Ketchup is delicious. Even if you spell it "catsup". It's just the best. John doesn't think so, he's a mustard kind of person. Ketchup is also awesome because it doubles as fake blood... fake blood you can dip your fries in!
It's late, can you tell?
Anyway, the last several days have all blended together in my head, so none of this is going to be chronological and it's really just going to be the highlights.
My brother Tyler came to see Ruthe. My mom may have bribed him with dinner, but he still came and held Ruthe for a quite a while. She was asleep, and after too long so was his arm! That happened to me today, too. Ruthe's big ol' head has a way of finding your nerves and pinching them juuust right!
Ruthe is such a well-behaved baby. Really. She hardly ever fusses. And when she does, her binky will calm her right down. If she's mad about needing her diaper changed, she'll tell you about it until you're done and she's clean and that's it. If she doesn't want to be swaddled she'll wriggle herself out of it. If she thinks you're boring or too loud or anything isn't exactly how she wants it she'll just fall asleep. [Or fake sleeping until all her demands have been met.] She's so well-behaved, in fact, that the nurses rarely check on her. They do their "cares" every three hours when she eats. They take her temperature, change her diaper, give her any meds she's scheduled for, and sometimes measure her girth or listen to her chest and belly. But that's really it. Sometimes when I go in to visit her I'll be there for an hour before I even see a nurse. One side of my brain tells me that's a good thing - because the nurses aren't expecting Ruthe to need any other medical care other than what's scheduled and normal. The other side of my brain is screaming, "Why are you not right here next to my baby at all times watching her like a hawk in case of an emergency??!'
After Ruthe's swallow-study, the speech therapists decided that they need to be the only ones giving her a bottle everyday. And then I heard that either them or the nurses could do it. And then the nurse told me it was only speech therapy. And then the speech therapist said she thought the nurses were still doing it on the days they couldn't. Long story short, Ruthe missed three days of bottle-feeds and I was one confused and upset mess of emotions. Obviously I want Ruthe to learn to eat from a bottle. And obviously I want a trained professional to be the one teaching her. My vote was always for speech therapy to come in everyday and work with Ruthe. I feel like that's more consistent than anything else, and will help her get the hang of feeding herself. [It's also a little bit because I spent twenty minutes watching one of the nurses trying to figure out how to assemble and use the special-needs bottle they prescribed Ruthe, and that just seemed a little wrong.]
Once a week they change out the feeding tube in Ruthe's nose. So the other night, maybe Monday, the nurse took out her old tube and replaced it with a new one. Ruthe HATED that. I'm sure it's uncomfortable in the first place, but the nurse didn't really listen when I said she has a cleft palate until he saw the tube curled up in Ruthe's mouth. The second try didn't even get it past her nose. Finally, after listening to her cry [and I mean really cry with tears and a red face and everything] for what felt like hours the tube was in, all the way, and the nurse could start her feed. Well, when I got to the hospital the very next day, Ruthe's feeding tube was going in her mouth. Ummm... why? Well, because the day-shift nurse knows that when a baby has a nasal cannula the standard procedure is to NOT put anything else in the baby's nose, to keep it from getting crowded or blocked or whatever. So she took the tube back out of Ruthe's nose and stuck it down her throat through her mouth. I was so confused, again. Thankfully I wasn't there while they were doing that again, because I probably would have just unhooked everything and taken Ruthe straight out of that dang hospital once and for all. I just couldn't comprehend why the nurse would think it was a good idea to put Ruthe through that kind of torture twice in twelve hours. And, talking to other nurses and doctors about it, I learned that if speech therapy is concerned that having the tube in her mouth will cause even more problems with her eating from a bottle and swallowing, they'll move it back to her nose.
The hospital has implemented a new security-system for visitors. In theory, it's a great system and I'm really happy with it. In practice, I have to stand in line for thirty minutes to get a visitor's badge. Standing in line isn't really the problem... it's standing in line behind so many unprepared people visiting moms and healthy babies that get to go home in a few days that really irks me. The security guards ask for a valid ID and the patient's last name and visitor's code. The ID is no problem, the last name is easy-peasy, the dang security code is where we hit the snag. My personal opinion is that if you don't know the code you should have to step aside and call the patient yourself to get it, so the next person in line can get through. Nope. The security guard looks up the patient's room number and calls up to ask them specifically if the visitors are welcome. And then takes their picture and scans their ID. It kills me. I have the least amount of patience standing in that line. And I've been asked by more people if I speak Spanish [and can explain the process to them] in the last three days than ever before in my life.
