Wednesday, January 26, 2011

About time.......

It's been a long time since we wrote an appropriate update. In fact, if I remember correctly we have not given any updates since our first visit, or two, to Loki's pediatrician (or as I mentioned before his "Child doctor").

A lot has happened in Loki's world since we moved to the Netherlands. Although we expected some regression in Loki's development due to the major transition, he actually has shown a pretty steady developmental path. In fact, more often these days, we actually see Loki reach new milestones without us constantly reinforcing, introducing, and encouraging him.

Loki is currently followed by one doctor, and thus far we have been quite impressed and happy with Dr. Draaisma. He referred Loki to the St. Maarten's Clinic, a rehabilitation hospital where children are offered a variety of services, ranging from a special day class for toddlers, a school for children with developmental and behavioral issues, a feeding clinic and a huge range of inpatient and outpatient adult services as well. For well over two weeks Loki saw a number of specialists who performed an even greater variety of tests on him, some repeated from the US, some new. In short, the assessment was as follows: Loki's cognitive development is age appropriate for his chronological age (24+ months) and so is the development of his receptive language (understanding). Loki made immense strides in his expressive language development and was tested age appropriately as well. This is especially impressive since he [A] started talking very late and [B] is raised bilingual. The main issues were noted during the assessment with the OT (ergo therapeut) and PT (fysiotherapeut). Loki's gross motor skills (walking, climbing, sliding, biking, etc.) are somewhat delayed. Fine motor skills show some gaps with amazing skills in stringing beats or holding a pen, but difficulties placing blocks on top of one another and using his hands and wrists without placing his underarm on a services for support. In addition, all agreed that Loki needs a little more time to process questions and is easily distracted by sounds. These are not major concerns, but certainly something to be aware of and keep an eye on, as they can impact his learning in school when he is older.

Because Loki is basically doing "too well" for the Maartens clinic preschool, he won't be accepted at their school. The rehab doctor wants to see Loki again in 6 months and possibly repeat all the tests. In addition, they did offer physical therapy services but also felt that, at this point in time, we are offering Loki what he needs and they suspect it won't offer much extra. We are okay with the outcome, especially since Loki was referred to the Torteltuin, a special needs group within a regular day care. As this is extremely expensive, we applied for special subsidies, which we were assigned a few days ago. Two full days of Torteltuin or "Torteltown" as dad likes to call it, will be paid for as well as approximately 15 hours to pay for extra support at home. While this is all incredibly good news, it does come with extra paperwork and spending much time on the administration.

Loki started "Torteltown" last week and he absolutely loves it. He has no difficulties saying goodbye to me, he loves to share stories about whom he played with, "Jimmy is favorite" and he even has been taking naps from day one. Loki is so, so ready to engage with other children, discover new toys and build relationships with other adults. I am very grateful that this little guy is making this transition smooth and graceful, much more so than I can say about myself. I yet have to find my groove when Loki is having these new experiences. Enough work to do, but I feel restless and have a hard time focusing. The process of letting go has begun......and when Loki casually says "dag mama (bye mama)" and offers me his bolletje (little head) for a kiss when I leave, I do need to take a deep breath.

The day care placement comes with some increased worries with the regards to germs. Loki's doctor was somewhat hesitant but agreed that Loki is ready to venture out into the world and only time will tell how well Loki is able to process all the viruses and bacterias living in green snotty noses and such!

On the medical front, Loki has undergone a kidney ultrasound (all looks great) and two urinalyses, one of which showed only a very low occurrence of proteinuria (or protein leakage in urine) and for the second we could not even get numbers because the occurrence was too low. Very good news indeed. Bloodwork thus far shows that, with the higher fluid intake (50% more than a child his age and weight), there are no signs of dehydration, so we will continue the same water intake as we have had for a while now. Loki underwent a photo study to assess his reflux and, unlike what was seen a last spring, he actually does have delayed gastric emptying, whichfinally provides us with a clear explanation about why he has reflux. It is such a relief to have an answer after almost two years of struggling. The less good news here is that the medicine they prescribed (erythromycin) to help his stomach process the food a bit faster did not work. The good news? Loki has been throwing up significantly less and, with that, he is eating more. He loves to try a huge variety of foods, but he continues to have a hard time swallowing anything with texture. But hey, we are happy with baby steps (even though Loki said today "no, Loki not a baby").

