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

What Should I Do?


katinagj

Recommended Posts

katinagj Apprentice

After a year of trying to get diagnosed with SOMETHING I've finally figured out that I actually do have some sort of intolerance to wheat. Other gluten foods, I'm not sure yet. Here's the story: starting in 8th grade I started having stomach issues, we(me and my parents) always thought it was dairy causing the problem, so I sort of avoided it in high school, and later figured out that dairy doesn't always affect me. A year ago after having severe bone aches, stomach issues getting worse, and very irregular always strange looking BMs(as well as being very fatigued and sore) I asked my doctor to test for celiac, even though as far as we know no one in my family has it, but we don't know a ton about family medical history so who knows. She said she wanted to do some other testing first before getting to the serious stuff. All blood tests came back normal except for a vit d deficiency which I am still taking supplements for because without supplements it wont stay at a normal level. I have gone to the doctor about 8 times since then, and still no celiac testing(though I sort of forgot about it being a possibility until now). Last week I went on an elimination diet to figure out allergies, which included going gluten free and dairy free. I cheated by eating a peice of toast, because I was starving and haven't quite got the hang of this diet yet. This was at about 8 pm, by the time I went to bed at 11 I had a severe headache, then woke up at 2:30 AM with such severe abdominal pain that I thought my husband was going to have to take me to the hospital. It got to the point of nausea, and I had to run to the bathroom twice to puke up toast(and it did still look like a big hunk of toast(sorry for the visual). The nausea and stomach ache stuck around for another hour while I sat on the couch sipping peppermint tea hoping I could go back to bed soon. Now I've just read that going gluten free before getting tested can affect diagnosis! I wish I had known this before...what should I do? I'm afraid to eat anything that could have gluten in it, since I am unsure if I got sick over gluten or if it was just the wheat...

ANY advice is helpful

ETA: I forgot to mention that after going onto this elimination diet I almost immediately felt better. My body aches stopped as well as stomach aches and strange bowels until I cheated on that piece of toast.

I also forgot to mention that we are trying to concieve and I had two early miscarriages in a row in september and october, that were completely unexplained. While I know that one early miscarriage is farely common, having two just worries me, and I don't want it to happen again, for obvious reasons. We have now hit our one year mark since we first started trying.


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



Celiac.com Sponsor (A8-M):



mushroom Proficient

After a year of trying to get diagnosed with SOMETHING I've finally figured out that I actually do have some sort of intolerance to wheat. Other gluten foods, I'm not sure yet. Here's the story: starting in 8th grade I started having stomach issues, we(me and my parents) always thought it was dairy causing the problem, so I sort of avoided it in high school, and later figured out that dairy doesn't always affect me. A year ago after having severe bone aches, stomach issues getting worse, and very irregular always strange looking BMs(as well as being very fatigued and sore) I asked my doctor to test for celiac, even though as far as we know no one in my family has it, but we don't know a ton about family medical history so who knows. She said she wanted to do some other testing first before getting to the serious stuff. All blood tests came back normal except for a vit d deficiency which I am still taking supplements for because without supplements it wont stay at a normal level. I have gone to the doctor about 8 times since then, and still no celiac testing(though I sort of forgot about it being a possibility until now). Last week I went on an elimination diet to figure out allergies, which included going gluten free and dairy free. I cheated by eating a peice of toast, because I was starving and haven't quite got the hang of this diet yet. This was at about 8 pm, by the time I went to bed at 11 I had a severe headache, then woke up at 2:30 AM with such severe abdominal pain that I thought my husband was going to have to take me to the hospital. It got to the point of nausea, and I had to run to the bathroom twice to puke up toast(and it did still look like a big hunk of toast(sorry for the visual). The nausea and stomach ache stuck around for another hour while I sat on the couch sipping peppermint tea hoping I could go back to bed soon. Now I've just read that going gluten free before getting tested can affect diagnosis! I wish I had known this before...what should I do? I'm afraid to eat anything that could have gluten in it, since I am unsure if I got sick over gluten or if it was just the wheat...

ANY advice is helpful

ETA: I forgot to mention that after going onto this elimination diet I almost immediately felt better. My body aches stopped as well as stomach aches and strange bowels until I cheated on that piece of toast.

