To those affected by a heart defect:

Breathing On Her Own…Again.

January 18, 2007 at 9:15 am by Mom & Dad

We couldn’t get to a computer last night to post an update for you, but no news is good news. She has remained steady as she has been weaned off of her blood pressure medicine and is being taken off the ventilator as we are writing this (they ask parents to step out of the room for that procedure). She will go back on oxygen only through her nose. We are still dealing with some tummy problems. Hopefully pulling her off the ventilator will help that and she will be able to stay steady breathing on her own.

Posted in Corrective Surgery | 2 Comments »

2 Responses

  1. Sierra Says:

    Way to go Haven! You are such an amazing little girl. Ofcourse, you have amazing parents. It’s in your genes. Keep fighting baby girl!! I am praying you right now! God touch this beautiful baby girl! Do miracles in her and through her. We love you and ask this in the name of your Son Jesus Christ. Amen. The three of you keep up the good work! It is amazing to see God’s hand at work.

  2. The Myers Gang Says:

    Hey,we love ya and are praying that things go through this time, so that this sweet baby girl is on the road to recovery for good. She is a tough little girl and she gets it honestly, you two are the greatest inspiration. Thanks for the updates.

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This site contains the story of Haven Leigh and serves as a source of hope and encouragement to anyone who has or knows a child born with HLHS, a congenital heart defect, or other terminal illness. Here, we show the rewards of nurturing and supporting a special child while celebrating her memory by sharing her story with others.

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