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

Gluten Free And The Holidays


hal2me

Recommended Posts

hal2me Newbie

Hello Everyone!

I'm new to this forum. Today I decided to register because of the upcoming holiday. Every year, my in-laws order Chinese food for Christmas dinner. They never offer to make anything for me or have something I can eat. I do bring my own food, but I feel excluded from the meal. It hurts my feelings that every year they do this and every year they ask me why I cannot eat the Chinese food. As I explain to them for the 100th time that I have celiac disease and cannot eat the food, my MIL says I am rude because I do not eat what they bought.

I am so angry because I feel like they do not listen to me at all. I do not expect them to have an entirely gluten free meal for me, but how hard is it to pick up some fruit or veggies so I can have something to eat? Every year while everyone is eating Chinese food, I am eating a peanut butter sandwich or some pasta with sauce I made at home while I get looks for not eating the meal. It sounds silly, but I feel excluded when I cannot eat what everyone else is having. Does anyone else feel like this? Especially at the holidays?

I've hosted dinner at my home in the past, but all they do is complain that the food does not taste good and that they have to be mindful of which butter tub to use.

Thank you for taking the time to read this.

Happy Holidays!


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



Celiac.com Sponsor (A8-M):



GFreeMO Proficient

I feel the exact same way. This year my sister is having lasagna, french bread and salad which I am sure will be gluteney from CC. There wont be anything that I can eat either. I am bringing my own food. I use to bring things to share but my bro in law wont touch my food and everyone else tries it but they never eat it. They nibble and push it around on their plates.

Just take your own food. Make something really yummy and warm it up in the microwave.

It's hard to feel so different...I go through the exact same thing.

tennisman Contributor

I feel sorry for both of you :(

hal2me I feel angry reading your post, it's really bad your MIL thinks you are rude because you can't eat the food. It's ridiculous how bad some people can be :angry: For christmas you should buy your in-laws a book about celiac disease :P

Happy Christmas :)

hal2me Newbie

Thank you both for the kinds words. It's nice to know that I am not alone with this.

kareng Grand Master

Thank you both for the kinds words. It's nice to know that I am not alone with this.

Where is their child, that you are married to, during this nonsense? Some in- laws will never like the person their child married. So you talking to them won't do any good. Your wife needs to step up here. Also, if you know it's Chinese, make something similar to take with you to eat.

hal2me Newbie

Where is their child, that you are married to, during this nonsense? Some in- laws will never like the person their child married. So you talking to them won't do any good. Your wife needs to step up here. Also, if you know it's Chinese, make something similar to take with you to eat.

Hi kareng!

Actually, I am the wife and my husband is their child :D You are right, talking to them never helps. My husband talks to them also and has tried to arrange it so we don't have to be there for dinner, but then he never hears the end of it. We are expected to be there for dinner. I took your advice and made some homemade chop suey to bring with me. The day of Christmas I'll cook some rice to eat with it. Thanks for the great idea!!

kareng Grand Master

Hi kareng!

Actually, I am the wife and my husband is their child :D You are right, talking to them never helps. My husband talks to them also and has tried to arrange it so we don't have to be there for dinner, but then he never hears the end of it. We are expected to be there for dinner. I took your advice and made some homemade chop suey to bring with me. The day of Christmas I'll cook some rice to eat with it. Thanks for the great idea!!

Sorry about the gender mix- up. :) I find it's easier if I can bring something similar to what they are eating....or a bag of Fritos and a Snickers bar .


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



Celiac.com Sponsor (A8-M):



cap6 Enthusiast

If I don't know what is being served then I call ahead and ask so that I can bring something similiar. Maybe that would help so you don't feel so left out. It's hard to always be different. I have been glutened at a gathering though for the last time. From now on I will be bringing my own food no matter what. It's just safer.

eatmeat4good Enthusiast

Hello Everyone!

I'm new to this forum. Today I decided to register because of the upcoming holiday. Every year, my in-laws order Chinese food for Christmas dinner. They never offer to make anything for me or have something I can eat. I do bring my own food, but I feel excluded from the meal. It hurts my feelings that every year they do this and every year they ask me why I cannot eat the Chinese food. As I explain to them for the 100th time that I have celiac disease and cannot eat the food, my MIL says I am rude because I do not eat what they bought.

I am so angry because I feel like they do not listen to me at all. I do not expect them to have an entirely gluten free meal for me, but how hard is it to pick up some fruit or veggies so I can have something to eat? Every year while everyone is eating Chinese food, I am eating a peanut butter sandwich or some pasta with sauce I made at home while I get looks for not eating the meal. It sounds silly, but I feel excluded when I cannot eat what everyone else is having. Does anyone else feel like this? Especially at the holidays?

I've hosted dinner at my home in the past, but all they do is complain that the food does not taste good and that they have to be mindful of which butter tub to use.

Thank you for taking the time to read this.

Happy Holidays!

