Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Puking Child... Whats Best Move? Brat?


VydorScope

Recommended Posts

TCA Contributor

Hope he's feeling better soon!


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



VydorScope Proficient

he did not nap very well. Hoping he sleep well tonight. He ketp everything down, but everythign is 1-2 bananas, some popsilces and fakorade. Thats bout all he had. Not had any more puking or ditry diapers at all.

He si a sleep now though

Fiddle-Faddle Community Regular

I hope he's feeling better and that you are getting some sleep! I think it's okay that he has no dirty diapers, but I do hope he has wet diapers--important that he stays hydrated!

VydorScope Proficient

Hoping tommorow goes well cause he has a Cubbies meeting after dinner. Kristi gonna stay home with him from church, I have to go because I am teaching this week, otherwise I would have stayed and sent her so that she could sing in the choir. :huh:

jerseyangel Proficient

Hope he sleeps well tonight :)

NoGluGirl Contributor
Glad to hear the fever is going down and he's feeling better....Its not fun for anyone when the kids get sick...My whole family has a nasty cold right now...ugh!!! :(

Dear Jules,

Sorry to hear you are all suffering! Colds are miserable! I still would take them anyday over the stomach flu! If I could go my entire life without catching a communicable disease, that is what I would pick! Poor little fella, Timmy. I take L. Acidophillus to protect me against bacteria and for viruses, particularly a cold virus or flu virus, I take Sambucol. It is black elderberry extract. It has corn syrup, but if you or your family members are not allergic to it, you could take it. This stuff boosts immunity up to 300 percent! Even if you contract a cold, it will be over in a week, instead of getting that nagging cough afterward and suffering for three weeks like my parents did last time!

Sincerely,

NoGluGirl :lol:

VydorScope Proficient

Son still has liquid stools, though not as bad, not puking any more, but not much of an atteptite, he is eating just not much. He does not show any dyhdartion symptons, but he does have the sniffiles.

Any thoughts? I know I am sick with a cold or somthing, but I think my stools are fine, guess I need get a diaper on to find out :lol:


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



jerseyangel Proficient

Sounds like a virus :(

That's pretty typical--starting out with stomach upset, vomiting and D--then moving into more of a cold. Is he still feverish? The only thing that I'd worry about would be his ears--sometimes Matt (my younger son) would get symptoms like this, and it would turn out to be an ear infection. He was a kid who didn't get the terrible pain, so we had to watch his symptoms carefully.

AndreaB Contributor
I know I am sick with a cold or somthing, but I think my stools are fine, guess I need get a diaper on to find out :lol:

:lol::lol::lol:

Add more food as he can handle and don't worry too much. Keep an eye on him and see if his temp stays down or spikes again.

VydorScope Proficient

Nope no fever. That seemed to have gone away after teh first day or so.

He ahs tubes in his ears so he should be okay on that point.

So basicly let him eat as he wants, and just wait it out? How long you think?

StrongerToday Enthusiast

Yep, keep him hydrated and let him eat what he wants when he wants. He'll be up and raring to go any day now.

AndreaB Contributor

Uuummm, if he wants to eat a candy and junk food diet I wouldn't recommend that. j/k I know he wouldn't do that. Make sure he takes something at every meal. With he eat broth? What has he been eating. Fruit is generally easy on the stomach as well as broth. Does his tummy hurt at all or just the general malaise and he doens't have much of an appetite. Whenever my kids go through this the really depressed appetite usually doesn't last more than two days and then they'll start picking up a bit. Put different foods in front of him and let him eat the quantity his stomach is asking for. If the really depressed appetite continues for a coupld more days you may want to consider taking him in. On the other hand, if he doesn't spike a fever again you may want to wait a little bit longer. Contact your ped/doc to see how many days they would want him to go before being seen.

Try to add more foods to create a variety, depending on his stomach. Broth with some meat and veggies, fruit, smoothies, applesauce (I know that's a fruit :P ).

jerseyangel Proficient
Nope no fever. That seemed to have gone away after teh first day or so.

He ahs tubes in his ears so he should be okay on that point.

So basicly let him eat as he wants, and just wait it out? How long you think?

Yea--that's about all you can do at this point. Go with his appetite, make sure he gets his liquids and this thing should run it's course pretty soon. :)

Fiddle-Faddle Community Regular

Cereal is usually a good bet at this point: Dora cereal, or gluten-free rice krispies. I can't remember--can he handle casein? If he can. skim milke might be easier on him than the high-fat stuff. If not, Vance's Dari-Free or gluten-free rice milk would probably be easier on the tummy than soy.

key Contributor

Tubes can get plugged. My son has tubes and he has an ear infection right now. This is only his second one in a year with tubes. He didn't puke this time, but he has in the past several times. If he is fussy, he could still have one. I am sure you would probably know, but just wanted you to know that they can still get plugged off.

