Posts filed under 'Family'
I just uploaded about 3 months worth of photos. I don’t really have much of an excuse for not posting them sooner. Time just got away from me, I guess. I have lots more to write about, and now that the pictures are out of the way, hopefully I’ll find the time to share. I’m also working on some video clips.
Updated 7/4/2008, by Neal: Now with even more photos! I just uploaded a bunch from last night. My brother Colin and his wife are in town, and I was a little crazy with my new camera. There’s a great series of Anna portraits there though!
Updated 7/5/2008, by Neal: Now with video! Turns out Flickr (the folks who host our photos) have started a new video service. I uploaded a movie of Anna dancing to “Happy Feet” there. Let us know how this works for you?
July 2nd, 2008
This weekend we took it easy. Anna’s managed to catch “hand, foot, and mouth disease” from some kid at daycare which means she’s running a fever and has a sore in her mouth that makes her not want to eat much (besides ice cream…). Surprisingly, though, she’s been in good spirits and sleeping pretty well despite it all. I’ve got a minor bug of some sort after running on almost no sleep for more than a week due to craziness at work, and Tara’s been running hard and feeling tired too. So we just basically hung out together and tried to relax.
Which makes Anna’s new favorite game all the more fun. It’s called “nap time”. Basically, she puts a pillow or two on the floor, asks Mommy and Daddy to lay down on the pillow, and insists that we close our eyes while she puts a blanket on, and off, and on, and off, and on, and off…
It’s the best game ever.
Updated: Here’s a photo of Colin and Roby playing “the best game ever” with Ms. Anna.
June 23rd, 2008
Dear Mama,
I love you so much!
Thank you for your smile and for all the hugs and especially the snuggles. Thank you for reading me books and playing games, for taking me on adventures, and even for the tickles. Thank you for letting me eat yogurt and cookies and beets and green beans. Thank you for helping me wake up when I’ve had a bad dream, and for coming and sleeping in my room when I’m not feeling well.
Thank you for spending so much time with me. I love being around you so much! Thank you for teaching me to do things with my left — I know that’s important even if it makes me frustrated sometimes. Thank you for your confidence in me, and for teaching me how to be big and good.
I hope someday I can be as big and good as you.
I love you Mama.
Anna Rose
May 11th, 2008
We just learned that Tara’s grandmother passed away earlier today. Anna Winifred Hess (our daughter Anna Rose was named after this great lady) would have been 92 in June. She passed very quickly and without any pain.
We were looking forward to a planned trip out to Kansas at the end of May to help her celebrate her birthday with her family — including her four grandchildren and five great-grandkids. I’m sure she would have loved to watch all the grand- and great-grandkids play together.
It’s too early for plans for a memorial service, but there’s a strong likelihood we’ll be heading home to Kansas at some point in the next week or so.
We love you and miss you terribly, grandma.
May 7th, 2008
There’s been a lot going on since we last posted, and I’m happy to report most all of it’s good news!
March opened with a change in the lineup here on Team Anna. Tara’s mom flew out from Kansas on Saturday (3/2) so that she could pinch hit for me while I flew back to Colorado for a week of face time at work. Poor Debbie was sick as a dog when she arrived, but fortunately it turned out it wasn’t anything a whole bunch of medication (procured from a local urgent care) couldn’t fix in a couple of days.
Tara and her mom had a pretty good time of things during the week I was away. Anna made good progress in her therapy and in other ways as well. She’s suddenly able to count to 5 most of the time (sometimes higher?), and has a pretty decent grasp on her ABCs for somebody who’s not even two yet! She’s talking up a storm — still mostly two word sentences, but wow, the vocabulary is impressive. Meanwhile: Her therapists were very happy with her progress, and she’s now used to the (crazy busy) routine, which means she’s sleeping and eating well. She’s mostly healthy, too, which is new and different for everyone.
Lots of work and a bit of the stomach flu kept me pretty busy for the week I was away. It was good to see my folks and Max on Thursday evening, and I managed to make a bit of money at the poker game on Friday. But I felt anxious the whole week and wanted to get back “home” to Birmingham. (It’s very hard to be away from Anna and Tara for that long — I have no idea how parents who travel regularly do it).
