Wednesday, March 25, 2015

Gratitude

 "Give thanks in all circumstances for this is God's will for you in Christ Jesus." (1 Thess. 5:18). I posted this verse on my refrigerator a couple weeks ago so that I would see it everyday. I have to remember daily to be thankful for every situation in my life. Some days this is easier than others, but it's amazing how just remembering to be thankful can completely change your attitude. 
    Just recently we spent two separate occasions in the ER at LeBonheur because Breckin's feeding tube came out. One time it was in the middle of the night so we spent 11:00pm-3:00am at the hospital, and the next time it took up our whole Saturday afternoon. In these situations though, instead of complaining, I tried to be thankful. I was thankful that I have a supportive husband to accompany me to these visits, and we actually used the waiting time to have some quality time together. I also was so thankful that we were only there with Breckin for something simple and not because she was sick or injured.
    Throughout this whole flu and RSV season, I have been so thankful that Breckin has stayed well. She spent 6 weeks in the hospital and had two surgeries while there and she stayed well. She never had any type of infection, virus, or even a cold. That is something to be thankful for even with a heart-healthy child! 
     I am so thankful for health insurance! Our LeBonheur stay in the NICU was an astronomical amount well over a quarter of a million dollars, and that was just the stay itself. That didn't include all the tests and labs and all the doctor's and surgeon's fees. Yes we have a high deductible, but that is nothing compared to what we would be paying if it weren't for insurance. I am also so thankful for the many many monetary contributions and gift cards from loved ones near and far and some people I don't even know. This has enabled us to pay bills, get groceries, buy diapers, and get Breckin's medications. God has completely provided for every one of our needs and it's amazing to see how he has worked through others to meet these needs.
     Everyday, I am thankful that Breckin has her feeding tube so we don't have to worry if she is getting enough nutrition. She may not be able to take all her milk by mouth, but we can give it to her this way. I am thankful that she has started to sleep through the nights most evenings. From everything I read before she was born, most heart babies aren't sleeping through the night for their first year. I am also so thankful she's gaining weight. This is another thing heart babies sometimes have a hard time doing, but she is steadily gaining and I'm loving all those fat rolls!
     I am also so very grateful to have such a supportive family, especially my husband. We make a great team, and I honestly don't know what I would do without him. He is very proactive in Breckin's care and it is so nice to be able to share the responsibilities with him. During the nights where Breckin wakes up several times, we usually take turns getting up with her. We may both be tired the next day, but at least we can both understand how the other is feeling. It's also nice having another person to help get the girls ready for bed at night and ready for church or school in the morning. I am in awe of all those single moms out there!
     It sounds crazy, but I am grateful that Breckin is able to undergo heart surgeries. There are babies who are born with her same heart condition whose hearts are too weak to withstand surgery. Their only hope for survival is a heart transplant. They then have to just wait for a heart to become available and in the meantime a lot of these babies are just "living" in the hospital for a while. So I am thankful that as many defects as Breckin's heart has, her heart is strong enough to withstand the repairs that it will need. 
    I could go on and on with so much more that I am thankful for, but these are just some examples of the things I am grateful for on a daily basis. New things constantly pop up in my day and no matter how negative or frustrating or unfair they seem, I try to be thankful for whatever comes my way. I know that God is sovereign and that He is good!

Love, 
Brooke

                Harper is such a sweet big sister
     
   
                                               Loving the smiles!
              Just want to squeeze those chubby cheeks!

