Wednesday, October 9, 2013

Jack's Birth Story



I woke up 2 years ago on this day and was tired of being told not to move, not to walk, not to worry, not to, not to…..  I spent much of the previous day in tears because I was tired of being on bed rest, stuck in a hospital room and away from my daughter.  Her tears made mine worse.  Frankly, I couldn’t believe that my water had broke so soon.  But, I guess one should have assumed that something like this would have happened given the history of my second pregnancy.  It’s probably safe to say that I was mildly depressed about this event, because I thought I was out of the woods with difficulties, troubles, problems, worries- you get my drift. 
As I attempted to start my daily routine that I had going for myself, I started praying my rosary, ordered my breakfast, countless fetal checks, and eventually a shower, I started to feel optimistic about my situation.  The nurse that day was so friendly, caring and really brightened my day.  As she helped me, along with Steve’s help, get ready to shower, I kept wondering what this next specialist was going to tell us.  The several neonatologists and other fetal specialist shared some pretty scary stuff with us.  We listened intently, asked all the right questions, prayed a lot, and appeared to be the most prepared couple in the hospital for this bundle of joy about to enter our lives, of course believing it’s all going to be completely perfect.  They shared some scary statistics with us for white, male babies.   We had another appointment that morning in the hospital at 9 AM with the fetal specialist from University of Cincinnati, Dr. Evans.  It was protocol, as were the countless other visits from specialists of all sorts for premature babies.  Worried….at this point, not so much.  I was confident that I prayed hard enough, did what the Dr’s told me to do during my pregnancy, I figured they were just following their protocol of keeping parents informed of potential outcomes or possibilities. 

They wheeled me to another room with “important equipment”, and an ultrasound tech along with Dr. Evans met Steve and I in the room.  Our baby looked perfect.  She looked amazing.  Her hair was floating in fluid, she was active, and looked happier than ever.  I was convinced our baby was a girl….and white girl odds are much better than white boys odds.  Our 45 minute appointment with him was enjoyable, especially when they had nothing but great things to say about the development of our baby, and how healthy she looked.  Steve and I enjoyed another look at our baby.  As much as we enjoyed our 45 minute appointment, the final minute of our appointment with him created much anxiety.  Dr. Evans was clear on his medical recommendation.  Our baby had to be delivered today.  We didn’t have a choice.  We weren’t expecting that, but the risks of keeping our baby in the womb were just too detrimental to their health.  Of course, doing what any great parent would do, we followed their directives.  Thankfully, I only ordered breakfast…I never was able to  eat it. 

Suddenly, my mindset changed.  I couldn’t get it out of my head.  This sweet baby girl was going to be born.  Steve and I prayed together, made many phone calls to make sure we had arrangements for our sweet 6 year old to meet her new sibling, and for family to be present for this wonderful event.  We prayed more.  Steve and I discussed our girl name again; we both weren’t agreeing on the same name.  As the day went on, my anxiety rose.  I worried.  I worried a lot.  I worried that my C-Section wouldn’t go as planned.  I worried that I wouldn’t walk again after my surgery.  I worried that Madeline wouldn’t make it in time to be there for Daddy to come tell her about her new sibling as soon as they were born.  I worried that our little baby might experience some of the THOUSANDS of issues they shared with us numerous times on the days leading to today.  The only way I could relieve my worry was to pray and cry.  I cried.  I cried a lot.  I was scared.  Very scared.  As the day went on, the nurse continued to be that foundation that I needed.  As she prepped me for surgery, she promised to be there for me while getting my spinal.  I cried through it.  I hugged her.  She knew I was scared.  She was there for me when my husband couldn’t be.  She reassured me of my amazing Dr., and the amazing team of Dr.’s that were present in the delivery room because our baby was premature.  It was overwhelming to see so many people in there.  Happy to see everyone there just for MY baby, but a very clear reminder that something could go very bad. 

