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I was never told low voltage electrical injury increases the risk for motor neuron disease, but I'm in the process of being evaluated for it. I cannot believe already growing bills & I can still breathe on my own & eat on my own. My insurance company is already denying test after test & even my wheelchair had to be purchased privately because without a diagnosis, they will not pay for a chair... and without assessments, I cannot get a proper diagnosis...
It's seriously not fair that people with ALS can have such insurance problems!
It's seriously not fair that people with ALS can have such insurance problems!