Our
most recent Wednesday clinic at Children’s was fairly productive. The two-hour albumin infusion Annaka now gets
every week, which moves much of the excess tummy fluid into her bloodstream and
is followed by a ten-minute Lasik infusion that flushes it out her kidneys,
worked well. The decreased belly size
allows her to breathe easier, which lets her do everything else easier,
too. She was super-talkative all evening
and spent a good chunk of time chewing on her toes, a normal baby privilege in
which she so rarely gets to indulge.
As always, we met with one of her doctors, who
classified her as “stable sick.” She
still needs a new liver, but she isn’t really getting any worse, or at least
not quickly enough to cause him concern.
Six weeks ago, however, this was not his diagnosis. When he saw her in the hospital during her
first bacterial infection of the summer, he said she would need a new organ
within two months. Well, we’re creeping
up on the two-month mark and as of right now her surgeons seem confident they
can wait for an organ more suitable for her size.
This is both good and bad. Obviously we want her to get the best organ
available even if it means being patient, and yes, we have struggled with all
the moral and ethical grayness that desire brings with it. At the same time, though, waiting is
hard. She is sick and we want her to get
better. Much of our lives are kind of on
a “pause” button. Her babyhood, like all
babyhoods, is fleeting. We have already
watched our other two children grow up too quickly, and so we are stuck between
this yearning to keep her little and an intense desire to wade through this
mucky season as quickly as we can.
As always, though, each visit to Children’s carries
with it yet another visceral reminder that things could be much, much
worse. It seems that in every elevator
ride, we meet yet another family struggling through a diagnosis we can barely
fathom.
I’ve mulled over Annaka’s ability to stay stable. Much of it has to do with the prayers, of
course, and her doctor called her a “fighter,” which I think is true. (Anytime I get close enough, she eagerly scratches
or slaps my face.) There’s more to it
than mere disposition, though. Annaka is
the product of great parenting, and what I mean by that is, she has the best
mom in the world.
I know I’m biased, but consider these facts:
For starters,
her mom is basically a nurse without the crazy hours and student debt.
JaLana’s
background in science, especially anatomy, and her almost manic attention to
detail makes her more than just a well-informed advocate. When the doctors or nurses throw around all
that medical terminology, JaLana actually understands what they’re saying. She asks questions that sound like they’re
coming from a med student because she has spent a crazy amount of time doing
research on Annaka’s condition and a thousand other potential conditions. Granted, this has meant she doesn’t really
sleep, but it also means that she can not only care for Annaka’s current needs,
she already knows what her needs might be weeks, months, years down the
road. So I’m not at all embarrassed to
say that my role in all this is to play with Annaka, change diapers, drive them
places, and wash the insane amount of bottles used each day. I teach English. I know my skill set, and it isn’t flushing
the Broviac.
Secondly, her mom is a grocery store.
JaLana chose to nurse our other two kids to good
results and was determined to do the same with Annaka. Buffeted by mounds of
research and multiple G.I. doctors telling her how good it was, JaLana has
endured the intense schedule that providing homemade milk has required, which
currently looks something like this:
Around 9:00 P.M. she expresses milk to put into
Annaka’s overnight bag. This milk is
fortified with a high calorie formula especially designed for babies with liver
failure. This milk is fed through
Annaka’s N.G. tube at a rate of 50 milliliters per hour. She is supposed to get 500 milliliters
overnight, so it’s a ten-hour session.
Around 10
P.M. Annaka receives 4 different medicines and her broviac line is flushed to prevent
a blood clot from forming in the line.
At 1:30 A.M. JaLana wakes up and expresses more
milk. This usually takes about fifteen
minutes. She then mixes the milk with
the formula and adds it to Annaka’s overnight bag. If JaLana is super-lucky she might be back to
sleep by 2:15 A.M., but this rarely happens.
At 5:00 A.M. JaLana wakes up to express more
milk. This milk will later be frozen and
stored for future use. She has to
express this milk, though, in order to keep her supply where it needs to be. If she slows down her schedule, her body will
stop producing. This summer she has been
able to go back to sleep after this, but starting next week, once school
starts, she will be up for the day.
Around 8:00 A.M. or so, she will express more
milk. This will become Annaka’s 11:00
O’clock bottle.
Annaka usually gets off her overnight feed between
nine and ten in the morning. Because of
nasal drainage, she throws up every morning.
Every day, without fail, she will throw up, often on me. Kind of gross,
but it’s the only way her little body can get rid of all the mucus that has
built up overnight. Somewhere between throwing up and her 11:00 O’clock bottle,
we give Annaka her seven morning prescriptions.
JaLana will express again around noon, depending on
the day’s schedule. Annaka usually
drinks anywhere from one to two ounces of her 11:00 bottle and then has to be
tube fed the remaining two ounces. Annaka
has to get four, four-ounce bottles during the day, each of which are fortified
with the high-calorie formula. Each
feeding usually takes about an hour, and is the only way she can gain any weight.
JaLana will express again in the late afternoon,
around 2:00pm. Annaka takes a bottle at
two and at five and at eight, so, from two to three, from five to six, from
eight to nine, she is being fed a bottle, most of it through her N.G.
tube. She is often asleep for much of
this; sometimes she is awake and tries to grab her tube, or, for extra good
measure, she fills her pants and leaks some on my lap.
JaLana will express again around 9:00pm to start the
cycle again. In a 24 hour period, we
freeze about ten, six ounce bags of milk.
It’s insane. If breast milk was
cocaine we’d have a yacht the size of a barn.
But hey, it absolutely has played a huge part in keeping Annaka as
healthy as possible, and all that frozen milk will also play a part down the
road.
Finally, her mom is in her face.
When Annaka sleeps during the day, saturated as she
is by intense sibling noise, JaLana often holds her so she stays asleep,
knowing she needs the rest. When Annaka
sleeps at night, JaLana takes the first shift on the couch. (Someone has to sleep next to her in case she
throws up at night, which she often does)
During the day, when Annaka is awake, JaLana makes sure she has some
kind of human interaction. This is how
babies learn best, and since Annaka has so few waking hours, compared to most
babies, JaLana tries to get the most out of them by reading to her, talking to
her, playing with her. I do too, of
course, but I would also be content to just pop her in one of those baby
jumpers on occasion. If JaLana has
anything to do with it, though, Annaka is getting talked to by someone.
Regardless, at the beginning of this summer, we
assumed the transplant would be complete before we went back to school. I think the doctors thought that too, but
here we are, less than a week from going back, looking forward to September and
hoping that with it comes a new body part.
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