We had a very calm weekend around Goleta this weekend. So calm, in fact, that we didn’t even remember until late Sunday that Rudy’s 10-month birthday was on Saturday. My convalescence had me begging off from any adventures for the short-term, but Rudy has had some notable ones of late to report.
Rudy had such a good time on his trek through the mountains with Nurse Aliza, that he was eager for more adventures. From the majestic Sierras, he headed to the idyllic wonderland that is Milwaukee where Donna took him to the Circus of America Parade, where 250 horses pulled wagons carrying the animals down the route (like those prima-donnas can’t walk?). Look closely, you’ll see him there on Donna’s arm.
Rudy thought the giraffe was cool; the clown creepy.
Rudy came home and wondered what all the hype was surrounding Comic-Con 2009 (as did we). Fortunately, two sweet nerds friends, Micheal and Cheryl, were glad to take him along. His big brothers are green with envy at how he got up close and personal with some of their heros.
Rudy fights with half a heart; Iron Man needs an Arc-reactor (wimp!)
Superman sports a tribute to a true super hero!
Kryptonite, baby!
Cheers Rudy! Here’s to many, many more months of adventure!
This may be a post to file under “too much information”, but seeing as we’ve posted 400 times in the last year it’s probably way too late for that. We had another medical procedure in our family today, but this time it wasn’t Rudy. While some of the folks in my office thought I was taking advantage of a 3-day weekend, my day started off with a 30 minute procedure on this table.
Very quick and efficient as far as doctor’s appointments go…yet permanently life-altering. Not sure if we’ve mentioned here before that a heart condition was arguably only the second biggest surprise surrounding Rudy. His penchant for beating the odds was there from the beginning given his deft maneuvering past countermeasures deemed 98% effective. But 2% probability is still probability. Shortly after Livy was born we had discussed taking more permanent steps, but that fell in a crack somewhere on “the list” between going to the dentist, updating the will and cleaning out the rain gutters. But trust me. We’re done.
Perhaps our family’s immersion in the medical world this past year has us in a place where such a procedure is discussed with surprising candor. A generation ago I suspect Daddy would have just been feeling under the weather for a day, but I learned that Trish felt differently when the kids greeted me in the driveway a couple days ago with giggles and all kinds of curious questions. Amazing how brutal things can sound when medical terminology is replaced with the lunch-table vernacular of elementary school boys and a conception of surgical precision has seemingly not progressed much past that of a Civil War field hospital.
In the consultation prior to my procedure protocol demanded that the doctor explain the finality of what one is about to undertake and assess whether the patient truly feels he is done procreating. In my case, his quick glance at the medical history alleviated any need for further questions (“Let’s see you’re 42, kids aged 12, 10, 7 and……..9 months! Sign here!”)
In one of the brochures they gave me to read, I was advised to take stock of my current offspring and determine whether my life would feel incomplete without any more. I don’t think it was to be read as a joke book, but I did find it funny. I was urged to take some time and take stock of the situation and my hopes and dreams. I have to confess, I didn’t do much of it then but this weekend of reclining and recuperating also affords some time for reflection. Final score: 3 boys, 1 girl. In terms of the Geyling family, amidst siblings who appear marginal in their ability to produce male progeny, I have done my part in producing three capable of carrying on the name. In terms of the species, I have done my part to propagate exceptional traits in my offspring—one of intelligence, creativity and rhythm; one of athleticism, charm and humor; one of grace, beauty and artistry, and one with matchless tenacity and perseverance.
You’re welcome!
PS. Note to any dinner guests in the near future—you might want to decline the peas.
Our family had two eventful weekends in one. First, Trish and Olivia got to go out to Kansas for a mini family reunion with the Wilsons. The highlight was joining Grandpa and “Team Wilson” for a 5k run/walk. Rudy joined along in spirit as G’pa Dick competed with a pair of Rudy’s “running socks” pinned to his number. Team Wilson dominated the course with Wilsons in the front of the pack, holding steady in the middle and bringing up the rear throughout the race and EVERYONE finished with a smile on his/her face. G’pa won bragging rights as the #1 male walker of the day with his good friend Bob coming in a close second! Olivia was determined to walk too and finished despite the heat and humidity…not quite sure what she thought of humidity (ha). She also experienced her first Midwest thunderstorm AND the thrill of catching never-before-seen lightning bugs!
Livy stretches with Grandpa and cousins Rachel and Emma before the race
Thumbs up at the finish line!!!
