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

Negative Test, Normal Ct Scan, Anything I Can Do?


torolf

Recommended Posts

torolf Newbie

Hey all, I


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



Celiac.com Sponsor (A8-M):



Emilushka Contributor

It sounds like whatever it is that you have, you can't tolerate gluten. I suggest you take that as reality and just go with it. The tests for Celiac are imperfect. It's worth it to talk with a GI doc to make sure you have the documentation in your chart, but if you're miserable with only a partial serving of breaded shrimp, I think you have your answer.

Please listen to your body. Let your guts heal. I hope you continue to feel wonderful on the gluten-free diet!

torolf Newbie

but if you're miserable with only a partial serving of breaded shrimp, I think you have your answer.

Please listen to your body. Let your guts heal. I hope you continue to feel wonderful on the gluten-free diet!

That's what I'm pretty much gonna end up doing. My parents don't even seem to think I have an issue, which sucks that they apparently don't believe me. :/

Skylark Collaborator

A CT scan does not diagnose celiac disease. If your doctor thinks it does, run screaming and get another doctor! There are blood tests, and an intestinal biopsy done by endoscopy. Hopefully you were tested for total IgA, as in that case the IgA versions of the tests are the correct ones. If you want to continue to follow up for a medical diagnosis, you would need to keep eating gluten and get the endoscopy. There are definitely celiacs with villous damage who do not show positive on the blood tests.

You are pretty obviously gluten intolerant if not celiac, and if you're going to eat a celiac diet it really doesn't matter one way or the other whether you are diagnosed. We don't get any help with the cost of gluten-free foods as folks do in Europe. You are an adult, and you need to make your own decisions about what to eat or not eat. Although it's nice to get validation, it really doesn't matter what your parents think. If gluten makes you sick, the sensible thing is to not eat it.

Emilushka Contributor

That's what I'm pretty much gonna end up doing. My parents don't even seem to think I have an issue, which sucks that they apparently don't believe me. :/

Nobody's perfect, including (obviously) your parents. In this case, I think you know what to do. I wish I could tell you that there's some magical thing you could do to change their minds, but really, it sounds like you just need to keep to the gluten-free diet and ignore them.

Sometimes the only thing you can do is take care of yourself and ignore the nay-sayers. It's OK. You're not alone - you have us!

SGWhiskers Collaborator

I just wanted to clarify that while the assistance with the cost of food may be less here in the US, there is a tax deduction available for us. Save your grocery store receipts and then get a comparison of what it would have cost for the same gluten items. Subtract the difference. If that totals more than 7.5% of your income, it can be used as a tax deduction (not tax credit unfortunatly).

Alternatively:

Deposit funds into your flexible spending health account and that cost difference can be deducted from the account. You don't need to meet the 7.5% standard. Before you deposit funds into the flex spending account, confirm that they honor medically necessary diets such as a gluten free diet in their allowable expenses.

With either of these two options, you will need a letter from your doctor stating celiac and a medically necessary diet.

It's up to you if a serious gluten challenge is worth going through just for the tax deduction. You will probably need to itemize each pancake mix, cereal, and flour if you use the flex spending account. A deduction will be reimbursed at roughly 30% of the cost difference vs a tax credit which is reimbursed at 100%, but is not available to us.

Skylark Collaborator

I just wanted to clarify that while the assistance with the cost of food may be less here in the US, there is a tax deduction available for us. Save your grocery store receipts and then get a comparison of what it would have cost for the same gluten items. Subtract the difference. If that totals more than 7.5% of your income, it can be used as a tax deduction (not tax credit unfortunatly).

In reality, I don't think anyone would spend 7.5% of income on difference between gluten-free and normal foods. It's too much of your paycheck with low income, and too much food to eat with high income. I can see possibly qualifying for the deduction in a year where you had extensive health problems and a lot of other medical bills.

That's good to know about the flexible spending, although I don't have that as a benefit right now.


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. - trents replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?

    2. - BlessedinBoston replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?

    3. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      14

      My only proof

    4. - Jmartes71 replied to Jmartes71's topic in Related Issues & Disorders
      14

      My only proof

    5. - marion wheaton posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,407
    • Most Online (within 30 mins)
      7,748

    H2HPizzaWagon
    Newest Member
    H2HPizzaWagon
    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

    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
    • marion wheaton
      Wondering if anyone knows whether Lindt chocolate balls are gluten free. The Lindt Canadian website says yes but the Lindt USA website says no. The information is a bit confusing.
×
×
  • 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.