Talked to our pediatrician today.
I started with "We are NOT okay here."
I pretty much laid it out. He's eating less and less. I used to be able to get him to eat in his sleep but even that is a struggle now. At night he'll eat 15 or 20cc and refuse more, then wake up starving again an hour and a half later, eat another 15 or 20cc and we start over.
I told her he DID gain some weight last week with the aid of the olive oil, but that sometimes now he's not wanting solid food either. (I think it's the olive oil.)
She said that she was getting close to the point of feeling like we needed to do something drastic like admit him to the hospital. I told her that I was desperate and if she felt like that would help us- we'd do it.
She wants to try one more thing. She wants us to try some Nutramigen AA hypoallergenic formula. If that doesn't work, then the next step is that she's admitting him to the hospital for a work up.
She assured me that she IS taking this very seriously and we WILL get to the bottom of it.
Just hearing her say those words lifted a weight. I finally feel heard.
Now I just have to FIND the formula (no one seems to carry it) and give it a try.
Wish us luck.
Wednesday, January 28, 2009
Talked to our pediatrician today.
Posted by David, Trish and Robbie Cox at 1:43 PM
Monday, January 26, 2009
Well, Robbie has finally gained some weight. He broke 10 pounds this week.
Our pediatrician has us adding olive oil to his food and feeding him solids as often as 3 times a day.
The olive oil looks disgusting but so far Robbie seems to tolerate it well. Fats are good for baby's brains, so it's not quite as awful as it sounds.
Unfortunately the feedings are about the same. If I'm really, really lucky I get 2 good bottles a day. The rest vary from almost nothing to an ounce.
The worst at this point is at night. He'll eat an ounce or less and then refuse more. Of course, he's then hungry an hour and a half later and wakes up crying. Takes another half ounce maybe an ounce and we start over again. This doesn't lead to much sleep for me.
He is gaining, so that's something, but it's such a battle to get there and I'm just not sure how long we can live like this.
As much as you hate to wish this on anyone else, it is sometimes good to know we're not alone. One of Robbie's NICU friends is going through the same thing. Lexi's mom made a post describing a feeding that sums it up all too well. Check it out here.
Other than that, he's about the same. Talking more and more, using his hands more and more. Still hates tummy time with all the fire he can muster so he still won't roll over.
If it weren't for the feeding woes, life would be great. Really, he's beautiful and sweet and funny.. he just won't eat. Unfortunately eating is the the most basic thing a baby needs to do so much of our time is spent in frustration in worry instead of playtime and joy.
Please keep praying that things turn around soon.
Posted by David, Trish and Robbie Cox at 7:09 PM
Thursday, January 15, 2009
Food wars continue. I don't even want to talk about it any more.
Suffice it to say that I'm exhausted.
But let's try to be more positive.
New things in Robbie's world:
He's getting better on his tummy. Tummy time is still a very short game because he despises (DESPISES) it, but I've been working on giving him the two minutes he'll tolerate several time a day.
This has helped him with his pushing up. He's always had really great head control, but he never even tries to push up because as soon as you flip him over he starts screaming hysterically. But we're not able to get him over and he'll occasionally even try to push up on his own.
If you put him up on his elbows, he can hold it for several minutes.
He's also getting more and more vocal. I'll upload a video later that you can hear him cooing. You won't be able to see much because it was darkish in the room and they always upload even darker, but you can hear him talking.
His latest thing is that any time something new is in his mouth, he starts talking. A new toy, my hands, his hands, whatever- he gets really vocal. He sometimes does the same thing when he's eating solids.
Which is another thing- solids are going pretty well.
So far he's had rice cereal, avocado and oat cereal. He's not too sure about the avocado. I think the consistency was a little odd for him. But we're not giving up. Avocados have LOTS of calories, so I'm hoping I can get him to love it. The rice cereal is okay but doesn't travel all the way through his system so well. The oat cereal, though- he really likes. And it's helping to keep him regular so it's a double bonus.
We're going to try the avocado again for a few days then I think we might try sweet potatoes.
I'm really focusing on vegetables that have more calories than breastmilk. Anything to give him a boost since he's still not eating. (Oh wait, we're not talking about that.)
