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

Only A Few Weeks In And Weary At Not Trusting What S gluten-free


Medz

Recommended Posts

Medz Newbie

I'm 6 weeks diagnosed by biopsy, and got glutened for the 2nd time this weekend. Out for lunch on Sunday I asked about every ingredient in the menu and was told what I could eat. I think the fries were probably cooked in oil that was contaminated. I spent Monday washed out with no energy and then on Tuesday morning had complete bowel emptying (sorry if TMI), which was the same as 1st time (which was due to my own carelessness) - almost exactly 48 hours later my guts reacted.

On the whole I'm not doing badly with coping, but when you're out it's a bit like roulette. Unless you go into the kitchen yourself how do you know they've got it right? I'm getting a little down at the prospect of never eating out safely again...

Plus a friend went out of her way to cook me gluten-free brownies but I think she put chocolate in that had gluten. She wouldn't have thought to check the choc when she'd sourced gluten-free flour etc. I haven't said anything as she was trying so hard.

Feeling like it's all a bit tough at the moment :(


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



Celiac.com Sponsor (A8-M):



YoloGx Rookie

Its really tough especially at first. Its best to just make and bring your own. I take a little zippered bag with blue ice in it and some munchies as well as a thermos wherever I go. You can thank your friend for the brownies and then later give them to someone else. At some point you may want to explain to her what you have to go through, or not depending on how close a friend she is.

There are a few restaurants that are aware of this kind of problem but not many. Depends on how much trouble you want to go to and if the whole restaurant thing is important to you or not. I often just eat my own food. Its possible to work with a chef and his/her crew, but it does take work and should be done ahead of time if at all possible. There are a couple of chains that feature a gluten-free menu: PF Chang and Outback. Even there though its a good idea to remind the server and cook and tell him/her you have celiac and he/she must be careful and wash hands etc.

Maggie Mermaid Apprentice

Sauces and marinades can be made with soy sauce or worchestershire sauce both of which contain wheat. Some restaurants use wheat flour as a thickener too. We always order the sauce on the side. Also learned the hard way to inquire as to whether the meat/chicken is marinated.

It's tough in the beginning, lots to remember and ask about.

You have a really great friend to be trying so hard for you. We have friends who know our situation and still bring only desserts that have gluten, they don't even bring plain old cut up fruit (how easy is that?). You can give her some gentle hints about baking gluten-free or just share them with others that can tolerate gluten.

Ahorsesoul Enthusiast

Be sure to tell the restaurant about your dinning experience with them. Either by email if they have it or by written letter. Not a point my finger letter but about how disappointed you were that some gluten was overlooked and made you sick.

Dada2hapas Rookie
I'm 6 weeks diagnosed by biopsy, and got glutened for the 2nd time this weekend. Out for lunch on Sunday I asked about every ingredient in the menu and was told what I could eat. I think the fries were probably cooked in oil that was contaminated. I spent Monday washed out with no energy and then on Tuesday morning had complete bowel emptying (sorry if TMI), which was the same as 1st time (which was due to my own carelessness) - almost exactly 48 hours later my guts reacted.

On the whole I'm not doing badly with coping, but when you're out it's a bit like roulette. Unless you go into the kitchen yourself how do you know they've got it right? I'm getting a little down at the prospect of never eating out safely again...

Plus a friend went out of her way to cook me gluten-free brownies but I think she put chocolate in that had gluten. She wouldn't have thought to check the choc when she'd sourced gluten-free flour etc. I haven't said anything as she was trying so hard.

Feeling like it's all a bit tough at the moment :(

Sorry you're experiencing this, but I've been there too. It is very frustrating to be sick, and it feels like playing russian roulette when you're just trying to eat! I'm relatively new to this and the gluten free diet, but it is wonderful to finally feel good!

Honestly, I'm one of those who used to be a bit unsympathetic towards folks with food intolerances, etc. With a background in science, I tend to discount personal accounts/observations as "anecdotal". (Ok, thanks for not calling me names!) :P This last year, I found myself with symptoms my physician couldn't seem to figure out. Having to share my own anecdotal accounts of my symptoms with him, and other specialists, I can finally relate. The conclusion is that I'm gonna have to be gluten free for life, but am still appalled at my pcp's and gastroenterologist's apparent lack of knowledge in diagnosing/treating celiac disease.

I finally got tired of getting sick 2 or more times a week trying to eat out at restaurants with gluten-free menus, so have stopped going out to eat for now. Stinks, as I'm bit of a foodie, and used to eat out (with my family) almost everyday. I also noticed that only when I am "paranoid" diligent in preventing CC at home, I don't get symptoms. Odd, isn't it? ;)

Tonight, I can say I've finally found a happy place, as I haven't been sick for a week now! Also found out (from a post on this forum yesterday) that I can have a snickers bar--my favorite candy I haven't had in months! Right now I feel great! I hate being sick, and everytime I get glutened life stinks, and then I wonder if I have a huge tumor inside.

I should mention that I'm the only one in my family of four that is gluten-free. Wife and kids are sympathetic, but I still don't trust them to fix food for me, due to cc. One day though...

Hope you feel better. Good luck! :D

tmbarke Apprentice

I know how difficult it is to have to struggle.........my coworker made a gluten free salad but didn't check the ham........I let him know and he appreciated the honesty (as he is learning and wants to include me in work parties)

I haven't dared to go to any restaurants...Maybe just for coffee talk, but even then will bring my own cup.

I thought about how I am going to miss the arby's french dip and the subway BMT or the burger king whopper jr!

But I also thought..........I can still duplicate.

