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

Starting the Gluten Challenge - Help


Ginger38

Recommended Posts

Ginger38 Rising Star

Not sure if this is the right forum to post this in but here I go:

I am starting the gluten challenge for an upcoming EGD and colonoscopy with biopsies. I have not done a gluten challenge before, as I fell through the cracks and was told to go off gluten before seeing an GI doc.
I am not excited about it. Gluten makes me very sick with all sorts of symptoms. I’m actually quite terrified of what this will do to me. I am also diabetic so I am concerned about that as well during this long process. I also have a few specific questions .. 

1. What is the minimum amount of time and minimum amount of gluten I need to consume to get a reliable biopsy? He said he will take about 5 biopsies while in there. He is also looking for Crohn’s disease 

2. Any tips for trying to function and work and be a mom and just survive during this process? I have terrible GI symptoms , increased reflux, not able to digest foods like salads and veggies, nausea, sour stomach, horrible bloating, diarrhea, gas, terrible exhaustion and brain fog, tachycardia, palpitations, rashes among others.

3. I also didn’t know if I should stick to a more bland diet and easier to digest foods since I’m intentionally harming my gut.

4.  Should I be taking or not taking anything during this time? Antacids, Imodium, gas ex, nausea meds, pain relief, probiotics, l-glutamine, all my vitamins? 

5. Should I go for the minimum amount of gluten or is it better to just pig out? 

Thanks in advance! Im really nervous about it all 


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



Celiac.com Sponsor (A8-M):



Ginger38 Rising Star

Is 5 weeks of eating gluten enough to get a reliable biopsy? 

Scott Adams Grand Master

Here is more info about how to do a gluten challenge for a celiac disease blood panel, or for an endoscopy:

Quote

"...in order to properly diagnose celiac disease based on serology and duodenal histology, doctors need patients to be on gluten-containing diets, even if they are causing symptoms, and this is called a "gluten challenge."

  • Eat gluten prior to celiac disease blood tests: The amount and length of time can vary, but is somewhere between 2 slices of wheat bread daily for 6-8 weeks and 1/2 slice of wheat bread or 1 wheat cracker for 12 weeks 12 weeks;
  • Eat gluten prior to the endoscopic biopsy procedure: 2 slices of wheat bread daily for at least 2 weeks;

and this recent study recommends 4-6 slices of wheat bread per day:

 

 

Ginger38 Rising Star
5 hours ago, Scott Adams said:

Here is more info about how to do a gluten challenge for a celiac disease blood panel, or for an endoscopy:

and this recent study recommends 4-6 slices of wheat bread per day:

 

 

Thank you for this information! 

knitty kitty Grand Master
(edited)

Hey, @Ginger38,

How are you doing?  

A Gluten Challenge recommends  at least 10 grams of gluten per day for a minimum of two weeks, but more is better.   Remember different foods can contain different amount of gluten.  Cookies and cakes have less gluten than chewy breads like thick pizza dough and artisan breads.  

Avoid salads and raw veggies as they are hard to digest.  Spicy and greasy foods should be avoided, too.  

Yes, well-cooked soft foods are easier to digest.  Crock pot meals or casseroles (chicken, or beef roast, veggies) are time savers when you're too ill to stand over a stove.  Cook the night before or overnight, and reheat if you're not home to monitor cooking.  

Small, frequent meals will help relieve the nausea and reflux.  Taking a magnesium supplement after meals can reduce reflux.  Eating a protein with the gluten may help some gastrointestinal symptoms.  

In half of Celiac people, the Casein in Dairy can cause an autoimmune reaction just like gluten does.  Some have found cutting out or adding dairy (depending on desired results) during a challenge helpful.  

Keep taking the B vitamins and stay hydrated.  The B vitamins are water soluble and are easily lost when we have diarrhea.  Stay well hydrated. 

