Friday, July 15, 2016

Happy Birthday Baby

Today is Atticus' first birthday! Between memories of the day he was born, to the realization that my baby is now a toddler, it's been a rollercoaster of feels all morning.












I've been thinking a lot about how we see things more clearly in hindsight and about having an eternal perspective. This past year has taught me a lot, and stretched me to lengths I didn't know I could go. Who knew you could live off so little sleep? 

One thing that has stood out in my mind is that God allows us to go through hard things. We have to or else we would never progress, but He will not abandon us in our time of need if we will remember Him. Looking back at this year I can see clearly the times when He was there. Sometimes it can be hard to see in a moment of pain or suffering when we are pleading for relief, and that is where faith comes in. We learn by trial of our faith. We put trust in the Lord, not that he will spare us from pain, but that He knows our pain and has a plan for us. He knows exactly what we are feeling when no one else does. And that someday, maybe not today, but someday if we continue to put our faith in Him it will be okay. Better than okay. It is by suffering that we learn JOY. 

We have been incredibly blessed, and I know that it is by the hand of the Lord. I know that we will continue to be tested. I also know that God loves me and wants me to grow, to learn empathy and humility. I also know that God wants me to have joy. This last Easter a simple thought came to me and has stuck with me ever since, choose hope. This is such a beautiful way to describe what it means to have faith and an eternal perspective. In the face of adversity, we choose to hope. 

Happy birthday to my baby. 

Love, Kember

“Press forward with a steadfastness in Christ, having a perfect brightness of hope, and a love of God and of all men. Wherefore, if ye shall press forward, feasting upon the word of Christ, and endure to the end, behold, thus saith the Father: Ye shall have eternal life.”
                                           -  2 Nephi 31:20

Saturday, January 16, 2016

Happy New Year! An Update on the Bensons

Atticus

www.laurenelizabethlife.com

Atticus turned six months old yesterday, he's growing and changing so fast. He got his first tooth on Christmas, and to be honest I was sad to see that toothless grin go. He is also sitting up by himself for extended periods which is fun. He hasn't rolled from back to tummy yet, but he's trying. We've started solids and so far, nothing too traumatic for him. Trying to comment on naps just makes me frustrated so we'll just leave it at that. He is sleeping better at night, sometimes only waking up 1x, sometimes 3 or 4x. It's a toss-up, really I never know what to expect. I am counting our blessings that Atticus hasn't shown any signs of infection or shunt malfunction. He is in great health and we thank the Lord every day that he is in our lives. We're starting to see a little personality come through. He's pretty shy and serious around most people, and will randomly take to someone really well. At home though, he's easy to make smile. I think Atticus is a sensitive soul, which comes with ups and downs, but I've learned that every week brings something new. Who knows what he will be like six months from now. We love little Mr. Benson.

Garrett

www.laurenelizabethlife.com
I couldn't be more proud of him. In December he finished his undergrad in accounting at UVU, and is loving his job. He is currently working full time in the accounting department at his company, and enjoying a break from school. He's also been working on some youtube videos on some of the accounting material he studied in his undergrad to help him stay fresh on the topic. Garrett is a wonderful daddy, my favorite part of the day is when he reads to Atticus (willing Atticus is still in a cooperative mood) before we put him to bed. This year has been such a rollercoaster for us, and I'm so blessed to have a man like him by my side. 

Kember

Still trying to figure out this whole mum thing. We are blessed to be in a circumstance where I can stay home with Atticus, and so that is where I am at. I spend my days changing diapers and negotiating naptime. Being a mom isn't all sunshine and rainbows, it's a big mish-mosh of heartwarming, heartbreaking, frustrating, unbelievable moments.  There are good days, and there are not so good days too. I am learning slowly to enjoy the good moments, and endure the not so good ones with faith in the Lord.

As always, we are a work in progress!

Love, The Bensons

"And finally, in all of living have much of fun and laughter. Life is to be enjoyed, not just endured." 
                                 - President Gordon B. Hinckley, Stand True and Faithful




Sunday, November 1, 2015

Atticus' Blessing!

