Home › Forums › Infant Reflux Information › Procedures › Endoscopies tomorrow
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July 30, 2008 at 2:31 pm #54778AnonymousInactive
Ok, so have the time & prep info for the procecedures (EDG & colonoscopy) tomorrow.
It’s @ 7:30am (1st procedure of the day!) & we have to be there @ 6:30am (leave the house @ 5:30am). So he can’t nurse past 3:30 am . It will be hard, but we’ll get through it.They said to do 1 Baby Lax enema @ bedtime.Anyone know where to buy that? I’m going to have to go w/ the boys by myself to get them b/c dh will be late getting home (we’re also buying a car tonight w/ all the mayhem going on ) so I’d like to only have to make 1 stop-lol.But since he can nurse up until 3:30am won’t he still have poop in his system?I called the children’s hospital & asked this question & she just said to do what the GI office’s instructions said & that it would be fine b/c they don’t like to do a lot w/ the babies… but the instructions are for babies 12mths & under. So are they assuming that those kiddos won’t be eating past bedtime (after the enema)? I called the GI office & they weren’t much help either.Oh, also… no IV or mask. They use a sedation drug & Evan will breath on his own, etc. So, that’s good to hear.July 30, 2008 at 2:36 pm #54780AnonymousInactiveGood luck Erin, I hope everything goes smoothly and you get some answers! Will look forward to hearing how it turns out.
Sorry, I’m not much help on the baby lax. I would likely phone around to some of the larger pharmacies (perhaps WalMart?) and ask if they have them in stock and perhaps to even set one aside for you.July 30, 2008 at 3:26 pm #54783AnonymousInactiveGood luck! I hope everything goes well. Look forward to hearing about it when you return!
July 30, 2008 at 3:37 pm #54785AnonymousInactiveGOOD LUCK!!!!!
July 30, 2008 at 4:05 pm #54787AnonymousInactiveSo, after 4 phone calls & more confusion…
The BabyLax enema is now Pedia-Lax enema & the instructions say “DO NOT USE UNDER 2 YRS OLD”. I called Ped GI office & they said if I can’t find BabyLax (well, I won’t be able to find it b/c THEY DON’T MAKE IT ANYMORE) then to only give Pedialyte from 3pm today until 3:30am… um, to a 2mth old? They said yes.Thankfully the Ped GI nurse called Walgreens & they said the Pedia-Lax enema will be fine.Then, I questioned about doing the enema before bedtime or to just wait to do it after his last feeding (@ 3:30am) & they said to do it after 3:30am… so that will be a good time .July 30, 2008 at 10:26 pm #54804AnonymousInactiveUrgh!!! I hope it all goes well….I will say a prayer for you tonight. Let us know how it goes. 🙂
July 30, 2008 at 10:43 pm #54807AnonymousInactiveGood Luck. I hope that those last few hours aren’t unbearable without being able to nurse him… Keep us posted.
July 31, 2008 at 4:43 pm #54845AnonymousInactiveSorry for the late update. When we got home earlier Evan & I laid down for a rest & JUST got up. I guess getting up @ 3:30am took it both out of us.
Anyway…
Evan did great & was such a good little guy. He slept until 2:45am last night (!!) so I fed him then & woke him again @ 3:30am to feed him. Then we woke him @ 4:30 am to do the enema. We left @ 5:30am & he slept the whole way up to the hospital so that was nice.
We arrived @ 6:30am & they pretty much prepped him starting right away… weight, height, temp, blood pressure, pulse, etc. He did have to get an IV but he was a trooper…& that nurse is talented finding his little vein. He got a little fussy around 3.5hrs (7am) but they have sugar water to dip the paci in & he really liked that. He actually fell asleep until 7:45am when they took him back.
He was in the procedures for about 20min, then they paged us & when we got to recovery he was sleeping on his little baby stretcher so peacefully. They had to wake him up after about 20min & he was groggy & out of it, but didn’t cry @ all. They wanted me to nurse him right away & I did, but he was really struggling b/c he was so out of it.
The EDG (upper endsocopy) showed everything normal & good. No irritation or ulcers from reflux & no esophageal thrush.The colonoscopy showed some inflammation & irritation (allergic colitis) most likely from Milk/Soy Protein Allergy but it’s almost all healed… only slight inflammation. He has a tear near the rectum so that’s probably what’s been causing the majority of the bleeding – although the inflammation could still be bleeding some too.He took multiple biopsies from both the EDG & colonoscopy. They will have the results in 3-5 business days & will call us. I think if I understand correctly that this will confirm if the inflammation in his colon is from allergic colitic or something else. It will also hopefully obviously rule out major problems.
So, basically Ped GI says to just keep doing what we’re doing. We have a follow-up appt w/ him in 4-6 wks (I need to call & make the appt).
Evan no longer has stinky gas. His diapers alternate b/w yellow & green and actually smell like a breastmilk diaper (finally). I will probably start adding things back into my diet in the next couple days.
We are still going back & forth trying to make a decision w/ his Prevacid. He gets really bad bloating & gas from the CaraCream (from either the corn syrup solids or sodium bicarbonate) so we went back to the capsules w/ pureed pears. He does better w/ this but strains quite a bit to get the pears out (probably just a lot of work for his little system still). Last night we went back to the solutab & gave that to him (so we wouldn’t have to enema out pears-ick) & he slept until 2:45am.. but we worry about him reacting to the lactose (milk) in them b/c of the Milk/Soy Protein Allergy. So…there’s not really an easy answer there. On the other hand, he hasn’t had any Prevacid today & hasn’t cried @ all since being home – so who knows-lol.
Thank you for all the support & prayers. Although we don’t really have any super definitive answers we do know some things we didn’t know.
July 31, 2008 at 8:14 pm #54854AnonymousInactiveat least things are moving in the right direction….:-) The biopsy’s should show you if the imflamation is from colitis or something else….so that will be good. As for the solutabs, I just don’t really know what to tell you there. Brianna had milk/soy allergy I think, but did fine with the solutabs…McKenzie couldn’t handle them, but I think you will see pretty quickly if he can’t handle them. And as for a milk/soy free diet…it will seem like a BREEZE! compared to what you have been through for the past month. Yeah for moving in the right direction!!!!
Oh one more thing…I have known MANY mom’s who didn’t have to give meds anymore once the food thing had cleared out…maybe that will happen with Evan!
July 31, 2008 at 8:25 pm #54855AnonymousInactiveErin,
that is such great news!!! I am so happy that you are finally getting somewhere. I will say about the solutabs and the lactose. Lactose is milk sugar not milk protein so he may do fine on them. If he doesn’t I would think it is more the aspartame that is upsetting him instead of the lactose… but it possible. Keeping my fingers crossed that you get good results from the biopsies.
July 31, 2008 at 9:33 pm #54862AnonymousInactiveOh Erin, great news! I have been thinking about you guys all day today. Keep us posted on the biopsy results.
July 31, 2008 at 11:48 pm #54869AnonymousInactiveGlad to hear everything went as smoothly as possible and that his gut appears to be healing! Thanks for the update!
August 1, 2008 at 9:56 am #54878AnonymousInactiveThanks for the update! I hope you get definite results soon so you can plan your course of treatment!
August 1, 2008 at 4:02 pm #54900AnonymousInactiveGlad everything went ok. Keep us posted.
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