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

The Unwanted Mystery Ingredient From Eating Out


Starving Amy

Recommended Posts

Starving Amy Rookie

I'm new to this game of minding gluten and eating out and dealing with "gluten free" things from sources behind a door. 

 

A month ago I thought my gluten free pasta made me sick from some sort of contamination. 

Turns out, I just don't handle quinoa well. That mystery is solved.

 

Today I had a full day of eating out. I am now broke, no moolah, and feel like poop. 

 

I had a "Pacific Love" shake from some juicer in DTLA. The only things in it that might have made me sick would be the royal jelly. I have read sometimes royal jelly is packed with gluten powder or capsules. I also added a "plant based protein." Perhaps it's quinoa based. I wrote for the answers. Here's to hoping they'll tell me. 

 

I felt unnaturally full after drinking that shake. That's usually a precursor to an episode but that feeling eventually passed leaving me feeling OK. But, again - I can't really be too sure as my symptoms come up and then hide themselves before returning. My flare-ups can be tricky to follow.

 

What I think is most likely the issue is an overpriced dinner I got bamboozled into having with friends at some spot in DTLA that's supposed to be all the things I'd want - vegetarian, vegan, gluten free… I had potato croquettes that were ordered for the whole table. I asked the waitress if they're gluten-free and she said, yes. I just looked at the menu at home and it says they also have "salted cod?" It was just a potato ball lightly fried with what seemed like light cheese inside… so this might be a problem. For the main coarse I ate a Brazilian chicken stew with okra served with polenta and black beans… nothing seems gluten about the meal - it wasn't even a stew… HEH... but …. ugh. I feel like I just walked into a pool of allergy causing hell. 

 

I wrote them too and told them I am pretty sick after my trip to their restaurant. I usually find most restaurants don't have the decent to write me back. I am always very courteous in my initial email so IDK.

 

So lame. I'm getting fearful of restaurants and angry at their owners. 

 

Does anyone else go through this? Can you share your experiences?

 


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

I avoid going out. I have sustained a lot of damage from celiac disease (anemia, fracture, etc) and I have another year or so to heal. I do not need any set backs. Does not mean that I can not go out and have fun. I attended a university basketball game with friends. I ate before I went, we went for dinner and then I treated myself with a bag of chips. Did I miss out? No! I had a blast with my friends ( and our team won!)

Keep a Go Picnic box in your car at all times to avoid breaking down and ordering foods that you have not researched.

glutenfreeliac Collaborator

For various reasons, I eat out quite a bit more than I'd like (if I had my way, I'd live in my kitchen. Alas.). I super-careful about ingredients, and ask a lot of questions. Since you ate at several different places and had a variety of foods, it's hard to say what may have caused the problems. If the croquettes were gluten-free (which I find odd, but maybe it was that kind of restaurant), it's possible there were seasonings on the food that were not. 

 

I tend to haunt restaurant websites, and, if necessary, I call during non-peak hours to discuss the menu in advance. If that's not possible, then I make it clear with every person I encounter that I'm gluten free. 

 

I've eaten out at many DTLA places, and have generally had great experiences. I say generally because, yeah, sometimes the food is way too pricey and the restaurants way too crowded. 

Starving Amy Rookie

For various reasons, I eat out quite a bit more than I'd like (if I had my way, I'd live in my kitchen. Alas.). I super-careful about ingredients, and ask a lot of questions. Since you ate at several different places and had a variety of foods, it's hard to say what may have caused the problems. If the croquettes were gluten-free (which I find odd, but maybe it was that kind of restaurant), it's possible there were seasonings on the food that were not. 

 

I tend to haunt restaurant websites, and, if necessary, I call during non-peak hours to discuss the menu in advance. If that's not possible, then I make it clear with every person I encounter that I'm gluten free. 

 

I've eaten out at many DTLA places, and have generally had great experiences. I say generally because, yeah, sometimes the food is way too pricey and the restaurants way too crowded.

Thanks for the suggestion of calling these places and asking them beforehand. It would be good to know just how serious they take people's illnesses.

I got a response from the juicer and it turns out they're using a protein powder that claims it's gluten free but its main bulker is brewer's yeast. So there's that. It says it's a vegetable based protein powder too but it has quinoa in it… Which I would consider a seed or grain. SO there's that too. I had a pretty uncomfortable reaction to it. The protein powder in question is called Garden of Life. I wrote them and told them I had a reaction to their product and it was probably the brewer's yeast. Very uneducated/dishonest of them.

