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

May Have Found A Huge Answer...but Still Confused (Possible Dairy Allergy)


zebaldwin

Recommended Posts

zebaldwin Explorer

I've had many chronic symtoms over the past probably 7 or 8 years...getting worse over the past 2 years.

The core symtoms are chronic nauseous, dizzy, headaches/migraines (nearly every day), general fatigue and weakness, and brain fog.

I've seen MANY doctors. Multiple GPs, multiple neurologists, a GI, an ENT, eye doctors, dermatologists, therapists, you name it. Have also had a brain MRI and have been tested multiple times for celiac (blood and biopsy, all negative).

For a while I thought it might be celiac and went on a gluten free diet for several months with no results whatsoever.

The past few months I sort of gave up.

About 3 weeks ago I decided to completely cut dairy out of my diet after reading an article on food allergy related migraines.

Well, my migraines disappeared for the most part. One night I ate pizza to "test" things out, and exactly 24 hours later the migraine hit.

So I came to the conclusion that I had diary related migraines with a 24 hour delay (which I've heard is common).

A lot of things clicked. When I was eating gluten free, I was dairy free for about a week, but re-introduced it so that I could get more protein.

One of the weeks I remember feeling pretty good I was in Ireland and ate no dairy that I can remember.

However, today I got the headache. Yesterday I ate absolutely nothing with any trace of dairy.

I guess my question is, what in Dairy would be giving me the headaches? Is it something that could be in other foods that I'm not aware of? Am I wrong that dairy is causing my problems since I got a headache today?

I got really really excited that I had at least a small breakthrough and figured out one of my problems...but today I am just depressed thinking of why the headache would be back.

I'd appreciate any input that anybody might have...sorry if this is a little vague. I'm trying to sum up A LOT in a few words.

Thanks guys!!


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



Celiac.com Sponsor (A8-M):



Lisa Mentor

I would suggest that you be tested with these:

The following are the celiac specific blood tests:

Anti-Gliadin (AGA) IgA

Anti-Gliadin (AGA) IgG

Anti-Endomysial (EMA) IgA

Anti-Tissue Transglutaminase (tTG) IgA

Deamidated Gliadin Peptide (DGP) IgA and IgG

Total Serum IgA

Are these the tests you had taken for Celiac? There is such as thing as Non Celiac Gluten Intolerance, meaning that you have symptoms of Celiac or Gluten Sensitivity, without testing positive. But there is no reliable test for that at this time.

If you like to be retested for Celiac, you must be on a full gluten diet for about three months. If not, you may go FULL gluten free (not sort of).

If you choose the diet, we can walk you through it. But it must be as 100% as possible. If you have no other options to relieve your migrane's, why not try. :)

....and welcome!

pricklypear1971 Community Regular

I've had many chronic symtoms over the past probably 7 or 8 years...getting worse over the past 2 years.

The core symtoms are chronic nauseous, dizzy, headaches/migraines (nearly every day), general fatigue and weakness, and brain fog.

I've seen MANY doctors. Multiple GPs, multiple neurologists, a GI, an ENT, eye doctors, dermatologists, therapists, you name it. Have also had a brain MRI and have been tested multiple times for celiac (blood and biopsy, all negative).

For a while I thought it might be celiac and went on a gluten free diet for several months with no results whatsoever.

The past few months I sort of gave up.

About 3 weeks ago I decided to completely cut dairy out of my diet after reading an article on food allergy related migraines.

Well, my migraines disappeared for the most part. One night I ate pizza to "test" things out, and exactly 24 hours later the migraine hit.

So I came to the conclusion that I had diary related migraines with a 24 hour delay (which I've heard is common).

A lot of things clicked. When I was eating gluten free, I was dairy free for about a week, but re-introduced it so that I could get more protein.

One of the weeks I remember feeling pretty good I was in Ireland and ate no dairy that I can remember.

However, today I got the headache. Yesterday I ate absolutely nothing with any trace of dairy.

I guess my question is, what in Dairy would be giving me the headaches? Is it something that could be in other foods that I'm not aware of? Am I wrong that dairy is causing my problems since I got a headache today?