Robbie is also falling more in love with his hands every day. Reaching for things, grabbing them- and that best part- putting things in his mouth. He's working on trying to control his paci and on the rare occasion that he does eat a bottle, he wants to have his hands on it so he can "hold" it.
He's also smiling and laughing more and more. Those are my favorite parts. Sometimes when he catches my eye and just beams I'm reminded all over again how incredibly lucky I am. The kid loves me. What more could a mom want?
He's also sleeping great at night. If we could get that issue we're not discussing under control, I have no doubt that he'd sleep through the night. He goes to bed about 11pm every night and sleeps until 9, 10, sometimes 11am.
Napping is still intermittent, but with a 10-12 hour stretch at night, even with getting up to (try to) feed him every 3 hours and pumping, I'm able to get enough sleep to function most days.
And of course, he's as handsome and adorable and precious as ever.
With that- pictures to prove it!
I finally decided this Bebe Pod thing isn't so bad after all.
It certainly is a different perspective up here.
You know, I think I really like it!
Daddy doesn't feel good so I'm keeping him company.
Boy, he's demanding. I need a nap.
My daddy is sooooo funny!
I have a new toy. Mommy says eventually my feet will touch the bottom.
It sure does taste good.
And it has cool toys!
Lookie what else I can do!
It sure is hard.
Mommy is trying to feed me this new stuff called "cereal." I'm still a little unsure.
And the "video" that's really just audio.
Posted by David, Trish and Robbie Cox at 6:25 PM
Tuesday, January 13, 2009
Well, OT just left.
For once she actually got to see Robbie's (not) eating in progress.
At 1:15, he acted like he was STARVING. He'd barely eaten at his 11:00 feeding, so that was entirely likely.
He was wide awake, so I knew he wouldn't eat, but I hoped.
So I gave him a bottle. He sucked on it like a mad man for about a minute and a half. Then he stopped.
He'd taken 10cc. (About 1/3 of an ounce)
That was about the time the OT showed up. I was still sitting with the bottle in the mouth. He gummed at it. And gummed at it. And gummed at it.
She asked if she could try and I passed him over.
For an hour she stimulated his mouth, tried different positions, played with him. She eventually took a break and did his stretches and tried again. He took another 10cc in that time.
He was finally getting drowsy.
I told her that he'd eat now and took over. Sure enough, he sucked down 60 cc (2 oz) in about 10 minutes.)
That's the story of my life. Try to wear him out, try to feed him. Emphasis on TRY.
But at least she got to really see what it's like.
So her theory is now this:
He's SO not oral-averted that he's actually the opposite. She said he's a bottomless pit of oral stimulation need. All he wants is oral stim. So much that all it takes is something in his mouth to make him happy. He can ignore hunger (eating only enough to turn off the hunger) as long as his need for oral stimulus is met.
Now, I'm not 100% sure this isn't all a bunch of mumbo jumbo, but it does make sense. He'll chew/suck on anything- his hands, toys, pacis, my hands- you get the idea. But he won't EAT.
Anyway, she did some vibration stuff on his cheeks. He LOVED that. He just laughed and laughed. So I guess if nothing else, he's having fun. The idea is that we need to try to "fill up" his oral need and then he can focus on something else.
Of course, I also talked to the GI's office twice in the last 2 days. It started as me calling to ask them to call in the script for the Prevacid solutabs (his reflux pain is IMMENSELY improved now- and no side effects from the lactose.) and ended up with me telling them he's still not eating.
It would be funny if it weren't so serious but the GI's office recommended and OT second opinion and the OT recommended a GI second opinion. No one really knows anything.
I'm not sure if I believe anyone can do anything at this point.
At this point my plan is to give the new drugs and new therapies until the end of next week to work. Maybe once he feels okay long enough, he'll have an appetite enough to want to eat. And we'll fill his oral stim "bucket" as best we can and see what happens.
If nothing gets better, I'm going for a GI 2nd opinion. I would like to see about something to stimulate his appetite and see if it helps.
If it doesn't, I'm not sure I have much choice about the G tube. I broke down into tears talking to the OT about it today.
I feel so emotional about it. It feels so drastic. I feel so guilty that I let them put one in in the first place, then guilty that I let them take it out and now it turns out he may need another.
