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

Very Frustrated!


Katie B

Recommended Posts

Katie B Apprentice

Hi everyone,

So, after being diagnosed as having IBS then having Celiac, then having small intestine bacterial overgrowth and perhaps not Celiac I'm left wondering what's what? I was also recently diagnosed with a pituitary disfunction so I can't produce vasopressin or cortisol - my endo. believes that since my pituitary is slightly smaller that it was attacked by an autoimmune disease... which would lead me right back to Celiac. Now my Gastro. wants me to eat gluten for 3 weeks and then he'll give me another blood test which may or may not show anything (tissue transglutamine, anti-gliadin antibody, anti endomysial antibody. I already tested negative for the other blood tests - test one showed I didn't have any antibodies and test two showed that my levels might be so low that I might not be able to produce the antibody. Test 3 - the scope showed that I had destroyed villi, however, the infection can result in the same destruction. I've been gluten-free for 3 months now and since I've been taking the replacement hormones (vasopressin and cortisol) am feeling great. I would like to get a final diagnosis on Celiac but fear that implications of being on gluten again. If I do have a diagnosis then I can qualify for a large tax deduction off of gluten-free foods. I can also know in the future what to look out for - and my doctors will be more aware as well.

Anybody else experience this? I guess at some point even if I don't get a firm diagnosis I'll just have to make a decision. There's no way I'm converting my kitchen back and forth and to be honest I'm getting quite used to eating gluten-free and don't even feel deprived...

Sigh... I know that the advice I'll get here will probably be skewed towards staying gluten-free but if anybody has a balanced view or has experienced something similar I would really appreciate your feedback.

Thanks!


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



Celiac.com Sponsor (A8-M):



Wolicki Enthusiast

Here's my opinion. Why not wait until you get the other issues under control, since symptoms can be misleading. Stay on your meds, get rid of the bad bugs. Once all that is done, then try out eating some gluten and see how you react. You will know pretty quickly if it is the problem.

Celiac is not one of those black and white diagnoses. Since the effects are systemic and doctors don't deal well with gray areas, many have been in the same situation. I hope you continue to feel better, whatever decision you make!

ravenwoodglass Mentor

If your total IGA is low eating all the gluten in the world won't give you a positive blood test. You have the gold standard for diagnosis, the villi damage and you feel better gluten free. IMHO your body has given you the answer. I do understand your desire for a firm diagnosis, it is too bad you have to literally (if you are celiac) poison yourself for up to three months to get that diagnosis. Do keep your doctor well informed of your reactions, if you have them, to the gluten challenge. Some doctors will diagnose based on the remission of symptoms gluten free and the recurring problems when the challenge is done. Hopefully if you react to the challenge that and the gold standard positive villi test you have already had done will be enough for the doctor to diagnose.

Another thing you could suggest to the doctor is that he rescope you now, since you have been gluten free and feeling better for 3 months. If when he rescopes the villi have repaired that should be diagnostic also.

michelley65 Rookie

I was also diagnosed with a small intestinal bacterial overgrowth about a year and a half ago.Ive been on different meds for it..and nothing seemed to help.I realized on my own that certain foods would aggravate it(bloating,gas constantly,diahrea,ect)..those would be bread,noodles,ect.I told my doctor about it and he said that the bacteria feed off the carbs and produce gas,so I started cutting way down on the foods that irritated me,and eventually(about 5 weeks ago)went gluten free.I feel so much better without it...and wonder now about my diagnoses of s.i.b.o.You mentioned that you can claim the gluten free foods with a diagnoses of celiac...what about gluten intolerance?I was tested for celiac and it came back negative,but I know Im sensitive to it and would like to claim my expenses.Might I add,when I was tested my doctors assistant told me that it was ok that I was gluten free for a week and also eating gluten light for sometime..it wouldnt make a difference..I know now that they were wrong..I might be celiac afterall and will never know.

Katie B Apprentice

Thanks everyone,

Sometimes it's just nice to share my frustration with people who understand. I know that there isn't a clear cut answer but at some point I just want to get healthy for good!

In response to Michelle - I've had two bouts of sibo and got rid of them by going on the specific carbohydrate diet. The first one I just scaled back everything and went gluten free and it disappeared. I started eating gluten again and it came back. After the second time I went on the specific carbohydrate diet and made my own lactose-free yogurt. I tried the antibiotic approach but while this was successful while I was on them once I was taken off I was back to having the infection. I've found that now I can eat rice, quinoa and other non-glutenous grains and the sibo hasn't flared up again. I think in the end I might never have an answer and I might just have to assume I have Celiac. It's certainly better than having another part of my body under attack - I'm not sure about being gluten-intolerant and tax deductions...it's definitely worth looking into though!

