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, email HLHS@mayo.edu.

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

PUBLIC PAGE
Thu, May 24, 2018 11:26am

New blog series featuring Gabrielle Wanek starting in June

By Suzanne R. Ferguson, @suzannerferguson

Gabrielle Wanek 1

We are very excited to announce that we will be featuring a new blog series by Gabrielle Wanek starting the first week of June. Gabrielle is a twenty-three-year-old born with hypoplastic left heart syndrome (HLHS). She will be uploading blogs about her experiences and answering questions. Check in each week for a new post and to ask any questions you may have for her!


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. The 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 the program at HLHS@mayo.edu to learn more.

 

Look forward to reading Gabrielle's story!

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