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11/08/2009
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Week 6 (end): Good News after a rough week!
posted on 04/20/2008

Smile We wanted to share some good news!  The boys still have a long road ahead and we pray we get no more infections (which we are at 7 now which is horrible since they are hospital related infections). 

Our Fantastic news:

Hunter:  Hunter has shocked everyone - he has responded so well this weekend and today his oxygen is now 30% (he was at 100% on Thursday and the doctors were not sure if he would make it through the night).  They also are taking him off the drugs that keep him paralyzed.  The paralyzing drugs were needed so he would not fight against the breathing machine (ossilator).  I gently put my finger in his palm today and he squeezed it three times showing that he was waking up from the drugs. It brought happy tears to my eyes as I filled with a feeling of relief.  He's still on the ossilator (we call it the jackhammer because it shakes his body) and his lungs are still severly damaged but he's showing amazing recovery.

Dylan:  We arrive at the hospital and the nurse says, go take a look at Dylan....  We peak in at him and we see he's now off his CPAP oxygen!  He still has a nasal canula just to give a tiny bit of oxygen in case he needs a boost but he's breathing room air essentially!  It's amazing to see how well he is doing.  He looks so happy!  Dylan also got a bath last night and the nurse left me a picture. I was my first time to see him without wires and the breathing CPAP.  I have to warn you - that that preemies on oxygen have two characteristics: 1. Oxygen cheeks: for some reason being on oxygen makes babies cheeks big 2. Pug nose:  Having the oxygen CPAP prongs taped to his face squishes his nose and makes it turn up like a pug nose... it will go back down in a few weeks they say.

Matthew:  He is doing well. He's not out of the woods because he has chronic lung disease too and still has the holes in his heart but he's been very stable.  He keeps his oxygen between 30-50%.  He got another infection  - our biggest complaint about the hospital is they have a higher infection rate that we would prefer, especially since infections are deadly to preemies...   It doesn't help that these guys are preemies and have very weak immune systems but we wish they would do more to prevent infection. 



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Week 6: Challenges to Overcome
posted on 04/17/2008

 
6 week Birthday: April 17, 2008

I wish I could say the past week had been smooth sailing. There are many things to be thankful for but Hunter’s condition has been on our mind 24/7.

Hunter: Hunter had a PDA ligation on last Friday 4/11/08. The surgery was successful at closing the hole but he has had a horrible recovery. His lungs have been damaged from weeks on the ventilator that has been helping him breath. He started out in this world so strong and not even needing help breathing. He unfortunately got an infection from his PIC line and that has made a huge ripple effect over the last weeks. The infection caused the PDA to open and it caused him to need extra help breathing because he was weakened by the sickness. The PDA did not close on his own so we had to do surgery because his oxygen requirements were so inconsistent. Prior to surgery he had already had chronic lung disease (basically his lungs are just damaged from the vent). So, after having surgery his lungs are just struggling even more. He’s been in a life/death situation this past week. Lungs do heal and grow so it is something that he can overcome but he is really really sick right now. I think this is the hardest thing in our lives to watch. To see your baby going from kicking and opening his eyes to now being under drugs to keep him paralyzed and just hope his little body can recover. There is still a lot of hope but we have a very long road ahead. So far so good, it has been one week since the surgery and today was a good day for him. His oxygen is down from 100% to 68%.

Weight: almost 3 lbs! (1345 grams) *note he is has not been weighted since his surgery
Length: 36cm ( 14.17 inches
)

Matthew: Matthew has been pretty steady which is surprising because he has more complex heart issues than Hunter. He has a PDA and a VSD, so, two holes in his hearts and a possible narrow aorta. I must add that these holes are completely normal in unborn children. These two holes are how the baby breaths when in the uterus. They are supposed to close at birth but with preemies they very often stay open. Matthew is still on the ventilator but he’s pretty consistent with his oxygen so there is no rush to do surgery. It would be nice if he could wait and do any surgery later when he is maybe 4 years old. Matthew is active and opens his eyes and looks your direction when you talk to him. He’s still the smallest but he’s not far behind his brothers. Matthew is just adorable and has a quiet strength about him. He seems a little more laid back than his brothers. He likes to hold your finger.

