Renly and Nick convalescing together.
(April 19, 7:13 pm) -- Early this afternoon I was able to pick up Renly, who is comfortable but pretty woozy after his surgery. Unfortunately he's cursed to wear a cone of shame for the next few weeks, but we're extremely glad that everything went so smoothly. I spent the morning assembling child gates to keep him off the stairs, but so far he hasn't shown much interest in wandering around.
Nick is doing great today. He got a good night's sleep, his pain is minimal, and we've both gotten pretty good at running IV meds.
Karen, for her part, is keeping busy even as she heals, repotting orchids and making a coffee cake for Easter.
Now that everyone's home and on the mend, we'll probably be updating more erratically, but there are still plenty of milestones ahead so do check back if you're interested.
Again, thanks to everyone who has shown so much love and support over the last weeks/months/years. We're grateful beyond measure.
-- Drew
(April 18, 2:22 pm) -- Just spoke to the surgeon at Friendship Animal Hospital. Renly completed his surgery and it went well. His tumor was huge -- the size of two fists -- but doesn't appear to be malignant, and they were able to remove it with no problems. (Yes, I requested a picture.) The second mass seems to have been a false alarm, and the doctors were able to close him up using a slightly less invasive procedure than we'd expected. Renly's waking up now and we should be able to bring him home tomorrow.
Once again, there's plenty of healing ahead, but I'm hugely relieved.
Oh, and Nick is doing fine too.
-- Drew
Renly, pre-surgery.
Renly's chest. The mass on the right isn't supposed to be there. His esophagus is the dark tube being pushed off center by the tumor. His heart is at the lower left.
(April 17, 11:04 am) -- Nick's settling in at home with varying degrees of comfort. Last night he had a fair amount of pain again, but hopefully we've got the medicine schedule straightened out to address that going forward. He's comfortable now, and he just received his first dose of IV antibiotics delivered by yours truly. Aside from accidentally spraying the room with saline at one point, it seems to have gone well.
We also, for context, wanted to share the other big story going on in our lives.
Last month, three days before Nick's surgery, I took Renly in for a check-up mostly because his nails were too long and I needed help trimming them. While listening to his chest, the vet was unable to find a heartbeat on his left side and suggested we do some x-rays. The scans revealed that most of Renly's chest cavity is filled with a large growth, which more tests have shown to be a thymoma -- a slow growing tumor emerging from his thyroid -- along with a smaller mass in his left lung. The doctors at Altas Vet on H Street and Friendship Hospital for Animals are both amazed that he hasn't had any trouble breathing; the growth is taking up the "vast majority" the space in his ribcage. In the attached image you can see his heart and esophagus pushed well off-center.
After consulting with several vets, we've decided that surgery is the right option. It's been agonizing because right now Renly seems fine (and has been feasting on chicken and rice for the past several days) but given his overall good health the balance seems to be in favor of intervention. All we can do is hope we're making the right choice. He'll check in at Friendship tomorrow at 6:30 am. If all goes well we'll see him on Saturday or Sunday. He'll be coned for the first few weeks, then we'll need to keep him quiet for another month or so as his ribs heal.
The result is that for the past week or so Nick and Renly have both been on prednisone. Nick got off gabapentin just in time for Renly to get on it. We'll see whose drugs cost more.
So, yeah, it's been a hard couple of weeks. We're eternally grateful to Nick's Aunt Amy for providing Renly with such loving care while Nick and I have been at the hospital. And I can't say enough good things about the doctors at Atlas Vet, in particular, who have been attentive and gentle with Renly and even better with me.
Send us good vibes and give your pets some extra love tonight.
-- Drew
Renly's been asked not to lick Nick's face or incision. He's working on it.
(April 16, 9:15 pm) -- This afternoon Nick was officially discharged from Georgetown, twenty-three days after he checked in. It was a long process, but we're both overjoyed to be home.
There's still plenty of healing ahead -- by my count Nick's got about two dozen pills coming his way every morning and evening for the foreseeable future, along with a bunch of IV meds I'm sure I'll be able to figure out -- but it's hard to overstate how transformative this surgery has already been.
