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Archived
Updates: SCVMC Rehab
Updates (Read chronologically from bottom to top) September 14,
2004 September 12,
2004 September 9,
2004 September 7,
2004 September 4,
2004 September 1,
2004 August 29,
2004 August 26,
2004 August 24,
2004 August 23,
2004 August 22,
2004 August 19,
2004 August 17,
2004 August 16,
2004 August 15,
2004 August 13,
2004 August 12,
2004 August 10,
2004 August 8,
2004 August 5,
2004 August 3,
2004 August 1,
2004 July 30,
2004 July 29,
2004 July 28,
2004 July 27,
2004 July 26,
2004 July 24,
2004 July 22,
2004 July 21,
2004 July 19,
2004 July 18,
2004 July 17,
2004 July 15,
2004 July 14,
2004 July 12,
2004 July 11,
2004 July 11,
2004 July 9,
2004 July 8,
2004 July 7,
2004 July 7,
2004 July 5,
2004 July 3,
2004 July 1,
2004 July 1,
2004 June 30,
2004 June 29,
2004 June 26,
2004 June 26,
2004 June 25,
2004 June 24,
2004 June 23,
2004 June 22,
2004 June 21,
2004 June 21,
2004 June 19,
2004 June 18,
2004 June 17,
2004 June 16,
2004 June 15,
2004 June 13,
2004 June 13,
2004
Santa Rosa: April
11th - May 11th
Early SCVMC rehab: May 11th -
May 20th
SCVMC ICU:
May 21st - June 10th
SCVMC Rehab (round two): June
11th - September 14th
Home in GV: September 14th - April 11th 2005
Home in GV: April 11th 2005 - August 26th 2006
My new life
4:33pm
As of 2:15pm this afternoon Jill is no longer a
resident of SCVMC! She's currently with my parents on the road headed up to
Grass Valley. We had a successful night in the "VIP House" yesterday with tons
of visitors. The VIP House is a little 2-bedroom house on the grounds of the
hospital that they sent patients, along with their families, to stay in for a
trial run right before discharge. She has had two incredibly hectic days getting
ready for the move. Just about every doctor that she has seen throughout her
stay at SCVMC came to say goodbye in the morning. For lunch, she hung out with
Jared (a fellow rehab patient) and Julie (a friend from rehab that was
discharged a while ago, but came back to see Jill off). I'm guessing that
tonight will be the most relaxing sleep session that Jill has experienced in ~5
months.
Administrative note...don't worry, I plan to update this page on
about the same frequency that I have been for the last few months. Even though
she is out of the hospital, Jill has lots of hard work ahead of her. I don't
plan to stop updating this site until Jill decides to take it on for herself...
-Dan
9:05pm
The big move is rapidly approaching... My parents
seem to have everything all set up for her return home on Tuesday. Jill will
start working with therapists up there on Wednesday (I think that maybe she was
hoping to get a few days off therapy but no such luck...oh well). She has
started the process of saying goodbye to all of her friends from the hospital.
Yesterday marked the 5-month point in Jill's recovery from her
injuries.
-Dan
9:50pm
Jill had a full day of rehab and visitors today as
usual. She has another off-site pass for this weekend. It will probably be used
to go over to the coast for lunch and some rest on Sunday. It is amazing that
she only has ~5 more days left at SCVMC. My parents have been working like mad
to get everything in line back home for her return. It will definitely be a
tough transition for the whole family, but we are all (especially Jill of
course) getting pretty tired of sleeping away from home and eating take-out.
In other news...Jill got to send off one of her long time rehab buddies
today. They have definitely been through a lot together - Congratulations Julie!
-Dan
9:56pm
Jill had a pretty good weekend. It was nice for her
to get an extra day off from therapy. The ~8 hour trip to Grammys house this
weekend went very well. The weather was beautiful for the bbq in San
Rafael/drive through the city. Lots of relatives came to hang out with us and it
ended up being quite the labor day weekend get-together. Jill's felt good enough
to socialize for a few hours before she had to take a little nap to recharge.
Coming back to all of the lovely sounds of the hospital wasn't so exciting in
the evening though. After a day of rest yesterday, she is back into the therapy
routine. Her schedule is getting pretty hectic as the therapists try to make
sure that everything is taken care of for Jill's discharge next week... After
she leaves SCVMC next Tuesday, Jill will continue to work on her recovery at my
parents house until she is able to get back out on her own.
-Dan
3:50pm
Jill has been doing pretty well for the last few
days. She gained some of the weight back that she lost last weekend and seems to
be feeling a bit better still. Yesterday she was able to push herself even
farther in the wheelchair than her journey on Wednesday (from her room out to
the patio). There are two really exciting pieces of news to report today...
