Friday, February 19, 2010

One Year Ago Today

At 9:15pm on 2/19/09, Sara and I were introduced to our daughter Olivia Anne. We were well aware that our lives would change forever, yet totally unprepared for the direction of change. Today should be a day of celebration and laughter, yet instead it will be a day of sadness and tears.

The last 12 months have been a roller coaster of emotion and stress. Even though we were exhausted the first 36 hours of our life with Olivia were perfect. We did not yet know that she had a heart defect, we did not know her liver couldn't clear itself of bile, we didn't know only one kidney would function. How sweet those precious hours of peace were. I can remember waking up to her 'hungry' cry during that first night, the pride I felt in being a father, the overwhelming urge to protect and defend, the reality of being a family of three now.

Not a moment goes by where Olivia is not front and center in our minds. The loss of those bright shining eyes and dimpled smile changed who we are forever. The torn fabric of our family might slowly be reworked and mended, yet always will the scar remain. We have made many new friends along our journey, while some old ones have faded away. The support we've received from friends, acquaintances, bloggers has been critical to our survival and will continue to be so in the future. I ask you now to keep us in your thoughts, not just today, but next week, next year, five years from now. Light a candle, Say a prayer, send a card, an e-mail, a phone call, acknowledgement that Olivia touched your lives keeps us going.

Peace,

Ben, Sara, & Angel Olivia

Goodnight My Sweet Angel.... Happy 1st Birthday

Thursday, December 31, 2009

Farewell 2009

2009 started with such hope and promise for the future, only to come to a sad end, turning the page on a year that changed our lives forever. No matter how sad, angry, or lost we feel, I would not trade one moment of the life we had with Olivia to make the pain go away. I'm just glad that 2009 will soon be a fading memory, ushering in a new hope with 2010.

Sleep well my sweet. Happy New Year Olivia. We Love you.

Monday, December 14, 2009

Alagille Tribute

Here's a video of our extended Alagille Family, put together so nicely by Julee Spalinger. At this time of year, please take a moment to reflect on what you have and what has been lost. If you are lucky enough to have fully healthy children count your blessings and don't take ANY time you have for granted.

Peace,
Ben

Thursday, November 26, 2009

Happy Thanksgiving Peanut!

We Love You & Miss You SO much....



Adele - Chasing Pavements

I've made up my mind,
No need to think it over,
If i'm wrong I aint right,
No need to look no further,
This ain't lust,
This is love but,

If i tell the world,
I'll never say enough,
Cause it was not said to you,
And thats exactly what i need to do,
If i'm in love with you,

Should i give up,
Or should i just keep chasing pavements?
Even if it leads nowhere,
Or would it be a waste?
Even If i knew my place should i leave it there?
Should i give up,
Or should i just keep chasing pavements?
Even if it leads nowhere

I'd build myself up,
And fly around in circles,
Wait then as my heart drops,
and my back begins to tingle
finally could this be it

Should i give up,
Or should i just keep chasing pavements?
Even if it leads nowhere,
Or would it be a waste?
Even If i knew my place should i leave it there?
Should i give up,
Or should i just keep chasing pavements?
Even if it leads nowhere

Should i give up,
Or should i just keep chasing pavements?
Even if it leads nowhere,
Or would it be a waste?
Even If i knew my place should i leave it there?
Should i give up,
Or should i just keep chasing pavements?
Even if it leads nowhere

Sunday, October 18, 2009

It Means Nothing

Sometime a song just hits home. I came across this song
when a friend posted it on Facebook shortly after Olivia died.
Somehow it just seems o capture a lot of what I can't seem to
express in my own words.

Did we lose ourselves again?
Do we take in what's been said?
Do we take the time to be
All the things we said we'd be
And we bury heads in sand
But my future's in my hands
It means nothing
It means nothing

You can find yourself a God
Believe in which one you want
'Cos they love you all the same
They just go by different names
When we fly our flag today
Are you proud or just ashamed?
It means nothing
It means nothing

It means nothing
It means nothing
It means nothing
If I haven't got you
If I haven't got you
If I haven't got you
If I haven't got you

And the sun sets in the sky
You're the apple of my eye
If the bomb goes off again
In my brain or on the train
I hope that I'm with you
'Cos I wouldn't know what to do
It means nothing
It means nothing

It means nothing
It means nothing
It means nothing
If I haven't got you
If I haven't got you
If I haven't got you
If I haven't got you

Sunday, September 20, 2009

Olivia Memorial Compilation

Here is a shortened compilation of pictures that were shown at Olivia's funeral.




