Monday, March 28, 2011

Challenges

By now, I have three draft blog posts, but none are finished. Perhaps my goal should not be to address everything, and to limit myself to what really matters at this point in time. I find this rather challenging, however. It is so easy to focus on the medical bumps in the road, and forget all the wonderful minor and major steps Loki takes. However, the reality is that many doctors' visits lie behind us and, most likely, quite some still lie ahead of us.

First, we know that many are anxiously awaiting news on Loki's recent 24 hour esophageal pH test. Dad already mentioned in our last post that this one came with issues, and I dare say it was one of the rougher moments since Loki left the NICU two years ago.

After thrice weekly feeding therapy, an infant follow clinic visit (of 4 hours), and meeting with the pediatric surgeon in two the weeks before, Wednesday we made our way to the hospital once again. Loki's reflux medicines were put on hold for 5 days in order to get a "realistic" result of how much reflux actually occurs. We noticed an increase in vomiting, coughing, and belching after a couple days. This was accompanied by a significant decrease in food intake by mouth. In most cases, the placement of the NG is not all that complicated. In fact, it is no different than what we used to do often at home before Loki had his g-tube. Unfortunately, our lovely nurse was unable to get the tube in. Each time--and she tried approximately 6 times in each nostril--the tube got stuck after 7 centimeters. Loki, who started off very courageous and optimistic screamed louder with each try. When the nurse decided to give it a break and ask for help Loki exclaimed "Hooray, all done." A young and very gentle lab assistent got teary eyed when he told Loki we were not quite there yet.

After a call from the nurse, we were able to get assistance from a radiologist doctor. Loki kept pushing his little face in my neck and on my face for kisses, and did not want to let go when I tried to put him back on the table, under the x-ray machine. It took four people, and all their strength to get the NG in. I had to push Loki down on the table with all my might to keep him still. This was without a doubt one of the most heartbreaking and painful moments during my life as a mother.

I remember so many moments in the NICU, promising Loki that, once he was home, the poking, prodding, tubes, and hospital pains would be over. I would protect, cuddle, and love him more than anything. To hear him scream "no mama, no mama, no no" while seeing the panic and fear in his eyes built upon a lot of guilt and pain I feel for him. I want to protect Loki from pain and discomfort. Yet in order to help him get better, I am the person who forces him down on the table, unable to save him from this harsh reality. The guilt and sorrow which I feel about this throughout recent days is just the tip of the iceberg, I suspect.

Once the tube was placed and secured, I was introduced to the little machine which registered what occurred during reflux. However, what I did not know was that every little detail needed to be registered manually as well as written down. Practically, this meant that every time we started or ended a syringe of food or water (which we do about every 15-20 minutes), we pushed the on and the off button and then wrote it down. When Loki went horizontal--whether it was to sleep, to have his diaper changed, or just to play-- or got up, I pushed another on and off button and wrote it down. Medicine needed to be registered as well as every "event" including abnormal (reflux) cough, vomit, spit up, cry, etc. Add to that Loki's desire to pull out the tube, and I was ready to completely fall apart by the end of the day. To top it off, he was a bit ill with diarrhea, needing his diaper changed about every 15 minutes. We were all exhausted!

Loki slept in our bed because we needed to ensure the tube stayed in and did not disconnect from its little machine, so we barely slept. The next day we went back to the hospital to release Loki from this torturous machine. The boy we took back home, fortunately, was completely different from the little man we brought in. He was excited again, happy, and talkative. Unfortunately the 5 day break in reflux medications has had a huge impact. We are counting up to 15 vomits per day, lots of stomach agitation when we give Loki a shot of food or water, and an average of three loads of laundry per day, as well as many mop jobs. To prevent dehydration, we have been giving Loki oral rehydration salts to keep his electrolytes balanced. During our visit to the pediatrician on Friday (hospital trip number three of that week), we collected urine, and we're awaiting the results. The good news during this visit was Loki's weight gain: at 11.8 kg, up from 11.2 kg two weeks ago (albeit on a different scale).

Today we met Loki's gastroenterologist for the first time. Unfortunately, all the vomiting cost Loki 300 grams and we are back at 11.5 kg. Doctor Gierenz took her time to get to know Loki's story, but unfortunately she did not yet know any results. We had a lengthy conversation about Loki's situation. Unlike what the pediatrician said, she believed there is a small chance that these reflux issues may still improve until Loki is approximately five years of age. Before she is willing to discuss the Nissen fundoplication, she wants a better idea about what exactly causes the reflux, and thus wants to await the results of the pH probe. In addition, we must check Loki's stomach content three times per day. This means that besides our regular notation of what goes in, we literally empty his stomach by using the syringe and see how much is still left. We push that back in, wait a minute and add the next shot. Needless to say, this is somewhat of a gross job. The doctor is willing to increase the Nexium to see what the impact may be and possibly to discuss with a nephrologist the option of using Motilium. That is a motility drug which is cleared through the kidney and is known for it's damaging impact, but can have extremely positive effects on stomach motility. Finally, it is likely Loki will undergo a gastroscopy, in which the stomach and esophagus are examined with a little camera. At that time, a biopsy will be done as well. (Apparently, there are cases of esophagitis caused by food allergies where a regular gastroscopy is not enough to observe the inflammation.)