Monica

VydorScope Proficient

Well he slept pretty good last night, fell alseep prbly an hour early so I think thats a good sign. Stools still not quite normal this am. About on avg how long do these things take to run thier course? Week? Month? Year? Century? :huh:

jerseyangel Proficient

Hi Vincent,

I was wondering how the little guy was doing.

My kids, if I remember correctly, usually felt a lot better in a week or so. Maybe not completely back to normal, but significantly better.

Not to be a pest, but if it gets toward a week, and he's still not doing much better, it might be a good idea to just have his ears looked at--better safe than sorry. Then, if it's just a stubborn virus, you'll rest peacefully. :)

Girl Ninja Newbie

I'd say that depends on each kid. My little brother stayed sick for 5 days or more when something knocked him down. My son is almost always better in 3 days no matter what he's dealing with.

Fiddle-Faddle Community Regular

I agree with GirlNinja--my kids are usually better in 12-24 hours, but every now and then, there'll be a particular vicious virus that knock'em flat for 3-5 days.

I don't know anything about ear tubes, but I did read in the paper yesterday that the medical community is FINALLY realizing that recurrent ear infections are not usually bacterial and don't usually need antibiotics. Apparently they had to do a big study before they would believe it.

The daughter of one of my friends had recurrent ear infections that my friend was finally able to trace to--no, not gluten, but CASEIN. The only other symptom she had was dark circle under the eyes, which her doctor said was a tip-off that a food allergy or intolerance might be going on.

Anyway, I'd push the broth if he'll drink it, with rice noodles in it if that will help, and maybe something like roast chicken? High protein and iron! If he doesn't have a problem with soy, stir-fried tofu with rice is easy to digest. Will he eat grilled salmon? Salmon is VERY easy to digest, and high in those Omega 3's and 6's.

Keep us posted! Hope he feels better. Hope you don't get it. Hope you are getting some sleep!

VydorScope Proficient

As for the tubes... we did try antibotics first, and they had no effect at all.. he almost lost his hearing, permenantly. The tubs saved him from that, bearly in time. I know they can get clog, and we have them check ever time we are in a doc's office and so fat so good... last check what his 3 year check up, in mid August.

Fiddle-Faddle Community Regular

Sorry, Vincent, I didn't mean to imply that medical intervention is never necessary! When it is necessary, we are lucky to have it!

I have another friend whose daughter is deaf in one ear. They have no idea what caused it or when it happened. . It wasn't picked up until she was in second grade.

I'm glad your little guy's hearing is okay!

Archived

This topic is now archived and is closed to further replies.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Jordan Carlson posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      Fruits & Veggies

    2. - wellthatsfun posted a topic in Gluten-Free Recipes & Cooking Tips
      0

      heaps of hope!

    3. - knitty kitty replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      6

      Help understand results

    4. - knitty kitty replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      10

      Insomnia help

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,994
    • Most Online (within 30 mins)
      7,748

