HLHS

The Todd and Karen Wanek Family Program for Hypoplastic Left Heart Syndrome (HLHS) is a research program with the goal of delaying or preventing heart failure for individuals with HLHS.

To learn more or to participate, please visit our website or contact HLHS@mayo.edu.

Follow the program on Facebook at Mayo Clinic HLHS, on Twitter @MayoClinicHLHS, and on Instagram at MayoClinicHLHS.

PUBLIC PAGE
Mon, Oct 7 9:37am

This Year’s Agenda for Feel the Beat!

By Brianna N. Tranby, @briannatranby

HLHS hearts

 

We’re in the home stretch – only five more days until Feel the Beat 2019! Be sure to RSVP if you haven’t already.

The agenda for the day is below.  And for those of you who can’t make it in person, we’re excited to share that we’ll once again have a livestream of the panels on our Facebook page! You can watch our Facebook Live video during or after the event on our page.

 


 

HLHS blog - agenda

 

 


Meet other people talking about HLHS or CHD on Mayo Clinic Connect – an online community designed to help patients and families connect with each other.  Our community is a safe space to share experiences, ask questions, find answers, and exchange support.  The discussion groups and topic pages are moderated to ensure that all posts are respectful, and Mayo Clinic Connect never sells or shares posted information to third parties.  Here are some you might like to follow:


The Todd and Karen Wanek Family Program for Hypoplastic Left Heart Syndrome (HLHS) is a collaborative network of specialists bonded by the vision of finding solutions for individuals affected by congenital heart defects including HLHS. Our specialized team is addressing the various aspects of these defects by using research and clinical strategies ranging from basic science to diagnostic imaging to regenerative therapies. Email us at HLHS@mayo.edu to learn more.

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Invite Others

Send an email to invite people you know to join the HLHS page.

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