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

Biopsy Normal


NateJ

Recommended Posts

NateJ Contributor

well, my biopsies from my colonoscopy and endoscopy came back 'normal'

The nurse said they removed 1 polyp that was benign. But other than that she didn't

see anything on there abnormal.

so I guess i don't have Celiac or anything else. just a make believe sore stomach and a fairyland

diareha.

I guess I just have to go through the rest of my life suffering now.


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



Celiac.com Sponsor (A8-M):



eatmeat4good Enthusiast

You could still be gluten intolerant. It doesn't show up on tests, but it still causes those symptoms. If you are gluten free...stay that way for a good while and see if your symptoms improve.

Bunch of people test negative but do way better gluten free.

Nothing to lose Nate....hang in there and stick with it.

ravenwoodglass Mentor

You should get copies of the reports even though she said they were 'normal'.

Now is when you try the diet strictly for at least a couple of months as false negatives are pretty common. Your damage could be patchy and in an area that was missed when they did the scope. There could also be changes that some doctors don't recognize as celiac related present.

lynnelise Apprentice

I agree with the above advice. Go on the diet 100% and see how you feel. IMO false negatives are so common that this is the only true test! If after a month or so you see no improvement then try an elimination diet. Something is causing your symptoms and frankly doctors are of little use. It's sometimes better to take things into your own hands! Good luck! Keep us posted on how you are feeling on the diet!

NateJ Contributor

Well so far I've been on the diet since Mar 6. and have seen little if any improvement.

I have been super strict about it too. I've only eaten out once and warned the waitress, she was very

cordial about it too.

I'm so frustrated and annoyed. The Dr. put me back on Questran as its the only thing that keeps m 'D' in check enough

for me to work. The Nuerontin has little if any effect that i can tell of.

I just walk around all day feeling like someone punched me in the gut over and over.

I'm going to stick to gluten free for now. at least until i see him on the 8th and probably beyond. I was

going to see a Nutrionist but I cant' really afford it. My next step would be an elimination diet.

Its hard to stay focused and not get depressed when you feel like utter crud all the time.

If it wasn't for my family i would probably give up.

thanks for the help and support. this place is a life saver.

Jestgar Rising Star

My next step would be an elimination diet.

Do try eliminating the big offenders: soy, milk, eggs, maybe corn. Also start writing down everything you eat to see if you can relate symptoms to food.

ravenwoodglass Mentor

Well so far I've been on the diet since Mar 6. and have seen little if any improvement.

I have been super strict about it too. I've only eaten out once and warned the waitress, she was very

cordial about it too.

I'm so frustrated and annoyed. The Dr. put me back on Questran as its the only thing that keeps m 'D' in check enough

for me to work. The Nuerontin has little if any effect that i can tell of.

I just walk around all day feeling like someone punched me in the gut over and over.

I'm going to stick to gluten free for now. at least until i see him on the 8th and probably beyond. I was

going to see a Nutrionist but I cant' really afford it. My next step would be an elimination diet.

Its hard to stay focused and not get depressed when you feel like utter crud all the time.

If it wasn't for my family i would probably give up.

thanks for the help and support. this place is a life saver.

Are you eating mostly whole unprocessed foods? Are you living with other gluten eaters and if you are have you taken the precautions we need to take to avoid cross contamination? You need your own toaster for gluten free breads, a new strainer for gluten free pastas and your own condiments, butter, nut butters etc. You should also avoid dairy for right now as until we heal most of us have a very hard time digesting it. If your significant other uses lipstick or chapstick type products do make sure they are gluten free. Also do check with the makers of any meds or supplements you take to make sure they are gluten free and be sure to avoid supplements that have wheat or barley grass. Things can be up and down for us especially at first. You had a previous post where you stated you had been better for the first 3 days of the diet but then went back on gluten so you could be tested. At least I think you said you went back on it. That is a good indication that the diet will help you but we do often find that we are more sensitive to very small amounts after we go gluten free so do take all the precautions that you can.

I hope your feeling better soon.


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



Celiac.com Sponsor (A8-M):



NateJ Contributor

Are you eating mostly whole unprocessed foods? Are you living with other gluten eaters and if you are have you taken the precautions we need to take to avoid cross contamination? You need your own toaster for gluten free breads, a new strainer for gluten free pastas and your own condiments, butter, nut butters etc. You should also avoid dairy for right now as until we heal most of us have a very hard time digesting it. If your significant other uses lipstick or chapstick type products do make sure they are gluten free. Also do check with the makers of any meds or supplements you take to make sure they are gluten free and be sure to avoid supplements that have wheat or barley grass. Things can be up and down for us especially at first. You had a previous post where you stated you had been better for the first 3 days of the diet but then went back on gluten so you could be tested. At least I think you said you went back on it. That is a good indication that the diet will help you but we do often find that we are more sensitive to very small amounts after we go gluten free so do take all the precautions that you can.

