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'Without Spinraza, I'm fairly certain that Zac probably wouldn't be here.' As the Scottish Government fast-tracks a treatment for spinal muscular atrophy, we spoke to Amy Cameron, who says the 'miracle' medicine saved her son's life. Read more: https://bit.ly/2GrT4cN | STV News
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220101 -- ZAOZHUANG, Jan. 1, 2022 -- A medical worker injects Spinraza to a 4-year-old child diagnosed with spinal muscular atrophy SMA at a hospital in Zaozhuang, east China s Shandong Province, Jan. 1, 2022. China is striving to improve the diagnosis and treatment of rare diseases. Recently, a tear-jerking video showing how a national health insurance negotiator helped cut down the bidding price of Spinraza from over 53,680 yuan 8,422 U.S. dollars per dose to 33,000 yuan went viral online and
220101 -- ZAOZHUANG, Jan. 1, 2022 -- A medical worker injects Spinraza to a 4-year-old child diagnosed with spinal muscular atrophy SMA at a hospital in Zaozhuang, east China s Shandong Province, Jan. 1, 2022. China is striving to improve the diagnosis and treatment of rare diseases. Recently, a tear-jerking video showing how a national health insurance negotiator helped cut down the bidding price of Spinraza from over 53,680 yuan 8,422 U.S. dollars per dose to 33,000 yuan went viral online and
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Spinraza, a recently approved drug for spinal muscular atrophy, has faced slow ramp-ups at hospitals and resistance by health insurers spooked by the $750,000 list price. http://bos.gl/cYgRNR5 | The Boston Globe
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