Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Sleepovers?


rami

Recommended Posts

rami Apprentice

So my newly diagnosed 8-year old would like to spend the night at his friend's house this weekend and I don't know how to feel about it. I hate to deprive him of some of the things I loved the most as a kid but I am terrified about this. I figured I could prepare his dinner and breakfast so there are no concerns but don't want to scare his friend's parents. Any thoughts for those with experience?


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



Celiac.com Sponsor (A8-M):



Mizzo Enthusiast

I would emphasize hand washing , no sharing of foods or anything that goes in the mouth ie: lip gloss, instruments , lollipops .

Provide all the food , and don't stress about it. (although we all did and do still ) LOL

Roda Rising Star

Ditto what Mizzo said. Both my boys spend the night with their friends and I send them their dinner and breakfast. I also send snacks that they can share. They both are pretty good at knowing what they can and can't eat. If offered they are allowed to eat fresh fruits/raw veggies, cheese sticks and known safe yogurts/fruit snacks/candy. I have explained the CC risk and the need to wash the fruits/veggies and hands before they are given to them.

Darn210 Enthusiast

My daughter usually eats supper before she goes. Takes dry cereal (chex) that she can add milk to for breakfast. She takes a snack to share (microwave popcorn and sometimes fruit chew snacks). She knows she can eat prepackaged safe items (string cheese sticks, yogurts, etc) but if your son isn't ready for that yet, tell him to only eat what he brings.

Whenever it is a "new" friend, I tell the parents what my daughter's reaction is (she gets nauseous and if really bad, vomits) so they don't freak out about the possibility of an anaphylaxis type event.

kvanrens1 Explorer

My daughter has a sleep over tonight. I checked with the Mom and they are having pizza and doughnuts (her daughter did not want birthday cake) so I made a gluten free pizza last night and pulled a gluten free doughnut out of the freezer and will send them with my daughter. I will also send lots of snacks and gluten free cereal bar for the morning (they are having monkey bread). Have not tried to make a gluten free version of monkey bread so the cereal bar will have to do :)

My daughter already feels "different" because of her diet. For her, it is important to have the gluten free version of the food they are having. Extra work and planning for me but so worth it for her health and happiness.

MitziG Enthusiast

My kids stay over all the time, they know the drill. They take a cooler full of snacks (I include extra for the other kid) and I usually make something kid friendly that can be microwaved- mac and cheese, pancakes, spaghetti..etc) I send a loaf of bread, some PB&J, gluten-free cereal and a bunch of fruit. Make sure to send the hot food in a micro safe dish so you don't have to worry about cc. Yes, its a pain, but the good friends' mmoms get used to it and understand. They appreciate not having to worry about poisoning my kid, and my kid loves all the gluten-free goodies that I don't usually buy (like expensive gluten-free chicken nuggets or ravioli!)

GwenO Apprentice

My daughter goes on sleepovers. She takes food with her and shares it with her friend No problems so far.


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



Celiac.com Sponsor (A8-M):



Juliebove Rising Star

My daughter usually eats supper before she goes. Takes dry cereal (chex) that she can add milk to for breakfast. She takes a snack to share (microwave popcorn and sometimes fruit chew snacks). She knows she can eat prepackaged safe items (string cheese sticks, yogurts, etc) but if your son isn't ready for that yet, tell him to only eat what he brings.

Whenever it is a "new" friend, I tell the parents what my daughter's reaction is (she gets nauseous and if really bad, vomits) so they don't freak out about the possibility of an anaphylaxis type event.

That is pretty much what we do too. If she does eat dinner there, I usually send something for her. She used to have one friend whose household was not only gluten-free but she and her dad shared many of their food intolerances. That mom and I had no problems with the other person preparing food because we didn't even keep stuff in the house that could be a problem. But other people don't always get it. One person was going to serve taco salads for dinner which would have been fine, but the corn tortilla bowls she was going to serve them in, also had wheat. People who don't have to avoid this stuff don't always get it. In the end, she opted for something else. I can't remember what. But I made the same thing for my daughter and sent it over.

One thing that my daughter has always been careful about is food that would be safe but it shared. She got upset at a party because they put out a lovely vegetable tray but there were also wheaty things that people were eating with their hands. So she couldn't eat the baby carrots and olives that she really wanted.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,803
    • Most Online (within 30 mins)
      7,748

    Nancy Larson-Kichak
    Newest Member
    Nancy Larson-Kichak
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      71.2k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Ann13
      I have the exact same symptoms for a couple of wks now but I've been taking Symbicort for quite awhile at this point. I read you can get yeast infection in the vocal cords so I may ask my Dr. for antifungal meds cos I cant wait for an ENT exam. Also read on this site the connection between Vit D and K2 deficiency and asthma...doesn't apply to me cos mine is from mold in a house years ago but still might try and see if my asthma improves. I am Celiac and gluten causes the same symptoms but it says this inhaler is gluten free and it only started acting up so that option is out. I use Ventolin on occasion but using that for many many years. For me I will see if can switch inhalers to a brand that doesn't affect vocal cords as much, Advair is NOT one of them, plus will try the supplements. Do not suck on menthol lozenges cos menthol dries out cords more...sleeping elevated and sucking on ice chips gets the swelling down...at night this can really help especially. I can't continue like this so will get on everything this coming week.  
    • Rhenriksen
      Did a little more research just now and found out that even though the max methane should not exceed 10. It is normal to be around 3 and not rise. Again, I was at 13 so this does make me a bit suspicious. This was done back in May of 2024. I do recall being put on 14 day Antibiotic called Rifaximin but I'm really not sure if it made a difference, but if it did, then the problems still came back:( 
    • Rhenriksen
      I did a SIBO Test about a year ago, and I barely elevated on the Methane portion (max was 10 and I hit 13). Dr wasn't too concerned.    
    • trents
      Have you looked into SIBO (Small Intestine Bacterial Overgrowth)?  Also, MCAS (Mast Cell Activation Syndrome)/histamine intolerance (they go together like a hand and glove).  Both of the above are common in the celiac community.
    • Rhenriksen
      So tough for me when my symptoms are asymptomatic. Only excessive gas, floating stools and occasional discomfort in my lower right abdomen. These symptoms do not change, regardless of how I eat too:(  I'm sure that next week the GI doctor will discuss my findings and pathology results with me. It's at that time I may push for an MRI or CT scan of the abdomen. I prefer the MRI to avoid unnecessary radiation too. 
×
×
  • Create New...