I hope your feeling better soon.

I've eliminated milk, corn, eggs, and gluten so far. no major changes to my symptoms yet.

I am eating whole foods and keeping a journal. I haven't been able to figure out anyone one thing that sets me off as I haven't had a 'good day' yet. Coffee for sure is a major problem for me. at least the work coffee is, so i quit that all together. I haven't checked on my meds yet. do the capsule ones have gluten?

I never did go back on the gluten, i was off for 14 days when i had my biopsy done. so maybe it was a false negative, not sure. I wish i could have spoken with the Dr. but he hasn't reviewed my results yet.

I definitely have some work still to do. The pots and pans might be a problem. and the condiments thing. I guess washing them in the dishwasher doesn't help get rid of it? i would think that hot water and such would blast the stuff?

thanks for the tips. I have much work to do

eatmeat4good Enthusiast

Many people use a dishwasher so that shouldn't be a problem, but with pots and pans used for cooking gluten you have to clean before they go into the dishwasher. (In my opinion) The medication yes, if one of your capsules has gluten in it and you take it every day, Wa La, sick every day. Also if your family isn't gluten free and you kiss them before they brush their teeth you can get sick. I didn't believe that one, but you watch...it is true. I tested it. ;) Little hands that ate cookies can get gluten on you and in you. I handed a cookie to my sister's kid and then happily munched on nuts thinking gluten free ain't so bad. Next day sick. If you touch gluten you have to wash your hands. Sanitizer isn't doing anything to gluten. Let's see, I think that is all the ways I have glutened myself aside from eating in restaurants supposedly gluten free. If you can get your whole family to go gluten free, you will stay a lot healthier. But at least have your own station where no gluten is allowed.

I got sick for two days after I de-glutened the kitchen and got rid of flour and products. If your wife bakes or I should say if anyone bakes, flour can hang in the air a long time and you can easily breathe it in and down your throat...and make you sick the next day. Also if you have pets, they can get you with their gluteny food. wash after feeding and don't let them lick you or feed them gluten free too.

It is overwhelming at first, but you will feel so much better if it really was any of these things people have listed and you finally figure it out.

Hang in there.

NateJ Contributor

Many people use a dishwasher so that shouldn't be a problem, but with pots and pans used for cooking gluten you have to clean before they go into the dishwasher. (In my opinion) The medication yes, if one of your capsules has gluten in it and you take it every day, Wa La, sick every day. Also if your family isn't gluten free and you kiss them before they brush their teeth you can get sick. I didn't believe that one, but you watch...it is true. I tested it. ;) Little hands that ate cookies can get gluten on you and in you. I handed a cookie to my sister's kid and then happily munched on nuts thinking gluten free ain't so bad. Next day sick. If you touch gluten you have to wash your hands. Sanitizer isn't doing anything to gluten. Let's see, I think that is all the ways I have glutened myself aside from eating in restaurants supposedly gluten free. If you can get your whole family to go gluten free, you will stay a lot healthier. But at least have your own station where no gluten is allowed.

I got sick for two days after I de-glutened the kitchen and got rid of flour and products. If your wife bakes or I should say if anyone bakes, flour can hang in the air a long time and you can easily breathe it in and down your throat...and make you sick the next day. Also if you have pets, they can get you with their gluteny food. wash after feeding and don't let them lick you or feed them gluten free too.

It is overwhelming at first, but you will feel so much better if it really was any of these things people have listed and you finally figure it out.

Hang in there.

well the kitchen is pretty much gluten free now. We went through it last night. Since I do most of the cooking anyway I dont' have to worry about anyone else contaminating it. The only stuff is prepackaged snacks and bread for my kids lunches that they pack themselves.

I am worried about the pills though. I called my pharmacy and they actually hung up on me!

I need two refills soon so I guess I'll have to go up there and ask them in person.

As far as the kissing my kids, etc... I'm willing to risk it. But its nice to know. Something I didn't think about really before.

Now if I can just get better for a day or two.....:(

frieze Community Regular

well the kitchen is pretty much gluten free now. We went through it last night. Since I do most of the cooking anyway I dont' have to worry about anyone else contaminating it. The only stuff is prepackaged snacks and bread for my kids lunches that they pack themselves.

I am worried about the pills though. I called my pharmacy and they actually hung up on me!

I need two refills soon so I guess I'll have to go up there and ask them in person.

As far as the kissing my kids, etc... I'm willing to risk it. But its nice to know. Something I didn't think about really before.

