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

Tested But Unsure


Jenilou

Recommended Posts

Jenilou Newbie

Hello everyone :)

I'm new to this site and new to a gluten free diet.

I have had symptoms relating to celiac for quite awhile now but didn't know anything about it until recently. I have been anemic for as long as I can remember. Also have other vitamin deficiencies for years. I have had digestive problems my whole adult life but recently in the last year they kept progressing. Lately I seem to have trouble now even eating some milk products. I have lost a total of 100 lbs in the last 3 years (was needed though) but only about 50 of it I really tried to lose, the other 50 came off easily. Anyway after my digestive problems progressed and I was losing weight without trying I decided to go to the doctor. At the beginning of June I had an upper and lower scopy. The doctor did a biopsy of my small intestine and he came back and said that my results were suspicious of celiac. I then went in for blood work and it came back normal. Has anyone else had this experience?

The doctor put me on a gluten free diet to see if that relieved symptoms anyway. I have been on this diet for less than 2 weeks now and I have never felt this good... and normal!!! So not sure what that means but I don't want to go back feeling like I did.

I am just confused why the blood work and biopsy came back contradicting themselves.

Btw.. Glad to have found this site.

Jenea


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



Celiac.com Sponsor (A8-M):



aikiducky Apprentice

The blood work is only reliable if you have celiac damage in the intestines that has already progressed very far. Otherwise false negatives are fairly common. There are a lot of people here on the board with a positive biopsy and negative bloods, and in that case, you should always go with the biopsy. Especially since you already know that the diet works for you.

Don't be disappointed or start to doubt the diagnosis if you get some set backs and symptoms return again. It seems to be normal to go up and down for the first year or so. Healing takes time, and it takes time to find all the possible hidden ways to get glutened. And healing takes time!

Pauliina

Jenilou Newbie

Thank you for the info! :)

Also another thing. I was talking to my parents today and when my mom went to the gastro today (she has ischemic colitis, no one else in my family has ever been diagnosed with celiac) and because of my recent discovery with celiac, she asked her doctor about me and told him about the contradicting results. He told her to tell me not to let a doctor pin my symptoms on celiac if I didn't have possitive lab results. There could be other reasons I was having problems.

So I guess maybe I will get a second opinion. Although I do feel better for the most part being gluten free.

Thanks again for the info.

Jenea

aikiducky Apprentice

With positive lab results, does he only mean the blood work? Because if he does he's just not well informed.

BTW you could request the lab report of the biopsy to see what exactly it says.

If you feel better gluten free that is also a piece of information to add to the mix...

Pauliina

gfpaperdoll Rookie

99.9% that your mom also has a gluten problem. If she were to go a on dairy free & gluten free diet - & grain light to start with, she might not have to go to the GI & have to listen to his ignorant advice. Well, of course you should have things like appendics, cancer, tumors, blockages ruled out. But if you have had workup by a GI I would assume that with an upper & lower scope that they checked all that stuff.

dietary trial is the ultimate test. So if you are feeling lots better - keep it up. Only thing is that you might find that you have an additional intolerance. Some people do & some don't. & then some people once they are gluten-free from 6 months to 1 year can add back in foods that they initially reacted to - just not gluten.

Good for you for going on the diet & finding this web site. Also, look for a local support group. They are everywhere & very helpful to find a gluten-free friend & local restaurant info etc. etc.

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 Ello's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Small Bowel Resection 12 inches

    2. - Ello replied to Ello's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Small Bowel Resection 12 inches

    3. - trents replied to Ello's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Small Bowel Resection 12 inches

    4. - Ello replied to Ello's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Small Bowel Resection 12 inches

    5. - trents replied to Ello's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Small Bowel Resection 12 inches

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

    • Total Members
      132,831
    • Most Online (within 30 mins)
      7,748

    ATownCeliac
    Newest Member
    ATownCeliac
    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

    • trents
      You might consider asking for a referral to a RD (Registered Dietician) to help with food choices and planning a diet. Even apart from any gluten issues, you will likely find there are some foods you need to avoid because of the shorter bowel but you may also find that your system may make adjustments over time and that symptoms may improve.
    • Ello
      I wish Dr’s would have these discussions with their patients. So frustrating but will continue to do research. Absolutely love this website. I will post any updates on my testing and results.  Thank you
    • trents
      Losing 12" of your small bowel is going to present challenges for you in nutritional uptake because you are losing a significant amount of nutritional absorption surface area. You will need to focus on consuming foods that are nutritionally dense and also probably look at some good supplements. If indeed you are having issues with gluten you will need to educate yourself as to how gluten is hidden in the food supply. There's more to it than just avoiding the major sources of gluten like bread and pasta. It is hidden in so many things you would never expect to find it in like canned tomato soup and soy sauce just to name a few. It can be in pills and medications.  Also, your "yellow diarrhea, constipation and bloating" though these are classic signs of a gluten disorder, could also be related to the post surgical shorter length of your small bowel causing incomplete processing/digestion of food.
    • Ello
      Yes this information helps. I will continue to be pro active with this issues I am having. More testing to be done. Thank you so much for your response. 
    • trents
      There are two gluten-related disorders that share many of the same symptoms but differ in nature from each other. One is known as celiac disease or "gluten intolerance". By nature, it is an autoimmune disorder, meaning the ingestion of gluten triggers the body to attack it's own tissues, specifically the lining of the small bowel. This attack causes inflammation and produces antibodies that can be detected in the blood by specific tests like the TTG-IGA test you had. Over time, if gluten is not withheld, this inflammation can cause severe damage to the lining of the small bowel and even result in nutrient deficiency related health issues since the small bowel lining is organ where all the nutrition found in our food is absorbed.  The other is NCGS (Non Celiac Gluten Sensitivity or just "gluten sensitivity") which we know less about and are unsure of the exact mechanism of action. It is not an autoimmune disorder and unlike celiac disease it does not damage the lining of the small bowel, though, like celiac disease, it can cause GI distress and it can also do other kinds of damage to the body. It is thought to be more common than celiac disease. Currently, we cannot test for NCGS. Celiac disease must first be ruled out to arrive at a diagnosis of NCGS. Both disorders require elimination of gluten from the diet.  Either of these disorders can find their onset at any stage of life. We know that celiac disease has a genetic component but the genes are inactive until awakened by some stress event. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% develop active celiac disease. The incidence of NCGS is thought to be considerably higher. I hope this helps.
×
×
  • 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.