Well, Atticus is 3 1/2 months old and we finally blessed him today! After everything that happened in the past few months, we finally felt confident about setting a date. It was such a great day.












I was a little stressed out about the whole thing, but everything turned out so well. Daylight saving ended up being a blessing in disguise, Atticus woke up "early" and so was able to get a nap in before the meeting so he was a little happier. It was also such a beautiful day with all of the leaves turning colors but still warm enough to be outside.

I was so happy that some of my family were able to make it and finally meet my little boy.  We didn't snag a photo of Garrett's family, but many of them came as well. Garrett did such a beautiful job with the blessing, it just touched my heart to see him bless our little boy.


“We should not need a hurricane or other crisis to remind us of what matters most. The gospel and the Lord’s plan of happiness and salvation should remind us. What matters most is what lasts longest, and our families are for eternity.”
                                                                       - Elder M. Russell Ballard

Friday, October 23, 2015

Mountains to Climb: An Update on Atticus


I want to begin first by expressing our deep gratitude to all of our family and friends who have kept us and our baby boy in your prayers. The love and support we have felt during this trying time has been incredible, thank you.

So then, an update on Atticus!

When I posted last we were waiting on an MRI, so I will start there. Atticus had to be sedated which meant that he had to fast prior to the appointment. At this point because he wasn't quite a month old he would also need to be under observation for 12 hours after sedation. Withholding food from a four week old baby is an incredibly frustrating experience for everyone involved.

On Tuesday, August 11th we drove up to Primary Children's Hospital where we were directed to the imaging/radiology department. They placed an IV in Atticus' hand and I carried him down the hall to the room where they would do the MRI. The nurse then directed me to a chair where I held him while she pushed the sedation drugs into his IV. Atticus was starving at this point so I watched his very frustrated face relax, and then handed his limp little body over to the nurse who took him back to do the MRI.

What you see here is a slice through the center of a ventricle. The fluid is the large white area. They are about 5x the size that they should be.


When the MRI was done we were taken to a recovery room where a nurse was assigned to monitor his vitals for a few hours after sedation. We were scheduled to meet with Dr. Kestle, the neurosurgeon who would be doing the operation should Atticus need it, after the MRI. I was very anxious to feed Atticus once he came out of sedation, but we were told to wait for the neurosurgery team to come meet with us before we fed him, just in case the surgeon didn't want him to eat. Well it ended up the team was about and hour and a half late to our appointment and consequently Atticus hadn't eaten in about 10 hours.

Garrett didn't know I snapped this photo, but I thought it was very sweet. Garrett is running on about 2 hours of sleep and is listening to some study tracks while calming a very hungry baby.

When we finally met with the team, the surgeon didn't even know we were waiting to feed Atticus, and gave us the go ahead. He informed us that he did want to do surgery the next day. We had packed some bags just in case, but it was still hard to process that our infant would be undergoing surgery within the next 24 hours. At this point Garrett and I were still undecided as to which surgery Atticus would get. We had two options, an ETV (endoscopic third ventriculostomy) or he could have a shunt system placed. He was a good candidate for both and both had various risks and benefits. This was the hardest choice either Garrett or I had ever made. One thing I didn't anticipate in becoming a parent was how hard it would be to make decisions, especially when the decisions you make directly impact another person's life in such a drastic way.

Preparing for Surgery
Ultimately after much thought and prayer, we decided that a shunt system would be the best fit for our little boy. A shunt system helps the fluid flow out of the blocked area of the ventricle. In Atticus' case he has a blocked duct that currently prevents the normal flow of fluid and causes his hydrocephalus. The shunt is placed into the ventricle, and a line is run up through his skull. There is a reservoir under his skin on the top of his head that holds some of the cerebral spinal fluid, this is so that if we suspect an infection they can tap into that instead of doing a spinal tap. There is also a small valve which regulates the flow of fluid, and then tubing which runs under his skin from his skull, behind his ear, and down under his abdomen where it drains into the cavity around his gut and is reabsorbed into the body.

