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

Just A Few Questions


karma

Recommended Posts

karma Newbie

Hello. I was just tested for Celiac, and the results came back borderline. I was a little confused has to what this meant? I called the advice nurse at kaiser and she said I should quit eating gluten soon as possible. I have been suffering from ibs for the past two years and a nurse friend of my mothers told me to get tested for Celiac. So can anyone let me know of any books that can be useful to me? When reading lables for food should I be looking for Gluten or Wheat? Thanks any help, advice, or knowledge is appreciated.

Thanks Again,

Karma


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



Celiac.com Sponsor (A8-M):



hez Enthusiast

Welcome to the board!

I really do not have any suggestions for books on celiacs. I learned most things on this board and other web sites.

Welcome to the world of reading labels, everytime. I would look for both wheat and gluten on product labels. Keep in mind wheat free does not mean gluten free.

My advice would be to keep it very simple for the first month. This allows time to research what words to look for and what companies you can trust. Remember that meats, seafood (real stuff, not the fake), fruits and vegetables are gluten-free.

As far as the boaderline question, I am not sure how to answer. My mom came back the same way. However, she had already gone gluten-free before the test which can mess with the results. For her, she tried the diet and could not believe how much better she felt. She is gluten-free and has never looked back.

Hez

EBsMom Apprentice

Danna Korn's "Living Gluten Free for Dummies" book is great! It will get you started in knowing what to look for on labels, which ingredients are safe, which are suspect, etc. I also like "The Gluten Free Bible", but Korn's book is the best "primer." If I could only buy one book, that would be the one. Good luck!

Rho

Eriella Explorer

Hello,

As far as books, I didn't have time to read any when I got dx-ed, so I have no recommendations.

With labels, look for an allergy warning label that says wheat and read the ingredients to look for barley, wheat, oats, and rye (and then re-read them at home to make sure you didn't miss anything). Then, also look for hidden gluten in: modified food starch (could be corn, potato, or wheat-- if it doesn't specify, don't use), natural flavors, artificial flavors, malt, spices, and broth/stock. Wal-mart and Wegmans label their generic products as gluten-free if they are, so it can be an easy place to start shopping. Also, for the first month or two, try not to use gluten replacement products such as bread, cookies, and the like. They are hard to digest, a lot of them taste like cardboard (although there is some really good stuff), and expensive.

What I recommend eating is very simple meals of eggs, rice, vegetables, fruit, and meat/fish. Keep spices to only McCormick (they don't add gluten) and I'd recommend cutting out dairy because lactase, the enzyme that digests lactose, is produced in the same villi that celiac destroys. Therefore, most celiacs are lactose intolerant for awhile. After a month of healing and researching safe foods, start introducing processed foods.

Some of my essentials are: Nutrition Kitchen soybean pasta, Tinkyada brown rice, ortega taco shells, Namaste cake mixes, and tortilla chips.

My weekly shopping list (ie cheap, healthy, gluten-free food) is: broccoli, carrots, lettuce, peaches, banana, canned pinto beans (to make refried beans), canned tomatoes (for pasta sauce, although many jarred sauces are gluten free), brown rice, Nutrition Kitchen soybean pasta, eggs, cheddar cheese (naturally low lactose), soy milk, McCormick taco seasoning, Mission corn tortillas, pork chops/chicken breasts/beef.

I normally eat grilled meat, broccoli, and rice; soy or rice pasta with sauteed veggies or tomato sauce; or tacos/burritos for dinner (I george forman the meat to get out the fat, then finish cooking it with the seasoning and beans). For lunch I eat leftovers or rice and beans. Breakfast is either an omelet or fruit with peanut butter.

I hope this helps!

stargazer Rookie

Hi Karma, were you tested with just the blood test? A biopsy is more accurate. You should try the gluten free diet and see how you feel. As for the labels, you have to look for gluten free, not just wheat because gluten is found in wheat, barley, rye, and oats (through cross contamination). There are several good books about Celiac disease that I found at Barnes and Noble book store (I'm sorry I can't remember the titles, it has been a while since I looked at them). I hope you feel better. :)

happygirl Collaborator

Actually, the biopsy is not necessarily more accurate, as the damage can be patchy, not enough biopsies may be taken, etc.

Check out the book in my signature, written by one of the leading experts on Celiac Disease.

I would obtain a copy of your records so that you know which tests were run. There is a full celiac panel, but many drs only run part of it.

If you want a consult with a GI, he will probably recommend a biopsy, which means that you will need to continue to eat gluten until the testing is finished.

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.