• Ads by Google:
     




    Get email alerts Celiac.com E-Newsletter

    Ads by Google:



       Get email alertsCeliac.com E-Newsletter

  • Announcements

    • admin

      Frequently Asked Questions About Celiac Disease   09/30/2015

      This Celiac.com FAQ on celiac disease will guide you to all of the basic information you will need to know about the disease, its diagnosis, testing methods, a gluten-free diet, etc.   Subscribe to FREE Celiac.com email alerts What are the major symptoms of celiac disease? Celiac Disease Symptoms What testing is available for celiac disease? - list blood tests, endo with biopsy, genetic test and enterolab (not diagnostic) Celiac Disease Screening Interpretation of Celiac Disease Blood Test Results Can I be tested even though I am eating gluten free? How long must gluten be taken for the serological tests to be meaningful? The Gluten-Free Diet 101 - A Beginner's Guide to Going Gluten-Free Is celiac inherited? Should my children be tested? Ten Facts About Celiac Disease Genetic Testing Is there a link between celiac and other autoimmune diseases? Celiac Disease Research: Associated Diseases and Disorders Is there a list of gluten foods to avoid? Unsafe Gluten-Free Food List (Unsafe Ingredients) Is there a list of gluten free foods? Safe Gluten-Free Food List (Safe Ingredients) Gluten-Free Alcoholic Beverages Distilled Spirits (Grain Alcohols) and Vinegar: Are they Gluten-Free? Where does gluten hide? Additional Things to Beware of to Maintain a 100% Gluten-Free Diet Free recipes: Gluten-Free Recipes Where can I buy gluten-free stuff? Support this site by shopping at The Celiac.com Store.

Iron
0

5 posts in this topic

I am newly diagnosed (1 month). I am iron deficient, as well as all the regular deficiencies Celiacs have. My dilemma is iron supplements cause constipation and that is what I am trying to get rid of. I just want to be "regular." My doctor advised me to wait to take iron until I am "regular" and take a multi vitamin, vitamin D, and Calcium. But I am worried about the iron. I am so tired and borderline anemic. I think iron would help, right? Any suggestions?

0

Share this post


Link to post
Share on other sites
Ads by Google:
Ads by Google:


I have that issue with iron pills, too. Didn't hurt me when I had diarrhea. as you heal, you will absorb the iron & B12 better. Make sure you take some sublingual ( put it under your tongue) B12. That helps your body use the iron you have. You might be able to just add iron rich foods to your diet. remember not to eat dairy with the iron food ( about 2 hours before and after eating the iron food).

Here's a list of iron rich foods

http://www.webmd.com/diet/iron-rich-foods

0

Share this post


Link to post
Share on other sites

If your physician is amenable, you can receive intravenous infusions to bring your iron/ferritin level up. This will help you feel better immediately, and once your gut heals, you should be able to absorb iron naturally. If not, you can receive the infusions on a regular basis. Some of us here on the Forum have done this. Your physician, however, may be unaware of this possibility (many are not), so you may need to educate him on its availability. If you have insurance, he can arrange for the infusion clinic at a local hospital to give you the iron infusions you need.

0

Share this post


Link to post
Share on other sites

Thanks for the suggestions. I am trying to be patient with feeling better. It is taking longer than I hoped (it has been a month - but lots of stuff I read said you could feel better in just 2 days of eliminating gluten). I just want to make sure I am doing everything right.

0

Share this post


Link to post
Share on other sites

In two days??! Wow, believe me, that would be extremely rare. It usually takes 6-24 months for most folks. My ability to absorb iron didn't return for four years.

0

Share this post


Link to post
Share on other sites
Ads by Google:


Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!


Register a new account

Sign in

Already have an account? Sign in here.


Sign In Now
0

  • Forum Statistics

    • Total Topics
      106,416
    • Total Posts
      930,442
  • Member Statistics

    • Total Members
      63,839
    • Most Online
      3,093

    Newest Member
    Cjm1985
    Joined
  • Popular Now

  • Topics

  • Posts

    • http://www.cureceliacdisease.org/faqs/ You can also find lots of information on celiac at the University of Chicago celiac site.  One test they suggest is the anti EMA antibodies.  I don't see that one listed in her results.  Probably because it is more expensive to do.  So they may have skipped it.  The other test they usually do is the total serum IGA levels, which is used to prove that the person's immune system actually makes IgA antibodies.  Some people don't make IgA antibodies, so the IgA tests are useless in them. It looks to me like she makes IgA though, if this is the serum IgA result. IgA 133 mg/dl Reference range 33-200 There are also gene tests they can do.  The genes indicate the possibility of developing celiac disease, not the automatic presence of celiac disease.  About 30% of people in the USA have one of the genes for celiac disease, but only about 1% develop celiac disease. Some of the celiac genes are associated with other autoimmune conditions besides celiac disease.  So there are lists of AI associated conditions with celiac disease.  Sometimes called related conditions. http://www.drschaer-institute.com/us/celiac-disease/associated-conditions-1051.html
    • Blood was drawn this afternoon... they said I could get results tomorrow or even the next day! I also have a GI appt scheduled for June 9th. I am so glad I will have at least some kind of answer pretty soon. I'll let you all know. Thanks again for being so helpful!
    • Thank you so much for those links, I will check into it. Her pediatrician told me this afternoon she is wanting to repeat the bloodwork since that one test was elevated. I'm relieved that her pediatrician didn't dismiss it like the other dr in the practice did.
    • http://www.houstonceliacs.org/ https://www.csaceliacs.org/csa_chapter_25.jsp You can check with these groups to see if they recommend any doctors in Houston.
    • I have been having issues with gluten for quite some time now and decided to go gluten free back in October, I finally got the celiac blood test a couple weeks ago and it came back inconclusive. My doctor referred me to a gastroenterologist who I saw today, she told me I'd have to eat gluten rich foods for 1 month and then have another blood test done....of it comes back negative she said I'd need to eat gluten another few weeks (up to another month) and then do a scope and biopsy....this would be hell on me as I have severe cramping and nausea when I am exposed to gluten.  I haven't actually eaten anything that is straight gluten like bread so I'm not sure what would happen. She gave me the option to hold off and continue my diet or go through 2 months of pure gluten exposure (and pain) my question is has anyone been faced with this? Should I just continue with my gluten free diet and assume I have it or is the diagnosis really that important? Doc says based on my symptoms and reactions I more than likely have it. 
  • Upcoming Events