The song is Somewhere Over The Rainbow/What a Wonderful World performed by Israel Kamakawiwo'ole

Thank you to everyone who has supported us and helped us through our ordeal. Everyone has been just wonderful in our time of grief. Sara and I are blessed to have such great friends. Thanks.

I'll keep posting every now and then so keep coming back.

Tuesday, September 8, 2009

Dragonflies

I am still at a loss for words to describe our current journey. Three weeks have gone by, yet every moment has seemed to drag by excruciatingly slowly. When Olivia was born in February our lives changed forever. Our regular routines and freedoms were thrown into chaos. Slowly over the next weeks Sara and I established nice routines all centered around Olivia - Feedings, Playtimes, Baths, Dr Visits, Medicines, Etc. We were satellites orbiting the center of our universe -- Olivia- a very bright star. When she left our world 3 weeks ago, our Sun, our Center, Our Focus was taken away. Sara and I lost our center, we lost our focus, we lost our Star. Hopefully someday we will find pleasure again in the freedoms that have returned -- finishing a meal uniterupted, sleeping in on the weekends, getting in the car w/o needing to 'load up.' These are freedoms we glady gave up and don't want back, but we have no say....

Needless to say, we have searched everywhere to understand why. We look for the tiniest little sign that things will be ok. The other day we were fortunate enough to experience one such event. Sunday morning 2 weeks after Olivia passed away I noticed a large number of bugs flying around our back pasture. When Sara and I went out to investigate, we were overwhelmed by Dragonflies. There were probably 200 or more flying around in our couple acre pasture. We stood out there and marveled at a spectacle we had never seen before. In the 10+ years I have lived in this same house, never had I seen this many Dragonflies in one area.

As we stood and soaked in this display of gleaming wings and darting bodies, one large Dragonfly came up to us. It had an iridescent green body with a purple/blue sheen to it's tail. The wings were a transluscent silver, gleaming in the warm sun. It hovered in front of Sara's face for a few seconds, then it moved over to me and landed on my left shoulder. Soon it took off and dissapeared into the rest of the Dragonflies.

While looking around on the internet about dragonflies, we came across some interesting facts. Native Americans believe that Dragonflies represent renewal and can be messengers from the spirit world. The story below was also found in our search, somehow it feels very appropriate.

The Dragonfly

Once, in a little pond, in the muddy water under the lily pads,
there lived a little water beetle in a community of water
beetles. They lived a simple and comfortable life in the pond
with few disturbances and interruptions.

Once in a while, sadness would come to the community when one of
their fellow beetles would climb the stem of a lily pad and
would never be seen again. They knew when this happened; their
friend was dead, gone forever.

Then, one day, one little water beetle felt an irresistible urge
to climb up that stem. However, he was determined that he would
not leave forever. He would come back and tell his friends what
he had found at the top.

When he reached the top and climbed out of the water onto the
surface of the lily pad, he was so tired, and the sun felt so
warm, that he decided he must take a nap. As he slept, his body
changed and when he woke up, he had turned into a beautiful
blue-tailed dragonfly with broad wings and a slender body
designed for flying.

So, fly he did! And, as he soared he saw the beauty of a whole
new world and a far superior way of life to what he had never
known existed.

Then he remembered his beetle friends and how they were thinking
by now he was dead. He wanted to go back to tell them, and
explain to them that he was now more alive than he had ever been
before. His life had been fulfilled rather than ended.

But, his new body would not go down into the water. He could
not get back to tell his friends the good news. Then he
understood that their time would come, when they, too, would
know what he now knew. So, he raised his wings and flew off
into his joyous new life!

~Author Unknown~


In the weeks to come I'll post a small memorial video of Olivia, keep checking occasionally, I'll keep the site active. Thanks again to everyone for their expressions of sympathy and support and of course to those who have donated in Olivia's name to The Alagille Syndrome Alliance. Take a moment to go there and donate $5 if you haven't. Thanks.

Thanks for listening.

Ben, Sara & Little Angel Olivia.

Sunday, August 23, 2009

Time for Reflection

Sara and I will be taking some time away in an attempt to recenter our lives. It won't happen in one day, one week, or even one year, yet we need to start the process.

We wish to thank everyone for their outpouring of prayers and support. It has helped sustain us through the darkest days we could ever imagine. Thank you we love you all.

