Tag Archives: odin

the eric update – day 53: supersized paci. yet another spit bath. first laundry load!

day 53: supersized paci

tonight, eric was upgraded to a really, really big paci, which is yet another sign that he’s getting to be a Big Boy. the pacifier is a special preemie, orthodontically-correct paci which the nurses claimed would be difficult to find outside the nicu. it doesn’t seem too difficult if you know where to look, but maybe there’s a difference that makes a difference that i’m not seeing. i’m sure someone can help me clear up the confusion. in any case, the supersized paci is a big step on the way to getting prepared for breastfeeding. it’s neat to see him start to suck on everything in sight when it gets close to feeding time, even though his feedings are coming through the feeding tube.

day 53: bearer of the ring

maybe someday, i’ll stop documenting every bath that he gets, but today was not that day. kris looked at me with a raised eyebrow when i told her that i was going to photograph yet another spit bath, but i just couldn’t quite bring myself to not take the pictures. hopefully you’ll still enjoy the fruits of my obsessiveness.

day 53: yet another spit bath. I.

no, this isn’t a mere product placement for johnson & johnson shampoo; it’s time for another “spit” bath! eric can’t have a full tub bath because his IV is in his arm, which makes it more difficult to keep water from infiltrating the line.

day 53: yet another spit bath. II.

first, the eyes must be scrubbed.

day 53: yet another spit bath. III.

and then the inside of the ear.

day 53: yet another spit bath. IV.

don’t forget the back of the ears. you don’t want any yeasty growths accumulating behind the ears.

day 53: yet another spit bath. V.

scrub his head!

day 53: yet another spit bath. VI.

rinse his head!

day 53: yet another spit bath. VII.

aahhhh. a brief respite from the rigors of the spit bath.

day 53: yet another spit bath. VIII.

a bath can be pretty tiring and one must yawn at least once during the process.

day 53: yet another spit bath. IX.

scrubbing bubbles.

day 53: yet another spit bath. X.

during the bath, eric decides that maybe the new, supersized paci would be a good way to help make the best of the situation.

day 53: yet another spit bath. XI.

it’s always nice to end a bath with a little fingergrab.

day 53: tucked in for the night.

tucked in for the night. well, not really, because the nurses will still be doing their nursing duties every couple of hours, but we like to imagine that he’s really settled in for a long night of restful sleep.

i think the muscle shirt with cars suits him well.

day 53: decreased nasal cannula flow

in one of the most subtle changes of late, eric’s nasal cannula air flow was decreased from 2 liters to 1.5 liters, which is a huge step forward in the process of getting weaned from the respiratory aid. the nurses thought he’d need to have his supplemental oxygen turned up to help offset the decreased airflow, but he didn’t, which they said was quite impressive.

the floating ball indicates the flow rate. when it gets to zero, he’ll be able to get rid of the nasal cannula altogether and be free of tubes up his nose!

day 53: his first load of laundry!

they also told us that, as soon as he gets the IV taken off of his hand, we can start bringing in his own personal clothes! the clothes he’s wearing now are special tops with velcro that make it really easy to get on and off in the event of an emergency, but soon he’ll be able to wear regular street cloths.

so, late in the night we did his very first load of laundry.

the eric update – day 52: still more postcards and gifts! and progress, micropreemie style.

day 52: hand on head with feeding tube. I.

today was another quiet day of making slow, steady progress. he’s increased his breastmilk feedings to 8 cc’s every two hours and appears to be continuing to tolerate them well. they will usually pull out up to 3 cc’s of undigested food before each feeding, but that amount doesn’t seem to be increasing as they up his total feedings, which is a good sign that his digestive system isn’t slowling down.

if he continues to tolerate the “bolus” feedings ( where they give him the breastmilk all at once, instead of a “continuous feed” where the milk is pumped in at a constant rate ), then they’ll keep adding a cc to the amount that they’re giving him every two hours. so tommorrow, i’d expect him to be on 9 cc’s every two hours. and given his wieght, he’d need to be getting about 20 cc’s every two hours to be on full feeds again ( meaning no additional parenteral nutrition from the IV ), which means he could have an intravenous line in for a ten days to perhaps two weeks. he’s having a little bit of trouble keeping a good IV and i think they might be running out of nice big veins; i suspect that sooner rather than later they might be forced to put the line in less attractive locations like his scalp.

day 52: hand on head with feeding tube. II.

we got some more postcards! and we’ve received lots and lots of gifts lately, from friends family and strangers, and i just haven’t had time to properly acknowledge them. i’m going to put pictures of everything up as soon as i get the free time, but in the mean time, please know that we’ve enjoyed everything we’ve received and are continually amazed at the new suprises that the mail seems to bring each day.