I realize that all of those things are complaints. But this was a very complain-y week for me so far. I finally hit that wall where I'm sick of the hospital and I feel like no one's doing anything and I'm sure I could take better care of Ruthe myself at home anyway and I just really really need things to be happening faster. It doesn't help that John isn't here, either. I just couldn't find anything positive about Ruthe being in the hospital. I asked John last night, in tears, why I couldn't just bring her home now with a little oxygen while she sleeps and her feeding tube for me to feed her with, and take her to the hospital once a day for an appointment with speech therapy.
There's a sign by her bed that has a checklist that needs to be completed before a baby can go home.
Ruthe's looks like this: The one in my head looks like this:
[X] I am in a crib. [X] I am in a crib.
[ ] I am gaining weight. [fatty] I am gaining weight.
[ ] I have passed my car-seat test. [sure] I have passed my car-seat test.
[ ] I passed the hearing screening. [whatever] I passed the hearing screening.
[ ] My family is ready for me. [YES!] My family is ready for me.
She hasn't actually had the hearing screening or car-seat test yet, but whatever. I don't care if she can hear me and her twelve pound head will fit safely in a car-seat, I just want to snuggle her.
But now I have my own checklist and here's how it's going...
[X] Ruthe's nurses check on her as often as necessary, and they do respond whenever her monitors alert them of a potentially risky situation.
[X] Ruthe is on the daily schedule for speech therapy to try bottle-feeding, and I can call to check the time of that appointment so I can be present to watch and learn.
[X] Ruthe isn't going to remember how horrible the feeding tube is, and the doctors and nurses know best how to deal with a baby that needs special considerations.
[X] Crazy people are much less likely to get past the new security-system to come in and injure or steal my baby. Also, it's better people-watching.
[X] The doctors are always there to answer my questions and listen to my concerns, but Ruthe's health care is their ultimate priority whether I understand their processes or not.
Showing posts with label diGeorge Syndrome. Show all posts
Showing posts with label diGeorge Syndrome. Show all posts
August 21, 2013
August 11, 2013
one month.
Ruthe Clementine is one month old! She was not a fan of her photo-shoot. It might have had something to do with the fact that we woke her up in the middle of her early-evening-nap... She was also a little mad at my mom, who told her that there would be cupcakes and then didn't deliver. I won't lie, I was looking forward to cupcakes, too.
We are just incredibly smitten with this girl. Everything she does is absolutely adorable. And she knows it. She thinks it's hilarious. I catch her every now and then with a little smirk on her face because she knows we're all wrapped around her tiny fingers. :)
I asked her nurse for her most recent weight, an last night she came in at a whopping 7lbs. 14oz.! If you remember, that's four ounces up from her birth weight. She was down to 6lbs. 8oz. at one point, so she's definitely headed the right direction now. Even if it is mostly in her chubby cheeks!
We also got the results back from her blood tests. The doctors were concerned that she might have some problems with her immune system, caused by the diGeorge Syndrome. All the tests came back completely normal! It is something that can change, so we'll have to have the tests run again after a while. And Ruthe will be referred to an immunologist for a follow-up, and possibly a closer look at all her immuno-globulin and t-cell levels. But for now we are just really happy that she's not going to be the-girl-in-the-plastic-bubble!!
AND we got a bow to actually stay in her hair!! She still only has that little Alfalfa-esque spike on the very top of her head, but it's finally long enough to collect all the hair into it a little tuft for a clippie.
We are just incredibly smitten with this girl. Everything she does is absolutely adorable. And she knows it. She thinks it's hilarious. I catch her every now and then with a little smirk on her face because she knows we're all wrapped around her tiny fingers. :)
I asked her nurse for her most recent weight, an last night she came in at a whopping 7lbs. 14oz.! If you remember, that's four ounces up from her birth weight. She was down to 6lbs. 8oz. at one point, so she's definitely headed the right direction now. Even if it is mostly in her chubby cheeks!
We also got the results back from her blood tests. The doctors were concerned that she might have some problems with her immune system, caused by the diGeorge Syndrome. All the tests came back completely normal! It is something that can change, so we'll have to have the tests run again after a while. And Ruthe will be referred to an immunologist for a follow-up, and possibly a closer look at all her immuno-globulin and t-cell levels. But for now we are just really happy that she's not going to be the-girl-in-the-plastic-bubble!!
AND we got a bow to actually stay in her hair!! She still only has that little Alfalfa-esque spike on the very top of her head, but it's finally long enough to collect all the hair into it a little tuft for a clippie.