Thank you to everyone has sent their love and support for the last three weeks. Our gratitude knows no bounds.
-- Drew
(April 15, 6:02 pm) -- All the signs pointed to discharge today, but apparently all the signs were wrong. The doctors need to make sure Nick's home care is set up before they'll let him go.
That seems to all be resolved at this point. We've been told by several sources that he's officially scheduled for discharge tomorrow, but ... well, we'll see. I'm done counting chickens.
In anticipation of Nick's return, Renly has arrived home to lead the welcome committee. I'm sitting on the couch with him now, and it's wonderful.
-- Drew
(April 14, 6:35 pm) -- A doctor from the infectious disease team stopped in this morning to share that they'd identified the bacteria causing Nick's infection and they're confident about the right antibiotics to treat it. He'll need to be on an IV for at least a few more weeks, so they installed a PICC line (a port in his arm that leads way into his chest and will be a lot more durable than the little ones they've been putting in and out of his arms) so he can get meds at home.
While we haven't gotten any official word, all signs are pointing to discharge tomorrow -- three weeks to the day after our arrival. We'll (hopefully) get final word in the morning, after which it will take most of the day to get everything in order.
Very much looking forward to getting Nick home. Right now there's a sink full of dishes that needs attending to.
-- Drew
Kaus Shipping De-Livers
Violet confirmed that the image in the lower left is NOT a tombstone. It's a sunset.
(April 13, 5:49 pm) -- Yesterday, my brother Bruce came down to check in on Nick, and he corroborates what I've been saying for weeks: Nick is looking great. We spent most of the day hanging around the hospital room, but also managed to get out for lunch and to check out the new record store in Unions Station before he got back on the train. (Congrats to me, the new owner of Breakfast in America.) He also delivered this beautiful piece of art from Violet, wishing Nick well.
This morning Karen and her son Max, along with Aunt Nancy, stopped in to say goodbye before heading back to Milwaukee. Karen's still got some soreness but is overall feeling good and ready to head home. She remains our hero. Max is unconvinced about applying to Georgetown for college, but I'm working on it. He's set on a school with a flight program, which Georgetown does not yet offer.
Nick decided to mark the occasion with celebratory "Kaus Shipping" t-shirts. (Kaus is the maiden name of Judy and her sisters. Kaus shipping refers to the family's habit of shuttling furniture, homegrown fruit, and family heirlooms from one household to another by hand rather than wasting money at the post office. This is, to our knowledge, the first liver delivery.) I think we all look pretty good.
Nick's been enjoying the visitors but looking forward to some new scenery. His veins have been so well poked that this afternoon they had to send in an IV expert to find a blood vessel they could actually get a tube into. After a while even she gave up and they're going to try again later with an ultrasound. I think I'd lose my mind being stuck with that many needles, but Nick is unperturbed.
All of Nick's numbers are going in the right direction, and it seems like his infection is under control. We just got a visit from the PA (one I like) who was able to lower some medications and confirmed that everything is on the right track.
Most importantly, today, for the first time in three weeks, Nick is wearing not just a shirt but actual, honest-to-God pants. I think he looks very dignified.
-- Drew
(April 11, 9:37 pm) -- This morning the interventional radiology team adjusted the placement of Nick's drain to address the infection they located in his abdomen. This was ... not fun. Despite getting pumped with enough Versed and fentanyl to knock out a horse, Nick managed to wake up (!!) during the procedure and felt a whole bunch of pain. Once he got back to the room and took a long nap, he felt better but was still sore for most of the afternoon and only clocked a few laps around the floor.
The uncontested highlight of the day was a visit from Hallie and Clover who updated us on school, discussed their upcoming birthdays and demonstrated new and creative hairstyles. Clover took advantage of our generous nurse, Meg, to get a some expert instruction in the medical arts, helping to empty and measure Nick's drain and remove some bandages.
Overall status remains consistent: progress continues to be good and we're feeling optimistic about getting home early next week.
-- Drew
Clover starts her medical training early.
Nick doesn't usually scowl like this, but, damn, he's looking good.