We are waiting to be scheduled for 24 hour pH study in order to see whether a Nissen Fundoplication would still be an option. With the rate his vomiting is decreasing, though, we probably would not choose to move to fast in this direction. Finally, this week another visit to the St. Maartens Clinic to visit with the feeding team. We made some movies, filled out a sh&*#@ load of forms and handed out yet another huge packet of reports. Also good news from the therapists overthere; Loki qualifies for three one hour sessions a week to address oral motor delays. Happy and daunting all at the same time. As we need for me to work, and I need for me to work in an interesting setting, three visits a week is a bit much. At the same time, they were very committed to addressing this asap as Loki is interested and still able to learn new skills quickly.

Then, in February Loki will be seen by the Infant Follow up Clinic in Nijmegen, which means we finally meet the neonatologist who helped us with our transition to the Netherlands. I am excited to meet her and excited to show off our little wonderboy!

Last but certainly not least, some fun information from "the Lowlands": Despite a cold, which he hopefully shakes off soon, Loki is doing incredibly well in many regards. It seems he is growing older, wiser, naughtier, and funnier by the day. He has an incredible social memory (e.g. in knowing people's names) and he loves to read books. One of his current favorites is Curious George, and I am proud to share that he sits through the whole story listening and sometimes commenting on what he sees. Loki pretends his animals and dolls can see, hear, talk, and have feelings, which causes for very interesting and entertaining scenarios and dialog. Loki is talking up a storm, and no we are not tired of it yet, thanks for asking. He usually uses 3 to 5 word sentences but sometimes we hear 6 to 7 and even 8 word strings. It is incredibly funny to hear Loki explain the world to himself and direct us around, see him test our boundaries, and dance around the house using booty and shoulder. Loki makes up games such as "tickle my toe, my booty, my hair" and he cautiously steps outside to discover the world. Lately, he finds a lot very "eng" (scary), despite the fact that we do not emphasize the "eng" aspects of his and our world. He is cautious when it comes to physical activities. At the same time, though, he is incredibly eager to learn and explores relationships with other people. Loki loves other children and they often appear in his pretend play scenarios. Without us really putting much focus on it, Loki just started picking up colors, with pink and green being his favorite and most consistent colors (brown, blue, and orange are often correctly named as well). A few days ago Loki was looking at a magazine and said "W." When I looked up he indeed pointed at a W. He also seems to know the O and sometimes the I. But his all time favorite is the K from "mama Kakhalijn" (yes, the second K included).

We understand and are happy with the input and assessment of specialists, but our own not-so-humble opinion: Loki is an incredibly fun, sweet, smart, handsome, enthusiastic and social little man who brings us more and more joy and, yes, I barely dare say so, less and less reason to worry constantly!

May 2011 be as healthy and happy as can be!

Saturday, January 1, 2011

Indiana photos

We need to write an update about Loki, and post a few videos. For now, here are photos from our recent Christmas trip to Indiana.

With Nana and Papaw:


First real snow play:


Family:


Happy face:


Coloring with Dad:


Lamps!


Mom prepares gift cards for the Holiday Gift Fund:


Cooking up a storm:


Dinner with Nana and two dogs:


Making dumplings with Nana:


With Cousin Taylor:


Wind with Aunt Alice:


With Papaw:


Up with Taylor:


Cousin Chloe may be Loki's biggest fan:


Gifts included several furniture sets for Loki's faerie forest lodge:


Isn't it time for a shot?


With Amber:


With Great-great-aunt Nancy


A sense of Indiana, #1: Morning from our house.


A sense of Indiana, #2: Lots of lights:

Sunday, December 26, 2010

Happy Holidays to all...

