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

Mexican Restaurants


mookie03

Recommended Posts

mookie03 Contributor

Hey guys,

when i first went gluten-free i understood that mexican was generally a "safe" food to eat if you are dining out bc they dont use much wheat in their food. But i was just wondering how safe it is. I mean, i know eating out is always a risk, but do u guys find that the tortilla chips are generally safe? And what about seasoning/spices? I know i should always ask but i find it difficult often to communicate w/ people in mexican restaurants- "no wheat"- "NO MEAT???" :P


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



Celiac.com Sponsor (A8-M):



tarnalberry Community Regular

actually, I worry most about mexican restaurants. cross contamination of the chips can be a big problem if they fry their own, as well as dealing with even the corn tortillas being heated up on the same grill as the flour. beyond that, I'm concerned about the sauces - enchilada sauce and other thickened sauces can be made with wheat - and meat that's been marinates - it often has soy sauce. if I can get plain, unmarinated, grilled meat with fresh veggies, and think I can communicate the tortilla issue, then I feel safe-ish, but not totally.

nothungry Contributor

I see that you are in NYC Mookie. Just north of Poughkeepsie in Tivoli there is an absolutely fabulous mexican restaurant, Santa Fe, that is part of the gluten free awareness program. It is a four star restaurant and almost their entire menu is gluten free. So, if you feel like taking a short drive upstate there is yummy mexican available.

Guest Rad

The Southwest is the heart of Mexican food country. Am very partial to New Mexico with all its' mom and pop restaurants going back 3 or 4 generations. It's just normal here to go to Mexican restaurants at least twice a week, maybe more. New Mexico is the Land of Enchantment, but it's also the land of a wonderful variety of excellent restaurants. The first words I said when finding out I had Celiac Disease were: no more burritos, no more sopaipillas (puffed fryed bread with honey), no more Mexican beer. Guacamole should be okay with corn chips. Am looking in a cookbook, and tamales look okay, but asking would be a good idea. There are Mexican seafood restaurants. And just made my first batch of refried beans; definitely have some to work to do, to get even close to the locals for taste. Did have a Naturopath tell me recently I am sensitive to hot spices, so between the two allergies am pretty limited to the the guacamole, refried beans, mild huevos rancheros, corn chips and mild tacos. Also am worried about cross contamination. Have made my own tortillas before and will try it with the gluten free flour. Anyone traveling to New Mexico, let me know as I have a list of great restaurants and places to visit.

Buenos Dias . . .

Dianna

celiachap Apprentice

I see that you are in NYC Mookie. Just north of Poughkeepsie in Tivoli there is an absolutely fabulous mexican restaurant, Santa Fe, that is part of the gluten free awareness program. It is a four star restaurant and almost their entire menu is gluten free. So, if you feel like taking a short drive upstate there is yummy mexican available.

Sounds good, but 95 miles, which is the distance from NYC to Tivoli, is not really a "short drive upstate". There must be some gluten-free Mexican places in Manhattan, or the Boroughs, that are decent.

I havn't used my Triumph Dining Cards yet, but when the weather gets better we'll see:

Open Original Shared Link

jkmunchkin Rising Star

Hey Ms. Met ;)

I've eaten mexican twice now and was fine both times. Although I admit the communication is a tad bit harder than some other restaurants. The 2 I went to are Rosa Mexicano (there are a couple in the city) and Casa Maya (in Scarsdale - in that shopping center by the A&P, next to Spiga).

mookie03 Contributor

thanks guys! Yea, that restaurant sounds really good but is quite far being that i dont have a car! I've been to Rosa Mexicano several times before dx (theres one right next to fordham law) but i havent tried it yet. I went to one mexican place in vegas and was ok, but i ate the chips w/o giving it a second thought and realized afterwards that there was a high chance of CC and i shouldnt have done that. I didnt get sick (and i am very sensitive) but that doesnt necessarily mean i didnt damage my body!

There are tons of mexican restaurants in NYC and ive always been a fan of the simpler things anyway (i dont like enchilada sauce or a lot of the other foods that may have gluten. My main concern is the chips! i cant imagine going out for mexican w/o being able to snack on them!!!


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



Celiac.com Sponsor (A8-M):



grantschoep Contributor

I have to add...

Open Original Shared Link

There is a great mexican place down the road from me. I must advertise them... they have been so great for me.

They have been great to me. I think all staff know me by now. I remeber when I first went their, one day, I had green chili on my plate delivered too me(their green chili has wheat) and it was intercepted by my waitress as the plate was being set down. She said something in spanish to the server(I only understand a little bit of spanish) and the plate was fastly removed and the next plate was announced as Gluten Free.

The server also said right away(when I first walked in and made the "uncomfortable gluten annoucement"), you probaly should not eat our corn ships, as they are made in the same vats as wheat things. That was cool.