August 7, 2013
days 27 and 28.
Ruthe is ALMOST too boring to keep posting about her every day. That, and I'm getting lazy.
Yesterday the speech therapist came to evaluate Ruthe's feeding skills. They tried feeding her with a regular bottle, and with a special-needs bottle for babies with a weak suck. Ruthe just can't quite figure out what the bottle is for. I'm sure if she knew how wonderful eating can be she would totally get on it! But as it is, she just can't suck well enough to get any milk out of the bottle, and then she has no idea that she needs to swallow the milk she does get. The therapist showed me how to squish her cheeks together while she's sucking to help her get better suction, so I try to do that every now and then with her binky. They're going to keep working with her, just once a day for now, to strengthen her mouth. This is really our only obstacle before taking her home, so I'm just a little antsy, but she can take her sweet time if she needs to. In can wait until she's ready. :)
Her surgeon also came in last night to take out her RA line. That was the IV going into her heart. She had been sound asleep for four hours (I know because that's how long we waited for the surgeon to get here.) so when the anesthesiologist came in to give Ruthe a little sleepy-juice we thought how perfect, she'll never even know what happened. Um... no. Ruthe woke up just as we were leaving and stayed WIDE AWAKE through the entire thing. It only lasted about three minutes, but apparently she was up and screaming at the doctor the whole time.
I don't blame her. They had to stop her feed at two o'clock, because they wanted her to have an empty stomach for the procedure at four. It didn't happen until seven-thirty. I'd scream through a procedure if I woke up that hungry, too! And the nurse didn't get her next feed started until after eight. Poor girl.
Today was nice and boring. I went over in the morning and got to hold her for a nice long time. The cardiologist did an echo to check out the bands and stent. Everything looked good. She was a little fussy at the beginning of it, but then she tooted [a lot] and was a peach for the rest of the time.
I asked one of the neonatologists that are in charge in the NICU if there are any specific questions I should ask when trying to pick Ruthe's pediatrician. The insurance company sent me a booklet of in-network providers and the pediatrician list is five pages long... Dr. Ramsay told me to make sure the pediatrician feels comfortable treating a baby with CHD, a cleft palate, and diGeorge Syndrome. I think it's ridiculous that Ruthe even needs a regular pediatrician. She'll be seeing her cardiologists at least every couple weeks for a while, she'll have physical and speech therapy, she needs to see an immunologist for evaluations and tests, and at some point we'll have to find someone to look at and correct her cleft palate. Surely one of those doctors could handle her shots and measurements. It's like they all want me to go crazy!
My parents went to the hospital this evening. Yesterday was the first time my dad held Ruthe, and my mom took a picture of the momentous occasion... and she apparently doesn't know how to use my dad's phone because the picture came out as a blurred view of his head. So tonight was take-two.
Someday we'll have her at home, and all our pictures won't be in those funky yellow parkas.
Yesterday the speech therapist came to evaluate Ruthe's feeding skills. They tried feeding her with a regular bottle, and with a special-needs bottle for babies with a weak suck. Ruthe just can't quite figure out what the bottle is for. I'm sure if she knew how wonderful eating can be she would totally get on it! But as it is, she just can't suck well enough to get any milk out of the bottle, and then she has no idea that she needs to swallow the milk she does get. The therapist showed me how to squish her cheeks together while she's sucking to help her get better suction, so I try to do that every now and then with her binky. They're going to keep working with her, just once a day for now, to strengthen her mouth. This is really our only obstacle before taking her home, so I'm just a little antsy, but she can take her sweet time if she needs to. In can wait until she's ready. :)
Her surgeon also came in last night to take out her RA line. That was the IV going into her heart. She had been sound asleep for four hours (I know because that's how long we waited for the surgeon to get here.) so when the anesthesiologist came in to give Ruthe a little sleepy-juice we thought how perfect, she'll never even know what happened. Um... no. Ruthe woke up just as we were leaving and stayed WIDE AWAKE through the entire thing. It only lasted about three minutes, but apparently she was up and screaming at the doctor the whole time.
I don't blame her. They had to stop her feed at two o'clock, because they wanted her to have an empty stomach for the procedure at four. It didn't happen until seven-thirty. I'd scream through a procedure if I woke up that hungry, too! And the nurse didn't get her next feed started until after eight. Poor girl.
Today was nice and boring. I went over in the morning and got to hold her for a nice long time. The cardiologist did an echo to check out the bands and stent. Everything looked good. She was a little fussy at the beginning of it, but then she tooted [a lot] and was a peach for the rest of the time.
