The Story of Nicholas' Early Arrival: No more feeding tube

Tuesday, April 7, 2009

No more feeding tube

Nicholas' NP discontinued his feeding tube today so all his feeds are by mouth only. He is allowed 85-90ml depending on how much he will eat. He is up to 10lb 2oz and is 19.7 inches long. He is going to start getting his vaccinations tonight and they will do one every night to space them out. He will get Tylenol and a surface novocaine to numb the area. They also give them sweeties which is a pacifier dipped in sugar water which stimulates the body's natural pain killer. That is nice because he wouldn't get any of that at the pediatricians office. They also lowered his oxygen to 1/4 liter. He is doing ok on it. He is satting in the high 80's and low 90's. Hopefully he will get used to it. His sats are supposed to be between 90-98%.

4 comments:

JCMatthewsApril 7, 2009 at 8:13 PM
Go Nick! Go! He's rounding 3rd and heading for home! I glad hear he had that feeding taken tube out. I know he needed it but it looked so uncomfortable...
ReplyDelete
Replies
UnknownApril 7, 2009 at 8:28 PM
Oh Nicholas, you are looking good! It won't be long now before you're home. Hugs to all of you!
ReplyDelete
Replies
Aunt PatApril 7, 2009 at 10:26 PM
We are jumping up and down with excitement for all three of you. Hope all things continue to go forward and Nicholas will be some soon. We will continue to keep you in our prayers.
ReplyDelete
Replies
The Adventures of DJ and KatelynApril 8, 2009 at 7:56 AM
So happy for you guys!!!It won't be long now he will be home. YAY!!!
ReplyDelete
Replies

Add comment

Preemie Experience

The Preemie Experience
The preemie experience is the shattering of all your dreams
For a normal, healthy delivery,
Of the ability to carry home a beautiful squirming bundle
After a short stay in the hospital.
It is lying there in your hospital room listening to
The happy sounds of whole families joined
Together by the birth of a grandchild, cousin, niece,
or nephew, and knowing that your
Child is miles away and may not survive long enough
For you to see or simply touch.
It is that first glimpse of a skinny, scrawny, not much bigger
Than a Barbie doll child
And feeling, fear, awe, and joy for such a fragile soul.
It is sitting by your baby’s “bedside” day after day,
Week after week, month after month,
Alternating between the emotional high of “Look, his eyes are open,” or “he’s crying!”
And the lows of “I’m sorry, something has shown up in the ultrasound,”
Or even “There is nothing we can do…”
It is hearing the alarms go off for the twentieth time in less
Than fifteen minutes because your
Child’s heart rate keeps hitting zero.
It is watching children dying around you, wondering if
Your child will be next.
It is hearing your child’s cry of distress as the nurses
Insert yet another IV and do another
Round of daily blood tests.
It is meeting other parents of children who are doing far better
And wondering, “Why me?”
And meeting parents of children who have just died,
And praising God for His mercy
To your child and feeling guilty because your child is alive
And someone else is grieving for theirs.
It is days of nightmarish testing and coping with less
Than positive results to the tests.
It is days of joy at seeing the first eyelash appear,
The child gain a whole ounce in one day,
And two bright shiny eyes look at you and into your soul,
And knowing that your child now recognizes you as Mama or Dada;
Or perhaps looks at you and does not see you at all…
It is that final hurdle before coming home!
It is the sorrow of waiting for the monitor company Representative to show you what to do
If the alarm sounds when your child is choking,
Gasping for breath, or simply dying.
It is the joy of just being away from all those nurses
And tubes and wires and beeps, and
Walking into the nursery you hastily prepared because,
after all,
The child wasn’t due for another four months!
It is thinking the nightmare is over…only to realize it still Continues in the form of
Such acronyms as PVL, RSV, BPD, CP and numerous others.
It is the final realization that those developmental delays
Have to be dealt with,
That reflux is a normal and unfortunate
occurrence in most preemies,
That the constant fight to gain weight is in direct proportion
To a preemie’s ability to do so.
It is watching a child struggle to pick up his or her head, sit, Crawl, or walk.
It is witnessing only silence when the child should be babbling,
Because the child cannot hear.
It is the mental images of a child running and playing
And communicating with others in a
Perfectly normal manner that are marred when you face years of therapy
In order to simply get the child to eat by himself or herself,
To talk or walk and then run.

The preemie experience is a journey…A journey through your soul in order to find the faith and strength to cope,
A journey of the mind when you face the emotional weariness,
A journey of the heart…to accept that, no matter what,

This child is yours,
And you will love this child no matter what.

The Story of Nicholas' Early Arrival

Tuesday, April 7, 2009

No more feeding tube

4 comments:

Sponsor Me at March for Babies!

Welcome

Blog Archive

Followers

About Me

Helpful Links

Preemie Experience

Counter