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

Restaurant Eating...is It A Possibility?


jewlr22

Recommended Posts

jewlr22 Newbie

Hello out there....

I am recently diagnosed with celiac through the blood tests...I have not been "scoped", or biopsied yet due to the fact that I have medicaid and it is very difficult to find a Dr. that will perform the procedure. I guess they don't pay enough.....Anyway...I am trying like heck to eat right, but I feel like such a downer on my family-we used to eat out all the time, not just junk food, but real food too, and now everything has changed....I am wondering first of all if there are any reccommendations anyone has to how you eat out or where to eat out and I am also wondering about putting the whole family (2- 10 year old sons and a wonderful dad ) on a gluten free diet. I am just concerned about their tastes---any suggestions there too??

I am starting to go into the depression I have heard goes along with such a drastic change in life, and really could use some support.

Thank you for listening........


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



Celiac.com Sponsor (A8-M):



bscarter46 Newbie

Hi jewlr22. I am not yet diagnosed but my doctor thinks I may also have celiac disease. I had both antibodies come back positive but the endomysial was negative. I'm still waiting on a call back from my doctor to see what this means. I have been reading a lot on this and I think there is a board about eating out and also you can go to the restaraunts websites and some have gluten-free menu's. The places so far that I have found with online gluten-free menu's are Wendy's, McDonalds, Outback Steakhouse, Chili's, Chik-fil-A, Steak N Shake and Burger King(has I think items containing wheat on their nutrition menu, not an actual gluten-free menu). If I do go on the diet my husband already says he will go on it with me. I think someone mentioned it is healthier than any diet. I am currently in a depression because it has been two years and even though I feel closer to finding out what is wrong with me, I also feel like we will never find out. I guess with the high antibody levels that I at least have a gluten intolerance, if not celiac. I hate the thought of going on the diet, but at least it is an answer and will get easier with time. Good luck and even though I don't know much, I hope I helped you some! Take care!

Guest jhmom

HI, if you have been dx through blood-work then there is really no reason to be scoped, you should be adhereing to a strict gluten free diet for life. For me I only eat at restaurants that offer a gluten-free menu because you never know what kind of spices are used or if they marinate their meats.

Here on the board there is a section "gluten-free dining and eating out", there are a lot of posts about certain restaurants that serve gluten-free meals and also posts in certain States.....

Here are some websites where you can look at gluten-free menus

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

Also I have heard PH Changs has a gluten-free menu

Guest gillian502

I wouldn't suggest eating out until all your symptoms have vastly improved and your antibodies have become normal. This will probably take 6 to 12 months, but I feel it's worth it. The less suspicious foods you eat, the faster you will heal. I've read that a lot of people here are comfortable eating at places like Wendy's and McDonalds...personally I wouldn't touch those places with a ten foot pole. I don't believe for one second that places like that are careful with cross-contamination issues; for goodness sake, there's teenagers running them! I would also say get the biopsy, just to confirm your diagnosis so you won't be fending off the drs. all your life telling you to just get one already, because they will do that.

hapi2bgf Contributor

I used to eat out a couple of times a week before celiacs and now I do not eat out as much - but I do go. For me and the people I know, eating out is as much a social activity as it is just getting a meal. In my own opinion, I will not let this diet force me to never eat out again. On that same note, I am very careful about where I go and what I eat, and when I go on trips I pack A LOT of gluten-free foods. But everyone has to make the decision about how to make this diet work for them and their life style.

Here's what I did when I was diagnosed. Maybe some of it will appeal to you.

1. Learn as much about the diet as you can and be able to explain it to someone who has no idea such a crazy disease ever existed. Be able to laugh about the disease - it puts the other people at ease.

2. Call you favorite restaurants between 2 and 4pm when they are slower and ask to speak with a manager. Ask if they have time now to talk to you about food allergies. Explain that you used to eat there regularly and your family really enjoys the food. You are trying to find one or two menu items that you can eat. Ask for plain non-marinaded meat with no seasonings, etc. Generally the managers have been extremely helpful to me. I have had managers pass me off to the regonal manager when they did not know the answers. And I have managers stand in the fridge and read lables.

