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In Logan's Memory | 
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In Logan's Memory A beautiful tribute to my angel Logan's valiant fight with HLHS. May he live on by touching others hearts!
This web site is dedicated to a little boy who even when he was still in the womb was read bible stories and prayed with. K.J. has HLHS and is awaiting his 3rd surgery. Come see our special boy, one look at his smile and blue eyes will steal your heart.{;}
This site is dedicated to Our son Conner. Conner was born with HLHS. he has had stage 1 norwood but will not be having the other 2 due to brain damage diagnosed after his first surgery. Dr's originally gave conner 8-12 months to live, he is now 2. Dr's now say he will most likely not live past 3. This site is filled with Pictures of him including birth, his flight to the childrens hospital his stay in the NICU, pics right after heart surgery and his stay in the PICU.
Hypoplastic Left Heart Syndrome This community is for families affected by HLHS. Surfing this community allows you to read about this Congenital Heart Defect, and how it has affected families all over the world.
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