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

What Types Of Cancer Does Gluten Cause?


Aleshia

Recommended Posts

Aleshia Contributor

hi, I was just thinking about all the issues in my family and how many people probably have/had celiac disease that was never diagnosed. my grandma on my dad's side died before I was born... I think she only like 50 and she died of stomach cancer and it had also spread to her liver and some other organs as well... she was also addicted to food, my dad said she just loved the texture and taste of it, so she ate not because she was hungry but just because it was so good. I don't know much else about her I think she was norwegian and part spanish and not sure what else.

do you think that could be celiac related??

also my grandpa on my dad's side had lymphoma and died when I was 12 and he used to get painful "rib attacks" he was 81 when he died. he was part french... and not sure what else german maybe?

my grandma on my mom's side has had so many problems. she had skin cancer that had to be removed. she was allergic to her own saliva for awhile and was very limited on what she could eat, I think she had a list of like 5 things she was allowed to eat and had to take drops to help with some of her allergies. she has fibromyalgia and seems to be getting alzheimers. some days she seems to be fine but other days she asks the same question like 20 times in 5 minutes. her antibody levels were sky high same as my grandpa on my dad's side. which they said was why she was allergic to so many things. she's french and irish/english I think. oh and she has osteoporosis too... she broke her foot once just by pulling her sock on too fast!

my grandpa on my mom's side had colon cancer, and he has osteoporosis, I'm not sure what other health issues he has, I know he doesn't eat much bread just because he is very consious of what he eats and his weight. I think he usually has oatmeal for breakfast and soup or something for lunch and I don't really ever recall him eating dinner but at bedtime he has a sliced apple and mixed nuts. anyway he is italian and scottish. oh and I think he had his gallbladder removed.

my mom has numerous issues, she is very moody and irritable and gets depressed alot. she gets bloated to where she looks 9 mo. pregnant (she's already quite overweight anyway) after eating and has a lot of tummy issues. she gets a blistery rash on her feet that itches like crazy and a lot more but I can't remember what they are. I keep trying to convince her she needs to get tested.

my dad has a lot of issues as well, he gets a weird bumpy yellowy looking rash on his legs, his feet are always swollen and he reacts to quite a few foods including eggs and dairy. he is morbidly obese but craves food so badly that he has a hard time dieting. he did really well for quite a while when hiw nd put him on a raw food diet. he had way more energy and a lot of his health issues went away. I think he initially lost 100 pounds but put most of it back on again. he has a lot of dental problems as well

my sister is also quite obese. she has numerous problems which were made worse by an abusive relationship. she was diagnosed with borderline personality disorder but her counselor now says although she has some of the same problems as that that it isn't actually that. she also has idiopathic thrombacitopenia (sp?) and dental problems. she gets infections very easily. she tried the gluten-free diet for a week and said she felt much better, then had noodles for lunch and was vomiting within 1/2 an hour then collapsed and was taken to the hospital with a kidney infection (I think... mabe it was liver?) she says she doesn't think that it was a reaction to the gluten that it was from the infection and that everyone came down with the flu a day or 2 later. she's probably right but I still think the gluten-free diet was helping her. she also gets the same "rib attacks" that my grandpa and my cousin and I also get.

sister's kids all have issues too. oldest has aspergers and gets those little bumps that look like permanent goosebumps. 2nd one gets migraines really often and is very irritable to the point of getting violent. shes really spacy too. youngest also gets migraines and has mood swings but not as severely as the middle child

anyone know if DSHS would cover testing???

anyway.... lots of health problems and just general not feeling well runs in my family.. I don't know if maybe we are just a bunch of complainers :rolleyes: or if there really is something serious there. celiac disease maybe?


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



Celiac.com Sponsor (A8-M):



ShayFL Enthusiast

Could it all be celiac? Well yeah, it could. But it could also be because in general most people just do not eat very well or take care of themselves. A lot of junky foods, sodas, etc. Taking OTC meds with every little sniffle or pain. Breathing in toxic environmental gunk. Chemical laden water. Bad relationships. Resentment. Trauma. Divorce. No exercise. Smoking. Drinking. Drugs. Constantly damaging their bodies. No, I dont think everything can be blamed on Celiac. But if you have the genes, it def. could play a role.

Ridgewalker Contributor

I understand your wondering, though. My mom's dad died of esophageal cancer, which was caused by years of untreated heartburn and acid reflux-- which are two symptoms I get right off the bat when I've been glutened. Was his problem actually untreated Celiac? In this case, I think the evidence piles up to a Yes answer. I inherited it from my mom... and I believe she inherited it from her father. Unfortunately, it's too late to find out for sure.

Ursa Major Collaborator

My grandmother died of stomach cancer, my mother of liver cancer, and my dad died of liver cancer also. Both my parents had all the symptoms of celiac disease, and so do most of my siblings (even though most of them deny it).

Undiagnosed celiac disease can cause cancer in any part of the digestive system. And it could also, indirectly cause skin cancer or other cancers, because a vitamin D deficiency caused by malabsorption can cause a lot of different cancers.

So, yes, all those problems you describe could be caused by celiac disease. Including Alzheimer's (advanced brain fog?).

