Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

General Questions


xphile1121

Recommended Posts

xphile1121 Newbie

I'm a student in CO, and I'm writing my research paper on celiac disease. Right before the semester started, I started getting sick after almost every meal. I still haven't been diagnosed (I want to wait until August between classes), but with all my research, I'm about 95% sure that I have celiac disease. I was just wondering if someone could answer a few really basic questions that I could use in my paper.

1. How long did it take for you to realize you had the disease? How were you diagnosed?

2. Has living with the disease affected your family much?

3. Is it difficult to cope when you accidentally ingest gluten? Are the symptoms worse after being off gluten for a long while?

4. Are you able to enjoy many of the same restaurants, just different menu choices?

5. Is there anything positive that has resulted from having the disease?

I would appreciate any help I can get.


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



Celiac.com Sponsor (A8-M):



Lisa Mentor

Many of your questions can be answered by doing a search here. All have been discussed at length once or twice ;) . This is a great resource, with boundless information.

xphile1121 Newbie

Sorry, I should have specified that I need 1 person's answers to all the questions. It's supposed to be kind of like an interview format. I tried to interview local doctors and have had no luck, plus I tried to get ahold of Elisabeth Hasselbeck via her gluten-free website, and I just got a generic response saying that her schedule didn't allow her time to answer. Any help would be appreciated.

ravenwoodglass Mentor

You may want to check and see if there is a celiac support group in your area. If there is you could go to a meeting and interview folks directly.

1. How long did it take for you to realize you had the disease? How were you diagnosed?

45 years I was finally diagnosed with the aid of an allergist and an elimination diet.

2. Has living with the disease affected your family much?

Yes. My children were watching me die slowly which was very difficult for them. It also was a contributor to the destruction of my marital relationship.

3. Is it difficult to cope when you accidentally ingest gluten? Are the symptoms worse after being off gluten for a long while?

Yes and yes.

4. Are you able to enjoy many of the same restaurants, just different menu choices?

Other diagnosed family members have had an easier time with this than I have. I have not been to a restaurant in years.

5. Is there anything positive that has resulted from having the disease?

Yes, I no longer live in pain and have seen many associated disorders go into remission.

OptimisticMom42 Apprentice
Hi, I know you only needed one interview but I wanted make sure that you understand that the hard work that has been done by people like Ravenwoodglass has made life so much easier for those of us who came latter.

1. How long did it take for you to realize you had the disease? How were you diagnosed?

Within weeks of seeking a Dr's advise. A co-worker and fellow celiac recognised it first and the immunologist agreed after the use of an elimination diet and repeated DH rash on elbows and knees when exposed to gluten.

2. Has living with the disease affected your family much?

They know a lot more about nutrition and miss some of thier old favorites that I haven't replaced yet.

3. Is it difficult to cope when you accidentally ingest gluten? Are the symptoms worse after being off gluten for a long while?

It's uncomfortable but it's less scary now that I know what is happening and how to respond. I've only been gluten free for about four months but my responces to gluten are refining. I can tell now when I get a small amount before I make myself really ill.

4. Are you able to enjoy many of the same restaurants, just different menu choices?

For now I'm staying clear of restaurants because I am still identifying intolerances like corn.

5. Is there anything positive that has resulted from having the disease?

Yes, I found a new hobby. I'm fascinated by the mind, body, nutrition connection. I love looking all this stuff up and finding little gems of information like that taking vitamin D can help my sensitive nose tolerate perfume and that gluten can cross the brain blood barrier causing anything from funny smells to epilesy and mental illness. Each person who researches and discusses this with another person who researches and ......... it's a positive thing, we are saving lives.

I would appreciate any help I can get.

You're Welcome

  • 4 weeks later...
LBethanyC Newbie

[EDIT: Just realized you only needed one. Oh well. Maybe it'll still do some good :P. Haha.]

1. How long did it take for you to realize you had the disease? How were you diagnosed?

I self-diagnosed myself long before I did the tests. Everything fit, and not eating gluten made me feel a hundred times better. Eating even a little would make me sick again. I was diagnosed by both my general doctor and a gastro who he brought in on my case. My blood tests came back negative twice, since I had cut gluten out for months before. We tried the old eat gluten, then not eat it, then eat it, then not eat it thing, and it convinced both doctors that I had Celiac. Then they diagnosed me.