First of all, Jill has been cleared to get back on a normal diet! She is no
longer forbidden to eat good things like dairy, chocolate, nuts, and legumes any
more! Her doctors want her to ease back into those foods slowly, but it is nice
for her just to get a taste of them. The other piece of good news is that she
got an "off site pass" for tomorrow. We are going to go up to my grandma's house
in San Rafael for the day. It should be nice and relaxing to get out of this
hectic place for a little while. And now...Jill has a message(I'm writing this
update from the hospital):
Thank you for everything during this hard
time. And, thanks to my parents and brother for everything. I love you guys!
-JILL (!) and Dan
9:58pm
Jill has been eating well this week and seems to be
done with the stomach problems for the time being. She still has to be on the
limited diet, of course, but she is eating in far greater quantities than over
the weekend. She had a lovely evening of visitors tonight. A big group of her
friends from both SJSU and Santa Clara joined her for dinner. She seemed to
enjoy the company quite a lot.
Her wheelchair mobility has improved
lately. She pushed herself on the long trek from her room to the other side of
the nurses' station before dinner tonight. In addition to her manual chair, she
has an electric chair that gets her around a little faster. I modified it so
that she has to drive with her "bad" hand (the right) and we have seen some
pretty impressive improvements to her right-hand fine motor skills since the
change.
-Dan
10:08pm
Jill actually had sort of a rough weekend. She came
down with a nasty little stomach bug on Friday night and it gave her trouble
until Sunday morning-ish. She didn't eat all that much and she had a hard time
getting any fluids down (that is, until the doctor on call threatened her with
an IV...). This evening she did much better though - for the first time since
Friday she actually wanted to eat and drink. The eating thing is further
complicated by her restricted diet (due to a medication that she is on, she
can't have all of the feel-good foods that have cheese, nuts, chocolate,
legumes...among other limitations). She really needs to gain some weight back,
but it's hard without being able to eat all of the good stuff...
In
addition to a case of the flu this weekend, she was a little bummed as well. We
are starting to plan for her return to my parents house and it gets her
thinking about how much her life has changed since the accident. The fact that
her memory and logic are getting much better makes it a bit more difficult to
deal with emotionally.
On a good note - despite the setbacks she
continues to work like mad on her recovery.
-Dan
10:29pm
?... So Jill will be moving back up to her old unit
tomorrow morning sometime. She will have her own room and the rumor is that
it'll be #43. There is no good explanation for her changing rooms and units all
over the place the last few days. I think that it all boils down to some
insurance issues and trying to find the right combination of therapists and case
managers. All of the moving is a pain but it's definitely keeping Jill on her
toes. She was doing extremely well tonight. Her right hand is still weak, but
she has definitely regained some of her fine motor control.
-Dan
11:27pm
Jill is all settled in down in the spinal cord unit
now (1st floor room 19). Her new room is a bit roomier than the ones upstairs,
and the spinal unit seems to be a bit more peaceful than the TBI unit is. It
will take a little while to get acclimated to the new nurses and a slightly
tweaked schedule, but Jill seems to be dealing with it well. After dinner
tonight we went up and visited some of her old buddies from upstairs for a
while. It is amazing how comfortable (?) we had become with that place after
being there for a few months...
-Dan
10:08pm
Jill had a nice day today. There has been a slight
change in plans for Jill's living arrangement. Apparently she will be moving to
the spinal cord rehab unit (directly downstairs from where she is now) within
the next few days. While she is far from being "healed" from her brain injury,
her doctors think that she will benefit more from the activities offered by the
therapists down on the spinal floor. It will be a big change for her - new
doctors, new therapists, and different patients to hang out with - but she is
definitely up for it.
-Dan
10:56pm
Jill had a very enjoyable Sunday with lots of
visitors and feasting. For lunch, some family friends from GV prepared a nice
big meal. We enjoyed the perfect weather out on the patio. After a short
afternoon nap, Jill had a long evening visit with some of her SCU buddies. They
brought another feast and we chatted and ate until well past her bedtime. Two of
her very close friends are moving away in the next few days and they decided to
have the send-off party at the hospital with Jill. It was hard for her to see
them go, but it was great that she got to spend such a nice evening with them.
Jill's stamina while socializing has improved quite a bit in the past few weeks.
She still gets tired, but lately she's been able to tough it out when she's
having a good time.
In other news...Jill has changed rooms and has a
roommate now (as of Friday morning). It was nice when she had her own room, but
at least Jill was friends with the new roommate before she moved in. The young
lady had her accident around the same time as Jill's, and they have become
friends as they work through similar issues in rehab. It is room #21 on the same
floor.
