3/28/2011

Jaylee's Art Show

Jaylee's Art was one of tow pieces chosen to be in the Warwick School District Art Show this year.  Grandma and Meg went to see it on display with us.
She wrote her name in a collage.




(we were interpretting her art in this last picture!)

3/23/2011

My week in pictures...
March 16-23, 2011
By Jackson Lee Stringham

















Life Sucks Sometimes!!

Just ask Jackson!!! From age 12-20 days, he slowly became sicker and sicker.  Luckily, he is a fighter and his body was compensating wondrefully, which saved his life... again!!  We knew something was wrong, just couldn't figure out what it was... I thought for sure his vesectomy site was infected.  But after a trip to the Urologist on day 14, we were reassured that we were just "paranoid".  After cutting dairy out of my diet, because of his fussiness and lack of interest in eatting, we found out from the visitting nurse that he was not gaining weight appropriately.  A trip to the Pediatrician found that he had LOST 3 ozs in 7 days, so we started on Soy Formula and returned the next day for more unuseful suggestions.  I was very frustrated, "knowing" that something was wrong but not knowing what it was.  I also felt that Jason thought I was just being way to overprotective... so I retreated to my room to watch TV and clean all day long.  By the evening on day 20, we decided to take him to the ER, even though we had been constantly reassured that he was not sick and we would prob be sent home to follow up with our Nephrologist after the weekend.  We watched and watched for signs of dehydration... there were none.  He was just irritable, not hungry, and pretty sleepy.  His mucous membranes were pink and wet, his fontanel not sunken, skin turgor good, and of course he was still peeing lots. He looked "good" for being so close to death! The ER staff kept saying that he wasn't all that sick, and after 20+ IV and blood draw attempts, they placed a NG tube to try to give "just a little fluid to see if it perks him up".  When his inital lab results came back, they were so off kilter that they were dismissed as hemolyzed and new labs were drawn.  All the while, internally, Jackson was crashing.  When he finally went limp in my hands and we screamed for the nurse, we were told that he was just fine, just exhausted from fighting the hospital staff.  I KNOW MY SON and knew things were not right.  When the repeat labs were just as bad, the PICU Dr came down with his staff, attempted 2 IV sticks and then literally ran him up to the PICU.  Dr Bob Tamburro was completely awesome, but being left in the waiting room for 1 hour after being told how serious the situation is, is unexplainable.  But, I will try... 
Your heart races constantly, your mouth is dry, you can't cry, you can't think, your belly feels ill, you feel like your floating in a surreal reality, your mind races from important details to mundane thoughts, you can't keep still, you pace the floor, you try to drink water to keep hydrated but it just makes you want to vomit more, you call your parents to update them on the seriousness, you pray, you pray and you pray, you beg to wake up from the bad dream, you worry about your older kids, you fall the the ground feeling completely helpless. 
We were informed of everything by Dr Bob... Jackson's sodium was 108 which caused brain swelling and irritablilty.  His potassium was also at a lethal level of 9.8.  He was tachycardic at 200-210, but afebrile.  He had been cool, clammy and mottled all week.  (Again, I had been reasured that his color was normal for an infant mulitple times)  He was started on albuterol neb treatments, kaexolate via NG tube, and iv Glucose/insulin to lower his K+.  They were only able to get a 24 g in his R AC at first so they kept treating his hyperK+ until it lowered enough to a level that would be safe for sedation and intubation and eventually a central line placement.  Dr Bob's critical thinking process was perfect!!!  Guess that's why he is a PICU Dr.  4 hours later, he was able to be sedated - it then took TWO hours to get him intubated and a central line in b/c his system was so collapsed, due to dehydration.  He was stuck mulitple times in the groin and then they were successful in his R IJ.  Saline bolus were then rushed into his little heart!!  You know Jackson... he ended up being over corrected - his Saline levels were increasing too quickly for Dr Bob's liking and he eventually needed IV K+ b/c his levels were too low!!!  You go Jackson!!  He did, however, need a blood transfusion after being HYPERhydrated - he has gained over 1 lb of pure water weight and looks almost unrecognizably pudgy.  He, again, was not able to open his eyes b/c of the swelling!!
He is now 22 days old... we've been moved to Hell, I mean the Pediatric floor, and he is stable.  He still is receiving BIG antibiotics since is urine and blood infections were resistant to many antibitoics!!  We cont to monitor his CMPS Q12' and he is receiving less and less IV fluids, as his PO intake increases.  We still have to "force" him to eat more than 1 oz at a time though.  He had spiked a 101' fever on day 21, but it has subsided.  His urine remains slightly coloudy (had been clear at home until day 19 but the Pediatrician felt that it was healing skin cells from his ostomy) but the Nephrology team thinks that it is just b/c his kidneys and ureters are still being cleaned out.  Of course, Dr Muchant called from Geissinger and talked to us for 1/2 hour - love that lady!! 
It's hard to keep everything straight now, just a few days and a few hours of sleep later.  The Ronald McDonald house is so very nice and I will start leaving my coins in their silly coin collector boxes from now on. 
I'm completely annoyed by the two other roommates and their families sharing Jackson's room. I'm worried about how long we'll be stuck in the hosp with IV antibiotics (prob 14 days).  Im worried that it will be a scary couple of years trying to maintain a healthy balance btwn his intake, output and Na+ supplement amounts.  I'm terrified that I'll let him get this sick again.  I'm exhausted.  But, of course I'm here typing away so that years from now I can remember the night we thought we lost Jackson...
Sunday March 20, 2011 @ 4 am.
The single worst day of my life. 