We were taken from the recovery room to the infant unit where he was admitted. He fed about three times before he had to fast again in preparation for the anesthesia the next day. Atticus began his next fast at 2:30 AM in the morning and around 7:30 AM the nurses came in to bath him. Sometime after 8:00 AM, we were finally ready to go. The nurses asked if we wanted to put him in the crib and wheel him down or if I wanted to carry him. I replied that I would carry him. We were taken down to a small room where we waited for the neurosurgery team to come and talk to us. We also met my parents there so they could see Atticus before he went in.

The team came in, and reassured us that Atticus was in good hands. I handed my baby over and just like that, he was on his way to surgery. We were taken to the waiting room where we found a small unoccupied office and my dad gave Garrett and I a blessing.  In the waiting room there was a mom of another child with hydrocephalus, his condition however was caused by genetic condition. I later spoke to our surgeon, he does not believe that it is a genetic condition with Atticus because there were no other abnormalities in his brain.

The surgery was fairly short, 1-2 hours, and went very well. We were taken down to OR recovery unit to see Atticus. As much as a tried to prepare myself to see him, I wasn't. I saw his little face, still so groggy from anesthesia, and I broke down in tears. Because he had a breathing tube during the operation his throat had been scratched. I could tell he was trying to cry, but it was more of a scratchy little groan. I remember being very upset at how cold he was and that he wasn't wrapped up very well. If you've ever been inside of an OR, they keep it very chilly and he was naked during surgery. Garrett asked the nurse if I could hold him. They handed Atticus to me and I just looked at his pale little face. He had three incisions, one on the top of his skull, behind his ear, and one on his abdomen. It was difficult to hold an infant knowing he had several incisions, monitors, and an IV stuck to him, but I was grateful I could. The nurse handed me a bottle of cold formula, which he didn't take.

Recovering from Surgery
We took Atticus back up to our room where he was attached to another set of monitors. He was given morphine for the pain, as well as percocet, motrin, tylenol, and a version of lortab for babies. He didn't eat for another 10 hours after coming out of anesthesia, and when he did it was slow going. At this point Atticus had been on IV fluids for over 24 hours, consequently his little body was all swollen with fluids. His recovery went well, with a few hiccups with his oxygen levels and some gas in belly.

2nd MRI Image
After his surgery they did another set of images with a different MRI machine. These images aren't as detailed and don't take as long, which did not require sedation (thank goodness!).  It was amazing to see the difference. Not too much, or too little. They want to see change, but not too quickly.

By Thursday, he was eating enough and wetting his diapers and was discharged. I was pretty surprised at how soon he was able to go home after brain surgery.  Modern medicine is incredible.

Leaving the Hospital
I wanted to make sure we got a "family photo" before we left the hospital. This was such an impactful experience for our little family unit, and while it's not the most glamourous photo I wanted to document this moment.

Atticus just passed his three month mark and I am happy to report that he is doing wonderfully! He will have the shunt for the rest of his life, and will need another surgery at some
Atticus at 3 Months
point to replace to tubing once he grows out of it. Hopefully, that is the only surgery he will need. He has a small chance of infection and a larger chance of blockage, if either of those happen then he would need to have the whole system replaced.

Every situation is different with hydrocephalus, but there is a chance he will have some type of learning disability. Whether that be social, emotional, reading, language, and what the extent will be we really don't know.  We are very hopeful for his future however, and as of right now he is hitting all his major milestones (smiling, lifting his head, eye tracking, etc.). He is even starting to rock (almost roll!) from tummy to back, which is so exciting for me!

We have a follow up appointment scheduled next month where they will do an ultrasound to check his progress and to make sure the shunt is functioning correctly. We are hoping to see a decrease in the size of his ventricles since the last image.

