Having been diagnosed with Multiple Sclerosis as a junior in high school 13 years ago, I’ve been on many medications for not only treatment of the neurological disease itself, but also for the life-altering symptoms and afflictions characteristic of MS.
I’ve been often told that MS won’t kill me, but the side effects of medicine and the complications of symptoms will.
Most recently, I began suffering from crippling pain, blurry vision, extreme fatigue, and what’s affectionately called, “cog fog.”
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