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

New To The Forum


Socaljim

Recommended Posts

Socaljim Newbie

Hi all,

I'm new to the forum. I had never even heard of celiac disease till 2 weeks ago.

My Dr. said to find out what had been causing my diarrhea for the past several years

he would do some blood tests. He called me last week and said that I "tested positive

for all the anti-bodies for celiac disease" ?? I wasn't sure what that meant. He spelled

it out for me so that I could look up great sites like this one on the net. I had

read on one of the other sites that the blood test was only 90% accurate. So I was hoping for

that 10%. Come on 10%. Then I had my endoscope / colonoscopy today at 11:00am PST. The Dr took a biopsy but said by the look of my small intestine (it was scalloped) even with out the results of the biopsy he was 99.9% sure I have Celiac Disease. Come on .1% :) I had been putting off going gluten free till I had the results of the endoscope. It seems like it is going to be very hard for me. I eat a lot of bread and pasta. I have been reading a lot of your posts and I have come up some questions I hope some of you can help answer for me since my follow up with my main Dr isn't for a couple weeks.

1)How common is it in your siblings and offspring? Both my sisters, a Niece and a nephew have symptoms. I


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



Celiac.com Sponsor (A8-M):



VegasCeliacBuckeye Collaborator

Jim,

Welcome to the board. Feel free to ask any questions you may have about celiac disease.

To answer your questions:

My mom has celiac disease. it is hereditary. My brothers refuse to get tested (they aren't the brightest folks in the world at times).

Depending on who you talk to, the blood tests vary in accuracy. However, if you test positive, you are probably positive. The majority of problems associated with it are "false negatives" not "false positives".

CC is a big deal and you will become educated about it as time goes on. You can still make your kids sandwiches, just make sure you wash your hands before you eat. Think of gluten as poison. If it touches something you eat or put into your mouth, don't eat/touch it (without cleaning your hands).

I had the same symptoms you had. It gets better when you go gluten free. I used to love regular beer, pasta and bread too. However, I havent purposely ate the stuff in 10 years. You will get the hang of it. Everyone complains in the beginning :)

happygirl Collaborator

Welcome to the board!

It sounds like you will have the gold standard of diagnosis...positive bloodwork with a positive biopsy.

The current statistics are that 1 in 133 Americans have Celiac. About 1 in 20 family members of a Celiac have Celiac. All Celiac experts recommend that ALL first degree relatives are screened via the blood test, regardless of symptoms/no symptoms. I would urge your family members to be tested.

Keep in mind that your kids may never have Celiac. Or, they may "get" it, but don't have it right now. You can develop it at any time....so a negative now doesn't mean they won't ever have it. On the other hand, they might always be ok.

Unless you have a wheat allergy, you can be in the same room, make a sandwich, etc. But you would have to wash your hands, not use the same utensils on your food, not make a sandwich for you with the same "dippables" that now have bread crumbs in them, etc. Gluten free means gluten free, not gluten lite. It is best to eliminate any sources of gluten that you are aware of. There are many on the board that would be equally as sick as pre-gluten free as they were if they weren't careful about CC.

I hope this is a good start for you. If you are looking for a good book, I recommend the one in my signature. It's my favorite :).

Oh---and to replace wheat pasta, try tinkyada (a rice based) pasta. Its great, and you can't tell the difference. www.tinkyada.com for info on it, but you should be able to find it at many stores.

Happy you found this site.....stick around and let us know what we can do. Best of luck!!!

Lisa Mentor

Hey Jim,

Your brighter days are just beginning. You have to jump through a few hoops to get there, but this is a new beginning.

Start simple: Fish, meats, rice, potatoes, fresh veggies, fruits. Dairy may be an issue for a time being. (lack of villi, absorbing issues)

Your best best is to read, read and read. We have product information, product warnings, recipies... the list goes on and on.

Gluten free does not mean a loss of life style, you just have to tweek it a little and know what to tweek.

This source is wonderful. No question goes unanswered.

Welcome and always feel free to ask a question..that's why we are here.

rinne Apprentice

Welcome Jim. :)

Ditto to the answers above.

Crystalkd Contributor

I'm 5 weeks into the diet. The first couple were the hardest. I use the pasta that has already been suggested and love it. I don't eat a lot of bread right now but Whole Foods has a good gluten free seclection of bread. I seem to be eating corn tortillas more now and they hold me over fine. I'm still trying to figure out the lactose thing. I didn't have any for the first two weeks but have been eating more of it and I don't think my body likes it right now. I had "grey area" blood work and neg biopsy but have been doing great on the diet. As long as I avoid cross contamination I feel better than I've felt in years! Don't lament for the things you can't have just find new ways to create them.

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. - Scott Adams replied to GlutenFreeChef's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      11

      Blood Test for Celiac wheat type matters?

    2. - Jmartes71 replied to annamarie6655's topic in Super Sensitive People
      4

      Airborne Gluten?

    3. - Wheatwacked replied to GlutenFreeChef's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      11

      Blood Test for Celiac wheat type matters?

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

    • Total Members
      133,128
    • Most Online (within 30 mins)
      7,748

    Susan Wales
    Newest Member
    Susan Wales
    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

    • Scott Adams
      I'm not saying that some celiacs won't need it, but it should be done under a doctor's supervision because it can cause lots of problems in some people.
    • Jmartes71
      I also noticed I get debilitating migraines when I smell gluten, wheat and its not taken seriously when it affects one in every way.Im still begging to properly be heard.I also noticed tolerance level is down the drain with age and life changes. I have been told by incompetent medical that im not celiac or that sensitive. Diagnosed in 1994 by gi biopsy gluten-free ever since along with other lovely food allergies. Prayers
    • Jmartes71
    • Wheatwacked
      trents:  Why some can tolerate european bread but not american bread.     I take 600 mcg a day.  Right in the middle of the safe range.   Groups at Risk of Iodine Inadequacy Though though the NIH does not specifically list Celiac Disease in this group, they state: "Iodide is quickly and almost completely absorbed in the stomach and duodenum. Iodate is reduced in the gastrointestinal tract and absorbed as iodide [2,5]."  That would certainly include malabsorption of Iodine due to Celiac Disease with resultant Iodine Deficiency. Vegans and people who eat few or no dairy products, seafood, and eggs People who do not use iodized salt Pregnant women People with marginal iodine status who eat foods containing goitrogens Deficiencies of iron and/or vitamin A may also be goitrogenic [51] https://ods.od.nih.gov/factsheets/Iodine-HealthProfessiona   1  
    • trents
      Wheatwacked, are you speaking of the use of potassium bromide and and azodicarbonamide as dough modifiers being controlling factor for what? Do you refer to celiac reactions to gluten or thyroid disease, kidney disease, GI cancers? 
×
×
  • 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.