-Dan
10:05pm
Today Jill got to cook dinner in a group with some
of the other patients and a therapist. They made taco salad and brownies. Jill
ate well and socialized as usual. It is still extremely difficult for her to use
her right arm for simple tasks though. She continues to work on it...
-Dan
11:04pm
It was another good day with lots of therapy for
Jill today. She got to go in the pool again today. Her muscles really seem to
respond well to the nice warm water. All else was pretty standard - therapy
during the day and visitors in the evening. Jill definitely enjoys her social
time...
-Dan
10:59pm
Jill did very well today. She had lots of therapy
all morning and then hung out with our aunt and cousin for the
afternoon/evening. My mom's big family has mobilized to keep Jill entertained at
the hospital since mom and dad had to go back to work (I can't believe that
school is starting already...). She dealt with their absence very well today. It
is really encouraging her to make steps towards independence. After dinner she
visited with some buddies and I. Not much new medical news these days (!).
-Dan
10:32pm
Jill had a very nice weekend with lots of visitors.
She has made some progress with pushing her wheelchair lately. It is still
extremely hard for her due to the stiffness of her right arm, but she is able to
move small distances. We went down to the ICU again tonight. This time we
actually got to go inside to see her old room. All of the nurses were extremely
excited to see her. She also got to meet the neurosurgeon that did her last
surgery. He was also very impressed with her recovery up to this point. One big
change for Jill is that our parents have to go back to work this week. She will
have relatives and buddies to hang out with (and me in the evenings), but it
will be different without the parents around (they'll still be around on
weekends of course). She is a little bummed, but it will let her become more
independent. She looks forward to going in the pool again this week. I think
that she'll get to swim 1-2 times per week or so.
-Dan
11:56pm
Jill had a great time in the pool today. She said
that it felt really good on her muscles to float around in the nice warm water.
She wore a floatation device and worked on her flexibility with the therapist.
All else is going well...
-Dan
10:10pm
Jill was doing really well tonight. She had some
visitors and seemed to have a grand old time. Her sense of humor is most
definitely intact these days. One very exciting piece of news is that she will
get to go in the pool tomorrow. The pool is used downstairs in the spinal unit
to help patients with flexibility and muscle tone. It will probably be a while
before she can really swim again, but I think that being in the water will help
her work harder towards that goal. She seems to be pretty excited about it. On
another note...thanks for the continued support from the Colorado Mason's. My
dad was out there last weekend for a funeral and they have been extremely
supportive through some tough times of their own...
-Dan
11:59pm
Jill is doing well today. She was pretty tired after
therapy and managed to fit in a pretty nice nap in the late afternoon (between
therapy and a few visitors in addition to my parents and I). She is completely
off of her most recent round of antibiotics as of Monday. This means that her
visitors no longer have to wear the little yellow hospital gowns when entering
her room (it was a precaution to keep from spreading the bugs to other
patients). Everything else seems to be plugging away as usual down at the
hospital.
-Dan
11:04pm
Jill is still doing extremely well. The last few
days have been full of therapy as usual. She is beginning to get the
functionality in her right hand back enough to push her own weelchair for small
distances. She is working extremely hard to get that arm working again. Today
(Sunday) was an epic day of relaxation for her. She slept in and ate all three
of her meals out on the porch to enjoy the day. The highlight of the day was a
lengthy rub-down from a family friend of ours who is a massage therapist. In
addition to sending Jill straight to heaven, it allowed her to relax all of her
muscles that were tired from a full week of therapy.
-Dan
11:13pm
Jill has had more good days lately. She has been
working hard and seems more determined than ever. Jill is starting to work on
"car transfers" with her physical therapist. This is the first step towards us
being able to take her off-site... Let's all hope that day comes
soon.
-Dan
11:19pm
Jill is back into the weekday grind of therapy. She
actually seemed pretty tired tonight, but her appetite is great and she's been
working really hard on her right arm.
She got some news on her planned
discharge date today. When she was admitted back in May, the date was set at the
middle of this month. Due to the fact that she is still showing significant
signs of improvement, however, that date is being pushed out 'till mid
September. It is a very good thing that her stay in rehab has been extended.
Despite the stress of living in a hospital environment, there is no way that
Jill could get the intensity and frequency of therapy that she gets here if she
was at home. It is great to look back at some of the earliest goals that were
set for her release...she has already surpassed many of those goals and
continues to improve each day.
-Dan
9:02pm
Jill had a pretty nice weekend. Saturday brought lots
and lots of visitors. In the morning she got to spend time with a bunch of
relatives and in the evening some college buddies brought her dinner and hung
out for a while. She was a trooper and stayed up in her chair for many hours. In
therapy yesterday she got to cook her own lunch (pizza). Today was a fairly lazy
day with no therapy. She just napped and lounged around...enjoying herself
thoroughly. The doctors continue to notch up the intensity/frequency of her
various therapy sessions so she definitely needs the rest...
