Wednesday, October 22, 2008

October 22, 2008 @ 7:18 pm AKA GERD Mania

My last post seems like ages ago. I can barely remember the last time I was able to lay Janna down flat for tummy time without her suffering from reflux and an aspiration attack. I’ve got a full out GERDling (gastroesophageal reflux disease).
The last month has seen many sleepless nights and many restless days with me trying to manage Jannas symptoms and researching strategies for managing GERD effectively.
I keep joking that Janna is the most expensive baby on our block. Here’s why:
Essential GERDling Gear:
  • Dr. Browns Bottles
  • Hypoallergenic formula (if not Breastfeeding)
  • Breastpump with storage bottles (still attemping to feed some breastmilk even if she can’t take it directly from the source.
  • Simply Thick™ to thicken feeds to help avoid asperation of vomit or excessive “spit-up” (commercial thickener for formula as intollerance of rice thickening only worsens symptoms for Janna)
  • 30 deg angle for sleeping (RESQ wedge) *very good investment!
  • 30 deg angle foam for chaning table *can get this cut at a foam shop
  • 30 deg pillow for feeding (pollywog brastfeeding pillow works when Janna’s symptoms aren’t too horrible)
  • babycarrier – one that doesn’t make me carry weight on my back for long (I own 4 different carriers now)
  • Hug me Joey – Infant car seat adapter (most infant car seats are seated too deep to be tolerated by GERDlings.)
  • Infacol (Simethicone to help with gas)
  • A multitude of burp cloths/ receiving blankets
  • 4 strain Probiotic (they need rebalance as the meds will put them off) we picked up a hypoallergenic formulation from Kirkland Labs in Oregon.
Meds
  • Novo-Ranitidine (Zantac) an H2 blocker that works intially for immediate relief but often will eventually stop working because the stomach develops more receptors to compensate for the blocked receptors that signal when to produce acid. (Tachyphilaxis) *www.reflux.org/reflux/webdoc01.nsf
  • Omeprazole/Lansoprazole. PPI or Proton Pump Inhibitors are the best for relief and chronically perscribed last because they are “off label” in Canada or not necessarily approved for use in infants. Studies at the university of Missouri have demonstrated the effectiveness and safety of PPIs for longer term therapy.
It’s been a tough haul but we are getting there. With thickened feeds she no longer spits-up/vomits 30mls of her feeding. With the proper meds I hope to stave off feeding aversion (which we were beginning to see signs of before we started the Ranitidine and it actually worked well for a few days!) We start Janna on the Prevacid w/Bufferbabies as soon as the Bufferbabies carrier for the Prevacid arrives from MARCI.
Even with her change table at 30deg I still have to perform the “quick change” to avoid reflux episodes and we can only lay her down on a 30deg sleeping surface 1hr after a bottle. She arches almost constantly now unless she’s drinking from her bottle. We did see a cessation of this while the Ranitidine was working.   We’re now back to the arching and her dose of Omeprazole (which we’ll keep her on until we have the Prevacid ready to go) still does not seem to help even after a week of being on it.

Again she was sleeping better in the first few days of Ranitidine dosing but she’s gone back to sleeping maybe 4-5 hours at night and usually being up most of the day with the exception of a 1 hour nap and a small handful of cat naps during and right after feeding for the past few days. Today has seen her have more sleep during the day than usual but it’s hard to tell if it’s due to omeprazole finally beginning to take effect or plain exhaustion. She fell asleep this afternoon twice during her bottle, once after the first 20mls and dozed for 15 minutes and then again after the next 20mls and stayed asleep for an hour and 20min. Falling asleep during her bottle is something we see quite often, and often after only the 20mls. I think this is because the liquid goes down her throat and gives her temporary relief and then the exhaustion kicks in and she falls asleep.


We’re still working on solutions, every week sees us trying something different or new.
These sites were very helpful:

www.pollywogbaby.com (for essential gear)
www.marci-kids.com the online home of the Midwest Acid Reflux Children’s Institute
www.reflux.org the PAGER site a non profit group dedicated to the provision of information and support to parents, patients and doctors about Gastroesophageal Reflux (GER).
www.infantreflux.org a forum for parents managing GERD symptoms in their children.

