Children with AFM struggle to live with debilitating disease: Part 1 | Nightline

“Nightline” follows two children who were diagnosed with the rare disease acute flaccid myelitis in 2018 and one woman who’s had it for a decade, and is helping others to overcome it.

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#Nightline #AFM #AcuteFlaccidMyelitis #Disease #Health #Children

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24 thoughts on “Children with AFM struggle to live with debilitating disease: Part 1 | Nightline

  1. What makes this different from polio? I went to school in the fifties with a kid who had had polio, and his left arm was withered, just as the limbs on some of these kids are. It's a paralysis, which is lifelong, so again, how does it differ from polio?.

  2. My heart broke in half when Camden’s dad said he is the only certified care giver so if something happened it’s all on him. For a parent to have to take this burden bc having professional help is not financial attainable is just cruel and there are sooo many families who are in the same situation for many different illnesses and conditions.

  3. So hard to watch a young child be stricken with something so scary. This made me go hug my 5 and 13 year old grandson. I just can't imagine how I'd cope with something like this. These parents are so strong. I truly hope they find a cure for AFM. Never even heard of this till now

  4. I bet Vaccines are the cause of this damn disease the first case was diagnosed in 2010 so what happened in that time? Where did this come from? God has nothing to do with it and prayer is worthless. They got to find out what changed in the DNA. DAMN VACCINES, I looked it up happens mostly 1to 8 years of age.

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