All Access DNA
All Access DNA
Podcast Description
What is DNA anyway? Should I consider genetic testing? Can my genes tell my future? All Access DNA honestly answers the questions you have about genetics, healthcare, and popular issues in precision medicine as it relates to our daily lives. We may even veer into territory that is no longer science fiction but science reality. Host Kate Wilson utilizes her genetic expertise and experience to interview leaders and specialists in genomic medicine and research. Join us as we bring you reliable, scientific information you can trust.
Podcast Insights
Content Themes
The podcast focuses on diverse themes including genetic testing, hereditary conditions, and precision medicine, with episodes discussing topics like dilated cardiomyopathy and inherited blood cancers, providing listeners insight into the challenges and advancements in genetic healthcare and patient advocacy.
Want to know more about your DNA? Curious about how your genes impact your health? All Access DNA honestly answers the questions you have about genetics, healthcare, and popular issues in genomic medicine. Host Kate Wilson utilizes her genetic expertise and experience to interview leaders and specialists in genomic health and research. Join us as we bring you understandable, scientific information about genetics!
Lori Jones shares her personal journey with Huntington’s disease, exploring its symptoms, family impact, and the importance of community and research. Lori shares with us insights into living with risk, making decisions about testing, and advocating for better understanding and treatment.
Keywords: Huntington’s disease, genetics, neurodegenerative, family impact, genetic testing, community support, research, memoir, advocacy
Key Topics:
- Genetic inheritance and risk of Huntington’s disease
- Family impact and personal stories of living with HD
- The importance of community, support, and advocacy in HD
- Current research, clinical trials, and future hope for HD treatments
Guest Bio:
Lori Jones has personally experienced the effects of Huntington’s Disease (HD) in her family and was instrumental in starting a Team Hope annual event in her area to raise awareness and support for research and community programs. She has been published in the Wisconsin HDSA Update Newsletter, and spoken in the public schools about HD, genetics, and presymptomatic testing. She has contributed short stories for Women in High Def by Diane Markins. A storyteller at heart, she regularly writes and speaks about her experiences with HD and many other topics to groups of all ages. Lori has three adult children and lives with her husband Chris in Wisconsin, when they aren’t escaping north to the Upper Peninsula of Michigan. “Spared: A Memoir of Risk and Resolve” is her first book.
Resources:
- Lori Jones’ Website
- Spared: A Memoir of Risk and Resolve
- Help 4 HD International
- International Huntington Association
- Huntington’s Disease Society of America
- Information on uniQure
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Note that this podcast is for entertainment and education and is not intended to be a substitute for professional medical advice. Please consult your physician with any questions you may have regarding your health.
The All Access DNA team includes: host, producer and editor Kate Wilson. The logo is designed by Designs by NKJ. Our Social Media Lead is Casey Lepley.
Disclaimer
This podcast’s information is provided for general reference and was obtained from publicly accessible sources. The Podcast Collaborative neither produces nor verifies the content, accuracy, or suitability of this podcast. Views and opinions belong solely to the podcast creators and guests.
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