Dear family and friends,

When we examine our lives as years, the last two have been remarkable for us. We spent Christmas 2008 in the Alta Bates NICU, looking forward to our tiny Loki coming home but not aware that kidney failure and feeding tubes were just around the corner. It was wonderful to spend the following Christmas at home with Loki. However, he needed much special care at that time, and we were exhausted.

Since then, Loki’s health has generally improved as the amount of care needed has decreased. His only surgery this year was to give him a new feeding tube, and when he was twice hospitalized for illness, each time was only for a couple days. Loki has also taken significant developmental steps. He is now a happy toddler, running, talking, playing more intricately, and especially laughing a lot. Despite the fact that we are not quite leading “normal parent” lives, we feel that we are inching towards some sort of normalcy.

Also this year, after talking about it for so long, we finally made the move to the Netherlands. This is obviously a big change in many ways. For example, we live in a small village outside of a medium-sized city instead of a major metropolitan area. Of course, this has been a large undertaking, consuming what little free time we had carved for ourselves. But it was clearly the right step, and it is wonderful living close to family.

As we are settling into our new lives in the Netherlands and as Loki’s care is getting easier, we very much look forward to a peaceful and calm 2011.

We thank you for your continued support and hope the upcoming year will bring you love and happiness.

With love and holiday greetings,

Loki
Mom
Dad

Friday, December 24, 2010

Report back from Team CA

It happened..... yesterday on Thursday December 23rd Team CA; Mascha and Amy, dropped by the Alta Bates Summit Medical Center NICU and handed out the books and gift cards we collected through the Loki Sky and his NICU Friends' Holiday Fund. In the mean while we, dad, Loki and myself, were celebrating Christmas a day early with our family in Indiana. Despite the Christmas cheer and children running around playing with their new toys, I couldn't help but have my mind drift off, now and then, to the NICU and the exciting event happening at the same time. Needless to say, I was eagerly awaiting report from Mascha and Amy.

As expected, they received many positive responses. Both families and nurses expressed their gratitude and several nurses mentioned last year's drive. Both Mascha and Amy expressed their excitement in being part of the drop off. As I remember from last year, it feels quite amazing to handout gifts and gift cards, knowing that it positively impacts a family going through a rough time.

The drive came and went, and my mind is already moving towards next year. We made it happen once, we made it happen twice, we will make it happen again.... my dream for the new year? Turning the Loki Sky and his NICU Friends' Holiday fund into a non-profit. Oh, think of all the possibilities this would add.....

Christmas 2008:



Christmas 2009:



Christmas 2010:



The girls before drop off, 2010



64 books and cards neatly wrapped by Mascha and ready to go....

Saturday, December 18, 2010

Funds closed.... but it will continue

Dear family, friends, friends of family, family of friends and perhaps even strangers,

We did it, we reached our goal of $1600 on the closing day of the Loki Sky and his NICU Friends' Holiday Fund. In fact, we almost doubled our initial goal with the $3000 we received from you. I don't think it will be easy to convey in a written message how incredibly grateful we are with the support we have received. Who would have dared to dream this?

With the money we were able to buy 64 $20 gift cards, 64 books, 14 $100 and 1 $50 gift card. Every family spending the Holidays at the Alta Bates Summit Medical Center NICU this year, will receive a gift card and a book accompanied by a letter from Loki and his Friends. Our California team, Mascha and Amy, will be handing out the gifts next week, many thanks to them for taking this on.

The larger gift cards will be handed out by the social workers at the NICU to families who are in need of extra financial support in order to buy a car seat, stroller, crib or other necessities to take care of their baby once they are home.

For those who intended to donate but have not yet had the chance to do so, please don't worry, we will continue to send the money towards the NICU to ensure families who need it most will receive the extra support.

For now I just want to say I am extremely pleased with the outcome and am looking forward to seeing and sharing pictures from our CA team this week! It would not have been possible without the 47 families and/or individuals deciding to donate, it would not have been possible with you! THANK YOU!

Loki Sky and his NICU Friends

Michael and Wagner, 25 weeksAnna, 31 weeks
Bennett, 31 weeksLoki Sky, 24 weeks
Foxen, 30 weeksGabriella and Alexandra, 24 and 25 weeks

Friday, December 10, 2010

And then some.....

