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

Food Phobias?


OBXMom

Recommended Posts

OBXMom Explorer

Are any of your children desperately afraid of trying new foods? Before he was diagnosed with celiac disease, we thought my 8 year old son was just the world's pickiest eater, but now we understand that he was in great pain all the time, and that his fears are the result of that pain. However, I am concerned now that his fears are so deeply entrenched that they may never go away. I would love to hear about other celiac children with similar fears, and any successful or unsuccessful attempts to deal with these fears.


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



Celiac.com Sponsor (A8-M):



gfgypsyqueen Enthusiast

I have an extrememly picky almost 8 yr old who was diagnosed with severe peanut and tree nut allergies at age 2. She is smart. She tells teachers, family, friends etc that she can't eat (blank) because it contains nuts. They assume she is correct, so she gets out of eating that food. In reality she just doesn't like whatever they were serving (mayo, potato, most meats, and the list goes on and on.) It took a solid 5 yrs to see a change in her attitude toward trying new foods. Now she gets an adventursome day and she will try a couple of new foods. But mostly, she sticks to the foods she knows and likes. Even when she does try a new food, most times she makes a horrible face and says it is awful for the first few times she eats it. Her best incentive for trying new foods is her bottomless pit of a little sister. Must keep up with the younger sister :P

I have Celiacs and so does the younger child. I can say, I would prefer a picky eater when it comes to food allergies and Celiacs. The younger child will try anything - food or not. UGH! Everything gets tasted!!!

I can tell you what didn't work for us easier than I can tell you what did work. (That's a smaller list)We talk about food, nutrition, and what food groups are required for a healthy meal. (She doesn't always eat it, but we talk about it.) :blink:

  • Make sure the child has comfort foods to eat when he has been glutened. Don't bother trying to get him to eat something new then.
    Do not try to force him to eat. My kids just dig in their heals and refuse.
    Get him involved in the cooking and purchasing of foods. (What he thinks is good will be different than what you think.)
    Make sure school lunch is cool and the safe snack box at school is full of stuff the other kids will really want and beg for.
    Offer tastes of everything.
    Insist that at least one bite of everything on the plate is tasted in order to get dessert. (That only worked in the last year for us)
    Once he heals a bit, insist that there is no food and little drink at least two hours before dinner.

Good luck with your picky eater. It has been a long battle for us. But we are finally starting to see the light at the end of the tunnel!!!

BTW, my own opinion is that some kids are sensitive to their bodies without knowing it and may have foods that they do not like because they make them feel bad or funny. For both of mine, we found additional food allergies/sensitivites through this.

dandelionmom Enthusiast

The first poster has some great advice! I just wanted to say that you're not alone struggling with this. We're just focussing on getting healthy, safe foods into her and we're hoping she'll outgrow the pickiness. She has to some extent already and has added to her list of okay foods.

We're just trying to stay patient and not put food stress on her because us pushing or stressing about food seems to make her worse. I keep telling myself that she'll try new things when she's ready.

NewGFMom Contributor

My son digs in his heels and will not try anything new most of the time. But he is very slowly adding things into his diet. He helps me cook all the time and has NO interest whatsoever in trying anything that we make. :D

But sometimes he surprises me with what he'll try.

However, his picky eating is really a blessing in a lot of ways. He never wants to eat what the other kids are eating. He's very happy to stick to his very short list of foods.

But as he heals, he adds about one new food every month or two. It just takes a really long time. The nutritionist we saw, wasn't too concerned with the nutritional issues with his diet. It's just kind of inconvenient when we travel.

Just want to let you know you're not alone. A lot of celiac kids don't like to eat a variety of foods. But in a lot of ways, that makes managing it a bit easier.

OBXMom Explorer

Thank you all for the suggestions and for the encouragement. I had not really considered that it is truly a blessing that my son is not tempted to try things that will hurt him. It is a very good thing to keep in mind.

Hoping all of our little ones someday enjoy a wide range of healthy foods-

Jane

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,806
    • Most Online (within 30 mins)
      7,748

    MoonBear
    Newest Member
    MoonBear
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      This article, and the comments below it, may be helpful:    
    • nanny marley
      Oh yes I can understand the tiredness after going threw all that, must be exhausting especially on the mind I have high aniexty so I can understand that , I wish there more easier ways for people to get help , I had a MRI on my spine some years ago without anything it was really quick and no prep , I understand the need for  them to see better with the bowel ,but you think they would use something a little less traumatic  for ibd sufferers on the bowels by now ,I hope your feeling better today 🙏
    • Colleen H
      I wonder if tingling burning feet are part of it.. I'm not sure if it's the med reaction that people with gluten intolerance get or the food we ate  It's frustrating because a person who did not want to admit to himself I had this condition wanted me to eat this chicken sandwich and now I'm stuck with a variety of symptoms plus now I'm hungry on top of it..  I'm new to this so I forget that "one bite" of the wrong thing can hurt us.😔. Do we stop eating if someone exposed us to gluten ??  My stomach is rumbling but my joints hurt ...  It's weird because I can feel the anxiety coming on.  I get joint problems ,  I don't know if anyone ever got hot flashes?? I suppose if it affects people head to toes you can get that too.   It's weird...hard to decipher what is what.   Also how long do I have to deal with this attack??  Makes me feel like not getting up out of bed.  I get too many symptoms which  horrible.  Thank you for your response..  
    • wellthatsfun
      as my last post stated, i was diagnosed via endoscopy on the 14th of june. i have been eating amazing home cooked meals, luckily, mainly cooked by my boyfriend who is extremely careful about contamination (and is an incredible cook at that). however, i find myself in a mental rut still. being 18, this is the time in my life where i should be exploring things, going out, having fun. yet every corner i turn i'm tortured by the amazing smell of something i can't have anymore. the wonderful sight of such yummy foods. it's near torture. if my boyfriend and his friend who lives with us buy something i can't have, they'll usually eat it outside of the house or the car or wherever we are - which is greatly appreciated - but even seeing a burger or chips or a sausage roll in their hands guts me almost beyond repair. i just wanna have it again too. i miss it. i feel left out and it makes me very sad all the time. it's not their fault. they are allowed to eat whatever they want to, whatever their intestines will allow. it just stings, bad. and i feel so ungrateful given i basically have a private chef who is doubly the love of my life. but it's just so hard. i know i'll adapt. i haven't given up hope.i just wanted to vent. thank you for reading
    • RDLiberty
      Thank you. I must have misinterpreted a study or something. Thank you for the clarification. Much appreciated. Almost three years into my celiac diagnosis and I'm still learning new things. 
×
×
  • 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.