Neuromyelitis optica (NMO) is a rare, lifelong illness that causes problems with your eyesight and your ability to move your body. It is an autoimmune disorder. This means your body’s defense system gets confused and mistakenly attacks healthy parts of your central nervous system.
This condition has gone by a few different names over the years. A long time ago, it was called Devic’s disease, named after Eugène Devic, a doctor who first wrote about it. In 2015, a group of international medical specialists changed the official name to neuromyelitis optica spectrum disorder (NMOSD). Even with the long name, most experts still call it NMO for short.
For a long time, experts thought NMO was just a rare version of multiple sclerosis (MS). Today, they know for sure that NMO is its own completely separate condition.
NMO is much more common in females than in males. In fact, about 80% to 90% of all people who get NMO are female. It most often shows up in adults who are between 30 and 40 years old. Kids rarely get it, making up only about 5% of all cases.
People of any race or background can get NMO, but it does not hit every group equally. It happens more often in people of African descent, and it can also heavily affect people of Asian descent.
NMO is a very rare condition. On average, only about 0.3 to 4.4 people out of every 100,000 have it. This means there are only a small number of cases across the globe compared to other common sicknesses.
To understand how NMO hurts the body, it helps to look at how your nervous system is built. Your central nervous system is made up of your brain and your spinal cord. The nerves that let you see, called optic nerves, are actually part of your brain too. The rest of the nerves that spread out to your arms, legs, and toes make up your peripheral nervous system.
Your nervous system sends messages back and forth using tiny electrical and chemical signals. These signals travel through special nerve cells called neurons.
NMO is a demyelinating disease that damages the protective myelin sheath. Without myelin, the nerve fiber is left bare, making it more susceptible to injury or dysfunction. NMO primarily attacks neurons in two main areas: the optic nerves that connect your eyes to your brain and your spinal cord, which serves as the main highway for nerve signals.
NMO causes symptoms in "attacks," meaning the problems appear and disappear. These flare-ups can last for days or even months. The attacks can be very strong and sometimes cause lasting damage, so some symptoms might remain even after the attack ends.The symptoms fit into three main groups:
This happens when your optic nerves get swollen and inflamed. Your eyes collect light and send signals through these nerves so your brain can create a picture. When the nerve swells up, there is not much room for it inside your head, so the swelling presses hard on the nerve. It is a lot like falling asleep on your arm until it goes numb, but it happens to your eyesight. Symptoms can hit one eye or both, causing:
This is swelling in your spinal cord. The swelling blocks the electrical messages trying to travel up to your brain or down to your muscles. If it blocks all messages, it is called transverse myelitis. The symptoms depend on where the swelling is located, and they include:
It is unusual for NMO to attack the main parts of the brain, but it can occur if it affects the brainstem or hypothalamus. The brainstem sits at the lower back of your head and controls automatic jobs you do not have to think about, like breathing and blood pressure. If NMO attacks the brainstem or hypothalamus, it can cause:
Just above the brainstem is your hypothalamus. This structure also handles automatic body processes. When NMO affects it, this can cause other body systems to malfunction, such as causing excessive daytime sleepiness.
Experts do not yet fully understand why people develop NMO. Some of the main reasons include:
Sometimes these immune mistakes occur right after a person recovers from a normal infection. About 15% to 35% of people with NMO were sick with an infection right before their symptoms started.
NMO is also more likely to happen if you already have another autoimmune disease, such as lupus, celiac disease, or Sjögren’s syndrome. While it does not seem to be a disease you directly inherit from your parents, genetics might make certain people more likely to develop it.
No, NMO is not contagious. It cannot spread from one person to another like a cold or the flu.
Unlike other nerve diseases, NMO has specific tests that can help prove you have it. Doctors use a few different tools together:
There is no cure for NMO yet, but treatments have come a long way. Because it is an autoimmune issue, treatment has two main goals:
The medications or treatments are used to treat neuromyelitis optica -
The biggest side effect of long-term NMO drugs is that they lower your body's natural defenses. Your immune system is supposed to fight off viruses, bacteria, and even bad cells like cancer. When you take these drugs to protect your nerves, you also lose some ability to fight off normal bugs.
People taking these medicines have a higher risk of getting severe infections or developing tumors. Because of this, you have to be very careful to avoid getting sick and stay up to date on vaccines for things like the flu, COVID-19, and pneumonia.
The treatment and recovery timeline for NMO can vary because many factors play a role. Your doctor is the best source of information on this. They can tell you the timeline most likely for your case and what you can do to help the process.
NMO attacks usually hit suddenly. You might notice your vision worsening over a couple of weeks, with eye pain and blind spots. Severe swelling in your spine can cause sudden muscle weakness or trouble peeing. If the swelling hits your neck, it can make breathing hard, which requires emergency help.
Because it is a lifelong condition, you will likely need to take immune-weakening medicines for a very long time to prevent these flares.
For almost everyone with AQP4 or MOG antibodies, NMO is a lifelong condition. You will have to manage it for the rest of your life. About 10% to 20% of people—usually those who do not have either antibody—only ever experience one single attack and never have another one. However, because doctors cannot predict the future, they usually recommend staying on medicine anyway.
In the past, the outlook for NMO was not very good. Today, things are much brighter because we understand the immune system better. Modern medicines can cut down the number of repeat attacks by 72% to 88%. The five-year survival rate is now very high, ranging from 91% to 98%.
If someone has a lot of attacks, they are more likely to have lasting trouble with walking or seeing. About 22% of people completely recover all their abilities after an attack, 7% do not get better at all, and the other 71% get mostly better but have to live with some lasting symptoms.
Because NMO occurs randomly and its causes are still somewhat of a mystery, there is no known way to prevent it or reduce your risk of developing it.
Living with NMO takes some work, but you can do it by focusing on a few key steps:
Because your immune system is suppressed, minor infections can quickly become major problems. You should get in touch with a doctor right away if you experience:
Tender Palm Super-Speciality Hospital offers advanced Neuromyelitis Optica treatment in Lucknow, India, at an affordable cost. We have a team of experienced neurologists, neuroimmunology specialists, neurophysiologists, and rehabilitation experts who provide accurate diagnosis, personalized neurological care, and advanced treatment for Neuromyelitis Optica. Our neurosciences team has extensive experience in successfully treating Neuromyelitis Optica in Lucknow, India.
Call us at +91-9076972161
Email at care@tenderpalm.com