I wonder how it will affect him long term. Will it make his oral issues worse? Will it make his reflux worse? Will he be able to run and jump and play like other kids? Will he always have stomach problems? And of course, there are the risks of surgery in general.
But I worry about not doing it as well. He's just not growing. While being small isn't the worst thing in the world, babies should grow. I worry about his health and his developement.
I broke out the exersaucer yesterday and he really likes it. But his legs are too short for his feet to reach even on the lowest setting and his arms are too short to reach any of the toys.
Right now he's doing well in every other area except this. But it can't be long before other areas start to suffer.
I just hate all of this and want him to get better.
For now, we just keep slugging along.
Posted by David, Trish and Robbie Cox at 4:54 PM
Saturday, January 10, 2009
I apologize for the delay in posting. It's been a very hectic week and this is going to be a long one, so it was hard to get to it.
We've survived our week of appointments. I'll get to them one by one.
Tuesday was OT.
It was frustrating, to be honest. There was a bit of double scheduling drama that involved getting Robbie and myself up hours earlier than normal only to be called and told the appointment was changed back to the afternoon. The reasons were good, but it's hard to be reasonable when you're exhausted.
Then she got here. The original plan was that our OT lady was coming with the head OT lady. Head OT lady couldn't come because of the aforementioned scheduling conflict.
Then when she did come all she wanted to talk about was thickening his feeds. I explained that I used the thickener for about 10 days with some limited success (that coincided with a new med refill which will be discussed later) but he didn't gain any weight at all during those 10 days. The thickener has no calories so it's basically watering down his food by 5% because I add 5ml to every 100ml of food.
She kept telling me to add the thickener after the milk. As though that has anything to do with it. HE DOESN'T FINISH BOTTLES. It's not like I can just feed him 5% more food. Don't I wish!
We basically talked in circles the whole time with her telling me to do something that I told her wasn't working. I switched nipples back to the Dr. Brown's preemie nipples and that seemed to help him control things a little better much the same as the thickener did. And it doesn't compromise calories.
In better news, we discussed his muscle tightness ("high tone") and how much improved his bending is. (Go us! I'm Robbie's personal trainer. We're a team.) and identified a hip thing that the PT back in the NICU pointed out. (His hip is wonky where it makes his toes on his left food point outward. My left leg does the exact same thing.) and what to do about it. He HATES that exercise, btw. He doesn't mind any of the other stuff, but that one upsets him.
She left and I mostly felt like I'd just wasted an hour and a half of my life.
Then came Wednesday.
Off to the pediatrician. Only when I got there (after fighting through rush hour traffic that threatened to turn me into a road-rage news story) I found that it was actually a nurse visit for his remaining vaccinations only. They didn't even weigh him.
I did see Dr. P in the hallway but only long enough for her to coo over his outfit and tell us she didn't want to see us again until his 9 month checkup.
I decided it was okay because the really important visit was the GI specialist on Thursday.
I then spent a day/night of hell with a feverish, cranky, clingy, miserable baby. Vaccines are fun.
Thursday found a more cheerful, less feverish baby and the GI doc visit.
I went to that appointment armed with a number of questions and suggestions.
I arrived at that appointment far earlier than expected so I swung by the NICU to say hello.
I ran into one of my favorite NNPs and one of the lactation consultants in the hallway. They cooed over how good he looks and the LC walked me to the NICU.
She asked about nursing. I was sad to tell her that he doesn't, but proud to tell her I'm still pumping and keeping up with his needs. (Easy to do when the kid doesn't eat, but let's not go there.) She was full of praise, which was nice.
A few of the nurses popped out to say hello and make eyes at Robbie. He made eyes back. He even smiled a few times and laughed once. As much as I do not miss living there, it was nice to see friendly faces.
Robbie looked into the NICU (we were out in the hallway) with a curious look. I wish I knew what he was thinking.
Then we were off to the appointment.
I have very mixed feelings about how it went.
I'll take my concerns point by point.
1) I wanted to switch from Prevacid suspension to solutabs (or some other form)
The suspension is very volatile and we always experienced a bit of a honeymoon period right after a prescription is filled. Then it tapers off. It's clear that the drug is breaking down.
