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

Chilis's New Menu

brendygirl

By brendygirl
in Gluten-Free Restaurants

Recommended Posts

brendygirl Community Regular
brendygirl
Posted

Usually when we go out to Chilis for lunch, all the people I work with get the soup and salad, except for me. (I can't tolerate cream, and I don't even like that cheesy baked potato soup they have.)

And, to be fair, I recently posted a minor rant on my blog here about Chilis and how they suddenly took the gluten free honey bbq sauce off the menu (so I couldn't order ribs), sabotaging a visit with my family over the holidays. It's ANNOYING that they change their menu every few months, so the printed ones in the folder I keep in my car are always incorrect and they always have to print me a new one.

However they won me over with the most recent menu switcharoo. Except for holding the croutons, I got to order and eat a "normal" meal and it was yum-OH!

I devoured the [b]"Bottomless Soup N Salad Express Lunch $6" Chicken Rice Lime Soup- flavorful

Chips and Salsa- chips are extra thin and yummy, salsa is fair

House salad with a honey-limey dressing- the bowl was shallow

which is perfect for scoping out any hidden croutons (for deeper bowls I have to dump it on a plate b4 eating to rake through and verify), the iceberg lettuce was shredded (not my preference), and the dressing was tangy and delicious.

The new menu (valid until mid-April) also listed tacos and several other items I'm looking forward to trying, as a Chilis is 5 minutes from my house.

The waiter wouldn't let me keep the menu, tho, and I'm too lazy to look it up right now to share the rest with you.

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

Celiac.com Sponsor (A8-M):


luvs2eat Collaborator
luvs2eat
Posted

Chilis is one of our faves... and one of the ONLY "chain" restaurants where we live (in the boonies!). I like their baked potato soup... just a little is so filling! As we do anywhere we go out to eat... we make friends w/ our server ("Have a seat and let me tell you about my food issues." ha ha) and I tell them, w/ a smile, that if there are croutons on my salad, I'll have no CHOICE but to ask that another be made. By the time they leave our table, I've said, "PLEASE, no croutons," about 5 times with a big smile and it totally works!

Isn't there another BBQ sauce for their ribs on their gluten-free menu? Seems to me I've had the original sauce.

redsidekick Apprentice
redsidekick
Posted

I also thought that the orignial bbq sauce for the ribs were ok. Really hope that hasnt changed.

The Chillis near me has always been very accomadating to me when I come in. In fact the last time I came in w/my family they sent a waitress from another section to serve us because she also has celiac and she was very helpful (She told us the chips and salsa were OK, I did not know that.

Sunny Side Newbie
Sunny Side
Posted

I'll have to check out the new menu and see what the choices are. I usually get the baked potato soup, sometimes with a side salad. I had no idea the chips and salsa were gluten free. I don't remember that ever being listed as gluten free on the menu. It's good to know.

MindytheOrganist Enthusiast
MindytheOrganist
Posted

I did not know the chips & salsa were gluten-free. I wrote to Chili's Corporate Office and was told the chips were NOT fried in a dedicated fryer and CC could occur.

I do believe Chili's is getting better with gluten-free options.

pugluver31902 Explorer
pugluver31902
Posted

I did not know the chips & salsa were gluten-free. I wrote to Chili's Corporate Office and was told the chips were NOT fried in a dedicated fryer and CC could occur.

I do believe Chili's is getting better with gluten-free options.

Yes, you definitly CANNOT have the chips and salsa. They are fried in the same fryers as all the breaded items, and they ARE NOT listed on the gluten free menu. The waitors get confused because the chips themselves are gluten free, but then they throw them in the fryer

MindytheOrganist Enthusiast
MindytheOrganist
Posted

Shoot! I was afraid of that. If only they could dedicate a fryer, it would put Chili's near the top of our list.

Of course, nothing comes close to Biaggi's.

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

Celiac.com Sponsor (A8-M):


buffettbride Enthusiast
buffettbride
Posted

Chili's is off our list now because they changed from the "original sauce" which was safe to a sauce that now has beer in it. They have removed ribs from the gluten-free menu altogether. What was so great about Chilis is that my daughter's fave meal pre-Celiac was from Chilis and it was awesome to not have to take away that from her too. Grrrrrrr. Bad Chilis. Bad.

Archived

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

Go to topic listing
  • Celiac.com Sponsor (A19):


  • Member Statistics

    • Total Members
      131,945
    • Most Online (within 30 mins)
      7,748
    Miyasato
    Newest Member
    Miyasato
    Joined
  • Celiac.com Sponsor (A20):

  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A22):



  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • Jacki Espo
      Covid caused reoccurrence of DH without eating gluten

      By Jacki Espo · Posted

      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      New Celiac Mama in My 30s

      By Mari · Posted

      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      My only proof

      By Mari · Posted

      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
      Does anyone here also have Afib

      By knitty kitty · Posted

      Fascinating.
    • DebJ14
      Does anyone here also have Afib

      By DebJ14 · Posted

×
×
  • 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.