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

In-Laws Do Not Understand


MyTummyHurts8

Recommended Posts

MyTummyHurts8 Newbie

Hi everyone,

I am new and this is my first post! I do not have Celiac disease, but I am what you would call self-diagnosed gluten sensitive. I figured it out by doing an elimination diet when I was 18, didn't care enough to really change until I did more research and read about all the damage I was most likely doing to myself. I am 26 now and have been gluten free for the past year (with slip-ups here and there, due to my own stupidity in not asking questions or reading labels more carefully). Anyway...

My husband is not gluten-free, but he is very supportive of my diet and tries to help me by using different utensils for his gluten foods and whatnot. I was pretty proud of him when we had Thanksgiving at his parent's house this past week. He was announcing to the family what they could and could not do to the gluten-free food I bought :-) It's hard to watch him eat sandwiches or stop for a donut, and I've asked him if he would ever consider being gluten-free with me... he isn't quite ready to give it up yet though.

I am feeling frustrated because his family thinks my sensitivity is just a joke, and that I'm pretending to be allergic to something for attention. They used an oven bake bag for the turkey at Thanksgiving and put flour in it, and I didn't know about it at first, but my husband knew that's what they normally do so he asked about it. They said, "It was only half a cup of flour, and we didn't think it would matter. It's not much. Can't she just peel the skin off and eat the meat? I didn't think a little bit of flour bothered her."

They've done similar things other times we have been visiting them. I usually just take my own food, or offer to make dinner for everyone.... although, I'm used to eating paleo/specific carbohydrate diet/gluten-free/sugar free, so when I make things and they try it, they sort of smile and say "Oh, this is... good" and reach for a box of mac n cheese.

I've tried to explain why I can't eat it and what it does to my body, but they don't get it and tune out when I start talking about it. How do you deal with your in-laws? Has anyone been successful in having gluten-eating family members really understand the need to be gluten-free and take it seriously? I'm open to advice and tips! :)

Thanks!


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

You are pretty new to this family. Is it possible they wouldn't really listen to anything you said? :blink: I just mean it may be the way they are and nothing to do with you & gluten sensitivity..

Because you are new to the family (Under 20 years of marriage is new to some families), I think its best if your husband speak up. Also, always bring your own food so you have something to eat.

I made one of those bag turkeys last year with some gluten-free flour. Don't remember if I used rice flour or some Pamelas mix and it worked great. If you think its worth it, you could send over a cup of the gluten-free flour ahead to use on the turkey.

Skysmom03 Newbie

We got one of kroger's frozen turkey's this year and it came with a gluten free gravy made from rice flour. Very good and couldn't tell a difference!

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. - Scott Adams replied to HAUS's topic in Gluten-Free Foods, Products, Shopping & Medications
      7

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

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

      Inconclusive results

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

      Inconclusive results

    4. - cristiana replied to HAUS's topic in Gluten-Free Foods, Products, Shopping & Medications
      7

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,436
    • Most Online (within 30 mins)
      7,748

    Vivien Armstrong
    Newest Member
    Vivien Armstrong
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • 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?
    • cristiana
      Thanks for this Russ, and good to see that it is fortified. I spend too much time looking for M&S gluten-free Iced Spiced Buns to have ever noticed this! That's interesting, Scott.  Have manufacturers ever said why that should be the case?  
×
×
  • 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.