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I Think I Have Celiac Disease


Cortneysmibro

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Cortneysmibro Rookie

Ok this post may be a bit long. I am pretty sure I have celiac Disease. I have been online researching for YEARS what might be wrong with me. I have though everything from narcolepsy to cancer. It all started about 4 years ago while I was pregnant with my third baby. But I just figured then that it was all just symptoms of pregnancy. The tiredness after eating, my heart would race and pound out of my chest. Constant headaches. My hands and feet would feel like they where asleep for no reason at all. I was constantly foggy headed and some times dizzy. But after the baby was born a few months went by and I was still not feeling better. Then I started having issues with my gallbladder. My mom who is diabetic told me to check my blood sugar. It was fine, yet I still got SOOO tired after eating. Over the next few years it got worse and worse. I had forgotten about the connection between eating and the tired spells since it was about 20 mins to an hour after I would eat that they would come on. Some times it was so bad that I could not keep myself awake no matter how hard I tried. And coffee only seemed to make it worse. I tried vitamins, getting more sleep, you name it. The only thing that seemed to help was when I tried a low carb diet to lose some weight. I am horribly over weight, and no matter what I seem to do I just can't seem to lose it. But I started feeling less tired and foggy and more like myself. My complexion cleared up and my skin seemed less read and blotchy. I got less headaches and woke up feeling refreshed in the mornings. But I started adding other low carb bread products and high fiber things back into my diet and slowly I started feeling crappy again. So after years and years of just going down hill and feeling worse and worse I finally went to the doctor. She tested me for some things and sent me to a therapist. They therapist says I am fine and thought I had a hormone problem. the doctor says no. I have reactive mono..... well the symptoms are getting much much worse.My joints are starting to hurt all the time. Most days I have HORRIBLE diarrhea. I get so foggy headed I can't keep a train of thought. My hand and feet are always cold and tingling. I am so so so tired all the time. No one believes that I feel bad. To everyone, including my husband I look fine. I keep telling him that there is SOMETHING wrong with me. That I just don't feel good ever. He thinks I am lazy,I eat to much and I am crazy :( But I'm not lazy. I am just exhausted. I want to try cutting out gluten and see if I feel better but I have a feeling it will be expensive and since my husband does not think I have a problem he will not want me wasting money on special food. I guess I could just stick to meat and veggies and fruit. I was just wondering if this sounds at all like that's what I may have? I have done SOOOO much research and this is the closest to how I feel. "sigh" I wish I could go to more doctors until someone listened to me. But I have no insurance. so I am stuck with the only doctor I can afford around here.


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kareng Grand Master

Did they check your thyroid? Are you anemic? Both things that make you feel tired & gain weight.

GottaSki Mentor

Hello and Welcome!

I don't have a great deal of time to post right now, but try not to lose heart when docs tell it is either stress, hormonal or depression. Trust your gut.

If you can have a celiac blood panel run before you give up gluten.

Your symptoms are very similar to mine and it took doctors along with me researching everything under the sun to find Celiac at 42 years of age...I was going to them with similar symptoms since my early 20s.

Hang in there...and trust your gut!

Cortneysmibro Rookie

Did they check your thyroid? Are you anemic? Both things that make you feel tired & gain weight.

thyroid is fine. That was one of the first things the doc checked out. I am anemic, but I have been since 2002. But that only explains the tired part. That does not answer everything else. :(

mushroom Proficient

You have not mentioned yet if your doctor has run a celiac panel for you. This is the first step in determining whether it is celiac disease. The celiac panel consists of the following tests:

Anti-Gliadin (AGA) IgA

Anti-Gliadin (AGA) IgG

Anti-Endomysial (EMA) IgA

Anti-Tissue Transglutaminase (tTG) IgA

Deamidated Gliadin Peptide (DGP) IgA and IgG

Total Serum IgA

If these tests have not yet been run you should ask your doctor to do them for you. If they have, can you post your results with the ranges the lab uses (if you do not have a copy of the results, you should get them - this should be done routinely for all lab testing). :)

Lori2 Contributor

Having a doctor run a celiac panel first would be preferable. However, with no insurance and an unsympathetic husband, going on the gluten-free diet is probably your only option. With your symptoms, I would certainly give it a try.

