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

Is It Normal To Still Feel Nauseous/stomach Pain After 2 Weeks Gluten Free?


cctaylor01

Recommended Posts

cctaylor01 Newbie

Hi there,

I'm new here. I've been gluten and dairy free for almost two weeks now. Though I have not been diagnosed with celiacs, I had been dealing with a whole slew of celiac/gluten sensitive type symptoms which, for over 8 years have never been resolved. An acupuncturist I was seeing to help with this said that she had all the same symptoms that I have and went gluten and dairy free, which has since made her feel like a normal human being again. I figured I would try the diet and see what results I got, considering I am willing to try anything at this point. It seems to be helping in many regards. Luckily the daily headaches/migraines seem to be subsiding pretty well already, along with a great energy level increase, less brain fog, less knee pain, somewhat better moving bowels, etc.

The problem is that I am still experiencing nausea and horrible stomach pain for hours after each meal. Is it normal to still be experiencing this. I know I haven't been on the diet for very long, so it's highly likely that I am just panicking and this is totally normal.

How long should it take for the stomach pain/gastro problems to start feeling better. I am sure this depends on the length and severity of symptoms, but does anyone have any words of wisdom for me?

Currently feeling super nauseous (sort of like there is food just sitting in my stomach) after eating only cucumber salad and some hummus 4 hours ago. Had gluten/dairy free waffles for breakfast with honey and 2 eggs and was nauseous shortly after that as well. Every couple days I am still taking the senna laxative to help move along my system, as the constipation is still a problem. Could that be causing a problem? The brand is Rite Aid's Senna Natural Vegetable Laxative.

Please help! Is it normal to still feel the stomach symptoms?

Thanks!


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



Celiac.com Sponsor (A8-M):



Chakra2 Contributor

It sounds like some of your symptoms are improving but others are not, right? That can be so frustrating. I'll pass on my general chronology of feeling better in case it might help. The basic message is that feeling better on a regular basis took a long time for me. At 2 weeks in I still felt rotten every day, even though some of my symptoms were already noticeably better.

MONTHS 1-3: Went gluten-free in January, undiagnosed (I didn't know anything about celiac disease, was just doing an elimination diet to find food allergies). GI symptoms improved within days (no more D, no more gas, pain or bloating). Other symptoms, like fatigue, mood issues and joint pain still present. GI symptoms would return frequently. I felt "allergic" to everything I ate. GI improvement was enough to keep me going though. Gradually I saw other improvement. I would have 2-3 good days, then 2-3 bad days. Or even more like 2-3 good hours, then 2-3 bad hours! Roller coaster for sure.

MONTH 3: BIG turnaround! After learning more about celiac disease and gluten intolerance, I dropped all dairy, soy, and corn. Also started probiotics and other supplements. Mood and energy issues improved. Joint pain got worse.

MONTH 4: honestly thought I had RA because joint pain getting so bad (and I'm only 33). Tested negative. Read about nightshades, dropped those. Pain vanished within days. Turned out those gluten-free subtitute foods had a lot of potato in them! Also started to absorb more of the info about how to avoid gluten. I started eating out less and being more careful to ask questions when I did, I got gluten-free dog food and treats, and switched all my bath products to gluten-free versions. Slowly but surely, started having way more good days than bad. GI symptoms return when accidentally glutened.

MONTHS 5-8: Life is good! I finally feel good for weeks at a time. I feel like it's such a new development though that I'm a little paranoid --don't eat out right now, don't eat at friend's houses. I know I'm probably being stricter than necessary but I've just felt bad for so long that I am cherishing my good days and don't want to do anything to mess them up! I'm hoping I get less paranoid about gluten as I go along.

To summarize, my advice is to keep up the good work! Your intestines might take months to truly heal and until they do you might still feel all kinds of lousy symptoms on and off. Check into other common food intolerances, and think about dropping those foods temporarily while you get better. A lot of the gluten free processed foods unfortunately have ingredients in them that can be related to other common intolerances. (FWIW, I have nausea as one of my symptoms and it took months to really go away -- now if i get a little gluten or a lot of potato it comes back.) Keep reading this board and other resources to learn more about how to avoid gluten in all its forms and how to avoid cross-contamination. I wish you luck -- the next few months may be your turning point too!

Chakra2

Heidi S. Rookie

It is different for everyone but there is a long detox and healing period if you are Celiac or gluten intolerant. It is not just a diet but a lifestyle.

2 suggestions:

1. start with an elimination diet. Boiled chicken and rice with water for 2 weeks. It is terrible but it is the best way to reset your system then add one food every couple days and see how each food makes you feel. Me I found out egg whites were another problem making me feel nauseous on top of being gluten free for example.

