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

Anxiety About Travelling Over The Holiday


gluten Tag

Recommended Posts

gluten Tag Rookie

Hi everyone! I'm new here and new (2.5 wks) to gluten-free.

I'm having some anxiety. I've just gone gluten-free and it feels pretty manageable in my home because I have a lot of control.

We are supposed to travel at the holidays to my in-laws in NY (we live in MA). I am really nervous about all this because

1) Im afraid of getting sick

2) Im just getting the hang of food and have still managed to gluten myself once. :lol:

3) I feel almost apologetic in going to someone elses house...like I don't want them to have to make concessions on my behalf. :(

4) Celiac Disease, in general, just makes me feel so self-concious. You know? Like I stick out because I am eating something different.

Does anyone have any suggestions or tips of what I could do to make this season a little more bearable? TIA.


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



Celiac.com Sponsor (A8-M):



MaryJones2 Enthusiast

Your anxiety will improve over time as you become more comfortable with the diet and dealing with situations like this. Since you are new to this I would recommend taking all of your food or preparing your food when you get there and make it similar to what everyone else is eating. It's pretty hard to accurately explain to someone else how to cook gluten-free food in their kitchen when you are just learning yourself without creating stress for you and the host(ess). Over time everyone will get used to you having different food and it won't be so uncomfortable.

Lori T. Newbie
Hi everyone! I'm new here and new (2.5 wks) to gluten-free.

I'm having some anxiety. I've just gone gluten-free and it feels pretty manageable in my home because I have a lot of control.

We are supposed to travel at the holidays to my in-laws in NY (we live in MA). I am really nervous about all this because

1) Im afraid of getting sick

2) Im just getting the hang of food and have still managed to gluten myself once. :lol:

3) I feel almost apologetic in going to someone elses house...like I don't want them to have to make concessions on my behalf. :(

4) Celiac Disease, in general, just makes me feel so self-concious. You know? Like I stick out because I am eating something different.

Does anyone have any suggestions or tips of what I could do to make this season a little more bearable? TIA.

Food is the toughest. Am still struggling too after 2 years but getting better at dealing with this part of the diet. Just wrote to another member with some of the same advice to you. Bring your own or look up stores too that are in the area and find gluten-free guaranteed safe prepared foods to take. I also have asked the hostess, especially family, what they are making and try to duplicate a plate of a few of the items to take for myself. Most of the holiday foods in a family are the same as what you would make for your family at home anyway, it is outside parties that can be the challenge. Offer to make a dish that you can eat but that everyone else can eat too. If they don't know you are gluten-free, they will never know. Just watch the serving spoons. Bring a serving spoon for your dish so that hopefully you won't get others mixing spoons and contaminate the dish. If you are staying for a period of days, try the web for local stores to buy some safe stuff for you. Do not know where in NY you are going, but I am in NY upstate, about 40 minutes from NYC and if you want, write back to monkeybusiness@hvc.rr.com and I can help you with stores near here. Good luck. This part DOES get better once used to it.

henny Explorer

I know how you feel!

I don't have any advice, other than be good to yourself. I'm still figuring out all this stuff myself and being shy does not help at all.

I love your username. Spreken sie Deutsch?

ang1e0251 Contributor

I've been on the diet for a year and I certainly felt exactly like you in the beginning. But after going to a couple of events and sitting very hungry, I promised never to put myself through that again. Last Saturday, we were invited to my sister's in law's T'gvg. Most people I've met but I not to where I want to explain my medical history. I told my sister I would be taking my own food. She started to argue that the turkey would be ok for me but I said in a few words that CC was going to be a problem. She didn't argue. I did take my own food. First I went through the line and found a few foods I could eat. Those satisfied me, I had eaten a snack before I went, and I ended never taking my own food out. It was a very nice time.

I would take or buy your own food and don't apologize if you decide to eat it. Just do it quietly and most people won't say anything, some won't even notice. I went to a flower show and brought out my own food. Another florist asked me about it and I explained, very short version, why I brought it. He asked my symptoms and I only said they are mostly digestive and not proper to mention here at the dinner table. He very kindly said he would rather eat what I had brought. Then the conversation changed and no more was said.

Most situations are going to hinge on your attitude. If you are casual about it and not upset, others will usually follow your lead. I usually don't feel the need to explain in depth to strangers but family I will tell as much as they are ready to listen to. Remember, your health, your choice.

Good luck on your trip and I feell confident it will all go well.

missy'smom Collaborator

If you can look up and find the local/area support group, they can be a good resource. They usually don't mind if people from out of town call or e-mail to ask questions about local shopping or dining. If they have a website, they may provide that kind of info. there.

gluten Tag Rookie

Thank you everyone for your replies. I don't know how long threads stay around here but if it's still around, I'll post in a couple of weeks and let you know how it went.

My in-laws are a bit sheltered. I think I'm the only person they know who has ever been allergic. To anything. :rolleyes:


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



Celiac.com Sponsor (A8-M):



blueeyedmanda Community Regular

If you are traveling through Upstate NY and you can stop at a Wegmans that is celiac heaven. They stock lots of gluten free products plus label all their house brand gluten free if it is.

gluten Tag Rookie
If you are traveling through Upstate NY and you can stop at a Wegmans that is celiac heaven. They stock lots of gluten free products plus label all their house brand gluten free if it is.

Thank you so much. I have a feeling there may be a Wegmans in LI.

Takala Enthusiast

If it's just a short casual get together, I just eat beforehand and bring a snack and drink water- and talk, I'm there for the socializing, not the food, and I don't think anybody minds. I accept that this is what I am, and this way I don't have to worry about eating something with gluten accidently. My metabolism is such that if I eat a high protein and fat meal before I go anywhere, I don't get hungry for hours anyway.

