Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Symptoms


newg

Recommended Posts

newg Apprentice

I had a negative blood test but my endoscopy was positive (my small intestine was has damage) so my doctor told me I have Celiac Disease. The ONLY symptom I have is feeling nauseous and since I have stopped eating gluten and wheat I have been feeling better but I still feel nauseous about half the time. Is this normal....how long does it usually take to feel better? Has anyone else had this symptom? Thanks :)


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



Celiac.com Sponsor (A8-M):



Lisa Mentor

Welcome:

You damage to you intestines too quite some time, healing will likwise.

Make sure that you are eating lightly seasoned food and check your lotions, shampoo, (lipstick?) and toothpaste.

happygirl Collaborator

Newg,

Welcome to the board! We are happy you have found us, amidst your diagnosis.

Yes, it is normal. How long have you been on the gluten free diet? It takes awhile to heal. For some, they see improvements but it takes months to get back to normal. Others heal and get better pretty quickly. Others see no improvements and then months later, get better.

Celiac is often referred to as a medical chameleon because there are so many symptoms, so many variances on healing times, etc. One person can have diarrhea, another constipation. One can have weight loss, another weight gain. Some have absolutely every symptom in the book, others only have the "classic" GI symptoms, others have relatively no symptoms (referred to as "asymptomatic Celiac" or "silent Celiac.")

So...the standard answer is....as much as anything is normal with this disease, yes it is normal. :P

Plus, the learning curve is steep with gluten free eating, so you might still be getting gluten through ingredients or cross contamination.

Let us know what we can do to help. Please feel free to PM me anytime!

Laura

NoGluGirl Contributor
I had a negative blood test but my endoscopy was positive (my small intestine was has damage) so my doctor told me I have Celiac Disease. The ONLY symptom I have is feeling nauseous and since I have stopped eating gluten and wheat I have been feeling better but I still feel nauseous about half the time. Is this normal....how long does it usually take to feel better? Has anyone else had this symptom? Thanks :)

Dear newg,

I am gluten intolerant and nausea has been my primary symptom. It is so hard to deal with. Since you have damage, chances are, the nausea you are still experiencing is due to your small intestine not being healed yet. It can take months or even years for it to completely heal if the damage is really bad.

On top of the nausea, I had such bad reflux I had to sleep practically sitting straight up. I also had poking pains all over my stomach, and the runs. My stomach also got so bloated and hurt, and I could not lose weight no matter what I did! About once a week, usually after I ate waffles, a peice of bread, or a poptart, or noodles, I would get so bloated and queasy, and would break out in a sweat, get extremely nauseated, start shaking and have diarrhea. Sometimes I got the dry heaves as well, on top of having so much gas I felt like I was having a heart-attack. I would shake really bad and my hands would go numb. Promethazine is the only thing that helped. Since going gluten-free, the reflux has reduced quite a bit, and I was taking Prilosec twice a day and it was unbearable even with it before the diet. Now I can even skip a dose and if I am late with it, it does not nearly kill me. This is a miracle in itself! The nausea has reduced to the point I can actually leave the house without taking my medication first! I have had more trouble with it returning since I did a course of antibiotics, but I have yeast candida as well. My tongue was going numb and my lips were swelling up too, before going gluten-free. It took only a few days before I saw results. I have to say it took a couple of weeks before I really noticed a difference. It was worth the wait. I hope to improve further soon. I hope this helped.

Sincerely,

NoGluGirl

P.S. I had a negative biopsy and bloodwork, but obviously it was not very accurate.

Ursa Major Collaborator
I had a negative blood test but my endoscopy was positive (my small intestine was has damage) so my doctor told me I have Celiac Disease. The ONLY symptom I have is feeling nauseous and since I have stopped eating gluten and wheat I have been feeling better but I still feel nauseous about half the time. Is this normal....how long does it usually take to feel better? Has anyone else had this symptom? Thanks :)

Have you eliminated dairy as well? People with celiac disease can generally not tolerate dairy until the villi heal, and many can't tolerate casein (meaning all dairy, because casein is the protein in milk) and won't ever be able to have milk.

So, eliminating gluten might be eliminating half the problem, and you might start feeling even much better if you get rid of dairy.

Another culprit could be soy. Dairy and soy are also known to cause villi damage and could be a problem on top of the gluten, or even instead of it.

So, eliminate those and see how you are doing. Then, after about a month, test them one at a time, to see if you react. If you do, you know to keep them out of your diet.

It can be tricky. You also may still have gluten somewhere sneaking in. Have you gone through all of your personal care products? You need to replace everything with gluten (wheat germ oil, barley extract, oat bran), and that goes for shampoo, conditioner, lipstick/chapstick, soap, toothpaste, lotions etc.

