The CUTEST big sister ever…

Rudy’s journey is draining on every member of our family in it’s own way, which makes me very grateful for when my kids have SUPER days.  Livy was excited to spend the day yesterday with Macey–said she was looking forward to it several times a day over the weekend, couldn’t stop talking about it afterward until she finally collapsed on the couch after dinner.  From the picture Greg posted on his blog, I think I know where her energy went…

http://www.zinkwazi.com/blog/index.php?showimage=1194

Thanks, Greg and Kim!  Perhaps a simple day, but oh-so-special for Olivia!

Happy 100th Birthday, Uncle Rixie!

Perhaps this is a bit off topic, but if there’s anyone worth making an exception for, it’s Uncle Rixie.  I think there are only two people in the world who can actually claim him as a legitimate uncle, but dozens who claim him as a surrogate uncle, parent or grandfather.  Long story, but when my father came to the US to attend Stanford as a freshman, he was taken under the wing of his Western Civ professor.  Dad became one of many people who learned that Rixie and his wife, Elliott, were very poor at keeping acquaintances, but very good at adoption.  With no children of their own, scores of fortunate people became their family.

I had Rixie’s big day noted on my calendar for some time and without question thought I’d be in the Bay Area with him to celebrate.  But not only do our circumstances make that difficult, but Uncle Rixie’s own health is such that he declined any celebration and isn’t feeling well enough to talk on the phone.  There’s so much good to say about him it’s difficult to know where to start, but anyone who has had the priviledge will understand my need to make mention of him. 

If you’ve lived one hundred years, you remember life before every family had a car or telephone.  You lived through two World Wars and saw 19 different US presidents (starting with Teddy Roosevelt!).  In Uncle Rixie’s case, the 100 years were filled with meaningful service to Stanford University and thousands of students in the classroom and as Dean of Admissions (how do you think I got in?).  While the milestone he’s achieved in his lifespan is impressive, more so are the scores of friends he’s made along the way.  I’m certain I am one of many who lament that we can’t celebrate him en masse today.

So tonight I no longer wish I could be in two places, rather in three.  It’s hard to beat sitting here in Santa Barbara listening to the unbridled laughter of three incredible kids, but I’d give an awful lot if I could have just a few minutes to be with Rudy at UCLA or to sit with Uncle Rixie in his apartment in Palo Alto.  Happy Birthday, Uncle Rixie!  Congratulations and thanks for everything!  I sure would love to work out a way to squeeze in a trip to the Bay Area.  But given the challenges we’re facing I didn’t want this incredible milestone for an incredible man to pass without some mention.

Missing the Munchkin

I checked the Mannings’ blog just about every time I walked past the computer today.  Just now, I came by and saw the post I had hoped I wouldn’t have to see.  Katie passed away this afternoon and I’m at a loss for words.  I only wish Alan and Vickie, who we only know through our blogs, weren’t on the other side of the country.  They have been courageous parents over the last five months and such a comfort to us.  Now we pray for peace and comfort for them as they mourn their little Munchkin.

Peace and Comfort to Katie, Alan and Vickie

It was such a comfort to be with everyone last night at the graduation.  In days like these, it’s good to be reminded of God’s power to work miracles and change.  More than that, it was such a blessing to be around people we love who we haven’t been able to see much due to the schedule we’ve been keeping.

No time for a big update now as this morning is going to be one of the rare times we’re all at home together, so we’ll make as much of those hours as we can before Trish and Grandma Jo head back to UCLA.  We’re still waiting to see if the fluid around Rudy’s lungs clears up enough so they can skip the surgery on Monday.  The fluid coming into the drains and the Xrays seem to indicate fluctuating symptoms, so please pray that it would be perfectly clear whether the situation demands surgery or not.

All of this seems so mundane and minor right now as our hearts are with Alan and Vickie at Yale who have come to the end of what can be done for their dear Katie as she battles HLHS.  As similar as our journeys have been, I can’t imagine what they are going through but send them love and prayer as they sit bedside and wait for peace or a miracle. 

This is a brutal monster we’re fighting.

Steady and Stable

Rudy had a strong day today.  His numbers held well and we heard few alarms.  One therapy that seems to be working well is the prescription of T3 for his thyroid deficiency.  You might recall that his thyroid function shut down a few weeks back, which would impact his overall vitality.  Having tried some other approaches yesterday they started T3 dosages which, along with the other medications, seem to be slowing the chest drainage.  Yesterday we had 120cc over 12 hours.  Today we have 90cc during the same period.  When I left on Monday it was somethingin the range of 240cc, so we have made clear progress.  Dr. Reemtsen has Rudy in the surgery queue for Monday, but we are praying the trend will continue so that we can cancel this one as well.