I got really really excited that I had at least a small breakthrough and figured out one of my problems...but today I am just depressed thinking of why the headache would be back.

I'd appreciate any input that anybody might have...sorry if this is a little vague. I'm trying to sum up A LOT in a few words.

Thanks guys!!

Casein and whey are milk products that are used in quite a few foods you wouldn't suspect. Learn about what milk derivatives are called and read labels (just like gluten). Also, its not uncommon to have more than one trigger and as you discover one you find another. Sucks, but is true.

Juliebove Rising Star

Are you sure there was no dairy? Did you read every label? Eat any prepared food? There is dairy in many canned soups, even in McDonald's fries. But there are plenty of other things that can cause migraines too. Wine and chocolate are two of them.

zebaldwin Explorer

I would suggest that you be tested with these:

The following are the celiac specific blood tests:

Anti-Gliadin (AGA) IgA

Anti-Gliadin (AGA) IgG

Anti-Endomysial (EMA) IgA

Anti-Tissue Transglutaminase (tTG) IgA

Deamidated Gliadin Peptide (DGP) IgA and IgG

Total Serum IgA

Are these the tests you had taken for Celiac? There is such as thing as Non Celiac Gluten Intolerance, meaning that you have symptoms of Celiac or Gluten Sensitivity, without testing positive. But there is no reliable test for that at this time.

If you like to be retested for Celiac, you must be on a full gluten diet for about three months. If not, you may go FULL gluten free (not sort of).

If you choose the diet, we can walk you through it. But it must be as 100% as possible. If you have no other options to relieve your migrane's, why not try. :)

....and welcome!

About a year ago I actually became a member here and was very active on the board, thinking I definitely had celiacs.

I got most of the tests you listed as well as a colonoscopy and biopsy.

On top of the that, on my own, I did a FULL gluten free diet for about free months (down to all new cooking utensils and shampoo) with ZERO positive results.

At that point I assumed it was safe to rule out gluten.

And like I said in the earlier post, the only long term relief from the headaches I've had in years was when I completely cut out dairy.

zebaldwin Explorer

Are you sure there was no dairy? Did you read every label? Eat any prepared food? There is dairy in many canned soups, even in McDonald's fries. But there are plenty of other things that can cause migraines too. Wine and chocolate are two of them.

For yesterday, I am sure. I checked every label. All I ate was oatmeal with water and sugar, a sandwich with turkey, lettuce and tomato on whole grain white with 100% natural potato chips, and then popcorn chicken and frozen french fries later in the day...checked he label and saw no dairy.

However, the day before, I had pasta with a SMALL amount of parmesan cheese. I guess there is a possibility it could be a 2 day delay...not sure

zebaldwin Explorer

Casein and whey are milk products that are used in quite a few foods you wouldn't suspect. Learn about what milk derivatives are called and read labels (just like gluten). Also, its not uncommon to have more than one trigger and as you discover one you find another. Sucks, but is true.

I actually was thinking that was a possibility too since I eat a lot of lunch meat and things with "caramel color, natural ingredients, etc etc" that I have read could contain casein.

However, over the past few weeks where I was headache free I did eat some of those things problem free...which is why I'm confused (and discouraged)


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



Celiac.com Sponsor (A8-M):



Lisa Mentor

About a year ago I actually became a member here and was very active on the board, thinking I definitely had celiacs.

I got most of the tests you listed as well as a colonoscopy and biopsy.

On top of the that, on my own, I did a FULL gluten free diet for about free months (down to all new cooking utensils and shampoo) with ZERO positive results.

At that point I assumed it was safe to rule out gluten.

And like I said in the earlier post, the only long term relief from the headaches I've had in years was when I completely cut out dairy.

There are several food that can attribute to migraines. I would assume you have researched those...cheese is one and MSG. Maybe you have found your answer.

I apologize if I have over looked some of your statements.

mommida Enthusiast

Usually with a reaction (intolerance) it is to the protein. The protein chain in dairy is casein. Maybe you notice the reaction to the amount of what you have ingested.