Tuesday, February 10, 2015

Experiencing Joy Through The Trials

    It has been four weeks now since we have come home from the hospital, and I feel like we are starting to settle in a little to our new normal. I won't lie to you though. The first two weeks after coming home, especially the second week, was pure awful! Breckin was fussing all the time. If she wasn't sleeping, she was crying. She was also up at night every couple hours and very difficult to console. It seemed like all she wanted was to be held all the time! It was taking us hours to feed her because we could not get her settled down to take her tube feeds, and she would push all her feeds back up her tube. We were sleep-deprived and dealing with a difficult baby on top of that. Everything about caring for Breckin was hard. Everything.
     I finally took her to the pediatrician and she put her on Zantac for reflux and a probiotic. I can't say that either of these things has been a life-changer, but things have definitely improved. Breckin is still waking up at night, but she does sleep about 4-5 hours at a time. Josh and I usually trade off getting up for the middle of the night feed, so we seem to be getting more sleep. She still is just a fussy baby. She hates being messed with. Changing her diaper, bathing her, and changing her clothes is not a pleasant experience for any of us. She also fights the bottle about every other feeding, and sometimes only takes a few milliliters of milk. Thankfully, we don't have to fight her to give her meds because we can give them in her tube. She is currently on four meds and a multivitamin, plus gas drops when needed. One of her meds is an antibiotic for a skin infection around her tube site, so this one will be gone in a few days.
     It's not like much has improved greatly since we got home, but I think the biggest thing is how God has changed my heart. I was not experiencing joy. I was not seeing this child as the blessing that she is. I would actually say out loud several times a day, "I can't do this!" And if you know me, that is not my nature. I am a strong-willed no-quitter person. I don't allow Harper to say the word "can't." To me, that is a curse word. When I set my mind to something, I accomplish it! However, I was relying on my own strength to handle things, and not giving it to God. I was not spending time in His word to get charged and fueled for the tasks of the day. So of course I felt like I couldn't do it. because I couldn't. I needed the Lord for strength!
     One morning I listened to one of our pastor's sermons from a while back entitled, "Faith in the Midst of the Storm." The sermon focused on the passage in Luke chapter 8 where Jesus and his disciples were in their fishing boat in the middle of the sea when a storm erupted. This is a short passage, but it has been a life-changer for me. I will never read this story the same way again. Brother Chuck made so many parallels to these verses that are so relevant and applicable to anyone's life today. I encourage you to listen to this sermon. It will change your way of looking at life's challenges. I learned from this passage and his sermon that I have to let Jesus come with me through the challenging times. I must abide with Him every single day by spending time reading the Bible and talking to Him. I also learned that going through a storm should be a time when my faith should grow. God's ultimate purpose is for my life to be conformed to that of Jesus Christ. I shouldn't allow this challenging time to come between me and the Lord, but to bring us closer. I need to see this time as opportunity for personal growth and as an opportunity to be there for others when they are going through a tough time.
     I do not know how I would make it through each day without Jesus in my life. If you are reading this and going through a storm in life, cling to the Lord. See this as a time to strengthen your faith and to be thankful to God for letting you go through this because of what He is going to accomplish in your life. If you are reading this and you do not have Jesus in your life and do not know Him as your Lord and Savior, I encourage you to let Him in. He knows that we are all sinners and not worthy of His love, but He gives it to us freely. He wants a relationship with us and wants us to spend eternity with Him in heaven. All we have to do is admit that we are a sinner, believe that He saved us from our sins by allowing His only son Jesus to die on a cross for us, and surrender our lives to Him.
     People have asked me how I go through this and deal with hard times like this and this is how. It is because I have accepted Jesus Christ as my Lord and Savior and commit to living for Him. That doesn't mean that life is going to be easy, or that it is ever easy to completely trust Him and live for Him. It is something that I have to constantly work on everyday, but it is so much better with Him! I can actually say I have true joy despite my circumstances, and that is something that I wish for everyone! Here is the link for the sermon I mentioned.: http://cfbconline.com/sermons#!/swx/pp/media_archives/116380/episode/21595
Also I encourage you to visit our church, First Baptist Church in Collierville, TN if you live locally and do not have a church home. We would love to have you!
   
Love,
Brooke

And of course my blog post would not be complete without some pictures of Little B!