In the meantime, we have made progress on sprints off the ventilator.  Yesterday and today, he cruised through two one-hour sprints each day, so thanks for your prayers and please pray that this trend will continue.  Nurses Filma and Denise got a bit carried away doting on Rudy today and ended up putting him in a “snuggle-up” and propping him way up so he could look around.  At first he seemed a bit dizzy, but it grew on him.  Now he looks regal; propped up a bit in a bit of a throne.

It’s 7:15 and Trish and I are going to drive up to SB tonight (yes, I wasn’t joking–our anniversary reservation is at Chick-Fil-A in Oxnard).  It will be fun to all be at home for the first time in a month.  We’re looking forward to a quick visit tomorrow from Trish’s mom.  In light of Grandpa’s radiation starting this week, we’re glad Grandma Jo can steal away for a couple of days to meet Rudy.

16 Years of Wedded Bliss…

"Oh, He shouldn't have!!!"This week, I based myself back in Santa Barbara because the extended absence from home was asking alot of Wilson, Max and Olivia.  Those of you in SB know what a perfect and clear week it was up there–good for the soul to look out all the way to the islands.  Great fun to be with Oma and Opa and the kids every evening after work, but I was also counting the days until Friday when I could come back and see Rudy.

In addition to seeing Rudy, I was also looking forward to being with Trish on our anniversary today.  They say it’s the thought that counts, so I came in and told her that I had thought of bringing her flowers, but they aren’t allowed in the ICU.  But I didn’t come in empty-handed.  On the way down here I came across the perfect gift–a trophy that says “BEST WIFE” on the plaque.  With great flourish, I pulled it out of the CVS bag and presented it to her.  She turned it over in her hands and looked puzzled until I realized I left the price tag on it (a steal at $9.99!).  Once it was removed the tears welled up in her eyes and she has been speechless since.  The only sounds she’s made have been the sobs everytime she looks at me or passes by her anniversary gift.  Nailed this one, baby–nothing but net! 

And it doesn’t end there.  While we’ll stick to our lunchtime regimen of soup in the cafeteria downstairs, I may just pamper her with extra crackers.  I just need to make sure I have enough left for the big anniversary dinner splurge at Chick-Fil-A on the drive home.  You better believe she can have two sides–waffle fries AND cole slaw!!!!  Sorry ladies; curb your envy–this dreamboat has left port!!

Hard to believe we’ve been married 16 years.  I can’t recall the course I envisioned we’d take, but so much of life is unexpected and that’s what makes it an adventure.  Even when some of the adventures include gut-wrenching challenges, there is such simple joy in having a companion to walk with.  We didn’t have much choice for where we could spend this anniversary, but the choice to laugh in the midst of it is one we won’t easily relinquish.  So HAPPY Anniversary to us!

happy anniversary

 

 

sitting with dad

Homage to a Hero: Dr. Brian Reemtsen

I’m usually not at a loss for words (as this blog would indicate), yet I’ve found it very hard to compose a tribute to the key member of Rudy’s team.  There’s a tinge of pathos in saying that my son has the greatest heart surgeon in the world only because it assumes as a given that his condition demands it.  I am sure no one here at UCLA would be offended by my saying that I would much rather Rudy have no need of any surgeon; but as that’s not our reality, it’s difficult to express the deep gratitude we have for Dr. Brian Reemtsen.

 

When we first learned of Rudy’s diagnosis of Hypoplastic Left Heart Syndrome we got several recommendations to seek treatment at Children’s Hospital Los Angeles (CHLA), but we discovered our insurance network was contracted with UCLA.  While we were willing to fight to any extent necessary to get Rudy the right care we also realized the wisdom in reserving our energy for the most important battles, so we decided to do some due diligence and investigate UCLA—at least to have some grounds on which to base an appeal.

 

As I’ve already written, the initial responsiveness of Gary Satou and Dan Levi served as a remarkable introduction to the team at UCLA.  Both spoke no ill of CHLA but also laid out what UCLA could offer—most importantly an expert surgeon, Dr. Brian Reemtsen, to do this very intricate surgery.  Just months before, Dr. Reemtsen had come from CHLA to build a top-notch Pediatric Cardio-Thoracic Surgery program in the new Mattel Children’s Hospital at UCLA.  They had high praise and said that they would speak with Dr. Reemtsen as he would certainly want to consult with us.  This willingness was driven home the next day when Susan, his assistant, called to let me know that Drs. Satou and Levi had already spoken to Dr. Reemsten and he instructed her to call immediately to again affirm that he would make time to see us whenever we could get to LA.

 

Our first meeting with Dr. Reemtsen in September was no let down from the hopes we had built up.  He took the time for a very thorough conversation, entertained any and every question and was straightforward about the challenging diagnosis we were confronting.  He was empathetic, realistic and hopeful; able to put things into understandable terms and patiently allowed us to digest information and repeated himself if we asked.

