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

Travelling On "Carnival Victory"


Deb350

Recommended Posts

Deb350 Newbie

I recently returned from a cruise on Carnival Victory. Carnival has on their website that they accommodate gluten-free diets. I did my research, as best you can, and saw 3 travelers blogs that said they had bread, pancakes, and french toast. After traveling all day and having to be careful of what I eat I looked forward to getting on the ship and having a late lunch. I went to the Main Dining Room only to be greeted by the waiter when asking for a gluten-free Menu that they didn't have one. He said I could have fruit and that they Maitre De would be coming to take my meal request for the "NEXT Day". I told him that this was unacceptable and that I would need to see her now. He then said you can have fish and steamed vegetables. I had a fruit dish to start, fish and steamed vegetables. When I asked what I could have for dessert, I was told fruit. I went to the front desk. Told them my dilemma. They sent me back to talk to Maitre De. She told me to come the next day for breakfast. They made me gluten-free pancakes which were nothing more than corn tortillas. I could not eat them. Absolutely gross! I went to lunch that day. Asked what I could have that didn't have soy sauce on it. I was told everything has soy sauce. Had to get the Assistant Maitre De and she told me that I could have soy sauce. Very scary! Needless to say I lost 3 pounds. Was absolutely starving. When we got off in St. Martin I headed for a restaurant where they understood everything about gluten-free and it was the first meal I had that was delicious in 6 days. This was my 40th anniversary gift and I this was my 14 cruise. The food was absolutely disgusting and they DO NOT have a clue about Gluten Free. Do yourself a favor and find a different cruise line.

  • 4 weeks later...

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



Celiac.com Sponsor (A8-M):



Deb350 Newbie

I wrote to the CEO of Carnival regarding my experience and below is their response:

Good morning Mrs. Bruno:

Mr. Arison has forwarded your letter to my attention for handling as concerns of this nature fall under my purview. It's my pleasure to respond on his behalf.

I'm sorry you feel that our call center agents and supervisory staff did not give your issues the attention they deserve. I can assure you that the concerns you've raised have been addressed by the appropriate management team and reviewed thoroughly. Nonetheless, we

  • 2 weeks later...
notme Experienced

well. coincidentally, we were looking at cruises the other day. for a very large group of us! i will not be cruising 'carnival' !!! you poor thing to have to starve the whole trip. thanx for sharing - obviously they don't give a crap about their customers...

  • 1 month later...
Tim-n-VA Contributor

I just finished a seven day cruise with Carnival (Glory). My experience was completely opposite from what Deb experienced.

I did talk to some of the staff and they generally have a contract for several months and then they rotate out. Just like any land based restaurant personnel turnover introduces risk.

  • 2 months later...
txgal748 Apprentice

We have been on two Carnival cruises this year. The second after my diagnosis. We do not eat in the dining room we eat at the buffet. I talked to the chef and he told me the main meat dishes in the carvery are gluten free and of course they always have salads and veggies. This ship also had an Indian restaurant for lunch in which most of the fod was gluten-free. For dessert I took my own chocolate.The chef said he could fix me gluten-free foods if I asked for him. Overall I was pleased with the service.

Archived

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

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

    • Total Members
      133,076
    • Most Online (within 30 mins)
      7,748

    Monica L
    Newest Member
    Monica L
    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

    • cristiana
      Thank you for your thoughtful contribution, @Tazfromoz. I live in the UK and the National Health Service funds free vaccines for people deemed to be at heightened risk.  I was pleasantly surprised to discover that as a coeliac in my 50s I was eligible for this vaccine, and didn't think twice when it was offered to me.  Soon after diagnosis I suffered mystery symptoms of burning nerve pain, following two separate dermatomes, and one GP said he felt that I had contracted shingles without the rash aka zoster sine herpete.  Of course, without the rash, it's a difficult diagnosis to prove, but looking back I think he was completely spot on.  It was miserable and lasted about a year, which I gather is quite typical. For UK coeliacs reading this, it is worth having a conversation with your GP if you haven't been vaccinated against shingles yet, if you are immunosuppressed or over 50. I have just googled this quickly - it is a helpful summary which I unashamedly took from AI, short for time as I am this morning!   My apologies. In the UK, coeliac patients aren't automatically eligible for the shingles jab unless they're severely immunosuppressed or over the general age for vaccination (currently 50+) but Coeliac UK recommends discussing the vaccine with a GP due to potential splenic dysfunction, which can increase risk, even if not routine for all coeliacs. Eligibility hinges on specific criteria like weakened immunity (chemo, certain meds) or age, with the non-live Shingrix vaccine offered in two doses to those deemed high-risk, often starting from age 18 for the immunocompromised.
    • Tazfromoz
      My understanding, and ex I erience is that we coeliacs are likely to suffer more extreme reactions from viruses. Eg we are more likely to be hospitalised with influenza. So, sadly, your shingles may be worse because you are coeliac. So sorry you had to go through this. My mother endured shingles multiple times. She was undiagnosed with coeliac disease until she was 65. Me at 45. I've had the new long lasting vaccine. It knocked me around badly, but worth it to avoid shingles.
    • hjayne19
      Hi all,  Looking for some advice. I started having some symptoms this past summer like night sweats and waking at 4 am and felt quite achy in my joints. I was training heavily for cycling for a few weeks prior to the onset of these symptoms starting. I have had low Ferratin for about 4 years (started at 6) and usually sits around 24 give or take. I was doing some research and questioned either or not I might have celiac disease (since I didn’t have any gastric symptoms really). My family doctor ran blood screening for celiac. And my results came back: Tissue Transglutaminase Ab IgA HI 66.6 U/mL Immunoglobulin IgA 1.73 g/ My doctor then diagnosed me with celiac and I have now been gluten free for 3 months. In this time I no longer get night sweats my joint pain is gone and I’m still having trouble sleeping but could very much be from anxiety. I was since referred to an endoscopy clinic to get a colonoscopy and they said I should be getting a biopsy done to confirm celiac. In this case I have to return to eating gluten for 4-6 weeks before the procedure. Just wanted some advice on this. I seem to be getting different answers from my family physician and from the GI doctor for a diagnosis.    Thanks,  
    • yellowstone
      Cold/flu or gluten poisoning? Hello. I've had another similar episode. I find it very difficult to differentiate between the symptoms of a cold or flu and those caused by gluten poisoning. In fact, I don't know if my current worsening is due to having eaten something that disagreed with me or if the cold I have has caused my body, which is hypersensitive, to produce symptoms similar to those of gluten poisoning.        
    • Churro
      I'm no longer dealing with constipation. I got my liver test last month and it was in normal range. Two years ago I did have a vitamin D deficiency but I'm know taking vitamin D3 pills. Last month I got my vitamin D checked and it was in normal range. I don't believe I've had my choline checked. However, I do drink almond milk eat Greek yogurt on a daily basis. 
×
×
  • 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.