Also, if you're eating gluten-free bread, have you bought yourself a new toaster? It simply isn't possible to clean your toaster well enough to be safe. The same goes for plastic colanders, wooden cutting boards and wooden cooking spoons, and scratched non-stick cookware.

newg Apprentice
Dear newg,

I am gluten intolerant and nausea has been my primary symptom. It is so hard to deal with. Since you have damage, chances are, the nausea you are still experiencing is due to your small intestine not being healed yet. It can take months or even years for it to completely heal if the damage is really bad.

On top of the nausea, I had such bad reflux I had to sleep practically sitting straight up. I also had poking pains all over my stomach, and the runs. My stomach also got so bloated and hurt, and I could not lose weight no matter what I did! About once a week, usually after I ate waffles, a peice of bread, or a poptart, or noodles, I would get so bloated and queasy, and would break out in a sweat, get extremely nauseated, start shaking and have diarrhea. Sometimes I got the dry heaves as well, on top of having so much gas I felt like I was having a heart-attack. I would shake really bad and my hands would go numb. Promethazine is the only thing that helped. Since going gluten-free, the reflux has reduced quite a bit, and I was taking Prilosec twice a day and it was unbearable even with it before the diet. Now I can even skip a dose and if I am late with it, it does not nearly kill me. This is a miracle in itself! The nausea has reduced to the point I can actually leave the house without taking my medication first! I have had more trouble with it returning since I did a course of antibiotics, but I have yeast candida as well. My tongue was going numb and my lips were swelling up too, before going gluten-free. It took only a few days before I saw results. I have to say it took a couple of weeks before I really noticed a difference. It was worth the wait. I hope to improve further soon. I hope this helped.

Sincerely,

NoGluGirl

P.S. I had a negative biopsy and bloodwork, but obviously it was not very accurate.

I take promethazine too! I try not to take it unless I have to because it makes me so tired!!! I am gluten-free (i think) and now I only get nauseaus about every other day. I'm hoping in a couple of weeks I won't have to take it anymore. Do you still take it? Thanks for the response...its nice to know someone else has the same symptoms as me!

newg

Mary Contrary Rookie

I had nausea for a bit as well, it really scared me at first when I was getting sick to my stomach usually in the middle of the night, I'd even have to get up and throw up...that coupled with the explosive D I thought I was in the throws of something horrible and life threatening...

I have had negative blood work and now going for a biopsy this coming week, but I have been off of gluten for 2 months now, I figured it out myself, my regular Doc was no help at all..and my symptoms are starting to subside...especially the horrible bloating and gas, it was gone in a matter of a week or so..the D is just now starting to go away. It doesn't even matter to me what they find or don't find next week, I am sure not ever going back to gluten. Also having a colonoscopy to be on the safe side..I am of that age anyway when a person needs one.

My regular Doc told me to eat toast... :blink:


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,843
    • Most Online (within 30 mins)
      7,748

