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

Is All Inclusive Possible?


joyjoy

Recommended Posts

joyjoy Rookie

my bf and I are talking about taking an all inclusive trip soon, but I have to admit I'm pretty scared. I've never had the biopsy, but I'm very sensitive to gluten and really want to avoid it.

I went to costa rica this past summer and stuck to eating fruit from the street markets that I prepared myself, and salads when we went for dinner in restaurants. I wound up with a bad reaction to something and cut the trip short.

I'm perfectly fine with eating fruits and salad since I've been vegan for 5 years and raw vegan off and on. my main worry is that at an all inclusive place, even if there is a ton of fruit, isn't there a good chance it's contaminated??? I guess I could call ahead, but it's often hard to find someone who speaks English. :(

any tips?

I also can't pack food (I think?) we'd be flying out from Canada, and I don't think they allow fruit taken over the border.


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



Celiac.com Sponsor (A8-M):



Newbee Contributor

Are you looking at a specific all-inclusive or just wondering about all-inclusives in general? I know there is one company that arranges gluten free vacations. They will talk to the place for the group to try and ensure no contamination. I used to do all-inclusives before I was diagnosed with celiac. Now I'm too nervous to try and go there if I have to negotiate with the staff.

joyjoy Rookie

I know

mushroom Proficient

I'd kinda just like a cheap last minute trip to a place that's full of uncontaminated fruit. that's all I need to be happy!

That's not exactly an easy ask :D I have no help for you, but wish you luck on your quest. :)

Newbee Contributor

My experience with all-inclusives is stuff gets messed up that shouldn't, but if you have celiac disease (or might have it) you have to ask yourself if it is worth it to take that chance with your health. Most people don't really understand how to handle food, etc. If it is only fruit you are going to eat and you can like take an apple and clean it yourself and prepare it or something like that seems like the risk would be low. Otherwise it seems kind of risky to me. If you find something safe though, let us all know! I'd love to do an all-inclusive again.

Melissa Palomo Apprentice

I would think fruit should be pretty easy to find that would be of little risk - at least anything with a skin (cut the skin off and don't eat it?) or rinse it before you eat it? I've not found it difficult to eat fresh fruit when traveling, for myself.

I bring lots of snacks and things when I travel - and the gopicnic meals, too. Non-fruit items are easy to pack and bring with you - that's what I would do as a backup plan.

joyjoy Rookie

thanks all! I guess I should at least wait for my enterolab results before getting ahead of myself. I really hope it's negative and only a gluten intolerance. it'll be so much easier to just avoid gluten rather than trying to avoid every little molecule.

I just need a vacation!


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



Celiac.com Sponsor (A8-M):



red island Newbie

I just got back from an all inclusive in Punta Cana. I would not do it again. The restaurant we went to the first night was great, I pulled out my spanish celiac card and everyone snapped to attention. I had all the waiters coming over to check on me and the chef made me a safe dinner. However we could not get into any restaurants the rest of the week and had to eat off the buffet. I saw kids handling rolls and then picking up food and then putting it back on the platter And and people using the ladles for a pasta dish to scoop up another dish. I had taken cereal and couldnt use the milk cause there were cherrios floating in it. The rooms in my resort had no kettles or microwaves so I ended up eating steamed rice and fruit plus the snacks that I had taken for the rest of the week. I got cc'd the last night and ended up flying home in the midst of a celiac reaction (fortunately it was mild).

I would check with the resort you decide you want to go to and make sure that you can be accomodated - I was not given the opportunity to talk to the buffet manager, everyone kept blowing me off. So in the future I would go with a resort that has rooms with kitchenettes so that you have the option of making your own food in a safe enviornment.And the next time I go on vacation it will be to a much higher quality resort.

joyjoy Rookie

great advice!

