If you ever call my house and I am holding Morgan Kate there is no doubt that you will be able to hear her. She makes noises non-stop. The only time she is quiet is when she is in a deep sleep. She grunts, groans, moans, etc. all the time. It's very rare for her to be completely quiet. Yesterday when we were at the eye doctor one of the nurses heard her and said, "Oh, she must be really mad or working on something BIG for you guys to handle later." Nope, not the case. If that were the case then I guess she is mad and "working on something" all of the time. I asked Dr. G about it today and she thinks some of it is caused by the reflux/stomach issues Morgan Kate is having.
Our appointment this morning went okay. Morgan Kate had only gained an ounce since Friday (8lbs 12.5 oz), but Dr. G was not concerned. The best part is - she's gaining. We talked a good bit with Dr. G about Morgan Kate's eating issues and we are going to try some new things. Dr G was great as usual and spent a lot of time with us.
Some of our issues:
1. MK has to be very still and quiet while we are OG feeding her. If she grunts, groans or cries it pushes the food back into the syringe and we have to stop.
2. The minute we start an OG feed she begins to arch her back, push on things, flail her arms, and fuss.
3. After OG feeding her she cries and continues to squirm and arch.
4. Her stomach makes horrendous noises, she has lots of gas, and she spits up frequently.
5. Bottles have not been going so well since the ear infection. Not sure if it's because of the infection or the fact that we have added rice cereal to her formula and it's now harder to get through the nipple. Go figure.
6. She will suck on the nipple a few times and then just stop.
7. If she is fast asleep she will not take a bottle at all.
These were the concerns we brought to Dr. G this morning and this is our current plan. With our luck, it's subject to change at any given time.
1. Stop the rice cereal. We need the formula to be thicker so that it stays down in her tummy, but we will have to use another substance. I can't remember what the substance is called but it has the consistency of formula and the minute it hits the stomach it thickens.
2. We are to give MK Levsin drops every six hours. These drops are given to babies with colic and babies with irritable bowel syndrome. We are hoping this is the trick.
3. Continue with her reflux medication.
4. Dr. G's office is trying to schedule an appointment for MK to have an upper GI done. They would like to get it done this week, but not sure how that will work out with the holidays. The upper GI might give us all a better idea of what exactly is going on.
5. After all of the above we may meet with a gastro doctor to get his/her take.
6. The very LAST resort would be for MK to have a surgical procedure to hopefully correct the reflux. This is the very last option and we are praying that we never get to this point.
We are trying to be positive and remain upbeat. We are just so tired of seeing our precious girl in so much pain. Feeding an infant is supposed to be a bonding time and a time for mother/father and child to relax and spend time together. There is NOTHING relaxing about feeding Morgan Kate. Every time she is due for another feed I find myself hoping and praying that Travis will just take over and I won't have to do it. It's that bad.
Her oxygen needs have been about the same, maybe a little less. She averages anywhere from 16ccs - 40ccs. She has a pulse ox attached to her foot and it tell us what her oxygen sats are. As long as they stay between 86 and 100 the alarm will not go off. However, the minute she drops to 85 the alarm begins to ding and it will continue to ding until she is able to pull her sats back up. Ninety-nine percent of the time she can pull her sats right back up. There has only been a few instances, very few, that we have had to turn her oxygen up to help her. The pulse ox is a big reassurance for me. I don't mind carrying it around or hearing the alarm go off. It gives me peace of mind. The only bad part about the pulse ox is there are a lot of false alarms. If Morgan Kate moves a lot or kicks her feet too much the pulse ox can't read and the alarm goes off. As I mentioned before, she moves a lot. Yep, you guessed it! And that means the alarm goes off. So, we spend a lot of time holding her down and trying to keep her foot still so that we can determine whether it's a true or false alarm.
I gave Morgan Kate her first dose of Levsin drops earlier today. After the drops I fed her and then she and I had "play time". She seemed really, really content and at ease. I put her on her "mat" and she kicked and moved and looked all around. She did an awesome job! She was on her mat for close to forty-five minutes or so and she was completely happy. She then had some tummy time and worked on holding up her head. After all the "work" she got to relax some in her new boppy chair that Kaky and Gdaddy gave her for Christmas. I am hoping that the Levsin drops gave her some relief and if that is the case, then terrific. It was a great afternoon and I am hoping that all the "work" and "play" will make her nice and sleepy for tonight. Wish us luck...
