Oct
04
    
Posted (The West's) in All Posts on October-4-2009

Ella has been doing much better since her return from the hospital. Overall, she is less fussy and irritable.  This just means that the pressure from her occluded SVC must have been causing some discomfort.

Every morning, we’ve had bloody noses since her procedure.  This is a side effect of her new medicine, Plavix.  It was so bad this morning that we finally called the cardiology department at the Children’s Hospital to ask for some direction.  The on-call doctor advised to skip her afternoon dosage today.  If we do not hear from a doctor by tomorrow at 2pm, we were instructed to call back for further direction.  We know that Plavix, along with her daily dose of Aspirin, is intended to help Ella from tissue re-growing into her SVC stints.  However, really bad bloody noses are not a great side effect.  We’re hoping to hear back tomorrow to see what we can work out.

Ella visited the pediatrician this past week.  We discussed her weight gain.  She went from 25.5 pounds in late July to 28 pounds at the hospital.  However, we weighed her again this past Thursday and she was 27.5 pounds.  This means that she likely had a bit of fluid on board prior to her SVC procedure.  In any case, Dr. Perry was happy with her weight gain.  At her 2 year check up, he stated that if she gained 4 pounds over the next year, that would be good.  However,  he tracked her weight on the growth curve and stated that for Ella, this increased weight gain is good.  So, he wants to keep her calories each day the same.

From there, we discussed changes to her food plan.  Dr. Perry would like to see her switch from an infant formula to a toddler formula, which has more of the minerals and vitamins that are age appropriate.  However, most of the toddler formulas are 30 k/cal per ounce.  Right now, Ella is on 26 k/cal.  When we’ve tried increasing the density of her food before, her tummy has given her grief. But it has been a year since we have tried and a year since her nissen surgery, so we think the time is right to try again.  We wanted to wait until her SVC was re-opened, but otherwise think that this is a good time to work towards this transition.

I suggested that we keep her on the same food and slowly increasing the calories, to see if she can tolerate the increased density.  This way, we know it is the density and not the food itself. One good part: since her caloric needs are sufficient, this means that her fluid volume will decrease if we can make it to 30 k/cal formula.  Just yesterday, we tried increasing the Ele-Care to 28 k/cal (1250 ccs).  So far, so good.  This is the first time that she has remotely tolerated a higher calorie food.  It is 100 ccs less than her 26 k/cal formula.  We’ve continued with 6 g-tube feedings per day.  Her body seems to like the smaller amounts, spread apart during the day.  With reduced volume, we can likely try 5 feedings per day when we’re ready to try 30 k/cal formula (1170 ccs).

We’ve still battled granulation tissue around Ella’s g-tube, so Dr. Perry took care of that for us.  Ella also received her flu shot.

We have an appointment later in the month for another follow-up echocardiogram, to check the flow of the SVC and make sure things look good.  Also, we have an appointment with an Ear, Nose, Throat specialist to check the fluid in Ella’s ears on Nov 6th.  We have a feeling this appointment might lead to another procedure, placing tubes in her ears.  But we also don’t know if the fluid in her ears might be causing discomfort along with less-than-perfect hearing.  So we’re hoping that this might be a way to eliminate this problem, especially as it relates to her hearing.


One time of day that Ella is still incredibly fussy is the morning. When she was younger, even 4 months ago, she would wake up happy and kicking in her crib.  She would smile at you.  Not any more!  Each morning now, she wakes up screaming and will not tolerate anything.  Not even a diaper change.  Once you pick her up or give her something she wants, she stops.  Wow, I know that these are terrible twos.  But I’ve also heard that age three can be even more challenging.  Yikes.

The last week, Josh was kept busy with contract work.  We’re thankful for the income and pray for continued guidance on His plan and will for our lives.

An excerpt from my devotional the other day that resonated with me:

Psalm 119:71 – It was good for me to be afflicted

It is a remarkable occurrence of nature that the most brilliant colors of plants are found on the highest mountains, in places that are the most exposed to the fiercest weather.  The brightest lichens and mosses, as well as the most beautiful wildflowers, abound high upon the windswept, storm-ravaged peaks.

One of the finest arrays of living color I have ever seen was just above Saint Bernard Hospice near the ten-thousand-foot summit of Mount Cenis in the French Alps.  The entire face of one expansive rock was strikingly vivd yellow lichen, which shone in the sunshine like a golden wall protecting an enchanted castle.  Amid the loneliness and barrenness of that high altitude and exposed to the fiercest winds of the sky, this lichen exhibited glorious color it has never displayed in the shelter of the valley.

As I write these words, I have two specimens of the same type of lichen before me.  One is from the Saint Bernard area and the other is from the wall of a Scottish castle, which is surrounded by sycamore trees.  The difference in their form and coloring is quite striking.  The one grown amid the fierce storms of the mountain peak has a lovely yellow color of primrose, a smooth texture and a definite form and shape.  But the one cultivated amid the warm air and the soft showers of the lowland has a dull, rusty color, a rough texture, and an indistinct and broken shape.