Hi, Katinagj, and welcome to the forum.

It sounds to me like you are a pretty good diagnostician yourself. As far back as a year ago you had your suspicions, and your doctor should have listened to you, particularly when you tested with a Vitamin D deficiency--a very large percentage of us have this symptom because our small intestines are damaged and we are not properly absorbing the nutrients in our food. By now, you probably have other deficiencies as well, and she should have known it could be associated with celiac with your other presenting symptoms.

If you have problems eating wheat, it is most likely (although not exclusively) a problem with gluten. And as you are aware you do need to be eating gluten for a proper test result. If you have been gluten free for only a week it is probably still not too late to get tested accurately. Two weeks would be too long. Can you call your doctor or her nurse or PA right away, tell her what has happened and ask her to order the testing (again!) right now, because you don't want to have to go back on gluten in order to be tested. By the way, it is common after a period free from gluten to have a more violent reaction to it when it is resumed. It's like your body has said, Ah, thank goodness we got rid of that stuff, and then when faced with it again, Oh No, Not Again! Two words of warning about testing:

1. If the bloodwork is positive she will probably want to order an upper GI endoscopy with biopsy (and you still have to eating gluten for that), and

2. It is possible that the test will come back negative--either a false negative, which seems to happen about 20% of the time, or because you are a non-celiac gluten intolerant, a condition some doctors are not even aware of, but which is just as bad for you as being celiac, and requires the same treatment--a gluten free diet.

Now, you do not have to do the endoscopy if you choose not to because it would probably take a while to schedule it depending on where you are and you would have to resume eating considerable amounts of gluten, or you could do the endoscopy without the gluten just to rule out any other condition. But I would think the way you have responded to the diet will have probably convinced you that you should not eat gluten again, whichever way the ball bounces.

That's my take on your situation. Good luck with making your choices.

katinagj Apprentice

Hi, Katinagj, and welcome to the forum.

It sounds to me like you are a pretty good diagnostician yourself. As far back as a year ago you had your suspicions, and your doctor should have listened to you, particularly when you tested with a Vitamin D deficiency--a very large percentage of us have this symptom because our small intestines are damaged and we are not properly absorbing the nutrients in our food. By now, you probably have other deficiencies as well, and she should have known it could be associated with celiac with your other presenting symptoms.

If you have problems eating wheat, it is most likely (although not exclusively) a problem with gluten. And as you are aware you do need to be eating gluten for a proper test result. If you have been gluten free for only a week it is probably still not too late to get tested accurately. Two weeks would be too long. Can you call your doctor or her nurse or PA right away, tell her what has happened and ask her to order the testing (again!) right now, because you don't want to have to go back on gluten in order to be tested. By the way, it is common after a period free from gluten to have a more violent reaction to it when it is resumed. It's like your body has said, Ah, thank goodness we got rid of that stuff, and then when faced with it again, Oh No, Not Again! Two words of warning about testing:

1. If the bloodwork is positive she will probably want to order an upper GI endoscopy with biopsy (and you still have to eating gluten for that), and

2. It is possible that the test will come back negative--either a false negative, which seems to happen about 20% of the time, or because you are a non-celiac gluten intolerant, a condition some doctors are not even aware of, but which is just as bad for you as being celiac, and requires the same treatment--a gluten free diet.

Now, you do not have to do the endoscopy if you choose not to because it would probably take a while to schedule it depending on where you are and you would have to resume eating considerable amounts of gluten, or you could do the endoscopy without the gluten just to rule out any other condition. But I would think the way you have responded to the diet will have probably convinced you that you should not eat gluten again, whichever way the ball bounces.

That's my take on your situation. Good luck with making your choices.

Thank you so much for the information! I read it and called my doctors office immediately, I am now waiting for a call back from my doctor. I was lucky I didn't end up on hold for 20 minutes. Luckily the last time I was in I went in through the walk in clinic and went to a different doctor than my original primary and the respresentative on the phone sent the order to him to okay. He seemed to listen a lot better than the other doctors I've gone to so I am hopeful that he will actually okay it.