-Dan
10:51pm
Jill had a great day yet again. This evening we took
a stroll to the other end of the hospital to bring her back to see the ICU
nurses. I think that it was good for her to see their reaction when she showed
up looking so great. One nurse came out of the elevator and paused there for a
minute with her mouth open she was so shocked to see Jill. Another exciting
event for the day was when her cast (right arm) got removed. They cut off a
section and put some more padding into it to make a splint. It seems to be more
comfortable than her old one. Today in OT before I came down she got to peruse
this very site on the internet. She emailed me at work to say that she approved.
-Dan
11:22pm
Jill had another very good day today. She had a long
discussion with my parents about Alan just before I arrived this evening. The
news has been tough for her, but it seems that some of the bad effects of her
brain injury (short term memory loss/reduced ability to concentrate) are
actually helping to damp out the initial emotional blow slightly. We are
extremely happy that the injury didn't rob her of the memories of what a great
guy Alan was.
Jill is really ready to get the cast off of her right arm.
She gets it cut off on Friday and is extremely excited about that...
-Dan
10:19pm
Jill had another productive day today - lots of good
therapy and socializing. Her memory has been gradually improving.
We had
our first discussion about Alan today. She was pretty upset about the whole
thing. She does remember Alan, but does not remember anything about the weekend
of the accident. It will no doubt take a long time for her to come to terms with
this terrible news.
-Dan
11:38pm
Jill had a pretty good day today. She is getting
lots better at being assertive with the hospital staff to get her needs met.
Today she got a big cast on her right arm to help it stay in the correct
position to heal. The cast will work in conjunction with an injection that she
got around a week ago to loosen up some of the tension in her wrist and hand.
The cast will be removed on Friday and used as a splint for a while therafter.
She continues to fight off this recent round of infections. They don't seem to
have any drastic effects on her mood and only reduce her stamina slightly.
Jill's appetite has been good and her therapy sessions have been productive.
-Dan
12:14am
Jill had a good day off today. She enjoyed lots of
lounging around and socializing. The infections that she has seem to make her a
bit more sleepy than usual, but overall she is in good spirits.
-Dan
10:45pm
Jill's condition is still improving daily. She
speaks more easily and is getting better about talking to her nurses and doctors
about her health needs. One minor setback is that she has come down with an
infection in her intestine. It doesn't seem to affect her mood all that much,
but we have to wear funny yellow gowns and gloves when we hang out with her.
Apparently this is a pretty common side effect found in patients that have taken
large quantities of antibiotics (the real irony is that the cure is ... you
guessed it - more antibiotics!). All of her therapy sessions have gone well
lately. Today in OT she got to use a computer for the first time since the
accident. She also works on pushing her wheelchair and assisting with her
chair-bed transfers. Her right arm is still very stiff, but she has definitely
improved its range of motion in the past few weeks.
-Dan
10:45pm
Jill had a pretty huge day today. Her doctors
finally cleared her to get rid of her back brace. It is amazing how much more
comfortable she seems to be without it. The scans taken last Friday show that
her spinal fractures are healing as well as can be expected. The other exciting
thing about tonight is that Jill actually got to leave the hospital grounds for
a little while. We went out to eat at an Italian joint a few blocks down the
road with 3 other patients and their families. This was Jill's first experience
with the real world since the accident so it was understandably a little
overwhelming for her. She dealt with it well, but she was extremely tired by the
time that we got back. She said that being in a wheelchair out in public kind of
bummed her out. One thing that is definitely still intact is her wit/sense of
humor. After we got back from dinner we had a great time chatting in her room
until bedtime.
-Dan
12:29am
Jill's doing well tonight. She is, however, still
waiting for the verdict on whether or not she can get rid of her back brace. All
of her docs have looked at it but now they want to get a second opinion from
some ortho guy in another part of the hospital. I'm pleased to see them take the
conservative approach...but Jill really just wants to get rid of that brace.
Jill's memory and brain function seem to be slowly improving still. It is sort
of tough though because, as she becomes more able to think about her situation,
she becomes more aware of the severe effects of the TBI that she is recovering
from (this makes it hard for her to see progress in her recovery at times).
Thank you all for supporting Jill through the ongoing recovery
process.
