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

Trying To Figure Out Family History


guy220d

Recommended Posts

guy220d Rookie

I am new to the celiac world (a year ago, I'd never heard of it) and exploring whether or not I have the condition. Unfortunately, I went on the gluten-free diet a couple of months before my blood tests (because I was feeling so bad), and the blood tests, according to my MD, came back negative. What I'm wondering about is my late father. 20 years ago, in his 60's, he was diagnosed with intestinal lymphoma (had a large section of his sm. intestine removed) and 10 years ago he was diagnosed with Hashimoto's thyroiditis. Two years ago, he was diagnosed with stomach cancer and died pretty quickly, last summer. Dad was never diagnosed with celiac disease. I know lymphoma and the thyroiditis can go along with celiac disease, but does stomach cancer? It seems like I've read in these celiac forums about other family members that have had stomach cancer.


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



Celiac.com Sponsor (A8-M):



Carriefaith Enthusiast

People with celiac disease that do not follow the gluten free diet have about a 40% increased risk of stomach cancer than someone without celiac disease or someone with celiac disease who is following the diet. Intestinal lymphoma is one of the types of stomach cancers associated with celiac disease. I'm really sorry about your dad :(

phakephur Apprentice
People with celiac disease that do not follow the gluten free diet have about a 40% increased risk of stomach cancer than someone without celiac disease or someone with celiac disease who is following the diet. Intestinal lymphoma is one of the types of stomach cancers associated with celiac disease.

Another factoid I've seen frequently on this site is that the vast majority of celiacs are undiagnosed (and therefore not following the diet). If this is the case, then how can the increased risk of cancer be quantified? Do oncologists routinely screen for celiac? Or can someone give me a reference to a study on cancer rates among non-compliant celiacs? I'd really like to read it.

Thanks

Sarah

jkmunchkin Rising Star
I am new to the celiac world (a year ago, I'd never heard of it) and exploring whether or not I have the condition. Unfortunately, I went on the gluten-free diet a couple of months before my blood tests (because I was feeling so bad), and the blood tests, according to my MD, came back negative. What I'm wondering about is my late father. 20 years ago, in his 60's, he was diagnosed with intestinal lymphoma (had a large section of his sm. intestine removed) and 10 years ago he was diagnosed with Hashimoto's thyroiditis. Two years ago, he was diagnosed with stomach cancer and died pretty quickly, last summer. Dad was never diagnosed with celiac disease. I know lymphoma and the thyroiditis can go along with celiac disease, but does stomach cancer? It seems like I've read in these celiac forums about other family members that have had stomach cancer.

You should not go on the gluten-free diet before having the blood tests done, especially if your gluten levels may not have been that high to start with. Otherwise the test will infact come back negative.

For instance when I was diagnosed 6 months ago my numbers where through the roof high. Now that I have been gluten-free for 6 months my numbers are almost normal. Gluten needs to be present in your body to show up on the blood test.

Try eating "normal" and taking the blood test again.

  • 2 weeks later...
happy4dolphins Enthusiast

HI, This is a really good question. I've been wondering some similar things myself. I run a duodenal cancer board (part of the upper small intestine) and wonder if there is a conncetion to some of these things.

-Nicole

  • 2 weeks later...
christianne Newbie

My maternal grandfather died of stomach cancer about 20 years ago. I was dx about 2-3 years ago (although the endoscopy was inconclusive). My father tested for Celiac and was found not to have it. My Mom has refused to be tested. My grandfather had stomach problems all his life so I wonder also if he had Celiac. He was only 64 when he passed away. They thought he had ulcers all his life. Not terriblyhelpful as far as proof goes, but a similar story.

tiffjake Enthusiast

My paternal grandmother died when my father was 12 years old. They told the family that she had non-tropical sprue, but nothing else about what that meant for the rest of the family. As far as my dad understood, she had stomach cancer. My dad and I have ALWAYS had stomach troubles. When I found out about my celiac, I told my dad, who has cut out the gluten and had a massive change in his life. I am not sure what would have happened to him if he didn't, or to me for that matter. But I know what happened to my grandmother. And since this disease is (or can be) genetic, I am not going to take the chance of having the same early death that she had.


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



Celiac.com Sponsor (A8-M):



guy220d Rookie

I had written in my original posting that my doctor thought my blood tests were negative for celiac anti-bodies. I've been suspicious of that for awhile, so I asked for a copy of the test results. I was a bit stunned when I read that my IgG anti-gliadin level was 21, four points over positive. I guess I shouldn't be stunned because I had to tell my doctor what the tests were for celiac disease. He was really uninformed.

penguin Community Regular
I had written in my original posting that my doctor thought my blood tests were negative for celiac anti-bodies. I've been suspicious of that for awhile, so I asked for a copy of the test results. I was a bit stunned when I read that my IgG anti-gliadin level was 21, four points over positive. I guess I shouldn't be stunned because I had to tell my doctor what the tests were for celiac disease. He was really uninformed.

