About Acute Flaccid Myelitis
Acute flaccid myelitis (AFM) is a rare but serious condition. It affects the nervous system, specifically the area of the spinal cord called gray matter, which causes the muscles and reflexes in the body to become weak. This condition is not new. However, the large number of AFM cases reported since 2014, when we first started our surveillance for this condition, is new. The risk of getting AFM varies by age and year. We have seen increases in AFM cases every two years since 2014 and mostly in young children. Still, CDC estimates that less than one to two in a million children in the United States will get AFM every year.
CDC understands that parents who have had a child diagnosed with AFM have many concerns and questions. AFM is a serious condition that can be difficult for children and their parents or caregivers. You are in the best position to be an advocate for your child. Talk to the doctor about any discomfort your child may have and ask about treatment options. Ask your child’s school about resources they may have to accommodate this illness. Spending time with others is also an important part of wellbeing and recovery. Encourage friends and family to spend time with your child if they feel well enough for visitors.
We invite you to share questions you have by sending them to CDC-INFO.
For patient resources, visit the Transverse Myelitis Association Resourcesexternal icon.
Most people will have sudden onset of arm or leg weakness and loss of muscle tone and reflexes.
Some people, in addition to arm or leg weakness, will have:
If you or your child develops any of these symptoms, you should seek medical care right away. Your doctor may collect information about your symptoms and send this information to their health departments. This is because CDC is asking doctors to be alert for patients with symptoms of AFM so that we can learn more about this condition.
AFM is diagnosed by examining a patient’s nervous system in combination with reviewing pictures of the spinal cord. A doctor can examine a patient’s nervous system and the places on the body where he or she has weakness, poor muscle tone, and decreased reflexes. A doctor can also do an MRI (magnetic resonance imaging) to look at a patient’s brain and spinal cord, do lab tests on the cerebrospinal fluid (the fluid around the brain and spinal cord), and may check nerve conduction (impulse sent along a nerve fiber) and response. It is important that the tests are done as soon as possible after the patient develops symptoms.
AFM can be difficult to diagnose because it shares many of the same symptoms as other neurologic diseases, like transverse myelitisexternal icon and Guillain-Barre syndrome. With the help of testing and examinations, doctors can distinguish between AFM and other neurologic conditions.
Learn more about the type of information that helps to determine if a patient has AFM or not.
We think viruses likely play a role in AFM. Since 2014, most patients with AFM (more than 90%) had a mild respiratory illness or fever consistent with a viral infection before they developed AFM. All the stool specimens from AFM patients that we received tested negative for poliovirus. Most patients had onset of AFM between August and October, with increases in AFM cases every two years since 2014. At this same time of year, many viruses commonly circulate, including enteroviruses, and will be temporally associated with AFM.
We detected coxsackievirus A16, EV-A71, and EV-D68 in the spinal fluid of four of 563 confirmed cases of AFM since 2014, which points to the cause of their AFM. For all other patients, no pathogen (germ) has been detected in their spinal fluid to confirm a cause. When a pathogen (germ) is found in the spinal fluid, it is good evidence that it was the cause of a patient’s illness. However, oftentimes, despite extensive testing of AFM patients, no pathogens are found in the spinal fluid. This may be because the pathogen has been cleared by the body or it is hiding in tissues that make it difficult to detect. Another possibility is that the pathogen triggers an immune response in the body that causes damage to the spinal cord. We are searching for what triggers AFM in some children who have had a fever and/or respiratory illness compared to most children who don’t get AFM.
There is no specific treatment for AFM, but a doctor who specializes in treating brain and spinal cord illnesses (neurologist) may recommend certain interventions on a case-by-case basis. For example, neurologists may recommend physical or occupational therapy to help with arm or leg weakness caused by AFM. CDC is working closely with national experts to better understand how to treat AFM and updated our clinical management considerations. We are also working to understand the long-term outcomes (prognosis) of people with AFM.
Since we don’t know the cause of most of these AFM cases or what triggers this condition, there is no specific action to take to prevent AFM. However, most children had a respiratory illness or fever consistent with a viral infection before they developed AFM. You can decrease your child’s risk of getting viral infections by having him/her:
- wash their hands often with soap and water,
- avoid touching his/her face with unwashed hands, and
- avoid close contact with people who are sick.
You can decrease the risk of spreading viral infections by:
- cleaning and disinfecting frequently touched surfaces, including toys and doorknobs,
- having your child cover coughs and sneezes with a tissue or upper shirt sleeve, not hands, and
- keeping sick children at home.
For more information on what CDC is doing, see our AFM Investigation page.