To those affected by a heart defect:

A busy day

March 21, 2007 at 8:47 am by Mom & Dad

Haven had an eventful day yesterday.  First of all, she was one sleepy baby.  She was asleep when we arrived in the morning.  She slept right through her morning shot, diaper changes, and even her physical therapy session!  So as we became more curious as to why this little baby was so tired, we began to notice that her heart rate seemed sort of stuck in one spot.  “Uh oh,” we thought, “we’ve seen this before.”  Well, we waited it out awhile, then her blood pressure dropped a little too low.  Then we new something was the matter.  The cardiologist came in, and thankfully since we’ve all seen this behavior before, we knew exactly what the problem was and what needed to be done.  Haven’s heart was stuck in an Atrial Flutter again.  Read the rest of this entry »

Posted in Recovery #1 | 1 Comment »

Holding Haven

March 20, 2007 at 9:05 am by Mom & Dad

Yesterday was a great day for us because we were able to hold Haven for the first time in about six weeks.  In fact, we were so excited about it that we forgot to put a post here on the site!  Some of our nurses and doctors were suggesting that if it were possible to get Haven and all her gear together, it would be a beneficial thing (for Haven AND mom & dad) to be able to hold her.  As you can imagine, it’s quite an ordeal to get her in a position to get out of the crib with all those tubes and wires (I think we counted 17), but our nurse was very willing to accomodate.  It was so nice to hold her again.  We were able to hold her for about two hours yesterday. Read the rest of this entry »

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If at first you don’t succeed…

March 18, 2007 at 9:53 pm by Mom & Dad

As everyone knows, perhaps the biggest issue that we have dealt with in Haven’s recovery has been the excessive amount of fluid that drains from both sides of her chest cavity.  While it’s true that this is perhaps not the most serious issue we’ve dealt with, it is certainly the longest lasting issue that is preventing her from moving forward with recovery and preperation for her second stage procedure (please refer to the HLHS page for more details regarding the second stage).  It has also been very perplexing because just about every doctor here has said that they’ve never encountered a Norwood baby (or any baby her size and age, for that matter) that has had such cronic chest fluid accumulation and production. Read the rest of this entry »

Posted in Recovery #1 | 4 Comments »

Flying Tubes

March 17, 2007 at 10:10 pm by Mom & Dad

If you’ve been to the “Pictures” page on the site, you’ve no doubt noticed the tape across Haven’s cheeks to hold the breathing tube in place.  Every so often, that tape has to be changed to ensure that the tube remains secure.  This is not as easy of a task as you might think.  It is at least a two person job and can be a little tricky.  Read the rest of this entry »

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Going, going…

March 16, 2007 at 4:15 pm by Mom & Dad

Haven’s chest drainage is still on the decline!  We are hoping this will continue throughout the weekend and maybe eventually stop althogether.  We are working on getting rid of the fluid all over her body which causes stress on her other bodily systems.  Other than that, we are trying keep her pain under control and keep her on the road to recovery… it’s been a long road, hasn’t it?

Mom and Dad are enjoying watching their baby grow and develop.  We forget sometimes that she is getting older even though she never leaves her bed.  We are thankful for the time we get to spend at her bedside as a family.  Thank you to the individuals and churches who have reached out to us financially to help us press on through this time.  Thank you also for all the correspondence and prayers- we know that we are in the thoughts of many people throughout the day and that’s a blessing.  We are glad that Haven is touching your lives as she is touching ours.

Posted in Recovery #1 | 2 Comments »

Only the good stuff…

March 15, 2007 at 4:56 pm by Mom & Dad

Yesterday afternoon, in light of some new light shed on a possible connection between Haven’s feedings and her chest drainage, they decided to switch her feedings from mom’s milk to a different formula that might be easier for Haven to digest.  Well, after a few hours of the new formula, Haven got very uncomfortable.  She struggled a good deal trying to tolerate the formula.  She’s such a trooper, but the formula just became more than she could handle.  So we stopped feeding her with that.  It appears that Haven likes to eat only the good stuff.  Read the rest of this entry »

Posted in Recovery #1 | 3 Comments »

On the right track

March 14, 2007 at 3:24 pm by Mom & Dad

Haven had a very restful night last night.  As you can imagine, we’ve been keeping a close eye on her chest drainage over the past couple of weeks.  In fact, we have a spiffy little graph that we plot our data on, and since we’ve done that some interesting connections have been made that should be very helpful in getting Haven to the place she needs to be.  For example, her chest drainage was considerably less after both of her chest surgeries, however, today we noticed the drainage was up a bit.  Well since we had this graph to compare her drainage amounts now with those of the last surgery, we noticed that the same thing happened then.  That seemed peculiar to us, and after wracking our brains a bit, we were able to draw a connection between her chest tube drainage and her feeding.  After both procedures, her chest drainage began to increase once we resumed feedings.  Interesting. Read the rest of this entry »

Posted in Recovery #1 | 2 Comments »

Update

March 13, 2007 at 11:48 am by Mom & Dad

We sincerely apologize for not being able to post any updates for the past couple of days.  It appears that the technical difficulties have been resolved.

Haven had a good rest of the weekend.  She continued to sleep quite a bit, but she was awake now and again and was very alert.  Monday afternoon they were able to take her back to the operating room for the procedure on the right side of her chest.  Read the rest of this entry »

Posted in Recovery #1 | 4 Comments »

Technical Difficulties….

March 12, 2007 at 10:15 pm by Uncle Justin

Some of you have been experiencing technical difficulties today viewing HavensHeart.net. There was a glitch in the blog which has since been remedied. Unfortunately, Jeremey and Alison were not able to post the news today because of the downtime.

Expect a post tomorrow about the goings on of today including Havens surgery (which turned out well).

Thank you for your diligence in checking the site,

Uncle Justin

Posted in Info, Uncategorized | No Comments »

Saving Up

March 10, 2007 at 9:00 pm by Mom & Dad

Haven had a good night’s rest last night.  The nurse said she didn’t even wink.  After a good bath early this morning, Haven slept ALL day today!  We assume she’s saving up for what will hopefully our last trip to the operating room for this hospital stay.  We had very nice weather today, so mom and dad went for a little walk this afternoon just get out and get some fresh air.  We can’t wait to be able to take Haven with us on our walks. 

Posted in Recovery #1 | 1 Comment »

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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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