-Dan
9:29am
I forgot about this for last night's update. Another
event plug: (same idea...different location) Some close family friends from
Grass Valley are throwing a fundraiser for Jill on July 20th (tomorrow!) from
11am-9pm at Lamppost Pizza (on Olympia Park Road - near Brunswick Rd./Hwy 49
intersection). If you are hungry for pizza and are in the Grass Valley area,
please stop by and mention Jill's name with your order. They will donate a % of
the sale to her trust fund.
On that note...thank you all for showing up
to the event in Davis. Based on the reports that I got, it was quite a
gathering. The kind folks at Lamppost said that, while they do these events
quite often, this was one of the most successful that they have ever seen. We
told Jill about it and she was blown away. It really seems to help her knowing
that so many people care about her and want to help throughout the recovery
process.
-Dan
8:51pm
Jill had a nice and relaxing day today. She loves
Sundays. We had a really mellow lunch down on the front lawn of the Rehab
Facility. This was the farthest that she has ventured from her room since her
trip over from rehab. Jill seems to be extremely hit and miss on her short term
memory. One thing that she remembered this morning was that she had a CT scan on
Friday. The scan was to check the status of the surgical procedure performed on
her back - she was interested in being able to get rid of the brace that she is
required to wear whenever she is up in a chair. Even though Jill's memory isn't
yet what it used to be, she still jokes around with us quite a bit. Today I saw
her shiver for a second and I asked her, "What was that all about?" She said,
"It either means that I am cold...(she pauses and looks over at my dad)...or it
means that I need a back massage right now."
-Dan
10:18pm
Jill is still putting tons and tons of effort into
her recovery. One of the things that she worked on today was balancing herself
while sitting on a flat bed. She continues to show significant improvements on a
daily basis. She shows more determination than ever to get her right arm working
again and even uses it to push her own wheelchair in therapy occasionally. Her
short-term memory is slowly improving.
-Dan, Mom, Dad
11:39pm
Jill is doing great yet again today. We talked a lot
about the accident this evening. She is still (for good reason) struggling to
come to grips with the severity of her condition. This process is definitely not
aided by her memory issues. Each time that the subject comes up, however, she
seems to get a bit more complete picture of her prognosis. Jill enjoys all sorts
of food these days. She isn't too excited about the hospital rations, but she'll
wolf down all sorts of take-out that we bring in from the "outside". She is also
working hard with her right hand. She signed a birthday card for one of the
other patients today and really wanted to work on using the right instead of
left hand. Eventually she gave up and signed the card with her left hand, but it
was really cool to see her making the effort.
A few weeks ago Jill said
that she would like to put a message of her own up in the updates section (she
decided that after I told her about how people get updates about her condition
through the site). I reminded her about it tonight and she dictated the
following to my mom. I was extremely impressed with the appropriateness of her
comments.
To all-
Thank you for your support for the past however
many months. I really thank you all for your support of my family. I am doing
well in a wheelchair. Thank you all for sending cards over the course of this
hardship. Thank you all for visiting this site. I couldn't have made it without
you - neither could my family.
Jill
-Dan
12:24am
As of today, Jill's feeding tube has been removed
and she is cleared to drink water. It is amazing how enjoyable a drink of water
can be after 3 months without...
-Dan
11:57pm
The rehab doctors are starting to talk about
removing Jill's feeding tube in the near future. She has shown the ability to
eat enough by mouth to sustain herself. Water-thin liquids are the only things
that give her any trouble these days. It is pretty exciting for her to get that
silly tube out of her belly. Everything else went as planned today. Lots of
tiring and painful therapy sessions...
-Dan
9:49pm
Jill had some more birthday festivities today. We had
cake and ice cream down in the courtyard of the rehab unit after lunch. She has
been craving chocolate cake for quite a while now. We are starting to notice
some small improvements in Jill's memory and logic from day to day.
-Dan
12:46am
Jill had a very full day today. The blood clot
filter went in as planned in the late morning. The procedure was done down in
radiology under a light general anesthetic and took around an hour and a half to
complete. She seemed to be relieved after it was all through. She was pretty
nervous about it last night and this morning. She was tired in the afternoon due
to lack of sleep and the lingering effects of the anesthesia, but still managed
a few reasonably productive therapy sessions. This evening she had a pretty
special feast after her nap. Jill was actually able to eat pizza! She had been
craving it for a while, so this was quite a monumental occasion for her. Her
therapists have finally cleared her for pretty much a normal diet (although she
is still not allowed to have un-thickened liquids and foods that are overly
difficult to chew).
-Dan
9:42pm
Jill had a lovely birthday today, and greatly
appreciated all of the visitors, flowers, cards, and gifts. We spoiled her with
various forms of real food (burrito, smoothie, candy, cheesecake, pasta....).
