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

Sound Like Celiac?


Tusofsky

Recommended Posts

Tusofsky Newbie

Hey guys. I found this forum while trying to do some research after my doctors (Family and the GI doctor I saw) mentioned Celiac to me.

I've always felt like I had a weak stomach, prone to stomach upset and diarrhea AND constipation things like that. I get tired easy, I go through what seems like RANDOM bouts of depression and anxiety (Especially in the last couple months) I eat a lot of bread, I'd say it's a big focus of my diet. Well, in November I got sick. Horrible vomiting, diarrhea, abdominal pain. I was in the ER overnight, they said I had a high white count (About 17,000) which usually indicates a virus so that's all I thought it was.

Starting a few weeks ago I was having sudden anxiety issues. Then on Feb 16th, I got sick again, same thing. Vomiting, diarrhea, a lot of abdominal pain. And it hasn't stopped. I've had sudden days where I think I'm better, but then I crash again fast. I was told I had a UTI (UTI from hell, it widthstood a round of Cipro, and now I'm on Macrobid). Last Wednesday my bloodsugar levels dropped to 21 (yikes) but have been fine ever since (staying in the 90s). I had an endoscopy yesterday because of suspected ulcers, but of course there were none, so my doctor took a biopsy to test for Celiac. But he barely mentioned it while I was in the recovery room, then he was gone (onto the next patient).

Now I feel constipated (despite having soft stools), I still have abdominal pain, mainly on the left side. I get spasms of pain on my lower back, and even on 8mg of zofran I get slammed with heavy nausea.

Of course, the past few days I've also been eating tortillas and toast to be easy on my stomach, which I know have gluten (the celiac wasn't mentioned to me till yesterday and then today by my family doctor) I was called today being told my bloodcells are small and a little pale, and I have a pretty severe iron deficiency. I know Celiac can cause problems with iron absorption.

I'm avoiding Gluten now, just to be on the safe side until my GI doctor gets back to me, but if they don't figure out what's wrong with me soon I'm going to scream lol It's been a rough, miserable two weeks. At least Celiac would be an answer. Though honestly I'm a little scared, which is why I'm posting here. My GI Doctor was very detached and not very patient friendly so he didn't exactly leave me feeling comforted.


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



Celiac.com Sponsor (A8-M):



GottaSki Mentor

Welcome!

Yes, your symptoms could very well be Celiac. At the very least it should be ruled out. Caution -- Do not remove gluten until you have had the Celiac Panel of blood work because if you remove gluten your body may not be producing the antibodies that show up in the blood work. Additionally, should you and your GI Doc decide to do an endoscopy to confirm Celiac diagnosis, you need to remain on gluten until that test is complete.

In addition to the celiac panel and iron...I suggest running all Bs, D, K, Copper, Ferritin and Zinc. Having very low vitamin/minerals in the body is one indication that you are not absorbing your nutrients which can cause many, many varied symptoms along with add weight to the Celiac Diagnosis -- the intestinal track becomes damaged in Celiac Disease - specifically the villi (fingerlike portion of small intestine that allows absorption of nutrients) become blunted.

Hope that was clear...sure many more will explain with perhaps better terminology.

Again welcome and hope you are feeling stronger very soon!

Tusofsky Newbie

Thank you for responding! He already took the biopsy yesterday, there just wasn't a lot of talk about it (I saw him for like 20 seconds after my endoscopy before he was gone in a flash) And my regular doctor is running labs off blood they took last week. So I'm hoping if I stick to rice, mashed potatoes, eggs and such, things that are easy on my stomach AND gluten free, I'll start feeling better. I've been missing way too much work because of this already.

They're putting me on an iron supplement, which I'm about to go pick up. It sounds like the lack of iron is causing some problems (Fatigue, joint paint, headaches... Possibly the anxiety? I've never had problems with anxiety before this year but I have battled depression before) but the abdominal pain, bloating, vomiting/nausea, diarrhea/constipation is still going unexplained for me unless I just also happen to have a nasty case of gastritis. Which may be case, I don't know at this point.

If I am told I DO NOT have Celiac from the biopsy, should I ask about a gluten-free (or less) diet anyway and see what they say? I've been reading it does help people with stomach problems, even if its labeled IBS. I really just want to get better...

GottaSki Mentor

A positive tTG IgA blood test confirms Celiac Disease -- but there are often false negatives. With your symptoms it can not hurt you to go Gluten Free -- it is not easy to make the transition long term, but well worth it if it brings health.