She completely agreed with that and gave me some samples of the solutabs to try - with instructions to call on Monday. If things are improved, she'll call in the script. If not- we'll completely change drugs, likely to Nexium.
1a) The solutabs use lactose as a binder and I was mildy concerned about that because of the theory that he doesn't tolerate dairy well.
She said we'd try it and see what happened.
1b) I asked about said dairy and if she felt it was necessary for me to continue to limit my dairy intake.
She said that we'd use the solutabs as a test. If by Monday things were going well, I could slowly add dairy back to my diet starting with cheese and yogurt.
Let me just say chhhhhhhhhhhhheeeeeeeesssssssse and yoooooooooooooogurt.
I don't really even like yogurt but right before I cut dairy out, I became addicted to the fat free vanilla Activia in a smoothie. Yum!
2) I asked about some sort of motility agent.
In babies with reflux and in babies with fundos, gastroparesis (slowing/stopping of some of the movement in the gut) is common. I thought perhaps if we can speed up his digestion that would help him not puke so much and make him hungrier.
I specifically asked about Reglan (yucky side effects) or Domperidone.
She shook her head. She doesn't think that's necessary at all. She said that IF we did that, she'd use a 3rd drug (I forget the name now) that would both speed things up and stimulate appetite, but it comes with a side effect of extreme drowsiness which obligates him to eat larger volumes when he's awake which isn't ideal.
I was a little annoyed at being dismissed w/o much of a discussion about the issue.
3) The non eating.
She mostly just nodded. In that "yes, that's what reflux babies do" way. I understand she sees this every day. But for me, this is MY kid.
I explained that he only eats when he's asleep and that I'm feeding him an average of 12 times a day to even get close to a reasonable amount of food in him.
She allowed that was a lot, but didn't comment further.
The real problem here is that he had gained 19oz in the 35 days since we'd been there. She finds that acceptable. Not ideal, of course, but as they've told me before- all they see are babies with stomach problems. They're used to sub-par weight gain.
The problem is that I know that he actually gained 17 oz in 21 of those days and has only gained 2 in the last 14. I'm concerned about the current trend continuing.
She pulled up his growth chart and said he's still got plenty of time to catch up (they want him caught up by age 2) and he was on his own growth curve so he was fine.
3a) I mentioned that the pediatrician had mentioned a G tube at one point and she just shook her head but didn't say much.
4) I asked if she thinks the fundo is causing some of his trouble with the volume intake.
She said no.
I think she's wrong. How can tying down part of a person's stomach NOT affect how it stretches?
5) I asked how much food he needs to protect his brain development.
This one made me cry. I've been so worried because he's already at a disadvantage in so many ways because he was so early.
Is my resistance to a G tube causing him more trouble? Am I risking his health further?
I was relieved at the answer. 100ml/kg.
At this stage that's 433ml/day. His worst days, he's eating just over 500ml. Relief. But at least I can keep that as a measure in my mind that if he's not hitting, I need to insist on seeing someone.
I should add that she looked at me like I was NUTS when I asked the question. I told her several times that I'm an anal retentive mother. She was warned.
I even made her write it down for me.
6) I asked her about the OT's beloved thickener.
She agreed that a non calorie thickener is probably not ideal. She said that if I want to thicken she'd recommend Enfamil AR instead.
I do resist that because he has SUCH a history of not tolerating formula that I hate to add anything in.
The other problem is that formula doesn't last.
Right now if he doesn't finish a bottle, I can save it for the next feeding. (Breast milk keeps well. It has great antibacterial properties.) but if it is mixed with formula, once he starts a bottle, it's only good for an hour. Which would mean pouring a lot of breast milk down the drain.
I'm currently producing about 22oz/day. He SHOULD be eating about 21oz/day. If he eats like he should, that doesn't leave much room for waste.
Plus he's proven that IF he will eat, he will gain on plain breast milk. (I won't even get into the latest information about melamine in formula.)
She wants to see us again in a month.
I left with the one thing I really wanted- a change in drugs. But I also didn't really feel heard. She did a lot of nodding. "Yeah, that's normal for a reflux baby." But I don't feel like she really got that he's not doing well.
In the end I decided to give the new Prevacid time to work and to go from there.
