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

Please Help Me Understand Celiac!


AmantHommes

Recommended Posts

AmantHommes Newbie

I have been trying to research this myself, but without much success from my time spent researching. I have recently been tested positive for Celiac by biopsy when doing an endo, my blood test came back as being "unable to test one way or another", which my GI doctor said happens in 1 in so many patients. Anyhow, so apparently, I have Celiac disease (I also have HyPOtyrhoidism) -- my question is -- is what does it do, if you ignore it, or even if you follow a gluten-free diet? I personally get SEVERE bloating, EXTREME pain in stomach, don't want to eat, can't sleep well, very bad heart burn, etc. BUT, does it cause any MAJOR issues, like heart, lungs, kidneys, brain, death, or anything like that, or what happens? If you FOLLOW your diet properly, do you still have outbreaks, problems, etc. or should it completely go back to how it would be without the disease? Just realllllly wish I understood this disease better -- because I keep failing to feel completely right. I have been spending about $1,000 per MONTH at the health food store to stock up on lots of gluten-free meals, foods and snacks -- but still get the nasty feelings sometimes (not always, but sometimes) -- I'm wondering if it is my thyroid pills, or what...? ALSO: even when I am FEELING good (no bloating, no upset stomach, feel hungry as normal, etc., my stool still remains softer than "perfect", and I poop too often -- maybe 2-4 times a day?)... Any and all advice is helpful -- because my doctor seems to not know as much as I would like -- he basically leaves it simply at "celiac disease, follow a diet period"... There seems to be much more to it than that.


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



Celiac.com Sponsor (A8-M):



Kamma Explorer

my question is -- is what does it do, if you ignore it, or even if you follow a gluten-free diet?

Here's what eating gluten can do to you in the long term if you are celiac:

1. Malnutrition

Even when patients are eating lots of healthy foods, they can become malnourished because the nutrients in the food are not being absorbed. Instead, the vitamins and nutrients are excreted in the stool. Malnutrition in untreated celiacs can cause weight loss, anemia, and vitamin deficiencies that may result in fatigue, stunted growth, neurologicial problems, and low bone density.

2. Decreased Calcium Levels and Osteoporosis

Calcium and vitamin D are lost in the stool instead of being absorbed into the body, leading to rickets in children, a type of kidney stone called an oxalate stone, as well as osteomalacia (softening of the bones), osteopenia, and osteoporosis. Interestingly, bone diseases can occur in people with milder forms of celiac disease who do not appear to have malabsorption. Bone density can actually improve once the gluten-free diet is started.

3. Lactose Intolerance

The enzyme lactase, which helps us digest the lactose in dairy products, is produced in the cells that line the surface of the villi in the small intestine. When the villi shrink and flatten in celiac patients who are eating gluten, lactase can no longer be produced and the patient develops lactose intolerance. Many celiac patients on the gluten-free diet find that once their intestines have healed, lactase production resumes, and they are able to tolerate lactose-containing products.

4. Cancer

According to most studies, long-standing untreated celiac disease leads to an increased risk of gastrointestinal cancer, such as lymphoma. Even with this increased risk, however, these cancers are rare in celiac patients. Some evidence suggests that in celiac patients who follow a strict gluten-free diet, the risk is no greater than in any other healthy person.

5. Neurological and Psychiatric Complications

Celiac disease has also been associated with depression, schizophrenia, anxiety, neuropathy, balance disorders, seizures, and severe headaches.

6. Miscarriage and Congenital Malformation of an Unborn Baby

Pregnant women who don't realize they have celiac disease (or who know they have it but don't follow a gluten-free diet) have nutrient absorption problems that can lead to miscarriage or congenital malformations, such as neural tube defects.

7. Short Stature

In children, undiagnosed celiac disease can lead to short stature. During childhood, it's crucial that children get the right nutrition to help them grow and develop. If they have unrecognized celiac disease and are eating gluten, the damage to their intestines will prevent nutrients in their food from being absorbed. Fortunately, if celiac disease is diagnosed in time, a gluten-free diet can sometimes help a child catch-up to a normal height.

Sources:

The National Institutes of Health.

pricklypear1971 Community Regular

And here's another bit....from what I've pieced together (as well as others), the longer you go without dealing with Celiac or any other ai disease, the more damage happens and the more likely you are to develop other ai diseases. Like Hashis. Or Lupus. Or arthritis. Or Sjogren's.

You may have another food intolerance - temporary or permanent. Many recovering Celiacs have a problem with casein/lactose (milk). Others have soy, corn, egg issues. Sometimes you just need digestive enzymes and probiotics to help your go system adjust.

Also, most of your shopping can be done at the regular grocery store- fruits, veggies, meats, legumes, herbs, spices. I visit the specialty stores for some items like flours, pastas, breads.