Gluten free products are expensive and are unnecessary. I personally can afford them, but do better without them. I stick to meats, vegetables, some fruit and then add rice, rice cakes, yogurt (I

Ninja Contributor

I've found the gluten-free products to be more of a nuisance than a help. Of course, it is nice to know they are there. Since, in science, there is claimed to be no such thing as true "zero" (in this area, anyhow), they allow a very small amount of gluten to remain in the product (<20pp). However, the more of that gluten-free food you eat, the more gluten gets into your system. This happened to me and it took awhile to figure it out. Luckily someone on here had posted about it!

Stick to the naturally gluten free whole foods; they're better on our bodies. :)

Good luck and don't be discouraged by the doctors. They say they've gone to medical school, but most seem to have just slept through it (lol). Either that or they need a "creative/outside the box thinking" degree in there as well.

~Laura


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Skylark Collaborator

You could definitely be celiac. It's common to have it come on in pregnancy. If you can get tested, you want to do that before you go off gluten. You have to be on a full gluten diet to get accurate results. If you feel better off gluten you're not going to want to eat the stuff for three months to be tested down the road. If testing is simply not an option go ahead and try the diet.

It's really easy to eat gluten-free on a budget. You just have to avoid the temptation to get the overpriced specialty breads and cookies. Rice, corn, and potatoes will be your starches instead. You can make totally "normal" dinners. Roast a chicken with some potatoes and serve with a salad (gluten-free dressing) and veggies. Your family probably won't even notice that it's gluten-free. Cook a couple extra potatoes and you can make eggs and home fries for breakfast the next morning. :)

A lot of family favorites like pot roast, beans and franks (I have yet to see gluten in a hot dog and Bush's has some gluten-free baked beans), homemade chili, stir-fry (use La Choy soy sauce or San J gluten-free tamari sauce), and chicken soup with rice are easy to make gluten-free. A big pot of vegetarian bean soup is only a few dollars to make and it makes a great meal served with homemade cornbread.

Here's my cornbread recipe.

Gemini Experienced

thyroid is fine. That was one of the first things the doc checked out. I am anemic, but I have been since 2002. But that only explains the tired part. That does not answer everything else. :(

The anemia that you have had since 2002 explains a lot more than just being tired. :o You know, I was anemic my entire adult life, from 18 to 46, when I hit the wall with Celiac and almost died. Yup....many a doctor blew me off and told me I was anemic due to heavy periods. The problem with that explanation is I never had a heavy period in my life, until I went through menopause.

I can understand your anger and frustration, believe me, so get back to a doctor and have them run the tests posted and make sure you gluten up for the testing. After they finish with that, go gluten-free immediately and give it a good 6 months because it takes that long for things to begin to get straightened out.

Your thyroid may not be alright either...they tend to screw that up too. It would be helpful if you had the results to post because it's common to have thyroid issues with Celiac also.

You don't need a doctors permission to eat whatever you want so if you choose a dietary trial, then go for it and don't look back. Dietary trials can be more revealing than many tests they do.

Cortneysmibro Rookie

Well I went ahead and just cut out gluten to see how I felt. I felt better almost immediately! What I thought was IBS, is GONE!!! No more headaches. I am not falling asleep or getting racing heart beats after eating! I am still very very tired and thirsty. My hands and feet are not tingling as much. I am still a bit fuzzy headed but I do not seem to feel as dizzy, or like the room is rocking when I turn my head. I did however discover that I must not be able to have soy either. I took a multi-vitamin this morning. With in 15 mins of taking it I was sicker then I had ever been from anything I have eaten. I started throwing up, got a horrible migraine, was so dizzy and fuzzy feeling. My body just tried to get everything out of it as fast as possible and in any way possible. :( It was horrible.It's been like 7 hours and I still do not feel 100% normal yet. SO I just learned that just because it says gluten free on the label does NOT mean that it will not make me sick. But other then that with or with out a diagnosis I think I will just stick to gluten free. I have not felt this good in years. I can only imagine how much better I will be a few more months down the road. I would love to go get tested but I honestly can't afford another doctor visit or more tests. I am already in dept to them for just shy of $1000.00 I can't keep adding more to it. I hate not having insurance. It stinks.

tom Contributor

Well I went ahead and just cut out gluten to see how I felt. I felt better almost immediately! What I thought was IBS, is GONE!!! No more headaches.