If you are in any way able, making any size donation to the Alagille Syndrome Alliance in Olivia's name will go a long way toward helping other families affected by this insudious syndrome. Thank you so much to the generous outpouring we have already seen.

Continue to check in here every once in a while, I still have some things I need to say.

Until then,

Peace to you all,

Love --

Ben & Sara & Our Little Angel Olivia

Sunday, August 16, 2009

Sleep Well

with your eyes of steel blue,
you pierced my heart.

with your red-golden locks,
you bound my heart to yours

with your toothless smile,
you stole my heart.

with your delicate fingers,
you held my heart.

with your laugh and giggle,
you tickled my heart.

with your cry,
you broke my heart.

with your silence,
you tore my soul asunder.

sleep well my angel,
you will be forever in our hearts.

OAH 2/19/09 - 8/16/09


Tuesday, August 4, 2009

Stuck in a Rut.... (Part 1)

... with babies we've found out that's not so bad of a thing.

Olivia has had a pretty hectic schedule for the last
2 weeks, leaving us all a little more or less frazzled :)

Week 1 itinerary:
  • Monday Evening:
The Disco Crib Experience - 10pm - ?
  • Tuesday:
8:20am U of M Liver Recheck
8:40am U of M Kidney Recheck
9:30am Vampire Blood Draw
12:30pm Kidney Ultrasound
1-3pm Eat Lunch, Nap, Travel Home
3:18pm Acquire another stuffed animal
  • Wednesday & Thursday:
Normal Routine @ Home & Grandma's






  • Friday:
Late Afternoon: Kansas & Missouri Huelsbergen Clan Arrive

Olivia was not impressed with all the new arrivals: My Father, Brother, Sister-in-Law, 2 cousins, 2 dogs and 1 bird. She gave them all "The Look" -- trying to decide if they were going to poke and prod her like most all newcomers (Docs and Nurses) do. She showed her dissatisfaction with numerous grumpy faces and crying. Great now my family thinks she's a complete grouch....
  • Saturday:
AM: Hang out at home & watch her cousins freeze in the unseasonably cold pool. Rianna and Lianna had a blast splashing in the water even with chattering teeth. At least the afternoon swimming session had some bouts of sun. (Pic to the right: Sara, Olivia, Grandpa Huelsbergen, & Rianna) The true Olivia started to make some appearances in the morning with a few smiles here and there, but the hustle and bustle still had her on guard - shooting "The Look" more than a
few times.
PM: The weather warmed up in the afternoon for a leisurely stroll around the grounds at Leila Arboretum. (Pictured to the left -- Myself, Olivia, Rianna, and Lianna in the background with a walking stick as tall as she is.) Everyone seemed to have a great time soaking up some sun and fresh air. Olivia really enjoys riding in her papoose,
it gives her a great vantage point absorb her surroundings. Over the last few weeks she is becoming much more aware of her environment - movement, sounds, & new objects. This walk proved to be just the ticket to put our little diva into a nice long nap. She didn't even make it home before she fell asleep. Home for a Barbecue and more sleep.


  • Sunday - "We're Going to the Zoo!"
AM -PM: I feel we're very fortunate to have a very nice Zoo here in Battle Creek - Binder Park Zoo. For a non-metropolitan area, this zoo is quite progressive and attempts to place animals into a more 'natural environment.' The plan for today was to make it to "Wild Africa" and feed the giraffes. Olivia's cousins were very excited about this Safari. We packed our things early and were ready to go when Olivia woke up from her morning nap. We haven't gone on too many outings besides Doctor visits and little shopping
trips, so this was going to be interesting. Olivia did quite well, all the people, new sounds, and smells did make her look a little wide eyed at times. While riding the tram to "Wild Africa" it became a little breezy and Olivia had some pretty priceless expressions on her face when she got a blast of the air. "Wild Africa" exhibit is laid out in about a 2 mile loop taking you by
an assortment of African Wildlife -- Giraffes,
Zebus, Wild Dogs, Monkeys, and Birds. A little sprinkle of rain didn't dampen anyone's spirits. A quick lunch in the cafe, an Ice Cream Cone for Rianna & Lianna, and it was time to head home. Olivia had reached her limit of stimulation and was letting the world know she was ready for a break.

PM: On to dinner at Clara's on the River, a nicely restored railroad station from the later 1800's. A nice evening out with close family, good conversation, and good food... what more could
we ask for. Olivia was able to suck on her bottle in style with three Grand parents, her aunt & uncle, her cousins, and of course her parents.... not that she really cared who was at the table as long as someone supplied the grub. It was a late evening before Olivia finally got to her own bed/crib, but she 'slept like a baby' once she was down.