A beautiful talk given by Elder Henry B. Eyring has come to my mind more than once since Atticus was born. "Mountains to Climb" where he talks specifically about faith building experiences. This has been a rollercoaster for our little family, and while I know we may not yet be through all our trials, I know that God has lifted us up and helped us to bear our burdens. I am grateful for the gospel of Jesus Christ, and I know that through Him we can do all things that the Lord would have us do.

"If we have faith in Jesus Christ, the hardest as well as the easiest times in life can be a blessing. In all conditions, we can choose the right with the guidance of the Spirit. We have the gospel of Jesus Christ to shape and guide our lives if we choose it. And with prophets revealing to us our place in the plan of salvation, we can live with perfect hope and a feeling of peace."
                                     - Elder Henry B. Eyring, Mountains to Climb








Thursday, August 6, 2015

Introducing Atticus Grant Benson: Our Story

When I imagined sitting down and writing out my son's "birth story" I couldn't have known that it would be so drastically different than what I had anticipated. It's taken me a few weeks to write this down because in all honestly, the last three weeks have been a whirlwind and some of the hardest of my life.

Atticus Grant Benson was born July 15th, 2015 somewhere around 9-11 PM. When I get the birth certificate, I'll have an exact time but in the midst of all that happened it's hard to remember all the details. He was a sturdy 8 lbs 6 oz and 20.5 inches long, and this is our story.

I had been experiencing some pretty intense back pain for several days, and this day was no different. On July 14th, a Tuesday, around 10:30 PM I decided to take a hot shower to try and relieve some of the pain in my lower back. This pain had been keeping me up every 40 minutes or so at night for several nights. As I stepped into the shower felt a gush, and suspected my water had broken. I hadn't felt anything like my Braxton hicks contractions so I decided to sleep through the night and if nothing had changed in the morning, I would go in and confirm with my midwife. Around 11 AM that next morning, July 15th, I went in and confirmed that my water had indeed broken. I was 38 weeks and 3 days. At this point I still wasn't experiencing what I expected contractions would have felt like. The midwife suggested we try some homeopathic options and castor oil to try and get things moving. I'm not a huge believer of homeopathics, but I was open to at least giving it a try. She inserting an IV lock and started my first round of antibiotics as I was GBS+, fed me the oil and placed something under my tongue, and sent me home. I had called Garrett to let him know that we would be meeting our baby boy that day, and he came home from work around 3 PM. We tried walking around, and climbing some stairs to try and get things moving, with no luck. At 4 PM, we returned to the birth center for the second round of antibiotics. The midwife suggested we try to physically induce labor at this point. After examining me, and bringing in a second midwife to try and confirm the baby's position, they informed me that they weren't sure the baby's head was facing down and wanted to do an ultrasound to confirm as they cannot deliver breech babies.

It was after 5 PM at this point, so after pulling some strings she was able to pull in a friend who worked at Utah Valley Regional to do an ultrasound for us. We drove down, praying the whole way that baby was in a good position so we could have the birth we had been planning from the beginning.

We met with the ultrasound tech, and held our breath as she began to scan my belly. She confirmed that the baby's head was head down, and Garrett and I felt a wave of relief as we celebrated in that brief moment. However, our victory was to be short lived. It slowly dawned on me that something was off when the midwives and the ultrasound tech did not share in our joy, and I heard one of them mentioning softly to the tech, "it's hydro, yes it looks like hydro". My heart slowly began to sink as the realization hit me, something was wrong. Trying as best I could to prepare myself for the answer, I finally asked aloud "Is something wrong with him?" Yes. Yes, something was wrong.

The hardest part about this time was that Garrett and I were given virtually no information, and were left to speculate about what we saw next. The ultrasound tech pointed out two large, black spots in our baby's brain. She told us that he had hydrocephalus, or fluid on his brain, and that I also had excess amniotic fluid. The fluid in his brain has caused his head to become larger than normal. We asked if this would affect his development, and she replied yes. That was all we knew for the next hour.

