
P





Wow, it truly is hard to believe that one week from today Rudy will celebrate his 1st birthday. All those months in the hospital I didn’t allow myself to look very far into the future and since we’ve been home, life has been so full and active I haven’t had much time to think about it…but here we are – a year later and getting ready to celebrate a major milestone. We may look a little tattered and worn but our family is certainly richer for the experiences of the last year and we are deeply blessed by the joy and laughter Rudy brings to the scene.
Our “Rudy’s Beat” community of family and friends has been a big part of the blessing of this past year through your prayers and encouragement. Because you are a significant player in Rudy’s journey so far, we wanted to extend an invitation to you to take part in a “worldwide” cyber-celebration. We invite you to wear Rudy blue (aqua), do something special or creative next Thursday, October 1st in honor of Rudy’s birthday and email us a pic of you celebrating. As if that isn’t fun enough, all cyber-guests will recieve a party favor so be sure to email us your mailing address too! Ha Ha
We have a tradition in our family of sending “cousin cash” to our nieces and nephews each year on their birthday…a small gift that the birthday boy or girl can pool together and get something they really want. For those who feel so inclined, in lieu of sending Rudy a gift, we’d like to invite you to send a small “cousin cash” donation to www.kissesfromkatie.org in his honor. Katie Manning, along with her parents, was and continues to be a source of inspiration to us and we would be blessed to see the very practical help her parents are providing to ICU kids and their families through their organization supported.
Locally, we’ve decided to keep things LOW KEY but if you happen to be in the Santa Barbara area, please join us at the McDonald’s on Fairview Ave. (ocean side off the 101 – and not just ANY McDonald’s, this is the birthplace of the Egg McMuffin! So, for those of you who don’t do fast food – Kelly- it’s kind of like going to a museum!) for a hot fudge sundae…we’ll be there Thursday evening from 6:30-8:00pm on the patio! Ha Ha
Okay, gang, get creative and LET’S PARTY!!!!

I think there’s consensus on the fact that Rudy is a superhero, but I’m not sure everyone grasps the full extent of his superpowers. Lately, I’ve been studying one carefully as it boggles the mind…he seems impervious to unbelieveable dips in his oxygen sats.
For those of you who aren’t heart parents or pulse oximetry geeks, normal oxygen saturation levels in humans are 92-100%. If you dip below 90% you get put on continuous oxygen. When normal humans get below 80%, function can become drastically impaired. Not much farther below that and they start to turn blue.
As an HLHS parent, you’re told that your child will have sats in the 70s and 80s prior to the Glenn. Rudy needs continuous oxygen to stay at that level, but the docs have told us that there’s no need to get neurotic if tanks run out, the power goes out and the concentrator doesn’t run (like it did last week), or we need to give him his bath. It’s not devastating for him to drop below that level for a period of time. We check sats regularly just to keep an eye on things and this is where Rudy’s superpower becomes evident. This week, I brought him in from the car and decided to check his sats while the concentrator warmed up. Here’s what I observed:




Good heart rate of 125. O2 sats of 35!!! Pink as can be. Smiling and laughing away. How does DeSat Boy do it? (Yes, it’s reading right). I’m expecting calls shortly from NASA and an Everest expedition or two as I’m sure they’ll be curious as to why they all need supplemental oxygen to function (pansies) while Rudy keeps right on giggling.
Fly on, DeSAT Boy!
Rudy thought he had breezed through his regular checkup with the pediatrician today.

Then things took a turn for the worse.

It’s relatively minor compared to all the other trauma he’s experienced, but no baby likes those blasted shots. (I know you’re probably picturing gut-wrenching screams, but remember–as much of a tantrum as this looks like–it was dead silent because of Rudy’s trach. That still surprises me every now and again when he gets really upset like he did today.)
But it wasn’t too long before he was the picture of resilience.

He’s got good reason to smile as Dr. Abbott gave him a big thumbs-up after his exam. He’s continued to put on weight–in fact, we think he set a new record by putting on a whole half pound in the last week. So he’s up to 17 1/2 lbs at a strapping 27 inches tall. His lungs sounded very good and clear. There’s significant relief for us in this realm as some of the docs decided it would be wise to do a test for cystic fibrosis because of some of the challenges Rudy’s been having with breathing and secretions over the last month. The team at UCLA did a genetic test last winter which ruled out everything but one minor anomaly. The consensus was that this probably meant it was 98% sure that Rudy didn’t have CF, but given the concerns about his respiratory function it seemed wise to be even more certain. So this week he got the sweat test which came back negative as well. Can’t say it didn’t produce a bit of anxiety for us to even have to run a test for another major health issue, but it’s great to have this ruled out. It gives us even more hope that Rudy will one day be able to breathe on his own. There’s not a major condition blocking him; he just needs time to get strong enough to go without the trach.
There are probably a few factors we can point to that seem to be helping Rudy breathe better. Getting bigger and stronger through his nutritional regimen certainly helps. There have also been some medication changes that seem to keep the secretions at bay. The cooler weather might also play a role–he did seem to have a hard time a couple of weeks ago when it was hotter in these parts.
We also think his spirits were boosted by a visit in our home from Nurse Aliza, though he probably had a hard time recognizing her without her blue UCLA scrubs.

