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

Avoiding Certain Places Because Of Gluten Intolerance


Rodmanj

Recommended Posts

Rodmanj Newbie

I haven't officially been diagnosed with Celiac, but I realized that I was gluten intolerant last November and have been on the gluten free diet ever since. My mom has Celiac, so I don't usually worry about whether or not there's going to be food I can eat when I'm home. However, since I've stopped eating gluten, I constantly find myself being afraid to go to certain places because I'm afraid that there isn't going to be anything for me to eat there, especially when I'm traveling. It's gotten to the point where I'm afraid to go to family functions because as understanding as many of them are about the gluten intolerance, I don't feel like they completely get it, and for the first time in my four years of college, I didn't go on a retreat with my Christian group that I looked forward to going on every year because there are so many people who go and I didn't think they would be able to accommodate me. Looking back, I get really mad at myself for missing out on these things because of my fear, and I was wondering if there was anyone else on here who gets the same way when it comes to leaving home.


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

You must take responsibility for having safe food! You cannot depend or expect others to figure it out and serve you safe food.

If you want to go on a church retreat, bring your own food. Don't expect them to " accomadate" you. Even if they tried, they probably wouldn't understand cc or that some oats are not gluten-free. Going to family functions, bring and fix your own food!

Sorry....it's time to grow-up my young friend!

Love,

Mom Karen

:D

Realized as I was typing this that this is the same stuff I am trying to tell my college son. Be responsible for yourself.

ciamarie Rookie

I think being afraid to 'stand out' or 'be different' makes it harder. However, you do need to take care of yourself but not become a hermit in the process; which is easier said than done. :)

A few years ago I went to a Women's retreat over a long weekend, and tried avoiding wheat (though I wasn't gluten-free, I was avoiding wheat...) and that was tough, but not impossible. I wasn't concerned about CC either, I just avoided the obviously wheat-filled items such as bread, pasta, etc. Since everything was served 'family style', avoiding CC would have been close to impossible, even if it came out of the kitchen gluten-free.

For something like that, even if you bring your own food, you'd have to be explaining to your table-mates why you're not sharing the food they're eating. And meal time is a big part of the social time, at least at the retreats I attended. So basically my advise would be that you'd need to get more comfortable with being different, and speaking up for yourself, asking questions, etc. That's easier if you're with people who already know you and are familiar with your 'issues'. But, you can do it! Stretch your comfort zone a bit, and it gets easier (though I'm still working on that myself).

It's possible that the retreat location has the ability to safely feed you, also. It wouldn't hurt (in future) to contact them and/or do a web search to find out if they can accommodate you, or their policy on bringing your own food, if they have a microwave you could use, etc. And, you can start a thread or do a search on here about what to look out for, what to ask, etc. when the need arises in the future.

SmnthMllrX Newbie

I know exactly how your feeling. Mainly when I travel I try and bring my own food along with me, but when staying in a hotel for a couple days and there is no refrigerator it's almost impossible. I hate going to my boyfriends family functions because his family doesn't understand and when I do bring my own food and prepare and cook it I almost always get sick from cross-contamination. I also dread going to out to eat to places that don't have a gluten-free menu because I hate trying to explain to a clueless waiter what gluten is.

I've been gluten free for about four years now and most of it gets easier, what hasn't gotten easier for me is allowing others to prepare my food. When I go away I do just as much research on what I'm going to eat as I do on the places I'm going to stay. But I'll admit that sometimes won't go places unless I'm not going to eat for a couple days. And there's no place on earth that's worth going to if I can't eat.

