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

Super Confused - Now What?


bluefey

Recommended Posts

bluefey Newbie

for four years I have avoided gluten - I knew it made a difference in how I felt if I didn't eat it.  I would sometimes because it was all I had left - or maybe somebody's birthday - but more often than not I didn't eat it...

 

In November I had a horrible pain in my upper abdomen that radiated into my back.  It had to be gall stones -- or so my doctor said. Went for an ultrasound - but nothing was there...    So then I had a CT scan -- still nothing    So then some blood work.  It came back that I had Celiac's -- this was not a surprise - like I said I knew gluten caused me issues...

 

So my doctor sent me to a gastroentologist  for more tests...  so I had a colonoscopy and endoscopy - with a biopsy....

I never heard anything about the results so I called today.   The nurse was very confusing.  She said that there was non-specific inflammation in the biopsy, but no indication of anything other than diverticulosis.  She told me to eat more fiber.  She also told me that I needed to have blood work done to determine if I had celiacs -- I told her that I already had blood work and that it said I did have celiacs - and that is why I went for the tests.   Her response was, "oh. well just eat more fiber- lots of grain."  I asked if this meant that I could eat gluten again, and she said she didn't know, but I should avoid seeds.   She made me an appointment in 3 weeks to talk to the doctor because she couldn't respond to my questions.

 

I don't know what to do now - to gluten or not to gluten that is the question... 

 

I believe I do have celiacs -- here is why

 

#1 if I eat gluten I have pain in my stomach within 20 minutes and my feet swell

#2 I lost 60 lbs recently without trying

#3 I have this crazy rash all over my legs that wont go away

#4 If I eat gluten I get headaches

#5 I have problem with bowel movements -- food frequently flows right through me or I might be constipated for days...

 

obviously I will continue to avoid gluten...   but there is a big difference between avoiding it and scrutinizing every single thing you eat to make sure it is gluten free and worrying about cross contamination.

 

any advice from you guys would be greatly appreciated... I just don't know what to think anymore...

 


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



Celiac.com Sponsor (A8-M):



Fenrir Community Regular

I would call and ask to talk directly with your GI doc because the nurse isn't explaining things properly. 

 

#1- biopsies can be negative and you can still have celiac.

#2- If you have had a tTG blood test done and it was positive, you most likely have celiac.

#3- Just because you don"t have stones does not mean you don"t have a gallbladder problem. I didn"t have stones but my gallbladder was causing me all sorts of issues. I had a HIDA scan that showed my gallbladder wasn"t functioning and was causing me pain. I personally think that celiac disease may have damaged my gallbladder. 

124chicksinger Apprentice

Don't eat the gluten, and don't eat the prescribed high fiber grain diet - you can get plenty of fiber without eating the gluten containing grains.  Eat an apple - high fiber.  Pineapple, high fiber. Strawberries, high fiber.  Even tho the strawberries have "seeds" it is okay to eat them. Diverticulosis doesn't collect the seeds within the pockets and get inflamed; that is an old notion that has changed.  Nuts and seeds like pumpkin actually help to "scrape" the intestines on elimination and aid in remedying diverticulosis, that is the current notion.  The nurse has given you contradictory incorrect advise. Get on the phone with the doctor asap.  If the doctor tells you a ) you have celiacs and b ) eat plenty of grains, go get your records and go elsewhere.   As to the gluten, stop indulging in it, ever, and start looking for all the hidden gluten and avoid it as well.  It takes a mere toast crumb to cause damage to your small intestine.  Take a probiotic too.    

 

I am new to this, but my issues are similar to yours as written, tho I have a negative diagnosis for celiac.  I am gluten free 4 weeks now.  Feeling better already.

 

Certainly, you will receive more helpful answers here from these wonderful people.  Take care.

1desperateladysaved Proficient

Greetings!

 

Were you eating gluten regularly before the endoscopy?  It is possible the gut had healed to some degree, or that the damage was missed.

 

Do you know if your nutrient levels are good?  Many people with celiac experience anemia or low vitamins B and D.

 

Look into avoiding all food without gluten and reading every label.  Celiac isn't just symptoms from eating gluten, but actual damage being done.  You likely will feel much better.

 

D

HavaneseMom Explorer

Hello,

If it were me, I would call and ask them to mail or email a copy of both your blood test results and your biopsy results. It sounds like the girl you spoke with on the phone wasn't very informed, and there may have been some terminology on the report that she didn't understand. It's always a good idea to get copies of all of your results and keep them in a file at home. It would be nice for you to know exactly what the report says sooner than the 3 weeks you have to wait for your appointment.

NoGlutenCooties Contributor

Welcome!

 

If you had a positive blood test and you get symptom relief from being gluten-free, then my money is on you having Celiac.

IMO... the nurse you spoke to sounds completely ignorant about Celiac and gluten intolerance. 

 

With Celiac, you cannot simply avoid "most" gluten and think that's good enough.  You need to be 100% gluten free.  No cheating.  No cross-contamination.  Otherwise your body produces antibodies and those little buggers literally kill you from the inside out.

bluefey Newbie

I have avoided gluten for 4 years -- after the diagnosis in November I have not had any gluten at all.  Everything I eat - even my medication is 100% gluten free - I study labels before I eat anything.  If I accidentally get gluten the pain comes back.  So, before the biopsy I had not been eating gluten for 4 months and the pain was gone.  Since then I did take medication with gluten, but I was so sick already that I didn't even think about if it had gluten.  The rash on my legs came back big time and my feet are swollen again!  The pain is back in my stomach.  I lost 14 pounds.  Pretty sure all of that is just from 10 days of medicine.   Until I went totally gluten free I was losing 4-5 lbs a week without trying.  I am still losing weight, but not as rapidly.  I take vitamins so my levels are not that bad. 

 

I don't plan to ever go back to eating gluten - no matter what the diagnosis of the biopsy says.  But if I don't have celiac then I need to find out what is causing all these problems.  I also won't be worried about cross contamination anymore.  I am just really confused why the nurse would tell me to eat lots of grain.  How does the blood work say I have celiac, but the biopsy said no?  and what is a nonspecific inflammation? 

 

 

Other than another biopsy - which cost me $1800 - how do I find out what is going on with my body?   Or should I just go by the blood work diagnosis?  just so confused now...


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



Celiac.com Sponsor (A8-M):



NoGlutenCooties Contributor

IMO... if you've been gluten free and had that kind of a reaction to the reintroduction of gluten then you are definitely Celiac and there's no point in doing a gluten challenge just to do a biopsy.  And without the gluten challenge, the biopsy would be meaningless - at least from a Celiac diagnosis standpoint.  "Nonspecific inflammation" just means that there was inflammation but perhaps not enough, or not severe enough, for someone at the lab to interpret it as bad enough to confirm Celiac.

 

My suggestion is to stay 100% gluten free and see how you feel.  You've already had testing to rule out a gallbladder issue - which is good.  With a gluten free diet you may find that the pain you experienced never comes back.  But if it does - definitely follow up with a doctor.

Fenrir Community Regular

Yes, if you cut out gluten and felt better I would just stick to a strict gluten-free diet and see if it goes well.

124chicksinger Apprentice

Its a shame the testing can't be more specific, especially the biopsies. It seems unless your intestines are riddled with damage, there is a chance the damage cannot be found.  Trust the blood work and your reaction to gluten.  As to the high fiber for the diverticulosis, you can get plenty of fiber without those "healthy whole (wheat)(rye)(barley) grains."  

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,555
    • Most Online (within 30 mins)
      7,748

    JMF
    Newest Member
    JMF
    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

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • 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.
×
×
  • 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.