Horrible bloating, diarrhea, gas, terrible exhaustion, brain fog, tachycardia, and palpitations can be symptoms of Celiac Disease, and also Thiamine deficiency.  Thiamine is needed to turn carbs into usable energy.  An increase in carbohydrates means a bigger demand for Thiamin (Benfotiamine).  

Most diabetics are deficient in Thiamine.  I have diabetes also.  Our kidneys don't absorb thiamine in the kidneys, so we lose a lot of Thiamine in urine. 

Metformin will block the Thiamine/Folate receptors on cells, preventing Thiamine and Folate from entering the cells, which can precipitate a Thiamine deficiency disorder.   

I was not a diagnosed Celiac when I was prescribed Metformin which contributed to my developing Thiamine deficiency.  Metformin is also a Sulfa drug.  It is not uncommon for people with Celiac Disease to develop Sulfite Sensitivity, a Type Four Hypersensitivity reaction, which can manifest as gastrointestinal symptoms and rashes.  Since switching to the AIP diet, I have been able to control my blood glucose levels with diet and Benfotiamine, and have discontinued antidiabetic pharmaceuticals.

For pain relief, a combination of Thiamine, Pyridoxine B6 and Cobalamine B12 have analgesic effects.  

I hope you get through okay.  We're all cheering you on! 

Eat a croissant for me!  

Edited by knitty kitty
Typo correction
Ginger38 Rising Star
On 8/23/2024 at 7:46 AM, knitty kitty said:

Hey, @Ginger38,

How are you doing?  

A Gluten Challenge recommends  at least 10 grams of gluten per day for a minimum of two weeks, but more is better.   Remember different foods can contain different amount of gluten.  Cookies and cakes have less gluten than chewy breads like thick pizza dough and artisan breads.  

Avoid salads and raw veggies as they are hard to digest.  Spicy and greasy foods should be avoided, too.  

Yes, well-cooked soft foods are easier to digest.  Crock pot meals or casseroles (chicken, or beef roast, veggies) are time savers when you're too ill to stand over a stove.  Cook the night before or overnight, and reheat if you're not home to monitor cooking.  

Small, frequent meals will help relieve the nausea and reflux.  Taking a magnesium supplement after meals can reduce reflux.  Eating a protein with the gluten may help some gastrointestinal symptoms.  

In half of Celiac people, the Casein in Dairy can cause an autoimmune reaction just like gluten does.  Some have found cutting out or adding dairy (depending on desired results) during a challenge helpful.  

Keep taking the B vitamins and stay hydrated.  The B vitamins are water soluble and are easily lost when we have diarrhea.  Stay well hydrated. 

Horrible bloating, diarrhea, gas, terrible exhaustion, brain fog, tachycardia, and palpitations can be symptoms of Celiac Disease, and also Thiamine deficiency.  Thiamine is needed to turn carbs into usable energy.  An increase in carbohydrates means a bigger demand for Thiamin (Benfotiamine).  

Most diabetics are deficient in Thiamine.  I have diabetes also.  Our kidneys don't absorb thiamine in the kidneys, so we lose a lot of Thiamine in urine. 

Metformin will block the Thiamine/Folate receptors on cells, preventing Thiamine and Folate from entering the cells, which can precipitate a Thiamine deficiency disorder.   

I was not a diagnosed Celiac when I was prescribed Metformin which contributed to my developing Thiamine deficiency.  Metformin is also a Sulfa drug.  It is not uncommon for people with Celiac Disease to develop Sulfite Sensitivity, a Type Four Hypersensitivity reaction, which can manifest as gastrointestinal symptoms and rashes.  Since switching to the AIP diet, I have been able to control my blood glucose levels with diet and Benfotiamine, and have discontinued antidiabetic pharmaceuticals.

For pain relief, a combination of Thiamine, Pyridoxine B6 and Cobalamine B12 have analgesic effects.  

I hope you get through okay.  We're all cheering you on! 

Eat a croissant for me!  