Granny Debbie made a fantastic Dora the Explorer cake for Anna’s early birthday (pictures to follow?), which we all enjoyed on the evening I returned. Then Sunday morning (3/9) it was back to the airport to drop off Debbie, who’s apparently deep in the throes of Anna withdrawl as I write this. (Thanks so much for visiting and for all your help!)
So that brings us to this week, our last week of therapy. Anna got her cast off yesterday, which was pretty mind-blowing for everyone involved. Anna was frankly a little bit confused, and kept acting like she was expecting us to put the cast back on. It made us both happy to let her know that the cast is gone (at least for a while). And it was great to finally give the girl a real bath with plenty of bubbles, no rush, and no smelly cast to put back on afterwards!
We were thinking of taking her out to someplace fun like Chuck E. Cheese’s or McDonald’s to celebrate. But the combination of three weeks of not being able to use her right hand plus a bunch of new books and toys from her early birthday celebration this past weekend meant that Anna was really much more in favor of sitting at home and playing in relative peace and quiet. And who could blame her?
Everyone was expecting today to be a really tough therapy day. Anna’s historically really bad about using her left hand after she gets her cast taken off, and the therapists were ready for a major battle. But the girl continues to surprise, and she’s been unbelievably good about using both her hands or even just her left hand when we ask her to. (That’s the new therapy focus: bi-manual exercises). There’ve even been a couple of moments when she’ll use her left hand for a task without even thinking about it! In general, though, today was a great therapy day, and the therapists are really happy with what they’re seeing.
Friday’s our last day of therapy. We’ll have a few solid hours of therapy in the morning, and then we’ll relocate to the clinic at UAB for Anna’s “exit interview”. Saturday we’ll try to pack, clean up, and hopefully get outside to do something fun since the Ides of March is Anna’s official birthday. Sunday we’ll need to be out of our apartment by noon, and grab lunch somewhere on the way to the airport. Tara and Anna fly back to Denver in the afternoon, and after getting them on the plane I’ll start the long drive back home (ETA: Tuesday).
It’s hard to believe we’ve made it this far, and that we were able to survive three full weeks of 24/7 casting and intensive therapy. But we’d do it all again in a heartbeat. The gains have been impressive, and on the whole the last three weeks have been enormously positive for Anna on many different levels. She’s able to turn her hand over much further than she was able to before (even with Botox), she’s able to isolate her pointer and thumb, use a fork independently to stab food, and sit cross-legged. Her core strength and strength in her left hand and arm have improved dramatically. And almost as importantly, she’s really done a truly fantastic job listening and learning to follow directions — a very large challenge for someone so little — and with tolerating all the long hours of therapy.
We’re so very proud of our girl!
March 12th, 2008
Cut to the chase: The tornadoes that threatened Birmingham missed us this morning. We’re all okay.
But we did spend some time hiding out in the bathtub very early this morning. I was very soundly asleep, oblivious to any danger when Kansas girl Tara woke me up at about 3:30AM, having somehow heard the sound of distant tornado sirens. We turned on the TV in time to see a major front bearing down on our location, with the backup weather folks from the local news stations in a panic about the whole affair.
So we quickly pulled on some clothes and decided that the bathroom off our bedroom was probably the safest location. I threw all the pillows in the house in the bathtub while Tara went and grabbed a very groggy and confused Ms. Anna. The two of them huddled in the tub for about 20 minutes (with me standing by ready to jump in if necessary) until about 4:10AM, at which point the front had passed over us with lots of wind and rain and thunder, but without manifesting any actual tornadoes.
We brought Anna into bed with us and I think she and Tara managed to get another couple hours of sleep before the therapists showed up at 6:45AM. (I can’t sleep if I’m up around that time, but it was nice to lay in bed and snuggle with the little girl).
I guess I didn’t think of Birmingham being prime tornado country, but this is the second scare now in as many weeks!
February 26th, 2008
Our first week of therapy is behind us.
Anna’s doing much better, health-wise. The steroids took effect almost instantaneously, and while she still has a runny nose and cough, at least she’s not croupy.