That's why I've made it a habit to always get copies of bloodwork results.

  • 2 months later...
lau Newbie
I am new to the celiac world (a year ago, I'd never heard of it) and exploring whether or not I have the condition. Unfortunately, I went on the gluten-free diet a couple of months before my blood tests (because I was feeling so bad), and the blood tests, according to my MD, came back negative. What I'm wondering about is my late father. 20 years ago, in his 60's, he was diagnosed with intestinal lymphoma (had a large section of his sm. intestine removed) and 10 years ago he was diagnosed with Hashimoto's thyroiditis. Two years ago, he was diagnosed with stomach cancer and died pretty quickly, last summer. Dad was never diagnosed with celiac disease. I know lymphoma and the thyroiditis can go along with celiac disease, but does stomach cancer? It seems like I've read in these celiac forums about other family members that have had stomach cancer.

Consider being tested to see if you carry the gene for celiac. I've found that only a gastroenterologist will know what test to order (I recall it's something like DQ2 and DQ8). If you don't have the gene, you can't test positive (antibody test) for the disease. If you DO have the gene, then you may have the disease or could one day develop it. I'm sorry to hear about your father--good chance he had celiac. If you find that you have the gene, I'd recommend you tell any first-degree relatives (siblings or children) that they should be tested too. Good luck.

  • 5 years later...
lilu Rookie

Also, be sure you get a test that show both the alpha and beta alleles (like Prometheus). The reason this is important is that while most people express as two whole genes: DQ_/ DQ_, you can actually have "hybrid" genes (ok, tried to explain here in layman's terms, but can't quite get it out). Do a search on DQ 2.5 "trans" and you'll see what I mean. The "whole genes" are called "sic" and the hybrids are called "trans", but they respond in the body in the same manner (increased risk).

Can someone else help me out here with a better explanation?

txplowgirl Enthusiast

Hi Guy,

I've wondered about the cancer too since it is so prevalent on both sides of my family. I've basicaly been sick my whole life and found out about the gluten connection 2 years ago. I was so sick that I didn't bother with the tests I went glutenfree immediately and like a lot of others really wish that I had tested before because i have tried to do a gluten challenge and I get about a week and a half into it before I have to quit.

Anyway, My mother's side, her only sister passed away last year to esophageal cancer, her four brothers passed from lung cancer, pancreatic cancer, and colon cancer. Her father passed away from stomach cancer. 3 of his sisters from lung, colon and breast cancer. There are over 9 first and second cousins who have had everything from colon to breast cancer. On top of several other problems ranging from Lupus, Ruematoid arthritis and thyroid problems. My mother lost her thyroid 40 years ago.

My father's side. I lost my dad to colon cancer, 2 of his brothers to stomach and lung cancer. I have 2 cousins who are brothers, 1 has kidney cancer the other has pancreatic cancer. One of their nephews who is 34 has liver cancer. Another cousin was diagnosed at the age of 29 to brain stem cancer. My grandmother to cervical cancer and her sister to lung cancer, their mother, my greatgrandmother to lung cancer. Several other first and second cousins ranging from colon, breast, non hodgkin's lymphoma and esophageal. As well as other problems ranging from thyroid, lupus, seizures, etc.

I truly believe this is all due to gluten.

So, this is why I stay gluten free. None of my family members believe this but i have managed to talk 2 cousins into going gluten free, so there is some progress but not much.

cap6 Enthusiast

I was not diagnosed until 2 years after my mom dies, however knowing what I now know I believe that she was Celiac. She suffered with gut issues all her life, had diabetes, fibromyalgia, intense itchy bumps on knees and elbows, severe bouts of constipation/diarrhea, restless leg, bruising, mouth sores and on the list goes. She was pretty much a mess and in constant pain. Her father had asthma, her mother diabetic and cancer runs through every generation. This is all the evidence I need to know celiac comes through her side of the family and in spite of all of this will my brother be tested or even listen. No!

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
      21

      My only proof

    2. - Jmartes71 replied to Jmartes71's topic in Related Issues & Disorders
      21

      My only proof

    3. - knitty kitty replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      44

      Supplements for those Diagnosed with Celiac Disease

    4. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      21

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,546
    • Most Online (within 30 mins)
      7,748

    Kkiloh
    Newest Member
    Kkiloh
    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