I would say "I am not trying to be rude when I don't eat your food, but people with Celiac disease are prone to developing intestinal cancers and I would like to be here for a few more Christmas's with y'all if you don't mind." Then I would smile, grab my salad and walk away. I might also say that "I have missed a few Christmas's before I knew what was wrong with me....and I'd rather not miss this one being sick thank you for understanding."

Just my 2 cents.

Jestgar Rising Star

Don't go. Your husband tells them he's tired of watching his wife be unhappy at Christmas and he's taking you out for dinner. You'll come to their house after everyone has eaten and spend some time with them then.

Any issues they have with it, the hubby responds with "I don't want to see my wife hurt. Wouldn't you do the same?"

TooManyHats Rookie

I intend on explaining things in reference to a peanut allergy. Would you expect someone with a peanut allergy to eat nuts? Of course not. Then why would you expect me to eat something that could potentially kill me? Say what you mean, mean what you say, and don't say it mean. Case closed. Smile and enjoy your meal.

CeliacMom2008 Enthusiast

I like Jestgar's idea! I would probably lean toward a response of "No, rude is being so insistent that I poison myself in front of you." I'm so sorry. I wish you could swing by my house and I'd give you a big plate of gluten-free cookies!!!

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. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    2. - knitty kitty replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    3. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    4. - Scott Adams replied to Russ H's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      KAN-101 Treatment for Coeliac Disease

    5. - Scott Adams replied to miguel54b's topic in Related Issues & Disorders
      1

      Body dysmorphia experience


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,156
    • Most Online (within 30 mins)
      7,748

    Shrub
    Newest Member
    Shrub
    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

    • trents
      This article does not address migraines at all.  Yes, red wine and sulfites are often mentioned in connection with migraine triggers. With me, any kind of alcoholic beverage in very modest amounts will reliably produce a migraine. Nitrous oxide generators, which are vaso dialators, also will give me migraines reliably. So, I think most of my migraines are tied to fluctuations vascular tension and blood flow to the brain. That's why the sumatriptan works so well. It is a vaso constrictor. 
    • knitty kitty
      Excessive dietary tyrosine can cause problems.  Everything in moderation.   Sulfites can also trigger migraines. Sulfites are found in fermented, pickled and aged foods, like cheese.  Sulfites cause a high histamine release.  High histamine levels are found in migraine.  Following a low histamine diet like the low histamine Autoimmune Protocol diet, a Paleo diet, helps immensely.    Sulfites and other migraine trigger foods can cause changes in the gut microbiome.  These bad bacteria can increase the incidence of migraines, increasing histamine and inflammation leading to increased gut permeability (leaky gut), SIBO, and higher systemic inflammation.   A Ketogenic diet can reduce the incidence of migraine.  A Paleo diet like the AIP diet, that restricts carbohydrates (like from starchy vegetables) becomes a ketogenic diet.  This diet also changes the microbiome, eliminating the bad bacteria and SIBO that cause an increase in histamine, inflammation and migraine.  Fewer bad bacteria reduces inflammation, lowers migraine frequency, and improves leaky gut. Since I started following the low histamine ketogenic AIP paleo diet, I rarely get migraine.  Yes, I do eat carbs occasionally now, rice or potato, but still no migraines.  Feed your body right, feed your intestinal bacteria right, you'll feel better.  Good intestinal bacteria actually make your mental health better, too.  I had to decide to change my diet drastically in order to feel better all the time, not just to satisfy my taste buds.  I chose to eat so I would feel better all the time.  I do like dark chocolate (a migraine trigger), but now I can indulge occasionally without a migraine after.   Microbiota alterations are related to migraine food triggers and inflammatory markers in chronic migraine patients with medication overuse headache https://pmc.ncbi.nlm.nih.gov/articles/PMC11546420/  
    • trents
      Then we would need to cut out all meat and fish as they are richer sources of tyrosine than nuts and cheese. Something else about certain tyrosine rich foods must be the actual culprit. 
    • Scott Adams
      I agree that KAN-101 looks promising, and hope the fast track is approved. From our article below: "KAN-101 shows promise as an immune tolerance therapy aiming to retrain the immune system, potentially allowing safe gluten exposure in the future, but more clinical data is needed to confirm long-term effects."  
    • Scott Adams
      Thank you so much for having the courage to share this incredibly vivid and personal experience; it's a powerful reminder of how physical ailments can disrupt our fundamental sense of self. What you're describing sounds less like a purely psychological body dysmorphia and more like a distinct neurological event, likely triggered by the immense physical stress and inflammation that uncontrolled celiac disease can inflict on the entire body, including the nervous system. It makes complete sense that the specific sensory input—the pressure points of your elbows on your knees—created a temporary, distorted body map in your brain, and the fact that it ceased once you adopted a gluten-free diet is a crucial detail. Your intuition to document this is absolutely right; it's not "crazy" but rather a significant anecdotal data point that underscores the mysterious and far-reaching ways gluten can affect individuals. Your theory about sensory triggers from the feet for others is also a thoughtful insight, and sharing this story could indeed be validating for others who have had similar, unexplainable sensory disturbances, helping them feel less alone in their journey.
×
×
  • 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.