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

Can Kids Go Nuts When Gluten Removed?


Mia H

Recommended Posts

Mia H Explorer

I have been struggling with my 4 1/2 year olds rashes for over 2 years. I finally found out that I am gluten and casein intolerant so I decided to take her off. She broke out from Kinnikinick (I also have a tapioca problem) so I thought maybe its the tapioca. So since Thursday (only 3 days now) she has been off and she has had tantrum after tantrum and does not care what she loses. (She even missed a friends birthday party yesterday and didn't seem to care!).

If it is withdrawal how long will this last? uuuuuuuuug

Mia


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

Don't know ... I seemed to feel like throwing tantrums when I got off gluten and casein!! :blink: Since it acts like a drug in your system, it sure seems like getting off a drug. Hang in there!

Daxin Explorer

I have read in other threads here, and experienced this myself.

Some of us do go through "withdrawl" syptoms when we went off gluten. This is due to the antibodies to the gliading etc being elevated. When your body is used to being on high alert for so long, it takes a while to reset itself, and can feel/act/appear exactly like withdrawl.

You and your children are not alone.

Mia H Explorer

I haven't had her tested yet, its so expensive to do Enterolab on your own. My husband has enough symptoms that he is going to get a blood test at the Dr next week. If that's negative (cuz he's been off gluten a couple weeks now and low gluten quite a while) we will test him at Enterolab, then next month our first child, then our youngest.

But the rashes are soo bad I can't wait for the test! I wanted to try diet change.

THanks for the replies.

Mia

Nantzie Collaborator

You can order individual tests at Enterolab too. I wasn't able to afford ordering everything all at once either. For me, my symptoms were so strong, and my response to just not eating gluten for a day or two was so dramatic that all I did was the genetic test ($150) just to make sure I was barking up the right tree and even was genetically capable of having it. My kids at the time didn't have symptoms, so I did genetic tests for them; my daughter a month later, and my son a few months after that. Then my daughter started showing symptoms a couple months ago so I got the gluten sensitivity stool test for her ($99 +$20 for shipping and handling - the stool sample has to be flown back next day air...) . And I just got the stool test kit for my son.

Nancy

mommida Enthusiast

You can find articles here at celiac.com that show gluten and casein have an opiate effect. (That is opium like heroin and) So if this is an individual that has been having this affect you are making them break an addiction. Withdrawal symptoms were very highly connected to children introduced to the gluten-free cf diet as a treatment for autism.

L.

Mia H Explorer

Well I will keep going than with her gluten-free/cf/tapioca & soy free diet and hope she calms down.

The thing about autism is interesting because she has had some interesting symptoms. When she was young I almost thought she has sensory integration disorder, couldn't stand sox, tags bugged her, certain food textures bug her. And she has STRONG reactions to everything like it's the end of the world. I was freaked out, I have never even met a kid like her before. She is a spirited child to say the least.

Anyone have a guess as to how long I should keep her on the diet? a month? I am hoping she will calm down in a week or so. She is harder than usual and that is saying something!

It's hard because everywhere we go people offer kids gold fish and pb & j sandwiches and milk.

Mia


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



Celiac.com Sponsor (A8-M):



eleep Enthusiast

My acute withdrawal symptoms lasted about a month or so. If you're serious about seeing how this works, I'd give it a good 4-5 months. I feel for your child as I had quite a few tantrums myself after going gluten-free -- upsetting, because I thought this was something that would instantly "fix" everything -- I wasn't prepared for the withdrawal and it nearly led me to believe that I was mistaken about the celiac and was actually going off the deep end (that's when I finally shelled out for the Enterolab testing).