2. Has living with the disease affected your family much?

Well, when I lived with my family, it did. It was very hard to get across to them that I couldn't have this, or I couldn't use that. My little sister even used to wave the food in my face and tease. However, none of them went gluten-free. My dad convinced himself he would for a few hours, after having a long discussion with me about what foods contain gluten, and how I felt after each reaction. He gets stomach problems too. But he went home that night and ate Bologna. Haha. Anyway, now I live on my own, and cook for myself, so they're free to do whatever they want. When I go to visit, which is rare, since they live 5 hours away (they usually visit me), I bring my own food and appliances, and cook my own meals in a dedicated area.

3. Is it difficult to cope when you accidentally ingest gluten? Are the symptoms worse after being off gluten for a long while?

It is very difficult for me to cope when I ingest it. I have always had a low self-esteem, but realized after cutting out gluten that it was all related to that, since I was constantly bloated. Whenever I ingest some, and bloat, I feel horrible about myself again. But once the reaction is over, I feel better again. For me, my symptoms became signicifantly worse after being off gluten for a while. Now even the tiniest crumb gives me a huge reaction.

4. Are you able to enjoy many of the same restaurants, just different menu choices?

I make a point not to eat out right now, as I am still healing. I would rather wait until I'm feeling better to test out restaurants, for fear of cross-contamination. But, of course, that is my own personal choice. It may never affect me, I just don't want to take the risk. Once I feel better, however, I will start trying to eat out at certain places, trying their gluten-free options.

5. Is there anything positive that has resulted from having the disease?

I lost all of my bloat weight, and started to feel a heck of a lot better when I cut out gluten :P. I don't eat any junk food anymore, or anything unhealthy really, so I have been eating very healthy, and that is undoubtedly great for my body. :).

Hope I helped! :).

LDJofDenver Apprentice

Hello xphile! First wanted to give you this link to the Denver Celiac Chapter (CSA chapter 17). Open Original Shared Link Aside from great info, past newsletters, etc., you may find an upcoming meeting where you could meet dozens of celiacs one-to-one.

1. How long did it take for you to realize you had the disease? How were you diagnosed?

Probably had it my whole life, but REALLY knew something was worse (terrible downhill slide, medical problems) past 5-6 years. Was diagnosed last year after 10 years of ASKING my doctor to test me because my adult son had been diagnosed with it. I changed doctors last year (out of immense frustration) and after new doc ruled out a bunch of other things he had in mind, he ordered blood tests for celiac disease. They came back positive.

2. Has living with the disease affected your family much?

Not really, it's just my husband and I and he's very careful. We have his and hers cutting boards, etc. But I catch him monitoring guests when we're preparing food/drinks, "no, you can't use that spoon in hers" etc. He's not a big bread eater, so that helps.

3. Is it difficult to cope when you accidentally ingest gluten? Are the symptoms worse after being off gluten for a long while?

To part A, yes at times. Feel nauseous, get stabbing belly/abdominal pains, and usually have to go to the bathroom several times. part B, oh my God yes! A&B: The glutening doesn't end that day, usually get all belly-swollen like I've gained 10 lbs overnight - that stays with me another week, sometimes two.

4. Are you able to enjoy many of the same restaurants, just different menu choices?

Yes, some. Found safe choices at my favorite Mexican restaurant Went early on an off-night, and so I could ask about food preparation and ingredients and together we came up with a few things. Same at a little Italian place we go to. And have since found quite a few that actually publish their own gluten free menu.

5. Is there anything positive that has resulted from having the disease?

Absolutely. My health is beginning to return. I sleep like I'm sleeping and not like I'm in a near-death coma :lol: My skin is WAY healthier, and healthier looking. And most of all, now I know what I've got and I can do something about it.


