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!
Flexibility, pain, and fatigue are part of hypermobility EDS. In this conversation, Dr. Taylor Kerrins discusses Ehlers-Danlos Syndrome (EDS), particularly hypermobile EDS, covering its definition, symptoms, diagnosis, and management strategies. He shares personal experiences with the condition, the challenges of obtaining a diagnosis, and the importance of physical therapy and exercise. The discussion also touches on genetic testing and available support resources for patients. Taylor emphasizes the need for ongoing research and understanding of EDS, highlighting the complexities of the condition and the importance of community support.
Key Takeaways:
- EDS is a connective tissue disease with various types.
- Joint dislocations are common in individuals with hypermobile EDS.
- There is no specific genetic test for hypermobile EDS.
- Exercise is extremely helpful but must be tailored to the individual..
- Support groups provide valuable resources and community for EDS patients.
- Ongoing research is essential for understanding EDS better.
Dr. Taylor Kerrins is a Clinical Assistant Professor of Medical Genetics & Genomics at the Medical University of South Carolina.
Please subscribe to this podcast on Apple Podcasts, Spotify, YouTube or wherever you get your podcasts to stay updated on new episodes of All Access DNA. Listen to past episodes on your favorite podcast play by searching “All Access DNA” or by streaming from our website at allaccessdna.podbean.com
Here are more resources related to today’s topic:
- The Ehlers Danlos Society
- Information on hEDS from the Marfan Society
- American Academy of Family Physicians handout from 2021
- The Norris Lab at MUSC
Any inquiries on the podcast can be sent to [email protected]
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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