More importantly, by Wednesday she was pretty much sleeping through the night. She’s working so incredibly hard in her therapy that sleep itself has become something of a reward. After working her little tail off for six straight hours between 7:00AM and 1:00PM, she really looks forward to her afternoon nap(s). And for the past three nights she’s been reluctant to read books and has flat out refused to have us sing songs before we put her to bed. “Do you want to read another book?” “No.” “Do you want Mamma to sing songs?” “No. Seep”, she says. “Seep”.
Therapy has been going very well, and we’ve accomplished a great deal in just one week. But it has not been an easy road. The therapists work the girl very hard, and during the first couple of days she put up quite a fight. I think Wednesday was our lowest point. Tara had to leave the therapy session for about an hour because Anna was having a total meltdown and refused to comply with even the simplest request. Tara and I and her therapists all agree that it’s incredibly important for us all to help Anna realize that she’s not going to get out of therapy just by throwing a fit, but knowing that doesn’t really make it any easier on anyone when the poor girl is throwing a tantrum because she’s exhausted and sick and frustrated and all we want to do is stop the damn therapy session and give her hugs.
But the perseverance has started to pay off. By the end of the week there were far fewer tantrums, and today (Saturday) she had an amazingly positive therapy session, with not a single tantrum and some real milestones. She’s now able to bear significant weight on her left arm independently for several minutes, she’s really improved her supination (turning her left hand over with her palm up and open), she’s doing amazingly well with her pincer grasp (thumb and pointer finger) with tasks such as turning pages of a book or picking up small objects, and she was successful, for the first time today, in independently stabbing a piece of food with her fork and bring it to her mouth. Almost as important: She’s now starting to grasp the concept of delayed gratification — that when we say “do X now and you’ll get Y later”, she understands enough to work through the difficult task at hand for the promise of a reward later. This is a Very Big Deal for someone not even two years of age, and extremely important to making forward progress in therapy sessions.
It’s been a very long, very tough week, though. Poor Tara’s now managed to catch a cold (due to lack of sleep and way too much stress), and nobody’s happy when Momma’s sick, let me tell you. I’ve been trying to keep up at work, but it’s honestly been much more difficult than I’d expected to be super-productive and engaged when I’m 1,300 miles and a time zone away and always a little bit exhausted from stress and lack of sleep. And while it’s been great to touch base with some family and friends by phone or video chats, it usually just reminds us how lonesome it can be here away from our home. We miss our family, our friends, and our usual routine. And of course we really miss Max.
After six straight days of therapy we get tomorrow off. We’re going to try and get out of the apartment and roam around a bit, though it’s also possible we’ll just relax at home. We’ll start our second week on Monday, with our therapists arriving extra early (to make up for lost time at the doctor’s on Tuesday) at 6:45AM! (Our therapists, it should be said, “kick ass” — to use the technical term — and we’re extremely happy with all they’ve done and are doing).
February 23rd, 2008
It’s official, Anna has croup! After yet another fun-filled night of little to no sleep and a couple of 15-minute sessions locked in the bathroom with the hot shower running, we decided to take her in to see the doctor. We went to see our therapist’s pediatrician at their “sick-kids” clinic. It seems Birmingham is having a massive flu outbreak, so the clinic was packed. Neal and I made frequent use of the antibacterial/germ-killing gel! It took us literally 2 hours to see the doctor. We were totally unprepared for such a long wait. We were moved into a small exam room where we tried to entertain the 2 year old for more than 1 1/2 hours! She told us multiple times, “Coat…door…go.” As time dragged on, we were all ready for “Coat…door…go.” The doctor tested her for strep and flu (both negative, thankfully), and finally gave us some steroids for the croup. We notice a difference in her cough already! Here’s hoping we have a good night.
In light of our lack of a good night’s sleep and Anna’s illness, we opted to cancel our therapy for this afternoon. We got in 2 1/2 hours before we left for the doctor - that leaves 3 1/2 hours that we will need to make up. They are very serious about making sure that Anna receives her 6 hours of therapy per day! I suppose if they have a method that works, they should stick with it. I have to admit that it all seemed a bit rigid today. My parental instincts wanted to say…”hey, back off…can’t you see she doesn’t feel well?” Every few minutes were filled with crying, which led to a runny nose, which led to a cough, with led to the barking, etc. etc. Surprisingly, she did quite well this morning despite her lack of sleep and nasty cough. She’s such a tough little thing.