I couldn't bring myself to look at Garrett. I felt so many emotions all at once. Fear, a lot of fear that I was going to loose my baby. Guilt, was it my fault? What could I have done differently? I had been so careful, not even taking a tylenol my entire pregnancy. Why hadn't we seen anything on the 20 week ultrasound? Panic, what did this mean for our baby? Was he going to be able to survive outside the womb? I stared up at the ceiling and tried to hold back my tears as my heart broke. Broke for my little baby, and for my husband. I felt so broken, like I had failed. This was what my body was designed to do, and I had failed. All I wanted to do was to bring him into the world safe and healthy, and I couldn't.

We left the ultrasound room and went to move our cars closer to obstetrics and gynecology. Finally having a moment alone in the car, Garrett and I were left to face the reality of what was happening. It hit us both hard, and we both wept openly for our little boy. Through tears, Garrett was the first to speak, "We'll love him no matter what, it will be okay."

As we walked hand in hand down the hall I couldn't hold back my tears. I cried as I was shown to a room, and instructed to put on the gown. The nurses asked if we wanted a moment alone, which we accepted. Garrett helped me with my clothes, gave me a blessing, and then we called our parents to let them know we were being admitted to the hospital. Garrett's parents would arrive about a half hour later, and mine later that night.

As the nurses began to monitor my belly, the midwives who were still with us pointed out that I was having contractions. I was shocked, because still wasn't feeling anything in my stomach. Then I realized, my back pain was my contractions and correlated with the spikes on the screen. I speculated later, that I had actually been in labor for several days.

We met with the doctor, who informed us that while vaginal delivery is always preferred, because of the hydrocephalus and baby's head size he was concerned what the trauma of a vaginal delivery would do to the baby, who still had not settled into my pelvis. Our plan for delivery had been a natural, unmedicated vaginal birth at a birthing center. When the doctor said the word cesarean, it didn't sink in. Everything had changed so fast it was hard to process. From the time we saw the ultrasound to the time I was on the table in the operating room, it was only about an hour.

Garrett's mom and dad arrived and Garrett and his father gave me and baby another blessing. My contractions were becoming more intense now, but I was able to walk myself to the operating room. A C-section was never in our plans, so I had not prepared myself for the experience. The OR was very cold and very white. I began to shake violently as I received the epidural and my wrists were strapped to the table. Garrett sat at my head and stroked my hair as the team prepared for surgery. Even when the epidural took effect, my upper body continued to shake violently through the entire procedure. I tried to hold back tears but could not. I had no idea what was about to happen, if we were even going to get to meet our baby boy. The NICU team stood by watching and waiting to take the baby should anything go wrong. One of the doctors asked me if I'd received a screening for gestational diabetes, as he suspected I may have had it due to the excess fluid.

I remember the moment we heard him cry, and I have never been so happy to hear a baby scream. I looked at Garrett and he asked me what I wanted him to do, stay with me or go with the baby. I told him to go with baby Atticus.

Garrett left the room and the doctors began to finish the surgery. As I mentioned, Garrett and I weren't given much information about our baby boy's condition. So when I saw Garrett come back into the operating room carrying a beautiful baby boy, I was shocked. He was so beautiful, I wish I could have held him. I remember asking in disbelief, "Is he okay?" Garrett put his little face next to mine, and all I could do was rub my nose against his.

One of the doctors said very calmly to me, "You're losing a lot of blood and your uterus is not contracting on it's own. If I can't get it to contract, I'm going to have to perform a hysterectomy." Not knowing what else to say, I numbly replied "Okay." He performed a suture where they roll the uterus up like a sleeping bag to manually contract it, which was thankfully successful. I lost 2 L of blood, during a c-section a woman usually looses about 500 ml. I know that I was blessed and that the Lord was watching over me during this time. I should be able to try for a VBAC (vaginal birth after cesarean) in the future.

They took Atticus back to the nursery while they moved me from the operating room to my recovery room. We were counting our blessings, our baby boy was okay. He was breathing, and eating, and pooping just like he should. They let him stay with us that first night, offering at one point to take him back into the nursery so we could get some sleep. We declined because all we wanted to do was be with our little boy.

