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

Celiac And Colon Polyps


natalieb

Recommended Posts

natalieb Rookie

Hi, I am 39 years old and very new to celiac but not new to living with autoimmune disorders, ie, thyroid disease. At around 32 I began experiencing what my gi doc told me was colitis. He then did a colonoscopy which showed that I had collangenous colitis. During that time I went from an energetic career woman to someone with numbness in her fingers, lethargy, colitis, pain in the upper left quadrant of my stomach, irritability, and severe leg pain. At 38, he did another colonoscopy and found an adenoma, it was benign, thank god, but I am terrified. After that I began listening to my inner self and got a hold of a doc at presby hosp in pgh. He was thorough and asked me every question under the sun unlike this other piece of work who put his kids through college by doing colonoscopies. Sorry but I can't contain my anger towards this highly regarded doc who couldn't do a simple blood test. Well, the doc at presby tested me for celiac and low and behold I had it. I am curious if there is anyone out there who has had colon polyps as well. I am so scared. Next May I will have another colonoscopy to see if any have dev. Is there anyone out there with these similarities? I have found no link whatsoever in what I have researched thus far. Help. Thanks, Natalie


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



Celiac.com Sponsor (A8-M):



gf4life Enthusiast

Hi Natalie,

Unfortunately, most doctors are like the first one you mentioned. I had never heard of Celiac or gluten, after 30 years of seeing dozens of doctors for GI related problems. Then when I came acrossed it one day and it sounded like me I asked for testing, and at first it seemed no one knew what tests to order, then they ordered the wrong ones, then when I finally got the right ones ordered(I had to take a list of tests in to my doctor so he knew what to order!) they came back negative. But long story short, more testing showed I did in fact have celiac disease and am much better off for knowing. I have already suffered too long, but should be able to heal, my children won't have to suffer so long.

Now as for the colon polyps, I did not have any during my recent colonoscopy (Thank God), but it is not uncommon to find in an undiagnosed celiac. Now I assume you are on the gluten free diet? So you should be feeling somewhat better, right. I would like to say that you will not have any more polyps, but I just don't know. I do know that you reduce your risk of developing intestinal cancer by staying 100% gluten free. So it is good that you be gluten-free, and good that your doctor recheck you in May, but it is not good for you to dwell on the thought of developing more polyps, or of it turning into cancer. It sounds like you have a great doctor and as long as you take care of yourself, then you are doing the best you can. The rest is in God's hands. I am glad you are here at this site. There are a lot of supportive people here and we are all in the same boat.

God bless.

Mariann :wub:

(my daughter really wanted me to use the heart smiley!)

angel-jd1 Community Regular

I don't know of a link between polyps and Celiac. It might be interesting for someone to research. I personally have diverticulitis. I also wonder if that has something to do with celiac.

-Jessica B)

wclemens Newbie

My father died of colon cancer, and so did his brother. My sister, brother, and I have all had colon polyps removed, none cancerous Thank God. I am the only one who has been on a gluten free diet, and I got a lot more serious about being careful to totally stay away from all gluten, milk, dairy, egg whites and yeast, which I am allergic to, after my colonoscopy.

The theory is that if my dad and his brother had been tested soon enough they would have been able to have the polyps removed without cancer developing.

You are wise to be concerned, and I feel that adhering strictly to a diet consistent with what you can tolerate (after of course learning what those foods are, and the list may be longer than what you think now) will certainly lessen your anxiety and apprehension.

Katie Couric is on such a campaign to rid this country of colon cancer, and my sister was so persistent that my brother and I went for testing. I had experienced colitis for years. I hope you find your path to good health and peace of mind. Please listen to what your body is telling you to avoid, and as the other writer mentioned, we are in God's Hands. He is faithful to help us each day. Welda

lucycampbell55 Rookie

I also had polyps found when they did my colonoscopy. None malignant. Thank God

I'm so new to celiac disease that I can offer no help as far as research is concerned. I just found out in November and what I have learned about the disease has come from the internet.

I have suffered indigestion problems for the last 30 years and got tired of being told they couldn't find anything, so I stopped complaining and just dealt with it the best I could. Since being diagnosed and going 100% gluten-free I have done fine. I am on medication for the damage to my stomach because of not being diagnosed sooner but have been told that If I stay 100% gluten-free my stomach will heal. It's just a matter of time.

Lucy

Guest ellcrys11

I had a colonoscopy in Jan of 2002. I had two polyps. One was ok but the other was precancerous. Both were remove. I was diagnosed with celiac disease in June of 2002. I feel real lucky that the dx was made. It has made my life simpler by going gluten-free but I don't get as sick any more.I would not go back to eating gluten if they paid me.

