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

Daughter Diagnosed Yesterday, Tons Of Questions


mom2two

Recommended Posts

mom2two Apprentice

After two positive blood tests, and two negative scopes in 2.5 years we just got my four year old's enderol lab results back yesterday. She was 23 for the IgA which was not surprising to me. I already know how to start cutting gluten out of her diet, thanks to many helpful messages here. What was surprising was her IgA anti-casein which was 15. It doesn't seem that high but according to them it is high enough to cut out casein. I don't even know where to start there, especially on top of the gluten! Do I cut it all out at once? What does that leave for her to eat?

Also, how do I explain to my very bright, but highly emotional four year old who LOVES food that she has celiac disease? I plan on getting some of the reccommended books for celiac kids off of Amazon but...any other advise?

Also, the gene analysis is confusing. It says she has one of the main genes that predisposes her to gluten sensitivity and celiac sprue, HLA-DQ2 or HLA-DQ8 -DQ8. (Subtype 2,7) What does that really mean? and what are people's reccomendations for the rest of the family getting tested. No one else is showing any symptoms at all. Sorry for all the questions I just don't know where to turn, and Dr. have been far from helpful.


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



Celiac.com Sponsor (A8-M):



Ursa Major Collaborator

There IS life after gluten and dairy, trust me. Your daughter will adapt, she is little. Was she tested for soy, too? Beware of substituting with soy, it could very well be a problem, too. And soy, as well as casein and gluten, can also flatten the villi.

Just explain to her that her tests show that she will get very sick if she keeps eating normal bread, and things that have milk in them (and tell her what those are). Then tell her that you will need to work together to figure out what she should eat now, because you love her very much, and don't want her to get sick.

You could together draw pictures of food she can still eat, and take those to the store to shop. It will be fun. Tell her that you will try different breads she can still have, and cookies, and pastas, to find the ones she likes. You can buy gluten-free flours and experiment with baking cookies, all kids love baking cookies. gluten-free cookies (at least the home-baked ones) are every bit as good as the gluteny ones. Some of the store-bought ones are fairly gross, but as I said, you just have to try different brands, until you find something your daughter likes.

She can still eat all meat, fish, vegetables and fruit, as well as nuts, seeds, several gluten-free cereals and many other things. Try rice milk (not rice dream, it is not gluten-free) or almond milk with the cereal.

AndreaB Contributor

Hi and Welcome! :D

My family is gluten, soy and dairy free. My husband and I are soy intolerant and my two oldest children and I are gluten intolerant. I am mildly dairy allergic.

I've posted some recipes under the following thread if you'd like to look.....Open Original Shared Link. I am a former vegan and have lots of recipes, although many have soy or gluten in them, others do not. I haven't really looked at adapting too many yet. Haven't been spending much time baking. I used to make all my own bread and stuff.....still make my own bread using Annalise Roberts cookbook. She uses dairy and eggs but I substitute for the dairy.

You'll want to cut the food out as quickly as possibe. Kids are resilient. Mine fought tooth and nail about our diet change. My oldest has finally gotten used to meat, my next oldest is still not cooperating very well. We've been gluten free since June but were gluten light before that (since April).

key Contributor

I am sorry your 4 year old has this. I am possibly going through the same thing. My youngest is 2 years old and has celiac disease. I have it. We tested my oldest son thinking, because he was only in the 10th percentile he may have it too. His came back completely normal.

My now 4.5 year old was always my biggest and appeared to be the healthiest child. He was in the 95th percentile for weight and the 75th for height. Then for the past few years he dropped the the 50th and the 25th. I thought that was ok, but was concerned because he was so gassy, had become a poor eater, irritable, etc. I asked the doctor 6 months ago if he should be tested and he said he "looked" healthy to him. Oh he complained of stomach aches on and off.

Then the other day, we are going through a period of the stomach aches, so I finally got him into see a new doctor here. I was shocked to find out he had lost weight since March and had dropped to the 10th percentile for weight. He had his blood drawn day before yesterday. I am terrified that it is something else. I can't believe he would have it too. I know relatives are at higher risk, but my blood tests were borderline positive and no one has believed me. I just was so sick I stayed gluten free. I never had the biopsy, because I had already been gluten free for 2 months when tested. My other son didn't either, because we were out of town and he was so sick we just put him on the diet.

THe doctor here says my 4 year old doesn't need a biopsy if the blood work is positive. She says it is obvious with his family history. She said she just went to a convention on celiac disease. I have already started cutting out gluten from his diet, because I want him to gain weight. I am worried about him having Type 1 diabetes too. It doesn't run in our family, but I read it can cause weight loss.

I am also worried about him being upset about his diet, but I will have to just substitute everything. We don't eat meat and that makes it doubly hard. We do eat dairy though.

Right now I am just really upset that I was never diagnosed for SO many years. Everyone of my 3 kids has something. THey are normal, but my one had a birth defect with his skull and had to have major surgery, the second was my one that was ok until now, my 3rd is small, probably has a genetic disease called NF1 and celiac disease. All of them are intelligent and handsome though! So i am greatful for that, but I just feel that if I hadn't had undiagnosed celiac disease while pregnant this wouldn't have happened.