She had lots of visitors which kept her nice and busy when combined with her
full therapy schedule. The physical/occupational therapists are beginning to
work with Jill on the muscle movements required to push her own wheelchair. This
is extremely difficult for her due to the lingering stiffness and range of
motion problems in her arms (especially in the right arm, which is nearly
immobile at this point...although it does seem to be improving slightly). In the
middle of the afternoon socializing session we got a bit of serious news about
Jill's medical condition. She will have a small "filter" inserted into a vein in
her abdomen to prevent a blood clot that has formed in her leg from traveling up
into her lungs. This commonly performed procedure for patients who are immobile
for a long period of time.
-Dan, Mom, Dad
11:58pm
More real food for Jill today. Instead of pureed
meals, Jill is now on the chopped food plan. This is good because it means that
her meals look (and taste) more like normal food. In addition to the hospital
rations, she got another smoothie today and some soft chocolates. The speech
therapist seems to be very impressed with how quickly Jill has re-learned her
eating skills. In other news, Jill got the cast on her left arm removed today.
She seemed pretty excited about having the cast gone. The hole from the trach
appears to be healing normally.
I am absolutely blown away when I look
back at how far Jill's come just in the past two weeks. She still definitely has
a long way to go - but she continues to fight like mad to recover from this
thing. Thank you all for your continuing support.
-Dan
9:05pm
Jill's trach is out! She seems to be talking ok still
(despite the doctor's warning that she may have troubles after the hardware
removal). When I talked to her tonight she was even more excited about the fact
that she got to eat a Jamba Juice along with her dinner. She has been getting
pretty bummed about her pureed mystery meals so the smoothie was a welcome
change.
-Dan
12:14am
Jill will have her trach removed tomorrow sometime.
The doc said that she'll probably have a hard time talking for a day or three
before the wound closes up. Jill is very much ready to get that thing out of
there. Also, an x-ray will be taken of her left arm/wrist to see if she can
finally get the cast off. Jill seemed to be in good spirits today. She ate well
all day (pureed food only still), and hardly requires tube feeding to supplement
her normal intake. Talking seems to be coming quite a bit easier for her these
days.
-Dan
11:39pm
Jill had a pretty good weekend. Her mouth and throat
muscles are starting to get used to eating again. The amount of tubefeeding that
she requires is greatly reduced. She had a few words with my parents about her
legs over the weekend. She seems to understand that something is terribly wrong
with them and has talked a little bit about being in a wheelchair. The regular
rehab schedule starts back up tomorrow. Hopefully this week she'll be able to
get rid of her trach and start eating some better food...
-Dan
1:06am
In just her second day of eating meals by mouth since
the accident, Jill has grown tired of the pureed mystery meat and mashed
potatoes - imagine that. She eats at least part of the meals like a good sport,
but has been asking for bigger and better things like chocolate cake, smoothies,
and pizza...and all sorts of other good stuff. The therapists are already
talking about trying her on very small and soft REAL, unblended food (like corn,
peas, or diced chicken meat) sometime within the coming week. Jill laughed a bit
for the first time today. It was not out loud, but it was definitely a prolonged
laughing spree. Jill's short term memory seems to be improving slightly although
it is still pretty sketchy. She still asks to go home with my parents and/or I
just about every evening, and has trouble understanding why she can't simply
leave the hospital. As she becomes more aware of her own condition she struggles
to comprehend the severity of the injuries that she has sustained.
A
quick programming note: I'm taking a few days away from computers this weekend
so I probably won't be able to do another update 'till Monday night or so. Have
a safe and enjoyable 4th.
-Dan
10:19pm
Jill had her first meal (by mouth) since the
accident today. For dinner she had some sort of pureed meat food, pureed cooked
carrots, and some mashed potatoes. That may not sound too appetizing, but Jill
was pretty excited about the mashed potatoes. They were the most normal thing on
her plate and she seemed really excited about being able to taste her food
again. She washed it all down with a little thickened cranberry juice. Over the
next few weeks the doctors will continue to give her food through her feeding
tube to supplement the relatively small amount food that she is able to eat.
Getting food in through her mouth is still quite a tough task. Her voice is
still getting stronger...
-Dan
10:30am
Jill is still doing quite well. She had lots of
visitors yesterday. She has been dealing with groups pretty well actually. The
only time that she seems to be indifferent about her surroundings is when she
has just been awakened from a nap (that is not too much of a change from before
the accident though...). I talked to her on the phone last night and I noticed a
definite improvement in her voice strength from my visit the day before. Her
therapists are starting to work with her memory and logic on a daily
basis.
An event plug: Members of our extended family in Davis are
throwing a fundraiser for Jill on July 14th from 4-9pm at Lamppost Pizza (on
Lake Blvd.). If you are hungry for pizza and are in the Davis area, please stop
by and mention Jill's name with your order. They will donate a % of the sale to
her trust fund.
