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

Not Sure What To Doo Now!


ericamricard

Recommended Posts

ericamricard Newbie

My 4 year old daughter has been sick for five months now. She is always telling me her tummy hurts and can't go to the bathroom. She was tested for celiacs and it was neg! The doctor told me that she was a holder. But she is on meds to make her go to the bathroom and that still doesn't work! She was tested for Cystic Fibrosis and she has the gene but not the disease!! Thank goodness!! Now are 23 month old was tested for the CF gene and she has the gene but also has a low iron count. Then my doctor told me her blood work came back postive for Celiac's. The only problem with Trinity was her iron...she has no problems!! The only thing that points to Celiacs is when she poops it is grayish and oily and that she has low iron. If anyone has had their child tested for everything under the sun and still can't go to the brathroom please let me know what to have her tested for! She thinks her tummy is always going to hurt and she will not eat! I am worried this will hurt her when she starts school. As for my other daughter any help on changing to the gluten free food would be a big help!

Thanks

mom in need

Erica


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



Celiac.com Sponsor (A8-M):



gfpaperdoll Rookie

The daughter that is constipated needs to be on a gluten free & dairy free diet right away the same as the other daughter. Negative celiac tests mean nothing, while a positive is a positive.

You should see improvement in both girls right away.

& P.S. If I can indulge myself & say how ridiculous for an MD to say a child is "a holder", oh geez...

if you want to test the one child that tested negative for celiac, just test her thru enterolab.com

Ridgewalker Contributor

Hi Erica!

For your younger daughter-- I know it's bewildering to think she has to go on a gluten-free diet when she seems healthy. But unfortunately, the facts that her poop is oily and her iron is low show that she is already suffering from malabsorption. That's the beginning of a whole host of malnourishment problems. She is extremely fortunate that this was discovered so young!

For your older daughter-- I agree with gfpaperdoll, it is absolutely worthwhile to try her on a gluten-free diet and see if she improves. Frankly, with the stomach pains, constipation, and a Celiac sister, she is very high risk. Blood tests have a significant percentage of false negatives, and that percentage goes up with small children.

Advice for going gluten-free--

The diet must be extremely strict. Your daughters' foods must not even come into contact with wheat, barley, rye, or oats- or any of their derivatives.

** Do not put their gluten-free bread in your old toaster, it will contaminate the bread. Buy a new toaster that is only for gluten-free bread. I keep a pretty kitchen towel over my gluten-free toaster, which keeps stray wheat crumbs out and keeps my husband from using it accidentally.

** Wooden spoons and bowls absorb gluten. Do not use them, or buy new ones for gluten-free cooking/serving. Ditto with pizza stones and cast iron pans.

** Gluten is extremely difficult, if not impossible, to remove from collanders, scratched non-stick pans, pastry brushes. The best thing to do is buy new ones for gluten-free cooking.

All of the above sounds horridly expensive, I know. Instead of buying everything at once, I bought as much as I could each week. It took about a month to get everything replaced. Do the toaster first!

No double-dipping a knife into mayo, peanut butter, jelly, mustard, butter, etc. If you swipe a piece of wheat bread and then dip the knife back into the jar, the jar is contaminated.

More advice on cross contamination can be found on this thread: Open Original Shared Link

Some of my kids' favorite foods are:

* Van's gluten-free Waffles. Check the front of the box for "gluten-free" because Van's also does wheat waffles. (Find at Whole Foods or some grocery stores.)

* Glutino Pretzels (Whole Foods)

* UTZ brand chips (Regular store)

* Pamela's Pancake and Baking Mix. Can make pancakes, cookies, muffins, many things with this good mix. (Whole Foods)

* Mainstream cereals that are gluten-free: Fruity and Berry Pebbles, Cocoa Pebbles, Trix, and Dora the Explorer Cinnamon Stars. Also, Envirokids Gorilla Munch is very good, kind of like Kix or Captain Crunch. (Envirokids is at Whole Foods and some regular stores.)

* Tinkyada Pasta. This is the only brand of gluten-free pasta that they really love. It's hard to mess Tinkyada up. Many other brands overcook very easily, and then are horrible. Another favorite brand on this board is Biaglut, but I haven't been able to find it anywhere. (Tinkyada can be found at Whole Foods.)

* My older son really likes EnerG tapioca bread, which we order online, but a lot of other people here hate it. My favorite gluten-free bread is one that I make from scratch. The recipe is here:

Open Original Shared Link All premade gluten-free bread benefits from being toasted. Even homemade needs to be toasted after the second day.

My 4-year-old is often constipated, and is afraid to use the bathroom as well. One thing I've done to help him is sit in the bathroom with him and sing songs. We also go through the alphabet and think of words that start with each letter. Sometimes we try to think of the silliest words, or animal words, etc. If he looks like he's trying to hold it, I'll gently flex his knees upward, which causes the butt muscles to relax a little.