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



Celiac.com Sponsor (A8-M):



hannahp57 Contributor

Hello i thought i might give another experience. for reference purposes i'll tell you about me first. i am a caucasian famale. i am 5'8" and weigh about 125.

now my celiac background:

1. I suffered symptoms throughout middle school and my first two years of high school. My symptoms got much worse at the end of my sophomore year. I went from 135 pounds to just over 100. My doctor told me it was acid reflux. the prescribed nexium did nothing. then my doctor went to a conference and heard about celiac disease. He came back with an info packet and told me this was my diagnosis. he then let me go about my business for a month then had me come back in. my symptoms had lessened slightly and i had gained five pounds back

2. It has affected my family some. we now spend quite a bit more on groceries and we have to be much more careful in the kitchen. as far as our daily lives though, i notice more differences than my husband does

3. It is very hard to cope when i acciedentally ingest gluten. first off the pain is overwhelming. secondly bacuse i blame myself as i am the one who is responsible for making sure foods are safe. i have definitely become more sensitive over the last three years ( i was diagnosed at 16 in july, i am now nienteen and this past month was 3rd anni! )

4. I have enjoyed a couple of restaurants. however, i have been glutened by restaurants twice, despite the menu option being listed as a safe choice for Celiacs and a discussion about my allergies to my server

5. There is a lot of positive from this diagnosis for me. i had never felt good before and just thought that was normal. too much info maybe but i had never experienced my digestive system functioning normally before this diet. now i also eat healthier and am more aware of what goes in my mouth. i also discovered i am allergic to MSG and it gives me quite a few problems.

Well maybe that was unnecessary but now you can maybe have a couple of comparisons. you can show how some are self-diagonosed, some diagnosed through tests, and some (like me) have doctors that hand them a piece of paper and send them on their way :P good luck!

shendler Rookie

1. How long did it take for you to realize you had the disease? How were you diagnosed? For at least 5 years I remember getting sick after every meal but within the past year it has gotten a lot worse. My test results were not conclusive in either direction and my doctor suggested going on a gluten free diet to see if it gets better.

2. Has living with the disease affected your family much? Nope.

3. Is it difficult to cope when you accidentally ingest gluten? Are the symptoms worse after being off gluten for a long while? It sucks to accidentally ingest gluten and for sure the symptoms get worse with time.

4. Are you able to enjoy many of the same restaurants, just different menu choices? No. I hate eating out now and would much rather prepare my own food. Besides having celiac I'm allergic to milk, eggs, certain fishes, certain meats so it makes eating out very challenging.

5. Is there anything positive that has resulted from having the disease? Feeling better and knowing I'm not insane.

belaugh86 Newbie
I'm a student in CO, and I'm writing my research paper on celiac disease. Right before the semester started, I started getting sick after almost every meal. I still haven't been diagnosed (I want to wait until August between classes), but with all my research, I'm about 95% sure that I have celiac disease. I was just wondering if someone could answer a few really basic questions that I could use in my paper.

Hello,

I'd be happy to answer your questions!

1. How long did it take for you to realize you had the disease? How were you diagnosed?

-I have had neurological symptoms since childhood such as moodiness, depression, brain fog, heightened emotions, trouble concentrating, cystic infection, cystic acne, and digestion problems. I have been tested once for Celiac and it came back negative. Doctors never recommended it - I had to ask for the test. I have self-diagnosed based on my symptoms along with a food journal of reactions to certain foods. I am convinced I am wheat and dairy intolerant as well as intolerant to many other grains, additives, etc.

2. Has living with the disease affected your family much?

-My Mother has celiac also, and has also never been tested "positive" for it. She knows because she retains a large amount of water and has horrible stomach pain/gastrointestinal side effects when she ingests a little gluten.

My family who is not gluten intolerant (brother and sisters) are supportive, but most of the time people don't understand the importance/significance of the disease unless they have it themselves. It takes a lot of explaining and educating, showing lists of exactly what foods we can't eat, etc. I remember being really upset for my last birthday because one of my family members bought me a torte that had gluten in it and didn't think to check for it. My boyfriend had no idea about the disease before he met me, and he has been supportive in making sure gluten containing foods stay out of the house when possible.

3. Is it difficult to cope when you accidentally ingest gluten? Are the symptoms worse after being off gluten for a long while?

-If I am doing really well and haven't come in contact with gluten, I can tell instantly if I've accidentally ingested some. The other day I ate some thai food that had gluten and I was foggy, irritable and extremely fatigued the following day. I recover pretty quickly though, as long as I abstain from eating at restaurants (I never know what's really coming in contact with my food) and cook meals at home for the days following the incident. I have also tried to enjoy beer, thinking that the alcohol and fermentation may have destroyed the gluten protein, but to no avail. I always have some type of reaction if I drink beer/liquor.