As some of you know we recently spent three days in the hospital with a sick boy. Nothing compared to the18 weeks after birth. Still, three days filled with worries, very little sleep and a very sad and miserable boy.

It made me realize even more how happy I am that, despite our transatlantic move and all the hectic it brings along, the Loki Sky and his NICU Friends’ Holiday Fund is happening again.

And how…

  • Thus far 32 families have donated and another 8 promised to do so!
  • Thus far we collected $1678, $78 over target which means extra money goes to families who have more intense financial needs!
  • Thus far Loki has eight NICU friends actively participating in raising funds one way or another!
  • Thus far 64 books have been bought and wrapped!
To those who are helping us make it happen THANK YOU from the bottom of our hearts. You are touching lives of families struggling with their babies’ health. To those who sent us their best wishes THANK YOU for your encouraging words. And for those still planning on donating, we are looking forward to your contribution!

Just as a reminder, the closing date is December 18th. However, we would like to encourage those who are still interested in donating to do so before this date, for planning purposes, e.g. whose names to write in the “People who made this possible” column!

To find out how to donate please go to: http://babylokisky.blogspot.com/search?q=Holiday+Gift+Drive

With warmth and gratitude,

The families of Loki Sky and his friends

Wednesday, December 8, 2010

Home!

After a bit more than 48 hours, Loki was released from the hospital. His fever greatly decreased today, and he was able to keep in about a half-day's worth of food. He was very happy to be home, as were we. We'll try to write a longer update soon.

Thanks for all your support during this latest challenge.

Tuesday, December 7, 2010

Hospital, again

I wanted to post a video this week but Loki had other plans. He got a fever on Sunday, which continued. By Monday he was not really keeping food in. A doctor visit led to the hospital which led to one night here, and now another. His fever has been above 38.5, to 39.2C (101 to 102F). He is generally able to hold down water, and the doctors are not concerned about dehydration or kidney stress, based on a positive urine test. But he will need to stay until he can process food and his temperature lowers.

Of course, he is always a trickster. I planned on going to Amsterdam for work this week but that is now uncertain. And we all have plane tickets to Indiana for Monday.

We will update as we can.

Update: fever up to 40.2 C or 104.4 F.

Tuesday, November 16, 2010

October and November photos

We've written little for two reasons. The good cause is that Loki generally has been doing well, and there is not much to report. Since moving, his development has really moved forward. He's a little boy now, running, talking with a vocabulary of over 270 words, sometimes even making 3 word sentences, being demanding, laughing, playing games, etc. This was very noticeable when we (finally) got our possessions from the US. These has been packed 10 weeks earlier, but he had clearly outgrown many of the toys.

The less good cause is that we are very busy with him, school, settling in, etc.

Among other things in these photos is Loki's second birthday. We kept the celebration small, as we were (and are) occupied with adjusting and settling. Although there are plenty of daily frustrations (both typical and "special"), Loki's birthday highlights that his health, growth, and happiness are blessings.

I will try to get some video together soon, and one of us will write about the many assessments, doctors, and such things.

Reading a birthday card, upside down:


Mom and I got him a train set. He pushes the cars around and says "chuckah chuckah chuckah":


Oma and Muus help blow out the candles:


Apron on:


Mitt and hat; ready to cook:


Loki loves the kitchen set to which Nana, Papaw, Oma H, Opa F, Tante Marieke, and Oom Martin all contributed:


Before it was cold and grey, we used our bike trailer:


And biked to the old walled village of Kranenberg, Germany:


We also walked through the woods:


Scarf:


Eating:


Hat:


A typical evening:



Finally, here are a few from Kyra's B-day party that she sent over. With Muus:


With Lova:


Drumming:


Matching:

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.
See videos.

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Loki's Holiday Gift Drive

Please consider donating to Loki's Holiday Gift Drive for the Alta Bates Summit Medical Center NICU. You can donate by Paypal or credit card here:





Click here for more information, including how to pay by check. For all posts on the Gift Drive, click here.