3/05/2011

My Twins

No one seemed to believe me when I said how much Jackson looks like Jenni...
atleast not until I found some of Jenni's baby pix.
He reminds me A LOT of his big sister... just look...

Jenninblle 2005
Jackson 2011 

3/03/2011

Jackson is Here!!

Jackson Lee Stringham3-1-2011
3 pm
8lb 10 oz
20 1/2 inch


*37 weeks 3 days
*Amnio to check for lung maturity at 0800
*Lots of contractions while waiting in L&D
*Csection scheduled for 1300'



*Nurse Anesthesist used to be hypnotist
*Spinal left me "numb" up to T4 - caused my BP and HR to bottom out, but it was great and only allowed me to feel pressures
*I heard the clamp clang together... yuck!
*Room was dead silent as they got ready to pull him out
*Jackson SCREAMED before he was even out of me!!!
*Jason peeked and almost jumped for joy when his belly looked "normal"
*Jason got to cut his cord
*I got to see him before he went off to NICU - I could NOT believe how big his cheeks were!
*We were told right away that he had a hypospadia but otherwise looked great. There was no evidence of a patenet urachus.
.*It took 45 minutes for Dr Muller to sew me back togehter, but my sutures have gotten many praises by nurses!


*Jason wheeled me over to NICU at 1700
*The girls, Grandparents, Mandy and Brian got to peek quickly at him in the NICU around 2030
*Jennibelle had been cleared by her Pediatrician to go see him with a dx'd sinus infection but she had gotten sicker on Fri so she struggled to not look or act sick in the NICU. (She was so cute!!)
*Jaylee seemed a little nervous, like she would break him!

(You can see how sick Jenni is feeling!!)
*On Weds morning (3/2/11) he was moved to the step down NICU.  I got to breast feed him.
*His creatnine went up to 1.1 after being 0.7 initially. Our AWESOME Nephrologist (Dr Muchant) explained that it could take 2 weeks for his Creatnine to level out.
*Jackson had 4 or 5 dirty diapers within the first 24 hours!
*He was peeing - Jason saw an actual pee stream when he was first born, I only ever saw drops on his penis.
*The Urologist (Dr Semfest) did a stat US and believed that he had a Post Urethral Valve and orded a VCUG for 3/2  to confirm the diagnosis
*The VCUG could not be done at 1500 b/c Dr Semfest could not advance the catheter up his urethra.  We were informed he would need surgery the next AM (3/3/11)(cystography with probable PUV clipping).
*An IV was started and he was NPO after MN before surgery
*He was so sweet before surgery... he is patient and gentle and he never cries!!  We got to old him in the pre-op area before they took him away.  We were both obviously nervous for him!

