26 April 2007
20 April 2007
13 April 2007
reflection
that is the most important thing. i am putting up some pictures from the past week since she has been home.
this was her going home outfit as we were leaving from the hospital. (i made her those booties when we were waiting during the surgery)
sleeping at grandma and grandpa's
the first bath we gave her. you can tell she's loving it! (incidentally, we gave her another one yesterday and she loved it!) you can see her scar here. i have started rubbing vitamin E oil on it, hoping it helps a little. we'll see as she grows up
peaceful again
here she is today, just before she fell asleep
06 April 2007
04 April 2007
03 April 2007
maybe thursday?
30 March 2007
so close...
28 March 2007
holding and feeding
27 March 2007
Update on Arianna
first of all, david and i want to thank all of you for your prayers for our family this past week. we have been so overwhelmed with the support of the body of Christ, people we know and even those we don't know.
david and i drove home last night and i am resting at home today. there is much to do, but my friend jessica came over and helped me out. david had to go into work at the country club today, and it will most likely open this weekend. this means that he will not be able to go to danville as much to see arianna before she comes home. but it is good in that he will finally be back at work and we will not need to rely on his unemployment checks anymore. i will be able to go down and see her alot this week due to other friends' willingness to drive me and spend their day with me.
i want to explain a little more about what arianna had and how she is doing. we finally found out the name of the heart defect that she had. it is called hemitruncus. every heart has a main pulmonary artery and off of that branches the left and right pulmonary arteries that bring de-oxygenated blood to the left and right lungs where it gets oxygenated and sent out to the body. what arianna had, was her right pulmonary artery was coming off of the aorta instead of the main pulmonary artery. this was, in turn, bringing already oxygenated blood to her right lung. because of this, the heart had to work harder to get the blood oxygenated through the left lung only. it caused alot of high pressure in her lungs and gave her pulmonary hypertension. we found out that it is a very rare defect and hard to find alot of information about. the dr. told us that in their research, they came across a study done in scotland about hemitruncus. in the last 29 years, they have only been able to find 9 cases of it. another dr. told us that in all of the thousands of births each year in boston, they only have 1 case of it a year. we also found out that her surgeon, dr. pourmaghadam (pour-ma-ga-dahm), has done 1 other surgery exactly like this before. at first, this was not very reassuring, but when we realized how rare this is, we felt that God had directed him to us since he has done it before. it is rare that a heart surgeon would ever get to operate on 1 of these cases, let alone 2. he did however, explain that essentially, the operation would be pulmonary reconstruction, and this is something that he does all the time. he went over in great detail what he would be doing, how exactly he would detach and reattach the artery and what they would need to do to her for this surgery. in order to prepare her for the surgery, after the anesthesia, they would cool her body down to 77 degrees to slow her metabolism and protect her organs. then they would put her on a heart and lung machine while they worked on her heart. when they were done, they would warm her body back up, suture her closed and then give her a blood transfusion. and then she would be done. when we saw her, she was a maze of tubes all over her. she had 7 lines directly connected to her heart still (3 tiny i.v.'s and 4 external pacemaker wires). she had 2 drainage tubes coming out of her abdomen that were draining excess fluid from around her heart and about 4 peripheral i.v.'s. she was also on a ventilator, which means she had a breathing tube down her throat. this all took place last thursday. as of yesterday, monday, she had all of those lines taken out of her except 3 i.v.'s. today, they took out another one, so she is left with 2. they have weened her off of almost all her medication and yesterday they started feeding her again. she had not eaten since i last breastfed her the morning after she was born, when they took her to danville. it had been over a week. the nurse let me bottle feed her for the first time yesterday, and she did ok. the dr. said it would be a learning process for her to know what to do. since then, the nurse has told us she is downing that milk every time feeding comes! she's doing really really well with it! this is the last thing she needs to do well in before they will let her go home. once she is established in her feeding and is getting enough calories and gaining weight, they will release her. dr. pourmaghadam also told us yesterday, that he wants the nurses to get her up to par with the feeding, 2 or 3 days, and then he wants me to stay at the hospital and room in with her and take over the feeding! it will be better for arianna and will help her recover even faster. so we are thinking maybe thurs. or fri. of this week, i will go down to stay, and hopefully, she will be able to go home early next week! the way she's doing, she should definitely be home before easter!
thank you again so much for all of your prayers. david and i have had the hardest week of our lives and still feel stressed out. it has been evident to us that we have been lifted in prayer. there were nights when we would break down and cry and not know how we could go on another day. and the next morning God would give us hope and comfort. i still have my emotional swings, as i am still dealing with postpartum hormones. i am trying to get my rest today, and hopefully will have enough strength to stay down there without dave. i don't know how i would've done this without him. he has been a rock by my side, even when we both cry. this trial has strengthened our marriage in a way that couldn't have happened any other way. and even though things are looking brighter, it is not over. arianna still is not with us, and we miss her. i would ask that you would pray that she continues to eat well and gain strength and that her heart continues to be strong. pray that david and i will have the strength to make it through another week without her and be patient until she is well enough to come home.