Thursday, January 22, 2015

First Week At Home

     We have been home for a full week now! Our days no longer consist of cafeteria food, waiting on doctors to round, the incessant beeping of monitors, showering in public restrooms, and living out of suitcases. I will however miss a few things from our 6-week stay at LeBonheur. I'll miss the oatmeal and pancakes for breakfast, spending hours binge-watching Grey's Anatomy on Netflix, the handful of wonderful nurses who loved on our baby, the free meal vouchers I got as a breastfeeding mom, and the memories that we made there with Harper. LeBonheur truly is a wonderful hospital that especially caters to children. When Harper came to visit us, she had so much fun getting books to read from the Family Resource Center (their library), walking down the hall of mirrors, watching a movie in the movie theater, eating in the cafeteria, and enjoying all the Christmas activities. The time we spent at LeBonheur was a very difficult time for our family, but it's also a time when we made a lot of memories that we will cherish forever.
     Being home has been so nice, but it has also been a big adjustment. Going from one to two children is a big change. Harper has become more needy lately and has been wanting me to spend more time with her than usual. This thrills my heart, but it also makes me a little sad since I have to split my time now. Breckin is not only a newborn, but a newborn who requires a little more care than usual. She eats every 3-4 hours like a regular baby, but for 20 minutes, she struggles with taking her bottle. This is due to her cleft palate, her heart defect, and her thickened milk which makes it more difficult to extract. Then, for the next 20-30 minutes, we put the remainder of her total feed in a syringe that is attached to her G-tube and this is taken by gravity. For her to tolerate her feeds, she must be calm and still which can sometimes be challenging. We also have to hook up an oxygen monitor to her twice a day to check her oxygen level. In addition to just feeding her, we have to mix breast milk with a fortifier for extra calories, and then thicken part of this to give in her bottle. After feeding, all the parts of her G-tube must be washed, and the area around the tube cleaned.
     The first full week since being home, I have felt like my life revolves around feeding Breckin. There are times when I get so frustrated and think how in the world am I going to live my life? How are we ever going to get out of the house and do something fun? How are we going to feed her when we are out in public? The past couple days we have been able to get out for a couple hours at a time, going to the park and visiting my co-workers, but we come back home in time to feed Breckin. I know that things will get a little easier, and I am hoping and praying that we will not have to use the G-tube for a long time. Right now Breckin is taking about an ounce and a half of milk in her bottle. My prayer is also that she continues to take more and more in her bottle.
     The other big adjustment of course is the lack of sleep. With Harper, this was not really an issue except for the first few weeks of her life. She started sleeping through the night at about four weeks, and we never really had to train her to do it. What I have discovered though is that we were in the minority. Most babies do not sleep through the night that early, and most don't usually do it until three months of age. I have to keep telling myself this when I'm awakened by a crying baby in the wee hours of the morning, and fighting fatigue throughout the day. I am so super thankful to have a wonderful husband who gets up in the middle of the night to do a feeding, letting me sleep. He has also taken care of both girls one day this week which allowed me to get a four-hour nap! So, things could be worse. I'm so grateful that Josh has a flexible job that allows him to help me out. I don't know what I would do without him!
     Things are going okay around here. We are going through most of the same things that other parents to new babies go through. I truly have to focus on the moment at hand. If I think about the future at all, even a few hours into it, I stress myself out. My daily prayer is just that God will supply me with exactly what I need when I need it. And so far, He has done exactly that. It is amazing to see how He is constantly working in our lives. When I feel like I'm at my wit's end and don't know how to keep going, He provides just enough strength to get me through the current situation. When I feel so worn and tired hat I feel like I can't do anything else, He provides rest. When I'm struggling with a whining toddler who insists on being pushed in a stroller, I'm given a stroller that can accommodate both kids. And when I'm completely overwhelmed by the medical bills that are already piling in, I am continuously supplied with financial support from friends, family, acquaintances, and even strangers.
     I truly feel blessed that God gave us this sweet girl to love and raise. I also feel ill-prepared and totally unequipped for the task. I try not to ask myself the question of "why?" I know that He has a reason for choosing Josh and I to be this sweet baby's parents. I just pray that I can show her the love that she deserves, and give her everything that she needs to live a fulfilling, happy life. "Now to Him who is able to do far more abundantly beyond all that we ask or think, according to the power that works within us, to Him be the glory in the church and in Christ Jesus to all generations forever and ever. Amen." (Ephesians 3:20-21, ESV).

