In the wake of Katie’s passing with grief and much concern for Alan, Vickie and their families, it is hard to know where to go with our own updates about Rudy…so many thoughts and feelings to process and yet, many of you are eager to know what’s going on today…I feel the need to post a more “thoughtful” update but for now let me just say that Rudy’s surgerical procedure has been cancelled. The doctors had me sign a consent form last night “just in case” but the xrays came back looking good and after the rounds this morning, they decided the procedure wasn’t necessary. I will share more later and, as always, thank you for your prayers!
Month: November 2008
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…
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!
Cuddle-bug

Okay, these pictures really don’t do him justice but I walked into Rudy’s room last night after the evening shift change to find the little guy snuggled so sweetly…Nurse Pam had run her tests, cleaned him all up and got him all settled on his side. He looked like such a big boy cuddled up to Pooh! Around 10pm he got turned to the other side and slept very comfortably and soundly all night long! So sweet!

Yesterday was uneventful…It was fun to see Dr. Robert back on the floor after a couple of weeks. Because Rudy’s surgical procedure was postponed, he spent the day just hanging out. He battled high blood pressure but didn’t seem too bugged by it. Yesterday was one of those fun days with Nurse Denise where he was awake and alert a good bit of the day but comfortable and not anguished. The fluid draining from Rudy’s lungs has remained the same…they will continue to monitor this the next couple of days and then decide whether or not to do the surgery on Monday. The big news of the day came when we got the test results back from the Infectious Diseases people confirming that Rudy is infection-free so the order came to take him off of three antibiotics! Yippy! He also had a couple of successful hour-long ventilator sprints again which is always encouraging so I believe the plan for today will be to continue exercising his lungs.
Rolf came back to UCLA early this morning and we will both head home to Santa Barbara late tonight for some time with the kids and the, always special, Rescue Mission Recovery Program Graduation tomorrow night.
Nov. 5: 5 weeks old today
Five weeks ago today our little Rudy was born. That means we’ve had five weeks of foot holding, hand grabbing and head rubbing on Rudy, five weeks of the yummy soup down in the cafeteria, five weeks of walking to and from the hotel every morning and late night, five weeks of listening to the beeps and alarms of monitors and medication dispensers hooked up to our son, five weeks of hearing a recap of the kids’ day by phone right before bed every night, five weeks of searching Rudy’s big blue eyes, five weeks of (almost) daily blog posts,etc, etc, the list goes on. Not knowing, really, what to expect when we started this journey, a five week timeline is about what we originally planned around. Well, five weeks have come and gone and now it’s time to regroup, adjust expectations, and focus on a “plan B” for the next unknown block of time.
I am where I was 5 weeks ago…unsure of what the next several weeks will bring and VERY unsure of how to plan for the unknown. In Rudy’s world, you take life one hour at a time and yet I have a family at home that has needs that go beyond the next hour and I’m finding it hard to function in both worlds. All this to say, it’s time to look ahead to some degree and it’s a little overwhelming.
Rudy had an uneventful 5-week birthday. Today’s focus, once again, was fluid output AND it has remained about the same-no change on average since yesterday. In regards to the procedure scheduled for tomorrow, there were no clear indicators whether or not to do it which led Brian (Dr. Reemtsen) to hold off and postpone until Monday giving Rudy a few more days to prove himself unworthy of another trip to the OR!!! Because we would prefer Rudy not undergo another surgical procedure if at all possible, we’re at peace waiting a few more days. Please continue to pray that the fluid draining from around his lungs WILL stop (making the surgery CLEARLY unnecessary). Thank you, thank you!
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.

Please Pray for Katie
Many of you have been following Katie Manning’s struggle and we just got a tough update on their situation. Please click here and pray for them today as Katie needed to be rushed back to the OR.
“Watching the President Show”
When Olivia called me this evening, I asked her what she was doing and she said, “Watching the President Show”. Yep, that’s what Rudy and I are doing as well. It’s Rudy’s first presidential election and he has been fast asleep most of the day. President-elect Obama is about to give his victory speech but, with all due respect, I don’t think Rudy cares much about such affairs…when he is awake, he looks as if all he cares about is to be tube and line free. Well, if the fluid around his lungs ceases to drain, he could get his wish to be free of at least 2 tubes…okay, I won’t go there yet but I can’t help but be encouraged. There hasn’t been much change since my post this morning…the fluid output has remained the same. No less but no more either. I’m praying that, come morning, there will be no output at all!
Rudy IS minus one of his arterial lines. The a-line that was in his left hand has been bleeding pretty consistently the past couple of days. This particular a-line was monitoring his blood pressure but has been in so long that it just started to wear out. For now, they have not replaced it and are relying on a little blood pressure cuff wrapped around his ankle. So, for tonight, his little hands are free. We’ll claim any progress we can! Thank you for your continued prayers!!!!! Love to all from Rudy’s room…


