How these parents of a child with a rare disease are making precision medicine work for them episode artwork

EPISODE · Sep 8, 2022 · 31 MIN

How these parents of a child with a rare disease are making precision medicine work for them

from pharmaphorum Podcast · host pharmaphorum

In today’s pharmaphorum podcast, editor in chief Jonah Comstock invites Drs Zachary and Geri Landman to tell their daughter Lucy’s story and the story of their new nonprofit Moonshots for Unicorns, which sets up a framework for parents in their circumstance to directly crowdfund research for rare single-gene disorders – starting with PGAP3.

Episode metadata supplied by the publisher feed · Published Sep 8, 2022

Embed this episode

NOW PLAYING

How these parents of a child with a rare disease are making precision medicine work for them

0:00 31:00

No transcript for this episode yet

We transcribe on demand. Request one and we'll notify you when it's ready — usually under 10 minutes.

No similar podcasts found.

Frequently Asked Questions

How long is this episode of pharmaphorum Podcast?

This episode is 31 minutes long.

When was this pharmaphorum Podcast episode published?

This episode was published on September 8, 2022.

Can I download this pharmaphorum Podcast episode?

Yes. Use the download control on the episode player to save the publisher-provided media file.
URL copied to clipboard!