Isn’t it the same with a Christian who is afflicted, storm-tossed, and without comfort?  Until the storms and difficulties allowed by God’s providence beat upon a believer again and again, his character appears flawed and blurred.  Yet the trials actually clear away the clouds and the shadows, perfect the form of his character, and bestow brightness and blessing to his life.



 
Apr
04
    
Posted (The West's) in All Posts on April-4-2009

Well, it has been a relaxing day hanging inside the house while the snow and wind was outside. It started last night with freezing rain which had a cool effect on the windows throughout today!

Grandma Eusey did some sewing mends for Ella, Josh & I played cards, Ella tried eating some pears, we had a blowout diaper…all a part of the fun of a snowy Saturday.

We’re hoping the weather improves tomorrow for our last day with Grandma Eusey.

P.S. We went to church tonight and reflected on the hindsight we now have. Two years ago today we found out about Ella’s condition. We always knew the Lord had a plan, but couldn’t imagine how much He would use this precious girl to further His Kingdom. Praise God for our miracle girl.



 
Sep
03
    
Posted (The West's) in All Posts on September-3-2008

UPDATE 12:30pm MST (by Josh)
Who would have thought 18 years ago, when I was sitting in my red 1967 VW Bug asking Tina to be my girlfriend, that I’d be sitting here in Denver with her and our miracle girl would be having surgery.

It was a bit emotional handing her over to the surgery team, but we confident in the care that she’s receiving. We prayed over her before she was whisked away and I think that was our breaking point emotionally.

We’re here in the waiting area now. Will update once we know more.

Trusting in Him for every step.

UPDATE 1:45pm MST (by Josh)
Got a call from the surgery team. Freaked me out at first because usually no news is good news. They just called to say everything is going fine and they’ll give us another update in about an hour.

Stay tuned…

UPDATE 3:54pm MST (by Tina)
It took awhile, but the Bun is in the recovery room. They are going to come and get us in 5 minutes so we can see her. She did fine through surgery and is extubated (yeah, no vent!). Thanks for all the prayers. We’ll give a more detailed update later.



 
Jun
21
    
Posted (The West's) in All Posts on June-21-2008

It was a gorgeous day in Colorado so we decided to plant some flowers. It was another step towards settling into our Colorado home.

And while we planted flowers, the Bun decided to catch some zzzs…



 
Jun
19
    
Posted (The West's) in All Posts on June-19-2008



 
Mar
02
    
Posted (The West's) in All Posts on March-2-2008


Yes…Bring Your Own Bottle. To heck with what the OT said. We tried the Playtex Vent-Aire and the Dr. Brown bottle.

At this point we’re thinking the Doctor got it right. We’ve only had a couple feeds with this bottle, but it appears like a lot less gas is being swallowed. Time will tell, and so will Ella.

We increased Ella’s volume of food today (70ccs per feed), and she took it pretty well, which is great. We did see some more retching, but not an increase that would cause us concern. As you can see from the picture above, our girl is getting pretty serious about making sure that bottle stays in her mouth.

Ella was pretty restless last night, which made for another sleepless night for Tina. Along with the regular scenario of a baby not sleeping through the night, it’s more complicated with Ella. For example, many times she ends up inadvertently removing the cannulas from her nose. Since she is so reliant on oxygen, it’s a matter of survival, not just an inconvenience. This is just one example of why the nights are so challenging. Ella stayed up a bit later tonight so we’ll see how well she does.

Although it was short, the Bun did get to see her “Aunt” Marla today. Always nice to have visitors.

Our next appointment is Tuesday with Dr. Kays. She’s having blood work done and we’ll be discussing the progress of her feeds to see if she has gained weight and / or if any changes need to be made.

One thing for sure…Ella is still cute as ever.

Sleep well tonight Bun…sleep well.



 
Feb
01
    
Posted (The West's) in All Posts on February-1-2008

Thank God, Ella slept pretty solid last night. Nobody was in the space next to us either, so we all got about 5 hours of sleep in. We’re still really wiped though because we’ve had minimal sleep overall during the last several days.

Our day started with the nurse practitioner giving us an update. This was great because we asked for more communication and we were getting it. Plus, the nurse practitioner is one that is part of the pediatric surgery team that works directly with Dr. Kays. All of this to say that she is a familiar face for us and is such a sweet person. We just love her. So, our day started with an update from her.

She knew our concerns and was doing her best to get them addressed. For example, we were a bit frustrated with the level of care in the Intermediate Pediatric floor. It was not appropriate for Ella since she has been having these “episodes” where she can down spiral quickly and become air starved, if she is not attended to quickly. So her first change was that she was moving Ella upstairs to the PICU (pediatric intensive care unit), where she can get more focused attention.

The move to the PICU was a good one. We feel like this is the right place for our girl. Plus, the room has a TV, which Ella has discovered. =)

Also, per the recommendation from the dietitian they’ve modified Ella’s formula. She’ll be receiving Pregestimil which will provide all her nutrition, but should be easier for her to digest than the Similac (they are concerned that the Similac might have caused some of Ella’s fluid retention issues, so they want to try a new one).