 

We were forewarned of some the personalities we might encounter when dealing with specialists and surgeons who deal with such complicated diagnoses.  We were warned that the greater the expertise, the more aloofness one might have to contend with.  We were briefed on skilled surgeons who excel in the operating room, but might be less than comforting at bedside (on the rare occasions they make an appearance).  I’m not sure what experiences fed these stereotypes, but meeting with Dr. Reemtsen quickly made it clear they didn’t apply here.

 

I spoke of the very strong recommendations we received for CHLA and Dr. Reemtsen took no offense at this, having nothing bad to say about his former employer and even encouraging us to investigate both options.  In making the case for UCLA, he held forth the promise that he would be hands-on involved in Rudy’s care from delivery to discharge.  His arrangement here is such that this is his only hospital and practice so he’s here every day and can remain very involved with his cases (contrasted to a specialized surgeon who might have patients in multiple hospitals and only pass through on an occasional basis).  He would be by the bed several times a day and constantly interacting with the treatment team in every development and decision.  He would be honest about our circumstances, communicate clearly and not give false hope.

 

It was a very encouraging conversation, at the end of which he pulled out his business card, wrote his e-mail address and cell phone number on the back, and made it clear that we should have no hang-ups about using it for any reason whatsoever.  No answering service.  No automated phone trees.  Straight to him.  I never ended up calling it but remember a few worried evenings in my office, as I tried to take in all the unknowns that lay before us, where simply picking up that card and turning it over to look at that number brought a sense of comfort and reassurance.  We were in good hands.

 

At the outset, I don’t think I would have been able to articulate an itemized list of qualities I would want my son’s cardio-thoracic surgeon to have.  As Rudy’s heart would be very small and would require very steady hands, I remember checking Dr. Reemtsen’s during that first meeting to make sure all the fingers were there and that they didn’t shake excessively.  Overall, I noted no obvious involuntary ticks but did wonder if it would be possible for me to hide in his closet and jump out just to see that he didn’t startle uncontrollably.  Other than that I didn’t have any sophisticated rubrics for evaluation.  Other doctors spoke highly of him and we wouldn’t expect UCLA to hire anyone with blemishes on their record (but I did check), so the main criteria for us to choose our expert had little to do with an educated analysis of his skills, but simply by how we felt about him.

 

While arrogance is not an attractive trait, when it comes to choosing a heart surgeon neither is too much humility.  You want self-confidence; a person who is well aware of their competencies and does not question them.  While the general population strives for well-roundedness, I prefer my heart surgeon to be somewhat out of balance—a bit too dedicated to work, unable to thwart perfectionist drives, never able to make enough time for hobbies, incapable of leaving work on time or stay away on a weekend.  Someone who will always remember that he’s dealing with MY baby—and that my world has come to a stop.  Someone who realizes that my medical training ended with high school biology, but I’ll be comforted to know relevant information in language I can understand.

 

I trust the number of interactions with Dr. Reemtsen documented in this blog communicates implicitly what is taking me a number of passes to state explicitly.  He is a person that exudes competence; who I suspect doesn’t give much time to things he can’t excel at.  He is purposeful and doesn’t give indication that much time in his day gets wasted, but has time to stop and be friendly.  He wears a mantel of importance, but carries himself without much fanfare.  His attention to his patients knows few bounds as demonstrated by the evening and weekend visits and the late-night phone check-ins I’ve overheard.

 

If the guy who holds my son’s heart in his hands demanded I call him “Spartacus”, I’d have no problem doing it, yet I love the way he introduces himself as “Brian”.  As isolating as life can be here in the CTICU addressing our key source of comfort as “Dr. Reemtsen” would keep him far more distant than we’d like.

 

I make no pretense that I’m motivated largely by my own self-interest in this whole journey.  I want the best outcome.  I want Rudy to have the best.  But this comes at a cost, and I’d be delusional if I thought I was shouldering more than a fraction of this.  In his devotion to our son, Brian has made our burden his (along with so many others here at UCLA) in ways that we never could repay.  We’d like to think we know what’s best for our kids and provide everything for them, but this experience has shown our knowledge and competencies to be shockingly finite.  So thank you, Brian, for having the expertise and skill we could never muster.

 

I also realize that others pay a cost for Brian’s round-the-clock devotion to Rudy.  On several occasions, we’ve heard Brian speak of the Reemtsen ladies.  As their husband’s and father’s commitment to my son undoubtedly makes for absences from them, we are so grateful.  May they realize now and in the future the profound hope he brings to families like ours through what he does each day.