Although I have progressively been feeling better, there have been a lot of ups and downs: I think the milder withdrawal effects actually went on for 2-3 months because it took an extra two months of that to finally be sure I had _all_ the sources of gluten eliminated from toiletries, vitamins and stuff like that. I also stalled on eliminating dairy because I didn't test for casein intolerance and I was in denial about how much lactose was still affecting my system.

eleep

Byte Me Apprentice
When she was young I almost thought she has sensory integration disorder, couldn't stand sox, tags bugged her, certain food textures bug her. And she has STRONG reactions to everything like it's the end of the world. I was freaked out, I have never even met a kid like her before. She is a spirited child to say the least.

Hi Mia!

My youngest daughter is VERY much like the way you describe your daughter! She is 12 years old now. She isn't quite as bad about things bugging her now as when she was little, but sometimes she still jumps up all of a sudden, says she can't stand to wear (fill in the blank here, lol) anymore, and changes clothes. Food textures, same thing here also. And talk about dramatic, LOL. That did get better for several years, but once puberty hit, it is back with a vengeance! Any little minor upsetting thing is a tragedy.

I have finally convinced all 3 of my kids, and even my mom :o to go gluten-free; I'll be interested to see if they experience any withdrawal-like symptoms. I'll keep you posted if they do.

Good luck, and I hope things get easier for you and your daughter soon :)

~ Jenn

mommida Enthusiast

I think the earliest you would be able to tell if the gluten-free diet is helping would be four to 5 months.

The best thing to do with kids is carry all the safe treats with you. All these offers of treats (sometimes for a reward for great behaviour) can be traded for the safe ones, and the diet doesn't seem like punishment.

L.

cmzirkelbach Newbie
Well I will keep going than with her gluten-free/cf/tapioca & soy free diet and hope she calms down.

The thing about autism is interesting because she has had some interesting symptoms. When she was young I almost thought she has sensory integration disorder, couldn't stand sox, tags bugged her, certain food textures bug her. And she has STRONG reactions to everything like it's the end of the world. I was freaked out, I have never even met a kid like her before. She is a spirited child to say the least.

Anyone have a guess as to how long I should keep her on the diet? a month? I am hoping she will calm down in a week or so. She is harder than usual and that is saying something!

It's hard because everywhere we go people offer kids gold fish and pb & j sandwiches and milk.

Mia

I just finished reading a book from the child's perspective on starting the gluten-free/CF diet. His name is Luke Jackson and his family started three children on the diet at once. I bought if off amazon .com, but the library may have it. It may be worth a read, to help you stick thru it. I have heard two weeks to several months before the benefits of the diet kick in, and they vary per child.

My son is Aspergers and diabetic, with one positive marker for celiac, (there is a correlation between diabetes and celiac). He is a much calmer child now, with fewer 'end of the world' moments. Homework used to take 1 hour of screaming, and 10 minutes to do it. By the end of last school year, the complaining reduced significantly. In fact, he has a fourth grade project due the first day of school, and he finished the reading portion and the first part of the writing already.

Mia H Explorer
I just finished reading a book from the child's perspective on starting the gluten-free/CF diet. His name is Luke Jackson and his family started three children on the diet at once. I bought if off amazon .com, but the library may have it. It may be worth a read, to help you stick thru it. I have heard two weeks to several months before the benefits of the diet kick in, and they vary per child.

My son is Aspergers and diabetic, with one positive marker for celiac, (there is a correlation between diabetes and celiac). He is a much calmer child now, with fewer 'end of the world' moments. Homework used to take 1 hour of screaming, and 10 minutes to do it. By the end of last school year, the complaining reduced significantly. In fact, he has a fourth grade project due the first day of school, and he finished the reading portion and the first part of the writing already.

What is the book called? That is reasuring news as to how the diet has helped in your family. That is great.

I hope we get similar results.

Mia

cmzirkelbach Newbie

The book is called "A User Guide to the gluten-free/CF Diet for Austism, Asperger Syndrome and ADHD"

The author is Luke Jackson. It is a quick read and pretty frank, with out being overly graphic.

Note: some of his info about gluten-free and celiac are wrong, but he clearly is not writing as an expert on celiac disease, only the changes the gluten-free/CF diet made for him and his brothers as autistics and asperger children.