Is gluten-free worth it? Yes. Your health will probably continue to decline on gluten. Don't ever think it can't get worse...it can and does.

The first 6 months are a wild ride. Your body will go through many changes. My bm's took 6 months to find a new "normal", so don't worry unless you notice a pattern of extremes - extreme D, C.

Do you know if your hypothyroidism is caused by Hashimotos? Hashis patients have swings between hypo/hyper. It's normal. You may be experiencing this. Also, if you are just starting supplamentation it may take a while to get the dosage right. Finally, you may need a different type of med. I'd give it a while and see if it levels out.

Kamma Explorer

Yeah, it's kind of grim if you don't keep eating gluten free.

I second what prickly said: eat the true gluten free food of vegetables, fruit, meat and seeds. It's cheaper and much more nutritious. Also, processed foods that are labeled 'gluten free' are not gluten free. They are allowed 20 ppm gluten in their products. Recent testing of random products claiming gluten free have shown that they can and do exceed this 20 ppm up to 200 ppm.

These levels are for the U.S. I live in Canada and up until 2010, Health Canada was still developing their levels and requirements. I'm still looking for what they have come up with.

AmantHommes Newbie

I've had hypothyroidism for years (about 15-17 years) -- it runs in my family. But I recently read on this board that many thyroid medications have gluten, so I'm worried about mine -- I honestly do not even know the brand of meds I am on for my hypothyroidism, I will definitely find out. I have been consuming many, if not mostly, processed "gluten-free" products, such as boxed meals, microwave bowls, etc. etc. I went to the regular grocery store tonight and bought a few meals of fresh meats, lots of fruits, a few veggies (broccoli and fresh green beans) -- so I'll see how I feel after switching to the "fresher" meals you cook yourself. I do still consume a LOT of cheeses and dairy -- it doesn't seem to bother me and I hope it doesn't, because honestly I'd rather have cheese than chocolate. lol What Kamma said is very interesting -- does anyone know how celiacs consuming gluten has affects on their brain/neuro system? I mean, it is weird how it can affect your mood, memory, mind, etc etc... I found out tonight that coffee and Coffee-Mate liquid flavored coffee creamer are both gluten-free, I hope they truly are, because I was once a Starbucks addict, until this celiac stuff, so I would adore being able to brew coffee and pour in some liquid Caramel White Chocolate creamer!

Any other advice, suggestions, meals, foods, recipes, etc. would be highly appreciated. You all have been very very helpful!!!

ALSO: What is best to eat for fiber and legumes & seeds?

Can't wait for the "normal" bm's... I guess that will come once my body is completely content with what I am putting into it. lol

trents Grand Master

Basically, Celiac Disease is an "auto immune" condition, meaning the body attacks its own tissues. In this case, we know that gluten triggers the body's immune system to attack the lining of the small bowel. The lining of the small bowel, when looked at under a microscope, is normally a highly textured surface with lots of little finger-like projections sticking up into the open area of the bowel similar to how stalactites and stalagmites line the walls of an underground cave. This creates a lot of surface area for the absorption of nutrients from the digested food as it passes from the stomach on its way to the large intestine. The immune system's attacks when gluten is ingested by a person with Celiac Disease destroy this texture over time and wear down the finger-like projections, thus greatly reducing the surface area where nutrients are absorbed. Instead, they pass on to the large intestine and are eliminated from the body in stool.

Theoretically, once you eliminate gluten from the diet the lining (i.e, "mucosa") of the small bowel heals and symptoms disappear. In real life this doesn't always happen as neatly and completely as we would like. There can be and often are several reasons for this:

1. Age. Celiac disease research has shown that going gluten free brings healing much more reliably in young people. After about age 35 the rebound of the SB mucosa doesn't happen as well. Age also has an adverse effect on healing in many or most diseases so this is not surprising.

2. Permanent damage to other physiological systems because of the length of time it takes to diagnose Celiac disease. It takes on the average 10+ years to diagnose celiac disease. Thus, nutrient deficiencies and other spinoffs of celiac disease damage organs and nerves over time and this may not be entirely reversible. The best example of this is bone density loss.

3. The great challenge of eliminating gluten from the diet. Most of us, despite all our efforts, still get "glutened" now and then. It is said that it only takes an amount of gluten the size of a quarter of a grain of rice to precipitate an auto immune Celiac attack in some people. These attacks can last for days or weeks. Gluten is not only in foods but in personal hygiene products and medicines, things that go into our mouths that you would never suspect as containing wheat products.

4. And then there is something called "refractory sprue" or Celiac disease that does not go into remission when gluten is eliminated. It does not respond to the usual anecdote of going gluten free. A certain percentage of Celiacs have this form. Its a mystery and doctors don't know why.