the eric update – day 51: saying goodbye to cpap. rumors of an isolette.

day 51: all nasal cannula, all the time

woohoo! he’s on all nasal cannula, all the time! and not alarming at all. o.k. he still has the occasional apnea or brady, but they’re all for reasons that don’t particularly concern the staff. he’s on 7 cc’s of breastmilk every two hours and tolerating it well – not great, but not bad either. Every so often they’ll pull a few cc’s of undigested milk out of his stomach before they introduce the new milk; if the amount that they pull out increases then they’ll slow down his feedings.

so, day 51 was a very, very good day. and there are whispers among the staff that, if he keeps up keeping up, then he’ll graduate to an isolette and ditch his radiant warming bed! amazing!

day 51: feet on palm

sometimes a simple shot can put into perspective just how small he still is.

day 51: hand grasping feeding tube

he often likes to grasp his feeding tube after milk has been introduced, which is sweet and sad at the same time.

the eric update – day 50: eric’s first tub bath! and even more nasal cannula.

day 50: eric's first tub bath. I.

the big news today was that eric got to have his first tub bath after weeks of “spit baths” with a washcloth. micropreemies are often none to impressed with bathing, as it just makes them cold, so it’s interesting to see his reponse. at first he seems like he might get quite unhappy with with the whole bathing thing, but he eventually settled in an waited patiently for it to be over. all the bathing was quite tiring, so after playing with a new toy that kris bought, he looked around for a bit and quickly fell fast asleep.

day 50: eric's first tub bath. II.

yes, it really does take that many people to bath a micropreemie, what with all the sensors and IV lines

day 50: eric's first tub bath. III.

at first, eric’s not too impressed with the whole bath experience.

day 50: eric's first tub bath. IV.

mama gets ready to apply some soap. he’s settled down at the point, resigned to fact that he’s not getting out of the bath anytime soon.

day 50: eric's first tub bath. V.

“you know, it’s fun and all to have so many women being so attentive, but could you pick up the pace a bit, as i’m getting pretty cold.”

day 50: eric's first tub bath. VI.

he’s getting dried off and decides that he’d like to hold the “graspy” toy that mama bought for him just a few hours earlier.

day 50: eric's first tub bath. VII.

getting a bath can be a very tiring event, so he has to try very, very hard to keep his eyes open.

day 50: eric's first tub bath. VIII.

yaaaawwwwwwwnnnnn. sleepy.

day 50: eric's first tub bath. IX.

or maybe not so sleepy. he puts off sleep for a few more moments and looks right at me.

day 50: eric's first tub bath. X.

o.k. yeah. i guess he really was sleepy afterall.

he’s up to 8 hours of nasal cannula, followed by 2 hours of cpap and handling it wonderfully, with very few alarms. i’d expect them to test out 24 hours of the nasal cannula very soon.

he’s still having trouble digesting the breastmilk as quickly as they’d like and he’ll typically have an alarm or two after feeding. the alarms after feeding are from the weight of the food in his stomach pressing on his vagus nerve, which helps to maintain his heartrate. the fact that his food isn’t moving along as fast as they’d like is aggravating the situation. at this point, there’s not much they can do, except watch him closely and obey the signs that he’s sending to take it slow with the feedings.

the eric update – day 49: eric’s 7 week birthday!

day 49: 7 week birthday kangaroo care

let’s all give odin a little birthday cheer, as it’s his 7 week birthday today! he gained a few grams and is now solidly in the 3 pound category at 3 pounds and 3.5 ounces. he also added a half a centimeter and is 38.7 centimeters or 15.25 inches, which means he’s added 3.25 inches to his length in the past seven weeks! woohoo! he’s rapidly being weened from the cpap and is on 6 hours of nasal cannula and 4 hours of cpap. since he’s doing so well breathing on his own, i suspect that within the next few days they’ll see if eric can go 25 hours on the nasal cannula. despite having to do more breathing on his own than ever, he’s throwing very few alarms; he only seems to alarm when the nurses are doing their “meanies” or when he’s put his head in a position that’s not conducive to breathing. his breastmilk feeds stayed the same as yesterday, as they’re pulling up more undigested food than they’d like to see, so they’re going to back off a bit on increasing the amount of milk that he’s receiving. you might remember that anytime digestion slows and milk starts hanging around, there’s an increased risk for a gut infection, so they’re just going to take things slow.

day 49: ouch!

the nasal cannula needs to be taped on his face to reduce the chance that he’ll pull it out and the process of repeatedly removing the tape when he goes back on cpap has made his skin a little raw. tonight, he even has a tiny bit of flesh pull away, which he obviously didn’t care for at all; nurse peggy put little pieces of what’s known as comfeel on his face to prevent it from happening again because open, irritated sores are not a good thing when you’re enduring a prolonged stay in the nicu.

