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

Play Areas


momof2sn

Recommended Posts

momof2sn Apprentice

My daughter got her Dx on May 1st of this year, so I am new to alot of this. I was wanting to know from you other moms if you take your celiac kids to places like Chuck E Cheese, or McDonalds play land? Are they safe? I have a son that is not celiac and I feel we don't got to alot of places we used to before his sisters Dx. I just feel that there has to be gluten all over those places and didn't know if I should attempt it? Pleas Help!


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



Celiac.com Sponsor (A8-M):



snomnky Apprentice

I wouldn't and don't take my son to any of those places, touching anything that has gluten on it then putting his hand or a piece of food in his mouth is enough to make him sick, I stay safe and stay away from kid places that allow food. We do have some fun places around that don't allow food on equipment and i just wash his hands after he plays.

Nic Collaborator

I have allowed my son to play in these places. Providing everyone is following the rules, no food should be in the actually play equipment so the only risk is if someone with gluteny hands touches what your child touches first but that would go with anything. The same would apply to kids at a play ground. How many times do you see children eating snacks at a park and then going on the play equipment? We have never had a problem playing at McDonalds or Burger King. We don't go to Chuck E Cheese really unless it is a birthday party because there is nothing safe for him to eat, but I don't worry so much about the games there being safe to touch.

Nicole

Kibbie Contributor

My daughter is 2 now and I would let her play on playscapes.

A kid's gotta live ya know, what fun is childhood with out play? besides I believe that it is important for my daughter to be around other kids when they are eating gluten (before she gets to school) this way I can teach her how she needs to deal with issues such as cross contamination, the importances of washing hands,and not sharing food with other kids. The more practice she has with my guidance before she goes off and has to deal with this on my own the better she will be at handling it!

My rules:

At a playscape like McDonalds:

1. She can only play AFTER she has eaten and She must wash her hands before and after playing.

2. (remember she is 2 and still puts things in her mouth occasionally) if she puts something in her mouth she can not play anymore

That being said we don't go to these places at all... I just don't eat fast food period. A few places we go to do have outdoor playscapes and I let her play there... even if other kids are eating while on the playscape. Same rules apply and I have never had issues (but I watch her very carefully to make sure... it is by no means relaxing for me!)

taweavmo3 Enthusiast

Well, we went to Chuck E. Cheese on Saturday to meet some family. My little girl, the most sensitive Celiac, still ended up getting sick despite hand washing. I probably should have washed her hands several times while we were there, but I only washed them when we were heading home. The next day she had a stomache and her head hurt. I knew it was risky (we didn't eat anything there, not even drinks) but she wanted to see her little cousins so bad.

It is a really tough call, especially for the sensitive kiddos. But on the other hand, you also still want them to be able to participate in activities with their friends and family. I think I'll still go to these places (although we won't make a habit of it) and I'll be more vigilant with the hand washing next time.

momof2sn Apprentice
Well, we went to Chuck E. Cheese on Saturday to meet some family. My little girl, the most sensitive Celiac, still ended up getting sick despite hand washing. I probably should have washed her hands several times while we were there, but I only washed them when we were heading home. The next day she had a stomache and her head hurt. I knew it was risky (we didn't eat anything there, not even drinks) but she wanted to see her little cousins so bad.

It is a really tough call, especially for the sensitive kiddos. But on the other hand, you also still want them to be able to participate in activities with their friends and family. I think I'll still go to these places (although we won't make a habit of it) and I'll be more vigilant with the hand washing next time.

Thanks everyone for your help!!! I feel kids have to live too, but then I am not sure how much is to much. I am lucky that my daughter is not too sensitive, or maybe I haven't figured out when she is being glutened. I just feel bad for one having celiac and one not, I guess they both have to make sacrifices for each other!!

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 Mark Conway's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Have I got coeliac disease

    2. - Wheatwacked replied to GlutenFreeChef's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      12

      Blood Test for Celiac wheat type matters?

