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

Celiac and dairy


BrittanyM

Recommended Posts

BrittanyM Rookie

Hi everyone! 

I got diagnosed last August after suffering from Mono. Since then things have been okay but not great. Still an icky stomach, started taking pre/probiotics and some vitamins. Now after a year a few months..for a week or two I’ve been getting migranes, sinus pressure and body aches? (Which is weird)..I’m currently putting myself on a dairy-free diet to see if it will help. I hope it does but the other part of me hopes it isnt dairy and maybe ive just glutned myself somewhere in the past week lol. I love my cheese, I can live without milk but cheese is my thing! Any sugguestions or help if anyone is dairy free and these were also their symptoms? Thanks! 


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



Celiac.com Sponsor (A8-M):



Victoria1234 Experienced

Could your probiotics or vitamins have gluten in them?

Ennis-TX Grand Master
33 minutes ago, BrittanyM said:

Hi everyone! 

I got diagnosed last August after suffering from Mono. Since then things have been okay but not great. Still an icky stomach, started taking pre/probiotics and some vitamins. Now after a year a few months..for a week or two I’ve been getting migranes, sinus pressure and body aches? (Which is weird)..I’m currently putting myself on a dairy-free diet to see if it will help. I hope it does but the other part of me hopes it isnt dairy and maybe ive just glutned myself somewhere in the past week lol. I love my cheese, I can live without milk but cheese is my thing! Any sugguestions or help if anyone is dairy free and these were also their symptoms? Thanks! 

Plenty of dairy free cheese, I make own cheese sauce, I buy dairy free cheese extracts, I make my own vegan Parmesan, and I buy dairy free cheese often. I love the new leaf cuisine diary cheese spreads, the smoked Gouda is to die for. I sometimes snack on daiya cheese like yesterday I had some Daiya Havarti and jalapeno slices with my omelette. Bit of a list at the end of this, note their are more options but the ones are things I have tried and are also soy free. The dairy thing is something most celiacs only have a issue with for a few months. Some have life time issues with dairy like me, I also went and watched a bunch of anti diary propaganda and did a bunch of research to convince myself to give it up when I became lactose intolerant 10+ years ago. >.> like why do human drink cow milk....same as drinking dog milk.,...both not for human consumption why drink it when it is meant for another species. Anyway just what I confirm with myself to no touch it.

Dairy Free Alternatives to Dairy Foods

Open Original Shared Link
^ Almond, cashew, coconut, blends etc.

Open Original Shared Link
^ More Almond, cashew, coconut, blends, they also offer yogurt and icecream alternatives.

Open Original Shared Link
^ They offer many coconut options, Yogurt, cheese, milks, icecream pints, icecream bars.

Open Original Shared Link
^VERY high end minimally processed almond milk, one the the best

Open Original Shared Link
^ NUT FREE, Dairy Free options of a rich milk alternative from yellow peas (legumes)

Open Original Shared Link
^Flax Based milk alternatives

Open Original Shared Link
^ BEST and least processed cheese spreads, cream cheese etc. I can eat these without any issues

Open Original Shared Link
^Offers Vegan cheese slices, cheese blocks, cheese shreds, pizza, CHEESE CAKES!, yogurt, s

Open Original Shared Link
^ Diary free and vegan, cheese, spreads, dips, dressings, condiments

Open Original Shared Link
*^ICE CREAM by the pint AND THEY SHIP IT TO YOU, Dairy free, soy free, sugar free, PERFECT bliss I suggest getting the gluten free pastry pack

PS I have a vegan bacon cheese sauce and a vegan queso dip on my recipe blog on my profile if you want to try them both are good in other recipes like the sauce makes a excellent base in potato gratin or broccoli casserole.