Another win for G'pa Dick!
Team Wilson
A rare "sibs pic" with big bros Rick and Steve 🙂
Back here in Goleta we had a full weekend of our own. Before I get into the details I have to mention the Rescue Mission graduation on Saturday night. We celebrated the achievements of a dozen heroes who completed their twelve months in the recovery program. Thanks Heather, Jessica, Kelly, Nanci, Rachel, Andrew, Ben, Cal, Edward, Jay, Morris, and Sergio for being examples of how intimidating struggles are best approached by leaning on the people God has placed around you and by taking things one day at a time. I love what I do in that it gets me a front row seat to watch lives transformed.
Stepping back from the profound, Wilson and Max declared this weekend to be a “DUDE-CATION” as all the females in the family had vacated the premesis. I was glad they took time to brief Rudy on the elaborate wild-man rites undertaken when boys find themselves separate from girls for extended periods of time (because I needed a refresher). Turns out there’s quite a bit of freedom to be taken with bodily functions and noises–and more extensive and detailed conversations regarding them than I ever thought.
On a true dude-cation, all meals must be eaten without utensils. Considering there was toast and sandwiches in good supply, this was easily done, but I thought there would be an exception made when it was time for lasagna. Turns out Max’s commitment runs deep, even when the melted cheese singed his fingers.
You laugh a lot on a dude-cation, which is always welcome. True dudes also laugh in the face of danger. While anyone can enter the pool the conventional way, it’s much more fun to do something daring:
WilsonMax
OK, I know. Responsible parents wouldn’t let their kids do this, but after you let them roll your six-day-old down into the OR for heart surgery your notion of what’s dangerous gets altered. Not to mention, it just plain ROCKS! Rest easy, there’s no picture of Rudy engaging in the ceremonial Dude-cation roof leap…yet. I guess you’ll be sending your kids to someone else’s house when you go out of town for the weekend.
Even though some kids with heart defects can’t go to upper elevations, Rudy went on a high-altitude adventure (kind of). Nurse Aliza spent the last few weeks hiking the John Muir Trail and took him along.
Thanks for sporting your handsome Rudy bracelet, Aliza–Rudy and Lance make good company. If anyone else happens to take Rudy on an adventure, we’d love to hear about it.
I think Rudy likes being home almost as much as we like having him here. We enjoyed seeing him make it through his first week ever without a doctor’s appointment. Given some of the med changes we’ve made over the past few weeks, we were curious as to what the report would be at his check-in with the cardiologist today.
We’ve gotten pretty good at reading chest Xrays, but echocardiograms are still very mysterious. The process involves sitting quietly in the darkened room waiting as multi-colored blips flash across the screen accompanied by the sound of rhythmic pulses. Lots of different measurements are taken and the print button is regularly hit when there seems to be a splotch worth capturing for posterity. Only when it’s all over does the verdict come–and this time it was a good one. Dr. Harake feels that there is nothing about Rudy’s heart function such that we need to schedule the Glenn. Rudy can keep on enjoying life at home and continue eating and getting bigger (today he weighed in at 15 lbs 5 oz!). His next appointment with the cardiologist is in early August so if his O2 sats remain in the 70s (today he came in at 77!) and there are no changes in his heart function between now and then, we have a real good chance of holding off on the Glenn until the fall.
As far as the lab work, we were very curious as to his Potassium level as this needs to be closely watched and balanced for proper heart function. Among the recent med changes, we discontinued Potassium supplements, so we were interested to see what his level was. Turns out you not only want to see a 4.0 on your kid’s school report card; it’s also the number you want to see when your checking the potassium level in his blood. And that’s right where it was–Rudy is doing great inside and out!
Today is a milestone day for Rudy. He turned nine months old! Nine months full like we never could have imagined. In looking back over the pictures since October, the way he’s developed is remarkable, but I’m also very aware of the traits that are taking shape inside him. In overcoming all that he has, Rudy has been a model of tenacity, perseverance, patience and contentment. I can look at him in one light and see a frail little baby; but then I look at the way his chest pumps up and down, stretching the various scars from all of the different procedures and I see toughness personified. He’s fought hard to get here and we are so proud of our little man.