3. Realize that eating out will be a bit boring compared to what you used to eat.

4. If in doubt of a restaurants ability to handle your diet (when you have no choice in where you are eating) bring a hot baked potato, cooked meat to add to a plain salad, and any dressing or condiments you might need. I stuff quite a bit in the diaper bag :P

Another concern is figuring out which family and friends want to learn how to cook something gluten-free and which ones just have no intention of dealing with it. To date, my friends are doing great cooking gluten-free and my family has no intention of dealing with it. So be it. I eat first or bring my own food to family events and make myself at home in their kitchen.

Best of luck!

  • 2 months later...
snoopini Newbie

Although there are places that have gluten-free menus, please be aware that they DO NOT always practice safe food handling. Subway for example does not wash their knifes after cutting rolls, plus the amount of crumbs around that place make me gag!! I frequent my local Outback BUT that was only after writing a very nasty letter to Outback after receiving croutons in my salad , or finding crumbs at the bottom of the bowl after eating my salad - SIX times this happened to me. I have spoken to the proprietor and he now knows that the food must be handled separately. Most people think that if we eat a little bit of gluten that's it's like being lactose intolerant. People think that you will have an upset stomach and that's it's not a big deal. Remember that ignorance is bliss, we are the ones who will be sick for a week, not them, they have no idea what it's like. I was also told by one of my local italian restaurants that I could bring my own pasta and eat their sauce, BUT after further investigation, I found out they use broth in their sauce which the chef had no idea had gluten in it. It's hard to eat out. I go to my local Wendys alot because their chili is supposed to be gluten free but if I go to the Wendys by my work I get sick...it's sad how many foods are gluten free but the handling of the food makes you sick. Just make sure the people know that nothing can touch the food as well, rinsing utensils isn't enough. I still have to remind my family of this as well!! Good luck! I'm sick today for some unknown reason....and my whole house is gluten-free!!

dkmb Newbie

With eating out you need to be pro-active and let the place you plan to eat at know your concerns. There are many posts as mentioned, on here about calling ahead, talking to the chef, and some people carry cards that tell about celiac disease.

My granddaugther just had a wonderful experience at the Jungle (like Chuckie Cheese). Her aunt called ahead and they said she could bring her own food. They brought a pizza with them on aluminum foil. The Jungle heated it up for her with a note that it was not to touch any other food in big letters!

It really can be a very healthy diet with the concentration more on fresh foods of all kinds, since you don't have to worry about hidden gluten. :D

DK


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



Celiac.com Sponsor (A8-M):



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. - Jane02 replied to HectorConvector's topic in Related Issues & Disorders
      314

      Terrible Neurological Symptoms

    2. - Jane02 replied to HectorConvector's topic in Related Issues & Disorders
      314

      Terrible Neurological Symptoms

    3. - knitty kitty replied to HectorConvector's topic in Related Issues & Disorders
      314

      Terrible Neurological Symptoms

    4. - trents commented on Amiah's blog entry in Amiah
      1

      Help!!

    5. - Scott Adams replied to HectorConvector's topic in Related Issues & Disorders
      314