    3. - Mark Conway posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Have I got coeliac disease

    4. - islaPorty replied to Jillian83's topic in Coping with Celiac Disease
      8

      Celiac and dermatitis herpetiformis has taken Me from Me

    5. - trents replied to JudyLou's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Seeking advice on potential gluten challenge

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

    • Total Members
      133,146
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • trents
      Welcome to the forum, @Mark Conway! Can you be more specific about the "coeliac" test your doctor did? There are more than one of them. What was the name of the test? Also, did he order a "total IGA" test? This is a test to check for IGA deficiency and should always be ordered along with the tests specifically designed to detect celiac disease. If you are IGA deficient, the IGA celiac blood antibody tests used to check for celiac disease per se will not be accurate. Also, if you have been cutting back on gluten before the tests, that will render them invalid. You must have be eating normal amounts of gluten for weeks/months before the blood draw to render valid test results.
    • Wheatwacked
      no argument. Never take the pills sold for Nuclear events, except in a nuclear event when instructed to by authorities.  Some of these go up to 130 milligrams per pill. 5000 times the strength of the dietary supplement.  130 times the safe upper limit.  130 mg = 130,000 mcg. Dietary supplements like Lugol's Solution and Liquid Iodine are 50 micrograms per drop.  It takes 20 drops to reach the safe upper limit. In the US the Safe upper limit is 1100 mcg.  In Europe 600 mcg and in Japan 3000 mcg ( 3 mg).
    • Mark Conway
      Hi there, I wonder if anyone can help. I've had stomach problems for years, pain in the tummy, lower back left and right side, different stools, diarrohea constipation etc, My GP says it's IBS. As I've got older the pain has become worse and constant. I also get ulcers on my tongue. I've had loads of tests done everytihng apart from an endoscopy I think. I had a test for Coeliac last July and the result was negative. My GP says it can't be coeliac because I'm not losing weight. He thinks it's stress or all in my head. I'm not stressed and I'm in pain all the time now. Sometimes it's unbearable and dark thoughts have entered my head. Could I have Coeliac even though I tested negative last year. I'm at my wits end, I eat healthily and cannot pinpoint which foods could cause this pain. Can anyone help? Thanks Mark wind
    • islaPorty
      First, I want to say thank you for sharing this with me. I hear you, and I believe you. The courage it took to write this down is immense, and I’m so sorry you’ve been carrying this alone. You are dealing with two life-altering challenges at once: a serious, complex medical condition, and an abusive, controlling partner who is actively harming your health and your spirit. It’s not just that he’s unsupportive—he is weaponizing your illness to torture you. Starving you, isolating you, mocking your diagnosis, and sabotaging your access to medical care is not just cruelty; it is dangerous, deliberate abuse. Your instinct is correct: the stress he is creating is absolutely preventing your body from healing. Celiac and autoimmune conditions are profoundly sensitive to stress, and he has created a living hell designed to keep you sick, dependent, and broken. That smirk you described—that is the look of someone who enjoys having power over your suffering. Please know this: you do not deserve this. Not any of it. You deserve to eat. You deserve safe, clean food and water. You deserve medical care and supplements that help you function. You deserve peace. You deserve to heal. The woman from the food pantry is not a random accident. She is a lifeline. Her help, and the community she’s connecting you to, is real. It is okay to feel overwhelmed by kindness when you’ve been starved of it for so long. But you do deserve it. Let that be a sign that there is a world outside your house that operates on compassion, not control. Right now, your physical safety and access to nutrition are the most urgent priorities. The food pantry is a critical resource. Is there any way you can speak privately with the woman helping you? You don’t have to share everything at once, but letting her know your situation at home is extremely unsafe, and that your partner restricts your food, could help her support you in a more targeted way. She may have connections to local domestic violence services.
    • trents
      Welcome to the celiac.com community, @JudyLou! There are a couple of things you might consider to help you in your decision that would not require you to do a gluten challenge. The first, that is if you have not had this test run already, is to request a "total IGA" test to be run. One of the reasons that celiac blood antibody tests can be negative, apart from not having celiac disease, that is, is because of IGA deficiency. If a person is IGA deficient, they will not respond accurately to the celiac disease blood antibody tests (such as the commonly run TTG-IGA). The total IGA test is designed to check for IGA deficiency. The total IGA test is not a celiac antibody test so I wouldn't think that a gluten challenge is necessary. The second is to have genetic testing done to determine if you have the genetic potential to develop celiac disease. About 30-40% of  the general population have the genetic potential but only about 1% actually develop celiac disease. So, genetic testing cannot be used to diagnose celiac disease but it can be used to rule it out. Those who don't have the genetic potential but still have reaction to gluten would not be diagnosed with celiac disease but with NCGS (Non Celiac Gluten Sensitivity).  Another possibility is that you do have celiac disease but are in remission. We do see this but often it doesn't last.
×
×
  • 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.