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 Melting Pot


Ginny

Recommended Posts

Ginny Rookie

Last weekend my husband and I ate at a Melting Pot in Philadelphia (It is a fondue style restaurant). I asked our server not to put bread on my plate because I had a gluten-allergy. She immediately knew what I was talking about and said that they had to make our cheese fondue differently (I guess they usually use flour in it to help it have a good consistency), but that they had a recipe to make it gluten-free. She recommended that my husband not dip his ravioli in the fondue until I was finished using it---I knew this, but I was impressed with her level of knowledge. Overall we had a wonderful experience there, and I didn't get sick. They were so accomodating! There are Melting Pots all over the country and it is one of my favorite places to eat.


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



Celiac.com Sponsor (A8-M):



NicoleAJ Enthusiast

Wow, I just assumed that Melting pot would be totally out of the question. I've made both cheese and chocolate fondue at home, but I never would have trusted it out of the house. It's nice to know that Melting Pot is so accomodating for celiac customers--I may have to give them a call and see if they are all so knowledgeable.

grantschoep Contributor

I just asked this question of the The Melting Pot down the street from my house, they said the gluten free list is specific to different stores, this reply is for one in Lousiville, CO, USA. There's not much there, but sounds like it could be done...

Gluten in Melting Pot Sauces and Products

Updated 10/06/06

We have been receiving questions from our guests regarding gluten in our products. Many people have allergic reactions to gluten, which is contained in anything prepared with wheat or wheat flour. Below is a list of menu items served at the Melting Pot that contain Gluten

or wheat flour.

Cheese Fondues:

All the cheeses for our fondues are prepped by blending with flour and contain gluten.

Unopened bags of shredded cheese from Roth Kase do not contain flour; they use potato starch for anti-caking which is safe for people allergic to wheat flour or gluten.

Gluten free cheese fondue can be made by taking the required amount of cheese directly from an unopened bag and in a clean bowl blending a small amount of potato starch into it. Taking care to label and store it separate from cheese station until needed.

The Cheddar Cheese fondue, Fiesta Cheese fondue, and some Featured Cheeses are made with a beer base, which contains gluten.

The cheeses can be made with a milk base as a substitute for beer.

No bread or crostini as they contain gluten also, serve extra fruits and vegetables. Tortilla chips can be served if the nutrition information states that they are gluten free.

Salads:

Our Salads and Dressings are fine.

Do not serve croutons.

Entrees and Fondue Cooking Styles:

Our broths contain gluten.

Fondue Bourguignon, which is a cholesterol free canola oil cooking style, is fine.

Both the Teriyaki Sirloin and the Teriyaki Sauce contain gluten.

Substitute tenderloin as a beef item where available, or substitute filet for an additional charge.

Do not serve either batter as they also both contain gluten.

Desserts:

The Cookies & Cream Marshmallow Dream and the Chocolate S

Guest cassidy

There was a post on this a while ago. I thought I was on to something when I remembered the Melting Pot. Apparently, it depends on your store. Some of them are very accomodating and others aren't willing to help at all. Since even the broth contains gluten I was leary of trying it because I wouldn't want to use oil and I might feel a bit weird about bringing in my own chicken broth. I still haven't called my local one but it might be worth a try.

jaimek Enthusiast

Ginny,

Exactly which melting pot did you go to? The one in Chestnut Hill, downtown or King of Prussia? I would love to go there, but I know there are numerous ones in the Philly area.

thanks!

elonwy Enthusiast

It very much depends on which location. In Southern California I got a resounding "no" from both locations, and corporate pretty much said "don't come in" but alot of people on the East coast seem to have had good luck. Things are different up here in the Bay Area though, I might see if there is one here.

Elonwy

Ginny Rookie

Jaimek,

It was the one downtown. Sorry I didn't reply sooner, it's been a while since I've been online. Good luck and enjoy!

Ginny


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



Celiac.com Sponsor (A8-M):



  • 1 month later...
gfsara1103 Newbie

I also had the privilege in going to the Melting Pot and having a gluten-free meal. In Pittsburgh,PA at Station Square is the one I went to. I called them ahead to see if I could bring my own bread on, which i did. They they preceded to cut up my bread to little square pieces just like the regular ones. Also, the waitress knew exactly how to make a gluten-free (no beer or flour) cheese fondue. She was very careful about it.. I'll never forget that wonderful experience. I can't wait to go again! It is pricey there, but well worth it. :D

jaten Enthusiast
Gluten in Melting Pot Sauces and Products

Updated 10/06/06

.....We have been receiving questions from our guests regarding gluten in our products. Many people have allergic reactions to gluten, which is contained in anything prepared with wheat or wheat flour......

