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

Coloscopy


skinnyminny

Recommended Posts

skinnyminny Enthusiast

I was at a celiac support group meeting last night and they were sayin celiacs need to have a colonoscopy every 2 years. I am only 19 years old, and I was wondering if anyone knows if this is necessary for someone my age, they were shocked to know I have NEVER had one.. please if anyone has any information about this let me know!


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



Celiac.com Sponsor (A8-M):



AmandaD Community Regular

I have celiac diagnosed by small intestinal biopsy and my doc has never recommended follow up colonoscopies (I originally just had a sigmoidoscopy)...Celiac doesn't affect the colon, persay, it's the small intestine. I think you occasionally may need a follow up small intestinal biopsy or EGD to check to make sure you are healing if you were having continuing symptoms...

A

I was at a celiac support group meeting last night and they were sayin celiacs need to have a colonoscopy every 2 years. I am only 19 years old, and I was wondering if anyone knows if this is necessary for someone my age, they were shocked to know I have NEVER had one.. please if anyone has any information about this let me know!
skinnyminny Enthusiast

That sounds right to me I was diagnosed 5 years ago and have had no follow up work other than a few check ups.

ravenwoodglass Mentor
I was at a celiac support group meeting last night and they were sayin celiacs need to have a colonoscopy every 2 years. I am only 19 years old, and I was wondering if anyone knows if this is necessary for someone my age, they were shocked to know I have NEVER had one.. please if anyone has any information about this let me know!

Celiacs can have a higher rate of adenocarcinomas and other cancers of the GI tract, but I believe this happens mostly with those of us who are undiagnosed for an extended period of time. Are you sure they said a colonoscopy and not a endoscopy? I could understand GI doctors wanting to do a endo every couple of years, to check if the villi are still healed, after all they don't get much money from us once we are dietary compliant and aren't sick anymore. <_<:D This is not something I would worry about unless your personal GI specialist said you need it for some reason, like for example you were not getting better on the diet.

IrishKelly Contributor
I was at a celiac support group meeting last night and they were sayin celiacs need to have a colonoscopy every 2 years. I am only 19 years old, and I was wondering if anyone knows if this is necessary for someone my age, they were shocked to know I have NEVER had one.. please if anyone has any information about this let me know!

I am now 28, and i had a partial-colonoscopy (not all the way through the entire intestines, just up to the colon...which didn't require sedation) and that was when i was 24, and I haven't needed one since. I have to say, your advice on this topic/issue is only as accurate as the person your getting your answers from. My point of view?? Why on earth would you allow a doctor to invade your intestines every two years when you know that the diet is working? You will heal fine so long as you stick to the diet and pay attention to any other food intolerances (especially as young as you are...knowing that the risks of cancer, etc. are minimal because the damage is only minimal due to your age). I personally feel it's being a little to over cautious to go every two years for a colonoscopy.

On another note, have you started to take any natural supplements to progress your healing process? L-Glutamine and Digestive Enzymes will help to heal you in half the time. They are not only available in a health food store, but they are over the counter in many other stores (although i do reccommend buying them from a health food store for risk free purposes ;) )

happygirl Collaborator

I must say, I've yet to hear of anyone recommending a colonoscopy every two years. Like it was mentioned before, the correct procedure to check for damage is an endoscopy, which checks the small intestine.

If they were in fact referring to an endoscopy (EGD), the "old" thinking used to be that follow up biopsies were necessary. Now, that is not the case.

Taken directly from Dr. Fasano's website (a leading Celiac researcher and physician) Open Original Shared Link

Do I need to repeat the biopsy once on a gluten-free diet?

If you are diagnosed based on positive serology and biopsy, and your symptoms improve once on a gluten-free diet, you do not need a follow-up biopsy.

The problem is that "old" thinking is hard to change. Many Celiacs who have had it for a long time have not caught up on recent research and continue to pass out information that came out long ago.