Today is an important milestone of a different sort. Our friends in the recovery community will be pleased to know that today is his CLEAN date. An unavoidable byproduct of what he’s had to go through is that Rudy has not lived a day of his life without narcotics…until today. In most hospitalizations, patients are able to use narcotics for limited periods without any lasting impacts, but given that he was there for seven months, five surgeries and all of the other pokes, prods and procedures, there was no way for him not to get addicted. In his last few months at UCLA, the team switched him over to methadone (the slower acting, longer lasting narcotic they sometimes use to help people get off heroin). Even this had to be weaned very slowly as Rudy had some tough bouts of withdrawal the times we went too fast. He came home on .3ml every 8 hours (which is already very little, but too much to cut cold turkey) and we have been stepping him down about .02 ml every 5-7 days. We brought him down to .03ml last week (a fraction of a teardrop) and cut him off today. We stood ready with the Tylenol in case he looked like he was struggling, but he didn’t require any of it. We’ll have to watch him for the next few days, but in the meantime I’m now looking for an age-appropriate big book in case we need to start working the 12 steps. Anybody want to be his sponsor?
It’s great to have our little addict in recovery, but that doesn’t mean medications aren’t a big part of our life. He’s still on 11 different prescriptions (for all you pharmacy geeks or heart parents: Digoxin, Captopril, Spironolactone, Diuril, Lasix, Albuteral, Atrovent, Levothyroxine, Aspirin, Bactrim and a Multivitamin). We do meds at 6am, 2pm, 6pm and 10pm. The biggest batch comes at 6am just after the food pump alarm goes off to signal the end of his overnight feeding–more reliable than an alarm clock. The other morning I had the presence of mind to snap a picture of our little pharmaceutical operation. Rudy will always be on some medications for the rest of his life, but we don’t expect it to be this many and we celebrate each time we get to move another bottle over to the dormant section of his tray. I think there’s five there now, so we’ve made some progress. Go, Rudy, Go!
Breakfast of Champions: Rudy's morning meds lined up and ready
Sorry for the delay between posts. The “no news is good news” maxim holds true. Been a great week here in Santa Barbara–some beautiful summer weather (sunny but comfortable in the 70s) came and we’ve been loving it. Max has been at track camp and Wilson at kayak camp, so they come home every day with tales of adventure. Throw in a good afternoon swim or two, end up sleeping well. Grandpa went back to Kansas to start his next round of chemo and Grandma stayed to keep an eye on Rudy and the rest of us.
Rudy’s pediatrician appointment this week affirmed what we’ve been suspecting. He’s feeding well and he’s growing (14lbs, 6oz). We’re seeing steady development as far as his motor skills, too. He looks all around now–instead of just looking down and to the left as he did when he got home from the hospital. He kicks his feet and grabs at things with his hands–usually he’s most successful at latching on to his O2 line or G-tube, so we need to keep things tucked in as best we can. Most mornings we find him having rolled over on his side during the night. All of this is relatively minor for most babies, but when we think of how many months we watched him lying prone in the hospital, we get a kick out of these new developments. Of course none of these have the emotional impact of his smiles, which he does quite often for us, but we’ll never tire of seeing more.
We’re excited to see Rudy make progress now that we are tied into the team from the California Early Start program, who has been doing assessments over the past weeks and laid out a plan of action for us this week. I’m not sure if Steven Covey wrote any material for infants, but Rudy now has a set of clearly defined goals, each with it’s own action plan of clearly articulated steps. Rudy may be behind developmentally, but how many infants do you know with goal/outcome/action plan sheets? Slackers, all of them.
These plans will primarily be carried out by two therapists who will come to our house twice weekly. Major goals we’re hoping to achieve by his first birthday include sitting on his own, taking food from a spoon consistently and developing some basic communication skills. We’ll likely have some regular exercises to reinforce the sessions with the therapists and also appreciate your prayers for these areas. As simple as these milestones seem, we will celebrate them heartily when we get there. As so much of our attention has been focused on Rudy’s viability, it’s encouraging to be working on some normal baby stuff.
I’ve seen the camera out quite a bit lately so I suspect Trish will have some pictures posted shortly. Thanks for checking on us.
While everyone was understanding, the only thing that would have improved Friday evening’s dedication service would have been for Rudy to be awake for more of it. We are really grateful for the way he has developed since bringing him home–he’s much more aware of his surroundings, looks all around (instead of just down and to the left) and is even starting to grab for things.
This week we’ll be getting our first home visit from the OT/PT team, but in the meantime I’ve gotten a bit of a jump on things with my own regimen. Click to watch a video Rudy’s latest trick:
As I posted briefly on Friday night, this weekend I’ve been very aware of the richness we find in the unexpected. We didn’t expect Rudy to join our family. We certainly didn’t expect him to have to battle like he has. I’ll go as far to say I hate that he has to battle like he does. I’m quite certain I’ll never get to a place where I can wholeheartedly say I’m grateful for his condition.
