<code id='888CAFDAD4'></code><style id='888CAFDAD4'></style>
    • <acronym id='888CAFDAD4'></acronym>
      <center id='888CAFDAD4'><center id='888CAFDAD4'><tfoot id='888CAFDAD4'></tfoot></center><abbr id='888CAFDAD4'><dir id='888CAFDAD4'><tfoot id='888CAFDAD4'></tfoot><noframes id='888CAFDAD4'>

    • <optgroup id='888CAFDAD4'><strike id='888CAFDAD4'><sup id='888CAFDAD4'></sup></strike><code id='888CAFDAD4'></code></optgroup>
        1. <b id='888CAFDAD4'><label id='888CAFDAD4'><select id='888CAFDAD4'><dt id='888CAFDAD4'><span id='888CAFDAD4'></span></dt></select></label></b><u id='888CAFDAD4'></u>
          <i id='888CAFDAD4'><strike id='888CAFDAD4'><tt id='888CAFDAD4'><pre id='888CAFDAD4'></pre></tt></strike></i>

          Home / entertainment / comprehensive

          comprehensive


          comprehensive

          author:focus    Page View:9
          Hiram Secrist (left), who has Duchenne muscular dystrophy, with his mother, Kristen Secrist (center), and his grandmother, Terrie Jordan. Courtesy Secrist family

          In mid-July, Kristen Secrist hopped on a call with her 5-year-old son’s doctor, who had urgent news: The first gene therapy had been approved for Duchenne muscular dystrophy. Her son, Hiram, would be a perfect candidate — if, she added, they could get him dosed in time.

          The treatment was approved only for 4- and 5-year-olds. Hiram turned 6 in three weeks. 

          advertisement

          “Oh, crap,” Secrist said to herself.

          Unlock this article by subscribing to STAT+ and enjoy your first 30 days free!

          GET STARTED Log In