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

Risk Of Cancer If I Continue To Ingest Gluten?


Silencio

Recommended Posts

Silencio Enthusiast

I cant find much about it online. My doctor told me to stay off gluten because I have a better chance of getting cancer if I continue to ingest gluten. I have been off gluten since I was diagnosed but im just wondering.


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



Celiac.com Sponsor (A8-M):



pain*in*my*gut Apprentice

I cant find much about it online. My doctor told me to stay off gluten because I have a better chance of getting cancer if I continue to ingest gluten. I have been off gluten since I was diagnosed but im just wondering.

Your doc is right. Here you go....

Open Original Shared Link

Skylark Collaborator

I cant find much about it online. My doctor told me to stay off gluten because I have a better chance of getting cancer if I continue to ingest gluten. I have been off gluten since I was diagnosed but im just wondering.

Wikipedia has pretty good info.

Open Original Shared Link

Don't worry though. Our risk of cancer drops to normal after about a year on the gluten-free diet. The enteropathy-associated T-cell lymphoma is pretty scary but it's usually only seen in people with advanced celiac disease who aren't on the diet.

Silencio Enthusiast

The reason I ask is because its kinda tough for me to know when I am glutened since I dont react to anything at all. The tests say I have it but I would never know it if I ate a regular piece of pizza or bread. I wouldn't do that but just giving an example.

pain*in*my*gut Apprentice

The reason I ask is because its kinda tough for me to know when I am glutened since I dont react to anything at all. The tests say I have it but I would never know it if I ate a regular piece of pizza or bread. I wouldn't do that but just giving an example.

Yes, that would be tough. I would think regular follow-ups with your GI for blood tests would be sufficient to make sure your numbers stay in the normal range and you are not accidentally getting glutened on a regular basis.

Skylark Collaborator

I agree. Take reasonable care and follow up with your doctor for blood tests and you will be fine. It's the people who go undiagnosed for all their lives who get cancer.

love2travel Mentor

The reason I ask is because its kinda tough for me to know when I am glutened since I dont react to anything at all. The tests say I have it but I would never know it if I ate a regular piece of pizza or bread. I wouldn't do that but just giving an example.

You and me both - I did not react to gluten, either. I have no clue whether I would now (have been off nearly a year) and not am about to find out. However, I was away for the past two weeks, visiting family (lots of little nieces and nephews) and have no idea whether I was glutened. I cooked about 95% of the meals myself and was very careful but still.

As others have mentioned, I was also told that the cancer risks are the same as non-celiacs after being off gluten a year.

My doctor has done bloodwork on me twice so far and both times were negative so I am doing something right! :)


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



Celiac.com Sponsor (A8-M):



come dance with me Enthusiast

The reason I ask is because its kinda tough for me to know when I am glutened since I dont react to anything at all. The tests say I have it but I would never know it if I ate a regular piece of pizza or bread. I wouldn't do that but just giving an example.

Wow that would be difficult. My 8yo ingested gluten over the weekend, trace amounts, and spent yesterday in bed holding her tummy screaming out in pain, so we can easily tell. You would have to be even more aware if your body doesn't tell you. I agree with regular checks. I take my dd for follow up blood tests but yeah, as you can see, I know when there is a slight slip up.

Silencio Enthusiast

You and me both - I did not react to gluten, either. I have no clue whether I would now (have been off nearly a year) and not am about to find out. However, I was away for the past two weeks, visiting family (lots of little nieces and nephews) and have no idea whether I was glutened. I cooked about 95% of the meals myself and was very careful but still.

As others have mentioned, I was also told that the cancer risks are the same as non-celiacs after being off gluten a year.

My doctor has done bloodwork on me twice so far and both times were negative so I am doing something right! :)

Yeah I go in for blood work every 3 months to see if everything is cool. Its almost that time again (first blood work since I was diagnosed) so I guess I will find out how well I have been doing with it. On another subject, im heading down to the Kinnikinnick store here in Edmonton to check out the new soft bread and buns that you informed me about in another thread.

come dance with me, I read stories all the time of people in so much pain over the slightest amount. I am pretty lucky not to have that.

BarryC Collaborator

Colo-rectal cancer runs in my family. I lost my Dad andtwo uncles in their 40's. I am 53, but I also lead a healthier lifestyle, no smoking, not too much booze. I wouldnt be surprised if their is a connection. They all ate lots of fatty meat slopped up with my Grannies home made bread. They all had the big bloated belly like I have, which is only now starting to soften up.

Silencio Enthusiast

I am pretty bad for eating alot of junk too. I am really skinny and cant gain much if I tried. I have never drank or smoked though

BeFree Contributor

"Our risk of cancer drops to normal after about a year on the gluten-free diet."

That's good to know!!!!

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. - cristiana replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

    2. - chrisinpa commented on Scott Adams's article in Skin Problems and Celiac Disease
      2

      Celiac Disease and Skin Disorders: Exploring a Genetic Connection

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

      My journey is it gluten or fiber?