If I do bring a main dish or dessert item it's something gluten free. It's easier to just put mine on a plate/bowl beforehand and pack that. I find the shortest answers are the best, if I feel like explaining anything, I just say "oh, allergies, this way I can enjoy myself and not think" and get on with it.

Well, yeah, technically this isn't correct, but I do have a lot of allergies, so it's not exactly being mistruthful, but the average person grasps that "allergy" word much more quickly than "oh, I have a form of gluten intolerance auto immune reaction that results not in my getting sick right away, but instead I don't want to have neurological symptoms like ataxia next week. " :blink:

My goals are simple- I just want to eat stuff that works for me without it being a big drama. The host may just want their cooking praised. This is what omnivore spouses are for. :lol:

We have a travel bag stocked with non perishable gluten free goodies we just throw in the car whenever we go anywhere.

In laws and family can be particularly, ah, tricky, because the other part of acceptance is that you have to accept a lot of them just won't "get" it and will not be able to grasp the concept- research shopping before you go, and pack as much as you can and be as self sufficient as you can.

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. - Florence Lillian replied to Florence Lillian's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      4

      Gluten-Mimicking Proteins that can affect some Celiac individuals.

    2. - trents replied to HectorConvector's topic in Related Issues & Disorders
      326

      Terrible Neurological Symptoms

    3. - knitty kitty replied to HectorConvector's topic in Related Issues & Disorders
      326

      Terrible Neurological Symptoms

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

      Gluten-Mimicking Proteins that can affect some Celiac individuals.

    5. - Scott Adams replied to HectorConvector's topic in Related Issues & Disorders
      326

      Terrible Neurological Symptoms

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

    • Total Members
      133,629
    • Most Online (within 30 mins)
      7,748

    EssexMum
    Newest Member
    EssexMum
    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

    • Florence Lillian
      Hi Scott: A wonderful, thoughtful explanation. Controlled human studies would be very interesting and quite informative. I have been eliminating certain foods and have narrowed it down considerably. Having other autoimmune diseases along with Celiac has become rather challenging. I appreciate your input, thank you. All the best, Florence
    • trents
      Hector, have you had a follow-up biopsy to check the progress of small bowel villous lining recovery after going gluten free?
    • knitty kitty
      @HectorConvector, Please try adding Niacin to your supplements.  Low Niacin has a connection with suicidal ideation.  Been here, done that.  Niacin made me feel better mentally and physically.  Omega Three fats will help, too. For pain, Thiamine, B12 and, Pyridoxine B6 have been shown to have analgesic effects when taken together.  I know this works because I've cracked some vertebrae and this combination relieves the pain.  I was prescribed opioids, but couldn't function or poop, so... I can highly recommend these vitamins for pain relief.   I adopted a paleo diet, the Autoimmune Protocol Diet which has been shown to improve intestinal health.  Improving intestinal health improves mental health because of the gut brain-axis.  Important neurotransmitter Serotonin is made in the digestive system.   Please Read... Association between dietary niacin intake and suicidal ideation: mediating role of C-reactive protein https://pubmed.ncbi.nlm.nih.gov/40859220/ Mechanisms of action of vitamin B1 (thiamine), B6 (pyridoxine), and B12 (cobalamin) in pain: a narrative review https://pubmed.ncbi.nlm.nih.gov/35156556/
    • Scott Adams
      Hi Florence, thank you for clarifying — and no worries at all about late-night writing. I appreciate you explaining that you’re specifically asking about gluten cross-reactivity, particularly the proposed immune cross-reaction between alpha-gliadin and certain non-gluten foods on a gluten-free diet. It’s an interesting and often confusing topic. The Vojdani & Tarash paper you mentioned did report antibody cross-reactivity in laboratory settings, which has led to a lot of discussion in the gluten-free community. However, it’s important to note that in-vitro antibody reactions (in a lab dish) don’t always translate into clinically meaningful reactions inside the human body. At this point, major celiac research centers generally conclude that true immune cross-reactivity to non-gluten foods in people with celiac disease hasn’t been clearly demonstrated in well-controlled human studies. That said, many individuals do report symptoms with foods like corn, dairy, oats, or others, and those reactions can absolutely be real — they just may involve different mechanisms, such as food intolerance, FODMAP sensitivity, separate immune responses, or individual gut permeability differences rather than molecular mimicry of gliadin specifically. If certain foods consistently trigger symptoms for you, keeping a structured food and symptom log and discussing it with a knowledgeable gastroenterologist or dietitian may help clarify patterns. It’s a nuanced area, and your question is thoughtful — we just have to separate what’s biologically plausible in theory from what’s been conclusively demonstrated in patients.
    • Scott Adams
      I’m really sorry you’re dealing with such intense burning pain right now. When symptoms get that overwhelming, it can feel unbearable and even trigger really dark thoughts, and that’s a sign of just how much you’ve been carrying — not a sign of weakness. It makes sense that you’d want to go back to a lower-carb, meat-and-vegetable approach if that’s helped reduce symptoms before; sometimes dialing things back to simple, whole foods can calm inflammation or gut irritation. At the same time, your safety and mental health matter just as much as the physical symptoms. If the suicidal thoughts are feeling strong or hard to control, please consider reaching out for immediate support — in the U.S., you can call or text 988 for the Suicide & Crisis Lifeline, or go to the nearest emergency room if you feel at risk. You don’t have to handle this alone. It may also be worth checking in with your doctor soon to review what’s changed and see if there are adjustments or treatments that could ease the burning pain more effectively. You deserve relief, and you deserve support while you figure this out.
×
×
  • 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.