Panda811 Newbie

I am not able to eat dairy and it has been over three years since diagnosis of celiac.  However, I am not lactose intolerant.  My symptoms are headache, neck and back pain l, congestion and swollen joints.  I have been told it is the protein in dairy for me versus the lactose.  I have also been allergy tested and do not have an allergy.  And like you...  I LOVE cheese.  Sometimes I go for it and just know that I will suffer the consequences.  Keep a food journal because I also react to corn, oats, soy and eggs.  All inflammatory foods to boot!  Good luck.

PTArt Apprentice

The casein in milk is very similar to the gluten protein, and over time the ammune  system can react to the casein as though it was gluten. This happens over time, and though you may have been able to consume dairy previously, you may have to avoid it now. Not good to suffer the consequences, it can do damage that you are not aware of.

 

kareng Grand Master
1 hour ago, PTArt said:

The casein in milk is very similar to the gluten protein, and over time the ammune  system can react to the casein as though it was gluten. This happens over time, and though you may have been able to consume dairy previously, you may have to avoid it now. Not good to suffer the consequences, it can do damage that you are not aware of.

 

Is there new legitimate research on this?  Please post a link.  I have not seen anything that proves that assumption.

knitty kitty Grand Master

There's this study...

Open Original Shared Link

On 12/12/2017 at 8:12 AM, kareng said:

Is there new legitimate research on this?  Please post a link.  I have not seen anything that proves that assumption.

 

On 12/12/2017 at 7:04 AM, PTArt said:

The casein in milk is very similar to the gluten protein, and over time the ammune  system can react to the casein as though it was gluten. This happens over time, and though you may have been able to consume dairy previously, you may have to avoid it now. Not good to suffer the consequences, it can do damage that you are not aware of.

 

 


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master
2 hours ago, knitty kitty said:

There's this study...

Open Original Shared Link

 

 

Knitty Kitty, 

Did you read and understand the study?  It did not say that milk proteins can trigger celiac disease (or mention cross reactions), but that they can cause an inflammatory response similar to what occurs in Celiac patients.  The study suggests this might be as a result of a leaky gut and other food proteins may cause the same effects.  We all know that celiacs tend to have too much zonulin causing “leaky gut” for a better term.  Foods, like corn, soy, etc. can cause the same effect (villi damage or symptoms)  as stated in the study.  

The milk proteins did NOT raise specific antibodies for gluten.  However, they can damage intestinal villi (as can many things besides gluten).  

Open Original Shared Link

The study suggests that if celiac disease patients are still experiencing symptoms they may need to look for hidden gluten or consider a milk (or another food) protein intolerance.  

We normally suggest to people who are not recovering fast on a gluten free diet to maintain a food/symptom diary to help indentify additional food intolerances or allergies.  After all, celiac disease is under the umbrella of Hypersensitivity (Type 4) and it makes sense that we would be more intolerant or allergic than the average person.  

kareng Grand Master
15 minutes ago, cyclinglady said:

Knitty Kitty, 

Did you read and understand the study?  It did not say that milk proteins can trigger celiac disease (or mention cross reactions), but that they can cause an inflammatory response similar to what occurs in Celiac patients.  The study suggests this might be as a result of a leaky gut and other food proteins may cause the same effects.  We all know that celiacs tend to have too much zonulin causing “leaky gut” for a better term.  Foods, like corn, soy, etc. can cause the same effect (villi damage or symptoms)  as stated in the study.  

The milk proteins did NOT raise specific antibodies for gluten.  However, they can damage intestinal villi (as can many things besides gluten).  

Open Original Shared Link

The study suggests that if celiac disease patients are still experiencing symptoms they may need to look for hidden gluten or consider a milk (or another food) protein intolerance.  

We normally suggest to people who are not recovering fast on a gluten free diet to maintain a food/symptom diary to help indentify additional food intolerances or allergies.  After all, celiac disease is under the umbrella of Hypersensitivity (Type 4) and it makes sense that we would be more intolerant or allergic than the average person.  

That's what I thought, too!  

I think a lorn of people are having problems with lactose.... not casein.  I know one of the above posters said low lactose foods were fine

 

Posterboy Mentor
On 12/7/2017 at 4:51 PM, BrittanyM said:

Hi everyone! 