***********
*Surgery lasted 1 1/2 hours... Dr Sempfest came to tell us that he did not find a PUV, like we expected... He found that his urehtra was a dead-end "urethral atrasia".  He then said "It is a lethal diagnosis, I don't know how he survived being a fetus"  Becuase of this, he had to make a vesicostomy... A hole in his lower belly that allow his urine to literally drip out of his bladder continuously.  The plastic surgery to repair his urethra and penis will be done around month 9 and then eventually his stoma will be closed up.  They are expecting that his urological swelling and dilation will subside some on it's own, now that the blockage has been relieved. The hole is about the same size as his belly button.
***********

*We will cont to monitor his Creatnine daily until he's D/C'd (3/4 or 3/5) Then we'll have out patient lab work done in Lancaster every few days and follow up with Dr Muchant weekly for a while.
He was in A LOT of pain after surgery (HR 200s, Resp 50, BP in the 80's, Arching back, crying...) The first thing his NICU Nurse said was "I will NOT ignore your son's pain", right before she sat on her big fat butt for 2 hours charting and never giving him his Tylenol.  Luckily, the next Nurse administered it right away!!
* It's 8 hours post op, he looks much more comfortable and has some bowel sounds so I will be able to feed him again soon.  He is not nearly as mottled and his color isn't as dusky.  It's obvious he feels better.

*Though this diagnosis is not a great one, it IS a diagnosis and it IS fixable and we finally have some answers.  I can't explain how good that is to us!!!!!


/\/\/\/\/\\/\/\/\/\/\/\/\\/\/\/\/\/\/\/\/\/\/\/\/\/\/\

Jaylee and Jennibelle absolutely LOVE him already!!! They have been very gentle with him and can not wait for him to finally come home! 
Grandma and Grandpa flew in from Seattle to spend some time with us and to care for the girls while we are here in the hosp.  They stayed up here in Danville for 2 nights at a hotel with an indoor pool
Nan and Poppop came up and spent two nights in the hotel too.
Mandy and her family came up for Jackson's delivery and ended up staying the first night so that Morgan could play with the girls and so that Mandy and I could hang out.
Meg drove up late at night on the 1st after work. She came to the hosp early on the 2nd to meet Jackson.
Everyone in Seattle has been calling and facebooking me to keep updated.






It is just amazing to me how many people care about this little boy and the rest of us.  People I barely know and have never even met have been diligently praying for us.  I honestly don't believe that I would be here, holding my son, without it.

I am exhauseted but want to keep everything straight.  I am already mixing things up and he's only 48 hours old.  I hope that he will one day realizes just how lucky he is to be here, and that we will never take our little miracle boy for granted!!  We hope to go home tomrrow evening!!

#################
I got to feed him tonight at 2000 and 2230.  He was awake for a little bit and just stared at us, taking us in while we inhaled every detail about him.  He's lost 14 ozs since birth, and looks a lot different.  is face is not nearly as swollen, though he's obviously parched from the anesthesia and it beaks my heart to see his dry lips and tongue.  We're hoping to go home tomorrow so, he'll be bottle fed tonight while I sleep and hopefully tomorrow my milk will come in and we can head home, as a family... JUST 4 days after he is born.  I've been wondering WHY God has blessed me with this boy.  Why did I get lucky enough to be his Mom?  Usually after I have a baby, I toy with the idea of L&D nursing.  These days I find myself wondering WHERE God wants me to go from here.  I feel like I make a difference at Bayada and love the realtionship I have with Emily and her family.  But maybe I could use this experience to help people in another foled of nursing?  Maybe all this is just eh pain pill typing?  Who knows... I am terrified that my Short Term Disability will be rejected and I'll have to return to work sooner than expected.  This is one of those days that
 I WISH MONEY GREW ON TEES!!!

We filled out the paperwork to have Home Health Nursing for a little while, though I'm not sure what the nurses would do, other than check on his stoma.  We've met with the Nurse Case Mgrs and have gotten and given lots of information regarding Medical Assistance Health Insurance and Social Security Disability Benefits.  This is all so new to me and it is so very confusing!!!

G'night!!