I wouldn't have had much sleep anyway, the nurses came in first every 15, 30, 60 minutes, then 2 hours to push on my uterus. They needed to make sure I was clotting enough and that my uterus was contracting. Even with the pain medication, this was the worst pain I have ever felt. One of the nurses was an angel and told me that I could dig into her arm with my nails if it helped. Strangely, it did. In addition to the nurses I had someone coming in to draw blood every few hours to check my hematocrit levels after losing blood.

Having him with us that night was a blessing. Garrett slept on the pull out bed and would change his diapers, and bring him to me to nurse. We got to be his parents that night and things felt almost normal for a little bit. The next day, we received a call from the NICU, letting us know they would be taking him for observation as babies with hydrocephalus are at risk of having sleep apnea.

Garrett went with him while I slept for a few hours. The nurse wheeled me up the the NICU later where I saw Garrett, sitting exhausted in a chair holding our baby boy. Atticus had an IV tube and monitors stuck all over him. The nurses let me know that his blood sugar had dropped during the night and they had to give him an IV line to help stabilize it. I nursed him and we cuddled for a little bit. We later realized that due to the blood loss and stress, my milk supply was very low. Ultimately, in an effort to get him out of the NICU as quickly as possible and bring his blood sugar up we ended up placing a feeding tube down his nose though which donated breast milk was pumped directly into his stomach.

This was a hard decision for me because I had wanted to nurse exclusively so badly, but couldn't. Like many other things that had happened, I didn't have a choice and had to do what was best for my baby. I didn't want to give up completely, so our routine became that the nurses would call me in my room everytime he would wake, which was about every three hours, Garrett would wheel me up to the NICU where I would nurse him for a few minutes, then pump while Garrett held him and he was fed through a tube. I met with several lactation consultants during this time, and was told later by my mother-in-law that one of them said to her that I would never be able to nurse. I am so glad they didn't say that to me, I was already pretty discouraged.

Atticus was in the NICU for five days, during this time they did an ultrasound on his head and then decided to do an MRI which he was sedated for. We met with the neurologist who let us know that he had been consulting with the neurosurgeon at Primary Children's Hospital. He believed that there may have been a small hemorrhage that happened sometime in utero, and that this may have caused a blockage in the duct that drains the ventricles of the brain, causing the hydrocephalus. This was the first bit of real information about his condition that we received. The good news, was that while in the NICU, his head hadn't gotten any bigger.

Initially, the doctors at Primary's wanted to transport Atticus via ambulance. The neurologist at Utah Valley however, didn't feel that was necessary and felt like if we could get him off the IV, and onto a bottle that he could discharge us after which, we could meet with the neurosurgeon at Primary's as an outpatient visit in a few days. On day four, it was time to discharge me. This was a hard time for Garrett and I because there were no available rooms for family members of NICU babies. We had been so diligent at staying as close as we could to Atticus, and now we had no choice but to go home for the night. We were both exhausted and emotionally spent. One of the lactation consultants basically had to kick us out. I was only able to leave because Garrett's mother came up to the hospital and spent the night sleeping in a chair next to Atticus. She made sure that he was being bottle fed so that we could take him home. I couldn't believe how difficult it was to leave that hospital that night, scarred and empty handed. Ultimately, it was the best thing we could have done. Once at home, I was able to relax and my milk began to come in more steadily.

Atticus responded well to bottle feedings and once he was successfully able to do so, he was discharged and finally able to come home. I would nurse him and supplement with formula, then pump to try and bring in my milk supply. Atticus has been home for two weeks now, and has been exclusively nursing for about a week.