Surgery started, I was still crying, worried out of my mind.  Having Steve by my side was the most comforting thing I could have had.  Seeing him smile at me as I lay helpless reminded me of just how special he is to me, my daughter, and the strength we need right now, literally.  He rubbed my tears, kissed my cheek and gave me the strength I needed to pull myself together.  We couldn’t wait to meet our baby girl.  

At 6:00 P.M sharp, our baby was born.  Dr. Aichholz tugged, pulled, shifted and tugged some more to get our baby out.  She was in no rush to get out.  We heard a nice squeal from our new baby.  And Dr. Aichholz announced , “IT’S A BOY!”  I laid there in SHOCK!  What!  How could this be!?  I wasn’t upset, I was thrilled, but immediately, I had a WHOLE new set of worries. And then, I looked at Steve and knew right away things were not good.  I couldn’t hear our new baby boy screaming anymore.  I could only hear rumbles of medical professionals working behind me, but no one was saying anything.  After what seemed like an eternity, a nurse shared with us that our little guy was having some troubles.  He was doing EXACTLY what those countless Dr’s told us that would happen.  She shared that they were doing respirations for our baby….he quit breathing.  He needed help.  After doing CPR, they knew that he needed to get some help.  They took him quickly to the Special Care Nursery at Christ Hospital.  There, he immediately was put on oxygen.  Dr. Melton, the neonatologist, was in charge of his care.  We were impressed with her during our meetings with her, and we were confident should would take care of our baby to get him healthy as quickly as possible.  Steve followed our baby boy, Jack, to make sure we knew what his medical needs were.  

I laid on the operating table filled with worry, and again was alone.  The nurse was my foundation while my husband was gone.  I needed somebody now, more than ever, but my son needed someone now more than ever, for the sake of his health.   
After several hours of being in the special care nursery, he was stabilized  with the support of a CPAP machine.  I was so sick after my delivery, I wasn’t able to visit him that evening.  It devastated me, even while I was vomiting.  I had to take Steve’s word that he looked ok and was acting ok.  My nurses didn’t even know how he was doing since he was with a whole different crew.  Steve shared pictures of Jack with me from his phone.  When I saw the first picture, I cried.  I kept praying.  The tubes looked scary.  This isn’t what I dreamed would happen.  I found myself in a place of disbelief, a horrible nightmare. But, sadly, this was as easy as life was going to be for Baby Jack for a couple of weeks.  As I was working so hard to pump to try to give Baby Jack “liquid gold”, I was filled with fears.  I didn’t know what to be scared of, but I did know that my little baby wasn’t alright.  I tried to sleep, but the alarm that went off every 3 hours on my phone so I could pump was really hindering my attempts at a good night’s rest.  We didn’t hear anything through the night from the special care nursery and we thought and hoped that this meant Jack started to show improvements.  

