Episode 4 features Lisa Ward, Jace Ward’s mom. We talked to Jace in episode 1 to get to know him and his journey more. Now, you can also listen to Lisa’s story about dealing with Jace’s diagnosis, being an advocate, and the ONC 201 extended access program they are very excited about.

Episode 4: Interview with Lisa Ward

Listen to families, patients, physicians, researchers, foundations, and others speak about their experience with DIPG. We aim to raise awareness by sharing different perspectives of a similar story and foster a sense of hope for this community. Whether you are someone who is new to DIPG and wants to know more, or someone who is already a part of this community, we hope these stories provide you with more insight. As always, we are stronger together!

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Episode 4: Interview with Lisa Ward

Episode 4: Interview with Lisa Ward