Many Celiacs were diagnosed on bloodwork alone---you will find many on this board. Heck, many Celiacs did not do bloodwork OR biopsy, but know that they do better without gluten in their diet.

So, unless you are having problems, then "usually" followup biopsies are not needed. Usually the first step, even if there are problems, is to run the bloodwork again.

Hope this helps clear things up. Does this help answer your question?

cmom Contributor

I have the celiac panel and small bowel series with follow-through every 3 years. I believe I am due in 2007 again. However, I am thinking of rejecting the small bowel series because the barium I have to drink may contain gluten. If I am mistaken about this, anyone may speak up to correct me.


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



Celiac.com Sponsor (A8-M):



trents Grand Master
I have the celiac panel and small bowel series with follow-through every 3 years. I believe I am due in 2007 again. However, I am thinking of rejecting the small bowel series because the barium I have to drink may contain gluten. If I am mistaken about this, anyone may speak up to correct me.

I had a CT of my abdomen recently with contrast, i.e., had to drink the barium milkshake. I inquired about it containing gluten on the day I scheduled the appointment. The radiology tech researched it and the next day had the info that it was gluten free. So, make sure you ask and get them to check it out.

Steve

happygirl Collaborator

cmom,

do you mind if i ask why you are having the barium/follow through? to check for other issues/maintenance (to make sure everything else is ok...no complications), I'm assuming, since it isn't used for Celiac testing. Wow-every three years---you are a better person than me :P I can handle lots of stuff...drinking that stuff was not one that went over well with me!!!

Due to non-celiac health issues, I had one this spring. I apparently wasn't her first Celiac and she knew that it was gluten free! So, I would recommend calling beforehand to have them verify it...but it looks like, at the very least, there are 'brands' of the stuff that are safe.

Hope this helps.

Laura

SanteeBay Rookie

I am 43 and was diagnosed 3 weeks ago. Positive blood and positve biopsy. I saw my doctor today and he wants me to have another endoscopy in 6 months, but I don't have to have another colonoscopy until I am 50 (WhooHoo!) You are lucky you found out when you are so young, unlike a lot of us who have felt terrible our whole lives and didn't know why..

Lisa Mentor
I am 43 and was diagnosed 3 weeks ago. Positive blood and positve biopsy. I saw my doctor today and he wants me to have another endoscopy in 6 months, but I don't have to have another colonoscopy until I am 50 (WhooHoo!) You are lucky you found out when you are so young, unlike a lot of us who have felt terrible our whole lives and didn't know why..

SanteeBay:

We have a lots of stories, a lot of histories and every one who posts here has a personal history. Many are know by us, who have been here a long time, and may suffer in silence. Do you reallty thing that we have not all walked in your shoes? <_<

"Lucky that you have found out...". I am glad that you found out why you were feeling so bad and happy that you have a conclusion.

There are some people here that have very serious side effect from un dx's celiac. Many are my friends and they are not so lucky.

Count you blessings, trust me. :)

cmom Contributor
cmom,

do you mind if i ask why you are having the barium/follow through? to check for other issues/maintenance (to make sure everything else is ok...no complications), I'm assuming, since it isn't used for Celiac testing. Wow-every three years---you are a better person than me :P I can handle lots of stuff...drinking that stuff was not one that went over well with me!!!

Due to non-celiac health issues, I had one this spring. I apparently wasn't her first Celiac and she knew that it was gluten free! So, I would recommend calling beforehand to have them verify it...but it looks like, at the very least, there are 'brands' of the stuff that are safe.

Hope this helps.

Laura

I have the barium/follow through to make sure I haven't developed any lymphomas or other problems. The last time I went in for one I already wasn't feeling well. Afterward, I became very sick. The hospital was about 45 minutes from my home. I had it coming out of both ends before I made it there. That's one reason I thought maybe the info I had was right about it containing gluten. I have wondered if it's really necessary though.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,543
    • Most Online (within 30 mins)
      7,748

    yfuvhg
    Newest Member
    yfuvhg
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.