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

How Common Is Celiac Without Symptoms?


Chaim9778

Recommended Posts

Chaim9778 Newbie

My daughter is 20 months old, and hasn't really had any symptoms of celiac other than she is small and only weighs 22 pounds. Between 2 doctor's appointments 4 months apart she only gained one pound. She was healthy weight at birth 7lb 6 oz, and height-wise is around 50 percentile, but has always been underweight. She has a first cousin, who is 13, and recently diagnosed with celiac, and a second cousin and his father (her great uncle) also have celiac...so it runs on my husband's side of the family. I read an article in Parents magazine as well and one story in particular was of a child who hadn't been gaining weight properly. Some with celiac never show symptoms, so I was most worried that she may have it and not be showing the symptoms. I have switched her to a gluten free diet for almost 2 weeks now and she has gained a pound or pound and a half depending on the day, in less than two weeks, and she hasn't been eating any more than she did before. She has never had any food allergies that I've seen other than a minor diaper rash from eating grapes or pineapple and that I assume was from the acidity. If she really has celiac and I would rather her become accustomed to not eating gluten now, rather than several years later like her cousin. I've read about a cheek swab test on these forums and am going to look into that as an option. Have any of you who have a child with celiac been diagnosed and have not shown symptoms? I wonder how common that is?


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



Celiac.com Sponsor (A8-M):



Mother of Jibril Enthusiast

Welcome to the group!

Having a blood relative with celiac disease is the greatest risk factor. It would certainly be interesting to do a genetic test... it's just a cheek swab and you can do it anytime.

Lack of growth is a common symptom of celiac disease in a small child, but there might be other subtle things that just seem "normal" for her. For example... have you noticed any changes in her personality? Has her appetite increased? Does she have any strange rashes that are going away?

happygirl Collaborator

According the medical literature, 'silent' or asymptomatic Celiacs are MORE common than those with what were considered "classic" symptoms.

There is a cheek swab for the genes: HLA DQ2 and HLA DQ8. However, about 30-40% of the American population has the gene. Only about 1% of the population is believed to have Celiac. So, just having the gene does not equal Celiac.

The gene test is not dependent on eating gluten/not eating gluten. However, the blood tests and biopsy, which are needed to diagnose Celiac, need to be done when the patient is consuming gluten.

Another point to keep in mind is that while many children are diagnosed with Celiac, testing at a young age increases the risk of false negatives - the testing isn't as strong for young children.

Genna'smom Apprentice

Hi

I am still in the not sure I believe celiac disease but my now 2 1/2 old daughter decided to stop eating in April of 08 and was down to 19 lbs.... She is now up to 26 1/2 lbs since going gluten free but she is also fighting us tooth and nail about not wanting to eat and is gaining weight due to a feeding tube and her starting to eat some food. We are so worried about what will happen when we try to cut back on the feeding tube or cut it out and she did not have any of the normal symptoms of a celiac person. The only way we found out was that she had biopsy done due to look ing for issues with her acid reflux and it came back that she had early warning stages but her immune system was so messed up at the time I am still not 100% convinced so we will wait till she turn 3 and the try giving her any and all foods and then see what happens.

Good luck but this is a great place for advice.

Chaim9778 Newbie
Welcome to the group!

Having a blood relative with celiac disease is the greatest risk factor. It would certainly be interesting to do a genetic test... it's just a cheek swab and you can do it anytime.

Lack of growth is a common symptom of celiac disease in a small child, but there might be other subtle things that just seem "normal" for her. For example... have you noticed any changes in her personality? Has her appetite increased? Does she have any strange rashes that are going away?

Hmm...her personality was a lot crankier from about 6 months on, before that she was never in a bad mood...I attributed that to beginning of teething but she also started oatmeal around 5 months of age, so that could have been part the moodiness too, if she does indeed have celiac. She has had eczema on her back which developed right when she turned a year old, and I thought that could be from the switch to cow's milk from breast milk, it has cleared up and is hardly noticeable except when it's really cold out, like the drier the air aggravates it a bit. She also had a rash/hives after she got her flu shot this year, it lasted 3 days, but she didn't have any rashes from it last year and received 2 doses since it was her first time, and this year the hives just from the one shot she did get. No rashes other than that. Her appetite would have days here and there where it would really pick up and my husband and I would think "Finally! She'll gain some weight now!" then it would taper off again. She never ate a lot of unhealthy foods, I'm big on lots of organic fruit and veggies, very limited sugar, etc...I am/was really big on whole grains, and fiber but may need to cut that out. Thanks for everyone's responses, very informative!

mftnchn Explorer

Gluten free is a healthy diet and ultimately you can make your own choice about it.

My thought is that you should seek out a sharp pediatrician and explain your discovery. Once she is gluten free no further testing for celiac is possible. Genetic testing only shows propensity, and you already know she likely has that due to family history.

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

    LowellFrancis
    Newest Member
    LowellFrancis
    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.