I got diagnosed last August after suffering from Mono. Since then things have been okay but not great. Still an icky stomach, started taking pre/probiotics and some vitamins. Now after a year a few months..for a week or two I’ve been getting migranes, sinus pressure and body aches? (Which is weird)..I’m currently putting myself on a dairy-free diet to see if it will help. I hope it does but the other part of me hopes it isnt dairy and maybe ive just glutned myself somewhere in the past week lol. I love my cheese, I can live without milk but cheese is my thing! Any sugguestions or help if anyone is dairy free and these were also their symptoms? Thanks! 

BrittanyM et al,

I just wanted to post this thread that might answer some of your questions about Casein/Dairy JMG had a similar question.

It has two livestrong links in it that explains well about the different kinds of Casein proteins.

I did not know there "types" of the casein protein but like you I knew I was reacting to dairy.

Open Original Shared Link

Open Original Shared Link

according to livestrong you are out of luck if can't live without cheese if indeed casein is your problem and not lactose.

from livestrong " There is no way to make cheese free of casein proteins. Do not eat cheese if you’ve been diagnosed with a milk allergy."

but there are lactose free cheeses and they will be labeled so like the gluten free things are.

I think the study Knitty Kitty linked studied Cow's Milk . .. it might be you don't react the same to goat's milk or goat cheese since these casein's are different from CM's caseins' according to livestrong.

who knew right?

I hope this is helpful.

posterboy,

Feeneyja Collaborator

Lactose intolerance occurs when you lack the enzyme (called lactase) necessary to properly break down the milk sugar lactose.  That undigested milk sugar cannot enter the body. But it then feeds gut bacteria producing gas, bloating, discomfort/pain.   There are no extra intestinal symptoms (this is an important point).

However, gut dysbiosis can ultimately be the result of lactose  intolerance (or any sugar intolerance).  Two things have been demonstrated to increase zonulin production (which opens the tight junctions, resulting in leaky gut): Gluten and Bacteria. SIBO (small intestine bacterial overgrowth), which can occur because of lactose intolerance, is essentially a bacterial infection of the small intestines and results in increased intestinal permeability (AKA leaky gut). SIBO can also damage the villi, making your ability to break down foods more compromised, feeding the SIBO/leaky gut cycle. 

With leaky gut you now have large proteins entering the bloodstream illicitting an immune response.  This is the cause of the extra intestinal symptoms and other protein intolerances.   

Its also worth noting that there is a fairly high prevalence of SIBO in those with celiac disease.

See this very informative lecture given by Dr. Fasano on the topic of intestinal permeability:

Zonulin, intestinal permeability and immune mediated disorders: facts and fantasies

Open Original Shared Link

 

knitty kitty Grand Master

"Activation of the adaptive immune system is one prerequisite for the occurrence of celiac disease and is reflected by the development of gliadin antibodies and auto antibodies. Our finding that, in a fraction of coeliac patients, CM protein challenge may induce an inflammatory reaction of the same magnitude, as did gluten challenge, may also suggest an innate as well as adaptive immune response to CM, and casein in particular. However, lack of increased serum antibodies to casein in our casein-sensitive coeliac patients may suggest that casein is less prone than gliadin to drive adaptive immunity."

Open Original Shared Link

Adaptive as well as innate immune response to casein is possible though not as common.  Casein can cause a reaction as severe as gluten.  

Open Original Shared Link

"Rich sources of celiac-disease-potentiating peptides were wheat gliadins, barley hordeins and rye secalins as well as low-molecular weight fractions of glutenin. In addition, amino acid sequences with a high degree of identity to the toxic peptides examined were detected in maize zein, oat avenin, protein of rice, yeast and chicken muscles, as well as β-casein and galanin."

Toxic peptides in corn and oats and casein and chicken.  Interesting.  Very interesting.  

  

 

knitty kitty Grand Master

Open Original Shared Link

Open Original Shared Link

Potatoes can aggravate leaky guts.