God Bless Everyone

Harriet

clare Newbie

One of the MANY tests I have had in the past four years in an attempt to diagnose my miscellaneous digestive complaints was a colonoscopy. The doctor found an unusual growth that didn't look like anything he had ever seen before, but which he assured me wasn't a polyp. In my followup colonoscopy two months before my diagnosis, there were two of these growths. I am supposed to go back in about 6 months to have them removed so I'm curious to see what the doctor will find this time now that I have been following a gluten-free diet...


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



Celiac.com Sponsor (A8-M):



  • 3 weeks later...
DawnM Newbie

Hi: I am wondering if my Mother in Law has undiagnosed Celiac Disease. She often complains of constipation. She was recently diagnosed with anal/rectal cancer. I asked my Mother in Law to be tested for celiac disease since it is a hereditary disease. She does not feel that it is necessary because she does not think she has it. I am praying that if she does have celiac disease, that the Dr.'s will do the testing, just to be thorough.

My sister in law also complains of stomach problems,pain, diarreah, the whole nine yards. She also refuses to be tested. She has had kidney stones, gall bladder removed and a hysterectomy. She is only 43 years old.

I HOPE neither has celiac disease, however, my son's diagnosed celiac disease had to come from somewhere!!! Anyone have any thoughts or recommendations to get them to be tested? Thank you.

seeking-wholeness Explorer

Dawn, I know how frustrating it is to have relatives brush off your concern for them! It's infuriating sometimes. The only wisdom I have to offer is frustrating in and of itself: remember that THEY are responsible for their own health! Once you have shared your concern with them (which you are totally within your rights to do), it is important to give them LOTS of time and space to process and consider what you have said. Sometimes, it will stick in the back of their minds and resurface months or even years later--when they are better equipped to approach the topic again. That said, I have heard that the latest issue of Reader's Digest has an article on diseases that are difficult to diagnose, including celiac disease. Giving your relatives a copy of the magazine or article may be a good way to broach the subject and lend credibility to your concerns. Good luck!

natalieb Rookie

Dawn,

How old is your son with celiac disease? I understand what it is like to have this situation as when I was diagnosed with celiac disease my doc told me to have my 9 yr. old tested as well due to the fact that she displays some classic symptoms. The test came back negative, but I noticed when she is gluten-free she does much better. anyhow, when I told my mother in law that I was going to have her tested she thought that I was out of my mind. In dealing with this, I have discovered that there are so many people out there who do not take this as a bonafide serious disease. It is a shame. Maybe that is part of the reason that they turn the other ear. Perhaps collecting as many articles on the subject, (Womans Day has an article about it as well in their Feb 17th edition), and presenting it to them. You will then have done all you can and must worry about your son. Obviously he got it from their side if your side of the family has no history due to the high genetic link. This disease however, still remains something that is in the dark. I actually had a friend tell me that once I healed my stomach that I could go back to have "a little" gluten here and there and guess what? She is a reg. nurse and has been for 18 years! Good luck. Remember though, you can only do so much and then guess what? It is up to them, they are big girls. Take Care. Natalie

  • 9 years later...
wartburg03 Rookie

I recently self diagnosed a gluten sensitivity and have been gluten free for 2 months. I waited until my celiac bloodwork came back negative but then went gluten free anyway. 2 days ago I had an upper endoscopy but I don'tknow if my biopsies would show celiac at this point even if I had it. I also had a colonoscopy (I'm a 32 yo female, not normally high risk, but my brother had 3 polyps removed at 26 about 5 years before he went gluten free). They did find and remove one and I'm awaiting those results as well. So I guess I'm saying that I don't know if I have celiac or non celiac gluten sensitivity, but I had a polyp so it's something to watch for. Good luck with your health!

kareng Grand Master

I recently self diagnosed a gluten sensitivity and have been gluten free for 2 months. I waited until my celiac bloodwork came back negative but then went gluten free anyway. 2 days ago I had an upper endoscopy but I don'tknow if my biopsies would show celiac at this point even if I had it. I also had a colonoscopy (I'm a 32 yo female, not normally high risk, but my brother had 3 polyps removed at 26 about 5 years before he went gluten free). They did find and remove one and I'm awaiting those results as well. So I guess I'm saying that I don't know if I have celiac or non celiac gluten sensitivity, but I had a polyp so it's something to watch for. Good luck with your health!

Just an FYI - you are responding to a 9 year old thread. I don't think any of these posters have been on in years.

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. - knitty kitty replied to dsfraley's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      12

      9 y/o Son Diagnosed with Celiac Disease; Persistent Symptoms: Does this Sound Familiar?

    2. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      1

      Second chance

    3. - cristiana replied to dsfraley's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      12

      9 y/o Son Diagnosed with Celiac Disease; Persistent Symptoms: Does this Sound Familiar?

    4. - Wheatwacked replied to dsfraley's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      12

      9 y/o Son Diagnosed with Celiac Disease; Persistent Symptoms: Does this Sound Familiar?

