<code id='D06D13734A'></code><style id='D06D13734A'></style>
    • <acronym id='D06D13734A'></acronym>
      <center id='D06D13734A'><center id='D06D13734A'><tfoot id='D06D13734A'></tfoot></center><abbr id='D06D13734A'><dir id='D06D13734A'><tfoot id='D06D13734A'></tfoot><noframes id='D06D13734A'>

    • <optgroup id='D06D13734A'><strike id='D06D13734A'><sup id='D06D13734A'></sup></strike><code id='D06D13734A'></code></optgroup>
        1. <b id='D06D13734A'><label id='D06D13734A'><select id='D06D13734A'><dt id='D06D13734A'><span id='D06D13734A'></span></dt></select></label></b><u id='D06D13734A'></u>
          <i id='D06D13734A'><strike id='D06D13734A'><tt id='D06D13734A'><pre id='D06D13734A'></pre></tt></strike></i>

          Home / comprehensive / comprehensive

          comprehensive


          comprehensive

          author:knowledge    Page View:83451
          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