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

Newly Diagnosed 16 Mo Old


mcarbone

Recommended Posts

mcarbone Rookie

Hi parents out there. My daughter was diagnosed with Celiac a couple of months ago. I am having a hard time trying to figure out if i make my 4 year old go gluten free or not. Up to this point i have not completely. Not sure what to do when he wants something that is not gluten free that i dont have the same thing that is gluten free for my daughter. Just wondering how others deal with this situations.


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



Celiac.com Sponsor (A8-M):



gfgypsyqueen Enthusiast

I don't think I follow the norm on this topic, but I'll tell you I do with my kids. Five food allergies spread between the three of us. There is just no possible way that I can justify making perfectly safe meals and snacks everyday that 100% safe for all of us. Just too hard and in my opinion, it sets a bad example. Maybe not bad, but definately a difficult mindset. What do you do when they go to school? Not everyone in the class will be eating gluten-free snacks just because of one child.

So to me, if you do not have Celiacs, you do not need to be on this diet. They can eat gluten-free at home and gluten when they go out and that will not cause any harm. And, my kids get similar, but NOT the same foods. Everybody gets a snack, but one might have Oreos and the other might have a gluten-free/CF donut. Everybody eats a hot dog for lunch, some have bread and some do not.

Oldest child developed nut allergy at 2. It is anaphylactic (big believer in MedicAlert bracelets from young ages). She is not a celiac. But turns out dairy was causing her significant problems. We found that out after she continually left yogurt out, which her sister ate and she is allergic to. Third time the baby ate the real yogurt the older child lost the right to have yogurt in the house. Same reason milk left. Shockingly the older child was severly lactose intolerant and we didn't know it. She is much better off without the milk and she does not leave ANY unsafe food around anymore :)

Youngest started having health and growth issues under 1 yr old. At 2, I demanded testing for Celiacs. After many arguements with Dr...eerrrr..it shouldn't be this hard......she was finally made gluten-free and CF and she no longer goes to that DR. She will be three soon. Happy, healthy, and doing good. Within 5 mths of being on the gluten-free/CF diet and being a toddler, she knows she cannot eat all foods and asks if a new food is safe for her. She tells people that offer her food that she needs special food. I love it.

The rules that work for us:

Buy everything possible that everyone can eat.

Lable all boxed foods so the kids can easily pick safe snacks.

No unsafe snacks at low levels that toddlers can reach.

No foods contain nuts in the house.

Some shared equipment with nuts food is allowed if no other options are available. The nut allergy child does not eat these foods.

All baking is gluten-free/CF/nut free.

Almost all dinners are 100% gluten-free/Cf/nut free. Pizza, pasta, and school lunches may or may not be gluten-free.

Strict no sharing of food rule.

Strict no double dipping rule.

Strict no food anywhere except at the table. (Eliminate the house of crumbs issue.)

Actually assigned seats at the table has been helpful. (Crumbs and germs from that child stay with that child. Yes, table are cleaned after each meal)

I've told the kids since they first got the diagnosis that certain foods hurt their tummy. They learn that for some people their bodies just don't like certain foods. Not everybody is a Celiac, not everybody has a nut allergy. But that is just food. They are healthy and so what if they can't eat EXACTLY the same as everyone else. We make safe chocolates that I can't buy for them. They go trick or treating and exchange Valentine candy, but they do not eat it. Safe candy bags are provided and I take out what item they can eat and bring the resat to work. We make and frost cakes and donuts. We make most things they want. As we go grocery shopping they learn to identify harmful foods/hidden foods like nuts. As they got older they learned to read labels. even my 2 yr old runs her finger along the ingredients list and then tells me it is good for her. She can't read!

As I said, I don't think I follow the norm in this mindset, but it works for us and that is key. Take what you can from above and see what works for you and your family.

Best of luck and your kids will figure it out pretty quick. It does get easier.

PS: the best bribery is paying the older child every time he/she is asked to give a food to the younger child that is not safe. As in the older child has to learn to read labels and spot the unsafe foods for the younger child. This happened once accidentally for us and the older child read labels aggressively every since!

zenmama Newbie

we are working on this as well. dd (15 mo) has Celiac and ds (3) only has seasonal allergys. While I dont mind gating gluten-free (I am also a vegetarian), Dh isnt a fan of it so we are woring out the kinks as we speak!