 

Dr. Reemtsen checking on Rudy
Dr. Reemtsen checking on Rudy

Pray for the fluid to stop…

The odd existence we’re living here make times of focused or extended prayer a challenge.  Today, like many days, we uttered a quick “Please, Jesus, let this be a calm day” as we stepped off the elevator on the 5th floor.  Unfortunately we were met with a bump shortly after we got here as we were having a check in with Dr. Reemtsen.  Alarms started to go off and, after a couple nonchalant looks at the screen (the usual first response), the tone got more concerned and then the inexplicable signal went off and six people were suddenly at the bedside dealing with the breathing tube.  Just a few minutes passed and, almost as quickly as they came in, everyone was gone.  No big deal–possibly just an obstruction in the breathing tube.  I’m glad there’s always a couple that check on us before going and we usually lie and go along with the “no big deal” line, but I don’t think we fool them with our ashen complexions and tears welling up.  I don’t think Rudy was ever in significant danger, but I don’t think we’ll ever get used to jolts like this.  Suddenly we’re both in need of comfort foods and are craving Big Macs and lots of french fries (you go to your happy place, we’ll go to ours).

The conversation with Dr. Reemtsen did set forth a plan for the week.  Rudy’s cardiac function continues to be very strong, so much that Dr. Harrison recommended that his next echocardiogram be at his discharge.  Everything they are addressing now has little to do with heart function, the biggest issue being the chylothorax (lymphatic fluid in the chest cavity).  The hope has been that the drainage into the chest drain would taper off, but that hasn’t been the case.  The medicine they’ve been giving him (Octreotide) should have worked by now, but they’re going to give it a few more days.  If there’s no change, the plan is to do another surgery on Thursday to ligate the thoracic duct.  Not a major surgery, but surely one we’d rather not see Rudy have to endure, so please pray that this would heal itself and the flow of fluid to the drains would stop.  So far we’ve seen fluids be very responsive to prayer so let’s channel the same effort that went into producing urine into the ceasing of lymphatic fluid.

Dr. Reemtsen feels that Rudy won’t make much progress until this can be corrected as all of his nutrition is likely just flowing out of his body into the drains.  They are also looking closely at his endocrine system as they are wondering if there’s some steriod deficiency or ongoing thyroid issues that are hindering his ability to move forward.  There’s also been consultation with the infectious diseases team as, though no significant cultures have grown, some of his symptoms (low blood pressure, occasional fevers) are making it tough to rule out).  In any case of extended hospitalization, the threat of infection emerges, so we’re praying against this.

That’s this morning’s update.  In the midst of it all, Rudy is lying very calmly and loves looking up at his aquarium.  I do wonder often what kind of thoughts are going on in his little mind through all of this.

Tougher Than the Rest

If your rough enough for love, baby I’m tougher than the rest.  —Bruce Springsteen

This lyric seems relevant tonight as we had another one of those afternoons that are all too commonplace in this process; one that stretches us and makes us realize that this process with Rudy takes toughness.  Just when you think you’ve been pushed as far as you can go, there’s another shove.

The chest drain went in smoothly and gave off lots of fluid, but Rudy’s low blood pressure was of concern all afternoon.  We went out to get some fresh air with the kids and shortly after we returned to the room the activity in the room suddenly picked up.  I still wonder how these ICU people communicate–first just a doctor and a nurse…then a second doctor…then more nurses and care partners.  The room stayed quiet, but focused and intense to where we could pick up that it would be best to pull out the kids and Oma and Opa out to make room for 8 people that were now at Rudy’s bedside.  The phones started ringing as other members of the team answered their pages and I could pick up the concern as I stood watching from the doorway.  I don’t think Rudy was in as much distress as some of the previous episodes and, probably in shorter time than it felt, they were able to find the right cocktail of medications to get his BP where it needed, but it was disheartening for me to watch.  He’s so fragile and delicate and the going is so slow that it really doesn’t feel like we’ve made much progress over where we were a week ago.  My kids were in the next room–they need us just as much as Rudy does.  Yet it’s so hard for me to focus my attention anywhere else.

That Springsteen lyric first came to me yesterday as we were watching the pediatric patients trick or treat down the hallway outside.  The staff had taken time to set up at different doorways so they could have as realistic an experience as possible.  The kids were cute, but I couldn’t take my eyes off the parents even though few of us were able to make more than a few seconds eye contact.  This wasn’t the Halloween they hoped for, yet they show up for their kids and enthusiastically wheel them down the hallway, making sure that IV lines don’t snag and that costumes can somehow be tied on around the medical equipment that needs to stay attached to their kids.  Some of them do it very tentatively and hesitantly and I hope that means that this holiday in the hospital is an anomaly.  But other parents move instinctively and maneuver the equipment with a second nature that makes it clear that this isn’t the first time they’ve had to do this.  These are the tough ones–tougher than the rest.  Who knew what our love for our kids would demand of us.