Weight: 2 lb 6 oz. (1210 grams)
Length: 37cm (14.57 inches)


Dylan: Dylan was the one that they didn’t know if he would make it on Day 1 because he was not able to breath on his own consistently. So, he had a rough start but he came from behind and passed everyone. He is not on the ventilator. He has a CPAP which is a little nose prong that shoots a little extra oxygen to him. H hates the blowing air in his nose so he constantly is fighting to take the CPAP off as you will see in the attached picture. It is so much fun to watch how he has these little tricks he has learned to push the device, kick it, or turn his head side to side and then surprise the nose prongs are out. Haha. Yesterday I watched him and he had them out completely for 30 minutes and his breathing was just a good as when he had them in. This is a great sign! Soon he will not even need his CPAP. He’s also infection free and has no IVs! Yeah! He is still eating through a tub in his mouth like his brothers but in the next two weeks he may get to start learning to take a preemie bottle. Dylan is feisty but has an angelic look about him. He looks just so sweet.

Weight:  3 lb 6 oz.   (1530.87 grams)

Length:  41 cm (16.14 inches)



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Week 4: The Boys are one month old!
posted on 04/03/2008

 
The boys are now 1 month old!
 
The overall big picture is going well for the boys.  They are all eating and growing.  They look just beautiful and you can tell they are recognizing mom and dads voices. They all have their eyes open and look around occassionally during the day especially when you talk to them.  That is one of my favorite times to just watch their eyes and think ahead to when they are 3 and running around the farm playing.  Also, you will see from the pictures that the boys are now getting some fat on them!  
 
Dylan:
 
weight: 1310 grams  (2.88 pounds)
length: 38 cm  (14.96 inches)
 
The one that started out strugglings so hard to breath is now doing the best of the three.  He's off the ventilator and nearly breathing room air (which is 21% oxygen).  He's getting full feeds and weighs almost three pounds!  He's very active and loves to try to kick the tubes and and pull his nose tube out.  He even squirms out of his bed.  They put them in a little cushion and then wrap them in to make them feel more secure, as they were in the womb.  He eventually wiggles his way out of it. You can see him put his hands at his chest (when he's on his tummy) and he's already getting some 'crawling' motions going. 
 
Hunter:
 
weight: 1310 grams (2.88 pounds)
length:  37.5 gram (14.37 inches)
He's also eating and growing. He and Dylan weigh the same and are both nearly 3 pounds.  The infection from two weeks ago really was a step back for him but he's overall doing well. We got good news that his PDA (hole in the top of the heart) has gone from very large to moderate so surgery is not urgent.  Still might be an option but it's a good sign to see the PDA closing.  Since the infection he's been on the ventilator to breath - we've been trying to wean him down to lower and lower settings but after weeks on the ventilator he has shown development of Chronic Lung Disease.  Sounds terrible but it's very common for preemies. The ventilator keeps them breathing and alive but .... it also damages the lungs.  It just wears and stretches out the lungs.  We hope that the lung damage doesn't get worse.  This is a condition that requires patience because it makes it harder for the baby to breath and makes them more dependent on the ventilator.  So, it's a slow weaning process.  The damage will heal over time.   Hunter looks good and seems to reall like having his dad hold his hand and his mom to hold his feet. 
 
Matthew:
weight: 1090 grams (2.4 pounds)
length: 35 cm (13.78 inches)
 
Also eating and growing well. Looking at the overall growth trends - he's done the remarkable.  He started at 1 3/4 pounds and he's nearly 2 1/3 pounds.  This is remarkable because his food increase was so much smaller than the other two boys because the doctors wanted to be cautious due to his heart.  he's now getting full feeds (which means that he's getting the full amount estimated for his weight).  This weekend he was doing very very well and then Monday morning he hit a road bump.  He may have gotten another infection (still waiting on test results)  but he's got alot of secretions (mucus) in his throat and lungs.  This makes it very very hard to breath and he has to be suctioned alot.  He (like Hunter) is still on the ventilator  and he also has shown development of chronic lung disease.  So, this latest development of having so much secretion and a possible infection doesn't help him.  It is still something that can be overcome.  The good news is that his heart is very strong and while he has the two holes in his heart (PDA and VSD) - he's been doing so well the doctors do not see it urgent to do any surgery.  We are meeting with the top heart surgeon today on Hunter and Matthew and hopefully determine our game plan.  They say PDA surgery is very common and not as scary as it sounds.... (but as a mom anytime you are told they are going to make an incision in your baby it is obviously stressfull...haha)
 
---
So, overall the fact that they have all grown so much in their first month is fantastic.  The Preemie roller coaster ride will not be perfect so you have to focus on the big picture that they are growing and eating and there will be roadbumps that the boys will overcome. 
 