This evening we talked online with “Henny” (Anna’s cousin, Henry) and aunt Jo. It was great to see them both, and made us realize how much we do (will) miss them. Anna became really upset when it was time for us to say good-bye. She just kept saying “Henny, Henny, Henny…no, Henny.” It was just very difficult to end the call. Both the kids seemed confused that they just couldn’t get together to play. Distance is a hard concept for the kidlets.
February 19th, 2008
A long, challenging day today, but things have gone amazingly well so far.
We had Anna’s initial evaluation and casting at 8:30AM at the UAB ACQUIRE program this morning. Anna did us very, very proud. All the doctors and therapists there were extremely impressed with how well she’s doing. Anna “passed” almost every evaluation they threw at her. It doesn’t mean she doesn’t have a ton to learn, but it does mean that she’s made some very significant progress in the last year and a half since her initial diagnosis, and it reflects well upon all the therapy we’ve put her through so far. This is truly a tribute to Tara for putting in so many long hours in doctors’ offices, hospitals, and therapy with Anna, and to the dear little girl herself for learning to endure and prosper despite it all.
During the therapy Anna was fitted for her new full arm cast. Tara had tried to prepare me for this ordeal, warning that based on past experience with her two previous castings “she’s going to scream bloody murder for as long as it takes”. Well, the good folks at ACQUIRE added a single, simple variable to the equation of putting a hard cast on an almost-two-year-old that made all the difference in the world: A Sesame Street video. Lulled into near unconsciousness by the psychedelic antics of that little red monster Elmo and his muppet friends, Anna hardly put up a fight and the new cast was on her arm in almost no time.
We’re very impressed with Anna’s new therapists as well. They clearly know what the heck they’re doing. Obviously they’ve got the casting and occupational/physical therapy parts down pat. But equally impressive is their understanding of the developmental psychology of the kids. Frankly, knowing what exercises to get the girl to do is only half the battle. The other half is figuring out a way to get her to want to do the exercises in the first place. So almost all the “therapy” consists of games, games, and more games, guided by a firm hand. (That bit is important too. I’ve already been ejected from the therapy sessions three times because I’m clearly the “softy”, and Anna tries to use me as a “safety net” when she’s upset with what the therapists are trying to get her to do — which, despite being a “game”, is rarely anything easy). Perhaps the most important thing is that Anna seems to really get along with her therapists, and they’re growing fond of her too.
After the morning session where we had the initial evaluation and the casting we went home for a quick lunch and to put Anna down for a nap. (The poor kid is still fighting a cold, which means she’s twice as exhausted as she normally would be, and it was a brutal morning for her even without a cold). Then our therapists showed up at our apartment with a truckload (literally) of “toys” and other therapy gear. They spent the rest of the afternoon “playing” with Anna, and they’ll be here at 7:00AM tomorrow morning right after Anna wakes up to continue the program. The goal is at least 6 hours every day (excluding naps) of one-on-one (actually, two on one since we’ve got an intern working with our primary therapist) therapy, 5-6 days per week for the next four weeks.
Overall we’re extremely happy with how everything’s played out so far. The main thing is that our therapy team really seems to “get it”. It’s not uncommon for folks to look at how “well” Anna’s doing and ask why we’re pushing her so hard. Today was a bit of confirmation from folks who really study this stuff that all our pushing has been necessary, that all the hard work has helped make an enormous difference in Anna’s capabilities, and that yes indeed there is a bunch more hard work to come.
But for the moment, we’ll allow ourselves to indulge in a feeling of accomplishment. When we asked what we needed to work on this evening our therapists recommended we just take it easy tonight, “let Anna do whatever she wants, and have her favorite food for dinner.” So we took a short walk together, and tried to relax over some pizza and a glass of wine/apple juice. It was over a year ago since we signed up to come on this adventure. It’s been a long year, and a long trip, and it’s a little hard to believe we’ve made it here after all. We’re happy to know that we’ve been doing well by our little girl, and to be in the company of folks who are experts in helping take her therapy to the next level. We now know this is a marathon and not a sprint, and that progress is measured in feet rather than miles, but today at least it feels like we’re on the right path and headed in the right direction.
