Shereese Hickson’s multiple sclerosis was flaring again. Spasms in her legs and other symptoms were getting worse.
She could still walk and take care of her son six years after doctors diagnosed the disease, which attacks the central nervous system. Earlier symptoms such as slurred speech and vision problems had resolved with treatment, but others lingered: She was tired and sometimes fell.
This summer, a doctor switched her to Ocrevus, a drug approved in 2017 that delayed progression of the disease in clinical trials better than an older medicine did.
Genentech, a South San Francisco, Calif.-based subsidiary of Swiss pharmaceutical giant Roche, makes Ocrevus. The drug is one of several for multiple sclerosis that are delivered intravenously in a hospital or clinic. Such medicines have become increasingly expensive, priced in many cases at well over $80,000 a year. Hospitals delivering the drugs often make money by charging a premium on top of their cost or adding hefty fees for the infusion clinic.
Hickson received her first two Ocrevus infusions as an outpatient two weeks apart in July and August. And then the bill came.
Keep reading.
[et_pb_section bb_built=”1″][et_pb_row][et_pb_column type=”4_4″][et_pb_text _builder_version=”3.10″]
This morning MPR broadcast a story that reporters have been working on for eight months. Federal law requires state to pay for nearly all drugs. This is an interesting story on how it all works. You can read or click the arrow below.
[/et_pb_text][et_pb_code _builder_version=”3.10″]<iframe src=”https://www.npr.org/player/embed/629575118/630008647″ width=”100%” height=”290″ frameborder=”0″ scrolling=”no” title=”NPR embedded audio player”></iframe>[/et_pb_code][et_pb_text _builder_version=”3.10″]
All 50 states and the District of Columbia were scored on more than 40 categories. The Commonwealth found 612 categories getting better, 259 getting worse in its 2018 report.