Thursday, October 14, 2010
Great News
More Prayers Needed
I was lucky enough to be in the NICU when the cardiology tech came to do the follow-up study (called an ECHO scan). He allowed me to watch and patiently answered my questions. It was amazing. I continue to be amazed at the things modern medicine has achieved that enable us to keep preemies alive. I feel like I am mooching off of the hard work and dedicated study of other people. It is costing a fortune, and it should. I think anyone who has researched enough to contribute to this process deserves to be paid a LOT of money.
The ultrasound showed her heart pumping well. It also showed her PDA vessel to be smaller, a good indication that the medicine has helped. Unfortunately it is still open with blood passing freely. So, the plan now is to give her another round of meds (possibly with two extra doses if the docs think it's worth a try, for a total of 5) and to re-evaluate on Friday. If the PDA is still not closed, or looking like it is not going to close, they will start talking about having it closed via surgery. In which case, they will have to fly her to St. Marks in Salt Lake where she will stay for the rest of her NICU life.
After the heart scan, later that night, I got a call from the Nurse Practitioner. She told me that after I left, Angelyn started having more apnea spells; deeper and longer ones that she wasn't able to pull herself out of. They decided they needed to put her back on the ventilator. Not considered a major setback, but a minor one. She will probably stay on the ventilator until her PDA is closed. Her body is having to work extra hard to be expected to use her lungs as a newborn, yet pumping her blood with a fetal heart.
I feel like we are at one of those (many) critical crossroads. In the next 24-36 hours she needs to respond to the medication well enough to convince the docs she can do it without surgery.
I know all things are in the Lord's hands and He can do all things. Please continue to pray with us.
~Emily
Tuesday, October 12, 2010
Preemie Update -- Your FAQ's Answered!
How is Angelyn doing?
The nurses always tell me she is doing great. She tolerates the CPAP (one step down from the ventilator) pretty well most of the time. Not that that means she's out of the woods. The doc is worried about the blood vessel present in unborn fetuses whose purpose it is to bypass the lungs. (Google Patent Ductus Arteriosis). When babies go full term, that blood vessel constricts and disappears. In preemies they have to watch it and give meds to help make sure it doesn’t reflux blood back into the lungs. Apparently her heart scan shows that hers is exceptionally large. When I asked the neonatologist if he was worried about it, he said “yes.” When asked if he was surprised about it, he said, “no.” Hopefully she will respond to the meds that treat it. We will have an update on her response to the medicine later tonight. He's worried because this NICU technically only accepts 28-weekers and above, simply because they don't have quite as immediate access to specialists should the need for surgery arise.
How early was she and how much does she weigh?
She was born at 27.5 weeks. That’s about 12 weeks early….or for those of you on the 9-month plan, she was 3 months early. She weighed in at 2 lbs 1 oz.
How long will she have to stay in the hospital?
Probably until close to her due-date (Jan 5). It all depends on how well she does. We could bring her home late December or early January.
How early did Adam come? Is all of this territory you have traversed before?
Angelyn is 2.5 weeks earlier than Adam was. He was born at 30 weeks. It is amazing how much my perspective has changed. Now I think Adam was a big baby and we would have been so thrilled if Angelyn had made it even to 30 weeks. The neonatologist was expressing to me today that the road with Angelyn will be different. She will have a much different set of challenges and complications because of that 2.5 week difference. However, one advantage is that with Angelyn I had time in the hospital to get all the treatments that give the preemies a boost before they come. I did not have time for those treatments with Adam. So, thanks to the steroids, her lungs are doing fantastic already (she is off the ventilator) and thanks to that horrible 48 hour magnesium drip, her head ultrasound came back completely clean.
Why do you have so much difficulty carrying babies full-term?
I have an abnormal uterus. Some call it “bi-cornuate” some call it “septated.” Basically, when the uterus forms, it starts out as two separate tubes which are supposed to fuse and become one, making the uterus a pear shape. Mine didn’t fuse all the way. So my uterus is a heart shape and has a wall that extends halfway down the middle. This wall is called the septum and it is less vascular than the actual uterine wall. If and when the placenta decides to try to implant on the septum, the risk for placental abruption skyrockets. Placental abruption (when the placenta tears away from the uterine wall) was the cause of both of my premature deliveries. It is extremely dangerous and can cause fatality for both mother and child. Modern medicine is truly a miracle and I am so grateful we are all still alive.