Having said all that, it's easy to get discouraged and just give up on going gluten free. But its really the only choice you have if you're a Celiac. Even if it only brings partial improvement we all have an obligation to do what we can do. If we will do that perhaps we can head off some of the problems that would accrue if we just ignore it. And, there is a lot of research being done on cures for celiac disease these days. Sooner or later someone will come up with something that's pretty effective I think.

Hope this helps.

Adalaide Mentor

I used a lot of the processed foods as I transitioned to gluten free since having what was "normal" for me helped me to cope. The longer I'm gluten free the more of those I cut out of my diet. I find that I feel a whole lot better eating meat, fruits and veggies. I keep my processed foods to a minimum, pasta which I would have a terrible time giving up and cereal and cereal bars. (Cocoa Pebbles, yum!) I eat a fair amount of brown rice and beans. (Which oddly now that I'm gluten free don't lead to extreme biowarfare anymore.) I imagine that after only 3 short months I'm still healing as I don't feel anywhere close to totally better and my pooping habits are still out of whack, although I no longer have emergency trips running for the bathroom and don't ever go so long without going that I feel like I'm dying. I've only lost about 10 pounds over 3 months but the pants I haven't worn in over a year suddenly fit which confirms that my bloating is gone. My fog is lifted enough that I can make it through a day and still remember that morning, at least most of the time.

As for the worst ill effect? I have just started the process of dental work I need. I was diagnosed with scurvy some 5 or 6 years ago and my teeth are in such bad shape I need something like 20 thousand dollars worth of work done. (Which is steep but I need 4 or maybe even 5 implants to replace teeth that I can't get bridges for.)

So anyway, my point is that it gets better but it takes time. Many here have shared stories of years and years of healing, which can be discouraging at first. On the other hand, once you are more successful with your diet you should notice at least some little things pretty quickly, and that for me is what keeps me on the wagon on my worst days of temptation. I also tell myself that after watching a grandmother die of intestinal cancer that it is certainly not a way I want to die. At just under 5 feet tall she weighed under 50 pounds when she died, no one should ever suffer that and if we can all do something to prevent it we should.


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



Celiac.com Sponsor (A8-M):



celiacandglutenfreehealth Newbie

First, I had thyroid cancer before being diagnosed with celiac, and at that time had a partial and then full thyroidectomy, so I am required to take a daily dose of thyroid medication to replace actually having one. My thyroid medication has no gluten in it, and has never caused a moment of issue (thyroxin).

Second, with respect to legumes, etc. for fibre - most legumes are naturally gluten free. Chick peas, black beans, kidney beans - all excellent - so enjoy those chili recipes, etc. Quinoa is a wonder food, so good for you and naturally gluten-free, not to mention super-fast to cook after those long work days.

Good luck in adjusting - it definitely takes time, but you will feel very good once you do.

Kamma Explorer

does anyone know how celiacs consuming gluten has affects on their brain/neuro system? I mean, it is weird how it can affect your mood, memory, mind, etc etc...

ALSO: What is best to eat for fiber and legumes & seeds?

Celiac presents primarily neurological for me. For the past three years I have had constant vertigo, exhaustion, and ataxia that progressed. Balance issues and looking like I was doing what they call the 'drunken sailor walk'. My brain was fogged out and I started to slur my speech. I had head titubations (head bobbing) and seizures out in public. The ataxia was / is torso rotations. (My upper body would start rotating/swaying in uncontrollable circles). I also have hyperacuity so sounds are extremely loud and distressful.

Others present with the neuropathy which affects their peripheral nerves.

For fibre, prunes are great! Also apples and pears have the most fibre of all the fruits. They are awesome to eat. Chick peas are great and home made split pea soup is a cinch to make. Just google a recipe. You might want to check out the Raw Food Diet or Paleolithic Diet. I've been doing the Paleo diet for two months now and am very happy with the results - I feel great and it's simple to do. Also...you might want to try quinoa.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,559
    • Most Online (within 30 mins)
      7,748