Is anyone else thinking the Melting Pot is missing somethings here? Barley? Rye? Oats...??? (whatever your stance on oats, according to a lot of research, it is true that about 10% of people with Celiac react to a protein in oats similarly to gluten)

Barley or malt is frequently used for flavoring, and the Melting Pots need to know that barley also contains gluten.

Rye? I had never run up against rye until about 6 weeks ago, in a restaurant in another town. A restaurant chef came out to talk with me. He, too, believed in what the Melting Pot statement says. This particular chef at a very nice restaurant (not MP) thought wheat was the only grain a Celiac/gluten-intolerant needed to avoid. In that circumstance, I avoided what surely would have been a glutening by giving him more information (he really thought he understood before). Of 3 of the dishes he was considering preparing for me, 1 contained rye (go figure) & 2 contained barley or malt.

  • 1 year later...
GFspouse Newbie
I also had the privilege in going to the Melting Pot and having a gluten-free meal. In Pittsburgh,PA at Station Square is the one I went to. I called them ahead to see if I could bring my own bread on, which i did. They they preceded to cut up my bread to little square pieces just like the regular ones. Also, the waitress knew exactly how to make a gluten-free (no beer or flour) cheese fondue. She was very careful about it.. I'll never forget that wonderful experience. I can't wait to go again! It is pricey there, but well worth it. :D

We had a similar experience at the Melting Pot in Lexington, KY last night when we celebrated our anniversary. I called ahead to inquire about the gluten-free menu. At first the response was a bit hesitant, but then she said she would do the research and call or email me back. Less than 24 hours later, I received the following email:

Recently the Melting Pot changed the bouillon they carried to a gluten-free recipe so that consumers like yourself could enjoy all that we have to offer instead of just the bourginnone cooking style (canola oil). Now every cooking style is available to you: Coq au Vin, Mojo, Court Bouillon, and as always, canola oil. We can also use certain brands of corn starch or potato starch (do you know where I can find this? Whole Foods?) that are gluten-free as well to 'flour' the cheese for the cheese fondue that you may order. (My favorite is the Caribbean cheese that we are featuring until the end of the month!)

I'm sorry that I couldn't be of assistance earlier, I just didn't want to tell you something wrong and not be able to accomodate your needs when you arrived.

Here is a list of items that you do not want to order however, as they are on the allergen list that we have made:

-Bread as a dipper with your cheese--you may get more dippers of any sort though to substitute!

-Croutons and Caesar dressing

-Teriyaki Sirloin

-Potstickers (These only come on the Pacific Rim but can be substituted as well as anything else)

-any ravioli

-Teriyaki Sauce

-Sesame and Tempura batters

-Cookies & Cream Marshmallow Dream

-Chocolate S'mores

-Cheesecake

-Brownies

-Pound Cake

-Graham Crackers

-Oreo Crusted Marshmallows

-Oreo crumbs

For your dessert dipper plate you can get all strawberries, we also carry fresh pineapple which is awesome in dark chocolate.

So, I called to make a reservation immediately. However, since I was booking with less than 24 hours notice, I decided to take an unopened bag of potato starch just in case she didn't get my reply email or hadn't had time to get it. I'm glad I did, because she hadn't received my email yet. They did use my potato starch and we had a WONDERFUL meal. The best meal I've ever had! And I loved the fact that I didn't have to worry that my spouse would get sick! They gave us extra fruit and veggies to replace the bread in the cheese fondue course. Then they replaced the ravioli with extra chicken in the meat course. For the desert course, we had plain marshmallow (instead of the Oreo-covered ones), strawberries, and bananas. They also placed an Anniversary card at our table with our names on it. Also, when I made the reservation they offered several celebration packages (for an extra fee, $10-55) such as roses, balloon bouquets, etc). The whole evening was extremely special!

Here is the email I got today, the day after we went:

Thank you so much for coming to see us Saturday night! It was very thoughtful of you to bring the potato starch, truly awesome! I'm very glad you and your hubby enjoyed yourselves and that the Caribbean cheese turned out to be great. I think we're actually going to make one today for ourselves with the potato starch and see if we can tell a difference. It's been suggested that we just go ahead and substitute it for the flour anyway with the amount of gluten allergies our restaurant has been seeing.

Again, thank you for the starch and thank you for coming in last night. We can't wait to have you again!