My daughter was starting to be reffered to a nuerologist for the possibility of abdominal migraines. You mentioned you had been to nuerologists, but was it ever discussed as a possiblity? (most testing needs to be negative and then the possiblity of abdominal migraines can be diagnosed off a checklist)

Are you keeping a very detailed food journal?

Juliebove Rising Star

For yesterday, I am sure. I checked every label. All I ate was oatmeal with water and sugar, a sandwich with turkey, lettuce and tomato on whole grain white with 100% natural potato chips, and then popcorn chicken and frozen french fries later in the day...checked he label and saw no dairy.

However, the day before, I had pasta with a SMALL amount of parmesan cheese. I guess there is a possibility it could be a 2 day delay...not sure

Most bread contains milk. I have a hard time finding any that does not.

zebaldwin Explorer

Most bread contains milk. I have a hard time finding any that does not.

freihofer's whole grain white doesn't have any milk

Juliebove Rising Star

freihofer's whole grain white doesn't have any milk

Must be something local. We don't have that here.

T.H. Community Regular

Hmmmm...

Perhaps you have a true intolerance rather than an allergy? If that's the case, amount may be a factor in whether you get a migraine. From what I remember from our allergist was telling us, it takes a few days for dairy to get out of our systems. So while dairy one day may be fine, or tiny amounts of dairy cc might be okay, you add them up over a few days and get whammied.

So if you, say, ate the cheese the day before, like you did this time, and then got just a little bit of contamination in your processed food the next day, that might be just enough to push you over the edge. I know you mentioned not having any dairy ingredients in your food, but could there be traces from dairy cc due to processing, by any chance?

Like perhaps the dairy free bread might have been made on an equipment line or in a facility that does have dairy, so it might get just a little bit of contamination. That sort of thing. Not enough to usually give you a migraine, but maybe with the little bit of cheese the day before, it was enough to zap you, you know?

I can't think of a lot of dairy things that might cause headaches that you wouldn't be noticing with other issues as well. Although cheese mold (that's used to make the cheese) can cause problems with some folks, so it might be worth checking to see if it's any dairy or if it's just cheese.

An elimination diet journal that also records amounts that you are eating might be useful. That was helpful to me when I ended up having an intolerance that was amount based - it IS hard to figure out, definitely! Because you feel like you ate it find one day, and then got sick the next. But if you can track amounts, or types of processing of dairy, perhaps that might have some of the answer for you.

zebaldwin Explorer

Hmmmm...

Perhaps you have a true intolerance rather than an allergy? If that's the case, amount may be a factor in whether you get a migraine. From what I remember from our allergist was telling us, it takes a few days for dairy to get out of our systems. So while dairy one day may be fine, or tiny amounts of dairy cc might be okay, you add them up over a few days and get whammied.

So if you, say, ate the cheese the day before, like you did this time, and then got just a little bit of contamination in your processed food the next day, that might be just enough to push you over the edge. I know you mentioned not having any dairy ingredients in your food, but could there be traces from dairy cc due to processing, by any chance?

Like perhaps the dairy free bread might have been made on an equipment line or in a facility that does have dairy, so it might get just a little bit of contamination. That sort of thing. Not enough to usually give you a migraine, but maybe with the little bit of cheese the day before, it was enough to zap you, you know?

I can't think of a lot of dairy things that might cause headaches that you wouldn't be noticing with other issues as well. Although cheese mold (that's used to make the cheese) can cause problems with some folks, so it might be worth checking to see if it's any dairy or if it's just cheese.

An elimination diet journal that also records amounts that you are eating might be useful. That was helpful to me when I ended up having an intolerance that was amount based - it IS hard to figure out, definitely! Because you feel like you ate it find one day, and then got sick the next. But if you can track amounts, or types of processing of dairy, perhaps that might have some of the answer for you.

Thanks Shauna! Ya...I'm still confused. I get a migraine usually without fail about 21 hours after eating dairy (mainly cheese)...yet some days where I didn't have cheese or anything dairy the day before I still get a migraine. So I am in the process of doing a daily, in depth food journal. (something I should have started years ago...but better late than never!)