As far as the croquettes and the food at Wood Spoon, we'll see. The place is the atypical highly rated, only because it's the fashionable hipster thing to do, hole in the wall. The boundless lemming reviews do not reflect what it really is. I do question everything I ate from them. I usually don't in the DTLA area but this place, who can't be bothered to have a real website, an email to write and discuss, a Facebook page, or to even have a functioning front house and wait staff - concerns me. I need to be better about not eating places where my friends think I should go. I just feel like I need my confirmed tests to hold in hand and smack them with while saying, "No - bad friend." ;p

 

I avoid going out. I have sustained a lot of damage from celiac disease (anemia, fracture, etc) and I have another year or so to heal. I do not need any set backs. Does not mean that I can not go out and have fun. I attended a university basketball game with friends. I ate before I went, we went for dinner and then I treated myself with a bag of chips. Did I miss out? No! I had a blast with my friends ( and our team won!)

Keep a Go Picnic box in your car at all times to avoid breaking down and ordering foods that you have not researched.

Yea after I finally get the tests done, I'll know how bad I am. My tested and confirmed gluten intolerant friend thinks I may have extensively hurt my intestines because of my other allergies and the intensity I am experiencing symptoms, now. She says if you go long enough the damage can trigger a litney of other issues. So, we'll see. If I have to eat indoors - fine. I'll save money and such. I usually take a bag of food with me but I also do not have a car, I share my sigother's so having a go box isn't always an option for me.

Gemini Experienced

Amy...brewers yeast and quinoa are gluten free. Ditto for royal jelly but as always, labels need reading or more questions need to be asked. It sounds like you need more food education before venturing out to eat.  Anything done as a croquette generally has breadcrumbs on the outside and probably were fried in a shared fryer.  Unless you asked specific questions about the stew you had, it may or may not be gluten free but I have never seen any stew in a restaurant that was gluten free. 

 

There is nothing wrong with a restaurant that does not have a website or a Facebook page. You can always pick up the phone and call them to speak to them directly about your food needs. Direct contact is better anyway. I know that can be challenging for the younger crowd but the world does not revolve around Facebook and the internet.  Once you learn how to question waitstaff and learn food ingredients, plus allow time for healing your GI tract, eating out becomes much easier.

KCG91 Enthusiast

My tactic if I have to eat out is always, always email the place in advance. I wouldn't arrive 'unannounced' and expect to eat safely (and I actually sent something back once because I wasn't happy with how they prepared it... I never thought I'd have the guts to do that)

 

I prefer email because I can make sure I ask all the questions I need to, and they can take the time they need to get the answers and come back to me. I usually say something like 'please can you tell me about how you prevent cross contamination in your kitchen' - leaving it open so they can show how much they do (or don't) know about it. I've had some really good responses (and subsequent good meals) this way - there are a few places I'd like to try that haven't replied but I'm going to follow them up with a phonecall I think. 

KCG91 Enthusiast

Just unravelled the comment above mine - count me out. 
 

[Edit: which has since been removed]


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



Celiac.com Sponsor (A8-M):



Starving Amy Rookie

Yea - I too do my research before. This, unfortunately, was a - "Hey I'm in town NOW…" no forewarning situation.  I really wish people were more considerate and let me know in advance when they were coming. 

 

But again - I really also worry about being a stick in the mud for everyone around me, too. I don't mind going somewhere everyone wants to eat as long as there's a salad, at least. I think going out to eat is just tricky. In the normal person's world, with healthy GI's, it's generally not one of those activities they plan out with much advance notice. 

 

As a former waitress I think the real issue is having respect, as a restaurant owner/staff, for health issues. It's like the nut allergy example. Everyone goes out to eat and should have that luxury. If you know you're serving people - you know they aren't all identical and that some have serious allergies. I have worked with two kinds of wait staff… ones who don't care about their customer's health and, imo, should be fired. and one's who understand and respect their customer's illness. If someone tells you they're allergic to nuts you better darn well be ready to serve that person or be able to say, I am sorry. No room for a mistake there. It's also a lot like a bartender serving coke when someone specifically asks for diet coke… if you ignore it and serve coke - and they're diabetic. Then you very well might kill someone. 