There are several people in the local SEPTA (Special Ed PTA) group that I attend that also swear by the gluten-free/CF diet.

For some kids, it is very rough in the beginning, because it is like going through withdrawal, but the overall improvements are worth it.

Jodele Apprentice

My oldest dd is having impulse problems and being hyper. She is also crying more. We have gone gluten-free for 3 days now. Is this going to get worse? :blink: First day of school is tomorrow. She is a Straight A student and I hope this does not harm her in learning. :(

Jodele

cmzirkelbach Newbie

Everyone is different, but the general trend is the first days are the hardest. She is going gluten-free because of gluten intolerance/celiac, not autism/ADS?

mamatide Enthusiast
So since Thursday (only 3 days now) she has been off and she has had tantrum after tantrum and does not care what she loses.

If it is withdrawal how long will this last? uuuuuuuuug

Mia

Hi Mia,

Sorry you're going through this... just wanted to share that my DD most defintely got worse than ever in the first week of gluten-free (and if it were me I'd leave the tapioca in her diet until you give gluten-free a little longer) - she was rolling around on the floor wailing in pain from her bloated belly. She was NASTY (and I mean nasty). Very very negative. Angry. She was worse than I'd ever seen her.

And then around 12-14 days, her poop turned dark and normal, and the very next morning she announced to me that the pain was gone. Completely gone. The day after that she started singing in the morning (something she did when she was an infant and that we hadn't even noticed she'd stopped doing -- until she started doing it again). She had a ton of energy (and she'd been energetic when she was on Gluten! She was veritably bouncing off the walls. She was happy and her entire body turned pink (after being so pale we could see all of her veins).

So my words of wisdom - stay the course. It will definitely get worse before it gets better but you need to be absolutely sure that it's all out of her system - fry pans, shampoo, conditioner, YOUR hand cream (which gets into everyone's food when you prepare it)...

Chin up and best wishes.

mamatide.

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. - trents replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      how much gluten do I need to eat before blood tests?

    2. - catnapt posted a topic in Related Issues & Disorders
      0

      anyone here diagnosed with a PARAthyroid disorder? (NOT the thyroid) the calcium controlling glands

    3. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      how much gluten do I need to eat before blood tests?

    4. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      Curious question

    5. - Amy Barnett posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Question

