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

Longhorn's Steakhouse


cdford

Recommended Posts

cdford Contributor

I have used our local Longhorn's (Hiram) as much as the budget will allow. One of the managers there had a friend who was a celiac patient and he was so careful that he caught the salad before it hit my table...the waitress had forgotten about the croutons. He even explained to her that she could not just remove the croutons and bring the bowl back. Would you believe they started a new salad bowl rather than risk cross-contamination.

They have great steamed veggies also. There is a grilled chicken dish with asparagus, mushrooms, and cheese that they can adjust by using fresh mushrooms instead of the marinated ones. The chefs here come out to my table when the manager is not there to watch over them. They have so far been very concerned and helpful. They actually commented that it was nice to get to create instead of just cooking by the book. I have not gotten sick from there yet.

I also contacted their regional offices and let them know what a great experience it was. I was told that several restaurants in the Atlanta area were meeting to determine the best ways to accomodate gluten-free requests. Maybe a special menu is in the works???

Donna


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



Celiac.com Sponsor (A8-M):



MySuicidalTurtle Enthusiast

I live just north of Atlanta and my brother and mother (who both have celiacs) eat pretty often at our local Longhorns. The manager is really helpful with them, too! A gluten-free menu would be awesome to have, especially since it will educate the staff just a little but more.

I am always afraid of the whole croutons thing and them just taking them off. I won't eat food if I think they didn't make it new. I am a cross-contamination freak.

cdford Contributor

I am so sensitive that I have to be a cross-contamination freak. I have called the regional or national offices of several restaurants over the last year and a half. Some of my comments were negative, but I go amazing responses from the positive comments. They were almost funny...as though they could not believe that someone would actually call to tell them what a great job one of their restaurants had done. One of these calls was when the VP shared with me the plans for a gluten-free menu or at minimum plans for meeting our needs. At least they are talking about it.

Donna

terri Contributor

I ate at the Longhorn in Chantilly Virginia and had a wonderful experience! The manager went back and cleaned the grill himself before cooking my food. They were gracious and understanding and I will definitely eat there again! :)

FreyaUSA Contributor

What did you order at Longhorn? I went there once and am not certain what it was, but I had a reaction (I think I ordered the barbaqued chicken salad, or something like that. Could the ranch dressing be Hidden Valley? Could the bbq sauce have gluten? Btw, it was so good :( ) My family would love to go there sometime, but I've been too afraid to take all my little celiacs there. :rolleyes:

terri Contributor

I had the peppercorn steak salad only without any sauce. I used my own salad dressing that I carry with me. I never use restaurant salad dressings or barbeque sauces, or any sauce at all for that matter. Better to be safe than sorry. I do encourage olive oil and fresh herbs and ground pepper, etc.

Boojca Apprentice

This is very interesting to me because when I wrote to them this summer the letter I got back was so NOT nice, and was the same "Go somewhere else to eat bc we can't make any adjustments for yoU" that most chains send. It just made me so mad that I now boycott Longhorn and in fact convinced my whole family and all our friends to do the same. I also wrote them a nasty-gram telling them about our boycott, and how they better get on the stick because in 2006 not only will they have to disclose their ingredients but they also are losing a lot of business to their competitors like Outback because they DO have a gluten-free menu.

Maybe that worked....

bridget


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



Celiac.com Sponsor (A8-M):



terri Contributor

Isn't it Logans Roadhouse that won't have a gluten-free menu? That was my understanding, that Logans, Applebees and Ruby Tuesday won't play ball. Maybe it is different in every state.

angel-jd1 Community Regular

I agree with bridget........they are not such a great place.......here is the response that I had gotten to them when I wrote in July

Dear Jessica,

Thank you for taking the time to write to us and for your interest in LongHorn Steakhouse. After consulting with our Culinary Team I find that I am unable to adequately address your concerns due to the fact that our restaurants source raw and processed ingredients from hundreds of providers across the United States. Many of these products are mixed by the provider or in the restaurant and the ingredients may change from time to time and batch to batch. Also, several of these providers use proprietary blends of seasonings which are not disclosed to the public. Therefore, it is not possible to provide an accurate list of gluten-free menu items. We understand the seriousness of your question and we regret that we are unable to provide the information you have requested.

Kind regards, Nikki Mechem

judy05 Apprentice

Is it true that restaurants have to display their ingredients?

I thought the bill only addressed food labels in grocery stores?

FreyaUSA Contributor
Isn't it Logans Roadhouse that won't have a gluten-free menu?

I regularly go to Logan's. The staff at the ones near me (I've been to two different ones) were incredibly helpful AND knowledgeable. We had one waiter who's girlfriend was celiac and he basically gave me the rundown on what's okay and what's not and had no problem checking on the what he didn't know immediately. The other times I've been, even without this great waiter, the staff have been very accommodating. Maybe it's just their corporate people that are pains.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,964
    • Most Online (within 30 mins)
      7,748

    Cbear
    Newest Member
    Cbear
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      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
      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
      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
×
×
  • 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.