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

Am I Harming My Other Kids By Going Gluten Free?


norahsmommy

Recommended Posts

norahsmommy Enthusiast

My youngest is gluten intolerant and I have made the house a pretty much gluten free zone because I kept contaminating her food. My two other girls have been sick almost constantly since I did this. They do get gluten at grandma's house and when we get occasional take out. My oldest is sick right now with either a weird bug or perhaps she has become gluten intolerant too? Tuesday night she wanted some chicken noodle soup for dinner and I had a can in the pantry. I made it for her and about halfway through she said her stomach hurt and didn't want to eat anymore. She went to bed soon after with a bad stomach cramp. Then in the morning she said she didn't feel good and threw up right after breakfast. My mom stopped by and brought her some saltines and 7 up and every single time she ate a cracker she would throw up. She threw up a couple of times at night but I really think it was because her stomach was so empty. This morning I gave her a handful of dry corn chex to snack on when she felt hungry. She kept those down. Then my MIL came over and gave her crackers and she threw up. I had to go to work with dh, and MIL watched the kids and she kept feeding her ritz crackers and dd kept throwing up. I gave her chex and she didn't throw up. So we will see what happens tomorrow. My oldest has had nothing to eat in 2 days except a couple of handfuls of chex and sips of 7 up or pedialite. My middle daughter just got over a bought of lots of diareah and vomiting 2 weeks ago. URG. I feel like my kids are never healthy! Oh and my baby just got over a horrible stint of constipation. She was miserable. I feel like I am somehow messing up my kids! Have I messed them up in some way by going gluten free for the most part?


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



Celiac.com Sponsor (A8-M):



Roda Rising Star

Gluten free isn't going to hurt the other kids. It sounds like maybe they may be gluten intolerent too since you mention your daughter threw up every time she had something with gluten. Something to think about. My kids eat all our meals together gluten free and they have not had any issue. However, my youngest son is officially gluten free tommorow. He had a positive tTg (negative 2 years ago) and I just found out about today. I'm not doing the biopsy for him, since it just seems to add up so he goes completely gluten free since I am diagnosed.

kareng Grand Master

Sounds like your kids might have gluten and, perhaps, other intolerances. My boys are teen & I am the only Celiac in the house. They eat a lot of gluten-free meals and are fine. Of course things like Bbq chicken, potatoes cooked with olive oil, green beans and ice cream are gluten-free.

Skylark Collaborator

A lot of us get more sensitive to gluten once we eat less of it. I wonder if your kids are gluten-intolerant and that's what is happening. Try taking all the girls gluten-free, including at Grandma's, and see if the mystery stomach illnesses don't clear up.

And by the way, you have not "messed up" your kids. People with normal gluten tolerance don't get more sensitive the way we do. They can go on and off wheat at will. Remember, diets used to be seasonal. We went months without certain foods, then ate them when they became available again.

norahsmommy Enthusiast

thanks guys, I just get a little paranoid at times because it seems like they are always sick. My youngest is totally gluten free (unless someone messes up) and she gets horrible constipation and painful bm's and crankiness issues when she gets a little gluten. When she gets alot ( a whole cracker or half a piece of bread) she throws up. She has been having really painful bm's all week and I hate to say I think my MIL fed her something wrong or contaminated. She spent all day 3 days last week at her house when I was taking my mom to visit my dad in the hospital after surgery. I stressed the importance of not contaminating her food but I doubt she took me all that seriously. However I was there today when she had a 20 minute screaming fit in pain trying to poop. So I think she gets it now.

mushroom Proficient

I have always found that the quoted figures of inherited celiac disease in families tend to run incredibly low. I think it highly probably that all your children are gluten intolerant and should be tested. And by the way, either you or your husband (or both) are also gluten intolerant because the gene(s) had to come from somewhere. Do not worry about harming your children by not giving them gluten; worry about harming them by giving them gluten.

Cypressmyst Explorer

It is stories like this that confirm my suspicions that everyone is gluten intolerant. Chances are very good that if Mother and Mother in law go gluten-free they will see improvements in their health too. Same goes for you and your husband.

My condolences on having so many sick kids at once though! Wow! You are not harming them by going gluten-free, you are helping them to not have mega problems later in life.


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

What is going on is by giving your little ones gluten occasionally you are doing gluten challenges. Their reactions are positive. It does sound like they also need to be strictly gluten free. Because they have been gluten light you would need to have them do a full out gluten challenge to have any chance of accurate testing. Even then they have a good chance of a false negative as childrens false negative rates are even higher than adults.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,857
    • Most Online (within 30 mins)
      7,748

    Sonya Haskin
    Newest Member
    Sonya Haskin
    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

    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
×
×
  • 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.