To those affected by a heart defect:

Update

April 23, 2007 at 6:50 am by Mom & Dad

As we progressed through Saturday, Haven’s urine output slowly decreased to practically nothing.  This was very concerning for everyone.  There is great concern as to just how much more fluid overload Haven’s body will be able to tolerate with such poor kidney function.  We spoke for a long time with the kidney doctor Saturday evening discussing dialysis and what that would look like for Haven specifically.  There are many many risks involved with that procedure espcially for someone with a major heart defect and liver failure; however, it may be her only opportunity to get past this point.

At that time on Saturday, it was much too late in the evening for something to be done so we decided to wait until morning to press the issue further.  When we came in Sunday morning, we (and everyone else) were surprised to find out that early that morning she had increased her urine output.  In fact, she did such a good job yesterday that by the end of the day she had more out than in for the first time in about a week.  This put everyone’s mind at ease; however, she is not making enough progress to move forward–just enough to not continue retaining large amounts of fluid.  So, talks about dialysis will continue today.  We are also expecting results back from the genetics tests this week as well.  Hopefully, over the next few days we can have some more information with which to make our decisions. 

Posted in Recovery #1 | 2 Comments »

2 Responses

  1. Laurie Says:

    Sweet little Haven…putting up such a big fight.
    Remember that Jesus loves the little children and is by her side.
    May you Jeremy and Alison also draw comfort and strength from all of God’s promises. Extra thoughts and prayers as you make more decisions this week as you get more information and results of some of these tests you are waiting for.
    As always,
    Love and lots of prayers!
    Laurie

  2. Marcia Says:

    Jeremey & Alison,

    Just wanted to let you know that
    you are all constantly in my prayers. Continue to rely on THE God of all comfort. He will always be there to see you through. God Bless.
    Love Ya,

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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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