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

Initial Diagnosis A Possible Gluten Problem?


songstressc

Recommended Posts

songstressc Apprentice

Hi Everyone, I am new here - learning to use post etc. My diagnosis is a maybe Gliadin count is 11. I am hoping some of you could share your histories and diagnosis. Were you diagnosed as a maybe and indeed were Gluten Intolerant? It is such a dramatic life

change - It would be great to hear if indeed I could be on the right track. Are you feeling better now?

Thanks for sharing :)


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

I had two family members who were only one point into the postive range on testing and went gluten free and saw a surprising difference in a number of issues. As for myself I never showed postive on a blood test and it was a real struggle to get diagnosed since the doctors would see the negative blood work and considered that negative to be a firm diagnosis that I didn't have celiac. The reality is that up to 30% of us show up negative on the blood tests even at the end stages. I was one of them. I was finally diagnosed 6 years ago and well my signature says it all. You have nothing to lose by trying the diet strictly for a couple of months UNLESS you are going to have an endo and biopsy if that is in your future do keep eating gluten until the biopsy is done.

GFqueen17 Contributor

i had GI problems for yearssss and my mom is celiac so she suggested i try going gluten free. i didn't think of getting a blood test first, i just went gluten free right away...and i felt much, much better! i did end up getting a blood test after about a week of being gluten free but of course it came back negative. i am not willing to go back on gluten just to get an accurate blood test. i know that every single time that i accidentally get contaminated with gluten, i get very, very sick...and that is all i care about.

Mother of Jibril Enthusiast
It is such a dramatic life change.

I went gluten-free on the recommendation of an allergist and I felt SO much relief from my abdominal pain. There was no way I wanted to try the "challenge." I could already tell that gluten was doing bad things to my body. That being said... at first I was hoping I was just a "little" intolerant. That maybe I wouldn't have to be paranoid about cross-contamination, lip balm, using the same toaster as my husband, etc... That's what my first post was about ;) Now that I've learned more, I really see the benefit to going gluten-free 100%. I feel great and I honestly don't crave gluten and dairy anymore! A bit of real ice cream would be nice, but I can live without it. I don't feel deprived. There are SO many good things to eat if you take the time to cook and explore new areas of the grocery store. People on this forum are wonderful about offering their advice and recipes :P

Welcome to the group!

songstressc Apprentice
I had two family members who were only one point into the postive range on testing and went gluten free and saw a surprising difference in a number of issues. As for myself I never showed postive on a blood test and it was a real struggle to get diagnosed since the doctors would see the negative blood work and considered that negative to be a firm diagnosis that I didn't have celiac. The reality is that up to 30% of us show up negative on the blood tests even at the end stages. I was one of them. I was finally diagnosed 6 years ago and well my signature says it all. You have nothing to lose by trying the diet strictly for a couple of months UNLESS you are going to have an endo and biopsy if that is in your future do keep eating gluten until the biopsy is done.

Thank you Ravenwoodglass for sharing - I really appreciate it. I feel better just chatting to someone - -ahh so many comfort foods gone! :huh: Your story is amazing- I was at the ND today and she said it is not a maybe and explained the false negative test that happens often. had to laugh as when I asked her to check my husband's gliadin - he was higher than me! Love the quote!

thanks,

songstressc Apprentice
i had GI problems for yearssss and my mom is celiac so she suggested i try going gluten free. i didn't think of getting a blood test first, i just went gluten free right away...and i felt much, much better! i did end up getting a blood test after about a week of being gluten free but of course it came back negative. i am not willing to go back on gluten just to get an accurate blood test. i know that every single time that i accidentally get contaminated with gluten, i get very, very sick...and that is all i care about.

thanks for sharing - I wonder how long it will take for my son to to change his ways? He has the same GI probs as I do. I asked the ND today if my count is higher or lower depending on what I have eaten and she said it does not make a difference and that most people have a false negative test. Oh well, carpe diem!

lizard00 Enthusiast

I'm in there with ravenwoodglass... I could be half dead and NEVER have positive celiac blood tests. Although, I am diagnosed.

A reaction is a reaction, whether it's a huge amount over the range, or just one or two points. Making antibodies to gluten doesn't happen if gluten is not a problem for you. Your ND is exactly right, false negatives are unfortunately not all that uncommon.

I can honestly say that I do not miss gluten at all! When I see it, it looks like poison to me. The only deprivation I have felt was a year ago when my life was passing me by. I discovered gluten to be a problem, and I ditched it and never looked back. There have been moments of frustration, moments of anger... all of the things you would expect. But in a situation such as this, you find the good. For me, I was unexplicably sick. Finding gluten was a <i>relief</i> because I didn't have to worry about taking drugs the rest of my life, or being constantly monitored for side effects...all that stuff no one wants to have to deal with. If I could control my health by removing a food, it wasn't so bad. So I chose my health, and it's much easier when it's a conscious decision.

Anyway, welcome to our club! We are always here to help, so please feel free to pick everyone's brains!


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



Celiac.com Sponsor (A8-M):



mommaofthree Newbie

I was just recently dx, 6 days ago now. I went in to see a GI because I believed I had IbS, they scoped and took biopsies and found that I had Celiac. However, I had more symptoms that I was just dealing with thinking I was getting Old ( I'm 27) and having 3 children just messes with your body. I had the skin rash, lost my period for months, had FHS tests that showed me at advanced menopause levels, and of course I was constantly exhausted and iron deficient. I saw 2 doctors for these issues and not one of them put it all together, not even my GI who believed I had IbS. She none the less was shocked.