    KimberlyS
    Newest Member
    KimberlyS
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Jordan Carlson
      Hello everyone! Been a while since I posted. The past few moths have been the best by for recovery for myself. I have been the least bloated I have ever been, my constant throat clearing is almost gone, I have stopped almost all medication I was prevously taking (was taking vyvanse for adhd, pristiq for anxiety,fomotadine/blexten for histamine blockers and singulair). Only thing I take now is Tecta. I also no longer get any rashes after eating. Things are going very well. Most success came actually once I upped my B12 daily dose to 5,000 mcg. I do have one thing I am un able to figure out and want to see if anyone else has this issue or has experience working around it. Ever since I was born I have always had a issue getting fruits and veggies down. No matter how hard I tried, it would always result in gagging or throwing up. Always just thought I was a picky eater. Now that my stomach and system has healed enough that I can feel when something is off almost istantly, I notice that after eating most fruits (sometimes I am ok with bananas) and veggies, my stomach instantly starts burning and my heart starts to pound and I get really anxious as if my body doesnt know what to do with what just enetered it. So I am thinking now that this is what probably was going on when I was born and my body started rejecting it before which caused this weird sensory issue with it causing the gagging. Hoping someone has some exprience with this as well because I would love to be able to enjoy a nice fruit smoothie once in a while haha. Thanks everyone!
    • wellthatsfun
      i know i've been rather cynical and sad about being fully diagnosed in june 2025, but my boyfriend has been consistently showing me the wonderful world that is gluten free cooking and baking. in the past couple of days he's made me a gluten free rice paper-wrapped spanakopita "pastry", plus a wonderful mac and cheese bechamel-ish sauce with gluten free pasta (san remo brand if you're in australia/if you can get your hands on it wherever you are).  those meals are notably gluten free, but mainly he's been making me easy gluten free meals - chili mince with white rice and sour cream, chicken soup with homemade stock from the chicken remains, and roast chickens with rice flour gravy and roast veggies. i'm a bit too thankful and grateful lol. how lucky could i possibly be? and, of course, for those who don't have someone to cook for them, it's quite easy to learn to cook for yourself. i've been making a lot of meals for us too. honestly, cooking is pretty darn fun! knowing basic knife skills and sanitary practices are all you really need. experimenting with spices will help you get on track to creating some really flavourful and yummy dishes. coeliac is a pain, but you can use it to your advantage. healthier eating and having fun in the kitchen are major upsides. much luck to all of you! let's be healthy!
    • knitty kitty
      That test is saying that your daughter is not making normal amounts of any IGA antibodies.  She's not making normal amounts of antibodies against gliadin, not against bacteria, not against viruses.  She is deficient in total IGA, so the test for antigliadin antibodies is not valid.  The test was a failure.  The test only works if all different kinds of antibodies were being made.  Your daughter is not making all different kinds of antibodies, so the test results are moot.  Your daughter should have the DGP IgG and TTG IgG tests done.   The tests should be performed while she is still consuming gluten.  Stopping and restarting a gluten containing diet can make her more sick, just like you refuse to eat gluten for testing.  Call the doctor's office, request both the IGG tests. Request to be put on the cancellation list for an appointment sooner.  Ask for genetic testing.   Celiac disease is passed on from parents to children.  You and all seven children should be tested for genes for Celiac disease.  Your parents, your siblings and their children should be tested as well.  Eating gluten is not required for genetic testing because your genes don't change.  Genetic testing is not a diagnosis of Celiac disease.  Just having the genes means there is the potential of developing Celiac disease if the Celiac genes are activated.  Genetic testing helps us decide if the Celiac genes are activated when coupled with physical symptoms, antibody testing, and biopsy examination. It's frustrating when doctors get it wrong and we suffer for it.  Hang in there.  You're a good mom for pursuing this!  
    • knitty kitty
      @hjayne19, So glad you found the information helpful.  I know how difficult my struggle with anxiety has been.  I've been finding things that helped me and sharing that with others makes my journey worthwhile. I like Life Extension Bioactive Complete B Complex.  It contains the easily activated forms of B vitamins needed by people with the MTHFR genetic variation often found with Celiac disease.   Avoid B Complex vitamins if they contain Thiamine Mononitrate if possible.  (Read the ingredients listing.)  Thiamine Mononitrate is the "shelf-stable" form of B 1 that the body can't utilize.  B vitamins breakdown when exposed to heat and light, and over time.  So "shelf-stable" forms won't breakdown sitting on a shelf in a bright store waiting to be bought.  (It's also very cheap.)  Thiamine Mononitrate is so shelf-stable that the body only absorbs about thirty percent of it, and less than that is utilized.  It takes thiamine already in the body to turn Thiamine Mononitrate into an active form.   I take MegaBenfotiamine by Life Extension.  Benfotiamine has been shown to promote intestinal healing, neuropathy, brain function, glycemic control, and athletic performance.   I take TTFD-B1 Max by Maxlife Naturals, Ecological Formulas Allthiamine (TTFD), or Thiamax by EO Nutrition.  Thiamine Tetrahydrofurfuryl Disulfide (TTFD for short) gets into the brain and makes a huge difference with the anxiety and getting the brain off the hamster wheel.  Especially when taken with Magnesium Threonate.   Any form of Thiamine needs Magnesium to make life sustaining enzymes and energy.  I like NeuroMag by Life Extension.  It contains Magnesium Threonate, a form of magnesium that easily crosses the blood brain barrier.  My brain felt like it gave a huge sigh of relief and relaxed when I started taking this and still makes a difference daily.   Other brands of supplements i like are Now Foods, Amazing Formulas, Doctor's Best, Nature's Way, Best Naturals, Thorne, EO Nutrition. Naturewise.  But I do read the ingredients labels all the time just to be sure they are gluten and dairy free. Glad to help with further questions.  
    • trents
      Welcome to the celiac.com community @pothosqueen!   Can you be more specific about which IGA test was run that resulted in 114 score and said to be "normal" and could you please include the reference range for what would be normal? By the size of that number it looks like it may have been what we call "total IGA" but that test is not usually run without also running a TTG-IGA. Total IGA tests for IGA deficiency. If someone is IGA deficient, then the celiac-specific IGA tests like the TTG-IGA will be inaccurate. Was this the only IGA test that was run? To answer, your question, yes, a positive biopsy is normally definitive for celiac disease but there are some other medical conditions, some medications and even some food proteins in rare cases that can cause positive biopsies. But it is pretty unlikely that it is due to anything other than celiac disease.
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.