Thank you so very much for all this helpful information!! I really appreciate it!! I am hanging in there as best I can. I have almost been constipated at times since starting the gluten challenge. Is that normal? 
I’m super fatigued and exhausted with brain fog and concentration issues. I’ve been itching. My allergies are all flared up. I feel like I’ve gained 10 pounds. Reflux has definitely increased. And I just feel sore and places are tender to touch, all over, especially my abdomen. I’m hungry like all the time. 
One of the biggest issues for me since starting the gluten challenge has been my blood sugars!! They have been so high and won’t come down much. Any idea why that is?? 
Thanks again for all your help!!! 

knitty kitty Grand Master

@Ginger38,

Magnesium citrate or Magnesium Glycinate chelates can help with the constipation. 

Benfotiamine will help with Gastroparesis, edema, reflux, brain fog and fatigue.  Benfotiamine won't lower your blood glucose, but it will help your body use insulin.

I take Bilberry supplements from Nature's Way to lower blood glucose levels.  I take one or two.  If you take Bilberry close to when you take Metformin, your blood glucose level can drop very low.  Be Careful!!!   

Be sure to stay well hydrated.  I found warm tea (no sugar) after meals helps with keeping things moving through.  Oolong tea is very relaxing for the anxiety.  Some people people say it has a laxative effect.   

Benfotiamine, B12 and Pyridoxine B6  when taken together results pain relief comparable to aspirin and NSAIDs.  (NSAIDs and aspirin will tear up your digestive system).

An antihistamine can help with the allergies. 

A hot water bottle works wonders on abdominal pain, too.

Sending encouragement.  Put your feet up and relax.  You'll be through this soon.  I'll be here if you need anything.


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



Celiac.com Sponsor (A8-M):



Ginger38 Rising Star
On 8/24/2024 at 1:23 PM, knitty kitty said:

@Ginger38,

Magnesium citrate or Magnesium Glycinate chelates can help with the constipation. 

Benfotiamine will help with Gastroparesis, edema, reflux, brain fog and fatigue.  Benfotiamine won't lower your blood glucose, but it will help your body use insulin.

I take Bilberry supplements from Nature's Way to lower blood glucose levels.  I take one or two.  If you take Bilberry close to when you take Metformin, your blood glucose level can drop very low.  Be Careful!!!   

Be sure to stay well hydrated.  I found warm tea (no sugar) after meals helps with keeping things moving through.  Oolong tea is very relaxing for the anxiety.  Some people people say it has a laxative effect.   

Benfotiamine, B12 and Pyridoxine B6  when taken together results pain relief comparable to aspirin and NSAIDs.  (NSAIDs and aspirin will tear up your digestive system).

An antihistamine can help with the allergies. 

A hot water bottle works wonders on abdominal pain, too.

Sending encouragement.  Put your feet up and relax.  You'll be through this soon.  I'll be here if you need anything.

Thank you!! What helps with this horribly painful  bloating??? Should I do a stool softener or gentle laxative for the partial constipation issue? And how much benfotiamine?? 

knitty kitty Grand Master

Magnesium supplements can help with the constipation.  Magnesium softens the stool.  Magnesium is often one of the minerals that can be deficient in people with Celiac Disease.

Start with 100 mg of Benfotiamine with meals.  I take a 250 mg Benfotiamine with two meals.  

Everyone is different and has different nutritional needs.  Find what works for you.

https://ods.od.nih.gov/factsheets/Magnesium-Consumer/

And...

https://ods.od.nih.gov/factsheets/Thiamin-Consumer/

Ginger38 Rising Star
7 hours ago, knitty kitty said:

Magnesium supplements can help with the constipation.  Magnesium softens the stool.  Magnesium is often one of the minerals that can be deficient in people with Celiac Disease.

Start with 100 mg of Benfotiamine with meals.  I take a 250 mg Benfotiamine with two meals.  