Now if I can just get better for a day or two.....:(

Gabapentin (Apotex, Greenstone)

these two generics and brand name neurontin are supposed to be gluten free, if your neurontin is not brand or made by either of those two other companies, all bets are off. good luck

NateJ Contributor

Gabapentin (Apotex, Greenstone)

these two generics and brand name neurontin are supposed to be gluten free, if your neurontin is not brand or made by either of those two other companies, all bets are off. good luck

Thats exactly what I'm taking. Gabapentin 100 MG cap Greenstone LTD

Where did you find that info?

I'm also taking Questran (Generic Cholestrymine sp?) and a Prevacid generic.

THANKS!

rosetapper23 Explorer

For medications, you can check www.glutenfreedrugs.com , but I ALWAYS call the laboratory directly that manufactures the pills. Sometimes the pharmacist is willing to make the call, but since I usually pick up prescriptions after work and the labs have closed already, I can get stuck with not knowing if something has gluten in it. Still, I place a call or send an e-mail to the company...sometimes someone will answer me late at night or over the weekend. With all the generics out there, you have to read your pill bottle EVERY time you pick up your usual prescription because they can switch companies on you. Be especially suspicious of red-coated pills (e.g., Claritin Red Tabs).

Also, are you using iodized salt? Many of us are sensitive to or outright allergic to iodine, so if yours is iodized, toss it and buy some non-iodized salt. Just a thought.

NateJ Contributor

For medications, you can check www.glutenfreedrugs.com , but I ALWAYS call the laboratory directly that manufactures the pills. Sometimes the pharmacist is willing to make the call, but since I usually pick up prescriptions after work and the labs have closed already, I can get stuck with not knowing if something has gluten in it. Still, I place a call or send an e-mail to the company...sometimes someone will answer me late at night or over the weekend. With all the generics out there, you have to read your pill bottle EVERY time you pick up your usual prescription because they can switch companies on you. Be especially suspicious of red-coated pills (e.g., Claritin Red Tabs).

Also, are you using iodized salt? Many of us are sensitive to or outright allergic to iodine, so if yours is iodized, toss it and buy some non-iodized salt. Just a thought.

I do used iodized salt, but no more than 2-3 times a week. Its not an everyday thing for me and depends on what I'm cooking. Usually I just put a dash in water if I'm boiling it for rice or something.

I will switch that too.

I checked out your list and all three of the brand names are on there that I take, but the generics are not. I guess I'll have to check with my pharmacy.

ravenwoodglass Mentor

I do used iodized salt, but no more than 2-3 times a week. Its not an everyday thing for me and depends on what I'm cooking. Usually I just put a dash in water if I'm boiling it for rice or something.

I will switch that too.

I checked out your list and all three of the brand names are on there that I take, but the generics are not. I guess I'll have to check with my pharmacy.

If you don't have the skin lesions then iodized salt is not going to be an issue for you. Iodine is only an issue for those with DH.

The label on your script bottle or the monograph that the pharmacy gives you should have the maker on it. It is best to call the maker if you can. If you put thier name and the words contact info in a search engine you can usually get the phone number. Generics can change binders at will so unless the company states that all their items are gluten-free it is best to check at each refill. I always tell the companies I have an allergy to wheat rather than celiac because some will consider wheat starch to be safe.

NateJ Contributor

If you don't have the skin lesions then iodized salt is not going to be an issue for you. Iodine is only an issue for those with DH.

The label on your script bottle or the monograph that the pharmacy gives you should have the maker on it. It is best to call the maker if you can. If you put thier name and the words contact info in a search engine you can usually get the phone number. Generics can change binders at will so unless the company states that all their items are gluten-free it is best to check at each refill. I always tell the companies I have an allergy to wheat rather than celiac because some will consider wheat starch to be safe.

No, i don't have any lesions. I think i would freak out if I did.

I have always had those bumps on the back of my upper arms. I read somewhere that is a symptom of Celiac. Can't remember where or what they call them.

I'm going to check my pills when I get home. I left two of them on there, but someone here confirmed my main one is gluten free for me yesterday. I'm more worried about the Questran powder and the prevacid cause those I can't find much info on.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,836
    • Most Online (within 30 mins)
      7,748

    RyanOB
    Newest Member
    RyanOB
    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

    • 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.  
    • Scott Adams
      Your concerns about Nando's cross-contamination practices are valid and important for the celiac community. It's disappointing that Nando's does not have stricter protocols for children's portions, especially given the risk of cross-contact with gluten-containing items like garlic bread. Cooking gluten-free items on shared surfaces, even if cleaned, is not safe for individuals with celiac disease, as even trace amounts of gluten can cause harm. While the adult butterfly chicken may be a safer option, the inconsistency in practices for children's meals is concerning. It's frustrating that Nando's headquarters did not take responsibility, but sharing your experience raises awareness and may encourage them to improve their protocols. Consider reaching out to celiac advocacy organizations to amplify your concerns and push for better standards. Always double-check with staff and emphasize the importance of avoiding cross-contamination when dining out.
×
×
  • Create New...