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

Melting Pot Littleton Co - A Glorious Gluten Free Meal


Michelle1234

Recommended Posts

Michelle1234 Contributor

This evening I went to the Melting Pot Fondue restaurant in Littleton CO expecting a good meal but having to forgo the bread with the cheese fondue and the brownies and cakes with the deserts. Boy was I wrong. My server informed me they had Deby's gluten free bread with the cheese fondue (they use a gluten free flower and milk for the base) which was very good. I also ordered the mandarin orange and almond salad minus the wontons. They offered me several choices of gluten free dressing. We had a nice veggie and meat meal (make sure to ask which sauces for dipping are safe) and then came the desert. I ordered the chocolate fondue with marshmallow mixed in and asked them to hold the cheesecake, brownies, graham crackers etc. I expect to get the bananas, strawberries, pineapple and marshmallows. Imagine my surprise when the plate came out also including brownies and sponge cake that my server informed me were Deby's gluten free products. At the end of the meal the manager came out to ask how I had enjoyed the products and let me know they were doing a trial for the nationwide chain. He indicated they knew how to keep cross contamination at bay by using fresh gloves, separate bowls etc. So if you live in the Denver metro area I recommend you go to the Littleton location and enjoy the meal while supporting the trial so hopefully they will go nationwide!

The Melting Pot

Littleton

2707 W. Main Street 80210

Phone: (303) 794-5666 [Fax]: (303) 794-0429

Best,

Michelle


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



Celiac.com Sponsor (A8-M):



Laurad- Apprentice

Holy cow, that's great news! That used to be my favorite restaurant before I went gluten-free, and now I'm super excited to go back!! Thanks for the info. B)

confused Community Regular

Makes me want to jump in the car and drive the 5 hours to go eat there for dinner lol

paula

tiffjake Enthusiast

Thanks so much for the info!! I can't wait to go now!!!!!

buffettbride Enthusiast

Holy cow how awesome! My DD LOVES fondue. We've eaten at La Fondue in downtown Denver, but pre-gluten-free. I've been meaning to check how to make going there gluten-free but I suspect we'll just start going to the Melting Pot. YUM!

Michelle1234 Contributor

I must admit I'm probably going back this weekend. The base for the meat and veggies was the oil instead of broth which was a bit heavy for me. I ended up just eating some of the veggies raw. As a result I think I'll order the cheese fondue, salad and then skip right to the desert. :-)

Cheers!

Michelle

angel-jd1 Community Regular

That sounds AMAZING!! I wish I was in CO!! Have some fondue for me.

-Jessica :rolleyes:

This evening I went to the Melting Pot Fondue restaurant in Littleton CO expecting a good meal but having to forgo the bread with the cheese fondue and the brownies and cakes with the deserts. Boy was I wrong. My server informed me they had Deby's gluten free bread with the cheese fondue (they use a gluten free flower and milk for the base) which was very good. I also ordered the mandarin orange and almond salad minus the wontons. They offered me several choices of gluten free dressing. We had a nice veggie and meat meal (make sure to ask which sauces for dipping are safe) and then came the desert. I ordered the chocolate fondue with marshmallow mixed in and asked them to hold the cheesecake, brownies, graham crackers etc. I expect to get the bananas, strawberries, pineapple and marshmallows. Imagine my surprise when the plate came out also including brownies and sponge cake that my server informed me were Deby's gluten free products. At the end of the meal the manager came out to ask how I had enjoyed the products and let me know they were doing a trial for the nationwide chain. He indicated they knew how to keep cross contamination at bay by using fresh gloves, separate bowls etc. So if you live in the Denver metro area I recommend you go to the Littleton location and enjoy the meal while supporting the trial so hopefully they will go nationwide!

The Melting Pot

Littleton

2707 W. Main Street 80210

Phone: (303) 794-5666 [Fax]: (303) 794-0429

Best,

Michelle


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



Celiac.com Sponsor (A8-M):



GeoffCJ Enthusiast

Anyone know if this is widespread? I'd love to go there.

Michelle1234 Contributor
Anyone know if this is widespread? I'd love to go there.

The manager said they were doing a trial for the national chain. As a result I suspect it isn't in the other locations yet. But that is also why I thought it would be good to spread the word. If they get a number of gluten-free customers they will see more value in expanding it to the other locations.

Best,

Michelle

steveindenver Contributor

Wow - what a great posting this is!I can't believe they're doing gluten-free fondue - good for them!!!

Cheri A Contributor

Yay! That's so cool! DH and I love to go to The Melting Pot!

tiffjake Enthusiast

Do you think they are doing it at the Littleton location too? I called and the manager said "yeah, we have gluten free stuff" but didn't know about Debys, so I think maybe they are ONLY doing it at the Denver location???

Michelle1234 Contributor
Do you think they are doing it at the Littleton location too? I called and the manager said "yeah, we have gluten free stuff" but didn't know about Debys, so I think maybe they are ONLY doing it at the Denver location???

Tiffany, yes the Littleton location was the one that I went to. Hope you have a great meal!