As we started the day on the Tuesday morning, Steve went right to see Jack.  He came in and nothing had changed, with the exception that Baby Jack was struggling more than he had the night before.  Steve’s eyes showed his fears, but his shoulders showed me that he was confident he was in good hands.  We decided that even though I was feeling lousy, extremely nauseated, it would be best for me to get in a wheelchair and see my bundle of joy.  It was a terribly painful ride after my C-Section and my nausea was pretty intense.  My pale skin was evident of that and the nurses in the special care nursery took notice right away.  They let me see Jack.  I cried.  I cried a lot.  My mind started wandering in all directions because I was so worried.  I could see his poor little lungs just laboring to work for him.  I took a picture because I was so happy to see him, but seconds after I had to leave.  The nausea overcame my body and I vomited several times.  I was so upset because I just wanted to sit next to my baby, but they wouldn’t let me.  They knew my body needed some time to recover and I needed to rest.  It ripped me apart inside to have to leave my baby.  Being wheeled back to my room, my emotions took over and I couldn’t control my worries.  I was overcome with tears.  Loud crying, bawling might be an appropriate term. 
After getting settled back in my room, 30 minutes later Dr. Melton came to talk to me.  She had a confident composure about herself.  But, she had glossy eyes.  I could almost see what was coming.  At 11 AM, I didn’t want to hear this.  I didn’t EVER want to hear this.  EVER, NEVER! Jack had something terribly wrong.  They had to perform a procedure that they were hoping was going to work.  We didn’t have a choice, it HAD to be done to keep him safe from more damage.  She was going to perform the procedure and report back to us after they could tell if there was a change.  Jack had developed a pneumothorax.  He now had air escaping his lungs and into his chest cavity because of holes in his lungs.  No one told us this could happen.   Shortly after she performed this procedure and having x-rays done every 5 minutes, it seemed, Jack was showing no signs of improvement.  We now had much more to worry about.  After performing a procedure 3 times, he needed some intensive support.  This came several hours later, and Dr. Melton told us we had 30 minutes to get him to Children’s Hospital before something life altering could happen.  The clock started.  She made phone calls as we panicked and made frantic, desperate calls for help from our family.  We needed support because we were crumbling.  The thought of our baby not making it wasn’t a possibility EVER, but now we were told that they are going to make every effort to keep him alive.   Our fears turned into nightmares.  The clock was still ticking.  10 minutes after Dr. Melton told us to get prepared to tell our Baby Jack good bye, she said that the Cincinnati Children’s Hospital Medical Center Neonatal Intensive Care Mobile Transport team was on its way.  She told us what to expect and told us we would be overwhelmed because of the amount of members that would be traveling with Jack just a few short miles up the road.   She also shared that they would be bringing Jack to my room in his isolette once the team had him stabilized so we could say our goodbyes.  There aren’t any words to describe this moment.  The intensity of this moment was clear with the raw emotions that Steve, Madeline and myself were experiencing, along with my mother.  No longer in shock because we couldn’t be, we continued to cry and prayed together for a good amount of time.  

Steve wasn’t allowed to arrive on the NICU floor at Children’s for about 2 hours after Jack left us because they needed to make sure that Jack was stable before anyone was with him.  Those 2 hours were terribly painful because we didn’t know anything.  Scared doesn’t describe our emotions, nor does panicked, worried, frustrated, angry, sad, or mad.  It’s a moment I NEVER want to live again.  We didn’t know if we did the right thing by having our 6 year old daughter there for that moment, but we knew that we couldn’t live with ourselves if she weren’t there if something terrible were to happen and she didn’t get to say good bye to her brother.  Hindsight, I wouldn’t change our decision.  It’s not what our 6 year old at the time needed to see, but our life had changed so drastically in 24 hours that we needed to do what was best for our family.  And, in reality, what she saw was nothing compared to what she was about to experience in the coming weeks with her little baby brother.  

Steve left us to be with Jack.  His mother came to be with me at the hospital while Madeline went back to sleep at home with my mother.  I again was alone.  I said goodbye to my newborn baby boy and just sent my daughter home with my mother.  I wanted nothing more than for her to sleep next to me in my uncomfortable, padless bed in the hospital room, but I knew that she couldn’t function the next day if I did that.  So, I cried all night long.  Steve finally called around 11 PM.  He had a shaky, shaky voice as he were choked up about something.  I knew then it wasn’t good.  Jack quit breathing.  He coded.  And Steve had to watch it.  After holding back his tears over the phone to communicate with me, he was able to tell me that Jack was finally resting peacefully and they had finally had success intubating him, and his chest tube was in place.  The machines were keeping him alive at this point, but Steve said he couldn’t believe how much better he looked already because his body could finally relax.  I wanted Steve to send a picture but he told me he couldn’t.  He didn’t want me to see a picture of Jack like this without standing by me.  