    • Mari
      I think, after reading this, that you areso traumatized by not being able yo understand what your medical advisors have been  what medical conditions are that you would like to find a group of people who also feel traumatized who would agree with you and also support you. You are on a crusade much as the way the US Cabinet  official, the Health Director of our nation is in trying to change what he considers outdated and incorrect health advisories. He does not have the education, background or experience to be in the position he occupies and is not making beneficial decisions. That man suffered a terrible trauma early in his life when his father was assonated. We see now how he developed and worked himself into a powerful position.  Unless you are willing to take some advice or  are willing to use a few of the known methods of starting on a path to better health then not many of us on this Celiac Forum will be able to join you in a continuing series of complaints about medical advisors.    I am almost 90 years old. I am strictly gluten free. I use 2 herbs to help me stay as clear minded as possible. You are not wrong in complaining about medical practitioners. You might be more effective with a clearer mind, less anger and a more comfortable life if you would just try some of the suggestions offered by our fellow celiac volunteers.  
    • Jmartes71
      Thus has got to STOP , medical bit believing us! I literally went through 31 years thinking it was just a food allergy as its downplayed by medical if THEY weren't the ones who diagnosed us! Im positive for HLA-DQ2 which is first celiac patient per Iran and Turkey. Here in the States especially in Cali its why do you feel that way? Why do you think your celiac? Your not eating gluten so its something else.Medical caused me depression. I thought I was safe with my former pcp for 25 years considering i thought everything I went through and going through will be available when I get fired again for health. Health not write-ups my health always come back when you're better.Im not and being tossed away at no fault to my own other than shitty genes.I was denied disability because person said he didn't know how to classify me! I said Im celiac, i have ibs, hernia, sciatica, high blood pressure, in constant pain have skin and eye issues and menopause intensified everything. With that my celiac nightmare began to reprove my disregarded disease to a bunch of clowns who think they are my careteam when they said I didn't have...I feel Im still breathing so I can fight this so no body else has to deal with this nightmare. Starting over with " new care team" and waisting more time on why I think I am when diagnosed in 1994 before food eliminated from my diet. P.s everything i went through I did write to medical board, so pretty sure I will continue to have a hard time.
    • knitty kitty
      @Scatterbrain, Thiamine Vitamin B1 and amino acid Taurine work together.  Our bodies can make Taurine from meats consumed.  Our bodies cannot make Thiamine and must consume thiamine from food.  Meat is the best source of B vitamins like Thiamine.   Vegetarians may not make sufficient taurine since they don't eat meat sources of taurine.  Seaweed is the best vegetarian source of taurine. Vegetarians may not consume sufficient Thiamine since few veggies are good sources.  Whole grains, legumes, and nuts and seeds contain thiamine.  Many of these sources can be hard to digest and absorb for people with Celiac disease.   You may find taking the forms of thiamine called Benfotiamine or TTFD (tetrahydrofurfuryl disulfide) and a B Complex will give the benefits you're looking for better than taurine alone.  
    • knitty kitty
      @Jmartes71, I went to Doterra's site and had a look around.  The Doterra TerraZyme supplement really jumped out at me.  Since we, as Celiacs, often have digestive problems, I looked at the ingredients.  The majority of the enzymes in this supplement are made using black mold, Aspergillus!  Other enzymes are made by yeast Saccharomyces!  Considering the fact that Celiac often have permeable intestines (leaky gut syndrome), I would be very hesitant to take a product like this.  Although there may not be live black mold or yeast in the product, the enzymes may still cause an immune system response which would definitely cause inflammation throughout the body.   Skin, eyes, and intestines are all made from the same basic type of cells.  Your skin on the outside and eyes can reflect how irritated the intestines are on the inside.  Our skin, eyes, and intestines all need the same vitamins and nutrients to be healthy:  Vitamin A, Niacin B3 and Tryptophan, Riboflavin B2, Biotin B7, Vitamin C, and Omega Threes.  Remember that the eight B vitamins work together.  Just taking high doses of just one, vitamin like B12, can cause a deficiency in the others.  Taking high doses of B12 can mask a Folate B9 deficiency.  If you take B12, please take a B Complex, too.  Thiamine B1 can be taken in high doses safely without toxicity.  Thiamine is needed by itself to produce energy so every cell in the body can function, but Thiamine also works with the other B vitamins to make life sustaining enzymes and digestive enzymes.  Deficiencies in either Niacin, Vitamin C, or Thiamine can cause digestive problems resulting in Pellagra, Scurvy, and Gastrointestinal Beriberi.   If you change your diet, you will change your intestinal microbiome.  Following the Autoimmune Protocol Diet, a Paleo diet, will starve out SIBO bacteria.  Thiamine keeps bacteria in check so they don't get out of control as in SIBO.  Thiamine also keeps MOLDS and Yeasts from overgrowth.   Menopause symptoms and menstrual irregularities are symptomatic of low Vitamin D.   Doctors are not as knowledgeable about malnutrition as we need them to be.  A nutritionist or dietician would be more helpful.   Take control of your diet and nutrition.  Quit looking for a pill that's going to make you feel better overnight.  The Celiac journey is a marathon, not a sprint.   "Let food be your medicine, and let medicine be your food."
    • RUKen
      The Lindt (Lindor) dairy-free oat milk truffles are definitely gluten-free, and (last time I checked) so are the white chocolate truffles and the mint chocolate truffles. 
×
×
  • 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.