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

Celiac Children And Bad Behavior?


debbie-doodles

Recommended Posts

debbie-doodles Contributor

Okay, so just 4 weeks ago my daughter's GI doctor took her off of her generic prilosec (she has reflux disease too) to see if she has outgrown the problem. My daughter got sick and wouldn't sleep, wouldn't eat, started throwing up and having diahrea and acting really cranky and bad. She seems really tired, but won't take naps or sleep at night. So I told the doctor and he told me to put her back on the prilosec. I did. Long story short, its been 2 weeks back on the meds and she is still acting really horribly. She seemed to get better for a day or two, but now its awful. She is not throwing up or having diahrea, but her behavior is terrible. This is not my little . :( I found out that she may have gotten some goldfish crackers from my sister on accident. Does anyone else notice that their children act out and throw tantrums and do things like pinch and bite and hit when they are glutened? My daughter has acted so good and sweet since she started the gluten-free diet back in April. And now this. Its been a month already and I feel like I'm gonna pull my hair out. Any ideas on how to deal with it? How long does it last??


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



Celiac.com Sponsor (A8-M):



Guest nini

actually one of my daughter's most noticeable symptoms prior to going gluten-free, was terrible behavior problems. Kicking biting screaming hitting thrashing about on the floor, etc... she couldn't help it... after taking her off gluten the behavioral issues disappeared. I think that if she got accidentally glutened I would probably see the same kind of behavior resurface.

Carriefaith Enthusiast

Gluten seems to really affect the brain. When I am glutened, I get brain fog, irritability, anxiety, mild insomnia, and nervousness. Those goldfish crackers may have been the source of the problem. The best thing to do is to make sure that she doesn't get anymore gluten. The longer she is off the gluten, the better she should get.

e&j0304 Enthusiast

My daughter definitely has behavioral problems when she has gluten. In fact, we were sent to a psychologist and then refered to a psychiatrist for her "behavioral problem" before we discovered her gluten sensitivity.

Since she has been off gluten she is so much better. However, she has had a coupld of accidents and her behaviors come right back. She is moody, cries, is clingy, and says she needs to eat constanty (which is how she was before). Her dr. and I think that her little tummy hurts and she interprets that as hunger.

I actually think she may have gotten some gluten today at her little Halloween party at school because this evening she has been awful and did actually say her tummy hurt. We'll see how tomorrow goes.

Good luck with your little one and I think you're right to assume it may be the gluten causing her behaviors.

taweavmo3 Enthusiast

Oh, that is a big fat YES for us!!!!! Emmie had a gluten accident 3 weeks ago, after being totally accident free for 3+months. Well, gluten had totally transformed my sweet baby girl into a different child. I would not have been surprised if her head had spun around.....she was throwing some hell raising temper tantrums. I had to call my mom to come over and watch the kids for a few hours, b/c I really needed a break from the screaming. Em would scream over every little thing, she was throwing things, biting, pulling her hair, hitting the wall, etc. She was like this pre-diagnosis, but not as bad. It was after this episode that I made our entire house gluten free, I wanted the stuff out of our home!

For us, the physical reaction lasts about a week (vomiting, fever), then the behavior starts up the following week. So, a two week period seems to be our recovery time. I have no idea how to deal with it....I usually just let it run it's course, but I still have consequences for her if she hits one of her brothers or me. Everything else, I generally let slide until she feels better.

Kasey'sMom Enthusiast

This is soooo great to help remind us that we're not the only ones who deal with this. My dd and I have the temperment changes as well. Things are tough around our house when we've both been glutened. :blink:

I remember when my dd first started having problems. Before celiac disease she was easy going and enjoyed simple things. Her tempermant can change within minutes. Our reactions last several days but it seems like after the first couple days she is able to control her emotions a little better. When our dd is gluten-free we have the a different child. Our house went gluten-free as well. I tend to let my OCD take over and I find it's one less thing for me to worry about..... atleast at home. :)

She got glutened at story time this week. She got a treat bag from another student. The bag had both gluten-free and regular candy in it. She didn't eat the candy but she played with the gluten-free candy and drank from a straw that was in the bag. I could tell within less than an hour she had gotten into something. Then the temper flared...........

Sometimes I just want to hibernate in our little gluten-free bubble at home. :rolleyes:

Indea88 Newbie

I have a new toddler since the diagnosis of Celiac and being gluten-free. I was being told he was autistic, spinning, screaming, biting, limited eye contact. My sons behavior now is nothng short of remarkable. There is a gut-brain connection.


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



Celiac.com Sponsor (A8-M):



tpineo Rookie

Yes, my daughter is a different kid. With gluten she is lethargic, irritable, very short fuse, whiny, and only wants to lie on the couch and watch tv. Without gluten, she is energetic, wants to play outside, has a longer fuse (for a 4 year old), and is just plain a happy kid. Tania

snoopylian Apprentice

There is a connection - a Dr. Jekle Mr. Hyde connection with my son. Malabsorbtion of nutrients = all kinds of problems, including behavioral. The behavioral problems use to go away about two weeks after the accidental glutenization until recently. I have a great book - Superimmunity for kids by Leo Galland, MD, starting on p 83 talks about behavioral problems and supplements. I found that due to the malabsorbtion my son had and his dairy free diet he was deficient in calcium. I give him liquid calcium magnesium citrate by bluebonnet. In the book the dr. also talks about probiotics. Probiotics (acidophilus is a common probiotic) help maintain a healthy intestinal track.

I use to take prilosec twice a day but after going on probiotics I no longer need prilosec. You can do some research on probiotics on the internet. I highly recommend it.

kimber Enthusiast

Hi

I think it may be the gluten as well as the reflux meds

My toddler (just turned 2) has had reflux since birth..we recently took him off meds and he did great for a week then drastically went down hill

From what I've been told after being off a PPi for 2 weeks, it can take at least 2 weeks to kick back in...then even more time to heal any damage that has been done

Hope your little one feels better soon, Kim

gf4life Enthusiast
actually one of my daughter's most noticeable symptoms prior to going gluten-free, was terrible behavior problems. Kicking biting screaming hitting thrashing about on the floor, etc... she couldn't help it... after taking her off gluten the behavioral issues disappeared. I think that if she got accidentally glutened I would probably see the same kind of behavior resurface.

<{POST_SNAPBACK}>

Nini,

I could have written this post (only substitute son for daughter!). You completely described how my son was when he was on gluten, and the behavior issues do come back when he gets glutened. Thank God that that has only happened a few times since going gluten-free. He is 11 and is remarkable in how well he handles the diet. He keeps himself gluten-free very well and is getting really good at reading his own labels. He HATES feeling the way gluten makes him feel.

God bless,

Mariann

  • 7 years later...
elsiemscharff Newbie

what I would have given to have known about this when my kids, now 28 and 30, were small. My daughter started being gluten-free about a year ago and told me to try it. I was stubborn, but after having severe allergies last spring, tried an elimination diet, starting with wheat.....omg. Bone Pain. Gone. Fuzzy Brain. Gone. Chronic Fatigue. Gone No kidding. Now that I put it together, ( my niece has celiac as do my two sisters), we are feeling great. Now....if i can only convince my son to do the same...

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,857
    • Most Online (within 30 mins)
      7,748

    LowellFrancis
    Newest Member
    LowellFrancis
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
×
×
  • 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.