Thanks for the response

mushroom Proficient

This is taken from a post you made in May 2011:

When I first heard about what celiacs was and its symptoms I was so excited. I have been sick for so long, with nothing even close to an answer.

Quick recap: my main symptoms include some digestive problems (upset stomach every morning, after some meals, etc. Bad brain fog for the last 6 or 7 months, bad/nauseous headaches almost every day for at least the last 2 years, weakness in my arms and legs, get chills easily, etc. and some other smaller symptoms. I got the blood tests for celiacs (before I went on the diet), they were negative.

I have been 100% gluten free for about 3 months now, and cannot pinpoint any positive changes. About half of that time I was dairy and soy free as well.

The brain fog is just the same (if not worse), I still get my headaches, and my digestive problems are actually worse than when I started.

I did not keep a journal of symptoms or anything, but I have sat down recently and looked back on everything and cannot see any progression.

Is all this still true today? Absolutely no change? (I went back to check out dairy and soy-free periods :) ) Just interested if anything at all has changed?

  • 3 weeks later...
inspired421 Newbie

Mushroom,great detective work!

Zebaldwin, what have you observed from your food & symptom log over the past 2 weeks?

  • 6 months later...
jstwnttbhealthy Newbie

my bet is on MSG!

Pegleg84 Collaborator

Hey

While I don't get migraines (as far as I know. I'm afraid one of these days I'll get whammied), last year I had a lot of trouble with dizziness, nausea, sinus pressure, what felt like a sinus/inner ear problem. After a bunch of test that determined there was nothing wrong with my ear, I did some reading and decided to cut out dairy. So much better! Not perfect, but much better. I'm pretty sure it's an intolerance to casein, as I can't have goat or sheep's cheese either. I also cut out soy and that's helped as well.

If it is a casein intolerance that's triggering your migraines, then I can imagine that even if you're avoiding it, just like gluten, small amounts have a cumulative effect and are slowly doing damage though you don't feel it until a while later. Also, like gluten, it takes time for your system to flush it all out and heal.

I'd keep it up. Be extremely careful what you're eating, and see if it gets better. For me, cheese is the hardest thing to replace, but I've been drinking almond milk mostly, using Earth Balance instead of butter or margarine (which might still contain casein. check!), and found this pretty decent "Parma veg" stuff that's ground nuts and kale and such, but make a good parmesan substitute. I've tried a couple vegan cheeses, but it's just not the same.

I think you've found what's bothering you. Just give it more time to settle out.

Cheers

Peg

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. - Scott Adams replied to Paulaannefthimiou's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Bob red mill gluten free oats

    2. - knitty kitty replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      High TTG-IgG and Normal TTG-IgA

    3. - trents replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      High TTG-IgG and Normal TTG-IgA

    4. - SamAlvi replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      High TTG-IgG and Normal TTG-IgA

    5. - Jsingh replied to lizzie42's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Son's legs shaking

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

    • Total Members
      132,868
    • Most Online (within 30 mins)
      7,748

    LMGarrison
    Newest Member
    LMGarrison
    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