9 comments:
woman----you have got some strength. It IS heart-wrenching and irritating, and joyful, and sweet all at the same time. Just make sure you play into your emotions--when you want to scream, scream and when you want to cry, cry. You and Travis are both in my prayers and I know things will get easier--you WILL have totally joyful times and I know God will continue to sustain you both as you do what is absolutely best for MK. Hang in there kid--one day you'll be sitting around a table with friends and talking about what a sweet and smart girl she is and remembering when she was "difficult". Even as I type I am reminded and reassured that God does not give us more than we can handle. You too are special to Him and He chose you as her parents b/c He knows you will be the best for her! Take Care
As I told you today, I will be praying for you as you work your way through this "hurdle". I know it seems once you conquer one obstacle, another one comes up, BUT, remember, this situation is temporary. Every day, Morgan Kate makes more progress and she will continue to because you and Travis are doing such an AMAZING job at this! I love you all and I hope you get some rest tonight.
i just wanted to tell you how excited i was (still am) that i got to see morgan kate the other night...even if it was just through the window:) you and travis are amazing parents...don't forget that! MK is a very lucky little girl. i'm very sorry that she is still struggling with her tummy, but i know you all will figure it out. i hope you are able to get some sleep tonight. we are still praying for you guys:)
xoxo
AA
I am so glad that you have a wonderful pediatrician. Levsin is a good drug for both babies and adults. We will pray that Morgan Kate's little tummy and intestinal tract will be receptive to the levsin. I know it is difficult for you and Travis right now but remember you guys are AWESOME parents and some day this will be only a memory. I pray on and off for you guys all day long. God brings you, Travis and Morgan Kate to my remembrance all day long. You and Travis are so strong. I am sure at times you and Travis do not think so but you are and I am so proud of you guys. Trust me it will get better. You and Travis have such a strong support system and know although we can not be there we are there in SPIRIT and in the spirit there is no distance.
I pray that God continues to touch you,Travis and Morgan Kate with His Spirit as You Travis and Morgan Kate all become stronger as a family. God knows our needs before we do. We Love you, Travis and Morgan Kate. Until we see you again....
Love,
Aunt Jan and MaMa
Hey! I am so proud of you and Travis. I know this is exhausting, but you are doing an incredible job as parents. Remember the joys are worth the work. You would be proud of Maggie with her wisdom teeth. She has been quite the trouper. We all love very much! Aunt Terry
Hey girl,
I have to tell you how much I admire you and Travis's strength through all of this. I know how hard it must all be and how tired you are, but you are hanging in there and have become a fantastic mommy! I hope that you all had a great Christmas and have a happy new year! Again, if there is ever anything you need, please let me know. I will pray that Morgan Kate's tummy issues subside and that things will only get better from here. Have a great night tonight as you ring in 2009 with your little girl, as I am sure she will be wide awake, ha:) Take care.
Lindsay M
Thanks so much for all the info you give us about Morgan kate.
My prayers will be for these current problems to get straightened out!!
You are doing so well, you amaze me with your stenght and faithfulness.
Sounds like she is going to be a talker!!
Take care and know many many prayers from so many people are offered up for you daily.
God has great power as you have said and he can handle all our needs and concerns.
Hope you all can get some rest!!!
We'll be praying that the new medicine will help. You and Trav are doing beyond phenomenal!!! I hope the 3 of you have a fun New Year's Eve...and Happy 2009!!! Love you guys, Kelly
Hey Heather! I haven't seen you in forever and had NO idea that you guys had been going thru all of this! What a BEAUTIFUL baby MK is --- and I'm sorry...she does look like Travis but babies change their looks! You guys are definetly in my prayers!! God will work things out for ya'll...he always does...just in His own way as you have obviously experienced! Now join facebook because I've been lookin' for you and Julie Smith to see what you had been up to! Liz pointed me in this direction. I have to say that as a nurse, you have done a great job of explaining things on your blog! :) Congrats on being home and I hope that 2009 continues to bless you, Travis, and Miss Morgan Kate! :)
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