Thursday, July 23, 2009

Olivia's Favorite New Song

Olivia will stop anything she's doing when this video comes on -- even though she doesn't really use a pacifier at all.

Be warned, it's a catchy (annoying) little tune you'll have trouble wiping from your mind the rest of the day.

Tuesday, July 21, 2009

Olivia & Her Disco Crib

We made our monthly pilgrimage to Mott Children's Hospital in Ann Arbor to check in with Olivia's Liver and Kidney specialists. We were able to schedule both clinics and her Kidney Ultrasound on the same day, making it much easier than having to make 3 separate trips of course. We have been spending the night before her appointments in a Hotel to avoid having to drag our butts out of bed before 5am and suffer the rest of the day.

Olivia actually travels very well. She likes her car seat, once we get in motion she tends to settle
right down . Consequently when we arrived to our hotel Olivia was well rested and ready to Parrrttaaayyyy!!! She was wound up and didn't want to settle down. We ordered room service, fed & changed Olivia, and got ready for bed. Last week Sara found a nice travel Crib/Bassinet (see picture) on E-Bay for Olivia so that Little Peanut would have a nice place to sleep, little did we know what we were in for. It plays lullabies and an electronically bastardized version of Pachelbel's Cannon - , it vibrates and has twinkling lights. After we placed Olivia in her new crib and turned out the lights ... finally bedtime or so we thought.... Sara and I look over to the crib and it looked like there was a disco going on. Flashing lights, swinging ornaments, and thumping feet -- all to Electronic Pachelbel's Cannon. Olivia has taken to lifting her feet and slamming them down onto whatever is in their way, last night it happened to be the end of the crib. This 'party' - punctuated with overtired baby wailing and foot thumping - lasted close to 30 minutes before she decided that sleeping was the best option. She was kind enough to let us sleep from 11pm until 5am without waking --- Yay!!

Our Tuesday started with a good weigh-in. Olivia easily topped 10lbs, tipping the scales at 10lbs 5oz! She managed to put on 1lb 3oz since her last Liver appointment. For her combination of Heart & Liver Disease everyone was very happy with this gain. Olivia got compliments from "Wow, she looks good" to "Hey you're getting some meat on those bones!" She actually fell within the normal desired growth rate! Obviously the new formula that she's been on for the last month has helped her a lot. She also seems to like it quite well, which, given all the crap we've had to medicate her with is a relief.

With her weight no longer an issue, we could turn to her other two issues on Tuesday's agenda: Itching and a Kidney Ultrasound. Over the last 2-3 weeks it has slowly become evident that Olivia's elevated Bilirubin values have are causing her to itch - she rubs her eyes with her
hands or rubs her whole face on our shoulders when she is being held. This is a very common development for anyone that has with severe cholestasis (bile build-up). We had been using Benadryl at night, but it seemed to be only helping minimally. Dr. Lopez wants us to try Hydroxizine (Atarax) to fight her itch, especially at night. During the day Olivia doesn't seem to itch too much, but when she starts to settle for the night, her itching starts, hopefully this new antihistamine will bring her some relief and make her drowsy enough to sleep through the night.

We capped off our visit with a quick detour to ultrasound land to settle a big question about her kidneys... Here's what I posted about our May visit with the Renal Team
The other semi-surprise today was that Olivia's Abdominal Ultrasounds (3 in total) taken over the last 2 months, don't all agree on the kidney findings. All the scans showed 'small' kidneys, but one -- the most recent one -- did not mention anything about a multi-cystic right kidney, while both the initial exams did make note of this finding. The possible problem here is that the Ultrasounds were not "Kidney Specific" but were more liver focused. A Kidney Specific Ultrasound has been set up for August to fully evaluate these discrepancies.
Our ultasonographer was able to get some very good pictures of Olivia's Kidneys. Her Right Kidney was obviously small
and not normal in consistency. We were able to see some of the previously described cysts on her right kidney. Her Left Kidney meanwhile "looked pretty much normal" according to the ultrasonographer. She did not feel that it was significantly smaller than it should be for Olivia's age. There were also no obvious cysts seen today. Mind you this was just the initial reading by the ultrasound tech, the study will still need to be read by a Radiologist, who will hopefully confirm these findings.


We've been graced with so many complications and negative developments over the last few months that today seemed to lift a great weight off our shoulders. This truly has been the best news we've received since, geeeze I don't know when. While Olivia has many more trials ahead, somehow the sun shone just a little brighter on the drive home today.