And we can't wait to come again! Thank you Jenny & everyone else at Lexington Melting Pot!

munkee41182 Explorer

Actually, this woman that use to work at the company both my fiance and i work at just left to go manage a Melting Pot in Burlington MA. She said that we should give 24 hours notice for gluten free meals. She brought up the "there is wheat flour in the cheese" etc....and I had said to her, "it's not just wheat, it'e barley, malt, rye, oats, etc" She said that she understood that, and other than the beer that they use in the cheese fondues...they don't use barley, malt, etc. Granted each MP may not be the same, but I at least feel safe to go to the one by us.

amberleigh Contributor

Our Melting Pot is REALLY good with food allergies. They have a huge laminated brochure type thing that they bring out that lists all the "no no's" for each food allergy and gluten/wheat is definitely on there. With that, we were able to select all 4 courses of the Big Night Out. I believe there are only 1-2 cheeses we can eat and 1 cooking fondue. I think the salads and chocolates are pretty easy though. With the dessert course, we always have them bring the fruit separate from everything else and then my husband just drizzles the chocolate over his "gluten food".

We've eaten there 3-4 times since I've been dx'd and no problems! It's one of our favorite places to go!

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. - RMJ replied to pothosqueen's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      Positive biopsy

    2. - trents commented on Scott Adams's article in Kids and Celiac Disease
      2

      New Study Reveals Age and Racial Gaps in Pediatric Celiac Testing

    3. - Russ H replied to pothosqueen's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      Positive biopsy

    4. - Scott Adams replied to pothosqueen's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      Positive biopsy

    5. - Scott Adams commented on Scott Adams's article in Latest Research
      3

      New "Glowing Bacteria" Pill Could Transform Gut Disease Detection (+Video)

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

    • Total Members
      133,000
    • Most Online (within 30 mins)
      7,748

    bonniebeebe143
    Newest Member
    bonniebeebe143
    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

    • RMJ
      I agree with @trents that the IgA you listed sounds like a total IgA, not celiac-specific, if 114 is normal.  Were any other antibody tests run?  
    • Russ H
      What you describe is seronegative villous atrophy (negative antibody tests but positive biopsy). It is uncommon in coeliac disease, and there are other causes, but the most common cause is coeliac disease. I would pursue this with your healthcare provider if possible. Based on clinical history, test results and possible genetic testing for susceptibility to coeliac disease it should be possible to give a diagnosis. There is a bit more here: Seronegative coeliac disease
    • Scott Adams
      If you are still eating gluten you could get a celiac disease blood panel done, but I agree with @trents and the gold standard for diagnosing celiac disease would be your endoscopy results. Is it possible they did do a celiac disease panel before your biopsy? This would be the normal chain of events. This article might be helpful. It breaks down each type of test, and what a positive results means in terms of the probability that you might have celiac disease. One test that always needs to be done is the IgA Levels/Deficiency Test (often called "Total IGA") because some people are naturally IGA deficient, and if this is the case, then certain blood tests for celiac disease might be false-negative, and other types of tests need to be done to make an accurate diagnosis. The article includes the "Mayo Clinic Protocol," which is the best overall protocol for results to be ~98% accurate.    
    • trents
      Actually, it would be more correct to say that the genetic potential to develop celiac disease is passed down from parents to children. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% of the general population actually do. But it is also true that the offspring of those who do have active celiac disease are at a considerably higher risk of developing active celiac disease than those of parents who have the genes but don't develop the disease. Some recent, larger studies put the risk at near 50% for the first degree relatives of those who have active celiac disease.
    • Jordan Carlson
      Hello everyone! Been a while since I posted. The past few moths have been the best by for recovery for myself. I have been the least bloated I have ever been, my constant throat clearing is almost gone, I have stopped almost all medication I was prevously taking (was taking vyvanse for adhd, pristiq for anxiety,fomotadine/blexten for histamine blockers and singulair). Only thing I take now is Tecta. I also no longer get any rashes after eating. Things are going very well. Most success came actually once I upped my B12 daily dose to 5,000 mcg. I do have one thing I am un able to figure out and want to see if anyone else has this issue or has experience working around it. Ever since I was born I have always had a issue getting fruits and veggies down. No matter how hard I tried, it would always result in gagging or throwing up. Always just thought I was a picky eater. Now that my stomach and system has healed enough that I can feel when something is off almost istantly, I notice that after eating most fruits (sometimes I am ok with bananas) and veggies, my stomach instantly starts burning and my heart starts to pound and I get really anxious as if my body doesnt know what to do with what just enetered it. So I am thinking now that this is what probably was going on when I was born and my body started rejecting it before which caused this weird sensory issue with it causing the gagging. Hoping someone has some exprience with this as well because I would love to be able to enjoy a nice fruit smoothie once in a while haha. Thanks everyone!
×
×
  • 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.