(April 10, 6:00 pm) -- Nick got a good night's sleep last night and had both a CT scan and a liver biopsy this morning. By the time his records were updated to allow food by mouth, the kitchen had closed for lunch. Luckily Nancy and Karen had made PBJs and Judy typically travels with enough food to provision a small army, so sustenance was available.
The biopsy results will take a while, but the CT scan shows what looks like an infection that the interventional radiology and infectious disease teams will be able to treat by repositioning his drain, running a culture, and prescribing a round of antibiotics. We'll be here through the weekend, but discharge next week is a good possibility.
There's also a fractured stent that the transplant team may need to address. So that's a thing, too.
In the meantime, we've started hanging photos of loved ones around the room to keep Nick's spirits up. And by "loved ones" I mean whoever happens to be next to Renly in a given picture. The nurses all agree that he is an extraordinarily cute dog.
Nick is approaching his extended stay with good humor, but he says he's starting to feel like he's "trapped in a combination of Groundhog Day and One Flew Over the Cuckoos Nest (without Nurse Ratched)." Indeed, all of the nurses here are lovely — though there is one PA I've got grudge against.
Hoping to see some doctors from the transplant team before I leave tonight, though they have an uncanny ability to show up the moment I step out of the room.
-- Drew
(April 9, 1:04 pm) -- Nick had a good day yesterday and again did laps around the floor, even with a reduced dose of antibiotics. There was also a brief dance party in the room, but, alas, I've been told not to share the video. The doctors are still trying to explain his elevated white blood cells though, so when he mentioned that he felt a slight pain on the right side of his chest they jumped on it, sending Nick for his first ever mammogram. (Which was emphatically NOT on my bingo card.) He got a clean bill of breast health, although he said that squeezing himself into position against the machine with a large abdominal incision was uncomfortable.
That seemed like a blip. His appetite was good and we watched Moonstruck on my laptop before I headed home. (What can't Cher do?)
Unfortunately, overnight his white blood cell count spiked, and he woke up with significant pain around his most recent drain site, radiating up to his shoulder.
The doctors need to get this under control, so today he's getting another chest x-ray and tomorrow a liver biopsy. Right now Nick's feeling pretty uncomfortable, so the pain meds are bumped up again. He's still sore, but it's manageable, and he's feeling sleepy since they kicked in.
Yesterday seemed to go so smoothly that I, at least, had pretty much accepted that he'd be home today. Apparently, it's not to be. It's a disappointing turn, but we're extremely glad he's dealing with this under the close care of doctors. Renly, our own chief medical officer, only ever recommends couch time and extreme licking.
Not making any predictions today. We'll see where the tests lead us.
-- Drew
(April 8, 9:38 am) -- Yeah, I'd like to know that too.
Nick's still got a little pain, but that's to be expected considering that he was sliced open and his viscera rearranged. Twice. He says he's feeling better and his mind is clearer than before the transplant, and he's doing dozens of laps around the floor. (For those of you who have seen him in the last few months, you know how huge this is. It used to be that he'd fall asleep mid-conversation. From now on if he does that you should be insulted.) All signs are that his new liver is adjusting to his body and working well.
The catch is that his white blood cells are elevated even though he's not showing any other signs of infection. Given all the anti-rejection drugs, that's something they need to keep a close eye on. They're going to fiddle with his antibiotics today to see what happens. So he'll come home ... soon? Soonish? He's extremely eager to be reunited with Renly, but receiving great care at Georgetown. We're in no rush.
At the risk of being repetitive, we're so grateful for all the love and support we've received throughout this process. Thank you, thank you, thank you.
-- Drew
I wanted to get a better picture of Karen earlier but she was too busy helping clean up from dinner to pose.
(April 8, 9:03 am) -- We’ve had so many inquiries about how cousin Karen is recuperating and we wanted to write a little update. Since being discharged from the hospital Karen has been staying at the Berning family home in Vienna. Her mom, a retired nurse and Nick’s Aunt Nancy (and godmother), has been taking excellent care of her while she regains her strength.