Save us a spot in your Disco Crib Olivia --- we want to join the party!


Tuesday, July 14, 2009

Odds & Ends

It's been a very uneventful 2 weeks so here are a few miscellaneous notes/thoughts that wouldn't make a separate coherent post. No Dr Visits for another week :) So next week should have reports from both Liver and Renal.

Olivia had a cardiology appointment 2 weeks ago, everything went very well. Her Echo showed no changes. Her function continues to be good, her Oxygen saturations are steady in the 82-82 range. Dr. Dohmmer was very happy with Olivia's progress. While UofM would like Olivia gaining weight faster, Dr. Dohmmer feels that her weight gain is good/acceptable for her combo Heart/Liver issues. We don't have to go back until end of July



Still trying to get the UofM team on the same page.
Renal & Liver aren't playing well together.... not that they are fighting, but they just aren't
talking as much as they need to for Olivia's sake. When one group makes a change in her medications or treatments it shouldn't be up to us have to inform the other group. This should be noted in her chart and be obvious to anyone reading them.... either things aren't getting put in the chart or they aren't reading the chart. Luckily we'll have our next meeting with BOTH Liver & Renal back to back next week. Maybe we can force the Dr.s to sit down meet each other, sing Kumbayah or something--- well let me dream at least.

  • Olivia's still gaining weight, she's now just over 10lbs., meaning she's put on 4.8lbs since her lowest weight w/o having her heart fixed and her liver malabsorption issues we think this is just dandy.. it doesn't matter what "Percentile she's at" what matters is that she's eating and growing w/o a feeding tube!



Olivia's getting excited about meeting her cousins from Missouri & her Grandpa from Kansas next week -- well in actuality O has no clue, but Sara and I are excited for her. If we get the pool warm enough, maybe she'll even get her first swimming lesson.

The Diva's finding her voice. She's been making cooing and gurgling noises for a while now, but over the last few days she's making a very distinct 'hiss/gurgle' noise when she's happy. We tried to capture it on the following video.

Just last night she started working on a second voice, a nice shrill squeal that I fear will develop in volume and intensity as she perfects it... ear plugs please. I managed to just catch a quick snippet of the sound here:

Do all Babies have a built in meal/food detector? Olivia can be in a deep sleep but as soon as Sara and I sit down to eat our meal, you can bet that Olivia will start screaming bloody murder. It doesn't matter if she's been sleeping for 5 minutes or 2 hours, she knows when we are about to eat. It doesn't matter if she's in her bouncy chair with us or across the house in her bedroom, that girl's got timing.

Many people have asked us "How are you doing and holding up?" Actually quite well. I like to describe what we're experiencing akin to a duck swimming on a pond: Nice and calm on the surface but paddling like mad below the water line. Of course that is a great simplification of my/our feelings, but for now that will have to do, there is much much much more to write on that subject, .... at a later date.


Once again Olivia, Sara and I would like to thank everyone for their continued inquiries, well wishes, gifts, meals and prayers; it's all greatly appreciated.

Tuesday, June 30, 2009

Alphabet Soup


When we took Olivia to her new pediatrician last week , we came away greatly impressed. O's Cardiologist had recommended Trestlewood Pediatrics in Portage (Kalamazoo) for her routine care - Vaccines, Runny Nose, Etc - basically anything not Alagille related. When we walked in an talked to one of the receptionists, right away she asked if Olivia was still seeing Dr. Dahmer (Cardiologist). As it turns out, her daughter was born with a severe heart defect 6 years ago and has been under her care ever since. I just those few sentences she made us feel welcome and gave us a positive inspiration for the day.

We were shown to an exam room by a nurse who took Olivia's vital signs; 9lbs 8oz & 23 1/4 inches
long -- our little peanut is growing... slowly but steadily. The clinic was neat, clean, and fairly new. Good first impressions. When Dr. Van Es came in and introduced himself he said "Well I've read a lot about Olivia from all the specialists so it's nice to finally meet her in person." Dr. Van Es spent the better part of an 1 hour talking to us about Olivia's history and treatments so far. Asking about her milestones and telling us what to expect over the next months. When is the last time you got 1 hour face time with a physician? We were very happy.