He has been gluten-free for almost 3 weeks now, and we are seeing lots of improvement! My older son has been gluten-free since the spring.

ericamricard Newbie

Thank you guys so much!! I is so hard to think my baby has Celiac's because she has been fine. Serria has been tested for celiac's an her bisopy came back neg. I have thought about just putting the whole family on a gluten-free diet just so nothing get mixed up with the sitter! She is smart and all but it would be so easy for anything to happen.I feel like after going to a GI doctor for 3 months they would have something by now...But all he says is she is a holder!!! That to me is well I can say what I want to... She trys so hard to go but she can't and she is on 8tablespoons of meds to help her!! That for a four year old is way too much!! Any info on what to do with her and make the change to gluten-free is welcomed!!

Thanks

gfpaperdoll Rookie

erica... what part of the country are you in? We can see if there is a support or ROCK (raising our celiac kids) group near you.

Of course I think that the easiet best thing is to take the whole house gluten-free. Those that want can eat gluten outside of the house. I think you will be amazed at how much healthier all the family becomes. Just feed them regular home cooked meals with plain meat, veggies, fruits, nuts & seeds.

for instance cook a big pot roast (just do not brown in flour or add a gravy mix) either cook with an onion, carrots, potatoes, or serve with rice veggies, and a salad etc.

check the recipe thread here for meal tips etc. anything specific you want to cook, just ask us & I am sure one of us makes it the gluten-free way. ! :)

check in & let us know how the kids are doing...

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,082
    • Most Online (within 30 mins)
      7,748

    NorasMimi
    Newest Member
    NorasMimi
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.6k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • DebJ14
      Good luck to you.  I would not get past that first slice of bread.  I would be vomiting and have diarrhea within 30 minutes and it would continue for hours and I would feel like I was hit by a truck for days.  My functional medicine doctor told me to stop taking Calcium and to significantly up my Vitamin D, add K2, lots of Magnesium, some boron and collagen.  This was all recommended after taking the Spectracell test for nutrient deficiencies.  Started doing this at 54 when diagnosed and at 72 no issues with the old bones.   
    • Recently diagnosed
      I live in Ottawa Canada and would be interested in a swap with someone who also has a gluten-free house. I’d love to swap out in winter for somewhere warm.
    • trents
      @KRipple, thank you for the lab results from your husband's celiac disease blood antibody testing. The lab result you share would seem to be the tTG-IGA (Tissue Transglutaminase IGA) and the test result is in excess of 10x normal. This is significant as there is an increasing tendency for physicians to grant a celiac disease diagnosis on the basis of antibody testing alone when the scores on that particular test exceed 10x normal. This trend started in the UK during the COVID pandemic when there was tremendous pressure on the medical system over there and it has spread to the USA. The tTG-IGA is the centerpiece of celiac disease blood antibody testing. All this to say that some doctors would grant a celiac disease diagnosis on your husband's bloodwork alone and not feel a need to go forward with an endoscopy with biopsy. This is something you and your husband might wish to take up with his physicians. In view of his many health issues it might be wise to avoid any further damage to his small bowel lining by the continuing consumption of gluten and also to allow healing of such to progress. The lining of the small bowel is the place where essentially all of our nutrition is absorbed. This is why celiac disease when it is not addressed with a gluten free diet for many years typically results in additional health problems that are tied to nutritional deficiencies. The millions and millions of tiny finger-like projections that make up the nutrient absorbing surface of the small bowel lining are worn down by the constant inflammation from gluten consumption. In celiac disease, the immune system has been tricked into labeling gluten as an invader. As these finger-like projections are worn down, the efficiency of nutrient absorption becomes more and more compromised. We call this villous atrophy.   
    • KRipple
      Thank you so much! And sorry for not responding sooner. I've been scouring the hospital records and can find nothing other than the following results (no lab info provided): Component Transglutaminase IgA   Normal Range: 0 - 15.0 U/mL >250.0 U/mL High   We live in Olympia, WA and I will be calling University of Washington Hospital - Roosevelt in Seattle first thing tomorrow. They seem to be the most knowledgeable about complex endocrine issues like APS 2 (and perhaps the dynamics of how APS 2 and Celiacs can affect each other). His diarrhea has not abated even without eating gluten, but that could be a presentation of either Celiac's or Addison's. So complicated. We don't have a date for endoscopy yet. I will let my husband know about resuming gluten.    Again, thank you so much for sharing your knowledge with me!
    • Jmartes71
      Ginger is my best friend, it helps alot with tummy issues..
×
×
  • Create New...