I'd love to just find a place that's near a market and eat fruit all week

smsm Contributor

Wait - what am I missing? Why is fruit dangerous? How is this fruit getting contaminated with gluten? I get that a buffet can have cc but I have asked for my own tongs in the past and that has worked. Is there something else I need to know? I am nervous now - why fruit from a market? I am going to crumble from frustration at this point - is there no way for me to travel still?

red island Newbie

The fruit at a buffet can be contaminated by people handling bread etc and then touching the fruit and putting it back (I saw this happen) But I took my fruit from the back of the platter and I was fine, I only got cc'd on the last day of my vacation and it wasnt from the fruit. Also my dietician told me that if I was worried about the fruit to just rinse it off with water before I ate it. Also there were always things like bananas and oranges that you had to peel so I ate lots of those.

dmb2151 Rookie

I went to an all inclusive in the Mexico this past summer, this was before my diagnosis but I knew that something was wrong with me prior to traveling. I got MUCH worse at the all inclusive. I was getting sick every night. Mid way through the trip I kept to fruit and mostly salads but did not get any relief. I'm pretty confident looking back that it was from gluten. I think most things contained gluten, and if they didn't, they were cross contaminated. I don't think I will ever do an all inclusive again. The cost of an all inclusive is great for all that you get, but it is not worth feeling that way on your vacation.

Good luck!

joyjoy Rookie

well i guess i dont have to worry after all... my enterolab test results came back negative... maybe i'm just gluten intolerant, who knows. but it sure doesn't explain why I react to the smallest bit of gluten!

so confusing

mushroom Proficient

Ummm, tell me again why it's less important to worry about gluten if you are merely gluten intolerant. To me gluten intolerance means you do not eat gluten, period. Same as celiac. Same reaction, same misery, just no diagnosis. You may not end up with the other autoimmune diseases that go along with celiac (although there is plenty of research aimed at determining whether NCGI is part of the celiac spectrum), but it willl ruin your vacation just as surely if you eat gluten.

joyjoy Rookie

i guess i just dont know enough about it to be honest. I assumed that if it wasnt celiac and just an intolerance that I wouldnt have to worry about things like my boyfriend's chapstick and getting him to brush his teeth after a beer... so i should still do that?

I mean like, if it isnt killing the villi in my intestines, and only making me miserable, then temporary discomfort isnt as bad as permenent damage?

mushroom Proficient

I mean like, if it isnt killing the villi in my intestines, and only making me miserable, then temporary discomfort isnt as bad as permenent damage?

Well, the problem with that is that we still do not know enough about NCGI. All the research that has been done up until the last year or two has focussed on celiac disease and assumed that NCGI was insignificant. But they are now beginning to recognize it as a separate disease entity and actually research it. I suppose I approach it from the perspective of what you don't know can hurt you rather than can't hurt you, probably because I am undiagnosed (self-diagnosed) because nobody thought to test me before I thought to try it to help my RA. So I do have a couple of other autoimmune diseases which developed many, many years (say 30) after I first developed my GI symptoms, and of course I will never know if I would have tested positive 30 years ago (or even today, since there is a 20% false error rate on the testing).

I suppose only you can decide if feeling good is worth avoiding gluten for (and potentially avoiding other problems) :)

joyjoy Rookie

oh it's definitely worth it... I'm just stumped on what I have to do. I mean it stinks to have to ask my bf to brush his teeth before kissing me :(

I guess I'm still just bummed out about the whole thing

mushroom Proficient

It's perfectly okay to be bummed out :) It is a big adjustment to make. But every day it gets easier, becomes more natural, just part of the daily routine until eventually you don't even really think about it (until someone else makes an issue of it, of course) :ph34r:

  • 1 month later...
marita6 Newbie

I've just come back from an all inclusive holiday. My only advice is even if you arrange everything to do with your diet before hand. Be extra vigilant with each meal and check with the staff. Even if you end up sounding like a broken record. People forget, or they just dont care enough. It's all in your hands. Have a great trip. Good luck.:-)

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,547
    • Most Online (within 30 mins)
      7,748

    gizmo1jazz2
    Newest Member
    gizmo1jazz2
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
×
×
  • 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.