<code id='E7E1DB729D'></code><style id='E7E1DB729D'></style>
    • <acronym id='E7E1DB729D'></acronym>
      <center id='E7E1DB729D'><center id='E7E1DB729D'><tfoot id='E7E1DB729D'></tfoot></center><abbr id='E7E1DB729D'><dir id='E7E1DB729D'><tfoot id='E7E1DB729D'></tfoot><noframes id='E7E1DB729D'>

    • <optgroup id='E7E1DB729D'><strike id='E7E1DB729D'><sup id='E7E1DB729D'></sup></strike><code id='E7E1DB729D'></code></optgroup>
        1. <b id='E7E1DB729D'><label id='E7E1DB729D'><select id='E7E1DB729D'><dt id='E7E1DB729D'><span id='E7E1DB729D'></span></dt></select></label></b><u id='E7E1DB729D'></u>
          <i id='E7E1DB729D'><strike id='E7E1DB729D'><tt id='E7E1DB729D'><pre id='E7E1DB729D'></pre></tt></strike></i>

          00:00
          00:00 00:00 LIVE
          buffering
          Replay
          LIVE
          00:00 / 00:00
          LIVE
          CC
          Opacity :
          Share:
          Close

          focus

          author:comprehensive    - browse:3618
          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

          hotspot