4. Are you able to enjoy many of the same restaurants, just different menu choices?

-Honestly, no. This may just be my problem, but I have tried to adapt and order meat and veggies or salads but a lot of times I know my food has come in contact with sauces or even frying pans and utensils that have been contaminated with gluten. I can tell by the way I feel after eating the meal within a few minutes to hours and especially the next day. I think the worst was when I woke up and couldn't hear out of my left ear!

5. Is there anything positive that has resulted from having the disease?

-Yes - I have lost a considerable amount of weight and gained much more insight about nutrition. For me personally, I have done a lot of research not just regarding gluten, but also foods that cause inflammation and other health problems. I went from a weight loss "plateau" of 165 pounds down to 150 pounds when I decided to go gluten free within just a couple of months. I think it was simply based on the fact that I not only strive to eat healthy, but also because Celiac disease pretty much nixes fast food for the rest of your life. Hardly anything at fast food chains is safe, and that was where I was eating at least a few times a week before my self diagnosis.

Hope this helps and I love answering the questions. :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,303
    • Most Online (within 30 mins)
      7,748

    Mary Rise Up
    Newest Member
    Mary Rise Up
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)

    • There are no registered users currently online

  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Wheatwacked
      How high is too high?  I take 10,000 IU vitamin D3 every day.  My blood is stable at 80 ng/ml (200 nmol/L).  Even at 10,000 a day it took 8 years to raise it to 80.  Higher levels of 25(OH)D in blood can moderate the autoimmune attack.  Vitamin D Is Not as Toxic as Was Once Thought Lower vitamin D levels have also been associated with increased OCD symptom severity.  This is a most dangerous popular belief. As mentioned you are suffering from vitamin and mineral deficiencies.  Part of the recovery, that is never explained by doctors, is replenishing your deficits.  Celiac Disease is a disease of malabsorption.  The Western diet is a diet of deficiency.  That is why many processed foods are fortified.  Gluten free foods are exempt.   "I’ve been completely asymptomatic since diagnosis."  There are 200 symptoms that can be caused by Celiac Disease and the malabsorbtion it can cause.     • "Floating, undigested stools for over a year now. Dont think its related to celiac as it was like this since im 17 and not 13-16( i got diagnosed at 13). " Many are misdiagnosed as gall bladder disease.  Choline is needed to create the bile salts needed to digest fat.  90% of our population is deficient.  Eggs and beef are the best source.  The RDA (minimum daily allowance is 500 mg to 3500 mg daily.  One egg has 27% DV.  Broccoli, chopped, boiled, drained, ½ cup only has 7%.  Low choline can cause Non Alcoholic Fatty Liver Disease.   Choline and Risk of Neural Tube Defects in a Folate-fortified Population; Could we be overlooking a potential choline crisis in the United Kingdom?;   Choline was formerly called vitamin B4.  I prefer phoshphatidyl choline for supplementation as it is the form we get in food.   • Chronic back pain started gradually, worsens with movement, lots of cracking/popping sounds.  Vitamin D deficiency may be linked to chronic back pain, But I took levothyroxine for slightly low FT4 levels.  I supplement Iodine by taking Liquid Iodine.  50 mcg per drop.  The RDA is 150 mcg to 1000 mcg in the US.  In Japan it is 150 mcg to 3000 mcg.  I take 600 mcg a day. Since 1970 the intake of iodine has decreased in the US by 50%.  Hypothyroidism has increased 50%.  Insufficient iodine leads to the thyroid gland working harder to produce these hormones, and if it cannot keep up, hypothyroidism can develop, according to the Mayo Clinic.   Iodine Insufficiency in America: The Neglected Pandemic.   I see improvement in muscle tone, healing, brain fog since taking the Liquid Iodine.  I could not eat enough seaweed. B1 stops the cramps in my feet B6 speeds up gastric empying and works on my freezing toes at night.  250 mg several times a day sometimes.  Also seems to be helping bowel regularity. 5 mg Lithium Orotate helped me with overthinking.   10,000 IU vitamin D to control autoimmune, mental health. 