So to close, we’re not out of the woods yet.  Not even close but at least I feel like we’ve found a marked trail.

Thursday, October 2, 2008

October 2, 2008 @ 12:45 am

After being negligent in updating the blog for over a month and receiving several inquires after little J I figured I’d better get to it.  She’s napping so I’ll take the opportunity.
Little Janna is keeping me on my toes.  She doesn’t cry and everyone says I should be grateful for that but I have mixed feelings about it.  We’ve had some friends share stories of their children as babes and I’ve discovered that not crying isn’t completely abnormal but it still bothers me a bit.  She’s very quiet for the most part and will let out the occasional sigh or vocalization and she does make a quiet “ahh ahh” sound when she wakes.  I hope to hear more of her little voice as the next month passes.
She’s pushing herself up at a 45deg angle during tummy time and almost able to roll herself over onto her back.   That makes me smile.  She does rarely give me a little glimmer of a smile herself from time to time but not often.
We’ve been working through some wicked acid reflux.  I can’t lay her on her back for long without having her spit-up which makes changing poopy diapers an interesting challenge.  Along with the reflux she has episodes where her eyes open wide, her face red and she pushes her chest upward and arches her back with her mouth agape. She looks like she’s trying her best to breathe and not choke.  The first time I saw this it scared me quite a bit.  When this happens I hold her upright and still and just talk her through it making sure she’s able to breathe.  We do this until the episode subsides.  I’d purchased several crib wedges to help keep her slightly upright while on her back they seemed to help a bit in the beginning but her symptoms only got worse and now they do not help.  As a result and to what I’m sure would be the horror of public health nurses and doctors everywhere; we’ve abandoned the normal “back to sleep” policy and she sleeps on her tummy or side with me always close by and my ears tuned into any sounds she makes.  I’ve gotten quite good at knowing what sounds could mean trouble.  After doing some research I discovered GER and found that she’s not alone in her symptoms.  We have a doctor’s appointment later this week and I look forward to discussing this and exploring strategies with her GP.
The breastfeeding never caught on.  Soon after we came home from the hospital she developed a bad case of thrush and was having difficulty feeding on a bottle so trying to BF was really not appropriate for her at the time.  It took several weeks for her to get over it and once she did we tried a bit again but in the end I decided it wasn’t worth pushing her to change from the bottle when I’d be going back to work in two months so I’ve kept the sessions relaxed and typically give up trying after 20 min.  She has nursed 3 times - but she is very difficult to get latched.  I’m still pumping.  Surprised?  I am.  Although I’m not as concerned about supply as we’ve got her on formula as well as expressed breast milk.  With her spit-ups and gas we’re still trying to find one that works well for her.  Her gassiness is worst overnight with her sleeping in 30-90 minute snatches between bouts of writhing, burping and spitting up before and after her bottle.  Our most recent choice has been Enfamil Gentlease.  I’m not sure it’s an improvement over anything else we’ve tried (we’re on our third formula switch) but it does have less lactose and the milk proteins are partially broken down so from a composition perspective it should be better for her.  I want to avoid giving her soy because from what I’ve read it can increase the risk of peanut allergy later on.
What else can I say - for the most part she seems like a “normal” if quite work intensive baby.  Here’s some photos to keep everyone an opportunity to say “aaaawe”.