But yet I’m so grateful right now.
Grateful that within that which has scared us like nothing else in our lives, we have found comfort. We have found empathy and companionship that truly lifts the soul. We have seen character, compassion and fortitude blossom in our kids. We’ve learned about our own endurance and ability to function in the midst of extended challenge. We’ve met people who amaze us in their expertise and devotion. We’ve been blessed and been made aware of God’s goodness in brand new ways.
I am so grateful for Friday night’s dedication celebration. Life can become a blur in the land of critically ill children. Stints in the hospital can go on indefinitely. One can emerge from one set of challenges only to face another. The goal of survival can trump a balanced engagement of life. Instead of feeling involved in things, you struggle with how much you’ve missed.
Having a clear milestone amidst the disorientation is precious to us. We were able to look back and rejoice over what Rudy’s overcome. We were able to set our sights forward and pray for his future—a thoughtful, hopeful prayer rather than a rushed and panicked one in a hospital hallway. We were able to be together with so many precious people who have helped us in shouldering this burden. So thank you to all for being a part.
In the calm weekend that has followed Friday night, I’ve enjoyed asking the kids what their favorite part was. Olivia gave us permission to share her journal entry for Friday (below) and we clearly see that it was a significant celebration for all of them. I so appreciated Walter’s observation on Philippians 4 that we find joy not because of life’s circumstances but often in spite of them. I loved Uncle Bob’s specific word to Wilson, Max and Olivia on how he has seen them respond to the circumstances facing our family. I loved the slideshow and the worship. Missed out on most of the food because I was having too much fun visiting, but love that Sydney and her team blessed us with the leftovers (those PB&J bars have got to be illegal).
A future blogger perhaps?
For those who couldn’t join us, we’ll work to get some pictures up and on-line shortly but in the meantime I’ll wet your whistle with the lyrics to the song we asked Marlin to sing (and in hindsight, we feel it was very unfair to ask anyone to try to sing in that room with very few dry eyes). As Trish mentioned in the program, it’s a song we’ve played in our house repeatedly around the birth of each of our kids as it’s been our prayer for all of them. All the more for Rudy on this week as a true smile has finally emerged:
Sunrise of your Smile–Michael Card
Reject the worldly lie that says,
That life lies always up ahead,
Let power go before control becomes a crust around your soul,
Escape the hunger to possess,
And soul-diminishing success,
This world is full of narrow lives,
I pray by grace your smile survives.
For I would wander weary miles,
Would welcome ridicule, my child,
To simply see the sunrise of your smile,
To see the light behind your eyes,
The happy thought that makes you fly,
Yes, I would wander weary miles,
To simply see the sunrise of your smile.
Now close your eyes so you can see,
Your own unfinished memories,
Now open them, for time is brief,
And you’ll be blest beyond belief,
Now glance above you at the sky,
There’s beauty there to blind the eye,
I ask all this then wait awhile,
To see the dawning of your smile.
For I would wander weary miles,
Would welcome ridicule, my child,
To simply see the sunrise of your smile,
To see the light behind your eyes,
The happy thought that makes you fly,
Yes, I would wander weary miles,
To simply see the sunrise of your smile.
The time of dedication ended with a prayer for Rudy from Philippians 4:4-7…we share a paraphrase of it below and ask, humbly, that you join us in praying these verses over Rudy that he may experience the richness of a life lived knowing the nearness and love of God.
Dearest Rudy,
Delight yourself in the Lord
Yes, and find your joy in Him
Be known for your gentleness and never forget the nearness of our God
And don’t worry – whatever is going to come
Just tell God every detail and the peace of God that no one understands will come to you
No, don’t worry
Just tell Him every detail and His peace will come to you.
It’s time we should be getting on to bed, but I don’t think I can end the day without posting something. Our time together at Rudy’s celebration reminded us that with the heartaches of this journey come a richness we wouldn’t have experienced otherwise. We have felt such concern and support from so many over the last eight months, so it was so moving to have so many precious people in the same room. Even more moving to see people make the drive from places as far away from LA, San Diego, Santa Cruz and Sacramento. Thanks to all who came, to those who participated in the service and put on the reception. More to come, but tonight our hearts are so full. Thanks everyone!