For some odd reason I was so nervous on the phone I could barely explain myself. How embarrassing. lol. My nerves like to act up when I least expect it. :/

katinagj Apprentice

Alright, so got my call back, and they set an appointment for me with my dr tomorrow. Luckily I am getting to see the same doctor I was seeing during my miscarriages, and I actually liked her and felt that she listened to me better. Now I need help figuring out what I should bring with me to convince her that I do in fact need to be tested, because they want me to talk over my symptoms with the doctor first. I am soo nervous now, I'm afraid they will decide not to test, since I've had drs deny me certain tests I asked for so many times in the past. And all I want is an answer...

So besides a list of my symptoms. Is there anything else I should bring with me?

GFinDC Veteran

You could also bring your family medical history on both sides, aunts, uncles etc... Celiac is an autoimmune disease, and they tend to run in families. So a history of autoimmune diseases in the family might persuade the doctor. If you google "celiac related condition" or "celiac associated condition", you will find lists of other autoimmune diseases that people with celiac sometimes have/get.

mushroom Proficient

You could also take along a list of some of the common symptoms of celiac disease (many doctors are not that familiar with them), like the list found here: https://www.celiac.com/articles/1106/1/Celiac-Disease-Symptoms/Page1.html

You might even have of these additional symptoms without being aware of it. I would help to highlight the symptoms you do have--make it easy for her.

Good luck!

katinagj Apprentice

Thank you so much for the help! I had an appointment with a dr that I have been trying to switch to my primary for quite some time. She was finally taking new patients. I brought in my list of symptoms and printed out and highlighted the symptoms I had from those pages including highlighting some of the responses that went along with my symptoms. She listened to me, and we talked over the symptoms, and she thought I had good reason to think I might have celiac disease. She also stated the possibility of lactose intolerance or IBD, but I got my blood taken just for the celiac test. When the blood results come in she is going to send me to a specialist(even if the test is negative). I am so happy that something is finally getting done, and that I may have an answer soon. Whether or not I will go back on gluten to do the endoscopy so that I could have a real diagnosis, I'm not sure. I'd like to have a diagnosis for when we have kids in case they had it, so it would be easier to get the dr to test them, but at the same time. I don't think I could handle eating wheat ever again after my severe reaction over the weekend....I guess we will see how things go! Oh my dr also thinks I have ADD, which I have also suspected for years, lol. But not worried about that one since I refuse to go on any of that medication.

Anyways, thanks again for the help, it is really appreciated!


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.

  • 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. - JoJo0611 replied to JoJo0611's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      CT with contrast.

    2. - Scott Adams replied to Ginger38's topic in Related Issues & Disorders
      2

      Shingles - Could It Be Related to Gluten/ Celiac


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,398
    • Most Online (within 30 mins)
      7,748

    Megannnnn
    Newest Member
    Megannnnn
    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

