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

How Many: Blood Tests Negative, But Celiac Or Gluten Sensitive?


Mmom

Recommended Posts

Mmom Newbie

Hi all,

I was wondering how many tested negative on blood panel but are indeed celiac or gluten-sensitive since much of what I've read here seems to indicate this possibility.

My blood test was negative for celiac, but 1.) I in no way eat the equivalent of 2-4 pieces of bread a day - I have always been a healthy fresh-vegetables-and-meat person anyway; and 2.) it seems that gluten exacerbates or brings back my stomach and bowel troubles.

Now, I haven't had problems until the last two months when in the beginning I felt I had a stomache flu that kept coming back! but I go from feeling sick to better and then sick again, and I'm losing weight - too much. I did feel better going gluten free for about two weeks but am guessing that is too soon to tell? All I know is that in a fit of perversity and upon the results of my negative blood tests I ate fried oysters and flour tortillas and now I am ill since. I should add that non-gluten fried food like bacon is very painful too.

My latest and greatest symptom and pain is the feeling that I have to defecate ALL the time. I actually feel pain in my lower colon area. No D lately but straining with bathroom visits and pain. Now have bleeding hemmoroids. Pleading with the primary doctor and begging for help for my pain has got me into the gastroentologist and he scheduled me for a colonoscopy in two weeks - the earliest. He suspects colitis. Don't have colon cancer in family hisotry but I have ALL the symptoms of it so I'm scared and freaked out.

Should I try enterolab? I'm trying to be gluten free now to see if I can feel better.


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

I ate wheat free but not gluten free for three years and came out negative on the blood panel. I came out VERY positive at Enterolab and get sick even when I get a minor cross-contamination.

dlp252 Apprentice

Well, my testing doesn't count since I did it AFTER I went gluten-free. I had both blood tests and biopsy, but neither my doctor nor I thought either would show anything...did it just for a baseline and because he was going to be in there (looking for damage from GERD) anyway.

I went gluten-free at the beginning of November and did see a little improvement. Then I decided to try the Enterolab testing--the results came back in December. They confirmed that I was gluten intolerant, casein intolerant and had one of the main genes associated with celiac. That was enough for me, lol.

I improved a lot more once cutting out the casein. The biggest two improvements are that I haven't had a sinus infection since October! I was getting them every 6 weeks, almost like clockwork...and I had pain in my knees almost contantly for several months...that has gone away too. My sense of smell is returning slowly but surely, and I have a bit of color in my checks again.

I'm still trying to figure out what ELSE I'm intolerant to to get rid of these last few nagging symptoms.

Becky6 Enthusiast

Both my daughter and i were neg but clearly can't have gluten. If we get the slightest cc we are very sick. Neither of us ate that much gluten prior to testing though.

Guest nini

my daughter's test was also negative, but she obviously has a major problem with gluten and has absolutely thrived on the gluten-free diet.

NSG Newbie

Blood work for both me and my daughter were negative - but after 16 years on a gluten-free diet - what else would they be! The slightest bit of gluten makes her sick and I am just getting over a full blown attack after an accidential ingestion. That's enough proof for me!

Smunkeemom Enthusiast

The doctor originally told me that my blood test was negative, but I found out 2 years later that it was positive, when I asked her about it she said "we don't like to put people on the gluten free diet unless they are really sick"

:angry:

I wonder how many "tested neg." but really had positive results.

moral of the story: ALWAYS get your actual lab results, never believe the doctor, always check it out for yourself.


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. - xxnonamexx replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      4

      My journey is it gluten or fiber?

    2. - cristiana replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

    3. - chrisinpa commented on Scott Adams's article in Skin Problems and Celiac Disease
      2

      Celiac Disease and Skin Disorders: Exploring a Genetic Connection

    4. - knitty kitty replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      4

      My journey is it gluten or fiber?