You may want to buy the book 'Good calories, bad calories' by Gary Taube. It might help your dad and sister especially (if they are willing to listen, that is).

The raw food diet will usually only temporarily help people lose weight, but since you can't keep it up for too long if your metabolism is out of whack (which apparently is the case for all obese people) it will all come back.

Because, you see, most obese people not only don't eat more than slim people, but most of them eat LESS, because they don't like being fat! If somebody sees a slim, muscular guy eat and eat and eat enormous amounts of food, people say, "Wow, he can put it away!" but if a fat person would eat HALF that, people will say, "That person eats too much and is a glutton!". And they claim the evidence is, that they are fat.

That is what I have to put up with. On a day when I thought I ate too much a couple of months ago, I actually went on the Internet to find a calorie counter (I've never counted calories before that), to see how many calories I consumed that day. I added everything, and even think I allowed for a little more than I ate, to make sure I didn't miss anything. It all added up to LESS than 900 calories, which is considered a starvation diet!

I have heard that I eat too much for so many years, that I have to make myself eat much of the time, because I don't like being fat. The problem is, that the less I eat the more I gain! But when I explained this to my husband, who is the one always telling me that I am eating too much, he said that I need to cut down more, because evidently 900 calories must still be too much for me then. I could have killed him!

Anyway, the book clearly shows that people with the mebabolic problem that leads to obesity can only lose weight on a very high protein, high fat (saturated), extremely low carbohydrate diet. Meaning, tons of meat (with the fat), cheese (if tolerated), butter, eggs and just a few vegetables. Nothing made with grain or starch at all, and no sugar, either. And basically no fruit.

dollamasgetceliac? Explorer

I do think it is Celiac disease related. And related to the food we eat and drink.

Compared to Europe a lot of people still smoke,hardly ever go to the doctor, they do not eat out as much as we do, their portions are smaller and their life style is based on a set schedule they eat what they are served, most of their food is made from scratch they walk to the store to buy food every day, I have never have seen anyone jog.

The ribcage pain I think I had that too, Inflamation of the tissue binding the ribs? I wonder if that is the same?

I am sure that Celiac is prvalent in Northern European countries , but I am guessing the onset of the disease is delayed , because they cook from scratch, and we eat Mystery Food.

veggienft Rookie

There are two types of autoimmune disease:

A. The immune system recognizes "self" tissue as a mimicking invader, and attacks it.

B. The immune system fails to recognize mimicking invaders.

Autoimmune type B is cancer, and it's age related. I believe people progress from type A to type B because the body sees that it's destroying its own tissue.

The immune system raises the threshold criteria for identifying invaders, and that results in the patient getting cancer.

What's the exact mechanism? I have a couple guesses, but that's all.

But the starting point has to be the gliadin protein. Type A autoimmune disease is molecular mimicry. We are constructed of proteins, and the only strong mimicking invader-protein we've found so far is gliadin. We've found it everywhere. We know how it invades, and how it mimics.

Accepting this premise, gliadin has to be the cause of the immune system raising its invader identification criteria ......has to be the enabler of cancer.

..

ShayFL Enthusiast

Yes, but how likely is it that "gliadin" is the only protein that can do this. My guess is there are thousands of them. As you are talking of "auto-immune" disease in general.


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



Celiac.com Sponsor (A8-M):



Ursa Major Collaborator
Yes, but how likely is it that "gliadin" is the only protein that can do this. My guess is there are thousands of them. As you are talking of "auto-immune" disease in general.

In reality it is lectins, of which gliadin is one (and the worst of the bunch).

veggienft Rookie
Yes, but how likely is it that "gliadin" is the only protein that can do this. My guess is there are thousands of them. As you are talking of "auto-immune" disease in general.

I can't say you're wrong. Beans make me much sicker, much faster, than wheat. Maybe like the big bear said, it's all lectins. We've just got a lot of genetic research on gliadin.

I lean toward the transition trigger being a lectin because gliadin's zonulin flood and associated gut purges into the bloodstream are documented. I'm guessing the hypoglycemia to type 2 diabetes transition triggers the sick body's raising of the invader recognition criteria. I think candida albicans is associated with that change. And candida surface protein structure is immune-identical to gliadin. For all I know, it's also immune-identical to other lectins.

Why do people without type2 diabetes get cancer? Other than people with cancers directly associated with lectins, I'm not sure they do. Like celiac, type 2 diabetes goes widely undiagnosed.

If I haven't put you to sleep yet, given time, I can throw more grey matter on the computer screen.

..

monkeypuss Rookie

this is interesting, i found an old purse from like 1930 in the loft, opened it and inside were the death certificates of all my ancestors on my nans side and turns out her father, his sister and their father all died of intestine or stomach cancers. she was celiac..just made me wonder if thats what caused it for em.

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 pothosqueen's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Positive biopsy

    2. - Scott Adams commented on Scott Adams's article in Latest Research
      3

      New "Glowing Bacteria" Pill Could Transform Gut Disease Detection (+Video)

    3. - trents replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      7

      Help understand results

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

      Fruits & Veggies

    5. - wellthatsfun posted a topic in Gluten-Free Recipes & Cooking Tips
      0

      heaps of hope!