I guess I was lucky to get the biopsy done first and the blood test second. After reading so many posts about not showing in blood levels.

I am on a crash course to learning everything I can about how to eat and I really appreciate all the information at this site!!

Krista

Antioch, CA.

songstressc Apprentice

Thank you - all of you who have taken the time to share your history/stories. I am very thankful for this site and the people on it. I have never taken part replying or talking on sites and it is surprising how great it feels to talk to others in similar situations. Happy Holidays to all of you whatever beliefs you follow and wishing you a fantastic new 2009! :D

IMWalt Contributor

I can identify with this. I was just looking at my test result of "3" for Iga. My GI told me that was a negative. I had been gluten-free for over 2 months when I first went to the GI, and she told me to eat gluten for 3 weeks and then we did the test. I did not eat much gluten during that 3 weeks, because I was not told I should eat a lot, and I did not like the side-effects. However, I went for a follow-up just last week, and she now feels that I do have celiac based on my positive dietary response and the fact that every time I eat gluten, either accidently or on purpose, I end up with the same old symptoms; gas, cramps, noisy stomach, D or loose stools. I don't understans the tests, but I do understand my GI tract.

Walt

luciddream928 Explorer
I can identify with this. I was just looking at my test result of "3" for Iga. My GI told me that was a negative.

I've had a question about this for a while - why does that number have to be above 10 to be a positive? Shouldn't it be, "either you have it or you don't"?

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. - nanny marley replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      22

      Insomnia help

    2. - knitty kitty replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      47

      My journey is it gluten or fiber?

    3. - Known1 replied to Jane02's topic in Gluten-Free Foods, Products, Shopping & Medications
      12

      Desperately need a vitamin D supplement. I've reacted to most brands I've tried.

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

      results from 13 day gluten challenge - does this mean I can't have celiac?

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,362
    • Most Online (within 30 mins)
      7,748

    Xpedit73
    Newest Member
    Xpedit73
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • nanny marley
      I do believe that people are under so much pressure up have a sleeping  pattern ,  with working and how households work these days , but in reality there is no wrong or right at to sleep , I believe your neighbour showed this with such a long life , I do exactly the same  at night many times so I hope I live into my nineties also , I have found one thing in life your body knows what's best so good to listen to wat it needs however unconventional that maybe 🤗
    • knitty kitty
      Try adding some Thiamine Hydrochloride (thiamine HCl) and see if there's any difference.  Thiamine HCl uses special thiamine transporters to get inside cells.  I take it myself.   Tryptophan will help heal the intestines.  Tryptophan is that amino acid in turkey that makes you sleepy after Thanksgiving dinner.  I take mine with magnesium before bedtime.
    • Known1
      I live in the upper mid-west and was just diagnosed with marsh 3c celiac less than a month ago.  As a 51 year old male, I now take a couple of different gluten free vitamins.  I have not noticed any reaction to either of these items.  Both were purchased from Amazon. 1.  Nature Made Multivitamin For Him with No Iron 2.  Gade Nutrition Organic Quercetin with Bromelain Vitamin C and Zinc Between those two, I am ingesting 2000 IU of vitamin D per day. Best of luck, Known1
    • SilkieFairy
      I am doing a gluten challenge right now and I bought vital wheat gluten so I can know exactly how much gluten I am getting. One tablespoon is 7g so 1½ tablespoons of Vital Wheat Gluten per day will get you to 10g You could add it to bean burgers as a binder or add to hot chocolate or apple sauce and stir. 
    • Wheatwacked
      Raising you vitamin D will increase absorption of calcium automatically without supplementation of calcium.  A high PTH can be caused by low D causing poor calcium absorption; not insuffient calcium intake.  With low D your body is not absorbing calcium from your food so it steals it from your bones.  Heart has priority over bone. I've been taking 10,000 IU D3 a day since 2015.  My doctor says to continue. To fix my lactose intolerance, lots of lactobacillus from yogurts, and brine fermented pickles and saurkraut and olives.  We lose much of our ability to make lactase endogenosly with maturity but a healthy colony of lactobacillus in our gut excretes lactase in exchange for room and board. The milk protein in grass fed milk does not bother me. It tastes like the milk I grew up on.  If I drink commercial milk I get heartburn at night. Some experts estimate that 90% of us do not eat Adequite Intake of choline.  Beef and eggs are the principle source. Iodine deficiency is a growing concern.  I take 600 mcg a day of Liquid Iodine.  It and NAC have accelerated my healing all over.  Virtually blind in my right eye after starting antihypertensive medication and vision is slowly coming back.  I had to cut out starches because they drove my glucose up into the 200+ range.  I replaced them with Red Bull for the glucose intake with the vitamins, minerals and Taurine needed to process through the mitochodria Krebs Cycle to create ATP.  Went from A1c 13 down to 7.9.  Work in progress. Also take B1,B2,B3,B5,B6. Liquid Iodine, Phosphatidyl Choline, Q10, Selenium, D and DHEA.     Choline supplemented as phosphatidylcholine decreases fasting and postmethionine-loading plasma homocysteine concentrations in healthy men +    
×
×
  • 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.