Wednesday, August 13, 2008

August 13, 2008 @ 7:54 pm

On the morning of day 13 during rounds I heard the news we’d been waiting for, for awhile.  The lead resident talked about transition to home and “rooming-in” for the evening.
You couldn’t have wiped the smile off my face.  That afternoon we went back to my Aunts to make sure I had a nap to prepare for my first night as mom with Janna by my beside.
The night went extremely well.  I found Janna to be easy, just requiring patience and persistence during feeds, our nurse for the night hadn’t ever had Janna in her care before and she seemed more nervous than I felt while preparing both of us for our night together but by the end of the night and her last check-up with us in the early morning she was giving me the “thumbs up” sign and she seemed quite satisfied with my ability to care for little J outside of the hospital.
That morning during rounds the resident signed the last bit of paperwork for release and we were given our referral numbers for a pediatrician and occupational therapist in Chilliwack, her RX for meds and one last bedside visit by the Neurologist that will be following up with Janna in 3-6 months time and we were on our way.
Janna’s first day at home was very nice.  I couldn’t get used to how quiet it was after all the hospital noises were both subjected to over the last week or so.  I imagine “little J” felt much the same.   So far so good.  I’m slowly trying to work in some B-feeding attempts during her more awake feeds and while she has latched and given a few sucks I think we’re a little ways from success yet.  I’m hoping we’ll both be able to figure it out by the end of the month with the help of the public health nurse.
It’s so great to treat Janna like a regular baby for a change.  We’ll be monitoring her development carefully with the help of her Occupational Therapist to insure that she receives any help she may need quickly.
I’ll post pictures once I have the chance to upload.  Taking care of a newborn while still expressing doesn’t leave a lot of time do manage things like blogs but we’ll do our best.  Thanks to everyone for their prayers and well wishes.  I’m sure they helped tremendously.


10 Comments »

  1.  
    1.  
      1. Simon Said,

August 13, 2008 @ 8:14 pm
Great news.
So happy Janna finally got to come home.
Sounds like she is doing wonderfully, you too.
Looking forward to seeing the 3 of you again soon.
Si
  1.  
    1.  
      1. Pam (Pam and Brandy) Said,

August 13, 2008 @ 10:21 pm
Oh Jenn, what a fabulous update! I’m so happy for you.
((HUG)) (so hard without smileys!)
Pam
  1.  
    1.  
      1. jen/peakwagger Said,

August 13, 2008 @ 10:38 pm
FANTASTIC NEWS Jenn!!!! Hope “little J” has an excellent first couple days home!
  1.  
    1.  
      1. Ashley (ALuv4Labs) Said,

August 13, 2008 @ 11:08 pm
I’m SO glad to hear she’s home, Jenn!
  1.  
    1.  
      1. Kathy (HunterBoozer) Said,

August 14, 2008 @ 8:55 am
Welcome home little one!!! This is fantastic news! Sounds like Little MIss J is heading in the right direction. That is awesome. Wishing you all the best,
Kathy
  1.  
    1.  
      1. Patty (stargazing1113) Said,

August 14, 2008 @ 12:40 pm
wonderful news! continued prayers and good thoughts SO happy to hear little Janna is at home
  1.  
    1.  
      1. Lynn Said,

August 14, 2008 @ 5:31 pm
How wonderful to hear Janna’s home with Mom and Dad where she belongs. The body was made to heal and love accomplishes much! I’m looking forward to meeting you Janna. Good work Jenn, you’re already a great MOM!
  1.  
    1.  
      1. Auntie Esther Said,

August 15, 2008 @ 1:09 am
Great news to hear that your night together went well… and good that you are still trying the B-feeding… We did that when everyone else was doing bottles… B-feeding was so handy, always the right temp… and we never ran out…. and it’s such a special thing that you can do for Janna and for yourself. Have fun!!!
  1.  
    1.  
      1. Janna Version 1.0 Said,

August 15, 2008 @ 6:14 pm
WHOOHOO! Getting back from a successful bomber trip to such fantastic news makes everything even better! Up for a visit in a day or two? I will be heading out of town either tomorrow or the next day.
  1.  
    1.  
      1. Jeremy Said,

September 17, 2008 @ 5:29 pm
So glad to hear she finally went home and things improved through those first two weeks. Any updates? I’ve been meaning the whole time to post a comment here to tell you that my thoughts and hopes are with you and baby Janna, and haven’t remembered to, so I hope this late comment will make up for it.
Hoping for the best,
Jeremy

