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

Five Year Old Celiac


Julia's mom

Recommended Posts

Julia's mom Newbie

My 5-year old daughter was diagnosed in September with Celiac. Her IgA came back highly positive and her small intestine which showed evidence of scalloping came back positive as well. My husband has been recently diagnosed as well.

The dilemma is that my daughter who was feeling so much better on her gluten-free diet for a month is now feeling intense abdominal, back and esophageal pain. We have a well scrubbed kitchen with only gluten-free products. She is not eating or drinking any dairy products and has low amounts of citric acid in her diet. We carefully package her snacks and lunch at school, and she has a vigilant teacher watching over her.

But still, she is in a lot of pain. The doctor's office recommended a PPI, for which I am not completely in favor and I have read the recommendations for nettle leaf tea, whole fennel seed, slippery elm, and flax seed. I am also uneasy about giving my child over the counter herbals that might be better suited for adults.

Does anyone have any recommendations? She is a bright girl who has learned how to read labels and take amazing ownership of her disease. Quite frankly she told us that she could not eat wheat for nearly 6 months, but we didn't get it!

Thanks for the help!


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



Celiac.com Sponsor (A8-M):



bear6954 Apprentice

My son is only two but I noticed too much sugar from fruits caused him stomach pain.

ang1e0251 Contributor

Your daughter sounds very astute. Have you asked her what is causing her pain? Maybe she has some idea, like before. If not, it might be a good idea to start a food journal for her. Write down everything that goes in her mouth as well as her symptoms. Maybe the reason will reveal itself. In the meantime, when I am glutened, I back off and go back to very simple basic foods that are gentle to my system. I eat very few processed gluten-free foods as I find I don't digest them that well. It feels like a stone in my gut.

It could be something new bothering her. That has happened to me a couple of times. I know it's so hard on you to see your child suffer. I hope the problem reveals itself to you soon.

dilettantesteph Collaborator

Like I said in the other post, do you know about stickers, playdoh and fingerpaint?

Julia's mom Newbie
Your daughter sounds very astute. Have you asked her what is causing her pain? Maybe she has some idea, like before. If not, it might be a good idea to start a food journal for her. Write down everything that goes in her mouth as well as her symptoms. Maybe the reason will reveal itself. In the meantime, when I am glutened, I back off and go back to very simple basic foods that are gentle to my system. I eat very few processed gluten-free foods as I find I don't digest them that well. It feels like a stone in my gut.

It could be something new bothering her. That has happened to me a couple of times. I know it's so hard on you to see your child suffer. I hope the problem reveals itself to you soon.

Thank you for your advice. In fact she told me the same tonight that gluten-free breads are troubling her. She is in so much pain and her physician said turn to the Internet to help. She just went to bed in horrible pain and crying. She has a large heated lavender pillow to help relieve some of the pain.

We tried slippery elm and pear juice yesterday and probiotics this morning.

We'll just keep trying! I think that we might have another culprit lurking in her foods.

Julia's mom Newbie
Like I said in the other post, do you know about stickers, playdoh and fingerpaint?

Thank you. I know that she is not playing with stickers and playdoh, however I would have to double check on the fingerpaint. I haven't seen any projects come home lately.

I just sent her to bed in pain. She is very cavalier which makes it harder to figure out when she is feeling ill. I am starting to have the impression, however, it is when she eats carbohydrates. During the day she eats carrots, apples, ham or turkey, and maybe a fruit roll-up...all screened to be gluten free. At night I will prepare on occasion a gluten-free pizza on its own sheet, gluten-free pasta, or something of the sort. For the most part I buy organic, gluten-free meats and cut with organic, washed vegetables. Tomorrow we are cutting out the carbs and getting allergy testing.

Thank you for your replies.

ang1e0251 Contributor

Last week I found I could no longer tolerate ham. I don't eat it that often so it took awhile to put that together. I also don't eat lunchmeats often. I believe I'm reacting to the nitrites/tates. There was another thread about those that made me notice. If she's eating those kind of meats frequently, that could be a culprit. I also avoid MSG. I'm not really sure I react to it, but it's just not good.

I eat corn tortillas in place of any bread products. I like it toasted. These sit very well with my system and are versitile.