Dr. Kays also made some dosing modifications to her Sildenifil and Bumex. He’s increased her Sildenifil by 25% and spread it out over increased delivery times, including the continuous feed at night (this is the heart medicine). The Bumex was also bumped up as of last night to 1 mg twice a day. This dose is more than we’d like to see Ella receiving on a regular basis, but it may help reduce her fluid retention in the short term. And because her labs look good, Dr. Kays is not concerned with this dose at this time.

It also looks like Ella is teething for real this time. This may explain some of her increased agitation. Our other theory is some possible strain in her GI system caused by the Similac. Either way, she’s been placed on a prophylactic dose of Tylenol and that seems to be helping her.

This is the plan for the weekend, and we hope it does the trick. So far, it looks like Ella’s numbers are going in the right direction, we’ll just have to see if this gets her to a place where we all feel comfortable taking her home. Keep in mind that she is still on 1 liter of oxygen.

We have had several NICU staff coming up to visit our girl. We’ve been so blessed by seeing their friendly faces and their love for our girl. They’ve also offered support to help us if we need it as well.

Ella is excited to see her grandpa tomorrow. Can’t wait for him to meet her.

Although our hospital journey has been extended, we know that we are right where He wants us to be today and that is a good feeling. Thanks for continuing to lift up all three of us to our Lord for His strength, mercy, and patience.



 
Jan
20
    
Posted (The West's) in All Posts on January-20-2008


Ella slept through the entire night for Nurse Janet. It was great because at shift change (7pm), Ella was drowsy. But instead of letting her sleep, Nurse Janet some kept our girl up a couple more hours. She did this by doing her hands on assessment, weighing her, and keeping her entertained with stories just to make sure she that would sleep through the night.

We got up early to see the Bun this morning and we snapped the picture above. Yes, we got up early because we have the feeling this might be our last weekend without Ella at home, so…

We decided to take a break and escape to Disney World, about a 2 hour drive from Gainesville. =) We spent the day at the Magic Kingdom park and left there to go have dinner at P.F. Chang’s (Tina’s mom had given us a gift card for Christmas). We’re going to stay the night in Orlando, and have breakfast with our friends (the Boemler Warings) tomorrow morning and then drive back to spend the day with Ella for the Martin Luther King holiday.

When we called throughout the day to check on Ella, she was doing great and having a good time with Nurse Kristen. It is refreshing to have Ella doing so well and maintaining the steps she has taken forward.

With all her great progress from this past week, it felt so good to just to top it off with some fun. We kept up with all the comments on the blog throughout the day from her phone. It was surreal to be at “the happiest place on earth” and to be blessed by everyone’s words at the same time.

As the slogan goes, Walt Disney World, where dreams come true. We feel that our dream has come true in the life of our baby girl. We praise Him for creating such a wonderful little girl and we’re excited to see how He continues to work in her life.

Thanks to all of you for how you have already participated in her life. As always, may she continue to be a reminder of Him and His call for us to trust Him, every moment of every day.



 
Jan
04
    
Posted (The West's) in All Posts on January-4-2008

Today was a rough day for Tina and me. Ella is doing ok at the moment, but we received a call this afternoon from the nurse practitioner requesting that we have a meeting with her, Dr. Kays, Dr. Drummond, and possibly a neurologist next Monday. This kind of request is not usually a good thing.

This suspicion was confirmed when she went into the details of why a meeting was scheduled. Ella’s CT scan revealed some concerns related to her central line (CVL), primarily the fact that it looks to be causing some occluding in her inferior vena cava (IVC). If you recall, Ella’s superior vena cava collapsed after coming off ECMO (SVC Syndrome), and the CT scan also showed that this is still the case.

The only reason our girl still has her central line is for her IV diuretics. This is why they want to switch her over to her getting all her meds via her G-Tube, so they can pull this line. Dr. Kays has ordered that they start trying this transition again tonight. Half of her diuretics will be given intravenously, and the other half through her G-Tube.

We hope that Ella tolerates this because this is one step closer to coming home. The next few days will be very telling.

Also, they’re planning on giving Ella an EEG on Monday morning to assess the pathways of how her brain is functioning. This, in combination with the MRI results should give a clearer picture of her brain and what she may be up against.

So we don’t know all the details, but we know there is going to be some heavy decisions in the coming days. The neonatologist has one perspective on what the next steps should be for Ella, while Dr. Kays maintains a different opinion. The purpose of the meeting on Monday is to openly discuss all the relevant factors related to Ella’s condition. Ultimately, it will require a decision on our part to move forward.

Please pray for wisdom and discernment during this time. We only want the best for Ella, as do the doctors and staff. Keep in mind that Ella has never been a text book case so there’s no hard and fast rules with how to approach her treatment. We trust that the Great Physician does know what’s best, and we desire to be obedient to what He puts on our hearts.

Psalm 32:8
I will instruct you and teach you in the way you should go;
I will counsel you and watch over you.

Psalm 16:7
I will praise the LORD, who counsels me;
even at night my heart instructs me.



 
Dec
21
    
Posted (The West's) in All Posts on December-21-2007


Ella had a rough day. We’re leaving this post short and sweet. It’s 2:30am EST and we just got back from the hospital. We’ll give more details tomoorw. In the mean time, please continue to pray for our baby girl.