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ATLANTA –
It is a disease that has no known cause, no treatment and no vaccine.
>> Read more new trends
Dozens of families across the country endure the horror of seeing a child go from happy and healthy to paralyzed and suffering.
That's exactly what happened to Aamira, 3 years old, who was diagnosed with acute flaccid myelitis.
>> Related: Mother says daughter has polio-like illness shows signs of recovery
Her mother, Reba Faircloth, told us that she was shocked by what the doctors had told her.
"They told me it was a type of polio, but it's not polio. That even hit me hard, "Faircloth said.
The Centers for Disease Control and Prevention have set up a working group that will bring together experts from different disciplines to determine the cause of MFA.
>> Related: CDC confirms 90 cases of polio-like syndrome, flaccid acute myelitis
In a press release, the CDC described the problem as a "critical public health problem".
The CDC has an entire section on its AFM website, it even starts reporting the number of cases each Monday.
The working group, composed of experts in science, medicine and public health, will also seek to determine the appropriate treatment and the measures to be taken to prevent it.
The disease is nothing new, but the peak of cases is. The CDC began to notice the increase in 2014.
So far this year, there have been 106 confirmed cases in 29 states, except five in children 18 years old or younger.
>> Related: Flabby Acute Myelitis: 7 Things to Know
Doctors say that most patients have cold-like symptoms before the disease degenerates into limb weakness.
The good news is that Aamira has progressively improved. After spending weeks in the hospital, she was finally able to walk alone.
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