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

    • Total Members
      133,322
    • Most Online (within 30 mins)
      7,748

    avery144
    Newest Member
    avery144
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • trents
      Under the circumstances, your decision to have the testing done on day 14 sounds very reasonable. But I think by now you know for certain that you either have celiac disease or NCGS and either way you absolutely need to eliminate gluten from your diet. I don't think you have to have an official diagnosis of celiac disease to leverage gluten free service in hospitals or institutional care and I'm guessing your physician would be willing to grant you a diagnosis of gluten sensitivity (NCGS) even if your celiac testing comes up negative. Also, you need to be aware that oats (even gluten free oats) is a common cross reactor in the celiac community. Oat protein (avenin) is similar to gluten. You might want to look at some other gluten free hot  breakfast cereal alternatives.
    • SilkieFairy
      After the birth of my daughter nearly 6 years ago, my stools changed. They became thin if they happened to be solid (which was rare) but most of the time it was Bristol #6 (very loose and 6-8x a day). I was on various medications and put it down to that. A few years later I went on this strict "fruit and meat" diet where I just ate meat, fruit, and squash vegetables. I noticed my stools were suddenly formed, if a bit narrow. I knew then that the diarrhea was probably food related not medication related. I tried following the fodmap diet but honestly it was just too complicated, I just lived with pooping 8x a day and wondering how I'd ever get and keep a job once my children were in school.  This past December I got my yearly bloodwork and my triglycerides were high. I looked into Dr. William Davis (wheat belly author) and he recommended going off wheat and other grains. This is the first time in my life I was reading labels to make sure there was no wheat. Within 2 weeks, not only were my stools formed and firm but I was only pooping twice a day, beautiful formed Bristol #4.  Dr. Davis allows some legumes, so I went ahead and added red lentils and beans. Nervous that the diarrhea would come back if I had IBS-D. Not only did it not come back, it just made my stools even bigger and beautiful. Still formed just with a lot more width and bulk. I've also been eating a lot of plant food like tofu, mushrooms, bell peppers, hummus etc which I thought was the cause of my diarrhea before and still, my stools are formed. In January I ran a genetics test because I knew you had to have the genes for celiac. The report came back with  DQ 2.2 plus other markers that I guess are necessary in order for it to be possible to have celiac. Apparently DQ 2.2 is the "rarer" kind but based on my report it's genetically possible for me to have celiac.  I know the next step is to bring gluten back so I can get testing but I am just not wanting to do that. After suffering with diarrhea for years I can't bring myself to do it right now. So that is where I am!   
    • catnapt
      learned I had a high PTH level in 2022 suspected to be due to low vit D  got my vit D level up a bit but still have high PTH   I am 70 yrs old (today in fact) I am looking for someone who also has hyperparathyroidism that might be caused by malabsorption    
    • catnapt
      I am on day 13 of eating gluten  and have decided to have the celiac panel done tomorrow instead of Wed. (and instead of extending it a few more weeks) because I am SO incredibly sick. I have almost no appetite and am not able to consume the required daily intake of calcium to try to keep up with the loss of calcium from the high parathyroid hormone and/or the renal calcium leak.    I have spent the past 15 years working hard to improve my health. I lost 50lbs, got off handfuls of medications, lowered my cholesterol to enviable levels, and in spite of having end stage osteoarthritis in both knees, with a good diet and keeping active I have NO pain in those joints- til now.  Almost all of my joints hurt now I feel like someone has repeatedly punched me all over my torso- even my ribs hurt- I have nausea, gas, bloating, headache, mood swings, irritability, horrid flatulence (afraid to leave the house or be in any enclosed spaces with other people- the smell would knock them off their feet) I was so sure that I wanted a firm diagnosis but now- I'm asking myself is THIS worth it? esp over the past 2 yrs I have been feeling better and better the more I adjusted my diet to exclude highly refined grains and processed foods. I didn't purposely avoid gluten, but it just happened that not eating gluten has made me feel better.   I don't know what I would have to gain by getting a definitive diagnosis. I think possibly the only advantage to a DX would be that I could insist on gluten-free foods in settings where I am unable to have access to foods of my choice (hospital, rehab, nursing home)  and maybe having a medical reason to see a dietician?   please let me know if it's reasonable to just go back to the way I was eating.  Actually I do plan to buy certified gluten-free oats as that is the only grain I consume (and really like) so there will be some minor tweaks I hope and pray that I heal quickly from any possible damage that may have been done from 13 days of eating gluten.    
    • Jmartes71
      So I've been dealing with chasing the name celiac because of my body actively dealing with health issues related to celiac though not eating. Diagnosed in 1994 before foods eliminated from diet. After 25 years with former pcp I googled celiac specialist and she wasn't because of what ive been through. I wanted my results to be sent to my pcp but nothing was sent.I have email copies.I did one zoom call with np with team member from celiac specialist in Nov 2025 and she asked me why I wanted to know why I wanted the celiac diagnosis so bad, I sad I don't, its my life and I need revalidaion because its affecting me.KB stated well it shows you are.I asked then why am I going through all this.I was labeled unruly. Its been a celiac circus and medical has caused anxiety and depression no fault to my own other than being born with bad genetics. How is it legal for medical professionals to gaslight patients that are with an ailment coming for help to be downplayed? KB put in my records that she personally spent 120min with me and I think the zoom call was discussing celiac 80 min ONE ZOOM call.SHE is responsible for not explaining to my pcp about celiac disease am I right?
×
×
  • 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.