I asked one of the neonatologists that are in charge in the NICU if there are any specific questions I should ask when trying to pick Ruthe's pediatrician. The insurance company sent me a booklet of in-network providers and the pediatrician list is five pages long... Dr. Ramsay told me to make sure the pediatrician feels comfortable treating a baby with CHD, a cleft palate, and diGeorge Syndrome. I think it's ridiculous that Ruthe even needs a regular pediatrician. She'll be seeing her cardiologists at least every couple weeks for a while, she'll have physical and speech therapy, she needs to see an immunologist for evaluations and tests, and at some point we'll have to find someone to look at and correct her cleft palate. Surely one of those doctors could handle her shots and measurements. It's like they all want me to go crazy!
My parents went to the hospital this evening. Yesterday was the first time my dad held Ruthe, and my mom took a picture of the momentous occasion... and she apparently doesn't know how to use my dad's phone because the picture came out as a blurred view of his head. So tonight was take-two.
Someday we'll have her at home, and all our pictures won't be in those funky yellow parkas.
August 2, 2013
day 23.
Ruthe has got all sorts of tricks up her sleeve! Or, in this case, up her chromosomes.
Our little nugget was diagnosed with diGeorge Syndrome. It's a disorder caused by a deleted portion of genes from her 22nd chromosome. There's a chance that it came from me or John, or that it occurred all on it's own. There are some other problems that Ruthe might have or develop, related to diGeorge Syndrome, but for now we're just happy to know where her heart defect and cleft palate came from!
And since we're dishing out the results of all Ruthe's recent tests, she's also positive for VRE. That's vancomycin-resistant enterococci. Enterococci is a bacteria most commonly found in the intestines that's become resistant to the antibiotic vancomycin. Ruthe's not sick from it, she just has the bacteria. She most likely got it from the hospital, although it could have been me or John or any of her many visitors. I'm not trying to point a finger, I just want to emphasize the fact that she isn't sick with an infection. someone could have VRE for their entire life and never develop an infection, or experience any symptoms because of it. If she does develop an infection from it though, it can be treated with different antibiotics.
Because she's VRE-positive, Ruthe was moved yet again. This time just to a new spot in the NICU. The NICU at Sunrice is divided into six[ish?] pods, and each of those pods has several wings, each housing three or four little nooks for babies. The wing that Ruthe was in when they got her test result back also housed a baby that could get seriously ill if they were exposed to VRE and developed an infection from it. Since Ruthe's such a trooper [and has way less machines to transfer along with her] we scooted her little bed into another wing at the end of the pod. We still have to wear all the isolation gear whenever we go to see her, and we'll have to until she comes home, but being at the very end of the pod is great! Ruthe's little nook is extra spacious, so we swiped a second rocking chair to keep in there for our night-time visits. :)
Ruthe's recovery - 15 minutes, one day, three days, and one week post-op. |
Our little nugget was diagnosed with diGeorge Syndrome. It's a disorder caused by a deleted portion of genes from her 22nd chromosome. There's a chance that it came from me or John, or that it occurred all on it's own. There are some other problems that Ruthe might have or develop, related to diGeorge Syndrome, but for now we're just happy to know where her heart defect and cleft palate came from!
And since we're dishing out the results of all Ruthe's recent tests, she's also positive for VRE. That's vancomycin-resistant enterococci. Enterococci is a bacteria most commonly found in the intestines that's become resistant to the antibiotic vancomycin. Ruthe's not sick from it, she just has the bacteria. She most likely got it from the hospital, although it could have been me or John or any of her many visitors. I'm not trying to point a finger, I just want to emphasize the fact that she isn't sick with an infection. someone could have VRE for their entire life and never develop an infection, or experience any symptoms because of it. If she does develop an infection from it though, it can be treated with different antibiotics.
Because she's VRE-positive, Ruthe was moved yet again. This time just to a new spot in the NICU. The NICU at Sunrice is divided into six[ish?] pods, and each of those pods has several wings, each housing three or four little nooks for babies. The wing that Ruthe was in when they got her test result back also housed a baby that could get seriously ill if they were exposed to VRE and developed an infection from it. Since Ruthe's such a trooper [and has way less machines to transfer along with her] we scooted her little bed into another wing at the end of the pod. We still have to wear all the isolation gear whenever we go to see her, and we'll have to until she comes home, but being at the very end of the pod is great! Ruthe's little nook is extra spacious, so we swiped a second rocking chair to keep in there for our night-time visits. :)