Hi all. I have not been diagnosed with ALS, however my suspicion is high based on the symptoms. I am a physician, but not a neurologist, and do not believe I am being paranoid. I can only hope I am wrong. I am having an EMG in two weeks, recommended by a neurologist without my asking for it. I respectfully ask those who have ALS if they recommend getting long term diability insurance now, which is not offered to those who have a diagnosis of ALS, and which I can always cancel later if I am, hopefully, wrong. I am not aware of what insurance will provide for the future.