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

Bleu Cheese


Sweetfudge

Recommended Posts

gfp Enthusiast
Hmmm, I love bleu & have missed it because of the could-be-gluten warnings. But I just had a thought... these molds that grow on wheat... could they possibly be advantageous to Celiacs? Maybe they actually digest & destroy gluten! I'm thinking they might be analogous to the bacteria that make yogurt more digestible for the lactose intolerant. It's probably just wishful thinking, but maybe our bellies need some Roquefort!

Hm but we have LSD available now so no need for ergot... :ph34r:

Seriously though I have the same thoughts....


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



Celiac.com Sponsor (A8-M):



TinkerbellSwt Collaborator

Wow.. i have learned a lot from this thread. I have always been wondering about the subject of bleu cheese. I love the stuff and was always afraid to try it. If I understood correctly, some bleu actually says wheat on it?

The ones that dont should be safe?

I might not be understanding this. Please someone simplify it for me? I get all kinds of confuzzeled.

gfp Enthusiast
Wow.. i have learned a lot from this thread. I have always been wondering about the subject of bleu cheese. I love the stuff and was always afraid to try it. If I understood correctly, some bleu actually says wheat on it?

The ones that dont should be safe?

I might not be understanding this. Please someone simplify it for me? I get all kinds of confuzzeled.

Basically it depends on the manufacturer.

For instance, some Roquefort is started of with a culture grown on rye bread whereas other's are naturally allowed to develop mould from the cave.

lovegrov Collaborator

One more thought on bleu cheese. Many folks, including those who make cheese, very seriously doubt that "gluten" would even transfer in a culture grown on bread. And if it does transfer, the percentage of gluten in the culture would be miniscule and the amount of culture used is so tiny that the resulting gluten in the cheese would be so minor as to not be measureable. You get more gluten every time you eat a processed food or eat out.

I can't prove this is true, but it makes sense to me. Bleu cheese iosn't even a blip on my gluten radar.

richard

gfp Enthusiast
One more thought on bleu cheese. Many folks, including those who make cheese, very seriously doubt that "gluten" would even transfer in a culture grown on bread. And if it does transfer, the percentage of gluten in the culture would be miniscule and the amount of culture used is so tiny that the resulting gluten in the cheese would be so minor as to not be measureable. You get more gluten every time you eat a processed food or eat out.

I can't prove this is true, but it makes sense to me. Bleu cheese iosn't even a blip on my gluten radar.

richard

I lean towards this myself, its not actually the bread they are taking just a scraping off the bread and i think they mostly say this for "advertising".. for instance Roquefort Papillion make a big deal about the traditional rye bread but quite how often they go back the the bread is not mentioned... they can just take some of the mould from one of the other cheeses... and do this more or less indefinately.

On the other hand Societe guarantee both their Roquefort cheeses are natually infected for the caves ...two different sets of caves and hence 2 different strains of the penecilin.

I'm not seriously worried about the Papillon but given an equal choice take the other, especially since the Bargnaudes is my favorite anyway...

eKatherine Apprentice

I read a recipe for making blue cheese at home where you innoculated the cheese curds with a slurry of your favorite blue cheese before hooping them.

VegasCeliacBuckeye Collaborator

Soory it took me so long to chime in, but between the computer troubles and my crazy week at work, I have been swamped.

Ok, here is the "skinny" on the issue.

When Bleu cheese was origianlly made (and made in some expensive cheeseries - Stilton, Maytag, etc), the culture that produced the bacteria to make bleu cheese was started on bread. The mold that was made (cultured) was then introduced to a certain cheese and then the bacteria would reproduce and have a reaction throughout the cheese (thus turning the cheese moldy or blue).

In the late 90's (and early 2000's), thanks to the internet, Celiac urban lagends and myths abounded and this one was incredibly popular. Afterall, if the bacteria came from bread, then the entire cheese has gluten in it right?

Wrong...

Most bleu cheese manufacturers now acquire their mold/culture via a scientifically made medium which is manufactured in gross and which allows them to produce massive amounts of bleu cheese (tons and tons).

Think about it, what is cheaper? Making the bacteria on your own with bread and then having people carefully remove gthe mold and introduce to cheese by hand....OR buying/manufacturing your own bacteria and having computers/machines to introduce the process and manufacture tons of cheese at half the labor cost???