Rodmanj Newbie

I've been thinking about it, and the real reason why I get nervous about staying overnight at a lot of places has more to do with me being prediabetic and less to do with the gluten intolerance. Like, my blood sugar drops really low if I go too long without eating (mostly between breakfast and lunch) and since most of my family doesn't have those kinds of problems, they don't understand that when I get like that I NEED to eat something, and it's gotten worse since I stopped eating gluten because there aren't as many "regular" foods I can eat and I can't just go somewhere expecting there to be something I can eat anymore.

kareng Grand Master

I've been thinking about it, and the real reason why I get nervous about staying overnight at a lot of places has more to do with me being prediabetic and less to do with the gluten intolerance. Like, my blood sugar drops really low if I go too long without eating (mostly between breakfast and lunch) and since most of my family doesn't have those kinds of problems, they don't understand that when I get like that I NEED to eat something, and it's gotten worse since I stopped eating gluten because there aren't as many "regular" foods I can eat and I can't just go somewhere expecting there to be something I can eat anymore.

Exactly, ! You have to bring something with you at all times, in case you need it. I keep packs of nuts in my purse or car. Always. Then you just take them out when you need to eat without waiting for someone else to find you something.

There are plenty of "Regular " foods you can eat. I just wouldn't trust others to keep them safe for us. You can get little packets of peanut butter or almond butter and eat them straight from the packet if needed.

cavernio Enthusiast

I know you have the best of intentions Karen, but telling someone its time to 'grow up' because they're unsure of how to deal with all the socialness around eating food is, ummm, well...Let's just say Rodmj could be a diagnosed 50 year old who was asking the same question. That he's concerned is the sign of maturity.

I'm not diabetic, but if I were I think I'd take to carrying around food with me at all times regardless of being a celiac. Carrying around food seems like the only option for you. And sure you won't always have access to a fridge, so it might be important to take to carrying around a merse or something that you can put fruit, carrot sticks, or nuts in, or other gluten-free snacks you can think of/find.

CC is going to be an issue pretty much all the time anywhere you go. As to your retreat, I'm not sure how it all works, but if it were me (well, I might not have gone like you if it were me!) and I went, I'd probably bring a bag of apples and only eat that all weekend.

I'm going to be going to a family BBQ in a month's time, and my mother-in-law, concerned as she is, wants to make something I can eat. She gave me a great idea that I'm currently using at home with my old pans. Aluminum foil. If I bring my own gluten-free food that needs to be cooked, I can just stuff it the foil and use the same BBQ no problem. (Although I really don't want to make an issue of it for 1 meal whatsoever, and just eat before I go and not eat when I'm there. But then people will feel bad for me and be start asking what they can get me, and it will be more awkward and a nuisance than if I just bring my own damned burger and bun.)


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



Celiac.com Sponsor (A8-M):



sallyalewis Rookie

I understand completely. I've been gluten free since February 2012, which isn't that long, and am headed on vacation with my parents and my sister's family. Instead of looking forward to a week at the beach, I've been worried about what was I going to eat, and what if I gluten myself? Also, I have quite a few allergies and I'm worried about being allergic to any sunblock I try, the ocean water making me break out, the pool chemicals ect....

I have googled local "Health Food Stores in the area and contacted them to ask if they are open, and if they carry the items I'll be needing.

I've been testing sunblock this week.

I'm trying to look forward to the fun, but know someone will say "You're allergic to SOMETHING else?!"

Good luck! :)

nvsmom Community Regular

I know this is even more of a hassle, but I find bringing extra food to share makes a slightly different diet less of an issue. I've been doing that for my "picky eating" kids for years. People are less likely to notice their pickiness when they are eating something that everyone else is.

Best wishes.

Cara in Boston Enthusiast

Check out the meals from GoPicnic. They are sort of like "lunchables" but shelf stable and they have several gluten free options. They are small and compact so they are easy to travel with and keep in your car or office. Not super healthy, but not too terrible. We use them for travel and my son keeps one at school in case he forgets his lunch.

Aside from that, we bring our own food to every event. I usually bring a dish to share and pack a complete meal for me and my son.

Cara

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,857
    • Most Online (within 30 mins)
      7,748

    LowellFrancis
    Newest Member
    LowellFrancis
    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

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
×
×
  • 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.