Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Kraft Blue Cheese Dressing


pnltbox27

Recommended Posts

pnltbox27 Contributor

i was reading the label on the blue cheese dressing from kraft and didnt see anything that looked evil, but i thought i read that blue cheese was a no no. any help would be great


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



Celiac.com Sponsor (A8-M):



psawyer Proficient

Kraft will clearly disclose any source of gluten. If you did not see it in the ingredients, it isn't there. Look for the specific words wheat, rye, barley or oats.

I can't offer personal knowledge on this product, I simply don't like bleu cheese so I don't use this dressing. There are only two or three Kraft dressings that are NOT gluten-free. We use the French and Golden Italian, but most others are also safe. If I recall correctly, the ones with gluten are a ranch and a caesar, but don't rely on me for this. It's Kraft, so just read the label.

ravenwoodglass Mentor
i was reading the label on the blue cheese dressing from kraft and didnt see anything that looked evil, but i thought i read that blue cheese was a no no. any help would be great

I would call the company and find out how the blue cheese is made and will they guarentee that it is gluten-free. There may not be any gluten ingredients per se in this but gluten is used in the formation of most blue cheese.

In addition you need to keep in mind that some of us, not all, will react to distilled gluten grain vineager so I always make sure that it is corn or wood derived. Many companies go with the idea that we can all tolerate distilled grain and will consider an item gluten-free even if it contains it.

I personally don't use Kraft products so I haven't tried this dressing since I am lucky to have a Wegmans near by that clearly labels everything that is safe.

Daxin Explorer

I can say from experience, that the Caeaer dressing has wheat in it. I am not sure about the blue cheese, but I think I rememebr seeing it on the list of products from Kraft that were okay!

VegasCeliacBuckeye Collaborator

I have eaten Kraft's Bleu Cheese Dressing regularly for 5 years with no ill effects (I am sensitive)

Chris

pnltbox27 Contributor

thanks guys for the help, i dont even eat the stuff , but was trying to understand reading the labels a little better. im still pretty new to this B)

larry mac Enthusiast

pnltbox27,

That's a new one. Can't wait till ya get to the stuff you do eat! Just kidding. That's a good question.

All the research I did convinced me it is gluten-free. I was wavering until I visited our gluten-free restaurant and discovered blue cheese on the menu.

Some of the bottled products at the store list wheat on the ingredients. Not sure what that's about. Perhaps they just got tired of all the phone calls and figured it was easier this way.

Never have cared for that stuff anyway. From time to time I'll find a restaurant that serves a good blue cheese dressing and buy some from them. Got that from my Mother. Soon as I started to drive, she would have me go to a place a few miles from our house and get some of their wonderful blue cheese dressing. Sometimes restaurant staff will act like they never heard of such a thing, but they soon enough get you some to go. Got spoiled I guess and just never could be satisfied with the store bought stuff.

I've been getting an excellant fresh made version from Central Market in Dallas, 1000% better than bottled!

best regards, lm


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



Celiac.com Sponsor (A8-M):



larry mac Enthusiast

pnltbox27,

Here's some reading from google:

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

And some previous threads:

Open Original Shared Link

Open Original Shared Link

best regards, lm

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      129,937
    • Most Online (within 30 mins)
      7,748

    kazzie21
    Newest Member
    kazzie21
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Your experience with gluten is actually not unheard of! Some people with non-celiac gluten sensitivity (NCGS) or even celiac disease report an initial ‘honeymoon phase’ during a gluten challenge, where symptoms temporarily improve before worsening again. This could be due to your body adjusting or even a temporary immune modulation. Since you’re only 2.5 weeks into the challenge, it’s possible more symptoms could reappear if you continue. Celiac testing (bloodwork and endoscopy) is most accurate after a full 6 weeks of gluten, so sticking with it for now is wise. That said, your joint/tendon issues (especially the Achilles stiffness) are interesting—they can be linked to celiac disease or other autoimmune conditions (like rheumatoid arthritis or even reactive arthritis). Have you been tested for celiac antibodies yet? If not, that’s the next step. If the tests come back negative, NCGS or another immune-related issue (like FODMAP intolerance or mast cell activation) might still be at play. It’s also worth noting that recurrent miscarriage and elevated liver enzymes can be linked to celiac (it’s often underdiagnosed in women with ‘atypical’ symptoms like yours). But if celiac is ruled out, a rheumatologist or a gastroenterologist who specializes in immune-related GI issues might help explore other possibilities (like Hashimoto’s, Sjögren’s, or connective tissue disorders). Hang in there—it’s frustrating not to have clear answers, but you’re doing all the right things by paying attention to your body and pushing for testing. Keep us posted on how the rest of your gluten challenge goes!
    • Jacki Espo
      Hi there @Pamp8  yes I've had dermatitis herpetiformis and a negative test for celiac and a negative biopsy. I had stopped eating gluten before taking the test.  I have had an inconclusive genetic (?) test.  I developed the same all body rash.  It was one of the worst experiences of my life and I am sorry you're experiencing it.  What helped me: 1). I stopped eating oats of any kind. 2). I also took some anti-biotics that were not prescribed for dermatitis herpetiformis but I read they could help. 3). Salty food exacerbates it for me.  Now I have a small flare up any time I get cross contamination like from french fries or a shared grill at a restaurant but it's not as bad as it used to be.  Wishing you relief soon. 
    • trents
      Welcome to the forum, @Pamp8! As to your first question, it is possible to have only the epidermal form of celiac disease but it is not common. Most people who have dermatitis herpetiformis also have damage being done to the villous lining of the small bowel.  As to your second question, most likely you are getting some gluten contamination from an unknown source on occasion that you are unaware of and are not suspecting. It could be something like in a medication or supplement you are taking or an oral hygiene product you are using or a spice you are using in your cooking. You might also look into a low iodine diet as iodine is known to exacerbate dermatitis herpetiformis. As to your third question, many who suffer from dermatitis herpetiformis find it is a stubborn problem and difficult to completely control.
    • Pamp8
      I'm new here, although in the past I know I've read some of the messages.   My doctor and I have long suspected that I have celiac. I have several other autoimmune illnesses. But, my celiac biopsy was negative, so I started eating a lot more gluten.  Over the last several years, I've had minor bouts of an extremely itchy rash that I was correlating to gluten, but it wasn't very bad and would improve in a short amount of time. Last year, I had a bout that was a bit worse, but it went away rather quickly, so I didn't think too much about it. Fast forward to this year. I have had a REALLY BAD case of it, for a few months, so I went to a dermatologist, and she diagnosed dermatitis herpetiformis without a biopsy. It was pretty obvious to her that it is dermatitis herpetiformis, but she said that if I wanted her to, she would do a biopsy. She said that I have just become more sensitized over time. She prescripbed Dapsone gel, which helps a lot, but I run out of it long before I'm eligible for a refill. So, I am going CRAZY. It is on my arms, legs trunk, everywhere, and it itches like chiggers. If I get even the slightest bit sweaty, it is so unbearable. I've been 100% gluten free since April, but it keeps flaring up. (I've been under intense stress, too.)  My questions are:  1.) Do many people have celiac without a positive celiac biopsy?  2.) How long will the dermatitis herpetiformis persist, even though I'm 100% gluten free? 3.) Is my story a common one? Thanks so much!
    • leenora
      P.S. I also suffer from Meniere's and Hashimoto's thyroid disease, osteopenia since 40 y.o. These all were diagnosed before the Celiac Disease! And I believe it is all interconnected.
×
×
  • Create New...