      Terrible Neurological Symptoms

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

    • Total Members
      133,582
    • Most Online (within 30 mins)
      7,748

    Kim RS
    Newest Member
    Kim RS
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Jane02
      Sorry, I just realized how old this thread is and only read the initial post from 2021. I'll have to catch up on the comments in this thread. 
    • Jane02
      Sorry to hear you're going through such a hard time. It would be worth looking into MCAS/histamine issues and also Long Covid. Perhaps there is something occurring in addition to celiac disease. It would be worth ruling out micronutrient deficiencies such as the b vitamins (B12, folate, B1, etc), vit D, and ferritin (iron stores). 
    • knitty kitty
      This sounds very similar to the neuropathic pain I experienced with type two diabetes.  Gloves and boots pattern of neuropathy is common with deficiencies in Cobalamine B12 (especially the pain in the big toe), Niacin B3, and Pyridoxine B6.  These are vitamins frequently found to be low in people with pre-diabetes and diabetes.  Remember that blood tests for vitamin levels is terribly inaccurate.  You can have vitamin deficiencies before there are any changes in blood levels.  You can have "normal" serum levels, but be deficient inside organs and tissues where the vitamins are actually utilized.  The blood is a transportation system, moving vitamins absorbed in the intestines to organs and tissues.  Just because there's trucks on the highway doesn't mean that the warehouses are full.  The body will drain organs and tissues of their stored vitamins and send them via the bloodstream to important organs like the brain and heart.  Meanwhile, the organs and tissues are depleted and function less well.   Eating a diet high in simple carbohydrates can spike blood sugar after meals.  Eating a diet high in carbohydrates consistently over time can cause worsening of symptoms.  Thiamine and other B vitamins like Niacin B3 and Pyridoxine B6, (which I noticed you are not supplementing), are needed to turn carbs, proteins and fats into energy for the body to use.  Alcohol consumption can lower blood sugar levels, and hence, alleviate the neuropathic pain.  Alcohol destroys many B vitamins, especially Pyridoxine, Thiamine and Niacin.  With alcohol consumption, blood glucose is turned into fat, stored in the liver or abdomen, then burned for fuel, thus lowering blood glucose levels.  With the cessation of alcohol and continued high carb diet, the blood glucose levels rise again over time, resulting in worsening neuropathy.   Heavy exercise can also further delete B vitamins.  Thiamine and Niacin work in balance with each other.  Sort of like a teeter-totter, thiamine is used to produce energy and Niacin is then used to reset the cycle for thiamine one used again to produce energy.  If there's no Niacin, then the energy production cycle can't reset.  Niacin is important in regulating electrolytes for nerve impulse conduction.  Electrolyte imbalance can cause neuropathic pain.   Talk to your doctors about testing for Type Two diabetes or pre-diabetes beyond an A1C test since alcohol consumption can lower A1C giving inaccurate results. Talk to your doctors about supplementing with ALL eight B vitamins, and correcting deficiencies in Pyridoxine, Niacin, and B12.  Hope this helps! Clinical trial: B vitamins improve health in patients with coeliac disease living on a gluten-free diet https://pubmed.ncbi.nlm.nih.gov/19154566/ P. S.  Get checked for Vitamin C deficiency, aka Scurvy.  People with Diabetes and those who consume alcohol are often low in Vitamin C which can contribute to peripheral neuropathy.
    • Scott Adams
      I’m really sorry you’re dealing with this—chronic neuropathic or nociplastic pain can be incredibly frustrating, especially when testing shows no nerve damage. It’s important to clarify for readers that this type of central sensitization pain is not the same thing as ongoing gluten exposure, particularly when labs, biopsy, and nutritional status are normal. A stocking/glove pattern with normal nerve density points toward a pain-processing disorder rather than active celiac-related injury. Alcohol temporarily dampening symptoms likely reflects its central nervous system depressant effects, not treatment of an underlying gluten issue—and high-dose alcohol is dangerous and not a safe or sustainable strategy. Seeing a pain specialist is absolutely the right next step, and we encourage members to work closely with neurology and pain management rather than assuming hidden gluten exposure when objective testing does not support it.
    • Scott Adams
      There is no credible scientific evidence that standard water filters contain gluten or pose a gluten exposure risk. Gluten is a food protein from wheat, barley, or rye—it is not used in activated carbon filtration in any meaningful way, and refrigerator or pitcher filters are not designed with food-based binders that would leach gluten into water. AI-generated search summaries are not authoritative sources, and they often speculate without documentation. Major manufacturers design filters for water purification, not food processing, and gluten contamination from a water filter would be extraordinarily unlikely. For people with celiac disease, properly functioning municipal, bottled, filtered, or distilled water is considered gluten-free.
×
×
  • 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.