2. check everything you use. Being gluten free means head to toe, it is an exhausting process. Check all products, anything touching your skin or ingesting, for wheat or wheat derivatives. This can take a long time, living gluten free takes purging your world of gluten as much as possible to limit exposure. You may be eating gluten free but are your pots, pans, silverware sterilized with no scratches in the coating?, shampoo, make-up, lotion, containing vitamin E (tocophernol)etc exposing you? Do you have crumbs in your silverware drawer? Dedicated new gluten-free butter, jam, etc? Do not stress, I am just trying to point out that two weeks is just the beginning, the fact that you ARE feeling better is a good sign. From what I read healing from each glutening takes the body up to 3 months to repair!!

Side note, I have never experienced constipation as a problem...so I can not comment on your stool softener, but from my experience watch out for "all natural pills" they can contain gluten in the binding of the pill.

sandsurfgirl Collaborator

It takes time to heal. There is a withdrawal period. The best thing you can do is use the search function and search for old threads on withdrawal. All sorts of crazy stuff happens for awhile.

I had improvements slowly over tim, but I didn't feel really good and pretty much symptom free until 6 months. Sorry to tell ya! I had like you do. Certain things improved and it was one step at a time.

Eat a clean healthy diet of veggies, meats, fruits, etc. Don't go nuts with gluten free carbs until you feel better. Let your body heal. Give it the raw materails to rebuild your gut.

At 2 weeks I was still bedridden, pooping literally 12 or more times, per day, having horrible crazy pains, dizzy spells so bad I couldn't drive, nausea, D then C and everything in between. The first two weeks I accidentally got glutened by things I didn't know contained it too so I guess I can't really say I was entirely gluten free yet at that point.

cctaylor01 Newbie

Very helpful to have someone describe specific changes over time. Very reassuring and encouraging. Thank you! I'm sticking to it and look forward to feeling as good as you do someday.

Claire

Skylark Collaborator

Also, keep a food diary. I had to go off gluten, soy, and dairy at first to stop the stomachaches. I developed tolerance again to soy and dairy once things healed up after maybe 6-9 months.

Marz Enthusiast

Stimulants cause havoc in my stomach - nausea, stomach pain, cramps... So maybe go easy on the senna (if it is a stimulant, don't know the "Rite Aid's Senna Natural Vegetable Laxative" brand) - you really shouldn't need it now that you've possibly figured out your problem. Stimulant laxatives are bad to take long term anyway, as your intestine becomes dependant on the stimulant to "keep things moving" so to speak.

Try magnesium supplements (if you don't have kidney problems) and natural fiber like psylium husks, prunes etc. If that brand is a fiber type laxative then ignore this comment :)

Soy and dairy could also be problems, I react to soy in the same was as gluten - terrible stomach pain. You could try an elimination diet or just keep track of all foods your eating and try find a pattern.


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



Celiac.com Sponsor (A8-M):



Marilyn R Community Regular

I'm new to the forum as well and greatly appreciate the wise words of encouragement from the previous posters on this thread. You give a wonderful gift of hope!

I work with the elderly and a couple of RN's from the West Indies ... they all swear that the best laxative is about four oz. of HEATED prune juice once a day when you're having that problem. And interestingly, I learned that blueberries contain the same ingredient as Kaopectate when D is the problem. I'm trying to stick with "real" nature and real foods vs. labelled stuff and that seems to help.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - trents replied to Mark Conway's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Have I got coeliac disease

    2. - trents replied to Mark Conway's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Have I got coeliac disease

    3. - JudyLou replied to JudyLou's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Seeking advice on potential gluten challenge

    4. - knitty kitty replied to JudyLou's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Seeking advice on potential gluten challenge

    5. - Wheatwacked replied to Mark Conway's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Have I got coeliac disease

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,152
    • Most Online (within 30 mins)
      7,748