I went to bed that night praying.  I don’t think I slept that night at all.  I couldn’t believe Jack was having such difficulties and wanted to take ALL of his pain away.  The next day Jack struggled with his chest tube and there weren’t any signs of improvement.  They were now talking about permanent damage to his lungs and the possibility of damaging all of his organs, including his heart, in his chest cavity because of the pressure.  I didn’t think things could get worse.  Another reminder from God that we’re not in charge.  Over the course of the next 3 days I was at Christ Hospital while  my baby was in Children’s Hospital.  These days required God to give me strength to get through each day because it was obvious I had no control over this situation.  It was all in God’s hands.  I prayed HOURS each day in hopes of just receiving 1 phone call from Children’s with good news.  It didn’t happen.  Finally, on the 4th day I was going to be discharged.  Two hours before I was discharged we received yet another phone call from the Dr. that Jack had developed another pneumothorax in his chest cavity, this time from his right lung and they had to perform another procedure.  I cried, screamed, hugged my husband in hopes of burying my worries in his chest, but nothing relieved my fears.  I begged the nurses to make my discharge quick.  I couldn’t take another minute of being away from my very sick baby.  I was convinced that if I arrived soon, Jack would show signs of improvement.  By 12 p.m., I was discharged and Steve drove me straight to Children’s.

Beyond the fear of the triple door entrance to getting to my son, I had to put my “STRONG MOM” cap on.  I needed it to be on for my newborn baby.  Steve steered me in the wheelchair to his pod- D, space 2.  And there he lay, sleeping.  I couldn’t keep my eyes off of him.  He was beautiful.  More than I even remembered from the 3 minutes that I had with him up to this point.  But the constant beeping, wires coming from every direction of his body and machines that decorated his bedside were overwhelming.  My "STRONG MOM" cap must have fell off somewhere.  They scared me.  He looked like a baby, but a really sick, sick baby.  I leaned over his bed, held his hand until I couldn’t stand anymore, and cried.  This isn’t what I was expecting at all.  I didn’t think he was this sick.  Clearly, the monitors all over his area said otherwise.  

1 month later our baby Jack was finally discharged from Cincinnati Children’s Hospital Medical Center.  He has taught us so much in his 2 years and we can’t wait to learn from him in the many years to come. The countless lessons that can be taken away from this are big and small, but if there’s one thing that I know for certain, God is in control.  We have been blessed with Jack and his very mild health concerns now, but if there’s something we remember each day, it’s that every single being on Earth is important and that each person is so special.    

Jack- Happy 2nd Birthday!  You’re a special little boy.  Your smile makes us giggle, your words make us chuckle, and your rising chest while sleeping reminds us just how fragile life is.  We love you!

Monday, May 21, 2012

Prayers for Jack, please

Well, tomorrow is the big day!  Jack is going to have tubes placed tomorrow afternoon at 1:30 p.m. at Children's Hospital Liberty Campus.  Dr. Charles Myer, III will be doing it, and we've heard nothing but great things about him.  Of course, anytime you place a child under anesthesia, you worry.  We are confident that everything will go wonderfully, just as planned, and the fluid that has been in his ear FOREVER will be removed, and hopefully Jack will be able to experience life without the discomfort of ear infections and fluid.  I do believe that the hardest part of the day, other than the worry of surgery and not being able to be with him, will be trying to keep him calm when we will no longer be able to feed him.  It's hard for parents to deny their children of food, and it's even more difficult with a baby because they don't have any ability to understand why we can't feed them.  But, I must remind myself, it's only for a short time, and the end result will help Jack's ears, his hearing and hopefully his sleep patterns. 

These past couple of months have been tough at times, but still very enjoyable.  If you haven't seen Jack in a while, he's quite the baby with a colorful personality!  His smiles, laughter and babbling makes the frequent trips to his bedroom in the middle of the night a little less difficult.  Steve and I are very sleep deprived and we hope to have Jack sleeping through the night sooner than later, but we remind ourselves how far we've come from the time he was born to now.  It's been a roller coaster, but each day gets a bit easier. 

Jack is now a sitting man!  We are super excited that he is making progress on his gross motor skills.  He still hasn't rolled from his belly to his back, but has rolled from his back to his belly.  We keep praying that he will meet the milestones.  He continues to work on his fine motor skills as well, as just as recent as these past several days, he's trying to use his pointer finger and thumb to grab tags!  These little things just thrill us!