Thanks for listening! At least I'm coming to the end of a very long process.

Black Sheep Apprentice

You have the gold standard for diagnosis, the villi damage and you feel better gluten free.

Those were my dr.'s exact words--the gold standard. Yesterday I had my 1 month app't. with her--1 month after having cut gluten from my diet, at her suggestion. I understand your desire for a "firm diagnosis", as I kept going back and forth on this, too, but my problem is, I don't have insurance. Which is why my doc didn't make me get tests! But I asked her yesterday about the tests, saying, "Without actually being tested, how will I know if I'm merely gluten intolerant, or a full-blown celiac?" And she said that if I really, really, want to, we can do the testing, but she also said, "The blood test is really nothing more than a screening. The biopsy is the Gold Standard for diagnosing, but really--does it matter? I mean, if you have all these health issues, and you cut out gluten and feel so much better, then your body has told you that obviously gluten was a big problem for you--does it really matter at that point what a test says?"

And I just sat there and thought about it a second and told her "No, you're right, it doesn't matter."

Not that all my health problems have suddenly and magically gone away--after all, it's only been a month! But, there's been enough of an improvement that I know for sure that gluten is poisonous to me, so that's all I need to know!

Although you did mention a tax deduction if you get a diagnosis....you must not be in the U.S.! So as someone who's self-employed, uninsured, and staring a this year's tax bill in the face at the moment, I can understand wanting a tax break. Still, let's say you don't get a firm diagnosis. No tax break. But, let's say you stay off gluten for a few months and find that bit by bit, you're starting to improve. Would the tax break still matter at that point?

I dunno, just something to think about. :)

ravenwoodglass Mentor

Hi everyone,

If I do have a diagnosis then I can qualify for a large tax deduction off of gluten-free foods.

Thanks!

I somehow missed this in my first reply.

If you are in the US please be aware that the tax break we get is not that great. We can only take a tax deduction after our medical expenses reach a certain percentage of our income. The year before my diagnosis that would have helped as we had 17 thousand dollars in copays for testing, specialists and drugs that did no good and in some cases a great deal of harm as at least 3 were pulled off the market while I was on them. I know that sounds like a lot for copays but my 'drug supply' of top shelf new drugs and trips to a very large hosptial and the MRI's, blood work at over a thousand dollars a pop for testing on 13 tubes at a time, the CT scans, the copays for neurologists, rhuematologists, different canes and supports for my joints etc all add up. Anyway since diagnosis 8 years ago I have needed a medical doctor about 10 times, mostly for checkups or early on for attempts at help with severe glutening and a severe sprain. Without being constantly sick I haven't even come close to the level of expense needed to take the tax break on the food. So in the end the tax break sounds good but for many of us it isn't something we can really take advantage of and feeling like a new painless person is to me worth much, much more than the little bit of a break the government would give us.


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



Celiac.com Sponsor (A8-M):



Katie B Apprentice

Yes - I can totally agree. My dietician also pointed out that if I don't get a diagnosis and in 30 years will I start to cheat a little, however, having something randomly malfunction in your brain is very scary and I honestly don't think I'll ever cheat. Besides, I really don't feel deprived - I can eat a lot more now than a year ago so things to me are looking better.

In terms of the tax deductions I am in Canada and I was just reading that if you save your grocery bills and create a chart then foods that you buy that are gluten-free - let's say bread - would then be deducted to the cost of a normal gluten-filled loaf of bread. Some people can get up to $800.00 back in a year.

However, I was thinking about this yesterday and again, who really cares about money when you have your health? If I were completely healthy, I would be able to work more (right now I'm on short term disability), I could probably cook more (so could maybe save a bit of $ on some overpriced gluten-free foods) and life would simply be better.

Thanks again for your responses. This forum has been amazing and it's great that so many people are so well educated about this disease. It's really becoming a movement and the stats show that we have a long way to go in terms of accurately diagnosing people.

Katie

michelley65 Rookie

I agree..who actually needs the diagnoses if you yourself know that gluten is the enemy!The tax break would be very nice to have..and I will still save my reciepts just incase anything changes,but for now all I can say is..."No more bellyachin!"

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,545
    • Most Online (within 30 mins)
      7,748

    WAY
    Newest Member
    WAY
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.