This is my first post here, so please be patient.
My husband was diagnosed with MS 10 years ago after optic neuritis took most of his sight.
He was on Betaseron until about six months ago, when he changed doctors, and was put on copaxone
because he kept having relapses.
Since going on the Copaxone he has lost his appetite, and eats very little. He says food just gags him. He has lost ...
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