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:
    Donate

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    2. - tiffanygosci posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Aldi Pueblo Lindo Yellow Corn Tortillas

    3. - tiffanygosci replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    4. - trents replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    5. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,974
    • Most Online (within 30 mins)
      7,748

    LRB
    Newest Member
    LRB
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Mari
      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
    • tiffanygosci
      Another annoying thing about trying to figure this Celiac life out is reading all of the labels and considering every choice. I shop at Aldi every week and have been for years. I was just officially diagnosed Celiac a couple weeks ago this October after my endoscopy. I've been encouraged by my local Aldi in that they have a lot of gluten free products and clearly labeled foods. I usually buy Milagro corn tortillas because they are cheap and are certified. However, I bought a package of Aldi's Pueblo Lindo Yellow Corn Tortillas without looking too closely (I was assuming they were fine... assuming never gets us anywhere good lol) it doesn't list any wheat products and doesn't say it was processed in a facility with wheat. It has a label that it's lactose free (hello, what?? When has dairy ever been in a tortilla?) Just, ugh. If they can add that label then why can't they just say something is gluten free or not? I did eat some of the tortillas and didn't notice any symptoms but I'm just not sure if it's safe. So I'll probably have to let my family eat them and stick with Milagro. There is way too much uncertainty with this but I guess you just have to stick with the clearly labeled products? I am still learning!
    • tiffanygosci
      Thank you all for sharing your experiences! And I am very thankful for that Thanksgiving article, Scott! I will look into it more as I plan my little dinner to bring with on the Holiday I'm also glad a lot of research has been done for Celiac. There's still a lot to learn and discover. And everyone has different symptoms. For me, I get a bad headache right away after eating gluten. Reoccurring migraines and visual disturbances were actually what got my PCP to order a Celiac Panel. I'm glad he did! I feel like when the inflammation hits my body it targets my head, gut, and lower back. I'm still figuring things out but that's what I've noticed after eating gluten! I have been eating gluten-free for almost two months now and haven't had such severe symptoms. I ate a couple accidents along the way but I'm doing a lot better
    • trents
      @Mari, did you read that second article that Scott linked? It is the most recently date one. "Researchers comparing rates of headaches, including migraines, among celiac patients and a healthy control group showed that celiac subjects experienced higher rates of headaches than control subjects, with the greatest rates of migraines found in celiac women.  Additionally, celiacs had higher rates of migraine than control subjects, especially in women. In fact, four out of five women with celiac disease suffered from migraines, and without aura nearly three-quarters of the time."
    • Mari
      As far as I know and I have made severalonline searches, celiac disease disease has not been recognized as a cause of migraines or any eye problems. What I wrote must have been 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.