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 Careful Is Careful?


bridgetsmommy

Recommended Posts

bridgetsmommy Rookie

Hi Everyone,

My 16 mo. old daughter has been on a gluten-free diet for one week (she was diagnosed with Celiac on 5/5/09 after the biopsy results of her endoscopy). The rest of the family is maintaining our usual diet and trying to do more gluten free meals when possible. I am just overwhelmed with all the possible "gluten contamination" issues and feel stressed and guilty. I am worried about any little crumb, but on the other hand, I know that gluten will happen, if not at our home, then everywhere else! My question is how do you all deal with it? How do you make sure you provide the safest environment for your child, while keeping things in perspective? Despite my fears, we've been doing our usual activities and I'm just watching her like a hawk. But, I won't always be there and need to learn to trust others and give myself a break. Any advice?

Also, we have a dog. I read that some people feed their animals gluten-free diets if there is celiac disease in the house. Is this a bit drastic?

I want to do what is best and healthiest but maintain some sense of normalcy. Like I said, I'm new to this and still in the fearful stage. I could use some support.

Thanks!


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



Celiac.com Sponsor (A8-M):



jmjsmomma Apprentice

The fearful stage is SO hard!!! My 5 year old was dx in Jan. My 4 & 2 year olds are negative, as are my husband and I. At first, I just had my son gluten-free. Now that we are 4 months into it, our home is about 95% gluten-free because we have found alternatives to just about everything. Granted, I live in Dallas where options are abundant, but all the gluten-free stuff is scarfed up by my younger two. Now, we have ONE gluten counter. I still use regular bread for the other two, and I only do it on that counter. We used to use separate colanders/utensils etc but we only use gluten-free pasta now. I use our regular oven if I'm going to make anything gluten, and we have a convection toaster oven that is gluten-free. It is so hard at first. It is a personal decision as to whether you have gluten or not in your home. As we went along in our journey, it was just easier to have "some" gluten in our home so our son could understand that he was not living in a bubble, and to feed our other smaller kids cheaply. But with that said it was a very natural transition to most of us being gluten-free given the wonderful options these days. I am not far past where you are now....if you need to chat feel free to email.

CeliacMom2008 Enthusiast

Regarding the dog food, we have gluten dog food in our house, but our son is almost 10. He isn't crawling around on the floor and then putting his fingers in his mouth. When he does play on the floor he knows he has to stay well away from where the dog eats. If he were a toddler I'd be finding the gluten free dog food.

Your question was how careful is careful...in our house we are extremely careful. To keep my sanity about cross contamination we maintain an almost entirely gluten free household. All meals are gluten free. The only thing gluten really is some cereal hubby and I eat after our son goes to bed - and we're very careful about it.

You're just getting into this. I don't know how sick your baby was before diagnosis. I can tell you that after watching my son get glutened our family does everything possible to make sure that doesn't happen.

You'll soon learn that gluten free is very doable, can be very nutritious, and very delicious. Once you get to that point it will be easier.

Jestgar Rising Star

It all does get easier, I promise you. Right now everything is new and there is so much to learn, but as pieces of this new approach to eating start to stick in your brain, they become habit, and not nearly so overwhelming.

Hang in there, and come here whenever you need a hand or an ear. :)

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Rogol72 replied to HAUS's topic in Gluten-Free Foods, Products, Shopping & Medications
      8

      Sainsbury's Free From White Sliced Bread - Now Egg Free - Completely Ruined It

    2. - Scott Adams replied to HAUS's topic in Gluten-Free Foods, Products, Shopping & Medications
      8

      Sainsbury's Free From White Sliced Bread - Now Egg Free - Completely Ruined It

    3. - Scott Adams replied to deanna1ynne's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      13

      Inconclusive results

    4. - deanna1ynne replied to deanna1ynne's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      13

      Inconclusive results


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,441
    • Most Online (within 30 mins)
      7,748

    Linda Boxdorfer
    Newest Member
    Linda Boxdorfer
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Rogol72
      @HAUS, I was at an event in the UK a few years back. I remember ringing the restaurant ahead to inquire about the gluten free options. All I wanted was a few gluten free sandwiches, which they provided and they were delicious. The gluten-free bread they used was Warbutons white bread and I remember mentioning it on this site before. No harm in trying it once. It's fortified with Calcium and Iron. https://www.warburtonsglutenfree.com/warbs_products/white-loaf/ The only other gluten-free bread that I've come across that is fortified is Schar with Iodized salt, nothing else.
    • Scott Adams
      In the U.S., most regular wheat breads are required to be enriched with certain B-vitamins and iron, but gluten-free breads are not required to be. Since many gluten-free products are not enriched, we usually encourage people with celiac disease to consider a multivitamin.  In the early 1900s, refined white flour replaced whole grains, and people began developing serious vitamin-deficiency diseases: Beriberi → caused by a lack of thiamin (vitamin B1) Pellagra → caused by a lack of niacin (vitamin B3) Anemia → linked to low iron and lack of folate By the 1930s–40s, these problems were common in the U.S., especially in poorer regions. Public-health officials responded by requiring wheat flour and the breads made from it to be “enriched” with thiamin, riboflavin, niacin, and iron. Folic acid was added later (1998) to prevent neural-tube birth defects. Why gluten-free bread isn’t required to be enriched? The U.S. enrichment standards were written specifically for wheat flour. Gluten-free breads use rice, tapioca, corn, sorghum, etc.—so they fall outside that rule—but they probably should be for the same reason wheat products are.
    • Scott Adams
      Keep in mind that there are drawbacks to a formal diagnosis, for example more expensive life and private health insurance, as well as possibly needing to disclose it on job applications. Normally I am in favor of the formal diagnosis process, but if you've already figured out that you can't tolerate gluten and will likely stay gluten-free anyway, I wanted to at least mention the possible negative sides of having a formal diagnosis. While I understand wanting a formal diagnosis, it sounds like she will likely remain gluten-free either way, even if she should test negative for celiac disease (Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If her symptoms go away on a gluten-free diet, it would likely signal NCGS).        
    • JoJo0611
    • deanna1ynne
      Thank you all so much for your advice and thoughts. We ended up having another scope and more bloodwork last week. All serological markers continue to increase, and the doc who did the scope said there villous atrophy visible on the scope — but we just got the biopsy pathology report back, and all it says is, “Duodenal mucosa with patchy increased intraepithelial lymphocytes, preserved villous architecture, and patchy foveolar metaplasia,” which we are told is still inconclusive…  We will have her go gluten free again anyway, but how soon would you all test again, if at all? How valuable is an official dx in a situation like this?
×
×
  • 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.