. .. .. ..

Awesome.

... I hate not having insurance. It stinks.

Reminds me to wonder how long the US will continue to be the only industrialized country that seemingly has no problem with putting ppl into your position.

It stinks.

Remember to vote this November, everyone. (Ok not *every*one)

tom Contributor

Forgot to comment on the multi-vit - some seem to have so many ingred it's tough to be sure which is a problem. Also, I've had them act differently depending on how much I ate w them.

That said, soy is pretty common in aggravating ppl w celiac.

Hope those other issues are improving.

Let us know. :)

Skylark Collaborator

That's great news that you feel so much better. B) I'd suggest you keep a food and symptom diary. That way if you react to something with a lot of ingredients or have delayed reactions you'll start to figure out a pattern.

adab8ca Enthusiast

Listen to your body. SO many of us were told "it's stress". I knew it wasn't freaking stress and that something was terribly wrong,so do you! I am SO happy that your gluten-free experience seems to be leading you in the right direction.

Many many healing hugs

AVR1962 Collaborator

Another thing that is not uncommon while pg is gestational diabetes. I had it with my 3rd child, made me quite sick. My iron levels were too low and my bllood sugar too high, not a good combo. Iron supplements and taking carbs out of my diet helped alot.

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    • catnapt
      thank you so much for your detailed and extremely helpful reply!! I can say with absolute certainty that the less gluten containing products I've eaten over the past several years, the better I've felt.   I wasn't avoiding gluten, I was avoiding refined grains (and most processed foods) as well as anything that made me feel bad when I ate it. It's the same reason I gave up dairy and eggs- they make me feel ill.  I do have a bit of a sugar addiction lol so a lot of times I wasn't sure if it was the refined grains that I was eating - or the sugar. So from time to time I might have a cookie or something but I've learned how to make wonderful cookies and golden brownies with BEANS!! and no refined sugar - I use date paste instead. Pizza made me so ill- but I thought it was probably the cheese. I gave up pizza and haven't missed it. the one time I tried a slice I felt so bad I knew I'd never touch it again. I stopped eating wheat pasta at least 3 yrs ago- just didn't feel well after eating it. I tried chick pea pasta and a few others and discovered I like the brown rice pasta. I still don't eat a lot of pasta but it's nice for a change when I want something easy. TBH over the years I've wondered sometimes if I might be gluten intolerant but really believed it was not possible for me to have celiac disease. NOW I need to know for sure- because I'm in the middle of a long process of trying to find out why I have a high parathyroid level (NOT the thyroid- but rather the 4 glands that control the calcium balance in your body) I have had a hard time getting my vit D level up, my serum calcium has run on the low side of normal for many years... and now I am losing calcium from my bones and excreting it in my urine (some sort of renal calcium leak) Also have a high ALP since 2014. And now rapidly worsening bone density.  I still do not have a firm diagnosis. Could be secondary HPT (but secondary to what? we need to know) It could be early primary HPT. I am spilling calcium in my urine but is that caused by the high parathyroid hormone or is it the reason my PTH is high>? there are multiple feedback loops for this condition.    so I will keep eating the bread and some wheat germ that does not seem to bother me too much (it hasn't got enough gluten to use just wheat germ)    but I'm curious- if you don't have a strong reaction to a product- like me and wheat germ- does that mean it's ok to eat or is it still causing harm even if you don't have any obvious symptoms? I guess what you are saying about silent celiac makes it likely that you can have no symptoms and still have the harm... but geez! you'd think they'd come up with a way to test for this that didn't require you to consume something that makes you sick! I worry about the complications I've been reading about- different kinds of cancers etc. also wondering- are there degrees of celiac disease?  is there any correlation between symptoms and the amnt of damage to your intestines? I also need a firm diagnosis because I have an identical twin sister ... so if I have celiac, she has it too- or at least the genetic make up for having it. I did have a VERY major stress to my body in 2014-2016 time frame .. lost 50lbs in a short period of time and had severe symptoms from acute protracted withdrawal off an SSRI drug (that I'd been given an unethically high dose of, by a dr who has since lost his license)  Going off the drug was a good thing and in many ways my health improved dramatically- just losing 50lbs was helpful but I also went  off almost a dozen different medications, totally changed my diet and have been doing pretty well except for the past 3-4 yrs when the symptoms related to the parathyroid issue cropped up. It is likely that I had low vit D for some time and that caused me a lot of symptoms. The endo now tells me that low vit D can be caused by celiac disease so I need to know for sure! thank you for all that great and useful information!!! 