Love,
Brooke
 Her first bath at home
 Ready for her check-up at the pediatrician's office
 A little half-smile
She's so sweet when she's sleeping

   

Sunday, January 11, 2015

Going Home Soon

     Breckin has had some ups and downs in the past week, but I believe that we are in the home stretch here in the NICU. After her G-tube surgery, we slowly worked up to her taking full feeds and she has been tolerating full feeds in her tube for the past several days. We do these feeds by gravity, which means that we pour her milk in a syringe that goes through her tube and it runs in over a few minutes. Before we do this, we offer her a bottle and whatever she doesn't take by mouth we put through the tube. She has been somewhat regressing this past week with her bottle feeds. It was like she forgot how to take a bottle. She was having trouble coordinating her sucks, swallows, and breaths. She would also get so agitated during feeds and would only take 5-15cc. I felt like we were starting over, and I was getting so discouraged. However, since last night, she began to take more in her bottle, and was getting less distressed during feeds. It was like God allowed her to improve at just the time when I was feeling down and discouraged.
     The other new aspect to her feeding is her obturator, which is her mouthpiece for her cleft palate. We have only used it a couple days, but so far it has not helped her. In fact, she doesn't take any of her bottle when this is in her mouth. She doesn't know what to do with the bottle when the obturator is in her mouth. She just kind of mashes on the nipple, and won't even suck. Many people have told us that it will take a while for her to get used to this. In the meantime, however, it is just very frustrating for both of us, and she does better without it right now.
   On Friday, the doctors said that if she does well over the weekend, we will be getting discharged next week. She has to be gaining weight and tolerating feeds which she is doing. We also have to do a 48-hour stay at the hospital to make sure we know how to do everything involved in Breckin's care. I am feeling so many emotions as we anticipate our homecoming. I am excited to get our family back together and to get to take care of my baby in our own home. I am also nervous about taking care of her and not knowing what to anticipate. When I think about the road we have ahead of us, it is so overwhelming! However, I know we serve the Most High God who is in control of everything. This is definitely not the path that we would have chosen for our family, but it is the one we are going down. I know God is going to take care of Breckin and get us through the challenging times with her. We are just so blessed to have her in our lives!

Love,
Brooke

Thursday, January 1, 2015

A G-tube For The New Year

     So we decided to go forward with the G-tube. This was not a decision that my husband and I went into lightly. I personally have gone back and forth so many times trying to decide what is the best thing for Breckin. When we talked with the doctor last week, he was not on board with it. He wanted to give it another couple weeks and wait for what's called an obturator. This is a mouthpiece that goes over the cleft in the palate to hopefully help her latch. The earliest this would even be started would be the second week of January, and it may not even be a solution to her feeding problems. So I decided over the weekend to put my foot down about not waiting for the obturator and to voice my feelings about the G-tube. Monday morning when the same doctor rounded, Josh and I brought up the G-tube again and our reasons for wanting to go forward with it. He pretty much immediately said yes I think we should go for it, and put in a consult with the surgery team. The fact that he was so much more on board with it only a few days later, made me feel even more that we were doing the right thing. 
     The next day, Breckin had an upper GI study to assess her anatomy and this was all normal. Later that afternoon, the surgical fellow came and talked with me about the surgery, and to make sure this was what we had decided to do. After confirming that yes this was something we have talked, thought, and prayed about, he told me that he believes we made a good decision. He said there is really no right or wrong way to go about feeding, but he said that babies tend to do better once they are home. This was just another affirmation that we were making the right decision for Breckin. There is usually another study that is done called a milk scan, which would assess if there is any reflux. Since Breckin has had no signs of reflux, they decided to forgo this study and go ahead with the surgery. It was scheduled for the next morning.
     So yesterday, on Wednesday December 31st, Breckin underwent her second surgery in just four weeks. Before the surgery, we met with the surgeon who would be doing the procedure. Her name is Dr. Williams and she told us that she is very good with G-tubes. This definitely put me more at ease. We watched our baby get wheeled back to the operating room again, and anxiously waited for the phone call to let us know they were done. Not even 45 minutes later, we got the call that the surgery went well and she was being taken back to her room on the NICU floor. 
     We came in to see her and the first thing I noticed was that she looked so long! It looked like she had grown in the short time that she was back there. The second thing I noticed though was that she had quite a bit of swelling on the right side of her head and face. Her ear was even shifted down due to all the swelling. The doctor told us that the scalp IV that they had started the night before had infiltrated and was leaking fluid into the soft tissue. They had already pulled the IV, but they said fluid would continue to leak out, and the swelling would take some time to go down. It looked awful, and I hated seeing her like that. It was almost worse than seeing her after her heart surgery. Luckily though with this surgery, she did not have all those lines and machines hooked up to her. All she has is an IV in her hand and the breathing tube in her mouth. 
     Today the plan is to wean her from the ventilator. She has definitely been more awake today and moving around when she's touched. They have started to go down on her vent settings, and have stopped giving her the morphine which is making her more sedated. They will just treat her pain with Tylenol and hope she will continue to wake up more. Her G-tube was clamped off this morning which means her gastric (stomach) juices will have a chance to just sit in her stomach. As long as this doesn't make her spit up or vomit, they will start feeding her this afternoon. The nurse practitioner said we can start feeding her with the bottle like before and give her the rest in her G-tube. We will start with small amounts and work our way up. The surgeon said that she would be up to full feeds in 48 hours if everything is tolerated. We are hoping that we will be able to go home next week!
     I hate that Breckin had to undergo another surgery, but I completely feel like it was the best thing we could do for her right now. I know that she will eventually get to where she can take a full bottle. She has the desire to eat, and she knows what to do. It's just a matter of her getting so tired that she can't finish her full amount by mouth. I think that once she grows and gets bigger and stronger, this will be an easier task for her. Our hope is that we won't even need to use the G-tube for long. I cannot wait to get our family of four back together under one roof. I am so excited to see what God has in store for our family in 2015! Happy New Year everyone! 

