#DIPGwontWait with Lisa and Jace Ward, DIPG Advocacy Group

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DIPG Advocacy Group co-founders Elizabeth Psar and Paul Miller join us to help give the background story to the group, how it formed and why; Also joining us is Lisa Ward, a new addition to the Admins of DIPG Advocacy Group, who’s son Jace Ward, a 20 year old pre-law student at Kansas State University, was recently diagnosed with DIPG.

Their ongoing journey has been central to this group’s petitioning for a Congressional Briefing, as Jace prepares to speak before Members of Congress and staff to the urgent need for greater awareness and research activity and collaboration for the deadliest pediatric cancer.

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