I’ll sign off tonight by remembering out loud that the real star of the show today, in every way, was dear little Anna. So strong, so smart, so charismatic, and so very patient. She truly made us proud to be her parents.
Sleep well, and dream sweet dreams, little one. Tomorrow is another day, and another set of challenges. But we’re here for you always. We love you.
February 18th, 2008
Not us! Last night was a very long night for Anna and me. Anna seems to have picked up some bug (or already had a bug) that took advantage of the fact that she had no sleep yesterday. She had a fever last night of 102 degrees. That, coupled with the fact that she’s in strange place in a pack-n-play, didn’t make for a particularly good night last night. I ended up sleeping with her in her room. There’s a queen-sized bed in her room, but I certainly wouldn’t know, as I was clinging to the very edge while Anna took the rest. She just wanted to be close, and kept insisting on sleeping on me. I generally like to sleep in a cool room, with a cool pillow, etc. The heat generated from Anna’s hot little body was not really conducive to good sleep for Tara.
So far today, Anna’s been a bit of a mess. She’s obviously exhausted, but not really wanting to take a nap. We finally insisted on the nap, and she’s going on 3 hours! She even managed to sleep through a pretty loud thunderstorm (I felt like I was in Kansas again! You just don’t get storms like that in Colorado.). Hopefully she can sleep off the worst of this bug. If not, we’ve been googling the nearest urgent care.
When she finally wakes up, we’re off to Target to spend some big bucks. You really take for granted the fact that you have condiments, spices, and what-not in your pantry. We don’t even have any dishwashing detergent to wash up the pots we’ve used.
February 17th, 2008
Thankfully, we all made it.
Despite some bad weather on Thursday morning (4 inches of snow in our driveway when I left), my three-day drive to Birmingham, Alabama went off without a hitch. Gloomy skies for most of the journey, but dry roads from Kansas to Alabama. Many thanks to Debbie and Rex in Towanda, Kansas for a fine steak and finer company on Thursday night, to the Days Inn in Fulton, Mississippi for being worse than I had hoped but better than I had feared, and to the makers of Red Bull for keeping me awake during the drive. I entered Birmingham around 9 o’clock this morning, and was unpacked in our new apartment before noon.
Tara and Anna made it to the Denver airport with time to spare, courtesy of my parents who got up much earlier than retired folk are wont to do in order to ferry their daughter-in-law and grandkidlet to DIA (thanks Mom and Dad!). Tara managed to get the folks at United to see reason and actually seat both mother and child next to one another (evidently the airline computers see no problem in seating a mother three rows away from her two-year-old daughter…), and the flight to Birmingham proved blessedly uneventful thanks in no small part to a portable DVD player and several “Dora the Explorer” videos.
Our apartment here is really quite nice, and we’re in a fantastic part of town (I felt quite under-dressed wearing only jeans and a t-shirt when I walked into the Panera at “The Summit” to use the restroom…). Most of all we’re happy to be together once again, and happy that this whole scheme worked out mostly according to plan.
We’ve got the day off tomorrow to sleep in, take a look around, and generally get our bearings. Anna’s ordeal starts Monday with her orientation, casting, and first round therapy at UAB.
February 16th, 2008
October? That’s the last time we’ve posted anything here. Seriously? Isn’t that a bit too long? Our bad. Boy howdy is it going to be hard to catch up, since so much has happened. November happened. December happened. January is in full swing. But here goes!
November
November was hard. Anna took part in her second casting session at Children’s Hospital in Denver. Which meant lots of miles and lots of hours in the new car for Tara and the girl. Three times a week Anna met with physical therapists at the hospital for “play time”. And then of course there was the cast she wore for all her waking hours for 20 straight days. The good doctors at Children’s also decided to try some Botox in Anna’s left forearm, in the hopes that it would help her work on turning her hand over palm-side up.
During this time it’s hard to say any of us were especially happy, for reasons that are probably obvious. And the results of all her therapy, while positive (she is able to turn her hand over more, she’s doing more with both hands, she’s way more dexterous with her left hand when casted, etc.), were far less dramatic than we’d seen the first time we participated in the therapy program. Progress, it seems, is now being measured in feet rather than miles.