I gave him the first solutab yesterday afternoon. Since then we haven't had any extended post-meal screaming episodes.
He even managed to his his food goal today. He's still pukey (I started him on avocadoes yesterday. Green puke is.....interesting.) but nothing is going to stop that. It's just about managing his pain.
The solutabs are a little bit of an annoyance because I have to dissolve them in water in a syringe. It's awkward and I'm worried about getting every drop into him. But anything that works is worth it to me.
(As an aside she told me just to put it in his mouth. Yeah-he swallowed it whole. I talked to a pharmacist friend and got better info.)
I'm really praying that this continues to be successful and as the days go on his stomach will feel better and better and his appetite will return and he will eat. And grow.
He's been stuck at 9lb 9oz for more than 2 weeks now. We're shootin' for 10 pounds.
Please pray for us!
Posted by David, Trish and Robbie Cox at 1:36 AM
Sunday, January 4, 2009
Well, let me see if I can catch every one up.
I apologize for the delay in updates. For some reason or other, I seem to have a lack of free time these days!
Robbie is now about 9 1/2 pounds. (I bought a baby scale for home.) After a really bad month of weight gain, he had a really good one and was just over 9 pounds at his last doctor's appointment.
Unfortunately, things have gone downhill in the last couple of weeks. He just doesn't want to eat. I can only get him to eat when he's really drowsy or downright asleep.
I've talked to doctors, therapists and a ton of other parents of preemies. It's not uncommon but no one can seem to fix it.
I've spent an embarrassing amount of money on different types of bottles trying to find one that would make him want to eat again but nothing seems to work.
The doctor brought up putting a G tube back in. (That's the tube that goes in through the wall in his stomach to feed him. He had one for 6 weeks but he was eating so well at that time that it was taken out as soon as it was safe to do so.)
I really, really, really don't want to do that.
Robbie didn't exactly take surgery well last time (you might remember that it took him 3 days to come out of anesthesia) and the G tube was really a pain in the butt to maintain. It leaked almost constantly and had to be adjusted frequently.
At this point our plan is talk to the GI specialist and the pediatrician this week and see what can be done. I'm fairly convinced that this is all a result of stomach/gastic pain. I'm not sure if it's the reflux or what exactly but he just doesn't seem comfortable.
He's gone back to crying anywhere from a half hour to an hour after nearly every meal (he'll wake up crying in pain.) It's absolutely heart wrenching. All you can do is pat him until it passes.
So I think it's time for new meds and maybe some more tests to see what is going on. I hate to put him through any more, but this can't continue.
In better news, he has started on solids this past week. The doctor encouraged us to start sooner than later hoping that he'd love food and would eat it even when he won't take a bottle.
He seems to like it. He hasn't QUITE figured out how to get it from the front of his mouth to the back. He's only 4 months adjusted age, so he's still fairly young to do so. But with enough gumming and a little help from mom he's eating about a half ounce at a time. I'm planning to try oat cereal next and then move on to vegetables.
Other than the horrible stomach problems, he's really doing well. He's really learning to use his hands well. The animals on his play mat have been taking regular beatings. He's starting to figure out how to hold his pacifier in his mouth and definitely likes to suck on his hands.
He's becoming more and more verbal. I've caught him "talking to" his swing, his toys and he definitely yells when he's angry. Not cries- YELLS. I'm afraid he might have inherited my temper.
We're now able to play more as well.
The only thing eluding us from his 4 month milestones is being able to roll over from his stomach to his back. That was one is challenging because his stomach hurts all the time, so it's hard to do a lot of tummy time. But it's something we'll be working with our therapists on in the coming weeks.
His pediatrician says he CAN roll over (at his last apppointment she was able to get him up on his arms and he flung himself backwards) but I don't think it counts if it's just an angry accident.
I'm really hoping that his stomach issues improve dramatically in the next few weeks. A lot of babies do improve around the 4 month mark (which he hit today!) Hopefully with some new meds and therapies we can beat this w/o another surgery.
We appreciate any prayers, good thoughts or sacrifices to the Gods that anyone wants to make. We need less stomach problems and more weight gain.
More pictures coming soon!
Posted by David, Trish and Robbie Cox at 9:27 PM