    5. - trents replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

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

    • Total Members
      132,696
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • xxnonamexx
      I read that as well but I saw the Certified Gluten free symbol that is the reason I ourchased it.
    • cristiana
      I agree, it so often overlooked! I live in the UK and I have often wondered why doctors are so reluctant to at least exclude it - my thoughts are perhaps the particular tests are expensive for the NHS, so therefore saved for people with 'obvious' symptoms.  I was diagnosed in 2013 and was told immediately that my parents, sibling and children should be checked.  My parents' GP to this day has not put forward my father for testing, and my mother was never tested in her lifetime, despite the fact that they both have some interesting symptoms/family history that reflect they might have coeliac disease (Dad - extreme bloating, and his Mum clearly had autoimmune issues, albeit undiagnosed as such; Mum - osteoporosis, anxiety).  I am now my father' legal guardian and suspecting my parents may have forgotten to ask their GP for a test (which is entirely possible!) I put it to his last GP that he ought to be tested.  He looked at Dad's blood results and purely because he was not anemic said he wasn't a coeliac.  Hopefully as the awareness of Coeliac Disease spreads among the general public, people will be able to advocate for themselves.  It is hard because in the UK the NHS is very stretched, but the fallout from not being diagnosed in a timely fashion will only cost the NHS more money. Interestingly, a complete aside, I met someone recently whose son was diagnosed (I think she said he was 8).  At a recent birthday party with 8 guests, 4 boys out of the 8 had received diagnosis of Coeliac Disease, which is an astounding statistic  As far as I know, though, they had all had obvious gastric symptoms leading to their NHS diagnosis.  In my own case I had  acute onset anxiety, hypnopompic hallucinations (vivid hallucinations upon waking),  odd liver function, anxiety, headaches, ulcers and low iron but it wasn't until the gastric symptoms hit me that a GP thought to do coeliac testing, and my numbers were through the roof.  As @trents says, by the grace of God I was diagnosed, and the diet has pretty much dealt with most of those symptoms.  I have much to be grateful for. Cristiana
    • knitty kitty
      @xxnonamexx, There's labeling on those Trubar gluten free high fiber protein bars that say: "Manufactured in a facility that also processes peanuts, milk, soy, fish, WHEAT, sesame, and other tree nuts." You may want to avoid products made in shared facilities.   If you are trying to add more fiber to your diet to ease constipation, considering eating more leafy green vegetables and cruciferous vegetables.  Not only are these high in fiber, they also are good sources of magnesium.  Many newly diagnosed are low in magnesium and B vitamins and suffer with constipation.  Thiamine Vitamin B1 and magnesium work together.  Thiamine in the form Benfotiamine has been shown to improve intestinal health.  Thiamine and magnesium are important to gastrointestinal health and function.  
    • trents
      Welcome to celiac.com @sha1091a! Your experience is a very common one. Celiac disease is one the most underdiagnosed and misdiagnosed medical conditions out there. The reasons are numerous. One key one is that its symptoms mimic so many other diseases. Another is ignorance on the part of the medical community with regard to the range of symptoms that celiac disease can produce. Clinicians often are only looking for classic GI symptoms and are unaware of the many other subsystems in the body that can be damaged before classic GI symptoms manifest, if ever they do. Many celiacs are of the "silent" variety and have few if any GI symptoms while all along, damage is being done to their bodies. In my case, the original symptoms were elevated liver enzymes which I endured for 13 years before I was diagnosed with celiac disease. By the grace of God my liver was not destroyed. It is common for the onset of the disease to happen 10 years before you ever get a diagnosis. Thankfully, that is slowly changing as there has developed more awareness on the part of both the medical community and the public in the past 20 years or so. Blessings!
    • knitty kitty
      @EndlessSummer, You said you had an allergy to trees.  People with Birch Allergy can react to green beans (in the legume family) and other vegetables, as well as some fruits.  Look into Oral Allergy Syndrome which can occur at a higher rate in Celiac Disease.   Switching to a low histamine diet for a while can give your body time to rid itself of the extra histamine the body makes with Celiac disease and histamine consumed in the diet.   Vitamin C and the eight B vitamins are needed to help the body clear histamine.   Have you been checked for nutritional deficiencies?
×
×
  • 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.