We had been told that he would be meeting with the neurosurgeon at Primary's the next Tuesday, which I was never comfortable with. I didn't feel like I knew enough about his condition and was afraid of waiting that long after they had initially wanted to transport him in an ambulance. We brought Atticus home on a Monday, and Wednesday was his first appointment with his regular pediatrician. At the appointment, Atticus' head measured two centimeters bigger which immediately had me concerned. All babies head's grow, but his was growing at a faster rate which indicates more pressure on the brain. His fontenelles are larger and more open to compensate for the increased pressure. This is why hydrocephalus is less scary for infants than for adults. They have more room to stretch. I had also noticed that his eyes were doing what is called "sundowning", another indication of increased pressure. I pushed for a sooner appointment and the pediatrician contacted the neurosurgeon at Primary's. We went up for an appointment the next day.

The surgeon let us know that he was concerned and felt that Atticus would need surgery. However, we met with him on his last day before moving to Canada. He said that he was 90% sure that we would do surgery the next week and so he booked the OR. The next week we came back for a follow-up with his partner, the surgeon who would ultimately be doing the surgery. This time, this surgeon wanted to wait some time and do another MRI to get a better picture of Atticus' condition.

So this brings us to the now. Atticus is home, and we have an appointment for an MRI at Primary's on Tuesday after which they will monitor him for 12 hours because he is so young. We then have an appointment with the neurosurgeon after to determine if they will want to admit him for surgery that day, or take another course of action.  We have two options at the moment, either they can do a shunt system which will likely need another surgery by the time he is three, or an endoscopic third ventriculostomy. The second option is more of a one time treatment, but has a significantly lower chance of success due to his age.

What his future will be, we do not know. There is a chance he could have developmental delays, or that he could be completely normal. The thing with hydrocephalus is that it can be caused by many different things, and so it's hard to tell what the outcome will be. We just have to wait and see with time.

I mentioned to Garrett the other day, you don't go through something like this and come out unchanged. This has been and still is one of the most humbling and difficult trials I have gone through. I am so grateful for the atoning sacrifice of Jesus Christ and the knowledge of the plan of salvation. God will never give us something we cannot handle, with his help. He gives us the experiences we need to help us grow.
"Don't be gloomy. Do not dwell on unkind things. Stop seeking out the storms and enjoy more fully the sunlight. Even if you are not happy, put a smile on your face. "Accentuate the positive". Look a little deeper for the good. Go forward in life with a twinkle in your eye and a smile on your face, with great and strong purpose in your heart. Love life."
           
                                                                   -Gordon B. Hinckley



Tuesday, June 30, 2015

36 Weeks: It's Getting Cramped in Here

6/30/15

Here we are at 36 weeks!


Well I'm in the home stretch now! I had my last day of work about two weeks ago, and have been prepping for baby boy to make his appearance. Honestly it couldn't have come at a better time, I am getting so uncomfortably large that working any longer wouldn't have been a fun experience. I have been reclining the drivers seat back further so that I can drive without rib pain, it works sometimes. 

I am feeling better since the last post, thankfully. I did have one spell of sickness this month but I don't know if it was disease (stomach flu) related or if I had a crazy bout of morning sickness return. Luckily, it only lasted about two days. Other than that, I have had some general nausea but not like the first trimester.  I am also starting to get some swelling in my ankles if I've been on my feet too long, but nothing too bad. 


Garrett's sisters and mom threw me a baby shower on Saturday. It was so great to feel all the love and support from friends and family, especially those I hadn't seen in a while. We did it during my family reunion so more of my family could make it. 

So I measured at 40 cm at my prenatal appointment yesterday. Ouch. Baby boy, please don't stay in too long, just long enough. It's getting cramped in there. 



Tuesday, June 2, 2015

32 Weeks: No Sugar Coating

6/2/15

This weeks marks 32 weeks, that's 8 months! And for your reference, pregnancy is 40 weeks, which means you are pregnant for more like 10 months. Not 9.


I don't feel like sugar coating anything this post so I'll just say it. I feel like crap. I've been sick in one form or another for the past 3 week - 4 weeks. My back is hurting a lot more this week as well. Mostly lower, some upper back. Baby is still doing well. Hopefully next post will be a bit more positive. I'm going back to bed now.