How are you feeling?
I am feeling much better. My arms look absolutely dreadful from all of those failed IV and blood draw attempts. I look like I’ve been either beat up or a heroine addict. My incision will be sore for a while but I am so grateful to be on track for a full and complete recovery.
How would you rate your pain on a scale of 1-10? “Say 8! Say 8!”
It has leveled out at about a 4 or 5.
How are the kids handling everything?
The kids are doing great! I miss them much more than they miss me. They have been to visit me twice and they seem to be having a fantastic time with all of their cousins and friends. They have minimal comprehension of what is going on. Peter knows we have another early baby and asked to see her. It is very likely that they will not be able to visit her in the NICU at all. I was nervous when they came to visit me last week that they would be sad and scared. I tried to present myself as normal-looking as possible. When they came, I was relieved. They didn’t seem too sad. Yet they were affectionate and told me they miss me and love me.
What can I do to help?
We have been blessed by so many willing, helping hands and we thank you from the bottom of our hearts! We are grateful to be in UT with so much family around, and our ward has really come forward with so many offers for help. If you are not close enough to do anything but pray, PLEASE continue. We have felt the power of your prayers so much through the course of this little life experience. We came close to delivering the baby even a week earlier but we felt that, as a result of the many prayers offered in our behalf, things began to stabilize and we got almost a full extra week of gestation time on hospital bed rest. (My doctor gave me this formula: every day in utero counts as two in the NICU). So, please know that your prayers are needed, felt, and appreciated. The Lord has blessed us so much up to this point and we are still just trying to trust Him and hope and pray for a good outcome. Truly, if He blesses us with a good outcome then it doesn’t matter what we have to wade through to get there.
Sunday, October 10, 2010
Well here she is
Angelyn Ricks
950 grams
35 centimeters long
(I'm giving the info out in metric because that's what hospital used and i figure it'll catch on and everything will be in metric soon. Especially 5Ks.)
Wednesday, October 6, 2010
Hospital Update
I find a certain irony in the knowledge that the longer I stay in the hospital, the better. Technically I am not due until January 5th! But right now we are going to focus on taking it one week at a time. Our goal is to make it to 28 weeks, which is the cut-off age for the NICU at this hospital.
The first two days I was here I was bombarded with every treatment and precaution known to medicine to help babies that come so prematurely. Steroids, magnesium, you name it. It was brutal but now it is over and we get to just play the waiting game.
I called my parents' on Tuesday to talk to the kids and was flooded with emotion and memories of the hospital torture I endured for each one of them. And now they are the greatest blessings in my life. I know there will eventually come a time when these next few months will all just be a distant memory.
In the mean time, we are just going to do the best we can to get through and be grateful.
Thank you so much for all your thoughts and prayers. We know we have really been blessed and have felt the power of your prayers in our behalf. We are so grateful that our baby is still in utero will praise and be thankful for every precious golden day she stays there.
Hospital Bedrest....how we got here.
Indeed, angels have watched over Emily today and we have relied on the Lord. As of this writing, things are calm. The baby's heart-rate continues to be strong and distinct. She must be a brave little trooper to put up with all the extra noise and the probing and the poking of her mother and we look forward to meeting her and introducing her to you. However, with your continued prayers, we hope that meeting will not happen for another few weeks. We are grateful for each of you and for your friendship and your prayers.
Monday, September 27, 2010
Highlights From Family Home Evening
Adam gave the lesson, which was a repeat of the talk he gave in primary. His performance tonight was more articulate than it was on Sunday. Still, the transcript has been included for you below because I'm good like that.
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A few days ago, Weston called me from work to ask me about a good time for an “appointment” either in Woodbridge or Alexandria (both about a...
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I love , love, LOVE the fall. It’s my all-time favorite season. The feeling and the smell of fall is so distinctive and joyful that it alw...
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It is cold outside. The van is in the shop. We are stuck at home. Today the boys wandered into the music room which doubles as the baby’s ro...