Karen went for a follow-up appointment this past Friday and met the physician’s assistant she will visit with virtually over the next two years. Her liver numbers are improving steadily and the doctors are pleased with her progress. However, she was told that her body has a lot of work ahead of it—regenerating two-thirds of a liver at a rapid pace is a lot of work!—and she’ll need naps daily for at least six to eight weeks.
I asked her what the worst part of the whole ordeal was and she responded that “nothing was too bad.” Although she admits that she doesn’t remember much of the first six days in the hospital, she did mention she wasn’t fond of the pain-inducing “incentive spirometer” she had to keep breathing into. Or the fact that each time she tried to order a meal she was told she had already called to order her food (she hadn’t) and that they would NOT be changing her request!
While they miss her, Karen’s immediate family back in Milwaukee is getting along just fine. Daisy (her 10-year-old daughter) even said the time is going by much faster than she thought it would.
Karen has been getting back into the swing of daily life—going for walks, spending time with extended family, playing games, showing off bruises, and even doing some unauthorized chores!
A little too much time sitting upright while extreme puzzling yesterday caused some discomfort today. That said, if you’ve ever considered donating your liver, Karen has one thing to say: “I’m fortunate to have a supportive family and employer that allowed me to put my life on hold so I could contribute a piece of my liver to Nick and experience a medical marvel. If you have the right support structure that works for you, I’d highly recommend considering a donation to save a loved one’s life.”
All of us continue to be in awe of Karen and her bravery, unselfishness, and generosity. Donating not just her liver but also several weeks away from her family, job, and home. She’s given ALL of us the amazing and immeasurable gift of many more (healthy!) years with Nick.
-- Stephanie
(April 6, 4:27 pm) -- Nick got a good rest last night and has plenty of energy today. Lots of energy -- he's chatting up the nurses, debating with doctors, showing off his scars to visitors, and doing so many laps around the floor that his mom had to drop out to take a rest. He attributes this to finally getting solid food for the first time in thirteen days. I say it's that plus, you know, the drugs.
A PA removed another of Nick's drains this morning, which leaves only one still flowing (the one draining bile from Friday evening). He's getting a dose of IV antibiotics at the moment, he's but spending more and more time unplugged from the IV tubes, which makes it a lot easier to move to a chair, get to the bathroom, or wander around the floor. Mostly, he's wondering if he can still buy a car* before Trump's tariffs jack up the prices. We had to remind him that he's not allowed behind the wheel for another month at least.
Because it's Sunday, we haven't see a surgeon today (at least not yet), but it sounds like Nick is likely to get another scan in the morning, at which point we'll hopefully be in a position to start figuring out a discharge plan. Fingers crossed.
-- Drew
* - Ugh. Yes, we're thinking of buying a car. It's a hybrid at least. But don't worry: I still plan on being an insufferable bike guy.
(April 5, 7:26 pm) -- There's not much update today, in part because I didn't roll into the hospital until after six o'clock. (I had things to do. Like sleeping and staring blankly at the wall.)
Overall, Nick feels like he's continuing to get healthier and all the blood numbers seem to back that up. We're keeping an eye on the bile leak, but the doctors generally seem pleased with Nick's progress. Things are a little quiet on the weekends, so we'll probably know a more on Monday.
-- Drew
Don't worry about Clover's temporarily removed mask. She assured us that she held her breath while posing.
(April 4, 4:38 pm) -- Nick's been feeling fine today and continuing to reduce his pain meds. More importantly, last night he got a visit from nieces Hallie and Clover, who answered one of the great medical mysteries of our age: how many staples does Nick have? According to their investigation, fifty-three.
We took all this to mean that Nick was on a glide path to recovery, but, alas, another scan revealed still more bile leaking into his abdomen. Again, the consensus is that while this isn't welcome news, it's just part of the process to be dealt with.
The plan is to do yet another scan (a percutaneous transhepatic cholangiogram, for those of you keeping track at home) to take a look around and likely install another drain. It's not a surgery, they assure us; it's a procedure. They just carted him away a few minutes ago.
In either case, it should be pretty quick -- not least of all because, as the nurse sent to fetch him made clear, he's the last patient they've got before the team can knock off for the weekend.