    4. - trents replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

    5. - trents commented on Jefferson Adams's article in Other Diseases and Disorders Associated with Celiac Disease
      6

      Celiac Disease Patients Face Higher Risk of Systemic Lupus

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

    • Total Members
      132,693
    • Most Online (within 30 mins)
      7,748

    Ali Zaib
    Newest Member
    Ali Zaib
    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

    • cristiana
      I agree, it so often overlooked! I live in the UK and I have often wondered why doctors are so reluctant to at least exclude it - my thoughts are perhaps the particular tests are expensive for the NHS, so therefore saved for people with 'obvious' symptoms.  I was diagnosed in 2013 and was told immediately that my parents, sibling and children should be checked.  My parents' GP to this day has not put forward my father for testing, and my mother was never tested in her lifetime, despite the fact that they both have some interesting symptoms/family history that reflect they might have coeliac disease (Dad - extreme bloating, and his Mum clearly had autoimmune issues, albeit undiagnosed as such; Mum - osteoporosis, anxiety).  I am now my father' legal guardian and suspecting my parents may have forgotten to ask their GP for a test (which is entirely possible!) I put it to his last GP that he ought to be tested.  He looked at Dad's blood results and purely because he was not anemic said he wasn't a coeliac.  Hopefully as the awareness of Coeliac Disease spreads among the general public, people will be able to advocate for themselves.  It is hard because in the UK the NHS is very stretched, but the fallout from not being diagnosed in a timely fashion will only cost the NHS more money. Interestingly, a complete aside, I met someone recently whose son was diagnosed (I think she said he was 8).  At a recent birthday party with 8 guests, 4 boys out of the 8 had received diagnosis of Coeliac Disease, which is an astounding statistic  As far as I know, though, they had all had obvious gastric symptoms leading to their NHS diagnosis.  In my own case I had  acute onset anxiety, hypnopompic hallucinations (vivid hallucinations upon waking),  odd liver function, anxiety, headaches, ulcers and low iron but it wasn't until the gastric symptoms hit me that a GP thought to do coeliac testing, and my numbers were through the roof.  As @trents says, by the grace of God I was diagnosed, and the diet has pretty much dealt with most of those symptoms.  I have much to be grateful for. Cristiana
    • knitty kitty
      @xxnonamexx, There's labeling on those Trubar gluten free high fiber protein bars that say: "Manufactured in a facility that also processes peanuts, milk, soy, fish, WHEAT, sesame, and other tree nuts." You may want to avoid products made in shared facilities.   If you are trying to add more fiber to your diet to ease constipation, considering eating more leafy green vegetables and cruciferous vegetables.  Not only are these high in fiber, they also are good sources of magnesium.  Many newly diagnosed are low in magnesium and B vitamins and suffer with constipation.  Thiamine Vitamin B1 and magnesium work together.  Thiamine in the form Benfotiamine has been shown to improve intestinal health.  Thiamine and magnesium are important to gastrointestinal health and function.  
    • trents
      Welcome to celiac.com @sha1091a! Your experience is a very common one. Celiac disease is one the most underdiagnosed and misdiagnosed medical conditions out there. The reasons are numerous. One key one is that its symptoms mimic so many other diseases. Another is ignorance on the part of the medical community with regard to the range of symptoms that celiac disease can produce. Clinicians often are only looking for classic GI symptoms and are unaware of the many other subsystems in the body that can be damaged before classic GI symptoms manifest, if ever they do. Many celiacs are of the "silent" variety and have few if any GI symptoms while all along, damage is being done to their bodies. In my case, the original symptoms were elevated liver enzymes which I endured for 13 years before I was diagnosed with celiac disease. By the grace of God my liver was not destroyed. It is common for the onset of the disease to happen 10 years before you ever get a diagnosis. Thankfully, that is slowly changing as there has developed more awareness on the part of both the medical community and the public in the past 20 years or so. Blessings!
    • knitty kitty
      @EndlessSummer, You said you had an allergy to trees.  People with Birch Allergy can react to green beans (in the legume family) and other vegetables, as well as some fruits.  Look into Oral Allergy Syndrome which can occur at a higher rate in Celiac Disease.   Switching to a low histamine diet for a while can give your body time to rid itself of the extra histamine the body makes with Celiac disease and histamine consumed in the diet.   Vitamin C and the eight B vitamins are needed to help the body clear histamine.   Have you been checked for nutritional deficiencies?
    • sha1091a
      I found out the age of 68 that I am a celiac. When I was 16, I had my gallbladder removed when I was 24 I was put on a medication because I was told I had fibromyalgia.   going to Doctor’s over many years, not one of them thought to check me out for celiac disease. I am aware that it only started being tested by bloodwork I believe in the late 90s, but still I’m kind of confused why my gallbladder my joint pain flatulent that I complained of constantly was totally ignored. Is it not something that is taught to our medical system? It wasn’t a Doctor Who asked for the test to be done. I asked for it because of something I had read and my test came back positive. My number was quite high.Are there other people out here that had this kind of problems and they were ignored? 
×
×
  • 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.