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. - Colleen H replied to Colleen H's topic in Coping with Celiac Disease
      2

      Gluten related ??

    2. - Jmartes71 replied to Jmartes71's topic in Coping with Celiac Disease
      4

      My only proof

    3. - AlwaysLearning replied to Jmartes71's topic in Coping with Celiac Disease
      4

      My only proof

    4. - AlwaysLearning replied to Colleen H's topic in Coping with Celiac Disease
      2

      Gluten related ??


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,076
    • Most Online (within 30 mins)
      7,748

    Deb baker
    Newest Member
    Deb baker
    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

    • Colleen H
      Thank you so much for your response  Yes it seems as though things get very painful as time goes on.  I'm not eating gluten as far as I know.  However, I'm not sure of cross contamination.  My system seems to weaken to hidden spices and other possibilities. ???  if cross contamination is possible...I am in a super sensitive mode of celiac disease.. Neuropathy from head to toes
    • Jmartes71
      EXACTLY! I was asked yesterday on my LAST video call with Standford and I stated exactly yes absolutely this is why I need the name! One, get proper care, two, not get worse.Im falling apart, stressed out, in pain and just opened email from Stanford stating I was rude ect.I want that video reviewed by higher ups and see if that women still has a job or not.Im saying this because I've been medically screwed and asking for help because bills don't pay itself. This could be malpratice siit but im not good at finding lawyers
    • AlwaysLearning
      We feel your pain. It took me 20+ years of regularly going to doctors desperate for answers only to be told there was nothing wrong with me … when I was 20 pounds underweight, suffering from severe nutritional deficiencies, and in a great deal of pain. I had to figure it out for myself. If you're in the U.S., not having an official diagnosis does mean you can't claim a tax deduction for the extra expense of gluten-free foods. But it can also be a good thing. Pre-existing conditions might be a reason why a health insurance company might reject your application or charge you more money. No official diagnosis means you don't have a pre-existing condition. I really hope you don't live in the U.S. and don't have these challenges. Do you need an official diagnosis for a specific reason? Else, I wouldn't worry about it. As long as you're diligent in remaining gluten free, your body should be healing as much as possible so there isn't much else you could do anyway. And there are plenty of us out here who never got that official diagnosis because we couldn't eat enough gluten to get tested. Now that the IL-2 test is available, I suppose I could take it, but I don't feel the need. Someone else not believing me really isn't my problem as long as I can stay in control of my own food.
    • AlwaysLearning
      If you're just starting out in being gluten free, I would expect it to take months before you learned enough about hidden sources of gluten before you stopped making major mistakes. Ice cream? Not safe unless they say it is gluten free. Spaghetti sauce? Not safe unless is says gluten-free. Natural ingredients? Who knows what's in there. You pretty much need to cook with whole ingredients yourself to avoid it completely. Most gluten-free products should be safe, but while you're in the hypersensitive phase right after going gluten free, you may notice that when something like a microwave meal seems to not be gluten-free … then you find out that it is produced in a shared facility where it can become contaminated. My reactions were much-more severe after going gluten free. The analogy that I use is that you had a whole army of soldiers waiting for some gluten to attack, and now that you took away their target, when the stragglers from the gluten army accidentally wander onto the battlefield, you still have your entire army going out and attacking them. Expect it to take two years before all of the training facilities that were producing your soldiers have fallen into disrepair and are no longer producing soldiers. But that is two years after you stop accidentally glutening yourself. Every time you do eat gluten, another training facility can be built and more soldiers will be waiting to attack. Good luck figuring things out.   
    • Russ H
      This treatment looks promising. Its aim is to provoke immune tolerance of gluten, possibly curing the disease. It passed the phase 2 trial with flying colours, and I came across a post on Reddit by one of the study volunteers. Apparently, the results were good enough that the company is applying for fast track approval.  Anokion Announces Positive Symptom Data from its Phase 2 Trial Evaluating KAN-101 for the Treatment of Celiac Disease https://www.reddit.com/r/Celiac/comments/1krx2wh/kan_101_trial_put_on_hold/
×
×
  • 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.