Many gluten free processed foods use potato starch.

  • 1 month later...
dopaminegirl Apprentice

I also can't have dairy but through a series of experiments and a lot of research I think I've pinpointed my problem. It may or may not be the same for you, but I thought I'd share. 

There are two kinds of beta-casein protein A1 and A2. We'll call A1 "bad casein" and A2 "good casein". The two proteins differ only in a single amino acid, but this is enough to make it so that they are processed differently in your guy. Bad casein is actually broken down into a casomorphin, which is an opioid peptide. That does not mean that milk gets you high, or is as addictive as heroin, or anything like that, it just means that it can interact with opioid receptors (which the gut has a bunch of).

It's worth noting that opioids cause constipation due to their interaction with the opioid receptors in the gut, and that a lot of people feel like cheese and dairy slow things down, but any connection between the two is pure speculation on my part at this point. 

Now here's where things get weird. The vast majority of milk cows in the western world are derived from Holstein-like breeds, meaning black and white cows. In a few select places, you'll see farms that use Jersey-type cows, or brown cows (Jersey cows produce less milk than Holsteins, but many connoisseurs feel it's a higher quality milk, particularly for cheese).  Holstein-like cows have A1 and A2 casein (bad and good), however, Jersey-type cows only have A2 (good casein), unless their genetic line involved a Holstein somewhere in the past, which does happen. 

A company in New Zealand figured out how to test their cows for these two genes, and selected their herd down to cows that specifically produce ONLY A2 (good) casein. You might have seen it in the store, it's called A2 milk. Some people have had a lot of luck with this milk, though it still doesn't solve the problem of cheese. 

I have suspected, due to trial and error and a few accidental exposures, that I have a problem with A1 casein, but not A2. In line with this: I am able to eat sheep and goat dairy without any difficulty, so at least I can still enjoy those cheeses! I am also fortunate because I'm apparently not too sensitive, as I can still eat cow-milk butter. The process of making butter removes *most* (read: enough for me) of the casein. 

However, if I eat cow cheese or a baked good with milk, I get really sick. It's a much faster reaction than if I get glutened. Within minutes I'm dizzy and tired and my limbs are heavy. I have to sleep for a couple of hours, and then, over the next couple of days, I'm vulnerable to moodiness and muscles spasms and stomach upset just as though I'd been glutened (though the brain fog isn't as bad).

I actually haven't tried A2 milk yet, mostly due to lack of availability (and motivation, I don't miss milk, I miss CHEESE). However, last year, when I was getting ready to go on a trip to Italy, I had a thought. Once, in the recent past, when I'd been testing dairy, I'd had a slice of parmesan cheese. Miracle of miracles, I was fine. I didn't feel a thing! I was so excited that I ran out and got some brie to eat as a snack. That did not go so well...

Turns out parmigiano reggiano is made from the milk of the Reggiana variety of cow which is, you guessed it, a brown cow (they say red). I did a little more research and found that dairies in Italy predominantly use brown cows. So I decided to try something.

As some of you may know, Italy is something of a haven for celiacs. It's one of the most gluten-free friendly places I've ever been. You can say "senza glutine" in the smallest little town and they don't even bat their eyelashes. You can buy gluten free foods in the pharmacy because they're considered a MEDICAL NECESSITY. If travelling-while-celiac freaks you out, go to Italy. Check out the website for the AIC (Italy's Celiac society), find some accredited restaurants, and GO NUTS.

While I was there, I decided to see if I could eat the dairy. I could. 

Friends, I ate gelato Every. Single. Night. after that. It was amazing. Between the dairy being safe for me and the preponderance of gluten free options, it was almost like I didn't have dietary restrictions. It was heaven. I want to go back and never leave. 

So that's my story. Almost too crazy to believe. 

TL;DR: Black and white cows make me sick, brown cows are my friends.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,959
    • Most Online (within 30 mins)
      7,748

    jenny44
    Newest Member
    jenny44
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.