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Emma Wrenn joins us to share her experience with her daughter Keira, who just passed away this last August as a result of her battle with DIPG, diffuse intrinsic pontine glioma. Keira’s case was public, and many of us around the world followed her story. Emma shares candidly what life is like now, what remain to be the greatest challenges to the DIPG experience, and the hope that her daughter’s life has given to research and progress for DIPG survival one day. Kenny from Michigan called in, having just lost his daughter to DIPG last May. Advocacy report focused on H.R.2008, Kids First 2.0, and H.Res.69, the National DIPG Awareness Resolution.
