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. - knitty kitty replied to Ginger38's topic in Related Issues & Disorders
      23

      Shingles - Could It Be Related to Gluten/ Celiac

    2. - knitty kitty replied to Charlie1946's topic in Related Issues & Disorders
      33

      Severe severe mouth pain

    3. - Bogger replied to Bogger's topic in Related Issues & Disorders
      2

      Osteoporosis: Does the body start rebuilding bones after starting a gluten-free diet?

    4. - trents replied to Charlie1946's topic in Related Issues & Disorders
      33

      Severe severe mouth pain

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

    • Total Members
      133,083
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • knitty kitty
      @Ginger38,  Are you taking a B Complex vitamin?  Vitamin D?  Thiamine in the form TTFD or Benfotiamine? I think increasing my B Complex vitamins and taking additional Thiamine and Vitamin C and zinc helps along with the Lysine.  
    • knitty kitty
      There's simple dietary changes that can be done to improve Barrett's esophagus.  There are vitamins that improve Barrett's esophagus --- most of the B vitamins! Reducing sugary foods and drinks will help.  A diet high in simple carbohydrates can deplete Thiamine and other B vitamins needed to process them into energy. Eating green leafy vegetables helps.  Green leafy vegetables are high in Folate and Riboflavin.       Dietary sugar and Barrett’s esophagus https://pmc.ncbi.nlm.nih.gov/articles/PMC5725502/#:~:text=The major finding of the,and sugar consumption [13].     Dietary intake of vegetables, folate, and antioxidants and the risk of Barrett's esophagus https://pubmed.ncbi.nlm.nih.gov/23420329/    Intakes of dietary folate and other B vitamins are associated with risks of esophageal adenocarcinoma, Barrett's esophagus, and reflux esophagitis https://pubmed.ncbi.nlm.nih.gov/24132576/    Associations between dietary folate intake and risks of esophageal, gastric and pancreatic cancers: an overall and dose-response meta-analysis https://pmc.ncbi.nlm.nih.gov/articles/PMC5689728/     Dietary vitamin B intake and the risk of esophageal cancer: a meta-analysis https://pmc.ncbi.nlm.nih.gov/articles/PMC6225909/#:~:text=A statistically significant%2C inverse association,an increased risk of EC.    Intake of Dietary One-Carbon Metabolism-Related B Vitamins and the Risk of Esophageal Cancer: A Dose-Response Meta-Analysis https://pmc.ncbi.nlm.nih.gov/articles/PMC6073467/    Dietary riboflavin deficiency induces ariboflavinosis and esophageal epithelial atrophy in association with modification of gut microbiota in rats https://pubmed.ncbi.nlm.nih.gov/32458157/    Association of Vitamin D and Parathyroid Hormone With Barrett's Esophagus (parathyroid needs Pyridoxine B6) https://pubmed.ncbi.nlm.nih.gov/30180151/   "let food be your medicine, let medicine be your food. "
    • Bogger
      Thanks for your reply I’m a nearly 69yr old female. My only medications are Fosamax and Lamotrigine for seizures. Thank you for that drugs.com link! There are soooo many common side effects for Reclast and almost nothing for Fosamax. Since it’s working well and I haven’t had any side effects from Fosamax (stomach bleeding, pain or upset) my doctor recommends it first over Reclast. Reclast is introduced into a vein thus bypassing the stomach which avoids all those stomach issues. But, once it’s in me, it’s there for a year or so. Any complications can’t be undone. With Reclast, I’m concerned about not being able to treat dental issues, several weeks of bone pain and the chance, although rare, of kidney damage. Plus all those other dozens of common side effects. It’s a very effective drug but looks pretty complicated to deal with. Hopefully I’m not just being a big chicken. In 2018 I fell and broke my ankle in two places. It took three screws to put it back together which is normal for that surgery. There was no mention of any difficulty or signs of bone loss. Thanks to my dog, I fell about a month ago onto a concrete floor with thin carpet. I landed on my left hip, then my spine, one vertebrae at a time, then clunked my head on the door frame. Twisted my wrist too. It was all in slow motion waiting to feel a crack that didn’t happen. Went to the ER tho. Amazingly, I didn’t even see any bruises. Thanks again for that link. I need to read through it some more. My doctor’s appt is next week when I’ll make the big decision.   
    • trents
      But for someone with Barrett's like @Charlie1946, long term PPI therapy might be necessary. 
    • Caligirl57
×
×
  • 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.