 

I know it's good to be on the defense in restaurants, I am learning the strategies, but I definitely think the ones who have no respect for their customer's should be weeded out too. It's beyond a matter of principal when there are real dangers on the line. 

 

 

 

My tactic if I have to eat out is always, always email the place in advance. I wouldn't arrive 'unannounced' and expect to eat safely (and I actually sent something back once because I wasn't happy with how they prepared it... I never thought I'd have the guts to do that)

 

I prefer email because I can make sure I ask all the questions I need to, and they can take the time they need to get the answers and come back to me. I usually say something like 'please can you tell me about how you prevent cross contamination in your kitchen' - leaving it open so they can show how much they do (or don't) know about it. I've had some really good responses (and subsequent good meals) this way - there are a few places I'd like to try that haven't replied but I'm going to follow them up with a phonecall I think. 

kareng Grand Master

Just unravelled the comment above mine - count me out. 

 

[Edit: which has since been removed]

 

 

It was inappropriate and removed.  Thank you for your thoughtful comment..

anti-soprano Apprentice

We are different, as celiacs.  This dilemma of going out with friends on the fly will always exist for us.  It will take time to figure out how you will deal with it.  Personally, I choose to put the focus on being out with friends.  It was difficult at first, eating plain rice at the Japanese restaurant, or just having a soda at the pizza place that doesn't have anything for me.  But I prefer NOT to dictate the restaurant choice when going out with large groups.  I just make do and enjoy the conversation- which really is more important.  It's not going to kill me and I can always get something later by myself.  I will always put my health above taking chances.  If the wait staff doesn't seem knowledgable or the restaurant doesn't look to offer anything I can eat, I simply don't eat.  Don't get me wrong- food is important to me.  I have broken down in tears after attending a business meeting involving dinner when I made arrangements weeks in advance in order to eat safely.  They had no idea and wanted me to go through the buffet and get whatever looked like it was gluten free.  Tears or rage!!!  It's not always a walk in the park.  But this is what we've got and some people have got it worse!

 

Ultimately, you are in charge of your health.  You can't depend on others and I wouldn't recommend asking merely "Is this gluten free?"  More pointed questions may be needed and lots of people ask to see ingredient lists.  You can eat mostly at home, but I don't think that will necessarily teach you what questions to ask- although it will allow you to heal and won't expose you to possible damage.  It's a learning process and you will determine your own limits and boundaries.  

 

Good Luck!

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. - Mari replied to Jmartes71's topic in Related Issues & Disorders
      21

      My only proof

    2. - Jmartes71 replied to Jmartes71's topic in Related Issues & Disorders
      21

      My only proof

    3. - knitty kitty replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      44

      Supplements for those Diagnosed with Celiac Disease

    4. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      21

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,545
    • Most Online (within 30 mins)
      7,748

    PatientOne
    Newest Member
    PatientOne
    Joined

  • Celiac.com Sponsor (A20):



  • Celiac.com Sponsor (A22):