Cheers!

Michelle

tiffjake Enthusiast
Tiffany, yes the Littleton location was the one that I went to. Hope you have a great meal!

Cheers!

Michelle

Sorry, I meant the Louisville location, that one is closer to us than Littleton....

a1sacch Rookie
This evening I went to the Melting Pot Fondue restaurant in Littleton CO expecting a good meal but having to forgo the bread with the cheese fondue and the brownies and cakes with the deserts. Boy was I wrong. My server informed me they had Deby's gluten free bread with the cheese fondue (they use a gluten free flower and milk for the base) which was very good. I also ordered the mandarin orange and almond salad minus the wontons. They offered me several choices of gluten free dressing. We had a nice veggie and meat meal (make sure to ask which sauces for dipping are safe) and then came the desert. I ordered the chocolate fondue with marshmallow mixed in and asked them to hold the cheesecake, brownies, graham crackers etc. I expect to get the bananas, strawberries, pineapple and marshmallows. Imagine my surprise when the plate came out also including brownies and sponge cake that my server informed me were Deby's gluten free products. At the end of the meal the manager came out to ask how I had enjoyed the products and let me know they were doing a trial for the nationwide chain. He indicated they knew how to keep cross contamination at bay by using fresh gloves, separate bowls etc. So if you live in the Denver metro area I recommend you go to the Littleton location and enjoy the meal while supporting the trial so hopefully they will go nationwide!

The Melting Pot

Littleton

2707 W. Main Street 80210

Phone: (303) 794-5666 [Fax]: (303) 794-0429

Best,

Michelle

That is the best thing ever! I think I would have cried tears of happiness!!!

  • 2 weeks later...
zachsmom Enthusiast

SO LIKE YOU JUMPED ON THIS RIGHT.... and told him millions of lives depended on this right? lol that is really great news I have two melting pots near me... I will ask if this is an option....

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. - cristiana replied to Scatterbrain's topic in Sports and Fitness
      5

      Feel like I’m starting over

    2. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      8

      My only proof

    3. - Wheatwacked replied to Jmartes71's topic in Coping with Celiac Disease
      8

      Related issues

    4. - NanceK replied to Jmartes71's topic in Related Issues & Disorders
      8

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,295
    • Most Online (within 30 mins)
      7,748

    LaniH
    Newest Member
    LaniH
    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

