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. - MauraBue posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Have Tru Joy Sweets Choco Chews been discontinued??

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

      how much gluten do I need to eat before blood tests?

    3. - suek54 replied to suek54's topic in Dermatitis Herpetiformis
      7

      Awaiting dermatitis herpetiformis confirmation following biopsy

    4. - knitty kitty replied to suek54's topic in Dermatitis Herpetiformis
      7

      Awaiting dermatitis herpetiformis confirmation following biopsy

    5. - suek54 replied to suek54's topic in Dermatitis Herpetiformis
      7

      Awaiting dermatitis herpetiformis confirmation following biopsy

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,260
    • Most Online (within 30 mins)
      7,748

    MauraBue
    Newest Member
    MauraBue
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • MauraBue
      Help!  My 5 year old daughter just stopped eating dairy and gluten due to her EoE and Celiac.  Her favorite candy in the world is tootsie rolls.  I did some research, and it sounds like these are the only options for finding something similar, but I can't find them anywhere to actually purchase.  Have they been discontinued??  Does anyone have another recommendation for a gluten-free/DF tootsie roll option?
    • catnapt
      I wonder how long it usually takes and if it is dose dependent as well... or if some ppl have a more pronounced reaction to gluten than others   thanks again for all the great info    
    • suek54
      Wow KK, thank you so much for all your attached info. I had a very quick scan but will read more in depth later.  The one concerning corticosteroid use is very interesting. That would relate to secondary adrenal insufficiency I think , ie AI caused by steroids such as taken long term for eg asthma. I have primary autoimmune AI, my adrenals are atrophied, no chance if recovery there. But I am in touch with some secondaries, so something to bear in mind. .  Niacin B3 Very interesting too. Must have a good read about that.  Im sure lots of questions will arise as I progress with dermatitis herpetiformis. In the mean time, thanks for your help.
    • knitty kitty
      Welcome to the forum, @suek54, I have Dermatitis Herpetiformis, too.  I found taking Niacin B3 very helpful in clearing my skin from blisters as well as improving the itchies-without-rash (peripheral neuropathy).  Niacin has been used since the 1950's to improve dermatitis herpetiformis.   I try to balance my iodine intake (which will cause flairs) with Selenium which improves thyroid function.   Interesting Reading: Dermatitis herpetiformis effectively treated with heparin, tetracycline and nicotinamide https://pubmed.ncbi.nlm.nih.gov/10844495/   Experience with selenium used to recover adrenocortical function in patients taking glucocorticosteroids long https://pubmed.ncbi.nlm.nih.gov/24437222/   Two Cases of Dermatitis Herpetiformis Successfully Treated with Tetracycline and Niacinamide https://pubmed.ncbi.nlm.nih.gov/30390734/   Steroid-Resistant Rash With Neuropsychiatric Deterioration and Weight Loss: A Modern-Day Case of Pellagra https://pmc.ncbi.nlm.nih.gov/articles/PMC12532421/#:~:text=Figure 2.,(right panel) upper limbs.&text=The distribution of the rash,patient's substantial response to treatment.   Nicotinic acid therapy of dermatitis herpetiformis (1950) https://pubmed.ncbi.nlm.nih.gov/15412276/
    • suek54
      Thank you all for your advice and the dermatitis herpetiformis article. The latter made me realise I had stopped taking my antihistamine, which I will restart today. The Dapsone has cleared the rash entirely but I still get quite a bit itching, absolutely nothing to see though. I know its notoriously hard to clear and its still relatively early days for me.  The iodine issue is very interesting. I do eat quite a bit of salt because I have Addison's disease and sodium retention is an issue. I also have autoimmune hypothyroidism, not sure how a low iodine diet would play into that? Because of my Addison's I am totally steroid dependent, I take steroids 4 x daily and cannot mount any defence against inflammation. I need to increase my meds for that. Now that I know what is wrong I can do just that if Im having a bad day. Life is very sweet, just so damn complicated sometimes! Hey ho, onwards. Thank you again for your advice.  
×
×
  • 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.