-- Drew
(UPDATE: April 4, 5:42 pm) -- He's back. He didn't even have to go to sleep through the procedure so got to watch it all on the monitor and chat with the doctors, which delighted him. They were able to remove the bile that had collected and expect the leak itself to resolve on its own. Nick says he feels better than when he went in.
(April 3, 12:32 pm) -- Last night before I went home, Nick announced that regardless of his dietary restrictions he was going to have a double espresso in the morning. He was committed to this plan, but as his accomplice, I was reassured when the nurses, and then doctor, signed off. This might the longest Nick has ever gone without caffeine, a record he's not interested in challenging anytime soon.
I did my best to get to the hospital in time for the surgeon's rounds this morning and got approval to show up before visiting hours, but by the time I arrived, coffee in hand, the doctor was long gone. The good news is that all reports are good, the numbers are (almost) all moving in the right direction, and the pain is under control.
In the most recent official surgery report, the surgeon noted that he had a "long conversation" with the patient's family after the procedure. Nick mentioned this, to which the doctor responded that we did "ask a lot of questions that didn't seem to be related your care." But honestly, if you had access to a world class transplant surgeon, who wouldn't ask about the feasibility of pig livers?
Our friends Haris and Sergio came by last night to play a round of Hearts. Despite a fairly substantial dose of drugs in Nick's veins, he made a credible showing. I got destroyed. (This morning, while discussing schedules, Nick remarked "Wow. The water is really high." He clarified that while he knew we were in the hospital together, he was also sitting on a porch watching waves come in. Sounds lovely.)
We just did five full laps around the floor, during which Nick allowed me to take the attached photograph, which he has cleared for public distribution.
-- Drew
Proof of life.
A plant even Drew can't kill.
(April 2, 2:42 pm) -- Nick got a good night's sleep last night (as did I, for what it's worth.) A little more abdominal pain, so they've ordered another round of x-rays. We'll see what comes back. All his blood numbers look good.
Nick was also able to take a walk around the floor this morning, during which he managed to unknowingly pull out his entire NG tube. I wasn't there to witness this, but as someone who was present for its insertion I cannot believe he was able to do this. It went 60 cm through his nose and into his stomach. Anyway, the doctors decided to keep it out, so we'll just write it off as an easy removal.
More intentionally, a PA just removed one of Nick's drains. We happened to have our niece Clover on the phone, who jumped at the opportunity to watch the entire thing, including an extreme close up of the process of stitching up the hole. Book your appointment now; she'll be your healthcare provider in twenty years.
Finally, congrats to Bruce, Linda and Violet who sent a plant that the doctors can't possibly object to.
-- Drew
(April 1, 9:26 pm) -- Today was a relatively quiet day. Nick's got a little pain, but generally comfortable. Still no food by mouth, but he was able to get up to a chair again for a while.
Most importantly, we were finally able to watch White Lotus from Sunday night.
-- Drew
(April 1, 7:52 am) -- The title says it all. Nick had a restful night and is feeling much, much better. Still some pain, but, as he says, it feels like pain he's supposed to have after a surgery. Both his surgeons just came by and are very pleased with how things went.
He is a little dopey, though. He just tried to rub his hands together and missed.
-- Drew
(March 31, 11:09 pm) -- Nick's still in recovery, but we connected with his surgeon who confirmed that everything went beautifully. There was, indeed, an issue with one of the bile ducts from the donated liver. They sewed it back and inserted a stent to take the pressure off the tissue while it heals -- a stent that apparently extends all the way through the liver and out of his skin(!) allowing the doctors to send in a camera(!!) to take a look around as needed. What a world.
We anticipate more pain around the incision site (and a fresh new set of staples,) but the hope is that by preventing the bile from leaking into the abdominal cavity, some of the other pain will be lessened. I'll be here through the night and am hopeful we'll both actually be able to sleep this time.
-- Drew
(March 31, 7:53 pm) -- We spoke to a doctor from the Transplant Institute this morning, and he gave some additional guidance for pain management. (tl;dr - More drugs.) This was welcome news, and Nick was able to get some good rest.
After Mike and Judy arrived, I snuck home to get a nap and take a shower, but just as I was heading back I got a call that Nick was heading back into surgery. Based on some elevated liver numbers, the team ran a new scan and discovered that bile is leaking into his abdominal cavity. Based on the quantity they don't think it's the bile ducts themselves, but the cut edge of the liver. They don't know for sure, though, so the only solution is to go back in, identify the leak, and sew it up.
This happens in about 30% of living donor transplants. Per the surgeon, it's not a surprise, but it's not a welcome development either.
Nick just went into the OR and should be back in recovery in about two hours. The plan is for his breathing tube to be removed before he wakes up this time and for Nick to be awake in just a few hours, but they'll do whatever seems safest. It's possible we'll be back to the ICU.
In any case, it's a discouraging step backwards, but Nick is clear that it's all part of the process.
Oh, and there's also some fluid in his lungs. Not a lot. But we'll worry about that tomorrow.
The good news (GREAT news) is that it looks like Karen will be discharged tomorrow! I'm more grateful for her every day and I know Nick is too.
Thank you again for all the love and support. If I haven't gotten back to you, please chalk it up to my disorganization not lack of appreciation. It means the world.
-- Drew
(March 31, 9:39 am) -- Last night was ... not great. Nick had a lot of pain and didn't get much sleep.
His intestines have -- presumably temporarily -- stopped moving food through his system. The doctors say that's not unusual, but, especially given his giant abdominal incision, it's also really uncomfortable. (On some level, I can't blame them. Check out the attached diagram. If you did that to me I'd stop working, too.) To make matters worse, opioids inhibit the digestive process; so the best tool to treat the symptom also worsens the underlying cause. Obviously, that puts Nick in a tough spot. He also can't have any pain meds processed through the liver kidneys* (like ibuprofen and naproxen), so that leaves opioids or Tylenol. I'm sure I'm oversimplifying, but there aren't a lot of great options.
Around midnight, they installed an NG line back through his nose to clear out his stomach, which helped, though installation wasn't a lot of fun. Anyway, that means his big step up to solid food is off the table. Nothing by mouth for a while.
Recovery, as I've been reminded, isn't linear.
The enormous bright spot is that the care Nick's getting at Georgetown has been terrific, in particular the nurses, who have been attentive, empathetic and relentlessly competent. I'd lay down in traffic for any one of them.
-- Drew
[* - Apparently it's the kidneys, which are doing all they can to cope with the immunosuppressants.]
A Roux-en-Y Hepaticojejunostomy, which includes a fair amount of internal remodeling.
(March 30, 2:02 pm) -- This morning one of Nick's liver numbers starting ticking up, which isn't good news, per se, but the doctor was clear that we shouldn't worry about it. Only today are the doses of immunosuppressants elevated to where they want them so we should expect the numbers to move around a little bit. Organ rejection, I've learned, isn't a binary; the doctors will be adjusting his meds for some time to come. It's just part of the process.
In better news, Nick is being moved onto solid food for dinner. (He had something he suspects was cream of wheat for breakfast, but he describes it as arriving in disc form, so better not to think too hard about that.)
Nick spent the morning reading through the official post surgery report and looking up new vocabulary words. The doctor noted that he felt an "excellent thrill" in Nick's hepatic artery, but it turns out that's the physical feeling of blood moving through a vessel, not an emotional reaction to Nick's specialness.
The doctor also shared that Karen's biliary ducts, which he sewed onto a section of Nick's intestine, were the size of angel hair pasta (!!) It's pretty amazing.
Nick's still a little wired, but they're bringing down his steroids, so he's starting to get a little more sleep.
Karen, for her part, was allowed to shower today. Nick wasn't, so we bought him some dry shampoo and are taking advantage of the endless supply of antiseptic wipes.
We were finally allowed to bring Karen flowers. Ironically, we thought they couldn't be delivered to her ward (just across the waiting room) so Nick was holding onto them until the surgeon saw them and promptly banned them from the room, (what with all Nick's immunosuppression and all.) But Karen can, in fact, have flowers, despite the very assertive signage saying otherwise. Anyway, they got to the right place.
-- Drew
(March 29, 3:39 pm) -- It’s day 5 and we’re starting to thrive! It’s been a pretty amazing few days seeing the things modern medicine can accomplish. Nick’s done a 180 in terms of energy since before the surgery. He takes laps around the unit in the middle of the night, reads aloud to us, visits Karen, FaceTimes with his nieces, and hardly sleeps (the steroids may be contributing to this a bit but it’s still nice to see him function again)
Nick is still on the all liquid diet (broth, jello, juice, decaf tea). Karen has moved onto “soft” foods. But the kitchen seems to keep screwing up her order and bringing her things she’s not supposed to eat. My guess is they will both have lost several pounds by the time they leave and not just in liver weight.
Karen and Nick have both been kept very busy these last few days. Dealing with nurse/surgeon visits, walking laps, removing dressings, navigating pain, trying to rest, staying hydrated, and regenerating livers. Karen even mentioned “these days in the hospital seem to fly by!” They appreciate all the well wishes and support but are too consumed to communicate much themselves. We’ll keep sharing updates for them in the meantime!
-- Stephanie
(March 28, 3:28 pm) -- I woke up this morning to discover that Nick had (1) sent an email to a national email list serve discussing tactics for the April 5 #HandsOff protests and (2) done ten laps around the floor without assistance. So at least we know the prednisone is working...
This morning the bandages came off for the first time, revealing this gnarly set of staples. It's called the Mercedes-Benz cut, but I don't think that does justice to just how long it is. A+ scar potential.
Nick's already stepping down his pain meds significantly and seems to be doing pretty well. I've received a thick binder of post-transplant guidance, so I've got a little light reading for the afternoon.
Karen is onto semi-solid foods. Nick hasn't moved off clear liquids, but judging by Karen's reviews I don't think there's much rush.
-- Drew
Working on developing fake stories explaining this scar. Sword fight? Gored by bull? Religious sacrifice?
(March 27, 3:28 pm) -- Just before lunch, Nick stepped down from the Intensive Care Unit (ICU) to the Intermediate Care Unit (...ICU?) It's all on the same floor, so the change is only about 40 feet, but it's another sign that everything's going smoothly. The doctors have encouraged him to walk as much as he can, so we just took two full laps around the new, but I want to be clear that the stretching exercises and balancing on one foot are entirely Nick's own idea and I take no responsibility. (I wish I was joking, but I'm not.)
-- Drew
(March 27, 10:54 am) -- Nick slept well last night and by the time I got here this morning they'd removed his central line IV (the one that goes in his neck.) It doesn't make much difference to him, but it does make him nicer to look at.
Around 10 his physical therapist stopped by and took Nick on a full lap (!) around the floor. Karen was occupied but on the next trip we're planning to repay her visit from yesterday. Looks like today will be more walking and another IV line coming out.
Pro Tip: Nick says that having a small booklight was extremely convenient last night and everyone should consider bringing one on an overnight hospital stay.
-- Drew
(March 26, 9:00 pm) -- Everything continues to be heading in the right direction, and we're getting great feedback from doctors.
I told Nick that I think he seems more energized and alert than he did before his surgery. He, ever the contrarian, promptly fell asleep.
This afternoon's big event was a visit from Karen herself, who walked all the way across the unit to check on Nick, who was overjoyed to see her. They both are, in my humble opinion, looking great.
Both of them have been given an "incentive spirometer" to encourage them to take deep breaths. It's going great except for when Nick forgets he's supposed to inhale and blows into it instead.
Just as visiting hours wrapped up, Nick was able to get up and do a half-lap around the floor. Considering that he was intubated less than 12 hours earlier, (and has an incision that's going to make one hell of a scar,) I am hugely impressed.
Another long, but extremely heartening, day.
Thank you all again for your support and messages. Nick's not online yet, but I'm passing them along, and he really appreciates all the love -- as do I.
-- Drew
(March 26, 2:41 pm) -- Not only is Nick enjoying a lunch of clear liquids, he's doing so while sitting in a chair.
This is all very exciting.
-- Drew
Nick asks for his glasses.
(March 26, 9:26 am) -- This morning at about 7:45 they took Nick off sedation and he woke up soon after. He did a great job with his breathing test and by a little after 9 they were able to remove the breathing tube. Not a fun process, but he did beautifully. Even before the tube was out he was asking questions and making jokes, though his first attempt was ... inscrutable.
All the tests are looking great, and his new liver is already working. Nick's bilirubin has dropped by about about half since the surgery. (If you've noticed he looked a little yellow in recent months, that's why. So this is excellent news.)
He's still hooked up to assorted drips and tubes, but the plan is for him to get up and walk (!!) today.
-- Drew
(March 25, 6:52 pm) -- I'm sitting with Nick in the ICU where he's hooked up to a LOT of tubes, but is resting peacefully now. Our nurse has been very gracious in answering my quetions. ("What's that? ... What are you doing THAT for? ... Is that normal?!") Karen is still waiting for a room in the ICU but is, I'm told, enjoying a popsicle and feeling pretty good, if also appropriately exhausted. We've got a nice view of the Georgetown campus from the window, though I regret to inform my classmates that they apparently tore down my sophomore dorm. Kids today...
I'll be here for a little while longer and will be here bright and early to get Nick's breathing tube out. I'll be honest, it doesn't look that comfortable.
(March 25) -- And he's done! All went smoothly and basically on schedule. The liver is in and sewn up to bile ducts, assorted veins and directly to his intestines. Lots of sewing. As of now (4:15) Nick's getting cleaned up and sent to the ICU. Once he's settled I'll get to see him, though he won't wake up until tomorrow morning at the earliest.
Thanks so much for all the kind messages. I'm so grateful for the support.
-- Drew
(March 25) -- Karen's surgery is complete as of 1:10. According to the doctor it went "very, very well." She should be awake later today, though it could take a while to get into the ICU...
-- Drew
(March 25) -- Just spoke to the nurses. As of about 12:30, all is going smoothly. Just about ready to say goodbye to the old liver for good.
-- Drew
(March 25) -- We got to Georgetown a little after 5:30 this morning and met up with Karen (our hero) before heading back to get prepped. Lots of doctors. Lots of paperwork.
Nick headed to the OR about 7:45. Surgery should last about eight hours.
-- Drew
(March 18) -- On Tuesday, March 25 Nick is scheduled to get a liver transplant at Georgetown University Hospital. We'll be posting updates here.
Nick has had a slowly progressing autoimmune liver disease called primary sclerosing cholangitis, or PSC, for more than 20 years. For most of the past two decades he’s been mostly asymptomatic, but now Nick has end-stage liver disease and is feeling the impacts, which are accelerating. A transplant is the only cure.
Most transplants involve deceased donors, but last year 604 liver transplants in the U.S. were from living donors. Thanks to Nick’s amazing, generous cousin Karen, who’s willing to give up part of her liver, he’ll be able to get a new organ without waiting longer and getting sicker before a liver becomes available.
The plan is for Nick to be in surgery most of the day on the 25th. After that he'll be in the ICU for two or three days, and assuming everything goes well, he'll be home after a little more than a week. This is a complex and major surgery, no doubt, but transplant medicine has come a long way in recent decades and Nick’s odds of a full recovery are good.
We’re fortunate to have access to the Georgetown Transplant Institute’s dream team of doctors with extraordinary expertise, including in living-donor liver transplantation in particular. As of this year Georgetown also has a fancy new transplant facility, which you can see in the accompanying video. (Nick’s hepatologist of the past 12 years, Dr. Rohit Satoskar, also shows up in the video—he’s the Institute’s medical director.)
Once Nick heads into surgery, Nick's sister Steph and I will coordinate messages for him, and we can also answer questions. If you don't have our contact info, you can reach us here.
Additionally, our friend Hannah has generously offered to coordinate a meal train to make sure we're well fed once we’re out of the hospital. If you'd like to take part, you can here.
-- Drew