I went into the ER with my second bout of "Bell's palsy" in less than two years. I am convinced that it has to do with lesions from MS, since the affected cranial nerve actually originates in the brain. My neurologist thinks it's just a coincidence, yet I haven't had any viral infections, as is common with Bell's.
Anyone else on here had MS related facial paralysis that mimics Bell's?
Anyone else on here had MS related facial paralysis that mimics Bell's?
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