Anonymous
I have MS and I’m on Social Security disability. A few years back when I started Medicare, the drug that I was taking for MS cost about $1200 per month. When Medicare Part D was passed, I thought “This is great, we got something.” In the time that we got Medicare Part D, the price of the drug I was taking went up to $2,600 a month. So even though I have that supposed benefit, I am always begging for prescription assistance and I spend the month of January trying to figure out how to fund that drug.
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