Glad you have already had the blood work along with endo. It will be interesting to get the pathology report to see if there is blunting of your villi along with biopsy info (the biopsies are often negative - depends how many and where the Doc took the samples).

I hope you start healing right away, but don't be discouraged if it takes awhile to notice improvement upon going gluten-free. It seems the longer we go un-diagnosed the more damage to our intestinal track -- hence longer healing times.

You have found the best place for Celiac/Gluten related questions...so many here helped me when I was ready to pull my hair out when first diagnosed as well as answered every question I've had along the way.

PS...you may want to add some fruit, vegies and meat the list...eating too many starches can be hard on the healing gut too...they are great gluten-free items...just make sure you keep it balanced.

Good Luck to you :)

Tusofsky Newbie

I'm eating banana, and egg too to try and have some protein. My appetite is very low right now, but I'm trying to keep myself fed lol

Thanks so much for your replies :) This seems like a really nice forum. I know I won't hear from the doctor over the weekend (Urg. I hate waiting on all these labs. Driving me crazy) but I'm starting my iron supplements they called in for me and gonna try and keep gluten free for the time being, hopefully I'll be okay for work this week. I've missed so much! But I'll post my results when they come in.

Tusofsky Newbie

Sorry if TMI, but I was constipated for the last few days (I hadn't had a bowel movement since Thursday morning, early and it was very small then I felt like I needed to go but I couldn't) now I'm back to having diarrhea :( I'm very scared about what's going on with me, I keep flying back and forth between being semi-okay (only thing consistent is my pain) and crashing to the ground. I just wish I knew what was happening...

Tusofsky Newbie

Apparently my family physician is NOT running blood panels for celiac and I'll need to have more blood taken now if I want that done, with my GI doctor. I guess it all depends on what my endoscopy says but. . Should I go back on gluten now just in case? I'm scared to because I don't want all my symptoms rushing back at me (I'm having constipation, pain, and dehydrating real easy now) but I'm scared of my nausea hitting me full force again, and the pain getting worse. But. I don't know. I feel really lost right now to be honest.


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



Celiac.com Sponsor (A8-M):



GottaSki Mentor

Apparently my family physician is NOT running blood panels for celiac and I'll need to have more blood taken now if I want that done, with my GI doctor. I guess it all depends on what my endoscopy says but. . Should I go back on gluten now just in case? I'm scared to because I don't want all my symptoms rushing back at me (I'm having constipation, pain, and dehydrating real easy now) but I'm scared of my nausea hitting me full force again, and the pain getting worse. But. I don't know. I feel really lost right now to be honest.

Check with your GI doctor. Was the endoscopy specifically for Celiac Diagnosis? If not he may not have taken the proper samples. If it was specifically for Celiac -- did they draw any blood before the endo? My Celiac GI always takes blood the day of the endoscopy to verify that I am not accidentally ingesting gluten.

I wouldn't go back on gluten if you are having improvement to your digestive symptoms -- post your endoscopy results in a new thread if you don't understand them...there are many in this forum that can help you interpret the results.

When you had blood run...did they happen to run B6, B12, D, Iron or other minerals (Ferritin, Copper, Zinc) -- being low or deficient in vitamins and minerals can indicate that you are not absorbing your nutrients due to intestinal damage caused by gluten.

Tusofsky Newbie

They didn't run any others, no. I got a call today and my biopsy did come back negative but NO it was not a specific to look for Celiac. So. I go in on the 13th, and I'm going to request bloodwork and try to get him to talk to me more in depth

It's frustrating to get a call "Found nothing, we don't know, sorry" then I have to be the one to be like "Can I have a follow up?" urg. Doctors why.

I haven't SEEN the biopsy results myself though, I'm going to request a copy when I go in. This was just over the phone.

GottaSki Mentor

Can't recall how long you have been gluten-free. You need to have been eating substantial amounts of gluten for several weeks before the celiac blood panel.

Tusofsky Newbie

It's literally only been 3 days, not even a full week. The vanishing of symptoms could even be a placebo effect (not everything went away, just lack of headache and nausea), I'm trying to keep that in mind. But considering I've always had digestive problems, and a few other symptoms that seem to be common in celiac's, I want to rule it out at the very least. Even while I was sick though, I was eating toast and the like, and prior, bread is a huge part of my diet (I adore pasta) but I'll talk to him about it and see what the doctor says. I'm seeing my family doctor as well, the day before for follow up on my UTI, and I plan on mentioning it to him, he's a billion times more patient friendly.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,553
    • Most Online (within 30 mins)
      7,748

    Jennifer CCC
    Newest Member
    Jennifer CCC
    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.