We have also seen an opthalmologist for Jack's left eye.  Indeed, there is something going on with his left eye, but we can't rule enough out to say exactly what it is.  Right now, they believe he either has an eye muscle problem or Duane's Syndrome.  We'll continue to see the opthalmologist on a bimonthly basis as she monitors his vision and movement with his eyes and follow with her recommendations to ensure Jack has the best vision possible. 

Sorry for the short update, it's been a while, but I gotta run!  We continue to pray, thank God for his blessings, and go to bed when Jack goes to bed!!!

Love and blessings to each of you and yours!

Monday, April 16, 2012

Some photos...some outdated! Enjoy !

Jack and his SMILE !
Jack adores Madeline

Jack after his 6 month shots.

Yup, he's a cutie!

Our 2 lovies!  We are so blessed.

Friday, March 30, 2012

Jack is making great strides!

This past week we had the opportunity to meet with Help Me Grow, a program through the state of Ohio for children showing delays in any or all areas of development.  They met at our home on Monday morning to do their assessment.  After the assessment they shared their results.  Steve and I were not surprised by them at all.  Jack is showing signs of progress in MANY areas, but there is a delay in his fine motor skills.  He qualifies for Occupational Therapy services.  We have been working diligently with Jack at home doing what we can, so this will only be an additional support for us and another person to add to Jack's team of people who want to see him do great things!  Right now the focus is on his grip, lifting his arms above his head and working on tummy time for many reasons.  We are working with him and seeing results, so it's been great to see his development! 

The biggest news of all right now for Jack is that he ROLLED OVER last night for the first time.  We are SO EXCITED about this!  He doesn't have it mastered and we are still working on his arms after he rolls over, but he has the strength to do it, which makes us very excited. 

I'll post pictures soon.....I promise! 

Thanks for your continued prayers, support and encouragement.  We appreciate it all!

Thursday, March 22, 2012

It's been a crazy month!

Whew.....I think it's safe to say that Steve and I are tired!  Jack has been making incredible strides, but it's been exhausting.  Shortly after Jack turned 4 months old Jack was back at the Dr. for a high fever, along with a cold.  Unfortunately, he had a double ear infection.  After 1 round of antibiotics his infection was cleared, but fluid still remained, and still does to this day, in both of his ears.  :(  We have been warned that since he has had an ear infection at such a young age, his chances of getting tubes are pretty high, given the fact that structurally his ear canals are very small, according to the dr.  But, bummer for Jack that we can't get tubes quite yet.  The protocol for getting tubes is 4 ear infections in 6 months time or fluid in the ears for 3 consecutive months.  So, we are in month 2 of fluid in the ears.  WE ARE PRAYING THAT THEY DO NOT BECOME INFECTED, and quite honestly drain on their own. 

Then, two weeks later, Jack started to show signs of being sick, AGAIN!  So, after 3 Dr. appointments in 1 week, it was determined that Jack most likely had RSV.  They didn't test for it, but he showed all signs of it.  So, 1 week ago we found ourselves in the Dr. getting a breathing treatment for Jack since he was wheezing.  It seemed to help, so they sent a Nebulizer home with us for daily breathing treatments.  He was NOT fond of those at all, but fortunately, we did see improvement.  We go back to the Dr. tomorrow to see if they hear the wheezing.  I think it's fair to say that we are ready for summer! 

For several months now, Jack has had difficulties in the evenings.  I wish I could say that it's gotten easier, but when having to listen to a screaming baby for hours each night, it's tiring, makes you want to cry and we feel so terribly that we can't make things better for Jack.  Fortunately, Steve and I make a great team and we are managing each night with support of each other, and we remind ourselves that it will get better, it just has to.  (Please....don't tell us it won't be for a while....not what we want to hear! :) ) When Jack screams, it's not a little cry for 10 minutes, it really does last for hours.  It's so hard on our entire family, especially Madeline because she just feels so badly for Jack and just wants him to stop crying; it makes her cry sometimes.  It's just hard when you don't know why they are crying and you can't find ANYTHING to get them to stop crying.  As soon as we think we find the secret, Jack finds a way to prove us wrong!  So, we continue to pray that those long evenings of many tears and screaming fits are going to end........SOON!