Everyone is different and has different nutritional needs.  Find what works for you.

https://ods.od.nih.gov/factsheets/Magnesium-Consumer/

And...

https://ods.od.nih.gov/factsheets/Thiamin-Consumer/

Thanks! The benfotiamine I have is 200 mg per soft gel??

Is there nothing much to help with the bloating? 

knitty kitty Grand Master

Your 200 mg Benfotiamine sounds fine. 

The best thing I found for the bloating is to follow the Autoimmune Protocol Diet (AIP diet).  The AIP diet has you remove carbohydrates from the diet.  If you remove carbohydrates, the intestinal bacteria that feed on carbohydrates and produce gas as an end product will be starved out.  More beneficial bacteria will replace them.  

The AIP diet removes all grains, veggies like corn and potatoes, and also beans (legumes) and pulses (lentils), ancient/alternative grains, and grasses (rice).  Also all processed foods are removed.  No processed meat like sausages.  The bloating symptoms improve quickly after a little while on the AIP diet.

The AIP diet reduces inflammation and gives the body a chance to heal.  Dairy and eggs are also removed as they can be inflammatory.  Nightshades (potatoes, peppers, tomatoes and eggplant) are removed because they promote zonulin production and increase intestinal permeability (leaky gut syndrome).

Just meat, veggies and some fruit.  Smaller meals closer together helps with hunger, as does including Omega Three healthy fats (olive oil, flaxseed oil, avocado oil, coconut oil).  

After the bloating and other symptoms abate, you can slowly add in more foods.  But be careful, if you go back to a high carbohydrate diet, the bloat causing bacteria may repopulate the gut and symptoms may return. 

Learning how to feed your tummy in a new way can take a great deal of mental adjustment, but it's very worthwhile.  You'll see the benefits quickly and you have lots of support here.

Scott Adams Grand Master

We've done an article on the AIP dies here:

 

Ginger38 Rising Star
On 8/29/2024 at 6:05 AM, knitty kitty said:

Your 200 mg Benfotiamine sounds fine. 

The best thing I found for the bloating is to follow the Autoimmune Protocol Diet (AIP diet).  The AIP diet has you remove carbohydrates from the diet.  If you remove carbohydrates, the intestinal bacteria that feed on carbohydrates and produce gas as an end product will be starved out.  More beneficial bacteria will replace them.  

The AIP diet removes all grains, veggies like corn and potatoes, and also beans (legumes) and pulses (lentils), ancient/alternative grains, and grasses (rice).  Also all processed foods are removed.  No processed meat like sausages.  The bloating symptoms improve quickly after a little while on the AIP diet.

The AIP diet reduces inflammation and gives the body a chance to heal.  Dairy and eggs are also removed as they can be inflammatory.  Nightshades (potatoes, peppers, tomatoes and eggplant) are removed because they promote zonulin production and increase intestinal permeability (leaky gut syndrome).

Just meat, veggies and some fruit.  Smaller meals closer together helps with hunger, as does including Omega Three healthy fats (olive oil, flaxseed oil, avocado oil, coconut oil).  

After the bloating and other symptoms abate, you can slowly add in more foods.  But be careful, if you go back to a high carbohydrate diet, the bloat causing bacteria may repopulate the gut and symptoms may return. 

Learning how to feed your tummy in a new way can take a great deal of mental adjustment, but it's very worthwhile.  You'll see the benefits quickly and you have lots of support here.

My current issues are this horrible feeling of being overly stuffed all the time which is causing reflux so bad I have vomit in the back of my throat. Like when I eat it just feels like here is no where for my food to go. Im miserable and can’t get relief.

Im also having issues with bathroom habits. One day I will be somewhat constipated, like I just don’t feel like I’m emptying my bowels completely but then the next day I am having horrible episodes of diarrhea multiple times a day. So idk what to do. I have many more weeks of this to go 😩😩

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now
  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,954
    • Most Online (within 30 mins)
      7,748

    Mabelie
    Newest Member
    Mabelie
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.