    • Scott Adams
      Oats naturally contain a protein called avenin, which is similar to the gluten proteins found in wheat, barley, and rye. While avenin is generally considered safe for most people with celiac disease, some individuals, around 5-10% of celiacs, may also have sensitivity to avenin, leading to symptoms similar to gluten exposure. You may fall into this category, and eliminating them is the best way to figure this out. Some people substitute gluten-free quinoa flakes for oats if they want a hot cereal substitute. If you are interested in summaries of scientific publications on the topic of oats and celiac disease, we have an entire category dedicated to it which is here: https://www.celiac.com/celiac-disease/oats-and-celiac-disease-are-they-gluten-free/   
    • knitty kitty
      @SamAlvi, It's common with anemia to have a lower tTg IgA antibodies than DGP IgG ones, but your high DGP IgG scores still point to Celiac disease.   Since a gluten challenge would pose further health damage, you may want to ask for a DNA test to see if you have any of the commonly known genes for Celiac disease.  Though having the genes for Celiac is not diagnostic in and of itself, taken with the antibody tests, the anemia and your reaction to gluten, it may be a confirmation you have Celiac disease.   Do discuss Gastrointestinal Beriberi with your doctors.  In Celiac disease, Gastrointestinal Beriberi is frequently overlooked by doctors.  The digestive system can be affected by localized Thiamine deficiency which causes symptoms consistent with yours.  Correction of nutritional deficiencies quickly is beneficial.  Benfotiamine, a form of thiamine, helps improve intestinal health.  All eight B vitamins, including Thiamine (Benfotiamine), should be supplemented because they all work together.   The B vitamins are needed in addition to iron to correct anemia.   Hope this helps!  Keep us posted on your progress!
    • trents
      Currently, there are no tests for NCGS. Celiac disease must first be ruled out and we do have testing for celiac disease. There are two primary test modalities for diagnosing celiac disease. One involves checking for antibodies in the blood. For the person with celiac disease, when gluten is ingested, it produces an autoimmune response in the lining of the small bowel which generates specific kinds of antibodies. Some people are IGA deficient and such that the IGA antibody tests done for celiac disease will have skewed results and cannot be trusted. In that case, there are IGG tests that can be ordered though, they aren't quite as specific for celiac disease as the IGA tests. But the possibility of IGA deficiency is why a "total IGA" test should always be ordered along with the TTG-IGA. The other modality is an endoscopy (scoping of the upper GI track) with a biopsy of the small bowel lining. The aforementioned autoimmune response produces inflammation in the small bowel lining which, over time, damages the structure of the lining. The biopsy is sent to a lab and microscopically analyzed for signs of this damage. If the damage is severe enough, it can often be spotted during the scoping itself. The endoscopy/biopsy is used as confirmation when the antibody results are positive, since there is a small chance that elevated antibody test scores can be caused by things other than celiac disease, particularly when the antibody test numbers are not particularly high. If the antibody test numbers are 10x normal or higher, physicians will sometimes declare an official diagnosis of celiac disease without an endoscopy/biopsy, particularly in the U.K. Some practitioners use stool tests to detect celiac disease but this modality is not widely recognized in the medical community as valid. Both celiac testing modalities outlined above require that you have been consuming generous amounts of gluten for weeks/months ahead of time. Many people make the mistake of experimenting with the gluten free diet or even reducing their gluten intake prior to testing. By doing so, they invalidate the testing because antibodies stop being produced, disappear from the blood and the lining of the small bowel begins to heal. So, then they are stuck in no man's land, wondering if they have celiac disease or NCGS. To resume gluten consumption, i.e., to undertake a "gluten challenge" is out of the question because their reaction to gluten is so strong that it would endanger their health. The lining of the small bowel is the place where all of the nutrition in the food we consume is absorbed. This lining is made up of billions of microscopically tiny fingerlike projections that create a tremendous nutrient absorption surface area. The inflammation caused by celiac disease wears down these fingers and greatly reduces the surface area needed for nutrient absorption. Thus, people with celiac disease often develop iron deficiency anemia and a host of other vitamin and mineral deficiencies. It is likely that many more people who have issues with gluten suffer from NCGS than from celiac disease. We actually know much more about the mechanism of celiac disease than we do about NCGS but some experts believe NCGS can transition into celiac disease.
    • SamAlvi
      Thank you for the clarification and for taking the time to explain the terminology so clearly. I really appreciate your insight, especially the distinction between celiac disease and NCGS and how anemia can point more toward celiac. This was very helpful for me.
    • Jsingh
      Hi,  My 7 year daughter has complained of this in the past, which I thought were part of her glutening symptom, but more recently I have come to figure out it's part of her histamine overload symptom. This one symptom was part of her broader profile, which included irritability, extreme hunger, confusion, post-nasal drip. You might want to look up "histamine intolerance". I wish I had known of this at the time of her diagnosis, life would have been much easier.  I hope you are able to figure out. 
×
×
  • 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.