It was a struggle and a great relief to make it through to Thanksgiving. Finally the damn cast came off! And while the airplane trip out and back as just as interesting and challenging as you’d expect it to be with a 21-month old, we did have a wonderful vacation out in Kansas. Anna loves her family there, and still talks daily about some of the fun she had.
December
December’s always crazy. But we managed to get our (fake) tree up, some lights on the house, and the Christmas music playlist rolling early this year. Anna started to make the kinds of Christmas associations that will probably turn her into a crazed, present-hungry, darling little monster between ages 3 and 12. Santa is “Ho Ho”, the ornaments on the tree remained fascinating for weeks, and candy canes, she discovered, are just about delicious. Cookies seem more available and more easily accessible for someone her age during this time of year, and lots of her toys and books got an update.
My brother made it out for the holiday, and it was great to spend some time with him and my folks. Also fantastic to see our Denver relative a couple of times — for whatever reason we’re not seeing them enough these days.
I have no idea how Tara managed it, but we did end up getting a holiday card out the door to folks on a few days after Christmas. Go team!
January
Recovery mode. Trying to catch up on some alone time with just ourselves. Trying to get back into the swing of things at work.
Anna’s doing just great. She’s “talking” up a storm. Mostly a lot of babbling, but in our experience that stuff usually precedes breakthroughs. She’s improving her pronunciation and speaking individual words much more clearly now, and she’s started doing an occasional two-word sentence (e.g. “Momma sit”, “Daddy move”, etc.). Anna’s increasingly more interested in the whole potty-training thing (also a big focus at daycare), and she’s making some progress there too! The girl has also been fairly healthy of late (knock on wood), which we attribute in large part to a switch from cow’s milk to soy milk for most of her daily milk consumption.
Tara’s working an extra half day now, which is a Good Thing since it means she’s less stressed about finding time in the late evenings to complete her “half time plus” assignment. This means Ms. Rose is spending a bit more time in daycare, but honestly she’s loving it. They’ve moved her up to a new room (somewhat ahead of schedule, I’ll add), and she seems to be happy as a clam with the bigger kids and all the new activities and toys and games. Last Wednesday was a bit of a milestone: The girl seemed somewhat reluctant to leave daycare and the plastic milk carton she and her friends were playing with at the time.
We’re also now starting to seriously look ahead to the Alabama trip in February. Notice I said look “ahead”, not look “forward”. For those of you not up-to-speed: We’ll be moving to Birmingham for four full weeks, during which time Anna will participate in an intensive constraint therapy program. “Intensive” means three full weeks of 24/7 full-arm casting, with therapy 6 hours a day for 6 days a week.
Frankly, I think we’re both a bit terrified about all that entails. (Anna, bless her heart, has no idea yet what’s in store…). But the flights are booked and we’ve confirmed we have a place to stay. Some good news: Tara’s mom will be coming out in the third week to help out while I return for a few days to put in some face time at work (thanks Debbie!).
Whew. That’s all for now. I know we’ve got pictures to post, but hopefully we’ll try to be more regular about those kinds of things in the near future.
How have you been?
January 20th, 2008
In the past week Anna has:
- had her eyes checked (everything looks good there)
- visited the new Children’s hospital
- met with the rehab doc who said she looked “just great”
- had her botox injections delayed until she’s seen next week by her OT down at Children’s
- had her hips x-rayed to determine if there is any problems with her hip development (everything looks good)
- tripped over a bronze bunny sculpture at Children’s and injured her left hand
- made a trip to urgent care on same day as trip to Children’s
- had hand/wrist/arm x-rayed 4 times to determine if anything was broken or torn (probably just a sprain)
- had her picture taken with Henry in their pumpkin costumes (not such a fun experience for anyone!)
- re-injured her hand
- played in the park a couple of times
- made another trip to urgent care to determine if she has another ear infection (unfortunately, she does)
- been re-weighed and measured: 27.2 lbs, and 35 inches long (big girl!)
- visited Oma, who returned home today after a 9-day stay in the hospital during which she had emergency abdominal surgery
That’s it, in a nutshell.