I know what you're saying....but Bronco, not everyone does that...some people still make bleu cheese the old-fashioned way, right?

That is correct!

Is it safe? -- This is the one that is up for debate.

Personally, I say yes. In a scientific sense, the likelihood that a bacteria grown from mold (which is breaking down the bread) and placed on/in/around cheese would somehow still have gluten left in it after the decomposition of both the bread and the cheese??? Seems remote to me. But we all make our own decisions.

anyway, I hope this somehow clears the issue up (though it could confuse the issue also - LOL)

For the record, I eat it all the time with no ill effects...

"they can take our bread, but they will never take our FREEDOM...or bleu cheese..."


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



Celiac.com Sponsor (A8-M):



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. - trents replied to Ginger38's topic in Related Issues & Disorders
      1

      Shingles - Could It Be Related to Gluten/ Celiac

    2. - Ginger38 posted a topic in Related Issues & Disorders
      1

      Shingles - Could It Be Related to Gluten/ Celiac

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

      Study Estimates the Costs of Delayed Celiac Disease Diagnosis (+Video)

    4. - Russ H posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      Coeliac UK Research Conference 2025

    5. - Rejoicephd replied to Rejoicephd's topic in Related Issues & Disorders
      5

      Basic metabolic panel results - more flags


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,375
    • Most Online (within 30 mins)
      7,748

    Sher Lee
    Newest Member
    Sher Lee
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • trents
      I don't know of a connection. Lots of people who don't have celiac disease/gluten issues get shingles.
    • Ginger38
      I’m 43, just newly diagnosed with a horrible case of shingles last week . They are all over my face , around my eye, ear , all in my scalp. Lymph nodes are a mess. Ear is a mess. My eye is hurting and sensitive. Pain has been a 10/10+ daily. Taking Motrin and Tylenol around the clock. I AM MISERABLE. The pain is unrelenting. I just want to cry.   But Developing shingles has me a bit concerned about my immune system which also has me wondering about celiac and if there’s a connection to celiac / gluten and shingles; particularly since I haven't been 💯 gluten free because of all the confusing test results and doctors advice etc., is there a connection here? I’ve never had shingles and the gluten/ celiac  roller coaster has been ongoing for a while but I’ve had gluten off and on the last year bc of all the confusion  
    • Russ H
      There were some interesting talks, particularly Prof Ludvig Stollid's talk on therapeutics for coeliac disease.    https://www.youtube.com/playlist?list=PLRcl2mPE0WdigRtJPvylUJbkCx263KF_t
    • Rejoicephd
      Thank you @trents for letting me know you experience something similar thanks @knitty kitty for your response and resources.  I will be following up with my doctor about these results and I’ll read the articles you sent. Thanks - I really appreciate you all.
    • knitty kitty
      You're right, doctors usually only test Vitamin D and B12.  Both are really important, but they're not good indicators of deficiencies in the other B vitamins.  Our bodies are able to store Vitamin B12 and Vitamin D in the liver for up to a year or longer.  The other B vitamins can only be stored for much shorter periods of time.  Pyridoxine B 6 can be stored for several months, but the others only a month or two at the longest.  Thiamine stores can be depleted in as little as three days.  There's no correlation between B12 levels and the other B vitamins' levels.  Blood tests can't measure the amount of vitamins stored inside cells where they are used.  There's disagreement as to what optimal vitamin levels are.  The Recommended Daily Allowance is based on the minimum daily amount needed to prevent disease set back in the forties when people ate a totally different diet and gruesome experiments were done on people.  Folate  requirements had to be updated in the nineties after spina bifida increased and synthetic folic acid was mandated to be added to grain products.  Vitamin D requirements have been updated only in the past few years.   Doctors aren't required to take as many hours of nutritional education as in the past.  They're educated in learning institutions funded by pharmaceutical corporations.  Natural substances like vitamins can't be patented, so there's more money to be made prescribing pharmaceuticals than vitamins.   Also, look into the Autoimmune Protocol Diet, developed by Dr. Sarah Ballantyne, a Celiac herself.  Her book The Paleo Approach has been most helpful to me.  You're very welcome.  I'm glad I can help you around some stumbling blocks while on this journey.    Keep me posted on your progress!  Best wishes! P.S.  interesting reading: Thiamine, gastrointestinal beriberi and acetylcholine signaling https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/
×
×
  • 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.