    Valerie Ensor
    Newest Member
    Valerie Ensor
    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
      Oats naturally contain a protein called avenin, which is similar to the gluten proteins found in wheat, barley, and rye. While avenin is generally considered safe for most people with celiac disease, some individuals, around 5-10% of celiacs, may also have sensitivity to avenin, leading to symptoms similar to gluten exposure. You may fall into this category, and eliminating them is the best way to figure this out. Some people substitute gluten-free quinoa flakes for oats if they want a hot cereal substitute. If you are interested in summaries of scientific publications on the topic of oats and celiac disease, we have an entire category dedicated to it which is here: https://www.celiac.com/celiac-disease/oats-and-celiac-disease-are-they-gluten-free/   
    • knitty kitty
    • knitty kitty
      Hi, @Ginger38, I've had shingles in the past.  I understand how miserable you're feeling.   Not only do i have the chickenpox virus lurking about, I also have the cold sore virus that occasionally flares with a huge cold sore on my lip when stressed or exposed to gluten.  The virus lives dormant in the nerves on the left side of my face.  It causes Bell's Palsy (resulting in drooling).  The cold sore virus is also in my eye.  My eye swells up and my vision is diminished permanently whenever I have a flare, so it's of the utmost importance to keep flares away and treat them immediately if they do happen so I don't lose any more vision.   I take the amino acid supplement L-Lysine.  Lysine messes with the replication of viruses, which helps the body fight them off.   I haven't had an outbreak for several years until this year when exceptionally stressed and contaminated, it flared up again. Lysine has been shown to be beneficial in suppression of viruses like the cold sore virus (a herpetic virus), the chickenpox virus (also a herpetic virus), as well as the HIV virus, and even the Covid virus.   I also take additional Thiamine in the form TTFD (tetrahydrofurfuryl disulfide) because Thiamine has antiviral properties as well.   For pain, a combination of Thiamine (like TTFD or Benfotiamine or Thiamine Hydrochloride), with B12 Cobalamine, and Pyridoxine B6 have been shown to have analgesic properties which relieve pain and neuropathy.    The combination of Thiamine B1, Pyridoxine B6 and Cobalamine B12 really does work to relieve pain.  I take it for back pain from crushed vertebrae in my back.  This combination also works on other pain and neuropathy.   I usually buy a supplement that combines all three and also Riboflavin B2 called EXPLUS online.  However, it's made in Japan and the price with the tariffs added makes it really expensive now.  But the combination of Thiamine B1, Pyridoxine B6 and B12 Cobalamine (and Riboflavin B2) still work even if taken separately.   I can't take Tylenol or ibuprofen because of stomach upsets.  But I can take the vitamin combination without side effects.  However, you can take the three vitamins at the same time as other pain relievers for added benefit.  The vitamins help other pain relievers work better. I hope you will try it.  Hopeful you'll feel better quickly. Interesting Reading: Thiamine, cobalamin, locally injected alone or combination for herpetic itching: a single-center randomized controlled trial https://pubmed.ncbi.nlm.nih.gov/23887347/ Mechanisms of action of vitamin B1 (thiamine), B6 (pyridoxine), and B12 (cobalamin) in pain: a narrative review https://pubmed.ncbi.nlm.nih.gov/35156556/ Analgesic and analgesia-potentiating action of B vitamins https://pubmed.ncbi.nlm.nih.gov/12799982/ A Narrative Review of Alternative Symptomatic Treatments for Herpes Simplex Virus https://pmc.ncbi.nlm.nih.gov/articles/PMC10301284/
    • Mari
      I think, after reading this, that you areso traumatized by not being able yo understand what your medical advisors have been  what medical conditions are that you would like to find a group of people who also feel traumatized who would agree with you and also support you. You are on a crusade much as the way the US Cabinet  official, the Health Director of our nation is in trying to change what he considers outdated and incorrect health advisories. He does not have the education, background or experience to be in the position he occupies and is not making beneficial decisions. That man suffered a terrible trauma early in his life when his father was assonated. We see now how he developed and worked himself into a powerful position.  Unless you are willing to take some advice or  are willing to use a few of the known methods of starting on a path to better health then not many of us on this Celiac Forum will be able to join you in a continuing series of complaints about medical advisors.    I am almost 90 years old. I am strictly gluten free. I use 2 herbs to help me stay as clear minded as possible. You are not wrong in complaining about medical practitioners. You might be more effective with a clearer mind, less anger and a more comfortable life if you would just try some of the suggestions offered by our fellow celiac volunteers.  
    • Jmartes71
      Thus has got to STOP , medical bit believing us! I literally went through 31 years thinking it was just a food allergy as its downplayed by medical if THEY weren't the ones who diagnosed us! Im positive for HLA-DQ2 which is first celiac patient per Iran and Turkey. Here in the States especially in Cali its why do you feel that way? Why do you think your celiac? Your not eating gluten so its something else.Medical caused me depression. I thought I was safe with my former pcp for 25 years considering i thought everything I went through and going through will be available when I get fired again for health. Health not write-ups my health always come back when you're better.Im not and being tossed away at no fault to my own other than shitty genes.I was denied disability because person said he didn't know how to classify me! I said Im celiac, i have ibs, hernia, sciatica, high blood pressure, in constant pain have skin and eye issues and menopause intensified everything. With that my celiac nightmare began to reprove my disregarded disease to a bunch of clowns who think they are my careteam when they said I didn't have...I feel Im still breathing so I can fight this so no body else has to deal with this nightmare. Starting over with " new care team" and waisting more time on why I think I am when diagnosed in 1994 before food eliminated from my diet. P.s everything i went through I did write to medical board, so pretty sure I will continue to have a hard time.
×
×
  • 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.