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

Cow's Milk Protein Allergy as childhood Symptom


Moonchild94

Recommended Posts

Moonchild94 Rookie

Hi everyone! 

I've been reading this site for a while now but saw a thread that really caught my eye and wanted to know some more info.

The thread was about a protein allergy in cows milk for kids, with mothers who had undiagnosed celiac, I myself was an infant who had that allergy when I was little. Did any of you who have been diagnosed with celiac, suffer from it? I have many other symptoms and am starting the diagnosing process in the next month or so as symptoms are getting much worse now. 

 

Any help is appreciated! 


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



Celiac.com Sponsor (A8-M):



Scott Adams Grand Master

Welcome to the forum! 

Many people with untreated celiac disease end up with casein (cow’s milk protein) intolerance and/or lactose intolerance, but not necessarily cow’s milk allergy, which is different.

In these cases cow’s milk can’t be broken down properly during digestion due to damaged villi in the intestines.

I had this issue and it went away ~2 years after I went gluten-free.

If you’re going to get a blood panel done for celiac disease don’t forget to continue eating ~2 slices of wheat bread a day until all tests are completed, otherwise you may end up with false negative results.

  • 1 year later...
DawnFL Newbie
On 8/1/2021 at 2:38 PM, Scott Adams said:

Welcome to the forum! 

Many people with untreated celiac disease end up with casein (cow’s milk protein) intolerance and/or lactose intolerance, but not necessarily cow’s milk allergy, which is different.

In these cases cow’s milk can’t be broken down properly during digestion due to damaged villi in the intestines.

I had this issue and it went away ~2 years after I went gluten-free.

If you’re going to get a blood panel done for celiac disease don’t forget to continue eating ~2 slices of wheat bread a day until all tests are completed, otherwise you may end up with false negative results.

I am Soo Upset that my doctor's office didn't tell me I needed to make sure I was eating wheat every day before the test! 
I even asked the lab technician who did the draw, "Does it matter that I haven't been eating much, lately?"  She said, "No.  It's a genetic test so it has nothing to do with food."    Now I'm confused & not certain what to expect.  

To the first part of this - I was Very sick as an infant & nearly died from milk allergy, according to my grandmother.  After I seemed to improve on Similac formula, & was old enough to begin eating solids, my grandmother packed me full as much food as I'd eat.  (grandma's often over-love through food)  I don't think I ever truly got over, or grew out of the milk allergy; not completely, anyhow.   But I do love cow's milk.  Not as much lately, because I seem to react to everything. 

Scott Adams Grand Master

For the genetic test eating gluten or not does not matter, for the blood antibody tests for celiac disease it does matter.

More info on this is here:

 

DawnFL Newbie
7 minutes ago, Scott Adams said:

For the genetic test eating gluten or not does not matter, for the blood antibody tests for celiac disease it does matter.

More info on this is here:

 

Hi, thank you so much, Scott, for your reply.  There is an awful lot to take in.  I've been run around the mulberry-bush, for over 2 decades, being told I had CFS, FMS, Hypothyroid, Vit D deficiency, Carpal Tunnel, RA & then told I couldn't possibly have RA.  It's been a nightmare.  Now, by gallbladder is shot, it has done some damage to my liver & I need the endo/ colonoscopy, Fibro Scan (liver) & H. Pylori testing & maybe something else.  Already had HIDA Scan & of course, they're willing to remove the gallbladder.   I'm not ready for that.
I tried to tell them for years, that I had something else going on, but it fell on deaf ears. 
Finally, the PCP scripted a Celiac Disease Panel Tissue Transglutimase IgG & IgA with Gliadin Antibody IgG & IgA.
This is the lab draw I just had, where the tech told me it had nothing to do with what I've been eating. 

I'm going to read through your article.  I think I've read it once, but I haven't been feeling well & not really retaining much info.

Thanks so much! 

Scott Adams Grand Master

At this point, given all the health issues you are having (many of your symptoms could be related to undiagnosed celiac disease), you may just want to try a gluten-free diet for a few months to see if it helps. If your test results end up positive your doctor may want you to do an endoscopy to confirm the diagnosis, which means you'd need to eat gluten daily for at least two weeks before that test.

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,688
    • Most Online (within 30 mins)
      7,748

    Princess.dfc
    Newest Member
    Princess.dfc
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.3k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • knitty kitty
      Yes, some people with Celiac do react to quinoa.  I know i do.  Apparently, two different "breeds" of quinoa can stimulate the immune system. Read here... Variable activation of immune response by quinoa (Chenopodium quinoa Willd.) prolamins in celiac disease https://pubmed.ncbi.nlm.nih.gov/22760575/#:~:text=Cultivars Ayacuchana and Pasankalla stimulated,for patients with celiac disease. And some of us react to corn (maize) as well. Maize prolamins could induce a gluten-like cellular immune response in some celiac disease patients https://pubmed.ncbi.nlm.nih.gov/24152750/   P.S. @Brook G have you thought about getting a genetic test done for known Celiac genes?  
    • Brook G
      People who are Celiac don't have a gluten response to Quinoa, but some people who are gluten intolerant do.  I react to quinoa just like I do to gluten.  Freddies/Kroger came out with their own gluten-free Bread and I didn't think to read the ingredients.  I couldn't figure out where I would have gotten gluten in my diet until I read the ingredients in their bread... QUINOA
    • trents
      Thanks for the additional information. I was thinking of asking you if your daughter was taking methylated vitamins since she has the MTHFR gene but you beat me to it. To answer the question you posed in your original post, as I explained, celiac disease does not damage the colon but the lining of the small bowel. If the damage is pronounced enough and the doc doing it is experienced, yes, the damage done to the lining of the small bowel can be spotted with the naked eye.
    • cameo674
      I could not locate the correct Gary Brecka video where he explains the methylation process and specifically states things about how people with the MTRR homozygous gene mutation are known to suffer from heartburn due to a weakened valve/sphincter where the esophagus and the stomach connect.  My brother had the youtube video sent to him from 10x health which is probably why I cannot locate it.     I will have read up on mast cell activation.  I do not know anything about it.  Tums is my preferred gerd treatment.  I always figured a little extra calcium could not hurt me.  
    • cameo674
      Trents: Due to a genetic mutation, my daughter has inherited from both parents she cannot process the Folic Acid provided in the fortified American grains.   An MD told her to avoid eating fortified grains.   My daughter makes the assumption that unless she makes the food item, that the baker used a fortified grain so she has been limiting her gluten intake since 2020.   Her Psychiatrist was who tested her for MTHFR gene issue because she suffers from depression and severe anxiety. The Psychatrist also instructed my daughter to supplement with a methylated version of folate once she knew my daughter was homozygous, because the methylated version bypasses the mutated gene step so her body can absorb it.  Low folate absorption impacts serotonin and dopamine production.  My husband and I also both have two other homozygous gene mutations that interfere with vitamin absorption: MTRR and VDR taq.  The first interferes with B-12 absorption which requires us to take a methylated B-12 vitamin and the second with Vitamin D absorption so we have to take higher doses to stay within normal levels.   My brother, who has the exact same gene mutations, went through 10x health genetic testing for vitamin supplements (paid by his employer) and received a huge report saying the same things about which types of supplements had to be taken.  Gary Brecka does videos on how these gene mutations impact the vitamin absorption pathways.       If my brother had not gotten his testing through work, he would never would have started his supplement journey.  His testing is what triggered my getting functional health testing that tested similar biomarkers to his.  Again the celiac testing was an add-on test that I did off the cuff.  
×
×
  • Create New...