Part 3 of 3: A long-form conversation with Lauren Holder, host of the Help4HD podcast and a rare disease advocate, who lives with Huntington's disease. Lauren and Susanna talk about how they think and talk about the possible futures when living at risk, the difficult path to having children, and the judgement they've experienced from others especially medical providers. 

Find the show notes for episode 20 here: https://www.geneticfrontiers.org/transcript-ep-20 

This episode is brought to you by The Tell Me Project, a story archive and a listening project where we host conversations with people about the meaning of genetic information in their lives. Follow Genetic Frontiers on your favorite podcast app, leave us a review, and connect with Genetic Frontiers on LinkedIn or Substack to join the conversation.