we were not able to find internet access in danville, so while i am away, david will keep his blog updated as much as he can. www.davidasiegrist.blogspot.com . he has a post there now with some more information you might like to read. i will leave you with a few pictures of our last week.
she would suck on our thumbs when she was hungry. it was hard to see her rooting reflex, trying to latch on to something to eat. this gave us both a bit of comfort.
these 2 pictures were taken the morning of the surgery. it was the last time we got to hold her and was a bit hard to say goodbye when they took her in.
22 March 2007
after surgery update
Everything went really well, according to the doctor. One of his nurses told Dave and La that the doc is a meticulous man and worked hard to make sure the surgery was without flaw. They were just going in to see Arianna, who is on a ventilator for the next 24 hours, to prevent her heart from overworking. The next 3 days are critical, as they doctors will be watching to see how Arianna's new heart and body are working since the surgery.
Please pray for Dave and La, who are not able to hold Arianna. (They did get a good 1/2 hour each this morning to hold and rock her to sleep before the surgery!) They will remain in Danville, until Arianna is able to come home. The soonest they'll be able to access internet may be on Sunday. Please continue to pray for them and the journey ahead.
ashley wittmer
21 March 2007
Baby Arianna's Surgery
This is Ashley Wittmer, writing on behalf of Laura. She and Dave have been unable to update this blog because there's no internet at the hospital, so i said i'd do my best to fill you all in on what's happening with Arianna Beth, their new baby girl.They've been at Geisinger Hospital (Danville, PA) since Monday and have meet with the pediatric cardiologist who will be performing Arianna's surgery. The surgery will begin tomorrow at 7:30aEastern and finish mid-afternoon. it will consist of the doctors opening her chest, cutting through the breast bone, adding cadaver (sp?) tissue to her tiny pulmenary artery and re-routing the artery. She'll be surviving on the heart and lung machine through the surgery and will need a blood transfusion when it's over.
The hardest part will be the recovery. They will be unable to hold Arianna for up to 14 days, while her body stablizes with her newly working heart. Please pray for Laura, who is diligently pumping milk for the baby and for Dave, who is standing by her side. They are doing ok and are encouraged by all the people who they know are praying for them (and for those who have given them physical and financial encouragement!). God will truly use this experience for HIS glory and we are trusting in that--moment by moment.
Ashley Wittmer
18 March 2007
a new baby
16 March 2007
the time has come...
15 March 2007
Italian Ice
last night, while on the way home from youth group, we passed by Rita's Italian Ice and saw that they were open! we felt spontaneous and fueled by our sudden thirst and the fact that we had a coupon for buy one get one free, we stopped. just in time too, it was 9 and they closed at 9, but they let us be the last customers of their first day open of the season. i got a mango misto, and let me tell you, it was heavenly! after the nicest spring-like day yet, this topped it all off. and i just saw on their website that next wednesday, march 21, they are giving away free italian ices at all of their locations in honor of the first day of spring! if i'm not in labor, i'm totally cashing in. i'm all for free stuff!
12 March 2007
blah blah blah
i can't decide what to do now. there are a few things i could do to tire myself out enough to sleep. i could wash the bath mat from the tub and scrub down the tub (it needs a good cleaning!), i could pack more stuff in my hospital bag, i could wash the dinner dishes, sweep and mop the kitchen floor, watch one of the movies we got out from the library, catch up on some ironing...i think i am trying to nest. which i've done a million times already. i'm tired of nesting. they always say that alot of women get nesting cravings just before they go into labor. well i've had nesting cravings for the past month and nothing's come of it. i'm going to go clean. i'll let you know how it all ends up. good night!
04 March 2007
Yea for pictures!!!!
02 March 2007
just sick
it ends happy! around 9:30 this morning they did some tests and found out that i was completely rehydrated and they were going to let me go. i still feel very weak and sick, but the chills and cramps and running to the bathroom are gone. i just have to stay on gatorade and bland foods for a while. lots of rest. we got home and i slept hard. nothing feels better than your own bed when you are sick. i love my bed!
david was absolutely wonderful throughout this whole thing! i needed help for so many things. every time i needed to get up to use the bathroom, we had to unplug the I.V. pump, unplug the fetal monitors and wheel the I.V. into the bathroom. he helped me every time. he got up last night to get me more blankets (when i had the chills) and help me turn over and tuck me in. i don't know what i would've done without him! right now he ran to the store to get me some more gatorade and food. i am so thankful for him!
so anyway, i am doing ok now. i need to recuperate some more, but i am much better than yesterday!