Hang in there. It takes awhile to adjust. Just wanted you to know that I have a 4 year old with this too probably.

Oh yeah, I say ALWAYS trust your mommy instinct. I have yet to be wrong! I am mad that I didn't test him six months ago. THe doctor talked me out of it, but he should have been tested "just because his brother and I have it"!

Monica

mom2two Apprentice

Thanks for all the good advice and tips. I would be totally in the dark without this message board. I wish others we'ren't going through the same thing but it is nice to know I'm not alone. Any advice on the casein issue? SHould we cut out gluten and casein together or do one first? ALso, where do I start with the casein? I've heard I shouldn't substitute with soy but are their cheese or yogurt substitutes? My daughter loves these two foods and practically lives on them!?!

fullofhope Newbie

I'd start with one (gluten) and then move to dairy. All at once could be too stressful for everyone. Alas I have not found a yogurt that isn't soy or dairy, and the same with cheese- maybe someone else has some source I don't know about, though!

We use bob's red mill mixes (pancake, brownie, and choc. chip cookie), envirokids cereal, pacific rice milk, enjoy life cookies, cereal bars, etc, and food for life millet and rice breads (frozen- they toast up yummy but you'll need a dedicated gluten-free toaster so you don't cross contaminate), and tinkyada rice pasta or quinoa (keenwah) pasta. I use rice flour or millet flour for things like chicken nuggets (although Ian's red banner makes good chicken nuggets and fish sticks). I'm just beginning to realize how many mainstream brands are gluten free (I'm finally calling companies and looking at websites) and our options are opening before us.

The AiA gluten and dairy free cookbook and special diets for special kids are wonderful cookbooks, and wheat free worry free or raising our celiac kids are both great books for info and recipes too.

We told our son that it was gluten, dairy, and soy causing him to feel icky and itchy, but look at all the yummy things we can still eat. I carry his favorites with me, esp when we are eating out or at the grocery store or a friend's house where there are likely to be things he will look longingly at, so he can have his gluten-free treats too. Usually what happens is everyone gets jealous of HIM because his treats look so good. :)

Best wishes,

janel

Nic Collaborator

My son was 4 when he was diagnosed. I explained to him that his body is confused and thinks that some of his favorite foods (I explained which ones) are poison and they are making him feel so sick. He understood it very well because he knew what poison was and I never had to explain it to him again. He now tells people when they offer him food that he can't eat that because it has gluten. He won't even touch food he can't have. He accidentally spilled a bowl of my nephews doritos the other day and he told my sister that he spilled them but he can't pick them up because he can't touch them. He has learned well, so will your child. Good luck.

Nicole


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



Celiac.com Sponsor (A8-M):



Guest nini

my daughter was dx'ed at three and now at six she is happy and healthy and thriving... focus on the things she CAN have, not on what she can't. Get the book Kids with Celiac Disease by Danna Korn, it will help A LOT. After she is gluten-free for a while she may be able to tolerate dairy again, so look at taking dairy out of her diet as a possibly temporary situation, if it turns out she isn't ever able to tolerate it, you will have gotten the hang of it by then.

In my signature there is a link to my web page, at the bottom of my web page is a link to the newbie survival kit that you can download, hopefully that will help you find some fun food choices for your daughter. It's all in how you approach it I think. If you see this dx as a good thing and that your daughter will now be healthy and you will be preventing her from a lifetime of illness it's easier to deal with than if you focus on OH NO I have to deprive this child of her favorite foods. You will find other foods that she will love. It gets easier.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,855
    • Most Online (within 30 mins)
      7,748

    Tara M
    Newest Member
    Tara M
    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

    • 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 .
    • Francis M
      Thanks. Since the back and forth and promises of review and general stalling went on for more than six months, the credit company will no longer investigate. They have a cutoff of maybe six months.
    • Scott Adams
      Is this the same restaurant? https://www.facebook.com/TheHappyTartFallsChurch/ Is it too late to take this up with your credit card company? Normally you have a few months to do a chargeback with them. It seems very odd that they are taking this approach with someone who is likely to be a regular customer--not a good business-minded way of handling things!
    • Scott Adams
      Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: The most common nutrient deficiencies associated with celiac disease that may lead to testing for the condition include iron, vitamin D, folate (vitamin B9), vitamin B12, calcium, zinc, and magnesium.  Unfortunately many doctors, including my own doctor at the time, don't do extensive follow up testing for a broad range of nutrient deficiencies, nor recommend that those just diagnosed with celiac disease take a broad spectrum vitamin/mineral supplement, which would greatly benefit most, if not all, newly diagnosed celiacs. Because of this it took me decades to overcome a few long-standing issues I had that were associated with gluten ataxia, for example numbness and tingling in my feet, and muscle knots--especially in my shoulders an neck. Only long term extensive supplementation has helped me to resolve these issues.        
×
×
  • 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.