He then did a very thorough exam -- which Olivia did take exception to -- finding nothing
remarkable outside of her known afflictions. Dr. Van Es made it a point to stress the importance of vigilance with 'The Diva', she walks a fine line health wise so any questions we have we should contact their office and they'll find an answer for us. He also made it an option to bring 'Her Majesty' in through the side door for her appointments, so she wouldn't have to wait in the main waiting room with any sick 'peasants.'.

Once the Dr. was gone it was time for the dreaded Vaccines.

Duh da daaaaaa ......


Olivia, having plenty of experience in the field of Pokeology, eyeballed the nurse as soon as she walked through the door. "The Look" is hard to describe, but it's very distinct. Olivia's facial expression doesn't really change, yet her eyes get slightly wider and steeled for the next event.A slight tensing of her body can be felt too. Her little Blue-Gray eyes observing every movement, rolling as far to the side of her head as possible as to not lose sight of her foe.

Olivia had only been given her HepB vaccine when she was born, all others had been postponed until now because of Olivia's Surgeries and hospitalizations. On this visit the Little Peanut (aka Little Turd), was subjected to an alphabet soup of vaccines: RV, DTaP, Hib, PCV, & IPV. This consisted of 1 oral and 3 jabs into her legs. I'm not exaggerating when I say jab, seriously it seemed like the nurse wound up to pitch a fastball with a needle & syringe. With
the little meat that is on O's thigh's, I was waiting for the needle to come out the other side and jab me in the leg.... Olivia's reaction I'm sure is identical to most infants/children's... there's a delay of 5 seconds or so before the stick registered in her brain, but the did she let loose a wail of pitiful proportions. Sara just commented again the other day that watching those vaccines was almost more difficult than holding her to get her blood drawn. Once the poking was over though, she quieted down quickly and slept most of the rest of the afternoon.

On our way home from this visit, it suddenly hit me that this was Olivia's FIRST wellness check-up. This Dr's visit had nothing to do Allagile, Tetralogy, or Kidneys!!!! Every visit up to this point had been to check something to do with her ailments. Only took us four months to get here, but hopefully before long I'll be writing more about these routine visits and normal baby milestones than her 'sick visits.'

Till the next time..... Olivia will be Chillin' in style.

Tuesday, June 23, 2009

Quest for the Golden Elixir.....

Sounds like a setting for an adventure novel or movie, eh?

Two intrepid and dedicated adventurers set out to capture a few precious drops of this liquor of life. Little did they know when they set out early yesterday morning what trials they would experience along the way. Armed with multiple little collection baggies they brave the heat and humidity of a typical Michigan Summer day. Quietly and patiently they set their trap.
Tick, Tock
Tick, Tock
Finally their quarry was sighted, a slight dribble, then a stream, yet somehow it managed to fully evade their specimen trap! Aaaargh, sticky tape failure and the prey ran off to the safety of a diaper pad... A chuckle or two was had about their equipment failure, but they quickly reset their specimen trap, not knowing when the next dribble of Liquid Gold would appear.
With carefully applied sticky tape & apparatus the two decided not to hover, because we all know "A watched pot never boils." A short time later to their surprise the Specimen Trap had been filled. To the adventurers dismay it was filled with a much larger quarry they weren't looking for, contaminating the desired Elixir beyond use. For the third time in as many hours, another specimen trap was carfully applied. Not too low, not too high, hopefully just right along the quarry's path.
Tick, Tock
{Theme to Jepoardy plays in the background}
Tick, Tock
Yet another equipment malfunction, allowing the Golden Elixir to escape capture. The intrepid adventurers made note to contact the trap manufacturer when they returned form the wilds and give them an earful about their product....
Over the next 14 hours, make shift and modified traps managed to catch everything but the needed liquid. A modified zip-lock baggie was used to cover the quarry's whole living area, but managed to catch only spit-up, projectiled from the other end of the hunting area. With each daylight fading fast and frustrations levels reaching a fever pitch, one final bid was made to slay this formidable opponent. With a careful and deliberate manner the Golden Elixir's retreat was cleaned, dried, and prepared. The final trap was applied, carefully the sticky tape sealed completely, allowing no escape.
With much jubilation, a short time later their quarry had been trapped. The rare specimen was quickly transferred into a transport container and rushed to the waiting scientists for evaluation. Fourteen hours after starting their 'simple task' of collecting a small specimen of Liquid Gold, the two adventurers collapsed into their bed at home, wondering what tomorrow would bring.
So who would have though the simple task of collecting a urine sample on little O, could have turned into such a fiasco. Moral of the story though is, stick with it and you'll get what you need in the end, even if it's 14 hours later....