-Dan
8:30am
Jill is getting stronger every day. She can project
her voice a bit more lately and she is building up the stamina to use her voice
for longer periods of time. She talked to my dad on the phone last night for
probably 5 or 10 minutes. Talking takes a great deal of physical and mental
effort still though. She appears to be noticeably drained after trying to use
her voice for brief stretches - but this is definitely improving. She had
applesauce again today. The docs had talked about removing her trach sometime
soon, but she still occasionally has issues with managing her phlegm. She has
been able to cough quite forcefully, but she still occasionally has to be
suctioned. Hopefully it'll be out in a week or so.
-Dan
8:37am
Jill had a big day of therapy yesterday as usual. She
ate some applesauce with the speech therapist. For the past few days Jill has
been alluding to the fact that she wants to eat real food... It will be a while
before she regains the skill to conquer solids though. The doctors were thinking
about taking Jill's trach out yesterday, but they decided to wait until she is a
bit better at coughing. We have seen her cough pretty forcibly, but the nurses
still have to suction her occasionally. Jill is still making great progress each
day...
-Dan
10:13pm
Despite the fact that Sunday is technically Jill's
"day off" from therapy, she continued to forge ahead with her recovery. She
attempted to teach herself how to throw a ball, and eventually was able to
propel it a foot or two with her left hand. I was extremely impressed given the
relative complexity of the act of throwing (grabbing the ball, getting her hand
going, and then letting go of the ball at the right time is not a trivial
thing). She was also able, with significant effort and some coaching from my
parents, to sign a b-day card for me and a "new baby" card for one of her close
work friends. Jill is still concerned, however, with the fact that her right
hand is essentially immobile still despite her efforts to get it working
correctly.
Even with all of the activity, she enjoyed a few afternoon
naps and chose to get up into her chair only once today. After a long bout with
the hiccups (first time since the accident - she was a pretty good sport about
it despite how uncomfortable it must have been) during the first part of her
chair session, she got neck massages from my parents and looked pretty darn
comfortable. Now Jill needs to rest up for the long week of rehab ahead...
-Dan
10:49pm
Jill had yet another great day today. She was a
little tired since she had some pretty intense physical and speech therapy
sessions throughout the day. Her voice is getting a bit stronger each day. She
is able to string a few words together every once in a while. She said that she
was hungry today and so one of the therapists let her have a taste of cranberry
juice. I told her that I was maintaining a website to update people on her
condition and she said that she wanted to put something on it from her. It
seemed to be a bit of pressure though, and she said that she couldn't think of
what to say. She continues to work extremely hard in all of her therapy
sessions.
-Dan, Dad, Mom
10:51pm
Jill continued to make great progress today. She has
increased the amount of sound that she is able to make. She actually vocalized a
few sentences today! Speaking definitely does not come easily, but when she can
muster up the energy she is able to string together a few words every once in a
while. Jill got to eat some yogurt today (1/3 container...vanilla). It was quite
a chore, but she got it all down and seemed to enjoy the eating experience. She
is now choosing what music to listen to and directing traffic within her room
(Jill said, "Mom, don't worry about it" when she was straightening up the room).
It was pretty hard to leave once again tonight. Jill was very clear about the
fact that she wanted to come home with us. It is heartbreaking to witness, but
it definitely feels like a step in the right direction.
-Dan
11:34pm
More good news today - Jill continues to work
extremely hard on her recovery. She was able to eat some applesauce today. She
had ice chips a few other times this week, but this is the first time that she
has eaten any type of food with her mouth since the accident. One especially
good moment from my visit was when Jill blew a kiss at her friend Heidi as she
left (before I was there she apparently blew a kiss to Grammy as well). She has
been working extremely hard to speak lately. She is able to move her mouth and
exhale so that it almost sounds like she is whispering, but no sound really gets
out (that's what I mean when I say that she "mouthed" something). Today while my
dad was talking to her on the phone she tried to say, "Hi dad. How are you?" She
mouthed it once or twice and then the last time was able get out a few sounds.
My mom and I were very impressed and my dad was even able to hear it over the
phone. The hardest (but probably most hopeful) moment of the day was, as my mom
and I left, when she mouthed, "I want to come home with you
guys."
-Dan
9:54pm
It was yet another great day for Jill today. Despite
being a bit sleepy (because she wanted to try to go a night without her sleep
medication last night), she had a productive day of rehab. Her trach is pretty
much "capped" all of the time now and she seems to be dealing with it quite
well. She was mouthing lots of words today, but is still having trouble making
sounds. She is becoming pretty effective at communicating using facial
expressions and nods.