Several months ago, Steve and I both started to worry that Jack was not developing properly.  He wasn't showing interest in really much of anything.  As our concerns increased, we decided to call upon Help Me Grow of Warren County.  Jack qualifies for such services due to his prematurity, as well as his medical diagnosis of Respiratory Distress Syndrome and Pulmonary Interstitial Emphysemia.  We've been searching high and low for support, from Dr. Google to family and friends that have experienced similar situations or who work in fields to help little kids and children like Jack.  We've received some great information, and daily Steve and I work with Jack, along with Madeline.  By the way....she continues to be the MOST AMAZING big sister to Jack.  With the "therapy" that Steve and I are doing with Jack, we are seeing great results that are promising for Jack's development.  One month ago he would scream seconds after we laid him on his belly for tummy time.  Now, we can keep him on his tummy for several minutes at a time!  And, while on his tummy, he can lift his head with the support of us "locking" his arms under his chest.  We've been working on his grip, and he is now picking up objects that are in his lap and bring them to his mouth!  It really is the little things that mean so much to us, and anyone that has experienced anything like this would probably agree with me.  Jack also is extremely social, loves to giggle, and seems to be very interested in the environment around him.  He is now looking to the left and right, which was something he wasn't doing 1 month ago.  With his strides and gains in the past month, it has shown us the importance of being diligent with his "therapy" at home and really makes us want to continue to help Jack.  It is all reassuring.   He's not rolling over, or even close to that, but we'll get there.  We are confident in that.  With the support of Help Me Grow, we're going to get Jack right where he needs to be!

And something so special to Steve and I is the relationship between Madeline and Jack.  It seems as though the two of them have an incredible bond. I believe it to be for many reasons.  I believe God has made Madeline one super, empathetic, caring, loving little girl who appreciates the gift of her brother, and Jack can see how much love is in Madeline's heart for him.  There are no words to describe how the two of them interact.  I can tell you though, when she is around, Jack responds so well to Madeline.  She is so calm with him, gentle and loving, and the nice thing about Madeline, she doesn't judge Jack, she doesn't resent the fact that he screams ALL of the time (it seems!), and she never questions why we do what we do, she just helps.  She is truly a gift from God to us.  This past year for her has been traumatic, with my pregnancy being so terrible to having a brother born with complications (which were SCARY for ALL of us), and yet she seems so happy to be where we are today.  She appreciates the family unit.  She appreciates Jack's smiles.  She appreciates the idea of being a big sister.  She is really very special to Jack.  Steve and I both adore their relationship and we know that the 2 of them connect in a way that we'll never understand, but we appreciate that!  It sure is amazing how insightful a 6 year old can be, and how much she can help our little guy develop. 

Big news for Madeline......she lost her 6th TOOTH on Tuesday evening!  She sure is a cute little girl without teeth!

We continue to pray for Jack and his development.  We also remind ourselves that Jack's issues could be much worse.  We pray for all the babies in this world, and we're thankful for the one we call our son.  We truly are blessed.
Thanks for all of your continued support, thoughts and prayers. 

Saturday, February 11, 2012

4 MONTHS OLD!

Well, today Jack is officially 4 months old.  It's hard to believe that he is 4 months already, but I must admit at the same time I feel like it's taken forever to get him to this age.  It really just depends on his day and how he feels.  At this point, I think it's fair and "safe" to say that he is having more good days than bad days.  We still find him struggling at times to catch his breath because of that STUPID reflux!  (If Madeline knew how often I used this bad word, I'm pretty sure she would have lots to say to me.)  He remains on 2 doses per day of Prevacid.  We are not really sure why some days he is better than others, but that seems to be a common problem for babies with reflux.  We have his 4 month check up today, so we will learn more and ask our million questions, like we always do. 