When all these tests and trials are completed, we may discuss the nissen fundoplication. This doctor thinks chances are that Loki's reflux is caused by gastric emptying rather than a less than optimal esophagal sphincter, which is what the Nissen fundoplication would address. Her reasoning is that Loki did not vomit from the very beginning, which is the case in most cases of straight-forward reflux. If she is right, the surgery could very well cause more problems.

Regardless of the cause and the treatment, we most likely have a long road ahead of us. Although we are inching back to what we know as "normal," the impact of this test has been scary. Loki barely shows any interest in eating or drinking by mouth, whereas before we had started to see the positive impact of his therapy. He gags and throws up with the littles pieces of jam in some yogurt and seems to have lost his taste for all the treats about which he had been so excited: chips, chocolate, applesauce, yogurt, ice cream etc. Even now, I do not feel that we have fully recovered. Dad and I both tense up when we hear Loki gag or cough. We can only sigh when the bucket and mop come out again. Seeing the same jackets repeatedly go into the laundry is completely frustrating. We are happy to see how resilient Loki is, but also painfully aware that every situation builds upon a large pile of traumatic events in this little guy's life. How can we protect him from more pain?

For now, we appreciate all the sweet calls and comments, and apologize for the lack of contact we have made. I am exhausted and worried about Loki's future. Even answering a phone call or email a message feels like a burden at times. With the sun coming out, the food staying in, and Loki returning to his happy and chatty self, I am sure you will hear from me again!

8 comments:

Kyra said...

Liefs, liefs, liefs!

What a heartbreaking story; if tears help, then mine are the first to enter tthis blog. Hope for better times and do call when you need to.

Kusje,

Kyra

fransje melief said...

Hey lieve Kathalijn, a heartbreaking story indeed, I am sorry for both you, Jesse and Loki, this was necessary to get a reality check on his reflux! What a hard time to be a mom & dad!! If there's a positive side to this, it would be that the "new" doctor has other ideas about what may cause his reflux, increasing chances of getting nearer to the truth. That doesn't mean the road won't be long of course. I am sure Loki will feel better in a few weeks and the therapy wasn't for nothing. Our weekend of fun may seem like a long time ago for you, but more will follow!

Love, Fransje.

Jolanda said...

Dear friend, I'm slightly speechless and the same tears that Kyra had are rolling over my cheeks. I wish there was more I could do for you! Hope to pop in soon, love you and our little hero a lot!

Love Jolanda

Richard en Maaike said...

Dikke kus voor jullie alle drie!

The Fitch-Jenett Family said...

Oh, honey. I am so feeling for you. The barfy, barfy, barfy days are godawful. Also, the holding down our little boys so people can do the unpleasant things they HAVE to do to them is hideous. I am so sorry that you are in this particular place right now. Ugh.

We send you big hugs and clean, fresh smelling thoughts!

Jaime (et al)

Suzan said...

En nou is het tijd voor goed nieuws! Heel veel beterschap gewenst! En heel veel liefs van ons 3-en,
Johan, Suzan en Phileine

Unknown said...

Dear Lijn,
Uff sounds very hard. Loki is a trooper and You both are wonderful parent.
Hoping for better days ahead.
Love Gracy

Anonymous said...

My heart aches for you guys upon reading this. I pray for the benefits of your commitment and love to show up as soon as possible. In the meantime, I bang my head against the wall in solidarity. I send you all a ton of love.
Esti

About Loki Sky

Loki Sky is a special little man. He was a very early micropreemie, weighing only 610 grams (1 lb, 5 oz) after 24 weeks, 3 days gestation, born to an American Father and a Dutch Mother in Berkeley, California on October 18, 2008.

On January 11, 2009, while still in the hospital NICU, his one kidney stopped working. It was repaired after three surgeries. After spending time in three hospitals in three cities, Loki came home on February 17. He struggled with eating, and then stopped in July, leading to 8 days in the hospital, a failure-to-thrive diagnosis, and a NG feeding tube. On October 10, a minor surgery installed a G feeding tube. Another procedure replaced it with a new one, and then again with a Mic-Key button in Jan. 2010.

In August 2010, he and his parents moved to the Netherlands.

Read about his first name.
Read & hear about his middle name.
See photos.
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