduce the activity of your immune system to help prevent relapses. These may include:
You may also be offered medicines to help with any ongoing symptoms, such as:
To help with symptoms such as muscle weakness and mobility problems you may be offered:
Neuromyelitis optica (NMO) is an autoimmune condition. It happens when your immune system attacks nerves in your eyes or your spinal cord.
It's not known what causes it. Sometimes it happens after a virus such as flu.
NMO is not an inherited condition. But it's more common in people with other autoimmune conditions, and those with close relatives who have autoimmune conditions.
It's more common in women and people of Asian or Black African origin.
If you or someone in your family lives with neuromyelitis optica (NMO) you can get support from charities including:
If you have NMO, your care team will pass information on to the National Congenital Anomaly and Rare Disease 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.