    SinnamonToasty
    Newest Member
    SinnamonToasty
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • trents
      And I agree with Wheatwacked. When a physician tells you that you can't have celiac disease because you're not losing weight, you can be certain that doctor is operating on a dated understanding of celiac disease. I assume you are in the UK by the way you spelled "coeliac". So, I'm not sure what your options are when it comes to healthcare, but I might suggest you look for another physician who is more up to date in this area and is willing to work with you to get an accurate diagnosis. If, in fact, you do not have celiac disease but you know that gluten causes you problems, you might have NCGS (Non Celiac Gluten Sensitivity). There is no test available yet for NCGS. Celiac must first be ruled out. Celiac disease is an autoimmune disorder that damages the lining of the small bowel. NCGS we is not autoimmune and we know less about it's true nature. But we do know it is considerably more common than celiac disease.
    • trents
      @Mark Conway, here is an article outlining the various tests that can be used to diagnose celiac disease. By far, the most popular one ordered by physicians is the tTG-IGA. But almost all of these tests are known by different names so the terminology will vary from place to place and lab to lab. The article gives common variant names for each test.  In addition to IGA tests there are IGG tests which are particularly useful in the case of IGA deficiency.  
    • JudyLou
      Thank you so much @knitty kitty! My feet aren’t dry or ashy and I don’t have a rash that gets scaly. It’s like very itchy/burning vesicles that are symmetrical - on both arms, both legs, etc. They actually feel better in direct sunlight as long as it isn’t really hot or I’m not exercising outside, but gets worse if I sweat (especially if the area is covered up). It’s not usually on the outside of my elbows and knees which seems more typical of dermatitis herpetiformis (unless it spreads there). It tends to first hit the inside of those areas. Interestingly, twice the rash broke out soon after eating an unhealthy meal and having an alcoholic drink (I only drink a few times a year, no more alcohol content than a glass of wine).  So I wonder if there is a connection. I’m halfway considering doing a gluten challenge for a few months to see what happens, knowing I can stop if I have any symptoms, and asking for a full celiac disease panel at the end. I really appreciate your thoughts! 
    • knitty kitty
      Welcome, @JudyLou, Your rash sounds very similar to the one I experienced.  Mine was due to a deficiency in Niacin B3, although I had deficiencies in other nutrients as well.  Celiac disease causes malabsorption of all the essential nutrients, but eating a poor diet, taking certain medications, or drinking alcohol can result in deficiency diseases outside of Celiac, too.  Symptoms can wax and wane depending on dietary intake.  I knew an alcoholic who had the "boots" of Pellagra, which would get worse when he was drinking more heavily, and improve when he was drinking less.   Niacin deficiency is called Pellagra.  Symptoms consist of dermatitis, diarrhea, dementia, and death (the four D's).  A scaly rash on the feet and hands and arms are called the "boots" and "gloves" of Pellagra.  Darkened skin around the neck exposed to the sun is Casal's necklace.  Poor farmers with niacin deficient diets were called "red necks" because of this.    Does your rash get worse if you're in the sun?  Mine did.  Any skin exposed to the sun got blistered and scaly.  Arms, legs, neck, head.  Do you have dry, ashy skin on your feet?  The itchiness was not only from the rash, but neuropathy.   My doctors were clueless.  They didn't put all my symptoms together into the three D's.  But I did.  I'd learned about Pellagra at university.  But there weren't supposed to be deficiency diseases anymore in the developed world.  Doubtful it could be that simple, I started supplementing with Niacin and other essential nutrients.  I got better.   One of Niacinamide functions is to help stop mast cells from releasing histamine.  Your allergist gave you doxepin, an antihistamine which stops mast cells from releasing histamine.   Since you do have a Celiac gene, staying on the gluten free diet can prevent Celiac disease from being triggered again.   Interesting Reading: These case studies have pictures... Pellgra revisited.  https://pmc.ncbi.nlm.nih.gov/articles/PMC4228662/ Steroid-Resistant Rash With Neuropsychiatric Deterioration and Weight Loss: A Modern-Day Case of Pellagra https://pmc.ncbi.nlm.nih.gov/articles/PMC12532421/#:~:text=Figure 2.,(right panel) upper limbs.&text=The distribution of the rash,patient's substantial response to treatment.   Cutaneous signs of nutritional disorders https://pmc.ncbi.nlm.nih.gov/articles/PMC8721081/#:~:text=Additional causes of yellow skin,the clinical features of Kwashiorkor.   Hello, @Staticgypsy, I would not recommend cutting so many nutritious foods out of ones diet.  Oxalates can cause problems like kidney stones, but our bodies can process oxalates out of our systems with certain vitamins like Vitamins A and D and Pyridoxine B 6.   People with Celiac disease are often low in fat soluble vitamins A and D, as well as the water soluble B vitamins like Pyridoxine B 6.  Focus on serving your granddaughter nutrient dense meals to ensure she gets essential vitamins and minerals that will help her grow. Micronutrient inadequacy and urinary stone disease: an analysis of the National Health and Nutrition Examination Survey 2007-2018 https://pubmed.ncbi.nlm.nih.gov/36976348/ Multivitamins co-intake can reduce the prevalence of kidney stones: a large-scale cross-sectional study https://pubmed.ncbi.nlm.nih.gov/38564076/
    • Wheatwacked
      This doctor is obviously under educated about Celiac Disease. Deficiencies that can cause oral thrush (Candidiasis) mouth ulcers: Thiamine B1 B12 Folate Zinc Vitamin C B2 B6 Iron Malabsorption Syndrome is often co-morbid with Celiac Disease causing multiple deficiencies of the essential vitamins and minerals.  Low or deficient  Vitamin D is almost always found in undiagnosed Celiac Disease. "Over 900 genes have been reported as regulated by vitamin D"  Possible Role of Vitamin D in Celiac Disease Onset  "The overall prevalence rate of vitamin D deficiency was 41.6%, with the highest rate seen in blacks (82.1%), followed by Hispanics (69.2%)."    Prevalence and correlates of vitamin D deficiency in US adults
×
×
  • 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.