  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • Mari
      I think, after reading this, that you areso traumatized by not being able yo understand what your medical advisors have been  what medical conditions are that you would like to find a group of people who also feel traumatized who would agree with you and also support you. You are on a crusade much as the way the US Cabinet  official, the Health Director of our nation is in trying to change what he considers outdated and incorrect health advisories. He does not have the education, background or experience to be in the position he occupies and is not making beneficial decisions. That man suffered a terrible trauma early in his life when his father was assonated. We see now how he developed and worked himself into a powerful position.  Unless you are willing to take some advice or  are willing to use a few of the known methods of starting on a path to better health then not many of us on this Celiac Forum will be able to join you in a continuing series of complaints about medical advisors.    I am almost 90 years old. I am strictly gluten free. I use 2 herbs to help me stay as clear minded as possible. You are not wrong in complaining about medical practitioners. You might be more effective with a clearer mind, less anger and a more comfortable life if you would just try some of the suggestions offered by our fellow celiac volunteers.  
    • Jmartes71
      Thus has got to STOP , medical bit believing us! I literally went through 31 years thinking it was just a food allergy as its downplayed by medical if THEY weren't the ones who diagnosed us! Im positive for HLA-DQ2 which is first celiac patient per Iran and Turkey. Here in the States especially in Cali its why do you feel that way? Why do you think your celiac? Your not eating gluten so its something else.Medical caused me depression. I thought I was safe with my former pcp for 25 years considering i thought everything I went through and going through will be available when I get fired again for health. Health not write-ups my health always come back when you're better.Im not and being tossed away at no fault to my own other than shitty genes.I was denied disability because person said he didn't know how to classify me! I said Im celiac, i have ibs, hernia, sciatica, high blood pressure, in constant pain have skin and eye issues and menopause intensified everything. With that my celiac nightmare began to reprove my disregarded disease to a bunch of clowns who think they are my careteam when they said I didn't have...I feel Im still breathing so I can fight this so no body else has to deal with this nightmare. Starting over with " new care team" and waisting more time on why I think I am when diagnosed in 1994 before food eliminated from my diet. P.s everything i went through I did write to medical board, so pretty sure I will continue to have a hard time.
    • knitty kitty
      @Scatterbrain, Thiamine Vitamin B1 and amino acid Taurine work together.  Our bodies can make Taurine from meats consumed.  Our bodies cannot make Thiamine and must consume thiamine from food.  Meat is the best source of B vitamins like Thiamine.   Vegetarians may not make sufficient taurine since they don't eat meat sources of taurine.  Seaweed is the best vegetarian source of taurine. Vegetarians may not consume sufficient Thiamine since few veggies are good sources.  Whole grains, legumes, and nuts and seeds contain thiamine.  Many of these sources can be hard to digest and absorb for people with Celiac disease.   You may find taking the forms of thiamine called Benfotiamine or TTFD (tetrahydrofurfuryl disulfide) and a B Complex will give the benefits you're looking for better than taurine alone.  
    • knitty kitty
      @Jmartes71, I went to Doterra's site and had a look around.  The Doterra TerraZyme supplement really jumped out at me.  Since we, as Celiacs, often have digestive problems, I looked at the ingredients.  The majority of the enzymes in this supplement are made using black mold, Aspergillus!  Other enzymes are made by yeast Saccharomyces!  Considering the fact that Celiac often have permeable intestines (leaky gut syndrome), I would be very hesitant to take a product like this.  Although there may not be live black mold or yeast in the product, the enzymes may still cause an immune system response which would definitely cause inflammation throughout the body.   Skin, eyes, and intestines are all made from the same basic type of cells.  Your skin on the outside and eyes can reflect how irritated the intestines are on the inside.  Our skin, eyes, and intestines all need the same vitamins and nutrients to be healthy:  Vitamin A, Niacin B3 and Tryptophan, Riboflavin B2, Biotin B7, Vitamin C, and Omega Threes.  Remember that the eight B vitamins work together.  Just taking high doses of just one, vitamin like B12, can cause a deficiency in the others.  Taking high doses of B12 can mask a Folate B9 deficiency.  If you take B12, please take a B Complex, too.  Thiamine B1 can be taken in high doses safely without toxicity.  Thiamine is needed by itself to produce energy so every cell in the body can function, but Thiamine also works with the other B vitamins to make life sustaining enzymes and digestive enzymes.  Deficiencies in either Niacin, Vitamin C, or Thiamine can cause digestive problems resulting in Pellagra, Scurvy, and Gastrointestinal Beriberi.   If you change your diet, you will change your intestinal microbiome.  Following the Autoimmune Protocol Diet, a Paleo diet, will starve out SIBO bacteria.  Thiamine keeps bacteria in check so they don't get out of control as in SIBO.  Thiamine also keeps MOLDS and Yeasts from overgrowth.   Menopause symptoms and menstrual irregularities are symptomatic of low Vitamin D.   Doctors are not as knowledgeable about malnutrition as we need them to be.  A nutritionist or dietician would be more helpful.   Take control of your diet and nutrition.  Quit looking for a pill that's going to make you feel better overnight.  The Celiac journey is a marathon, not a sprint.   "Let food be your medicine, and let medicine be your food."
    • RUKen
      The Lindt (Lindor) dairy-free oat milk truffles are definitely gluten-free, and (last time I checked) so are the white chocolate truffles and the mint chocolate truffles. 
×
×
  • 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.