I’ve got new photos…I just need to post them. I can’t wait for Thanksgiving.
October 28th, 2007
Since my last entry I’ve posted at least a couple batches of photos. Make sure you check them out! They extend far beyond those found on the front page of this site.
Just a quick update…yes, we are all still alive and kicking! I know it has been a long time since I updated the blog; I guess we’ve been a little busy. Here’s a brief list of what’s been going on: Anna’s been walking around a lot lately - it’s become her primary mode of locomotion at this point; she’s had another ear infection; she’s been fitted for a new Dynamic Ankle Foot Orthotic (DAFO) for her left foot, so that she will hopefully walk correctly (heel-toe, not toe-heel); I was sick for a couple of weeks; Neal was sick for a couple of weeks; Granny and Papa came to visit; Anna played a lot with Henry; she’s been increasing her vocabulary substantially; Neal received a promotion; and we recently purchased a new car. Doesn’t sound like a lot when you write it down, but it seems like we’ve been very busy lately.
September, October and November are gearing up to be extremely hectic months. If she isn’t already, Anna will be fed up with doctors and clinics (I’m sure I will be too, and I’m not the one being poked, pulled and stretched). We have Anna’s 18 month check-up coming soon (she’ll be 18 months in a little more than a week!). And then we have all of her specialist appointments - neurologist, opthamalogist, neuropsychologist, and physiatrist (rehab doctor). We’re coming up on the one-year anniversary of Anna’s diagnosis. It’s hard to believe that it has been only a year. Sometime in October we’ll also be having Anna’s 6-month reevaluation for her IFSP (Individualized Family Service Plan). This is basically a powwow among Anna’s therapists, our early intervention service coordinator, and us where we discuss Anna’s progress and our goals for the next 6-month period.
In late October Anna will be receiving her Botox treatment. No, she doesn’t have wrinkles. Doctors often use Botox in children with cerebral palsy to relieve/reduce spasticity (high muscle tone) in select muscle groups. The physiatrist will be injecting Botox into several of Anna’s arm muscles. This will hopefully allow her to strengthen the opposing muscles that aren’t able to do much because of those muscles with high tone. Of course, this makes Neal and me more than a little nervous. I mean, the stuff is poison. And she’s still so little. They say that the injections are painful, which makes me feel terrible for putting her through this. I guess the one saving grace is that she probably won’t remember this (?). I certainly hope she doesn’t.
After the Botox treatment, Anna will begin her second round of constraint therapy at Children’s in Denver. As a reminder, this is a 3-week intensive therapy program where Anna’s good arm is casted in an attempt to make her use her affected arm. We see an occupational therapist down at Children’s 3 times per week, and we do a lot of work at home. She wears the cast from the moment she wakes up until she goes to sleep. Fun!
Anna has made a lot of progress since her last round of constraint therapy in March/April. Since we finished up the first round in April, we’ve continued to wear the cast all-day for 2 days per week and during each and every evening meal. It will be interesting to see what goals we establish for this phase. The treatment period will last right up to the Wednesday before Thanksgiving. I’ve been joking about the fact that this year we will have something for which to be truly thankful: a few cast-free days!
September 7th, 2007
I just learned that my uncle, Mike Steadman, passed away quietly last night just a few days short of his 65th birthday.
Mike was a great guy who managed to maintain his sense of hope and humor throughout many years of treatments for stroke and, finally, cancer. I’ll remember him, in particular, for the paintings he produced in his later years, and for the wonderful poem he composed and read at his grandson Ben’s funeral last spring.
Mostly I’m feeling terribly sad for his wife Margaret, my cousins Dean, Pete, and Pat Steadman, and for little Madie who’s lost both her brother and now her grandfather in such as short span of time. The Steadmans are some of the strongest, most loving, most positive, and best people I’ve had the good fortune to know. It just seems unfair that such good people have had to endure so much pain of late.
There will be a service for Mike this weekend. You can find more details on my cousin Dean’s blog.
To Margaret, Dean, Pete, Pat, Madie, Peggy, and all the rest of the extended Steadman family: We love you so very much. You are all in our thoughts and prayers.
June 27th, 2007
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