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:
    Join eNewsletter
    Donate

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Mari replied to Jmartes71's topic in Related Issues & Disorders
      15

      My only proof

    2. - Rejoicephd commented on Jefferson Adams's article in Gluten-Free Cooking
      1

      Your Complete Gluten-Free Thanksgiving Plan: Recipes, Tips & Holiday Favorites

    3. - marion wheaton replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Are Lindt chocolate balls gluten free?

    4. - trents replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Are Lindt chocolate balls gluten free?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,422
    • Most Online (within 30 mins)
      7,748

    HAUS
    Newest Member
    HAUS
    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

    • Mari
      Years  ago a friend and I drove north into Canada hoping to find a ski resort open in late spring,We were in my VW and found a small ski area near a small town and started up this gravelled road up a mountain. We  got about halfway up and got stuck in the mud. We tried everything we could think of but an hour later we were still stuck. Finally a pickup came down the road, laughed at our situation, then pulled the VW free of the mud. We followed him back to the ski area where where he started up the rope ski lift and we had an enjoyable hour of skiing and gave us a shot of aquavit  before we left.It was a great rescue.  In some ways this reminds me of your situation. You are waiting for a rescue and you have chosen medical practitioners to do it now or as soon as possible. As you have found out the med. experts have not learned how to help you. You face years of continuing to feel horrible, frustrated searching for your rescuer to save you. You can break away from from this pattern of thinking and you have begun breaking  away by using some herbs and supplements from doTerra. Now you can start trying some of the suggestions thatother Celiacs have written to your original posts.  You live with other people who eat gluten foods. Cross contamination is very possible. Are you sure that their food is completely separate from their food. It  is not only the gluten grains you need to avoid (wheat, barley, rye) but possibly oats, cows milk also. Whenever you fall back into that angry and frustrated way of thinking get up and walk around for a whild. You will learn ways to break that way of thinking about your problems.  Best wishes for your future. May you enjpy a better life.  
    • marion wheaton
      Thanks for responding. I researched further and Lindt Lindor chocolate balls do contain barely malt powder which contains gluten. I was surprised at all of the conflicting information I found when I checked online.
    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
×
×
  • 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.