Love,
Brooke


Before her surgery yesterday just resting peacefully
 Day one after surgery-no more NG tube!

Friday, December 26, 2014

Feeding and feeding

     We have been back in the NICU for almost two weeks now. Breckin did so well after surgery that she no longer needed to be in the cardiovascular ICU. She has been doing so great since her heart surgery. Her respirations are so much better now-she breathes maybe 30-40 times per minute instead of 80-100. Sine being back in the NICU, we have mainly just been working on feeding by mouth. Because of her cleft palate and her heart defect, she has difficulty taking her full volume by mouth. She also was aspirating on her milk after her surgery. This means that the breast milk was going down her trachea to her lungs, which was why she would just give up eating after a few swallows. Our speech therapist is the one who saw the signs of this and ordered what is called a modified barium swallow. During this test, it showed that she aspirated on the breast milk in her bottle. So, a thickener called nectar was added, and this solved the problem.
     Since the swallow study, we have been feeding her with the thickened breastmilk. We are also adding fortifier to the milk to give her extra calories. As of today, she has surpassed her birth weight by a few ounces so she is back to gaining weight. We have been working on giving her as much volume by mouth as she will take. She was eating every three hours and it didn't seem like she was getting hungry enough, so we changed it to every four hours and that seems to have helped a little. She is now taking about 40-45cc pretty consistently by mouth. This is about 1 1/2 ounces. Her goal is to take 70cc by mouth every 4 hours or 60cc by mouth every three hours. We have come a long way, but I still feel like we have a long way to go.
     We have had so many great nurses here who have truly loved on our baby, and for that we are so grateful. However, because so many different nurses rotate through, I feel like there is some inconsistency. Every nurse has their own way of doing things and their own way of feeding Breckin. When Josh and I are here, we will feed her, but through the night, we let the nurses feed her. I feel like this is when she loses ground. It is just very frustrating being here day in and day out knowing the only thing keeping us from going home is her eating. I know that she will eventually get there, but I'm afraid it could take several more weeks for that to happen.
     We have recently been considering the idea of getting a gastrostomy tube or G-tube. This is a feeding tube that goes directly into her stomach. We can still do what we're doing now-offering her milk by mouth and then give the rest in her tube. However, we can go home with the G-tube and continue to work with Breckin at home. The G-tube is a simple procedure, but it is another surgery that Breckin would have to undergo. This is my only hesitation with going ahead with this. I hate to put my baby through another surgery where she will undergo general anesthesia, but I feel that Josh and I can make more progress with her at home.
     I have seen God working so much in Breckin's life, and I am just ready to get her home to actually start living life with her. We are so blessed with her and she is such a joy in our lives already. I know we have a long road ahead of us filled with many more doctor's visits, surgeries, therapy, and challenges down the way. However, I know that God is going to be with us through it all. I never thought I would make it past that first week here. I thought I would lose all hope, but my hope is continuing to be renewed each day that we spend with our baby girl.


