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Abby Meyer, MD: Why screen for CMV?

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Manage episode 460013057 series 3586396
Content provided by Cochlear North America. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Cochlear North America 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://staging.podcastplayer.com/legal.

Spend the next few minutes with us to learn from Dr. Abby Meyer, pediatric ENT at Children's Minnesota, as she fills us in on what Minnesota is doing to implement universal screening for cytomegalovirus (CMV). You'll hear about their ongoing research, how data is driving patient care, and how they are educating families about CMV.
For more information about CMV, please visit these resources:
CMV and Congenital CMV
National CMV Foundation

If you enjoyed this episode, please press the subscribe button, give us a rating and a review. We’d love to hear from you.
The views of the interviewees in this podcast are their own and do not necessarily represent the view of Cochlear North America and Cochlear Limited.
This material is meant for health professionals – if you’re a consumer please seek advice from your health professional about treatments for hearing loss. Outcomes may vary and a health professional will advise you about the factors which could affect your outcome.

  continue reading

13 episodes

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iconShare
 
Manage episode 460013057 series 3586396
Content provided by Cochlear North America. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Cochlear North America 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://staging.podcastplayer.com/legal.

Spend the next few minutes with us to learn from Dr. Abby Meyer, pediatric ENT at Children's Minnesota, as she fills us in on what Minnesota is doing to implement universal screening for cytomegalovirus (CMV). You'll hear about their ongoing research, how data is driving patient care, and how they are educating families about CMV.
For more information about CMV, please visit these resources:
CMV and Congenital CMV
National CMV Foundation

If you enjoyed this episode, please press the subscribe button, give us a rating and a review. We’d love to hear from you.
The views of the interviewees in this podcast are their own and do not necessarily represent the view of Cochlear North America and Cochlear Limited.
This material is meant for health professionals – if you’re a consumer please seek advice from your health professional about treatments for hearing loss. Outcomes may vary and a health professional will advise you about the factors which could affect your outcome.

  continue reading

13 episodes

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