    • JoJo0611
      I didn’t know there were different types of CT. I’m not sure which I had. It just said CT scan with contrast. 
    • Scott Adams
    • Scott Adams
      I had the same thing happen to me at around your age, and to this day it's the most painful experience I've ever had. For me it was the right side of my head, above my ear, running from my nerves in my neck. For years before my outbreak I felt a tingling sensation shooting along the exact nerves that ended up exactly where the shingles blisters appeared. I highly recommend the two shot shingles vaccine as soon as your turn 50--I did this because I started to get the same tingling sensations in the same area, and after the vaccines I've never felt that again.  As you likely know, shingles is caused by chicken pox, which was once though of as one of those harmless childhood viruses that everyone should catch in the wild--little did they know that it can stay in your nervous system for your entire life, and cause major issues as you age.
    • trents
    • Clear2me
      Thanks for the info. I recently moved to CA from Wyoming and in that western region the Costco and Sam's /Walmart Brands have many nuts and more products that are labeled gluten free. I was told it's because those products are packaged and processed  in different  plants. Some plants can be labeled  gluten free because the plant does not also package gluten products and they know that for example the trucks, containers equipment are not used to handle wheat, barely or Rye. The Walmart butter in the western region says gluten free but not here. Most of The Kirkland and Members Mark brands in CA say they are from Vietnam. That's not the case in Wyoming and Colorado. I've spoken to customer service at the stores here in California. They were not helpful. I check labels every time I go to the store. The stores where I am are a Sh*tshow. The Magalopoly grocery chain Vons/Safeway/Albertsons, etc. are the same. Fishers and Planters brands no longer say gluten free. It could be regional. There are nuts with sugar coatings and fruit and nut mixes at the big chains that are labeled gluten free but I don't want the fruit or sugar.  It's so difficult I am considering moving again. I thought it would be easier to find safe food in a more populated area. It's actually worse.  I was undiagnosed for most of my life but not because I didn't try to figure it out. So I have had all the complications possible. I don't have any spare organs left.  No a little gluten will hurt you. The autoimmune process continues to destroy your organs though you may not feel it. If you are getting a little all the time and as much as we try we probably all are and so the damage is happening. Now the FDA has pretty much abandoned celiacs. There are no requirements for labeling for common allergens on medications. All the generic drugs made outside the US are not regulated for common allergens and the FDA is taking the last gluten free porcine Thyroid med, NP Thyroid, off the market in 2026. I was being glutened by a generic levothyroxin. The insurance wouldn't pay for the gluten free brand any longer because the FDA took them all off their approved formulary. So now I am paying $147 out of pocket for NP Thyroid but shortly I will have no safe choice. Other people with allergies should be aware that these foreign generic pharmaceutical producers are using ground shellfish shell as pill coatings and anti-desicants. The FDA knows this but  now just waits for consumers to complain or die. The take over of Wholefoods by Amazon destroyed a very reliable source of good high quality food for people with allergies and for people who wanted good reliably organic food. Bezos thought  he could make a fortune off people who were paying alot for organic and allergen free food by substituting cheap brands from Thailand. He didn't understand who the customers were who were willing to pay more for that food and why. I went from spending hundreds to nothing because Bezo removed every single trusted brand that I was buying. Now they are closing Whole foods stores across the country. In CA, Mill Valley store (closed July 2025) and the National Blvd. store in West Los Angeles (closed October 2025). The Cupertino store will close.  In recent years I have learned to be careful and trust no one. I have been deleberately glutened in a restaurant that was my favorite (a new employee). The Chef owner was not in the kitchen that night. I've had  a metal scouring pad cut up over my food.The chain offered gluten free dishes but it only takes one crazy who thinks you're a problem as a food fadist. Good thing I always look. Good thing they didn't do that to food going to a child with a busy mom.  I give big tips and apologize for having to ask in restaurants but mental illness seem to be rampant. I've learn the hard way.          I don't buy any processed food that doesn't say gluten free.  I am a life long Catholic. I worked for the Church while at college. I don't go to Church anymore because the men at the top decided Jesus is gluten. The special hosts are gluten less not gluten free. No I can't drink wine after people with gluten in their mouth and a variety of deadly germs. I have been abandoned and excluded by my Church/Family.  Having nearly died several times, safe food is paramount. If your immune system collapses as mine did, you get sepsis. It can kill you very quickly. I spent 5 days unconscious and had to have my appendix and gall bladder removed because they were necrotic. I was 25. They didn't figure out I had celiac till I was 53. No one will take the time to tell you what can happen when your immune system gets overwhelmed from its constant fighting the gluten and just stops. It is miserable that our food is processed so carelessly. Our food in many aspects is not safe. And the merging of all the grocery chains has made it far worse. Its a disaster. Krogers also recently purchased Vitacost where I was getting the products I could no longer get at Whole Foods. Kroger is eliminating those products from Vitacost just a Bezos did from WF. I am looking for reliable and certified sources for nuts. I have lived the worst consequences of the disease and being exposed unknowingly and maliciously. Once I was diagnosed I learned way more than anyone should have to about the food industry.  I don't do gray areas. And now I dont eat out except very rarely.  I have not eaten fast food for 30 years before the celiac diagnosis. Gluten aside..... It's not food and it's not safe.  No one has got our backs. Sharing safe food sources is one thing we can do to try to be safe.        
×
×
  • 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.