Archive for September, 2007

Laura Is Growing Up

Wednesday, September 26th, 2007 by Jeff

Laura continues to grow up (and up and up and up). She is getting taller and harder to carry, seemingly every day a little more.

This fall Laura started home school, with mom as her teacher. Recently she’s begun learning how to read, and is doing great!

Laura continues to take gymnastics and swimming classes, too. She surprised me the other day by standing on her head, up against the wall, without any help. I don’t think I can do that!

Laura is also enjoying going to church and learning about Jesus. She recently learned a great song that says “Oh who made everything? God did, God did”.

We’re really proud of Laura and happy to see her growing up into a “big girl”! She’s a great big sister, too!

Here’s a couple recent pictures of Laura. There are more in her photo album.

Helen’s Recovery - Two Weeks Later

Wednesday, September 26th, 2007 by Jeff

Helen continues to do very well at recovering from her heart surgery two weeks ago. In fact, if you didn’t look inside her shirt to see the incision, you would not be able to tell.

She had a checkup visit with the cardiologist today, and everything checked out fine. She has gained almost 12 ounces in the 2 weeks since the surgery, so that is really great! She is eating and drinking really well, and she is pretty much back to the same level of mobility (creeping and rolling).

Please continue to keep little Helen in your prayers, that there will be no issues that come up, and that she will continue to grow and thrive.

Here’s a recent picture of Helen:

Helen’s Homecoming

Monday, September 17th, 2007 by Jeff

I’m really happy to let you all know that Helen is coming home from the hospital today! The cardiologist saw her this morning and gave the ok.

Helen will need some gentle care for the next few weeks, but she is really doing well. Thanks for all your prayers…we really appreciated it!

Update on Helen

Saturday, September 15th, 2007 by Jeff

Helen has left the ICU and moved to a regular pediatric care unit. She had some fluid around her lungs on Friday, but that has subsided. All in all she is doing very well! She’s eating solid foods and she has been playing with toys on the floor. She’s no longer tethered to the bed by all those tubes & wires, so Rachel has been able to walk around with her.

There’s no definite word yet on when she’s coming home, but it may be as early as Monday. Thanks for your continued prayers!

Here’s a couple pictures of Helen from today (Saturday):

Helen’s Recovery

Thursday, September 13th, 2007 by Jeff

Helen continues to recover in the pediatric intensive care unit (PICU) at Children’s Hospital in Minneapolis. She had her chest tubes and ventilator tube removed this morning. She was moved to a more private room so she could have fewer distractions. She was awake during much of the day, but she was kind of crabby and we tried to get her to sleep more. Every time she was offered a drink (glucose water only at this point), she sucked it down very quickly, which is a good sign (since she has never been a very fast bottle drinker).

The nurses think she’ll leave the ICU either Friday or Saturday; from there she’ll go to a regular care unit in the hospital.

Here’s a picture of Helen with Rachel holding her. You can tell that Helen is not quite herself yet:

Successful Heart Surgery

Wednesday, September 12th, 2007 by Jeff

We are very relieved to report that Helen’s surgery today was very successful and her prognosis is very good. She had the surgery at Minneapolis Children’s Hospital to fix her heart defect. She had a ventricular septal defect, which is a hole between the pumping chambers.

After meeting with the anesthesiologist, surgeon, and several of the nursing staff, we went into the OR with Helen at about 1:00 pm today. We were there when they put her to sleep and then we said goodbye to her. After about an hour of preparation, the surgery itself began around 2:00 pm.

At about 3:15 pm we got word that the surgical team had been able to successfully close the defect. A patch was not needed; the stitches alone were enough to close it. They also removed some excess “muscle bundles” that could later obstruct the valve. At that point Helen was taken off the heart-lung machine and an echocardiogram showed that the hole had been completely closed, with no leakage.

At about 5:00 pm we were allowed to visit Helen in the Pediatric ICU. She is laying on a bed and she looks so very tiny on it. She has a large bandage over the incision where her chest was opened to access her heart. She has many tubes and monitoring devices on her little body. Helen is currently sedated and is on a ventilator; they are telling us that the ventilator will probably be removed on Thursday morning.

It is hard for us to see Helen in this helpless state, but the nursing staff is very competent and kind to us, and very good at explaining what they are doing. Rachel has enjoyed “talking shop” (as a former ICU nurse), although there’s a lot of differences between pediatric and adult ICU care.

We appreciate all the prayers that have been spoken on our behalf. Thank you so much! Please continue to pray for a quick and event-free recovery for Helen. She will likely be in the ICU for a couple more days, and then spend another few days in a regular nursing unit until she is discharged, sometime around the middle of next week if all goes well.

Helen’s Upcoming Surgery

Monday, September 10th, 2007 by Jeff

As many of you who are reading this may know, our newly-adopted daughter Helen has a heart condition called VSD (ventricular septal defect). We had an appointment with a pediatric cardiologist in late August at the Children’s Heart Clinic in Minneapolis, and after taking a careful look at her heart and discussing options, we agreed that she will have open heart surgery. It is scheduled on Sept 12th at 1:00 pm. Please pray for little Helen and for us as we care for her. We have been told that she will be in the hospital (Children’s Minneapolis) for 5-7 days after the surgery. Rachel will probably stay at the hospital most of the time. Jeff will take some time off work but may go in to work some days (we’ll see). Laura will spend some of her time with her grandparents and/or aunts and probably some time at home with Jeff.

This is not really a surprise…we’ve known all along that Helen would probably need surgery to repair this defect (which is a hole between the two ventricles in the heart). The surgery is not without some risk, although it’s a procedure that is done quite often and the surgical teams are very skilled. We really don’t have an option to not do it…without the surgery her heart would keep working harder and harder and eventually she could have congestive heart failure and permanent lung damage. So we leave it in God’s hands and trust that he will take care of little Helen and make her well.

Thank you for your prayers.

Here’s a recent picture of Helen.  Go to her photo album for more pictures.

If you’re interested in learning more about VSD, these are good resources: