Hana’s Heartversary

On Sunday two weeks ago, May 28th, we celebrated Hana’s very first Heartversary – one year with her new heart.
It turned out to be a wonderful celebration! We invited some of our local friends and supporters for a big picnic in Golden Gate Park. We were even lucky enough that some of Hana’s medical professionals came! This was a party to celebrate life (Hana’s) to give thanks (to you – all of our supporters) and to commemorate the donor. I think its this last point that really has me thinking these days. It has been a year since the donor family lost their small child and made the courageous decision to donate their heart. Not a day passes where I don’t stop and think of them, hope they are able to find some peace and maybe some solace in their decision.

I wish we could have had a chance to have all our family, friends and family from everywhere come to the party. You are what has carried us through! On that note, you may wonder how we managed to pull off having a huge party with a four-week old baby. Our local village here in San Francisco is that answer! A small group of our friends rallied together and took care of all the party details, I just took care of all the big things before the arrival of Corrina. It was amazing. All Paul and I had to do was just show up on the day of the party! Balloons, tents, chairs, tables, food, drinks, a cake, picnic blankets all just showed up at our reserved party spot and all of these wonderful woman (it was mostly the woman, but I know the husbands helped too) have their own toddlers to run after! This is such a perfect example of how important our village is and what an impact they make on our lives.

For our family, life is moving along, especially with the addition of Corrina to our family. Hana is doing great thanks to the medical professionals who dedicate their lives to these kids. This past week she had her one year clinic visit. Coincidentally she was checked out by the original director of the heart transplant program (now semi-retired). There was a tiny bit of concern over Hana’s persistent cough and runny nose (they are thinking possibly allergies) although it doesn’t seem to bother her at all and her lungs sound perfectly fine. We were able to drop two of Hana’s medications – Valcyte and Amlodipine. As long as Hana’s blood pressure stays within normal range she can stay off of the Amlodipine. Hana’s weight gain has been good (thank goodness for all the great summer produce!) She has her annual biopsy in a week, which will be more invasive than any other biopsy since they will look at both the right left sides of the heart (its normally just the right). It will be an all day affair at the hospital. Let’s hope and pray for zero rejection and ideal heart pressures.

I can’t believe it has been a year already. Thank God. What a miracle.

I’m sorry this update is getting posted so late, it has been really hard to find time to sit down at the computer when you have a newborn (and you don’t fall asleep). Corrina is six weeks old today!

I do have something exciting to share in the next or so. It brought tears to my eyes. I hope you like it too!


She picked out her outfit for the day.
Hana is signing, “Good Job”.


This amazing cake was made by our friend Carole! Amazing!
Our friends Isai and Alison from Tamalitos Catering did all the food.
Take a heart. Sign your name. Say a prayer or well wish. Drop it in the frame.
The cookie decorating bar.


This is The Amazing Rachel, our kid entertainment. She was truly amazing!


Grandpop helps Hana fly with her butterfly wings (Thanks to the Amazing Rachel).


The Amazing Rachel had all the kids captivated.


Paul says a few words of thanks before we cut the cake.

Our great party planning crew!

Patient Hero

We have two special things to share with you! The first one is that on April 30th, Hana became a big sister! Corrina Mae Yago arrived after a fairly quick and easy delivery. My mother was here for a few days before the birth and several weeks after to help everyone with the transition. Hana has been really great with her baby sister and is very sweet. She is feeling the pull away from me (to take care of a baby) and has been understandably emotional but really, she’s handling it like a champ!

All of this made Mother’s Day really special for me – I had my two girls and my own mother and we didn’t have to spend it in the hospital (like last year)!

So far life with a newborn has been pretty good – I say that and I fear that Corrina’s fussiness has not yet completely shown itself. The last few days has included those crazy, fussy late afternoons/evenings that challenge your mental health! Before that and while my mom was here we did get out and about and helped Hana have some fun. Hopefully I’ll still be able to get out of the house for some fun outings with Hana and Corrina.

This brings me to our second special share – in about a month will be the annual Summer Scamper fundraiser race for the hospital and Hana will represent the hospital’s Heart Center as the Patient Hero! You can read Hana’s Patient Hero bio by clicking on this link:
You may remember that last year, just a week after being discharged from the hospital after her transplant, Hana attended the Summer Scamper – you can read about it in “A Great Summer Scamper“. We are putting together another “Hana’s Heart” team and you can donate to our team by clicking on the link below:
If you would like to join our team, please let me know! I will be walking in the 5K with Hana. Although I would love to run the 10K again this year, I think it is too soon after having a baby to be running!

We are VERY excited to have Hana represent the Heart Center and to support their continued research into treating children like Hana. Because of them, Hana has survived her hospitalization and thrived in life. Because of all they have done for Hana and our family we have enjoyed an amazing year together outside the hospital – that’s right, its been almost one year since Hana’s heart transplant! Hana has never been stronger, happier or healthier! She has been eating and gaining weight and enjoying all the activities a toddler should get the chance to enjoy! She is living life!

As I write this, it is the last evening of my life as a thirty-something. Tomorrow I enter a new decade. As I reflect about back on my thirties, but more this last year of being 39, I feel like this last year has been the best of my life – Hana finally got her gift of life, we all got to move out of the hospital, we got to move home after being at the Ronald McDonald House, we got to live life (with Poppy) back at home in San Francisco, we got to add a new baby to the family. All of this happened in the last year. It is all so incredible to me. It has taken a village of people to help us get here and we are incredibly grateful! I am excited for our adventures of the next decade!


A Special Announcement 

This update is long overdue, so I apologize. I have been incredibly busy and exhausted which will all make more sense when I tell you our special announcement. But, first things first, let me tell you how Hana is doing!

Hana has had some ups and downs. The highs are very high and the lows haven’t been bad enough that she had to be admitted to the hospital, but she got kind of close. The first two weeks out of the hospital were amazing! She was eating a ridiculous amount of food on top of getting three tube feeds a day so her weight jumped up. Then each week after that we would drop a feed and she also stopped eating so much at the same time. She was incredibly happy and had a huge jump in her speech development. My mother came out to help out for four weeks. Hana loved that.

The first two weeks of my mom’s visit were also great. She had slowed in her eating but was still doing well. She finally weaned off her steroid after nine months. About 48 hours after her last dose, coincidentally the day after pulling out her NG tube, she was not right. Her blood pressure was really low and she was kind of lethargic and sleepy. I was also away all day (first time since she had her transplant) so Paul and my mom handled talking with the team at Stanford. By the time I got home she perked up and seemed much better the next day. But things started up and down after this – with more GI symptoms, a few vomiting episodes and diarrhea. She would have a bad day then a better day followed by another bad day. We took her back to Stanford and the retested her for adenovirus, which came back negative (it would have been very unlikely she had it again). They said if she got worse or if she didn’t have intermittent good days then they would admit her to the hospital for observation. We avoided this but ended up putting the NG tube back in to keep her hydrated.

This persisted for a good ten days but fortunately Hana seemed on the mend for the last few days of my mom’s visit. My mom was here for four weeks! The illness made me kind of anxious because I was dreading spending more time back in the hospital. This last week Hana has been really great, playing and singing. We just need to encourage more walking, running, jumping and climbing- it seems she has not quite gotten back to where she was in December. Hana also had another heart biopsy in early March. This was her regularly scheduled biopsy, since her last one was in December. Her heart pressures were the same and her biopsy result was a 1a. Hana has always gotten a zero for rejection but they treat 1a the same as zero so 1a is good news. Her next biopsy is her one year biopsy! This will be more invasive as they go all the way into the left side of the heart (right now they only go into the right side of the heart and don’t go any further) and the recovery time is longer (she will spend several hours in the short stay unit afterward).

So, as I said earlier, we’ve been incredibly busy. My mom was out for the month of February and we, along with an organizer, finally went through all the chaos of piles, boxes and bags of things building up over the last year or more and got some projects done around the house. We still had stuff we put aside to make room for Hana’s big, first birthday party. I was slowly making progress on all these things but not fast enough for our approaching deadline. This is part of our special announcement.

So here it is, (drumroll please) projected for May 3rd, Hana will become a big sister! That’s right! We are expecting another girl in about six weeks! We are very excited and nervous. The nervousness is about caring for Hana, with all her needs, and a newborn. But Hana will be almost one year post-transplant and things should be (and already are) much easier. We are also nervous that this new baby will have a perfectly healthy heart even though we were told the chances of her having dilated cardiomyopathy is so low that they don’t recommend against having more children. I am getting extra ultrasounds and I also had a fetal echocardiogram and everything looks great! I think this is why we delayed announcing anything – we wanted to know more information on the health of the baby. But by the time we knew things were looking good Hana had gotten sick and then we were preoccupied with her hospitalization. We are getting more excited with each day! I think Hana is going to be a great big sister!

I must add that this time of year – February and early March is hard for me and even more so this year. It’s the time of year when we were shocked by the news and events of Hana’s heart failure and our lives and what we thought parenthood would be like forever changed. I have a very hard time looking at photos of Hana leading up to her being diagnosed with heart failure and hospitalized and I can now see in her baby face the signs that we all missed. It breaks my heart. Going through and organizing all the stuff in the house, including Hana’s baby stuff, reminded me again of that time and it has been very emotional, more so than I imagined it would ever be. There is more lingering sadness and grief than I thought. I guess the imprint on my heart, from this time, is much deeper than I realized. Even now, writing about it is very hard.

I don’t want to linger in past trauma, not when there is so much promising life to live, but sometimes these things have a way of grabbing hold of you until they run its course. So, I’m letting it run its course, slowly, and hoping it doesn’t create any additional and unnecessary drama. 

We have so much to look forward to. We have so much to be grateful for! Thank you, everyone for all your support!

This video is Hana saying hi to her nurse practitioner, Jenna, from Hana’s days on the Berlin Heart.

 A Bittersweet Homecoming 

After a little bit of drama Hana was discharged and we got home early this afternoon (Saturday). The drama involves the lab at Stanford and the Kaiser pharmacy (unrelated dramas). We’ve been waiting on the second negative adenovirus PCR to be cleared to stop the Cidofovir treatments and go home. Everything else with Hana’s condition was resolving or resolved. The resident was working hard to get all our discharge stuff ready so we could go sometime on Friday. She was also working with the lab to get that last test result. We were all hoping it would be negative, of course, and they agreed to hold off one day on her scheduled Cidofovir infusion to get the result so she didn’t get an unnecessary treatment.

The lab promised a result by the end of the day Friday. After repeated calls nothing had come by 5pm and the answer we got was that whoever ran the test didn’t use enough blood from the vial that was sent and therefore they couldn’t get a result. They didn’t need more blood, they just needed to run it again and since it was already Friday end of day it would have to wait until Monday. This was obviously not okay with a number of people as it would mean at least two more possibly unnecessary days in the hospital and the risky Cidofovir treatment all because someone made a mistake in the lab. It took the attending physician to make some calls to ensure someone stayed late and ran the test again. The result came in some time after midnight – another negative!

The other drama with the Kaiser pharmacy was less severe. The resident talked with someone at the Kaiser pharmacy to ensure we would be able to get three medications we needed upon discharge. Two of them were just medications that had expired over the four weeks in the hospital. The person at the pharmacy said they would be ready. The pharmacy called to tell me they would be ready that afternoon. They called Paul when they were ready to be picked up. Paul went Friday night to pick them up and they only had one ready. He was told to go to a different pharmacy to pick up the others the next day. Today our friend went to pick up the prescriptions while I packed up the room. They didn’t have what they needed to fill either prescription and gave her a hard time saying we should have picked them up yesterday (why? If they don’t have them and can’t fill them). I hate having to come up with threats and ultimatums but it had come to this. In the end they begrudgingly called around and found out Kaiser in San Francisco could fill them. We shall see if that happens.

Now we are home! We ended up having way too much stuff at the hospital that we now have to unpack! Hana was cranky about leaving because I think she knew things were changing and she didn’t quite understand what “going home” was going to mean. Once we got in the car she was pretty happy and once we got home she got right to work playing with her toys and discovering the Christmas presents that she had been too sick to enjoy (she still has a few to unwrap!). She is running around the house and talking up a storm. I’m exhausted, way more than I thought, and it’s going to take at least a few days to get things settled. But we are HOME and it’s amazing. Thank you to everyone who helped keep us fed, sent cards and gifts! It’s helped tremendously.

I call this homecoming bittersweet because across the country, from the hospital where I was born, my grandfather is also being discharged into hospice care at home. After a traumatic car accident eight years ago where a man was trying to kill himself by running a red light at 70mph and hit my grandfather’s car, my grandfather has battled lots of very painful and complex medical conditions. In the last week, some new problems emerged that have caused a lot of pain and their treatment interfere with  the maintenance of other conditions. It’s very hard for me to digest all of this while being exhausted and dealing with Hana’s own hospitalization. It’s also really hard to be so far away especially when we’ve been unable to visit our families back east for two years. It feels really hard.

Skin, And Good News

I’m ready to get out of here! Hana is dealing better than me and she hasn’t even left the room in weeks. Today I’m going to start weaning the amount of iPad watching, although she does that naturally too, as she gets interested in doing more things. I’m starting to get frustrated with the state of things.

The pediatric dermatologist came to look at Hana’s skin. He was concerned about the unusualness of it and so recommended a skin biopsy and additional tests. We were able to do the biopsy right in the room, about 30 minutes later. I sat in the recliner and held Hana in my lap while the nurse, resident and attending dermatologist did took the biopsy sample from the front of her thigh and then stitched her up. She did get lidocaine first and Tylenol but she still screamed on and off. About 30 minutes after it was all finished Hana was  practically dancing around the room talking and laughing! 

Since the biopsy, Hana’s really been mostly back to her usual self. She is laughing and playing and singing and climbing a little. It’s hard because she is often attached to some wires and tubes and therefore limited. Her appetite has been good, although the variety of what she’ll eat isn’t that great. 

On the downside, Hana is still having high heart rates, bloating, and high blood pressure. Her neutrophils count is improving and so they restarted her Cellcept. Her Tacrolimus levels have still not been stable so we need that to be working better. Once she is off the Cidofovir, they can restart some of her other meds, including her enalapril which will help lower her blood pressure.

The pediatric dermatologist checks her skin every day. Today he said he was very pleased as her wound sites are looking much improved. It’s so weird to see wounds appear without any (outside) trauma. The skin is coming off and she is bleeding over the underlying bloody looking areas and so we have to keep them covered for now. I know they are very sensitive and hurt Hana. So far, there have not been any notable results, other than ruling out most scary things. The dermatologist is heavily leaning towards adenovirus causing transient changes to her clotting which caused injury to some small blood vessels. They are going to consult with hematology who may need to get involved based on a few more test results we are waiting on. It’s very strange to thing that Hana’s blood may be clotting too much when, for months on the Berlin Heart, they thinned her blood so it wouldn’t form clots and this was never a problem. It’s still puzzling why her rash appeared over her old lovenox injection sites and where her hospital ID band was on her ankle.

As I feel Hana’s health is getting back to normal, I ask the question, “When can we go home?” I know we have to wait on certain things, such as having stable Tacrolimus levels, but I understand the reasoning. But when I ask if we can finish the Cidofovir infusions at home I get a “no” or “but she has to be hyperhydrated”. I say, “So what?” Hana so far handles the treatment and hydration just fine. I think a nurse that came to the house for the treatment could certainly handle giving her IV saline along with the Cidofovir. That would be better than being in the hospital another week. Give me reasonable explanations for “No.”

As I’m writing this the resident has come in to tell me that Hana’s adenovirus PCR was run on Monday and came back NEGATIVE!!!! Now we need another negative today (she, the resident, is going to see if they can accelerate getting the results) and maybe we can go home this weekend!

Three Weeks

We have now been here for three weeks! Everyone thought it was going to be two or three days. We are all getting weary of being in the hospital. The good news is that Hana is doing much better, for the most part. It still feels like two steps forward and one step back but at least that’s still overall progress.

Over the weekend Hana started walking and playing around the room, not just sitting in bed or in the wagon. She’s a bit wobbly on her feet and I want her to get her strength back so I’ve been pushing her a bit to play standing up. Her mood has been better – laughing, smiling, playing and singing. Her diarrhea is gone. Her appetite has greatly improved, although still almost entirely starches. 

I thought I was going to have to go to battle over Hana’s NG tube feeds but the attending physician (the head of the transplant cardiologists) stepped in and reassured me that his end goal was the same as mine and in the meantime he really thinks she needs the extra nutrition. Their goal is only 50% total calories from tube feeds and I can live with that, especially since she probably needs the extra help right now. They’ve also been very willing to listen to what I think about her feed schedule and the amount of Pedialyte versus formula. I think it’s been going fairly well. Hana is still battling with a lot of bloating but that seems to be getting better. 

So I feel we’ve taken a bit of a step back too. Hana is now anemic from all the blood they’ve taken recently, so she is now getting liquid iron which makes you feel really terrible. We’ve started putting it in her formula mix so she gets it over several hours which has made it better but it is more iron than they typically prescribe. Yesterday Hana’s hematocrit was so low that she got a blood transfusion. Ordering a blood transfusion is never a trivial thing for pre and post transplant patients. About an hour into the transfusion the rash that cropped up about a week ago suddenly got much worse looking. It also looks the worst in the area Hana still has lingering bruises from lovenox injections (while on the Berlin Heart) AND under her hospital ID band on her ankle. The rash could still be from the adenovirus but these latest developments are odd so now we are waiting on a consult from dermatology. Hana tossed and turned and had screaming fits all night long. I think the rash is starting to really bother her. So today we are both VERY tired! In addition, Hana’s weight is up significantly from yesterday, not a good thing. She looks swollen again, her respiration rate, heart rate and blood pressure have been high.

So at this point, we have a nice list of things to resolve before getting out of the hospital. We need Hana on a good nourishment and hydration plan with oral eating and tube feeds. Her Tacrolimus level needs to be stable. She needs to restart her Cellcept and a few other meds as soon as she is not neutropenic. Of course, she needs to test negative twice in a row for adenovirus so we can stop the Cidofovir treatments and I’m thinking at this pace, she will test negative twice before we got the other things resolved! Hana’s bone marrow, liver and kidneys all need to keep up with all the extra load they’ve had to carry. Hopefully we can get her back to health without any more complications.

Disappointing Results 

We got Hana’s adenovirus results back and they were both higher this week than ever before, in the 30,000’s. This was very troubling to us and I started to feel like maybe things were careening out of control. But I kept reminding myself that Hana seems much better, so that should count for a lot. Still, it was a bit stressful.

They’ve been playing with Hana’s feeds schedule since she’s been sleeping so poorly at night and I always felt she did better not getting continuous feeds overnight. When Hana sleeps poorly, I sleep poorly. The GI doctors said Hana’s digestive system is more mature so she may be able to handle things that she didn’t handle well before. So we’ll see, but I still think Hana needs gut rest at night when she’s sleeping, that’s when humans are supposed to get gut rest. 

Other than her half Pedialyte, half formula feeds Hana has been eating more foods. Toast, rice, noodles, carrots and crackers. Apparently pancakes do not qualify as conforming to a lactose-restricted diet so I’m not allowed to order them, despite getting the GI doctor’s approved. Today Hana had NO diarrhea for the first time in weeks. She still has tons of bloating and gas and her heart rate and respiration rate have been quite elevated. I’m hoping that she is truly on the mend.

Now, getting back to the adenovirus results, the resident had already spoken for the Infectious Disease doctors about Hana’s results. They said ‘they have seen this before’ and ‘let us know if her results are still not going down after next weeks results’. So, they don’t sound concerned. They are the experts so I’m giving them a bit more time to prove themselves. They also said there is some lag time between when a patient’s symptoms lessen and when the test results reflect this and the most important thing is that she is starting to feel better. Now, this makes more sense to me. Lastly, as it was explained to me about the test results numbers, the increase from the last test result of 15,000 to 30,000 is not significant. It may sound like a lot but it isn’t and there is margin of error too. If her results went from 15,000 to 250,000 then that would be significant. This made me feel much better. Of course, I’d like the results to be ZERO. We want to get out of here! The hospital has been a madhouse lately.

Too bloated, feeling miserable

Now we NEED to get some rest!

Smiles and Crackers

So the morning after Hana’s fever her mood improved dramatically. She still wakes up cranky and sleep has been problematic but yesterday (Tuesday) she actually smiled! I was so surprised.

I think this was the most encouraging development for the medical team too. During rounds they discussed delaying her next Cidofovir treatment by one day so that they could look more into drug reactions. So it ended up being a quiet day with just playing with toy food and licking Pedialyte popsicles. She had no more fever or rash. She seemed in a much better mood all day and did well with playing and talking. She continues to have lots of gas and a distended stomach.

Today (Wednesday) followed a very restless night of sleep. Overnight they transitioned Hana off her TPN (IV nutrition) and increased the amount of Pedialyte she got through her NG tube. Hana seemed in good spirits, relatively speaking, with more smiling, playing and singing. As the day wore on she did seem much more cranky for food. She would get frustrated with her toy food and then cry.

Two GI doctors came to see her and felt it was a good time to start half strength formula/Pedialyte tube feeds. They said there is never a guaranteed time when it’s safe to start and sometimes you just have to try and test how things go. After Hana’s Cidofovir treatment finished they started her on the half Pedialyte/formula feeds. An hour after that she was crying so much for cookies that I decided to give her a cracker. She nibbled it nice and slow. Then I gave her another. Over the next three hours she ate six packages of crackers (saltines). She was pretty happy about it! Now we wait to see if she throws up or gets more diarrhea. Hopefully not and we can get out of here in the next few days or so. I know I need to get out of here and get some sleep! I’ve been completely exhausted!

Some Pins And Needles

Yesterday (Sunday) was pretty low key and boring. Hana got her Cidofovir treatment So there was a little extra activity but nothing notable. Today (Monday) was much different.

Hana woke early and cranky. She’s crying for food – pancakes, noodles, cheese. I’ve been a little worried about her distended stomach (from gas) as it seems to be a new symptom. I’ve also noticed her heart rate and blood pressure creeping up and although they are within an acceptable range it seems there should be an explanation as to why. The attending physician noticed this trend too and ordered an echocardiogram to be done today to check Hana’s heart function. In other news, Hana’s neutropenia seems a little bit better.

Hana and I got busy with her toy food. I put the bedside tray over her crib and sit her up. This is probably why it took me a little while to notice the rash. She didn’t have the rash in the morning during rounds. I called the nurse who came to look. Then the resident came and looked. Besides pink mottled skin and dots on her legs and arms (nothing on her abdomen, chest or back) she also had swollen and purple/red knees. Then the cardiology fellow came to look just as I was turning the lights out for nap time. Everyone seemed concerned and asked if Hana was having trouble walking or standing or itching or pain. She didn’t seem any different to me.

I finally got Hana to fall asleep and they showed up to do the echocardiogram. Hana never sleeps through echocardiograms. Then the GI fellow showed up and said that Hana was not ready to start any formula today and possibly tomorrow. She said they treat kids who have had liver transplants for adenovirus all the time and it just takes a long time to recover. She also said we would be here at least another week.

After that the heart failure/transplant fellow showed up to look at Hana’s rash. She ordered Benadryl. By the time she left, I knew there was not going to be any napping for Hana today. Later, after the Benadryl, the attending and fellow showed up and by that time the rash and knee swelling was starting to look better. The theories so far are – a delayed drug reaction to the Cidofovir, a reaction to adenovirus, a drug reaction to something else, a new infection. They need to watch and manage it carefully. They may need to pre-treat Hana with Benadryl before the next Cidofovir dose, which is tomorrow (Tuesday).

I wish that were the end of it. When the night nurse came in to do her assessment, Hana had a mild FEVER, 100.9. You never want to have a fever when you have lines going directly into your bloodstream because this could mean bacterial infection which can be lethal. Sigh. So then the nurse was gone for a long time, as she talked with the fellow and got all the stuff she would need. Then she came back and drew blood for testing and culture. Then we placed a bag to catch urine if Hana pees (sometimes this works, sometimes it doesn’t). Then the new TPN and lipids (the IV nutrition) were hung up and then the IV antibiotic (zosin) was started and by the time this was all finished it was late and Hana was so incredibly tired and cranky. It is now late for me and Paul too. Luckily we already got some preliminary blood test results back and the fellow came in to tell us that so far it’s not looking like a bacterial infection. This could still mean a drug reaction to go with the rash or maybe another viral infection on top of the adenovirus. This hospital is filled to the brim with contagious sick kids right now. It’s so bad that they are having kids share rooms that they normally would NEVER have share a room.

So we’ve been a little bit on pins and needles. In all of this I forgot to mention that Hana tried to eat playdough earlier in the day, she is so sadly desperate for food. She cried so hard when I swiped it away. I am both the bad guy and her comfort – how confusing that must be for her.

I also want to mention that a friend of ours, another little girl with cardiomyopathy and a few months younger than Hana, was admitted to the CVICU last night. She suddenly had a seizure and turned blue. She has no history nor known risk or reason to have a seizure so I can only imagine how intensely scary it was. She had two more seizures, one in the first ER and another in the Stanford ER. Her poor brother had to witness the intensity of the first seizure – as his parents thought they were going to lose his sister. That’s a lot for a little kid to handle. Please keep her and her family in your thoughts and prayers.

Pedialyte popsicle

Two Positives

Today we got two positives. I wish two positives were a good thing but when you are talking about viruses, that is not the case. Both of Hana’s adenovirus blood tests came back for positive for high levels of the virus. The way I understand it, and I could be off a bit, her initial blood test came back at 7,000 last Thursday. Then they drew a level this past Wednesday which came back 25,000 and another this past Thursday which came back at 15,000. The cardiology fellow (admittedly not an Infectious Disease Doctor) interpreted this to mean that Hana’s adenovirus got worse after the initial test and first few treatments of the Cidofovir then peaked at 25,000. Now it is on its way down which is why the latest test came back at 15,000. I hope she’s right.

This was disappointing news for us, but it makes sense because Hana’s symptoms seemed to follow the same trend. Today they started IV nutrition for Hana so that she starts to get something as her gut rests. My understanding is that GI will check in Sunday and make recommendations based on her progress. Tomorrow (Sunday) Hana will get another Cidofovir infusion. They also did another dose of IV Magnesium today. All these things started to get to me today as I worried about things tumbling out of control. It would only take one small thing to really push Hana over the edge – another contagious infection or a PICC line infection or who knows what. I think seeing Hana feeling so down and out for so long was getting to me and I wondered if that’s how parents of kids fighting cancer feel. 

I was able to get out of the hospital for a bit while Paul stayed with Hana. I was too exhausted to do much or even go for a walk. But I did feel a bit better when I returned and I came back with a toy for Hana. She hasn’t wanted to play with toys for many days – she’s been watching her musical cartoons on the iPad, so I was hesitant to get anything. She’s been picking songs about food. Then she started picking videos of adults playing with toy food (it’s ridiculous, who are these people?). I normally change these videos when they come on but I was desperate so I let her watch them. Besides I wasn’t able to engage her in any of the iPad apps I had downloaded for her. So, the toy I brought back was wooden toy food. She LOVED it! For the rest of the day she would sit up for short spells and play with the toy food and play dough. She would even pretend to eat it and say, “Yummy!” I thought toy food would just make her feel worse since she can’t eat, but I guess not?

Hana seemed to perk up in the afternoon, overall. She even asked to have popsicles. We were tipped off that the Emergency Department had Pedialyte popsicles and yesterday one of the nurses went on a mission to get some for Hana. She only wanted the blue popsicles. Yesterday we found more Pedialyte popsicles at the drug store so I got some and put them in the freezer. Still today she would only touch the bright blue Pedialyte popsicles! She only eats them in very small amounts but at least it’s something. Yesterday Hana didn’t really ask to eat or drink but today she did. It’s so hard to deny her.

While I was out today, the attending cardiologist stopped by and talked with Paul. He said it is not unusual that it is taking so long for Hana to overcome the adenovirus and they usually expect two weeks of Cidofovir treatment. Then the side effect of the adenovirus is the GI problems and that can take a few weeks to resolve (although I don’t anticipate we would have Hana in the hospital the entire time). This all made me feel a little better. It will take more patience and the challenge of figuring out how best to nurture Hana through this.