We have officially transitioned him to 3-6 month clothing, so he is only 1 month behind in clothing, which really doesn't matter.  As for his adjusted age, Steve and I are still seeing him progress as if he were 11 weeks, not his actual age of 17 weeks.  That is definitely the hardest part to deal with, not because we are worried that he is behind, but we felt like he was so "stagnant" with what he was doing for such a long period of time, it seemed as though time never moved.  But, we can certainly see changes now.  Jack, when he is feeling well, is a very happy, delightful baby to be around.  He has a very low key personality and LOVES, LOVES, LOVES to be around people.  He enjoys being talked to and the attention, so his time at the babysitter's house is enjoyable for him.  He flashes beautiful, charming smiles at us, even at 3 or 4 A.M. when we have to feed him.  We are certainly blessed.  Hopefully, this will continue as he gets older and feels better.... :)

Last weekend we finally had Jack baptized in our church, St. Margaret of York.  It was beautiful.  Jack let out a nice little prayer of his own when he was baptized.  He was baptized in the hospital when he was born because at that time we were told that he was struggling.  We wanted to make sure that God was there with him at all times, and he certainly has been!  We were blessed to have all of our family here for the baptism, which made it even more special.

We had his 4 month check up yesterday afternoon.  It went well, as we expected.  We asked many, many questions, as our Dr. always expects from us, and we continue to move forward.  Typically, at this age babies are able to eat rice cereal or start thinking about introducing solid foods.  Since Jack isn't "acting" like a typical 4 month old, we are postponing this for a couple of months.  She expects that we will be able to determine if he is ready for solid foods at his 6 month check up.  However, we are going to begin to put a very small amount of rice cereal in his evening bottle, to start.  The hope is that this will help his reflux.  Unfortunately our little guy is still greatly affected by his acid reflux.  Yesterday she did tell us that since his reflux is so severe, we probably won't see much of an improvement, if any until after his 6 month mark.  We just feel terrible for Jack, because when he is having issues,  you can tell how uncomfortable and painful it is for him.  If only we could take the pain away from him.  We discussed everything.....from his diapers to his bottles to his smiles and head control.  Since he doesn't have complete head control, we have to continue to work on that.  The horrible part of this is that we cannot put Jack on his tummy very often because it causes him to spit up ALL of what is in his belly and it's uncomfortable for him, so we do lots of standing with him, along with him laying on our chest to help him lift his head.  I can honestly say that this is something that I have stressed myself out about, but with practice and time, he will get it.  STUPID REFLUX!  We discussed increasing his meds, but the Dr. doesn't want to increase it because of the age that he is and he is already taking the equivalent of 1 adult tablet each day.  We continue to pray each day that it gets easier for him. 

As for his weight, he weighed in at 12 pounds, 11.5 ounces.  He was 24.75 inches long.  His weight puts him in the 11th percentile, his height a whopping 44th percentile and his head circumference is 27th percentile.  She seemed very satisfied with his growth, especially with how bad his reflux is.  We continue to feed him Nutramigen....yes, a formula that NEVER has coupons, never goes on sale, and is so costly that we spend more money to feed him than we do ourselves.  But.....we can say that it makes him happier....and IT IS ALL WORTH IT!  Unfortunately, that is all we knew with Madeline, so at least our kids are consistent and require the same food... ;) !!

Madeline continues to be the BEST big sister one could ever ask for.  Not a day goes by that she doesn't comment on her little brother, how much she loves him and how cute he is.  Steve and I are so thankful that she is open to him, loves him and has yet to show us any signs of jealousy.  He certainly requires alot of attention, but she always finds a way to make it work for all of us.  She sure is a special little girl!  As for being little, she is still pretty tiny, weighs close to 37 pounds (on a good day), and lost her front tooth!!!!

Until next time, we'll keep praying for Jack, his friends at Children's Hospital and all the kids in this world.







May God Bless each of you.