    • trents
      Welcome, @catnapt! The most recent guidelines are the daily consumption of a minimum of 10g of gluten (about the amount found in 4-6 slices of wheat bread) for a minimum of two weeks. But if possible stretching that out even more would enhance the chances of getting valid test results. These guidelines are for those who have been eating gluten free for a significant amount of time. It's called the "gluten challenge".  Yes, you can develop celiac disease at any stage of life. There is a genetic component but also a stress trigger that is needed to activate the celiac genes. About 30-40% of the general population possesses the genetic potential to develop celiac disease but only about 1% of the general population actually develop celiac disease. For most with the potential, the triggering stress event doesn't happen. It can be many things but often it is a viral infection. Having said that, it is also the case that many, many people who eventually are diagnosed with celiac disease probably experienced the actual onset years before. Many celiacs are of the "silent" type, meaning that symptoms are largely missing or very minor and get overlooked until damage to the small bowel lining becomes advanced or they develop iron deficiency anemia or some other medical problem associated with celiac disease. Many, many are never diagnosed or are diagnosed later in life because they did not experience classic symptoms. And many physicians are only looking for classic symptoms. We now know that there are over 200 symptoms/medical problems associated with celiac disease but many docs are only looking for things like boating, gas, diarrhea. I certainly understand your concerns about not wanting to damage your body by taking on a gluten challenge. Your other option is to totally commit to gluten free eating and see if your symptoms improve. It can take two years or more for complete healing of the small bowel lining once going gluten free but usually people experience significant improvement well before then. If their is significant improvement in your symptoms when going seriously gluten free, then you likely have your answer. You would either have celiac disease or NCGS (Non Celiac Gluten Sensitivity).
    • catnapt
      after several years of issues with a para-gland issue, my endo has decided it's a good idea for me to be tested for celiac disease. I am 70 yrs old and stunned to learn that you can get celiac this late in life. I have just gradually stopped eating most foods that contain gluten over the past several years- they just make me feel ill- although I attributed it to other things like bread spiking blood sugar- or to the things I ate *with* the bread or crackers etc   I went to a party in Nov and ate a LOT of a vegan roast made with vital wheat gluten- as well as stuffing, rolls and pie crust... and OMG I was so sick! the pain, the bloating, the gas, the nausea... I didn't think it would ever end (but it did) and I was ready to go the ER but it finally subsided.   I mentioned this to my endo and now she wants me to be tested for celiac after 2 weeks of being on gluten foods. She has kind of flip flopped on how much gluten I should eat, telling me that if the symptoms are severe I can stop. I am eating 2-3 thin slices of bread per day (or english muffins) and wow- it does make me feel awful. But not as bad as when I ate that massive amnt of vital wheat gluten. so I will continue on if I have to... but what bothers me is - if it IS celiac, it seems stupid for lack of a better word, to intentionally cause more damage to my body... but I am also worried, on the other hand, that this is not a long enough challenge to make the blood work results valid.   can you give me any insight into this please?   thank you
    • trents
      The biopsy looks for damage to the mucosal lining of the small bowel from the inflammation caused by celiac disease when gluten is ingested. Once you remove gluten from the diet, inflammation subsides and the mucosal lining begins to heal. 
    • Theresa2407
      Our support groups in Iowa have tried for years to educate doctors and resource sites like this one.  We have held yearly conferences with continued education classes.   We have brought in Dr. Murray, Dr. Fasano, Dr. Green and Dr. elliott.  In those many years we may have had 2 doctors attend.  We sent them information, with no response.  I talked to my personal doctor and she said their training for Celiac was to show them a skinny man in boxer shorts and a huge stomach.  Saying if you see this, it is Celiac.  If it isn't in their playbook then they don't care.  Most call it an allergy with no mention of our immune system.  There is so much false information on the internet.  Then people don't understand why they can't get well and are acquiring more immune diseases. I mention this site to everyone.  Scott has working hard for the Celiac community.
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