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

    • Total Members
      132,998
    • Most Online (within 30 mins)
      7,748

    SpoonedMango
    Newest Member
    SpoonedMango
    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
      If you are still eating gluten you could get a celiac disease blood panel done, but I agree with @trents and the gold standard for diagnosing celiac disease would be your endoscopy results. Is it possible they did do a celiac disease panel before your biopsy? This would be the normal chain of events. This article might be helpful. It breaks down each type of test, and what a positive results means in terms of the probability that you might have celiac disease. One test that always needs to be done is the IgA Levels/Deficiency Test (often called "Total IGA") because some people are naturally IGA deficient, and if this is the case, then certain blood tests for celiac disease might be false-negative, and other types of tests need to be done to make an accurate diagnosis. The article includes the "Mayo Clinic Protocol," which is the best overall protocol for results to be ~98% accurate.    
    • trents
      Actually, it would be more correct to say that the genetic potential to develop celiac disease is passed down from parents to children. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% of the general population actually do. But it is also true that the offspring of those who do have active celiac disease are at a considerably higher risk of developing active celiac disease than those of parents who have the genes but don't develop the disease. Some recent, larger studies put the risk at near 50% for the first degree relatives of those who have active celiac disease.
    • Jordan Carlson
      Hello everyone! Been a while since I posted. The past few moths have been the best by for recovery for myself. I have been the least bloated I have ever been, my constant throat clearing is almost gone, I have stopped almost all medication I was prevously taking (was taking vyvanse for adhd, pristiq for anxiety,fomotadine/blexten for histamine blockers and singulair). Only thing I take now is Tecta. I also no longer get any rashes after eating. Things are going very well. Most success came actually once I upped my B12 daily dose to 5,000 mcg. I do have one thing I am un able to figure out and want to see if anyone else has this issue or has experience working around it. Ever since I was born I have always had a issue getting fruits and veggies down. No matter how hard I tried, it would always result in gagging or throwing up. Always just thought I was a picky eater. Now that my stomach and system has healed enough that I can feel when something is off almost istantly, I notice that after eating most fruits (sometimes I am ok with bananas) and veggies, my stomach instantly starts burning and my heart starts to pound and I get really anxious as if my body doesnt know what to do with what just enetered it. So I am thinking now that this is what probably was going on when I was born and my body started rejecting it before which caused this weird sensory issue with it causing the gagging. Hoping someone has some exprience with this as well because I would love to be able to enjoy a nice fruit smoothie once in a while haha. Thanks everyone!
    • wellthatsfun
      i know i've been rather cynical and sad about being fully diagnosed in june 2025, but my boyfriend has been consistently showing me the wonderful world that is gluten free cooking and baking. in the past couple of days he's made me a gluten free rice paper-wrapped spanakopita "pastry", plus a wonderful mac and cheese bechamel-ish sauce with gluten free pasta (san remo brand if you're in australia/if you can get your hands on it wherever you are).  those meals are notably gluten free, but mainly he's been making me easy gluten free meals - chili mince with white rice and sour cream, chicken soup with homemade stock from the chicken remains, and roast chickens with rice flour gravy and roast veggies. i'm a bit too thankful and grateful lol. how lucky could i possibly be? and, of course, for those who don't have someone to cook for them, it's quite easy to learn to cook for yourself. i've been making a lot of meals for us too. honestly, cooking is pretty darn fun! knowing basic knife skills and sanitary practices are all you really need. experimenting with spices will help you get on track to creating some really flavourful and yummy dishes. coeliac is a pain, but you can use it to your advantage. healthier eating and having fun in the kitchen are major upsides. much luck to all of you! let's be healthy!
    • knitty kitty
      That test is saying that your daughter is not making normal amounts of any IGA antibodies.  She's not making normal amounts of antibodies against gliadin, not against bacteria, not against viruses.  She is deficient in total IGA, so the test for antigliadin antibodies is not valid.  The test was a failure.  The test only works if all different kinds of antibodies were being made.  Your daughter is not making all different kinds of antibodies, so the test results are moot.  Your daughter should have the DGP IgG and TTG IgG tests done.   The tests should be performed while she is still consuming gluten.  Stopping and restarting a gluten containing diet can make her more sick, just like you refuse to eat gluten for testing.  Call the doctor's office, request both the IGG tests. Request to be put on the cancellation list for an appointment sooner.  Ask for genetic testing.   Celiac disease is passed on from parents to children.  You and all seven children should be tested for genes for Celiac disease.  Your parents, your siblings and their children should be tested as well.  Eating gluten is not required for genetic testing because your genes don't change.  Genetic testing is not a diagnosis of Celiac disease.  Just having the genes means there is the potential of developing Celiac disease if the Celiac genes are activated.  Genetic testing helps us decide if the Celiac genes are activated when coupled with physical symptoms, antibody testing, and biopsy examination. It's frustrating when doctors get it wrong and we suffer for it.  Hang in there.  You're a good mom for pursuing this!  
×
×
  • 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.