day 49: pacified. I.

eric’s getting much better at coordinating his sucking and breathing; a mere week ago, he’d alarm when a pacifier was in his mouth for more than 15 or 20 seconds, but now he can keep the pacifier in as long as he’d like. since he’s doing so well, nurse peggy said that it’s a good time to introduce a pacifier during his breastmilk feedings so he can begin to associate sucking with feeling of food in his stomach. this is but the first step in a long process of getting his used to having to coordinate the sucking, swallowing and breathing that must occur for real breastfeeding, so it’s a big step.

day 49: pacified. II.

sometimes he has trouble keeping the pacifier in his mouth with the tubes in the way, so peggy has “illegally modified” the paci by notching it so that the tubes can stay where they need to stay and he can more easily keep it in his mouth. nurse peggy is thoughtful like that.

day 49: longhair

eric’s hair is getting so long that it’s growing over his ears!

the eric update – day 48: gifts! last transfusion? no alarms (except pops induced)!

day 48: loose cannula

there’s no doubt about it. we’re back to the ho-hum days that are mostly filled with kangaroo care.

eric is being transitioned from the cpap to the nasal cannula much more quickly than previous attempts. today, they altered his schedule to alternate between 4 hours of cpap and 4 hours of the cannula. amazingly, he only had 2 brady’s (bradycardia, or slowing of his heart rate ), the entire day and both were while he was on my chest, which, of course led to endless jokes from kris and nurse jan. both brady’s were due to his head slowly getting into a position that made it difficult for eric to breath. of course, whenever eric’s on my chest he seems to enjoy putting his head in the position that will lead to a brady. i imagine that he thinks it’s a fun game to have me move his head in the correct position, only to move it slowly and imperceptibly back to the wrong one. over and over we play the game and sometimes he wins and has a brady.

eric also likes to tug on his nasal cannula, pulling the prongs out of his nose. if he weren’t doing so well breathing on his own, we’d know when the prongs were out of his nose, as his blood oxygen levels would start to decrease. but since he is breathing so well, we don’t see the “desat” and only later discover that his prongs have been out for as long as 10 or 15 minutes at a time, which is yet another sign that he’s getting stronger.

day 48: eric meets babo the ugly doll

some longtime friends, matt and erin, who we haven’t seen in awhile came into town this weekend bearing gifts! eric was happy to receive his new ugly doll, even if the nurses were all a little perplexed as to what an ugly doll was and why on earth anyone would want to buy one. but we don’t care what they think, since eric and the ugly doll got along quite famously and found themselves in long, heated discussion about which of them was taller.

day 48: eric and babo discuss who's longer

clearly, the ugly doll has no grounds for his assertion that he is, in fact taller than eric.

day 48: eric's new handcrafted knit cap

in addition to giving him the ugly doll, they also gave him a cap that erin knitted with her very own hands! the nurses were all very impressed that the cap was knit by a nicu rookie, since it can be tough to make the cap snug, but not too snug, and it should also be quite stretchy in all directions to accomodate the various forms that his very malleable head might take on from day to day. there’s a bit bucket of “discards” in the waiting room outside the nicu that have been knitted by volunteers but that haven’t passed the quality control inspection from the nicu staff, but eric’s cap won’t be in it, because it’s about as perfect as you could want it to be. thanks!

day 48: diaper change from pops. I.

there’s nothing special about the fact that i’m changing eric’s diaper, but i couldn’t remember ever providing photographic evidence to dispute any lingering suspicions that i might be trying to shirk diaper changing duties.

day 48: diaper change from pops. II.

it’s a bit more tricky to change his diaper these days, since it is seemingly impossible to not get the velcro on the diaper stuck on the shirt before you get all the cords and lines out of the way.

day 48: diaper change from pops. III.

as i change his diaper, it strikes me that as odd to think that some day we’ll actually change his diaper and not have to worry about pulling out IV or feeding lines or detaching sensors.

day 48: diaper change from pops. IV.

it occured to me that i’ve only casually mentioned his intravenous feeding and having discussed at greater length a very important element of how well eric is doing.

day 48: total parenteral nutrition.

so it’s time for a short course in parenteral nutrition, where parenteral refers to food that enters the body through a blood vessel. in what is known as total parenteral nutrition, all of the essentials ( carbohydrates, protein, fat, vitamins and minerals ) are delivered directly through an IV line in one of eric’s veins.

