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

Diagnosed Celiac: Is This Typical/normal?


rockette

Recommended Posts

rockette Newbie

First I will say thank you for any help and replies! I will try to make this short. I'm 38 female. Was told I had IBS for years. In January, I developed acid reflux. Meds didn't help that much. Had an endoscopy biopsy (out of state as I was gone from home for 2 months) in march and was told I have celiac and "go gluten free and u will feel better!". That was all I was told. In April I went to a Gastro doctor in my home town and I was asked to go on gluten challenge so they could run the blood tests. 3 days of gluten was all I could take. I am to the best of my knowledge gluten free for 3 months. I use my own newly bought cookware, Tupperware etc. I changed all my hair products that contained wheat. I read every label etc. I do not believe I am accidently eating gluten. I am also dairy, corn and oats free.

I have been having these bouts of nausea that come and go with a hungry type feeling/pain that is not relieved by anything. Anti nausea meds help but not enough. I have recently had a CT, MRI, ultrasound to see if anything wrong. Everything is fine. All my bloodwork comes back normal.

So now to my question: have any of you experienced nausea that seems to come and go for a few days at a time while your body is still healing? I know I am only 3 months gluten free and that it can take months to heal and feel better. But geez! This nausea is the worst. That is my main complaint: nausea. No diarrhea or anything else. Also wanted to mention I am seeing a dietician who is knowledgeable in celiac and she said my diet looks good, just need to get more protein.

Thanks in advance for responses!


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

Some of us have additional intolerances like to soy and dairy. Maybe you could try doing a diet and symptom journal and see if any pattern appears.

saintmaybe Collaborator

First I will say thank you for any help and replies! I will try to make this short. I'm 38 female. Was told I had IBS for years. In January, I developed acid reflux. Meds didn't help that much. Had an endoscopy biopsy (out of state as I was gone from home for 2 months) in march and was told I have celiac and "go gluten free and u will feel better!". That was all I was told. In April I went to a Gastro doctor in my home town and I was asked to go on gluten challenge so they could run the blood tests. 3 days of gluten was all I could take. I am to the best of my knowledge gluten free for 3 months. I use my own newly bought cookware, Tupperware etc. I changed all my hair products that contained wheat. I read every label etc. I do not believe I am accidently eating gluten. I am also dairy, corn and oats free.

I have been having these bouts of nausea that come and go with a hungry type feeling/pain that is not relieved by anything. Anti nausea meds help but not enough. I have recently had a CT, MRI, ultrasound to see if anything wrong. Everything is fine. All my bloodwork comes back normal.

So now to my question: have any of you experienced nausea that seems to come and go for a few days at a time while your body is still healing? I know I am only 3 months gluten free and that it can take months to heal and feel better. But geez! This nausea is the worst. That is my main complaint: nausea. No diarrhea or anything else. Also wanted to mention I am seeing a dietician who is knowledgeable in celiac and she said my diet looks good, just need to get more protein.

Thanks in advance for responses!

There are a couple things that come to mind that wouldn't show up on standard assays in a doctor's office.

One is pyroluria, which is I admit, controversial but gaining ground as being accepted in the medical community. In this disorder, one product of hemoglobin biosynthesis that is not excreted in affected individuals binds preferentially to zinc and B6, causing deficiencies of these nutrients. Treatment includes large doses of zinc, B6, and black currant seed oil. A pyroluric person has difficulty making metabolic use of Omega-3 fatty acids, and should also consume more Omega 6 fatty acids and arachidonic acid.

Some top symptoms of pyroluria are morning nausea and a tendency to skip breakfast.

Another possibility might be leptin/insulin dysregulation, which are the hormones that control when you get hungry, when you feel full, and how your body processes the nutrients that you eat. If you are leptin resistant, you might feel hungry at strange times, after you eat, or at odd hours of the night. The fix to this is to go grain/starch light or free, and eat protein, fibrous greens, fruit, nuts, and seeds. The goal is to switch from a glucose metabolizing diet to a ketone diet, which incidentally leaves you feeling less a slave to food, and might help you lose weight (if you need to).

Note that the above two problems are not mutually exclusive (they can both be true), and dovetail nicely with your dietician's recommendation of getting more protein.

mommyof4 Apprentice

I may not be the best one to reply because I am 8 months since diagnosis & I still have some issues we are "figuring out".

However, nausea was a big thing for me those first months...I was on Zofran for the nausea...which helped some, but I still struggled with it. I know that feeling of being desperate to try anything to help...soooo off to a chiropractor I went. He's not the "bone crackin" kind of chiropractor, but he works more with muscles. I only had to go a few times & he worked muscles in my neck...I also had many procedures done during the diasnosis stage...4 endoscopies in total, CT scans, MRI's...the chiropractor suggested that sometimes the way the neck is manipulated can cause nausea. For me, as soon as I went & had my neck worked with a few times, I was able to stop taking the Zofran. I have no idea if it was the chiropractor that helped or just time that helped.

I've read that nausea can be an effect of Celiac...I still will have some nausea, but not like it was at the beginning. You are still only a couple months post-diagnosis. I also agree with the previous post about watching for other food intolerances, although it sounds like you are pretty careful.

Hang in there...I know how much of a life change all of this is! I've told my husband many times that I don't mind the diet change...I just want to feel 100% "back to normal".

rockette Newbie

Thank you. I will look into the things that were suggested. I do have to say that my nausea comes and goes but when it is here it is here for a few days straight at the least. I am now on day 6 with no relief. Go to bed with it and wake up with it. This is my longest bout of it so far. I also am taking zofran and it does help take the edge off but doesnt make me completely functional. I keep telling myself how I know that I new to this and it takes time! But it is just hard when I feel so sick.

Also, I did stop soy for a few weeks and didnt notice an improvement. Maybe I need to go off of it for longer. I find the whole food intollerances and figuring out which ones are triggers to be hard to do.

I have not ever seen a chiropractor before but who knows! I would do whatever it takes to make me feel even close to normal again. I think I will see a naturopath next.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,549
    • Most Online (within 30 mins)
      7,748

    Blough
    Newest Member
    Blough
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)

    • There are no registered users currently online

  • 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.