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

    • Total Members
      133,562
    • Most Online (within 30 mins)
      7,748

    Hannah Kelch
    Newest Member
    Hannah Kelch
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • knitty kitty
      I found some articles that illustrate the immune reaction to casein and gluten. Bovine milk caseins and transglutaminase-treated cereal prolamins are differentially recognized by IgA of celiac disease patients according to their age https://pubmed.ncbi.nlm.nih.gov/19290628/   Gliadin and Casein Metabolism: Synthesis of Gliadomorphin and Casomorphin and Their Biological Consequences https://www.researchgate.net/publication/397908713_Gliadin_and_Casein_Metabolism_Synthesis_of_Gliadomorphin_and_Casomorphin_and_Their_Biological_Consequences   Effects of milk containing only A2 beta casein versus milk containing both A1 and A2 beta casein proteins on gastrointestinal physiology, symptoms of discomfort, and cognitive behavior of people with self-reported intolerance to traditional cows’ milk https://pmc.ncbi.nlm.nih.gov/articles/PMC4818854/#:~:text=Results,lactose tolerant and intolerant subjects.   Casomorphins and Gliadorphins Have Diverse Systemic Effects Spanning Gut, Brain and Internal Organs https://pmc.ncbi.nlm.nih.gov/articles/PMC8345738/   Brain Opioid Activity and Oxidative Injury: Different Molecular Scenarios Connecting Celiac Disease and Autistic Spectrum Disorder https://pmc.ncbi.nlm.nih.gov/articles/PMC7407635/  
    • Mari
      Ijmartes71 I  son't think you are crazy by any psycoligical s=defination but you are obsessive. you may have considerable brain fog  , a problem that affects celiacs and many other people. . With this obsession you have abd being braun dogged you arw not abke to take any advice people are giving you to help you. To take advice you need to reduce your anxieties abd think more clearly. .Stop taking your herbs for at least one week because some of them will have side ellectsif you take them too long. You can add them back if you don't notice any good changes. Be more careful about being strictly gluten free.  
    • cristiana
      Just to say that I too was hesitant to come off dairy products completely @dsfraley.  Milk, yoghurt and soft cheeses definitely caused bloating.  This bloating gave me rib and pelvic pain, and I remember  the pain was so horrible at times it was almost a sick feeling., kind of like the sort of aches you get with flu.   Milk, yoghurt and soft cheeses also gave me diarrhea, but I noted I could still eat small amounts of hard cheese like cheddar without any issues. Re: milk, my gastroenterologist told me at that time that I could just by lactofree products, and should be fine, but when my gut was still very damaged they went right through me regardless. Thankfully I am able to tolerate milk very well again, although I have noted that too much of it can have a slightly laxative effect. The other thing that made me feel off were heavy iron supplements, which contributed to bloating and diarrhea.  In the end a GP told me to take ferrous gluconate, which is a much gentler supplement, with water an hour before breakfast in the morning.  That was helpful.  If your son is supplementing  (which needs to be under medical supervision as too much iron can cause issues) Floravital fruit syrup is another alternative, but make sure you don't buy Floradix as it contains gluten. Lastly, all oats, soya products and certain pulses also made my stomach sore.  Apart from the oats (which need to be certified 'pure' aka gluten free ones) I was able to eat these things again some months after adopting a gluten-free diet. I would say keeping a food diary might be worth a try, noting any negative symptoms following eating.  Patterns start to emerge which might otherwise be difficult to identify.
    • trents
    • Wheatwacked
      Anyway, I have no problem with grass fed milk other than the price.  Maybe I should move to Ireland or New Zealand.  They're the only countries that don't feed grains to their cows to increase milkfat and milk volume. A side note: I just came back trom the vascular surgeon about the scan of my carotid arteries done last week.  A year ago I had over 90% stenosis in the right artery and 80% in the left.  Tcar procedure done in the right with a stent.  The results today were right side downgraded to Moderate stenosis and the surgeon did not expect to see as much improvement on the left. (untouched). I must be doing something right.  Recheck in six months.   Mucosal reactivity to cow's milk protein in coeliac disease This paper proves that cassein is the protein in cow's milk is the trigger but the study did not differentiate as grass fed milk.  I haven't found any studies specific to grassmilk. The study does not differentiate alpha or beta cassein.  Google says: some clinicians speculate that grain-based proteins could potentially pass into the milk, though scientific studies typically find no detectable gluten or gliadin fragments in bovine milk regardless of the cow's diet. So given alpha cassein as the trigger, grass fed A2 cassein; thought to be easier to digest and less likely to trigger the specific inflammatory pathways associated with standard commercial dairy; plus the omega 6:3 ratio of grain fed milk is 5.8:1 vs grass fed ratio of 1:1, grass fed milk is less inflammatory.  
×
×
  • 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.