day 48: lipids

despite all the active research that has gone into parenteral nutrition and fact that it’s probably one of the greatest reasons that eric has been able to keep growing despite suffering from pneumonia, i can’t help but feel that the bag of fluids look suspiciously like gatorade and the the syringe surely must be filled with lard and not some state of the art blend of short chain lipids as they claim.

day 48: another feeding

day 48: eric's 16th transfusion

eric received three more transfusions today which brings him to a grand total of 17 thus far. he needed the transfusions because he still has a hard time making new blood as quickly as he breaks it down and they’re talking a lot of samples out to keep close track his immune blood counts while he has pneumonia. we were told today by nurse jan that, if things went as they expected, today’s transfusions would be the last he’s likely to receive during his stay in the nicu!

day 48: checking his lungs

eric’s lungs are sounding so good that it’s not really clear whether they’d still would say that he has pneumonia. in other words, he might just be fully recovered!

day 48: pooh borrows the cap

it’s interesting to note that while we were free to explore giving “directed donations” ( where we give the blood that eric would receive ), we didn’t because it apparently takes so long to process and screen the donations that they often get the donations back after they are no longer needed. also, the screening criteria for neonatal donations is so rigorous ( i.e. can’t have any antibodies for many common ailments ) that it’s often difficult for the parents to pass the screening test. so while the staff would never prevent us from giving blood, they’ve always strongly hinted that it’s easier, safer and faster to just get transfusion from their trusted pool of special neonatal donors.

day 48: ending the day with a little 'roo

because they have to monitor his blood pressure and other vitals closely during the transfusion, there’s no kangaroo care to be had during the process. of course, kris wasn’t going to let let three transfusions get in the way of lots of kangaroo care, so she simply had to time the sessions differently than normal. speaking of timing, while you might think that we can just waltz into the nicu and do the ‘roo, in addition to having to work around the transfusions, we also have to be aware of the nurses rounds which occur every two hours. and it’s also nice to get the kangaroo care in while he’s on the nasal cannula as the cpap mask can have a hard maintaining a good fit while he’s doing the ‘roo. so there’s quite a few “knowns” that we have to deal with in addition to the usual array of “unknowns”, such as getting kicked out abruptly in the evening, just after kris had settled in with eric, to prepare for two new admits.

the eric update – day 47: 3 pounds! no ROP ( yet )! the return of the nasal cannula!

day 47: 3 pounds! I.

wow! a mere 16 days after hitting 2 pounds, eric weighed in at 1370 grams tonight! or 3 pounds 0.3 ounces! it’s absolutely stupendously amazing that he’s gained a whole pound in such a short time, especially when he’s been so sick.

day 47: 3 pounds! II.

i guess he really does have the snowdeal genes, since putting on weight has never really been a problem for generations of snowdeal men. it’s amazing to see how quickly his appearance is changing on a day-to-day basis with the weight gains.

day 47: plumpy.  I.

eric is also getting 4 cc’s of breastmilk every 2 hours. he has a long way to go to be considered on “full feeds”, as he’d need to be getting about 19 cc’s of milk every two hours before they’ll discontinue his IV completely. still, he’s making great progress and seems to be tolerating the milk quite well.

day 47: plumpy.  II.

and he has a mere 2 days left on his antibiotic regime to treat the pneumonia and suspected sepsis. interestingly, after all the hullaballoo surrounding the sepsis it appears that the gram negative stuff they found in the yeast culture was likely a contaminant. i guess that’s the way it works sometimes.

day 47: back on the nasal cannula. I.

also, the eye doctor came by for his regular ROP checkup and didn’t detect any sign of abnormal blood vessel growth in his retinas. while this is great news, the doctor felt the need to warn us that not only was eric not out of the woods – he wasn’t even in the woods yet! now that’s some smooth bedside manner. he then stated matter of factly that eric’s most vulnerable stage will be between 33 and 39 weeks and that most 24 and 25 weekers will develop stage I or stage II of the condition. so, once again, while we’re extremely happy that his eyes are fairing well, his next few checkups will be the ones that will really give a better idea of if he’ll develop ROP.

day 47: back on the nasal cannula. II.

and just as we suspected, they’ve started testing eric out on the nasal cannula again, with 2 hours of nasal cannula, followed by 6 hours of cpap. and despite my many attempts to miminize the appearance of one of the side effects of the cpap mask, sometimes it’s impossible to hide the conehead that he can get from the tight cpap straps pushing against his very soft head.

he seems to be tolerating the nasal cannula very well and is continuing his streak of remaining alarm free! that’s right – he hasn’t had a single incidence of apnea or bradycardia. it really is hard to believe that he’s showing such great improvements in such a short period of time. i guess it’s hard to remember that things can get better just as quickly as they can turn for the nurse. such is the way of the nicu.