I wanted to just share and set expectations for everyone. Preemies have very weak immune systems and they often take 1-2 years to develop strong immune systems.  Due to this, it is so critical to keep illness away from them.  We want to show them off more than anything and have visitors but it is not a good idea because more people means more opportunity for exposure (now and even later when they are home).  Just be sure and let us know if you are sick or if you have been around someone sick to try not to expose us or the three boys so none of us get sick.  Infection and illness are very very serious and can be deadly to preemies born before 30 weeks.
 
Thank you for your love and support and all the prayers and well wishes.  It means the world to us and the boys. 
 
love,
Kim
 
PS.  More good news.... we had two healthy foals born this weekend.  Two colts by King Arthur out of our Contender mare.  One more foal on the way, which I think is due in May.


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Week One: First week!
posted on 03/14/2008

Week One: end of week
1 week old
 
The boys are doing very well but just have little things they have 'grow through' since they were born so premature.  They are all breathing on their own.  Dylan was not but in the last two days he's catching up and now trying to pass his brothers. haha. Matthew is struggling a little with his breathing/heart but is doing just fine.  He just needs a little time for all his body parts to grow.  Hunter is the little champ, he's smallest and the fiesty one.
 
We got to hold Dylan for the first time yesterday.  He's the biggest boy of the 3.  We are just so proud at how well  he's doing considering he was in pretty critical condition on day one with his breathing. 
 
Drum roll..... Their full names are:
 
  • Hunter Keith Hodgson
  • Matthew William Hodgson
  • Dylan James Hodgson
 
You will notice that the middle names are after the following people
  • Keith - Keith,  (Guy's Dad)
  • William - Guy's middle name
  • James - Larry's middle name (Kim's Dad)
 
I'm turning in all the official paperwork this morning! 
 
Keep the boys in their prayers - we feel very confident that they will sail through this Neo Natal Intensive Care with flying colors over the next two months but they are premature and still have to grow and their organs have to adjust to being 'in the real world'  In can be a bit of an emotional rollercoaster watching and wishing you could do more to help them but they are in the best possible hands at Texas Childrens.  Guy's medical background comes in very handy as he asks many questions to understand all aspects of test, procedures, etc.  We are getting good at changing preemie diapers and checking that their little nose prongs that give them a little extra oxygen are well positioned. 

March 10, 2008

I know everyone is curious about the triplets.  So far so good!  They will be in the NICU for probably 2 - 3 months but they are in the best possible hands to get them to grow.  Premature babies usually finish out the pregnancy term (40 weeks) in the NICU. 
 
Today was one of the best days of my life.  Today was the first day for me to hold two of the boys.  Hunter and Matthew are doing very, very well (above average) and I got to do what they call Kangaroo care.  Basically let them sleep on the bare skin of your chest. Both Guy and I got to do this and it is such an amazing experience.  They are just so tiny it’s a little scary at first because you don’t want to hurt them …but you quickly realize they are not as fragile as you would think.  You immediately see their heart rates slow into a relaxed state.  I can’t describe the feeling but it is amazing.

Dylan continues to improve.  He’s doing well but still not breathing on his own yet.  He is going to just need more time to catch up to his brothers.  Each day we are seeing more improvement.  He’s not at the point where I can hold him yet but I am able to let him hold my finger and he seems to love that.  He’s a fighter and seems determined to catch up.
 
I want to thank everyone for their friendship, support and prayers.  The boys are doing very well and just need more time to grow.  The Texas Children’s NICU is an amazing place.  Obviously every parent would rather their newborn be going home but it is truly an world renowned facility.  The doctors and nurses are so caring and have so much experience with premature babies - it definitely is a comfort knowing that each of the Hodgson triplets has a whole team that is nurturing them and helping them grow! 


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