    Chanwill
    Newest Member
    Chanwill
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.4k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Dawn Meyers
      Hi I have celiac disease and the dermatitis herpetiformis rash Also other autommune diseases.  I have had bad side effects to all the vaccines I have had and now my Doctor wants me to have the pneumonia vaccine.  I am concerned because of some of the bad side effects I have had in the past example Hep B after shot couldn't  move arm for several months.  Flu shot and COVID was sick right after shot. Told not to get anymore. My lung is inflamed and have a cough I can't seem to get rid of. Very concerned 😟. 
    • knitty kitty
      @Manaan2,  I'm so happy to hear you're going to try thiamine and magnesium!  Do let us know the results!   You may want to add a B 50 Complex with two meals of the day to help boost absorption.  Thiamine interacts with each of the other B vitamins which are all water soluble.   When supplementing magnesium, make sure to get sufficient calcium.  Calcium and magnesium need to be kept in balance.  If you choose a calcium supplement, take two hours apart from magnesium as they compete for absorption.  Take Calcium with Vitamin D.  Vitamin D helps calm the immune system.   For pain, I use a combination of thiamine, B12 Cobalamine, and Pyridoxine B6.  These three vitamins together have analgesic effects.  My preferred brand is "GSG 12X Takeda ALINAMIN EX Plus Vitamin B1 B6 B12 Health Supplementary from Japan 120 Tablets".  Alinamin is another form of thiamine.  It really is excellent at relieving my back pain from crushed vertebrae without side effects and no grogginess.   Look into the low histamine version of the Autoimmune Protocol Duet (Dr. Sarah Ballentyne, a Celiac herself, developed it.)  It really helps heal the intestines, too.  It's like a vacation for the digestive system.  Add foods back gradually over several weeks after feeling better.   I'm so happy to have pointed the way on your journey!  Let us know how the journey progresses! P. S. Add a Potassium supplement, too.  Potassium is another electrolyte, like magnessium, that we need.
    • Manaan2
      @knitty kitty I can't thank you enough!  My husband and I already started looking into those supplements.  We definitely plan to give it a try.  We've been against the Miralax since it was originally advised by PCP, but because of the level of pain she experienced on a daily basis, we decided to try it.  We've made many attempts to gradually decrease but due to her pain and related symptoms, we've kept her on it while trying all sorts of other dietary adjustments pre and post diagnosis specific to food; so far none of those efforts have made a significant difference.  I will definitely share how she's doing along the way!
    • BIg Nodge
      Hi, I have recently embarked on the gluten-free journey. I have what to me seems like a somewhat confusing set of test results and symptoms. I have been impressed by the accumulated knowledge and thoughtfulness as I browse this forum, so I figured I'd make a post to see if anyone can offer any insight. I know there are many posts like this from new users, so I have tried to do my baseline research first and not ask super obvious questions.  I'm 43, overall very healthy. No history of gluten sensitivity or really any of the classic GI symptoms. About three years ago I started to experience intermittent bouts of fatigue, chills/cold intolerance, and shortness of breath/air hunger (sometimes feels like a hollowness in my chest, hard to describe). The symptoms over time have become fairly significant, though not debilitating, I am able to exercise regularly and am fairly physically active, continue to perform well at work. But for example I have gone from someone who consistently ran hot, was always cranking the a/c, to someone who wears a down vest inside at work in winter and get chills if the a/c even blows on me in summer. I get tired and lose energy even when getting decent amounts of sleep, and have to have my wife take over on long drives that I could previously handle with no problems. More generally when I am experiencing these symptoms they seem to crowd out space in my mind for focusing on my family, my hobbies/activities etc, I sort of withdraw into myself.   I happened to be experiencing these symptoms during an annual physical with my PCP a few years ago, he observed post nasal drip and suggested it was allergies and that I treat it with claritin. At first it seemed to respond to claritin (though not zyrtex), but over time I became unsatisfied with that answer. There didn't seem to be any seasonal rhyme or reason to my symptoms, and I felt like I was on an endless loop of taking claritin, then stopping, not being sure if it was even making a difference. I did eventually get allergy tests and found modest allergies to dust and pollen, which didn't feel like a smoking gun.  I then started seeing a natural medicine doctor who was much more willing to explore my symptoms via testing. The first thing that came back abnormal was elevated thyroid peroxidase antibodies/TPOs, 137 IU/mL vs a reference range of <9. At the same time my thyroid panel showed normal thyroid hormone levels. So it appears my immune system is attacking my thyroid even though it is working fine. I got a thyroid ultrasound at the time, it was clear, but with some abnormalities such that they suggested I get is scanned again in a year. These are certainly risk factors for a thyroid autoimmune disease, though my thyroid seems to be working fine for now.  From here my doctor considered celiac due to the murky thyroid/celiac links, so we did a panel. Results were as follows: TT IGA <1 U/ml, TT IGG <1 U/ml, deamidated gliadin IGA 24.6 U/ml, deamidated gliadin IGG <1 U/ml, IGAs 170 mg/dL. Readings greater than 15 considered high by my lab for the first four, my IGAs are within reference range. So basically just the deamidated IGA popped, but my IGAs are normal. I also notice on the tests that my thyroglobulin was high, 86.7 ng/ml vs a range of 2.8 - 40.9.  My doctor suggested that it certainly wasn't conclusive for celiac, but it was possible, and likely that I have some sort of gluten sensitivity. She suggested going gluten free and seeing how I felt as opposed to doing a biopsy. The best theory I can come up with is perhaps I am a silent celiac or just have a gluten sensitivity that doesn't produce immediate GI symptoms, but is still doing damage and over time has caused leaky gut. So now gluten is getting into my blood, and my immune system is attacking it but also mistakingly attacking my thyroid.  So that's what I did, went gluten free in October. It's been about four months, and I am really not feeling any difference. I still get the same symptoms that come and go. My bowel movements may be a bit more regular, but it was never a major issue before so I would consider that a minor improvement. I know that it can take a while to see improvements, and I am going to remain gluten-free and see how I feel. But I am definitely questioning whether I really understand what is going on, and am open to any thoughts or suggestions from the forum. Sometimes I wish I just went ahead with the biopsy before going gluten-free. While I would certainly be down to start drinking IPAs again ahead of a biopsy, you know, for science, I feel like at this point I would be throwing away four months of work and am better off staying the course and seeing what happens. But I'm really not sure.  I know there is a lot of thyroid knowledge on these boards, along with the celiac expertise, so I'm curious if this resonates with anyone's experience. And I'm interested in what sort of timelines people have experienced in terms of feeling improvements for some of these non-GI symptoms like chills, SOB, brain fog etc. Thanks in advance. 
    • cameo674
      Does it taste like black licorice?  It said it was chewable.  I do not like that flavor.     Since the burn at the back of my throat is there everyday, I usually only take something when it is unbearable and keeping me from ADL especially sleep.  
×
×
  • Create New...