Monday, August 11, 2008

August 11, 2008 @ 9:40 am

Little Janna continues to show us signs that she’s improving.  The nurses have changed her feeding from a scheduled every three hours to more “on demand feeding” leaving up to 4 hours between feedings to give her a chance to tell us she’s hungry.
She seems to be able to do this well enough on her own in the late morning to early afternoon before and after that time she still seems to need help to wake-up.
Her pheno dose is gradually being moved back to her last evening feeding (11pm-12pm) so that we can let her sleep a little longer overnight and not have to struggle with feeding a sleepy baby.  We’ll need to wake her at 4-5am for the first morning feeding.
She has a definite ”wake and play” time between late morning and early afternoon.  She’s making noises and actually crying in her little way.  She’s looking around and will look straight at mom or dad or the nurse during a cuddle and feed and seems to also like staring at the overhead lights.  The nurses think she’s ready to try breastfeeding today during her more awake feeding times.  It will be great if she and I manage to move to that method of feeding as expression of breast milk via pumping isn’t all that fun and takes quite a bit of time and effort.  Perhaps one of these days I’ll find the time to add an “Adventures in Lactation” diary page to give everyone a glimpse of the little absurdities that are involved in “expressing myself”.
So we’re getting there, the only thing holding us up from release is the monitoring of her SP02 readings.  Back around 6 days ago when the pheno was still quite high in her system she had a dip in her readings just after dylantin dose which the doctors think could have been attributed to the dylantin but the policy is when this happens with a newborn or small baby they have an observation period of 7 days to insure it doesn’t happen again before releasing from hospital.

6 Comments »

  1.  
    1.  
      1. Lynn Said,

August 11, 2008 @ 10:37 am
She’s so beautiful! Hopefully she’ll be breast feeding soon Jenn. You’re giving her the best by “expressing yourself”. Thinking of you daily.
  1.  
    1.  
      1. Pam (Pam and Brandy) Said,

August 11, 2008 @ 2:05 pm
Sounds like she’s making lots of progress! I can’t wait to hear that you’re heading home with her.

Saturday, August 9, 2008

August 9, 2008 @ 12:42 am

Today saw more improvements in Janna’s level of alertness.  She’s now looking around with those deep blue-gray newborn eyes of hers, staring at faces and at light sources overhead.  She’s also finding her voice more and more and actually had some fussy moments today.  I didn’t mind them one bit.

She had her day “10″ MRI today - they squeezed her in early as this time of year the MRI is closed for maintenence.  Wendy the specialized nurse for the Neurology team said little J was also a little fussy for her before the MRI so she took the time to feed her and settle her in a bit.

I gave Janna two feedings today and she went through them even better for me than she had in the past.  It was no longer necessary to support her chin and encourage her to latch.  She’s now seemed to figure that out on her own.  She was alert enough today to have a bit of a “playtime” consisting of just making noises with her, looking into her eyes when she stared up at me, holding her hand and giving her lots of love and cuddles.

One of the Neurologists expressed interest in following Janna’s progress after we are discharged.  He wanted to insure we have access to all of the support we require and basically said his door is always open to us.

So things look good for a discharge soon.  There are a few metabolic test results to come in and it sounds like they want to continue to observe little J a few days longer just to make sure she’s on the right dosage of anti-seizure meds (Pheno) before they send us on our way.

5 Comments »

  1.  
    1.  
      1. Lynn Said,

August 9, 2008 @ 1:11 am
I appreciate this blog so much, thank you for keeping us informed Jenn and Tim. Janna looks so wonderful in your arms!
  1.  
    1.  
      1. Pam (Pam and Brandy) Said,

August 9, 2008 @ 5:01 pm
I’m glad she’s showing so much progress! It would be great to have access to the neurologist - if any problems do develop you’ll be able to get help immediately!
I’m looking forward to hearing that Janna’s on her way home.
  1.  
    1.  
      1. Janna 1.0 Said,

August 9, 2008 @ 6:43 pm
Janna! You look so cute and sweet and it was so lovely to meet you. I will be through Vancouver, and then Chilliwack on around the 15th and would be so tickled to see you and your ma n’ pa.
xoxoxoxoxoxooooo
  1.  
    1.  
      1. Cathy (Cozncrew) from the lab board Said,

August 9, 2008 @ 8:28 pm
It is wonderful to see that there are some improvments in Janna’s level of alertness. This sounds to me like it is a good sign of things to come. I hope that things continue to go well and your sweet baby is home where she belongs.
Our thoughts and prayers are with you all.
Cathy