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

I Feel Like I'm Trying Too Extract Teeth With A Spoon While Hitting My Head Against A Brick Wall.


Coinkey

Recommended Posts

Coinkey Apprentice

So, I got my lab results back. The first walk-in doctor I saw ordered a Celiac panel, he didn't talk much but at least he listened and considered what i said. then he went on holiday and won't be back till the end of the summer. :( My results came back and they called me to go in and discuss the results. New doctor, he talks more and listens less. My results are negative for TtG but everything else is normal except ferritin and vitamin D. He says "if you feel better when you don't eat gluten then keep that up. It's not worth bothering with a biopsy at this point because most of the time tests for celiac are negative." okay, so true. Except for the fact that he tells me all of this as he is backing out of the room and walking away. Thanks dude. So, I walked out of the room with him and kept asking some questions, "so if all those test are negative, why does it hurt so much when I eat gluten? What does the slightly low ferritin level mean?" Then he says, "just keep eating gluten free, maybe the problem with gluten will go away eventually" and walks away. I walked out rather frustrated. So, yeah, I'll keep eating gluten free because I am a totally awesome person without it but it's frustrating that the doctors don't answer questions and that the tests are negative. It's all in my head then. One day I'll wake up and eat toast for breakfast and be absolutely fine, that's what the doctor seems to think. I just need someone to tell me I'm not insane, it's not all in my head and also what those ferritin and vitamin D levels are (both "low").


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



Celiac.com Sponsor (A8-M):



lucia Enthusiast

You're the opposite of insane. Sounds like you're doing a really good job of taking care of yourself, despite the obstacles. Did you know that on average it takes 9 years in the U.S. for a celiac to be diagnosed after getting symptoms? The American medical community is simply not very good at dealing with celiac - diagnosing it or treating it. I suggest reading this article focused on Dr. Peter Green who is an expert on celiac at Columbia University Medical School. He's pretty great. Here is a relevant section of the article.

Celiac disease is a master of disguise because it may strike any section of the small intestine, with each section being responsible for the absorption of different vitamins and minerals and associated with different biochemical changes in the body. Even the most diligent doctors have difficulty spotting it.

Kay DH Apprentice

So, I got my lab results back. The first walk-in doctor I saw ordered a Celiac panel, he didn't talk much but at least he listened and considered what i said. then he went on holiday and won't be back till the end of the summer. :( My results came back and they called me to go in and discuss the results. New doctor, he talks more and listens less. My results are negative for TtG but everything else is normal except ferritin and vitamin D. He says "if you feel better when you don't eat gluten then keep that up. It's not worth bothering with a biopsy at this point because most of the time tests for celiac are negative." okay, so true. Except for the fact that he tells me all of this as he is backing out of the room and walking away. Thanks dude. So, I walked out of the room with him and kept asking some questions, "so if all those test are negative, why does it hurt so much when I eat gluten? What does the slightly low ferritin level mean?" Then he says, "just keep eating gluten free, maybe the problem with gluten will go away eventually" and walks away. I walked out rather frustrated. So, yeah, I'll keep eating gluten free because I am a totally awesome person without it but it's frustrating that the doctors don't answer questions and that the tests are negative. It's all in my head then. One day I'll wake up and eat toast for breakfast and be absolutely fine, that's what the doctor seems to think. I just need someone to tell me I'm not insane, it's not all in my head and also what those ferritin and vitamin D levels are (both "low").

Low "ferritin" (iron) and vitamin D levels are common in Celiac disease, the iron suggests anemia. Actually low D is common in the general populace. I caught the flu last Sept and a couple of weeks later had bad reactions to bread, such as stiff joints, muscle aches, D, lethargy, brain fog, etc. I went off gluten in November, and then had the Celiac Panel in Jan. It was negative (due to gluten-free probably), as well as a panel two years ago (because of a rash like DH that is now gone after 6 month gluten-free). I had a endoscopy and biopsy that were also negative, these were probably also false negatives because there was only 1 biopsy and I was gluten-full for only 1 week. As the previous poster indicated, even GIs have poor knowledge of gluten enteropathy and they tend to dismiss symptoms as something else. Mine said I only (only!) have a 10% chance of Celiac because I am HLA-DQ8 positive. He dismissed ALL of my symptoms as due to diverticulitis (infected pockets in colon). Needless to say my colon was fine. He never gave me a diagnosis for the gluten problem. You have to do what is best for you. If gluten makes you sick, then listen to that. Doctors spend too much time believing test results and not enough listening to patients and their symptoms. Getting used to gluten-free is a huge life change. I went into a big grocery store today to see if they had frozen dinners I could buy for lunches. Strange experience wandering the aisles and knowing that there is little that I can eat without getting sick. Once you are over the grieving process and frustrations, gluten-free is a much better life change. We're eating much better than when we ate breads and processed foods. Try to find a doctor that listens to you; they are like every other profession in terms of their abilities and not.

  • 2 weeks later...
notme Experienced

boy, i guess i really got off easy with my doc, then. i have been having digestive problems for years and was misdiagnosed by other doctors. i had been feeling progressively worse to the point of not eating very much because it was such a pain in the butt (lol - sry couldn't resist) i didn't even go in to complain about my intestinal issues. i have high blood pressure and had to go for my six-month check. i was down to 110 lbs (am 5'8" always been thin but my weight hung right around 125 or so. my dr. (he is a D.O. not even a GI dr.!) asked me what was going on. i said same old, same old. i have sucky guts. so he looks at the rash on my scalp and asked me exactly what happens when i eat. i said sometimes i'm ok and sometimes the meal moves through me like a freight train. he writes down "celiac disease. gluten-free diet. align" on a prescription pad and hands it to me. i said, dude. that's not happening! i am making my annual trip to nj where i am eating nothing but pizza. and drinking many beers. he just looked at me a little sideways and told me to pay attention to what i am eating/drinking when i get sick. well, whattayaknow. there it was. it took me a few months of denying it but last weekend i was really, really sick. and really, really tired of being sick. i feel 1000% better!! and pretty glad my doc is a smart guy. especially after reading on here that so many have been misdiagnosed!

Wenmin Enthusiast

Maybe your doctor didn't know enough about the gluten intolerances to answer your questions and this was his quick escape. Find a doctor that specializes in Celiac Disease, maybe you won't feel so neglected as you did this time and he/she will feel more confident answering your questions...

Wenmin

Archived

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


  • 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

    • 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.        
    • Mmoc
      Thank you kindly for your response. I have since gotten the other type of bloods done and am awaiting results. 
×
×
  • 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.