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

How To Explain Celiac To 4yo


Nantzie

Recommended Posts

Nantzie Collaborator

I was just wondering how everybody explained celiac to their child. My daughter just turned four. She only has mild to moderate symptoms; D that doesn't seem to hurt/worry/bother her, mild tummy aches and appetite issues, dark circles under her eyes and some behavior issues that may or may not be related to celiac. In other words, things that are more worrisome for me than her.

I know that she's old enough to understand quite a bit. I am ordering a couple of books for her from Amazon - Eating Gluten-Free with Emily and The gluten-free Kid. They are geared toward kids who are a little older, but I think they'll work. I think they'll also be good in helping me figure out how to explain this to her school.

I was just wondering how everyone else approached this with their kids.

Nancy


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



Celiac.com Sponsor (A8-M):



Daxin Explorer

I think you're on the right track with the books! It can be tricky with kids, explaining things that seem over their head.

I find just being striaght up sometimes helps as well. Kids are sometimes a lot smarter than we give them credit for. :lol: Try just being as direct as possible...she may surprise you. :huh:

Guest nini

I got Danna Korn's book "Kids with Celiac disease" and used her recomendations

chewymom Rookie

My daughter will be four next month and has symptoms just like what you describe! She occasionally complains of tummy aches, has non-painful diarrhea, etc. We tested her using Enterolab, and it came back that she is gluten sesitive/intolerant.

I haven't put her on a gluten-free diet yet, mainly because her symptoms are so mild and bother me more than her! I would love your feedback once you've done this for a bit. I'm dreading pulling some of her favorite foods, not to mention trying to be in control of what others feed her!! :blink:

jayhawkmom Enthusiast

My daughter just turned 5. We bought her Gluten Free with Emily and No More Cupcakes and Tummy Aches.

I've done a lot of explaining, discussing, and doing everything possible to be positive about it. Instead of saying, "NO you can't have that" -- I try to remember to say things like, "Sure, that is yummy - but how about we have this instead, it doesn't have gluten in it."

I keep positive, but continually reinforce the "no gluten."

My daughter's blood tests came back as inconclusive, but we went on to have the endoscopy because of the constant tummy aches and "D." Turns out that she had ulcers in her small intestines, and we never would have known that without the endoscopy. I immediately pulled all gluten from her diet, and she's a million times better now. She's not completely better, but she's growing again...and that's awesome!!

On June 13th - she weighed 30 lbs and was 39" tall. (her 3 year old friend is taller and heavier) And, when she went for a follow up visit the other day, she was 33 lbs and 40.5" tall!!!

Nic Collaborator

I was actually very straight foward with my son. He was diagnosed at 4 years as well. He did have some pretty bad symptoms (constipation mainly). I explained to him that his body is confused and thinks that gluten (I explained that gluten is all of the cookies,cakes, cereals, pasta, and breads that he eats) is poison and that is why he is so sick. He really did understand. Now at 5 I have no problem with him understanding that he cannot eat or touch any food without me or someone designated as a food giver for him says it is ok.

Nicole

TCA Contributor

I told my son that some foods are what makes his tummy hurt and he needs to ask me before he eats something. He knows that here at home everything is safe, but when we're away he needs to ask. He's 3.5 and it works well for us!


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



Celiac.com Sponsor (A8-M):



Luvs to Scrap Apprentice

My son will be 4 in Sept. When he got diagnosed in June we told him that gluten (or wheat, oats, barley and rye) made him sick just like they make Daddy sick. He now will only get to eat foods that are safe for him and Daddy. We only offer him safe things at home obviously but we have been working on him needing to ask before eating something when we are away. I was so proud of him last Sunday when he told the children's worker at my parents church that he couldn't eat the animal cookies. He tells people he can't eat wheat and after reading Danna Korn's book I have been trying to teach him the wheat, oats, barley and rye thing. I think he understands pretty well for his age. It really helped here that he had a parent he could be like. (You are gluten free too aren't you, Nancy?) We totally played that up and Luke loves eating Daddy's special stuff. :) Kendra

Nantzie Collaborator

Thanks everybody for all the great advice. I ordered Kids with Celiac Disease, as well as the other two books. I'll have to play up the "Just Like Mommy" thing. I never mentioned my gluten intolerance to her before because she has always been such a picky eater that I didn't want her to tell me she was brocolli intolerant or something. :lol: I found out from some other parents though that their celiac kids ended up not being picky anymore after going gluten-free. Fingers crossed on that one..

I did talk to my daughter's preschool today. I decided to just go ahead and make gluten-free versions of whatever they're having for lunch/snacks. That way I won't have to worry so much, and they won't have to deal with it either. I'm going to put together some information for them sometime in the next couple weeks and have a meeting with the director and her teachers.

For the record, all they did was write it all down on her information card. They didn't say I needed to bring a doctor's note. They just said they wanted as much information on it as I could provide them with.

Wonder if they'll provide me with my own filing cabinet? <_<:lol:

Nancy

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. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    2. - tiffanygosci posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Aldi Pueblo Lindo Yellow Corn Tortillas

    3. - tiffanygosci replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    4. - trents replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    5. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,979
    • Most Online (within 30 mins)
      7,748

    Susan Upchurch
    Newest Member
    Susan Upchurch
    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

    • Mari
      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
    • tiffanygosci
      Another annoying thing about trying to figure this Celiac life out is reading all of the labels and considering every choice. I shop at Aldi every week and have been for years. I was just officially diagnosed Celiac a couple weeks ago this October after my endoscopy. I've been encouraged by my local Aldi in that they have a lot of gluten free products and clearly labeled foods. I usually buy Milagro corn tortillas because they are cheap and are certified. However, I bought a package of Aldi's Pueblo Lindo Yellow Corn Tortillas without looking too closely (I was assuming they were fine... assuming never gets us anywhere good lol) it doesn't list any wheat products and doesn't say it was processed in a facility with wheat. It has a label that it's lactose free (hello, what?? When has dairy ever been in a tortilla?) Just, ugh. If they can add that label then why can't they just say something is gluten free or not? I did eat some of the tortillas and didn't notice any symptoms but I'm just not sure if it's safe. So I'll probably have to let my family eat them and stick with Milagro. There is way too much uncertainty with this but I guess you just have to stick with the clearly labeled products? I am still learning!
    • tiffanygosci
      Thank you all for sharing your experiences! And I am very thankful for that Thanksgiving article, Scott! I will look into it more as I plan my little dinner to bring with on the Holiday I'm also glad a lot of research has been done for Celiac. There's still a lot to learn and discover. And everyone has different symptoms. For me, I get a bad headache right away after eating gluten. Reoccurring migraines and visual disturbances were actually what got my PCP to order a Celiac Panel. I'm glad he did! I feel like when the inflammation hits my body it targets my head, gut, and lower back. I'm still figuring things out but that's what I've noticed after eating gluten! I have been eating gluten-free for almost two months now and haven't had such severe symptoms. I ate a couple accidents along the way but I'm doing a lot better
    • trents
      @Mari, did you read that second article that Scott linked? It is the most recently date one. "Researchers comparing rates of headaches, including migraines, among celiac patients and a healthy control group showed that celiac subjects experienced higher rates of headaches than control subjects, with the greatest rates of migraines found in celiac women.  Additionally, celiacs had higher rates of migraine than control subjects, especially in women. In fact, four out of five women with celiac disease suffered from migraines, and without aura nearly three-quarters of the time."
    • Mari
      As far as I know and I have made severalonline searches, celiac disease disease has not been recognized as a cause of migraines or any eye problems. What I wrote must have been confusing.
×
×
  • 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.