Also - I just updated the main page with some new
visitation info...here it is so that you don't have to click back and forth:
"The best time for visitation is 4-8pm on weekdays. Jill is in the "Neuro Rehab"
unit Rm. 49 (second floor in the "old" section of the hospital). Weekends tend
to be more crowded, mostly with Jill's fantastic (and huge) extended family, so
if you're from the area try to come on the weeknights."
-Dan
10:12pm
Jill had another good day today. She is still
communicating with her head extremely well. She also was trying to use speech
more today even though her trach was not plugged. I talked at her on the phone
tonight and my mom said that she was mouthing words back to me the whole time
(she still is physically unable to talk due to her trach). Also, she is becoming
much more active with her left arm. My mom said, however, that Jill seems to be
worried about the tension in her right arm. When the therapist was working on it
today, Jill implied that it hurt her to work on the arm, but that she wanted to
press on with the therapy anyway. Keep it up Jill...
-Dan
10:21pm
Jill had a phenomenal night tonight. For the first
time since the accident, Jill was really actively communicating with us. She was
smiling, nodding her head yes and no, and making all sorts of other facial
expressions. Becky, Kina, Danh, and I were blown away to see the way that she
reacted to our stories/conversations about past events. It also appears that
Jill can smell now. She got a new trach in today that seems to route more air
through her nose. We had her choose which kind of hand lotion for us to put on
her based on smell (she really liked two, but turned her nose up at the third
one...). The doctors will cap off her trach and try to get her to make sounds
during her upcoming speech therapy sessions. Based on how she's doing currently,
it seems that she probably has the mental capacity to talk, but I'm not sure
that she has the muscle control yet. She appears to be having periodic muscle
spasms in her neck and jaw. This could also explain some of the frowning that
she does from time to time. Regardless, I left her room in awe tonight. She
seems more determined than ever to work hard to bring herself back. Her tenacity
appears to be paying off...
-Dan
7:50am
Jill had lots of family in town yesterday to hang out
with. She was up in her wheelchair with her neck brace off for ~90 minutes. It
is apparent that she has to work pretty hard to keep her head up, but it's
impressive that she still can hold it up at all after 2.5 months in bed. She was
very attentive with all of the visitors around. Towards the afternoon she seemed
to get a bit uncomfortable. She developed a bit of a fever and was having some
phlegm issues. Overall she is really making good progress
lately.
-Dan
9:39pm
Jill didn't seem to be feeling quite as well today,
but really worked hard in therapy and enjoyed her visitors. She displayed a
variety of emotions today. We think that she is becoming more and more aware of
her surroundings as the time goes by.
-Dan, Dad, and Mom
9:25pm
Jill had yet another good day today. She has been
pretty expressive with her face lately and that trend continued. We asked her to
stick her tongue out at her dad this afternoon and she was able to... then she
went on to do it twice more just for fun. She is also extremely attentive when
the nurses come in to work on her. She has really taken an interest in what they
are doing lately.
-Dan
8:35pm
Jill was able to eat some ice chips today. This is a
big step towards eventually being able to eat on her own. Her head control is
improving daily and the speach therapist started to teach her to nod "yes" and
"no". The doctors upped her sleeping and seizure medications today. She has been
having issues with getting really sleepy during her therapy because she has not
been getting much rest at night. Her hands are getting more flexible. More
smiles today for the doctors as well. Good progress these
days...
-Dan
10:58pm
Jill was doing pretty well again tonight. She smiled
a few times - and was able to lift her head off of the pillow to look around the
room. She really seems to enjoy visual stimulation within her room (things like
people moving around and the TV being on). It is good to see her beginning to
become more aware of her surroundings.
-Dan
5:31pm
The news is more of the same from the hospital these
days. Jill is becoming much more consistent with her responsiveness. Also, she
doesn't have to wear her neck brace while she's in bed these days. Sorry for the
brief updates lately, I have been sick since last Friday so I haven't been able
to see her first hand.
-Dan
9:42pm
Jill had a really good day today. She smiled quite a
few times throughout the day (in response to my parents and to some of her
college buddies). In addition, she was able to follow a few simple commands -
things like looking a different objects throughout the room and opening her
mouth for the nurses. She is a great deal more expressive with her face and just
seems more alert in general. Keep it up Jill...
-Dan
10:02am
Jill is all settled in at rehab now. Now that she
has the internal shunt the therapists are able to tilt her bed up for long
periods of time. She has been pretty alert over the last few days as well. She
tracks her doctors and visitors pretty well with her eyes as they move around
the room. Another bonus about her return to rehab is that this time she got her
own room...for now anyway.
-Dan