But I humbly suggest that the most significant development has come from another fit of innovation. There has been periodic mention made about humidifying things a bit for Rudy as a 2l/hr oxygen flow can dry patients out. You might recall that we had a compressor from home health that gave him mist, but no matter how we tried to rig this to run in tandem with the oxygen concentrator we couldn’t keep his sats anywhere near where they needed to be. A couple of weeks ago, it got tiring to watch him fight with such thick secretions so I started to think back on some of the setups I studied for days on end back in the ICU. I suspect the “right way to handle this” would be to work with the home health company on this, but I wasn’t up for the prospect of navigating phone trees, getting the necessary order from the appropriate doctor and then arranging and waiting for delivery. A second approach would be to find it on the internet (which was quick, easy and probably half the cost of home health), but it seemed that even $30 for a rather simple contraption that would take 5 days to arrive wasn’t preferable.
So, I went for a third option, which involved grabbing an empty saline bottle (which we have in good supply thanks to the last time I took matters in my own hands), getting some drip irrigation tubing from the garage, and spending 89 cents in the plumbing medical supplies aisle at OSH. Less than an hour later after a bit of drilling and cleaning, the hum of the concentrator was accompanied by the pleasant bubbling sound of Rolf’s Wonder Humidifier taking that nice oxygen and giving it a sweet, sterile bath before it made its way to the mask. Rudy thinks it’s yummy.
I held off reporting on this exciting innovation right away even though it seemed his secretions became much more manageable in short order. They’ve stayed that way ever since we started using the RWH, so it’s a keeper. Anyone know a good patent attorney? Between this and the smashing success of the PRS, I’m not sure how much longer I’ll be needing my day job!

Since school started, the pace at home has picked up and time is FLYING by. There are so many new experiences for Rudy about which we’ve wanted to post but they are happening so fast and a big snowball is starting to form…rather than go into lengthy descriptions of all the fun, I’ll let the following pics speak for themselves.






I just had to post the following link to a radio interview my dad did this week. If you have a minute, it’s a great interview for a wonderful cause. Dad is participating in the Head for the Cure 5K Race/Walk (www.headforthecure.org) on September 13th in Lawrence, KS in support of brain cancer research. Although he will be starting a new chemotherapy regimen this month, his doctor has given him the go-ahead to participate with a few precautions in place. Once again we cheer, “Run, Grandpa, Run”!!!
To hear the interview, click here, and then click the “Dick Wilson KLWN Radio” Bar to start!
Since we’re on the subject of links…here’s one more for you. Rudy made Greg Lawler’s photo blog again (not like we’re counting or anything!)…boy, do I wish I had his gift for capturing precious moments. Click Here!
We’ve reached another milestone…Eleven Months! Trish’s computer has been sidelined briefly with a virus, and with it some cool pictures that would make for a celebratory post, but we certainly didn’t want this day to pass without some acknowledgement.
Unfortunately, Rudy had to mark this day with an unscheduled visit to the pediatrician. His lungs have been pretty congested for the last couple of days–or “junky” for those of you who deal better in medical lingo. He’s been a bit uncomfortable, but I’m not sure if he’s worse off than his parents who’ve had to suction him about every 20 minutes around the clock. On the immunologist’s recommendation last week, we did change up a few things with his breathing treatments, but perhaps this was too abrupt. So, we’re going to do a bit more gradual transition introducing Singulair to abate secretions and more slowly wean the inhaler treatments. Breath easier, Rudy, Mom and Dad would like more sleep.
Due to the equipment issues I don’t have any pictures of Rudy handy, but while we’re celebrating birthdays let’s welcome Alyssa Johanna Geyling, Rudy’s new cousin who was born yesterday. In addition to her stellar good looks, she also demonstrates remarkably good taste in fashion accessories at a young age.

So we don’t have any new pictures of Rudy ready to post right now (but we have a sure classic coming), but Wilson and Max thought it would be cool to post some skateboarding pictures from the last week of summer vacation on Rudy’s Beat. What does this have to do with Rudy or HLHS? Absolutely nothing. But they are cool.


If skateboarding is cool, how much cooler is finding a taratula at the skatepark?

While we were in the neighborhood, I humored my wife’s recent obsession with Micheal Jackson coverage by making a swing by the Ranch.

Hard to believe school’s back in session. We made the most of the summer.