 Christmas Eve
 Doing some feeding with her big sister and the speech therapist
Snuggle time with mommy

Monday, December 15, 2014

Breckin's First Heart Surgery

     Breckin had her first heart surgery last Tuesday evening on December 9th, just 6 days after being born. The cardiac surgeon, Dr. Knott-Craig was thinking it would be two to three weeks before she needed it, but she was showing that she was over circulating too much and was ready for it sooner. One of the conditions that Breckin has is called double outlet right ventricle which causes too much blood to be circulated to the lungs. This causes her to work too hard to breathe. So, at about 4:30 that evening, we walked with our little girl to the surgical floor, kissed her goodbye, and handed her off to strangers. It was one of the scariest moments in my life. The thing I kept thinking was, how in the world am I going to be able to do this two to three more times?
     The surgery only took a couple hours and Dr. Knott-Craig was so pleased with the outcome. He said the pulmonary band they put in place was a perfect fit. It was just loose enough where she could grow into it, but not too tight where it wouldn't last long. He also said she only lost about two teaspoons of blood so she didn't need to receive any blood.
     We transferred to the cardiac ICU that evening where our sweet girl was lying in her bed hooked up to all kinds of monitors and intubated to help her breathe. Her nurse, Morris, would be taking care of her all evening. He was so great to explain everything that was going on and give information about every piece of equipment she was hooked up to. He stayed in her room with us that evening and watched her every move. It was a little awkward getting up to pump every three hours with a strange man in my room, but I was glad he was there. The next morning, he said the night went great with no complications. He only gave her one dose of morphine, and she never required anything but a dose of Tylenol the next day.
     I am truly amazed at what my sweet girl has already gone through since being here. Besides having heart surgery, she has had more needle sticks than I can count, multiple tubes in her nose and throat, several IV lines inserted, and she even suffered a terrible wound on her ankle from a blister that opened up. She has been such a trooper and I am humbled by her strength. All of the nurses comment on how strong she is, and I am so grateful for that.
     Since her surgery, she has done so well from a cardiac standpoint. She was intubated for about 36 hours after surgery because she was just unable to wake up and breathe on her own. After that, however, she was back to her old self of being feisty and demanding :) The biggest hurdle that we have faced since surgery has been her not eating. The next three days after being extubated were just awful. She was hardly taking anything by bottle, and not seeming to make any progress from one day to the next. I was feeling so hopeless and sad about this. I know this is our last task before getting to go home. She has to be eating!
     Today, thanks to our wonderful speech therapist Amy Clare, we had a breakthrough! At her morning feeding, she noticed that Breckin looked like she was aspirating her milk. She worked quickly and within 20 minutes, we had her downstairs doing what's called a modified barium swallow. They took an x-ray of her being fed to see if she was aspirating the breast milk. After a few swallows, they saw that she was aspirating. To fix this problem, they thickened her milk with stuff called nectar to prevent it from going down her trachea. The first feeding with the thickened milk seemed to go okay. Amy Clare fed her and said she was doing great coordinating her suck, swallow, breathe actions. She only took about 7cc at that feeding, but Amy Clare was very pleased with this. At her next feeding, I was on my own. We had a nipple that had been cut at the top to make the hole larger to try to help Breckin get more milk. At this feeding, she was much more interested in eating and she ended up taking 17cc-more than half of what she took at her last feed! I was definitely one proud mama!
     I am so thankful for everyone's prayers and I can totally see God doing amazing things in Breckin's life. She has been in this world not even two weeks and already she is making a lasting impact on so many people. She has more strength already than I imagine I ever will. It's strange even saying this but despite all of her health problems, God has truly blessed her. She is already such a blessing to me and I cannot wait to get her home and live with her as a family of four.


Love,
Brooke


   Getting her barium swallow test
Right after her heart surgery