    • cristiana
      Hi @Scatterbrain Thank you for your reply.   Some of these things could be weaknesses, also triggered by stress, which perhaps have come about as the result of long-term deficiencies which can take a long time to correct.   Some could be completely unrelated. If it is of help, I'll tell you some of the things that started in the first year or two, following my diagnosis - I pinned everything on coeliac disease, but it turns out I wasn't always right!  Dizziness, lightheaded - I was eventually diagnosed with cervical dizziness (worth googling, could be your issue too, also if you have neck pain?)  A few months after diagnosis I put my neck out slightly carrying my seven-year-old above my head, and never assigned any relevance to it as the pain at the time was severe but so short-lived that I'd forgotten the connection. Jaw pain - stress. Tinnitus - I think stress, but perhaps exacerbated by iron/vitamin deficiencies. Painful ribs and sacroiliac joints - no idea, bloating made the pain worse. It got really bad but then got better. Irregular heart rate - could be a coincidence but my sister (not a coeliac) and I both developed this temporarily after our second Astra Zeneca covid jabs.   Subsequent Pfizer jabs didn't affect us. Brain fog - a big thing for people with certain autoimmune issues but in my case I think possibly worse when my iron or B12 are low, but I have no proof of this. Insomnia - stress, menopause. So basically, it isn't always gluten.  It might be worth having your vitamins and mineral levels checked, and if you have deficiencies speak to your Dr about how better to address them?    
    • knitty kitty
      @NanceK, I do have Hypersensitivity Type Four reaction to Sulfa drugs, a sulfa allergy.  Benfotiamine and other forms of Thiamine do not bother me at all.  There's sulfur in all kinds of Thiamine, yet our bodies must have it as an essential nutrient to make life sustaining enzymes.  The sulfur in thiamine is in a ring which does not trigger sulfa allergy like sulfites in a chain found in pharmaceuticals.  Doctors are not given sufficient education in nutrition (nor chemistry in this case).  I studied Nutrition before earning a degree in Microbiology.  I wanted to know what vitamins were doing inside the body.   Thiamine is safe and nontoxic even in high doses.   Not feeling well after starting Benfotiamine is normal.  It's called the "thiamine paradox" and is equivalent to an engine backfiring if it's not been cranked up for a while.  Mine went away in about three days.  I took a B Complex, magnesium and added molybdenum for a few weeks. It's important to add a B Complex with all eight essential B vitamins. Supplementing just one B vitamin can cause lows in some of the others and result in feeling worse, too.  Celiac Disease causes malabsorption of all the B vitamins, not just thiamine.  You need all eight.  Thiamine forms including Benfotiamine interact with each of the other B vitamins in some way.  It's important to add a magnesium glycinate or chelate supplement as well.  Forms of Thiamine including Benfotiamine need magnesium to make those life sustaining enzymes.  (Don't use magnesium oxide.  It's not absorbed well.  It pulls water into the intestines and is used to relieve constipation.)   Molybdenum is a trace mineral that helps the body utilize forms of Thiamine.   Molybdenum supplements are available over the counter.  It's not unusual to be low in molybdenum if low in thiamine.   I do hope you will add the necessary supplements and try Benfotiamine again. Science-y Explanation of Thiamine Paradox: https://hormonesmatter.com/paradoxical-reactions-with-ttfd-the-glutathione-connection/#google_vignette
    • Wheatwacked
      Your goal is not to be a good puppet, there is no gain in that. You might want to restart the ones that helped.  It sounds more like you are suffering from malnutrition.  Gluten free foods are not fortified with things like Thiamine (B1), vitamin D, Iodine, B1,2,3,5,6 and 12 as non-gluten free products are required to be. There is a Catch-22 here.  Malnutrition can cause SIBO, and SIBO can worsen malnutrition. Another possibility is side effects from any medication that are taking.  I was on Metformin 3 months before it turned me into a zombi.  I had crippling side effects from most of the BP meds tried on me, and Losartan has many of the side effects on me from my pre gluten free days. Because you have been gluten free, you can test and talk until you are blue in the face but all of your tests will be negative.  Without gluten, you will not create the antigen against gluten, no antigens to gluten, so no small intestine damage from the antigens.  You will need to do a gluten challange to test positive if you need an official diagnosis, and even then, no guaranty: 10 g of gluten per day for 6 weeks! Then a full panel of Celiac tests and biopsy. At a minimum consider vitamin D, Liquid Iodine (unless you have dermatitis herpetiformis and iodine exasperates the rash), and Liquid Geritol. Push for vitamin D testing and a consult with a nutritionist experienced with Celiack Disease.  Most blood tests don't indicate nutritional deficiencies.  Your thyroid tests can be perfect, yet not indicate iodine deficiency for example.  Thiamine   test fine, but not pick up on beriberi.  Vegans are often B12 deficient because meat, fish, poultry, eggs, and dairy are the primary souces of B12. Here is what I take daily.  10,000 IU vitamin D3 750 mg g a b a [   ] 200 mg CoQ10 [   ] 100 mg DHEA [   ] 250 mg thiamine B1 [   ] 100 mg of B2 [   ] 500 mg B5 pantothenic acid [   ] 100 mg B6 [   ] 1000 micrograms B12 n [   ] 500 mg vitamin c [   ] 500 mg taurine [   ] 200 mg selenium   
    • NanceK
      Hi…Just a note that if you have an allergy to sulfa it’s best not to take Benfotiamine. I bought a bottle and tried one without looking into it first and didn’t feel well.  I checked with my pharmacist and he said not to take it with a known sulfa allergy. I was really bummed because I thought it would help my energy level, but I was thankful I was given this info before taking more of it. 
    • Wheatwacked
      Hello @Scatterbrain, Are you getting enough vitamins and minerals.  Gluten free food is not fortified so you may be starting to run low on B vitamins and vitamin D.   By the way you should get your mom checked for celiac disease.  You got it from your mom or dad.  Some studies show that following a gluten-free diet can stabilize or improve symptoms of dementia.  I know that for the 63 years I was eating gluten I got dumber and dumber until I started GFD and vitamin replenishment and it began to reverse.  Thiamine can get used up in a week or two.  Symptoms can come and go with daily diet.  Symptoms of beriberi due to Thiamine deficiency.   Difficulty walking. Loss of feeling (sensation) in hands and feet. Loss of muscle function or paralysis of the lower legs. Mental confusion. Pain. Speech difficulties. Strange eye movements (nystagmus) Tingling. Any change in medications? Last March I had corotid artery surgery (90 % blockage), and I started taking Losartan for blood pressure, added to the Clonidine I was taking already.  I was not recovering well and many of my pre gluten free symptoms were back  I was getting worse.  At first I thought it was caused a reaction to the anesthesia from the surgery, but that should have improved after two weeks.  Doctor thought I was just being a wimp. After three months I talked to my doctor about a break from the Losartan to see if it was causing it. It had not made any difference in my bp.  Except for clonindine, all of the previous bp meds tried had not worked to lower bp and had crippling side effects. One, I could not stand up straight; one wobbly knees, another spayed feet.  Inguinal hernia from the Lisinopril cough.  Had I contiued on those, I was destined for a wheelchair or walker. She said the symptoms were not from Losartan so I continued taking it.  Two weeks later I did not have the strength in hips and thighs to get up from sitting on the floor (Help, I can't get up😨).  I stopped AMA (not recommended).  Without the Losartan, a) bp did not change, after the 72 hour withdrawal from Losartanon, on clonidine only and b) symptoms started going away.  Improvement started in 72 hours.  After six weeks they were gone and I am getting better.  
×
×
  • 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.