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Living in the Shadow of Huntington Disease & the HTT gene. Demystifying Genetics with Kathy Langley

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Manage episode 467288784 series 2313219
Content provided by Matt Burgess. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Matt Burgess or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ppacc.player.fm/legal.

Kathy Langley opens up about her family's struggles with Huntington disease, sharing her personal journey from the silent pain of knowing her father's condition to advocating for awareness and support in the community. She highlights the emotional complexities surrounding genetic testing decisions and the need for improved education on HD within the healthcare sector.
• Kathy’s early experiences with her father's HD symptoms
• The emotional impact of discussing HD in the family
• The dilemma of wanting children while facing genetic risks
• Insights into the testing process and its psychological effects
• The role of stigma and the importance of awareness
• Advocacy for education on HD for medical professionals
• Support mechanisms for families affected by HD
• Kathy’s efforts to raise awareness through social media

Support the show

Demystifying Genetics is sponsored by TrakGene
https://www.trakgene.com/

  continue reading

Chapters

1. Demystifying Genetics with Kathy Langley (00:00:00)

2. Family Impact of Huntington Disease (00:00:01)

3. Advocating for Huntington Disease Awareness (00:18:03)

4. Exploring Family History for Huntington Disease (00:30:00)

36 episodes

Artwork
iconShare
 
Manage episode 467288784 series 2313219
Content provided by Matt Burgess. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Matt Burgess or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ppacc.player.fm/legal.

Kathy Langley opens up about her family's struggles with Huntington disease, sharing her personal journey from the silent pain of knowing her father's condition to advocating for awareness and support in the community. She highlights the emotional complexities surrounding genetic testing decisions and the need for improved education on HD within the healthcare sector.
• Kathy’s early experiences with her father's HD symptoms
• The emotional impact of discussing HD in the family
• The dilemma of wanting children while facing genetic risks
• Insights into the testing process and its psychological effects
• The role of stigma and the importance of awareness
• Advocacy for education on HD for medical professionals
• Support mechanisms for families affected by HD
• Kathy’s efforts to raise awareness through social media

Support the show

Demystifying Genetics is sponsored by TrakGene
https://www.trakgene.com/

  continue reading

Chapters

1. Demystifying Genetics with Kathy Langley (00:00:00)

2. Family Impact of Huntington Disease (00:00:01)

3. Advocating for Huntington Disease Awareness (00:18:03)

4. Exploring Family History for Huntington Disease (00:30:00)

36 episodes

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