Simply put, I would never say any chain/ethnic/whatever is safe. Is completlly based on the staff. Especially if its a non chain type store. Learn the staff. Teach the staff. and of course, when they do well tip em nice.

Mahee34 Enthusiast

you always have the mexican chains like qudoba and chipotle that have gluten free options.......i know they can't compare to an authentic mexican restaurant but sometimes are a nice substitute!

mytummyhurts Contributor

I don't know if you have a Chevy's were you are. They may just be on the West Coast. But they have a gluten free list here Open Original Shared Link as well as many other restaurants on that site. The chips there are fried with wheat containing items, so they are a no-no. I know what you mean about them being hard to resist. I used to love chips and salsa at Mexican restaurants.

I had a mexican place I used to love and I don't eat there anymore because they don't speak English that well and I don't like eating out much at all anymore. You could learn the Spanish word for wheat. I did that with beans, because it was hard to get across "no beans" so I went back and said "no frijoles" and they totally understood. But, of course, it's not as simple as no wheat. Otherwise our lives would be much easier, right? ;)

Spanish word for wheat is: trigo

Gluten: gluten :lol:

free translator here:

Open Original Shared Link

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,563
    • Most Online (within 30 mins)
      7,748

    Bob Madden
    Newest Member
    Bob Madden
    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

    • Scott Adams
      Oats naturally contain a protein called avenin, which is similar to the gluten proteins found in wheat, barley, and rye. While avenin is generally considered safe for most people with celiac disease, some individuals, around 5-10% of celiacs, may also have sensitivity to avenin, leading to symptoms similar to gluten exposure. You may fall into this category, and eliminating them is the best way to figure this out. Some people substitute gluten-free quinoa flakes for oats if they want a hot cereal substitute. If you are interested in summaries of scientific publications on the topic of oats and celiac disease, we have an entire category dedicated to it which is here: https://www.celiac.com/celiac-disease/oats-and-celiac-disease-are-they-gluten-free/   
    • knitty kitty
    • knitty kitty
      Hi, @Ginger38, I've had shingles in the past.  I understand how miserable you're feeling.   Not only do i have the chickenpox virus lurking about, I also have the cold sore virus that occasionally flares with a huge cold sore on my lip when stressed or exposed to gluten.  The virus lives dormant in the nerves on the left side of my face.  It causes Bell's Palsy (resulting in drooling).  The cold sore virus is also in my eye.  My eye swells up and my vision is diminished permanently whenever I have a flare, so it's of the utmost importance to keep flares away and treat them immediately if they do happen so I don't lose any more vision.   I take the amino acid supplement L-Lysine.  Lysine messes with the replication of viruses, which helps the body fight them off.   I haven't had an outbreak for several years until this year when exceptionally stressed and contaminated, it flared up again. Lysine has been shown to be beneficial in suppression of viruses like the cold sore virus (a herpetic virus), the chickenpox virus (also a herpetic virus), as well as the HIV virus, and even the Covid virus.   I also take additional Thiamine in the form TTFD (tetrahydrofurfuryl disulfide) because Thiamine has antiviral properties as well.   For pain, a combination of Thiamine (like TTFD or Benfotiamine or Thiamine Hydrochloride), with B12 Cobalamine, and Pyridoxine B6 have been shown to have analgesic properties which relieve pain and neuropathy.    The combination of Thiamine B1, Pyridoxine B6 and Cobalamine B12 really does work to relieve pain.  I take it for back pain from crushed vertebrae in my back.  This combination also works on other pain and neuropathy.   I usually buy a supplement that combines all three and also Riboflavin B2 called EXPLUS online.  However, it's made in Japan and the price with the tariffs added makes it really expensive now.  But the combination of Thiamine B1, Pyridoxine B6 and B12 Cobalamine (and Riboflavin B2) still work even if taken separately.   I can't take Tylenol or ibuprofen because of stomach upsets.  But I can take the vitamin combination without side effects.  However, you can take the three vitamins at the same time as other pain relievers for added benefit.  The vitamins help other pain relievers work better. I hope you will try it.  Hopeful you'll feel better quickly. Interesting Reading: Thiamine, cobalamin, locally injected alone or combination for herpetic itching: a single-center randomized controlled trial https://pubmed.ncbi.nlm.nih.gov/23887347/ Mechanisms of action of vitamin B1 (thiamine), B6 (pyridoxine), and B12 (cobalamin) in pain: a narrative review https://pubmed.ncbi.nlm.nih.gov/35156556/ Analgesic and analgesia-potentiating action of B vitamins https://pubmed.ncbi.nlm.nih.gov/12799982/ A Narrative Review of Alternative Symptomatic Treatments for Herpes Simplex Virus https://pmc.ncbi.nlm.nih.gov/articles/PMC10301284/
    • 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.
×
×
  • 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.