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



Celiac.com Sponsor (A8-M):



gfpaperdoll Rookie

I would not give her the gluten free grains until all pain is gone, or at least 6 months after going gluten-free. some people cannot tolerate those grains. You can make a peanut butter cookie with sugar, peanut butter (1 cup each) & 1 egg. It is an old standard recipe. There are other recipes with no grains. check out the SCD diet, I think their web site is called pecan bread, sorry not sure. You can google it.

A lot of people do not tolerate tapioca flour. try sorghum flour & coconut flour - but IMO they are all cross contaminated, although I order direct from the mill & use them only occasionally...

try white rice only - get organic if you can & wash it before cooking. Also try the Mission Brand White Corn Tortillas as a sub for bread. You can even make a pizza on them. Cut in 4ths & fry in coconut oil for chips... heat them in a skillet with coconut oil & put PB & Jam & bacon & roll up for a good anytime snack.

also think about getting her checked for H. Pylori & get the doctor to check her appendics. It is common for us to have appendic problems, & gall bladder problems.

Even if she is not having a definite problem with dairy, I would cut out dairy for a minimum of 6 months. & no soy, nobody needs soy.

I hope this is somewhat helpful. & that she is better soon. That stomach pain is the worst there is.

climbmtwhitney Apprentice

Hello.

Another idea.....Have you noticed a pattern with soy or corn? Many of the gluten free/casein free breads contain them. Also, if you're eating pizza, are you using a soy cheese? I, myself a Celiac, am in horrible pain from soy in any amount. (And, I think corn is about to go too.) And, my 10 yr old daughter, also Celiac, gets horrible stomach pain from an overload of soy such as Gluten-free Casein-free pizza made with soy mozzarella.

My doctor told me that once the gluten & casein are out of the diet, often other food intolerances can rear their ugly heads. When your gut is stripped from the gluten (leaky gut), then proteins from other foods can leak through your gut and your body reacts by creating antibodies and causing distress. And, soy and corn happen to be two biggies that bother a lot of people. Also, I agree with the other posters that tapioca flour/starch bothers many too and it's in a lot of Gluten-free Casein-free breads. Also, if your using Kinnikinnick breads, many contain pea protein which happens to bother me as well.

Anyway, I really do hope you figure it out quickly. I know first hand how hard it is to see your little ones suffering. We are awaiting an official soy result on my daughter since she also starting going south after 2 1/2 months of being Gluten-free Casein-free. It's so hard, but hang in there. I bet with a food diary and help from your smart daughter, you'll figure it out soon.

Best,

Sonya

Julia's mom Newbie
Hello.

Another idea.....Have you noticed a pattern with soy or corn? Many of the gluten free/casein free breads contain them. Also, if you're eating pizza, are you using a soy cheese? I, myself a Celiac, am in horrible pain from soy in any amount. (And, I think corn is about to go too.) And, my 10 yr old daughter, also Celiac, gets horrible stomach pain from an overload of soy such as Gluten-free Casein-free pizza made with soy mozzarella.

My doctor told me that once the gluten & casein are out of the diet, often other food intolerances can rear their ugly heads. When your gut is stripped from the gluten (leaky gut), then proteins from other foods can leak through your gut and your body reacts by creating antibodies and causing distress. And, soy and corn happen to be two biggies that bother a lot of people. Also, I agree with the other posters that tapioca flour/starch bothers many too and it's in a lot of Gluten-free Casein-free breads. Also, if your using Kinnikinnick breads, many contain pea protein which happens to bother me as well.

Anyway, I really do hope you figure it out quickly. I know first hand how hard it is to see your little ones suffering. We are awaiting an official soy result on my daughter since she also starting going south after 2 1/2 months of being Gluten-free Casein-free. It's so hard, but hang in there. I bet with a food diary and help from your smart daughter, you'll figure it out soon.

Best,

Sonya

Thank you. This is very helpful information. Yesterday she thrw up her hands and said "I'm done with this!" which scared me a little until she started laughing again. So far laughing is still the best medicine. She feels better and and forgets about her stomach.

Thanks for the explanation about the leaky gut and exposure to other proteins. That makes a lot of sense. Thus far I have noticed reactions to gluten-free cookies and pizza the most. She does well with chicken, rice, bananas, blacks beans, and apples.

This forum's recommendations have been outstanding for us. Julia is always on board with changing her diet around and doesn't feel entitled to anything unless her brother gets something. We are creating a food journal and a tummy chart to understand. We are learning quickly.