I'm learning to get my hands into the baking of bread and rolls.........I can have that whole hamburger again.....and some french dip!

I live with a non gluten-free brother and so far, he doesn't mind my food - in fact, says it's easier to go to the bathroom.......(TMI....sorry)

I just found recipes to make my own noodles too........homemade chicken noodle soup with thick noodles! mmm

You can still use marinade for your own meats too - lime juice, gluten-free spices (I use italian blend) and a bit of oil with gluten-free lite soy sauce (optional).

I'm fortunate to find out that in Allendale Mich, a gluten-free restaurant will be opening up! From one gluten intolerant to another......I'm positive it will be safe......and I'll be able to eat out again!

Once you can duplicate your favorites, eating out will be just a budget buster!

Good Luck

Tena

homemaker Enthusiast
Sauces and marinades can be made with soy sauce or worchestershire sauce both of which contain wheat. Some restaurants use wheat flour as a thickener too. We always order the sauce on the side. Also learned the hard way to inquire as to whether the meat/chicken is marinated.

It's tough in the beginning, lots to remember and ask about.

You have a really great friend to be trying so hard for you. We have friends who know our situation and still bring only desserts that have gluten, they don't even bring plain old cut up fruit (how easy is that?). You can give her some gentle hints about baking gluten-free or just share them with others that can tolerate gluten.

Just a note...if you cook yourself ....Lea & Perrins


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



Celiac.com Sponsor (A8-M):



ang1e0251 Contributor

I'm sorry you had to go through that. It is tough to eat out. I'm lucky to have found a couple of local places to eat a dish or two. I can't have anything too exciting but I'm looking forward to eating at a fancy Italian place in Ft. Wayne that has a gluten-free menu. It's pricey so I'm saving up but it will be great!

You know it just takes time to accept this new lifestyle. You are going to have a time going through all the feelings you get about the changes. We have so much emotion attached to our food. I remember watching a show about gastric bypass and the woman was crying because she could not partake of most of the Thanksgiving meal. I had never considered the emotional attatchment to food, family and traditions. Now I am living that same story. After two years, I have accepted it for the most part. I'm still a little miffed about family attitudes but I'm working on that. I don't like letting someone else be in charge of my happiness.

You'll be OK and I promise it will get easier. Treat yourself with safe food but also look for personal rewards that do not involve food; buy flowers,(my personal favorite, I'm a florist!), go for a hike, play with your pet, buy that expensive perfume you've been wanting, or how about a charm bracelet and every month you are gluten-free, you add a new charm! It's a great life and we have a condition that is manageable so fight on, girl!

tmbarke Apprentice
You'll be OK and I promise it will get easier. Treat yourself with safe food but also look for personal rewards that do not involve food; buy flowers,(my personal favorite, I'm a florist!), go for a hike, play with your pet, buy that expensive perfume you've been wanting, or how about a charm bracelet and every month you are gluten-free, you add a new charm! It's a great life and we have a condition that is manageable so fight on, girl!

I love your positive outlook! Simple rewards!

I'm going to start doing that one!

As depressing as it gets...........it would be a great coping mechanism.

Kinda like "SHOPPING THERAPY!"

Medz Newbie

Thanks all for support and advice. Feeling a bit brighter about it today after I made some halfway decent gluten-free bread for lunch. I think I'm just coming down after the initial relief at being diagnosed and finally knowing what was wrong and what I could do about it, and now the reality of day-to-day living with it is sinking in a bit.

I like the bracelet idea. When I gave up smoking I rewarded myself for each successful month, so why not the same for going gluten free!

Diva1 Enthusiast
I'm 6 weeks diagnosed by biopsy, and got glutened for the 2nd time this weekend. Out for lunch on Sunday I asked about every ingredient in the menu and was told what I could eat. I think the fries were probably cooked in oil that was contaminated. I spent Monday washed out with no energy and then on Tuesday morning had complete bowel emptying (sorry if TMI), which was the same as 1st time (which was due to my own carelessness) - almost exactly 48 hours later my guts reacted.

On the whole I'm not doing badly with coping, but when you're out it's a bit like roulette. Unless you go into the kitchen yourself how do you know they've got it right? I'm getting a little down at the prospect of never eating out safely again...

Plus a friend went out of her way to cook me gluten-free brownies but I think she put chocolate in that had gluten. She wouldn't have thought to check the choc when she'd sourced gluten-free flour etc. I haven't said anything as she was trying so hard.

Feeling like it's all a bit tough at the moment :(

I feel its a bit tough for me too a this moment...just gluten free for one month doing better but its hard to eat out .its like eating with anxiety hoping that you are not going to be glutened....i guess its live and learn, I'm glat to have read your post it makes me feel better to know that I'm not alone with this

Diva

mbrookes Community Regular
I feel its a bit tough for me too a this moment...just gluten free for one month doing better but its hard to eat out .its like eating with anxiety hoping that you are not going to be glutened....i guess its live and learn, I'm glat to have read your post it makes me feel better to know that I'm not alone with this

Diva

You are far from alone, my dear. Our name is legion.

One thing... because of the very nature of Celiac Disease it will have a great deal of control over you, but don't let it take over your whole life.

Part of eating out is the social side, which I contend is necessary for mental health. The simple fact is... be as careful as you possibly can and you will still get a dose of poison occasionally. Suffer through and start again. No guilt, anger or any other negative emotion will speed your recovery, so don't waste the energy.

(Feel free to roll your eyes and call me Pollyanna. I've always been like this and don't expect I'll change any time soon)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,549
    • Most Online (within 30 mins)
      7,748

    Blough
    Newest Member
    Blough
    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.