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

Iron Deficiency Anemia And Celiac Disease


TamaraG

Recommended Posts

TamaraG Newbie

- Hello all :) I'm newww. I have had many health problems like you all sense I was a child. I have been developing new symptoms and I'm tired of not knowing what is causing it all. I am afraid of going to the doctor and them dismissing me thinking I'm a hypochondriac! I don't want to waist their time.

- Here's my short list ;) I was diagnosed with Iron deficiency anemia 2yrs ago. I have had this sense I was a kid cause I have always felt tired, dizzy, and week and my heart pounds anytime i stand up. As well as I always ate ice and had to go to the doctor a lot with pin worms from eating endless amounts of yummy dirt lol. Around this time I was also diagnosed with depression.

- Not sure if this is related, I have also had chronic UTI's and chronic dehydration and sciatica and have been to the ER with headaches due to the left side of my brain swelling a few times. Now I'm developing IBS. My older brother has also been diagnosed with IBS. (Heard celiac disease can be in the family). Now after I eat anything I get terrible bloating and gas and a lot of times when I do need to use the bathroom I'm doubled oven in pain and trying to move quickly to the bathroom. This has become a way of life for me.

- These new symptoms started after I got married 3yrs ago and boy was it a hard start to say the least! I now have to go to therapy to control my irritability, anger and ongoing depression. Here's the rest: Pins and needles in my fingers and toes, gas, bloating, if not loose greasy stool then foul smelling pellet stool, never broke 109lbs no matter how hard i try, fatigue, periods went from heavy to hardly spotting (cant take birth control), tried having kids (no luck), ulcers in my mouth,back pain,shortness of breath, chest pains sometimes,swelling hands,legs and feet, and my enamel is wearing away more and more.

Does this sound like just anemia with some unrelated problems?

Thnx Tamara :)

if needed" 5'4

104lbs

VERY PALE :P


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



Celiac.com Sponsor (A8-M):



ShayFL Enthusiast

It sounds multi-faceted to me. Have you been tested for Celiac? Thyroid? Parasites? Iron/Ferritin lately? Vitamin D? B vitamins? Calcium and Magnesium?

I understand not wanting to go to a Dr. all too well. But if you have insurance, you really should take the time to try to find a good one that will help you. Osteopathic MDs are often good, Naturopaths if you have them.

You can get all of these blood tests on your own through places like directlabs and healthusa. But be warned, they are expensive and add up quickly. If you have the money, you can do this to find out about your nutritional status. But why not let insurance pay for it?

MaryJones2 Enthusiast

Anemia affects a lot of different functions in your body so it's possible that what you describle is realated to years of chronic anemia but it might be a good idea to have your other vitamin and mineral levels checked as well as your thyroid. I can't quite tell from your post if you are celiac and are on a gluten-free diet. If you aren't it might not be a bad idea to try it for a while and see how you feel. I think a lot of folks will also mention that you should cut out dairy initially too to relive some of the IBS symptoms.

There is a study out there worth reading on the topic of iron deficient anemia and celiac disease.

TamaraG Newbie

Anemia affects a lot of different functions in your body so it's possible that what you describle is realated to years of chronic anemia but it might be a good idea to have your other vitamin and mineral levels checked as well as your thyroid. I can't quite tell from your post if you are celiac and are on a gluten-free diet. If you aren't it might not be a bad idea to try it for a while and see how you feel. I think a lot of folks will also mention that you should cut out dairy initially too to relive some of the IBS symptoms.

There is a study out there worth reading on the topic of iron deficient anemia and celiac disease.

[/quote

To give some more info:

I'm a military spouce so i have the insurence its just that i can only see one doctor. And she looked at me for lupus once and literaly LOOKED AT ME and said hmm i dont think you have anything wrong with you. I was thinking about hitting the ER cause once again this one doctor is always booked and I cant seem to get in with her. I think the people in the ER would look at me like I was crazy haha. I have been checked for diabeties and my thyroird, it was all normal. They did say I was malnurished and under weight and to eat more. I eat a lot does not help. I think I will get my blood checked again maybe it is something like B12 deficiency. I just want an answer im sick of this the iron did not help me. And to top it off they didnt even care why I had this deficciency they just said I was severly anemic here take this and go home. haha lordy:P

CarlaB Enthusiast

Check out this symptom list and see if it rings any bells. Sorry you're so sick. I totally understand. :(

Open Original Shared Link

jerseyangel Proficient

Hi Tamera and welcome :)

I had just about all of the same symptoms as you do. I was frequently dizzy, tired and pale as a child. As an adult, I was severly, and persistantly anemic, had the tingling & numbness, the diarrea, nausea, difficulty getting pregnant, tooth enamel problems, chest pain (due to reflux, in my case), and many other symptoms. I was debilitated enough by age 48, that I had to quit my job.

Anemia is a very common symptom of Celiac--I would strongly suggest you do go to your doctor and tell them you would like the Celiac Panel run. You need the full panel:

Anti-Gliadin (AGA) IgA

Anti-Gliadin (AGA) IgG

Anti-Endomysial (EMA) IgA

Anti-Tissue Transglutaminase (tTG) IgA

Total Serum IgA

Don't change your diet prior to testing, you need to be eating gluten for the test to be accurate. Celiac is genetic, and many of us were diagnosed with IBS--sometimes for years--before finally finding out it was Celiac. It's very telling that your brother has also been diagnosed with IBS.

I don't know if you have Celiac, gluten intolerance that may or may not be associated with another condition, or something else entirely. I would start with the bloodwork and go from there.

Best of luck!

Ursa Major Collaborator

Despite what a lot of doctors think, there is no such a thing as 'just' anemia. There is always a cause for anemia, and it needs to be found. Otherwise you will be treating a symptom if you only treat anemia.

I agree, with your IBS (not a valid diagnosis either, since it is a collection of symptoms that have a cause that needs to be found) and anemia and everything else you describe, it could well be celiac disease.

And yes, another possibility (which doesn't rule out celiac disease even if you have it) is Lyme disease. A lot of the symptoms are the same.


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



Celiac.com Sponsor (A8-M):



nora-n Rookie

I agree with everyone that posted here, and want to add that I think that some doctors don't do anything unless you come back again. They maybe think your complaints are just a passing thing, and will only take you seriously if you keep coming back.

If the doctor is not gonna order any celiac tests, you can order your own gluten intolerance tests through Enterolab but you have to pay privately I think in your case.

Or, if you really cannot get the doctor to listen, and if you have no money to get testing done, you can go completely gluten-free and see if you get better. It took me 7 months and then the fatigue was gone one morning.

If you are celiac, you definitely will get osteopenia in the end and you might get some more related illnesses.

Look into lyme too. There is a young person here on the forum with anemia due to lyme too. Food intolerances too.

nora

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,962
    • Most Online (within 30 mins)
      7,748

    AlissaW
    Newest Member
    AlissaW
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.