Wendy

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Russ H's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      KAN-101 Treatment for Coeliac Disease

    2. - Scott Adams replied to miguel54b's topic in Related Issues & Disorders
      1

      Body dysmorphia experience

    3. - Scott Adams replied to Colleen H's topic in Related Issues & Disorders
      2

      Heat intolerant... Yikes

    4. - Scott Adams replied to Jmartes71's topic in Coping with Celiac Disease
      1

      Related issues

    5. - knitty kitty replied to Sarah Grace's topic in Related Issues & Disorders
      23

      Headaches / Migraines and Hypoglycaemia


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,149
    • Most Online (within 30 mins)
      7,748

    dvyoung
    Newest Member
    dvyoung
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      I agree that KAN-101 looks promising, and hope the fast track is approved. From our article below: "KAN-101 shows promise as an immune tolerance therapy aiming to retrain the immune system, potentially allowing safe gluten exposure in the future, but more clinical data is needed to confirm long-term effects."  
    • Scott Adams
      Thank you so much for having the courage to share this incredibly vivid and personal experience; it's a powerful reminder of how physical ailments can disrupt our fundamental sense of self. What you're describing sounds less like a purely psychological body dysmorphia and more like a distinct neurological event, likely triggered by the immense physical stress and inflammation that uncontrolled celiac disease can inflict on the entire body, including the nervous system. It makes complete sense that the specific sensory input—the pressure points of your elbows on your knees—created a temporary, distorted body map in your brain, and the fact that it ceased once you adopted a gluten-free diet is a crucial detail. Your intuition to document this is absolutely right; it's not "crazy" but rather a significant anecdotal data point that underscores the mysterious and far-reaching ways gluten can affect individuals. Your theory about sensory triggers from the feet for others is also a thoughtful insight, and sharing this story could indeed be validating for others who have had similar, unexplainable sensory disturbances, helping them feel less alone in their journey.
    • Scott Adams
      The most common nutrient deficiencies associated with celiac disease that may lead to testing for the condition include iron, vitamin D, folate (vitamin B9), vitamin B12, calcium, zinc, and magnesium.  Unfortunately many doctors, including my own doctor at the time, don't do extensive follow up testing for a broad range of nutrient deficiencies, nor recommend that those just diagnosed with celiac disease take a broad spectrum vitamin/mineral supplement, which would greatly benefit most, if not all, newly diagnosed celiacs. Because of this it took me decades to overcome a few long-standing issues I had that were associated with gluten ataxia, for example numbness and tingling in my feet, and muscle knots--especially in my shoulders an neck. Only long term extensive supplementation has helped me to resolve these issues.      
    • Scott Adams
      I am so sorry you are going through this; it sounds incredibly overwhelming and disheartening to be dismissed by the very medical professionals you're turning to for help. It is completely understandable that you feel lost and exhausted, not just from the relentless physical symptoms like the leg pain, stomach issues, and profound fatigue, but from the psychological toll of being told it's "just IBS" or that you need a therapist when you know your body is signaling that something is wrong. While it's true that a normal tTG test can indicate that celiac disease itself is being managed from a dietary perspective, it is a major oversight for your doctors to ignore your other diagnoses like SIBO, a hernia, and Barrett's esophagus, all of which can contribute significantly to the symptoms you describe. You are absolutely right to be seeking a new Primary Care Physician who will listen to your full history, take your Barrett's diagnosis seriously, and help you coordinate a care plan that looks at the whole picture, because your experience is not just in your head—it's in your entire body, and you deserve a medical team that acknowledges that. I had hernia surgery (laparoscopic), and it's not a big deal, so hopefully you can have your new doctor give you some guidance on that.
    • knitty kitty
      Some people have difficulty processing tyrosine.  Cut out the nuts and cheese and see if there's any difference.  Everyone is different. This study shows that tyrosine can affect our brain with detrimental effects as we age. Neuro-Cognitive Effects of Acute Tyrosine Administration on Reactive and Proactive Response Inhibition in Healthy Older Adults https://pmc.ncbi.nlm.nih.gov/articles/PMC6084775/ "In conclusion, we show age-related effects of tyrosine administration especially on proactive, not reactive, response inhibition, accompanied by signal changes in dopamine-rich fronto-striatal brain regions. Specifically, we observed that tyrosine’s effect on brain and cognition became detrimental with increasing age, questioning the cognitive enhancing potential of tyrosine in healthy aging."
×
×
  • 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.