500 mg Thiamine - neurologic symptoms 500 mg Nicotinic Acid - increase capillary blood flow 500 mg Pantothenic Acid - creates energy from glucose Krebs Cycle 1000 mcg B12 - creates hemoglobin for oxygen transport 500 mg Taurine - essential amino acid, a powerful antioxident that we make indogenously so it is officially labeled "Conditional Essential" as Choline used to be, but not enough when sickness increases inflammation. reduces Reactivite Oxygen Species (ROS are are free radicals.). 840 mg Phosphatidly Choline x 3 - essential for fat digestion, gall bladder, liver, brain fog, cell membranes, prevent congenital spinal defects (along with B6, B12, folate, Taurine. Iodine - muscle tone, testosterone, hyper and hypo thyroid, slow healing.  600 mcg of Liquid Iodine.  Sometimes twice a day, usually added to a drink.
    • Scott Adams
      I completely understand the frustration of finding reliable gluten-free ingredients—it's exhausting when trusted products disappear or companies don't respond to safety inquiries. For teff flour in bulk, check out Azure Standard or Bulk Foods; both often carry gluten-free grains in larger quantities and clearly label dedicated facilities. For soy flour, Anthony's Goods tests for gluten and offers bulk options, though always verify their current certifications. For beans, peas, and lentils, Palouse Brand is a great choice—they're GFCO-certified and transparent about their farming practices. As for lentil elbow macaroni, Explore Cuisine offers similar pastas, though cross-contact policies vary. When companies don't respond, I lean on third-party certifications (GFCO, NSF) or stick with brands like Jovial or Edward & Sons that prioritize allergen safety. It's a constant hunt, but hopefully these leads help! Have you tried local co-ops or ethnic markets for teff? Sometimes they stock bulk African or Indian brands with clear labeling.
    • Scott Adams
      Beans in desserts are a fantastic way to add moisture, structure, and protein while keeping recipes gluten-free. Black bean brownies are a classic, but other beans like adzuki and pinto can also work well—adzuki beans are naturally sweet and often used in Asian desserts, making them great for cookies or cakes. Lentils, especially red lentils, blend smoothly into batters and can replace flour in recipes like blondies or muffins. Since you’re allergic to chickpeas, you might try navy beans or cannellini beans for a milder flavor in vanilla-based desserts. For less crumbliness, blending cooked beans into a paste helps bind the dough, and adding a bit of xanthan gum (if tolerated) can improve texture. If you’re experimenting, start with recipes that replace half the flour with bean purée before going fully flourless. Have you tried using aquafaba (bean liquid) as an egg substitute? It works wonders in gluten-free baking too!
    • lmemsm
      This may make you feel better about cross-contamination: https://nationalceliac.org/celiac-disease-questions/do-i-need-new-designated-pans-plates-and-utensils/ https://theceliacscene.com/rethinking-cross-contamination-no-need-to-be-so-careful/ I use Tom's of Maine or a toothpaste that states it's gluten free.  I have allergic reactions to some toothpastes so some of the toothpastes in health food stores are usually safer for me. They're typically gluten free as well. Spices can contain cross-contamination from gluten.  There are a few lists online of spices that are safe for celiacs.  I also grow my own herbs and use them in place of store bought when I can.  I think Badia lists their spices as gluten free and Spice Lab has some gluten free too. Knitty Kitty has a great point about nutritional deficiencies and B vitamins.  I got a lot of aches and pains when I got off gluten.  I tried to replace wheat with other healthy grains like teff, buckwheat and sorghum.  Limiting one's diet too much and not getting enough vitamins, can make someone feel worse.  A lot of the gluten free foods in the stores are made with lower quality ingredients than the wheat varieties.  I try to replace all my foods with homemade options.  Then I know the quality of the ingredients and which vitamins I may be high or low in.  Probiotics or prebiotics can help with bathroom issues.  Better to get them in foods if possible and not pill form.  My doctors keep recommending magnesium too.  It's not supposed to be taken alone, but they don't seem to care about that.  It's easy for vitamin D to be low too.  That was another thing doctors told me to take.  Unfortunately, they didn't monitor it and it went too high.  Again, better from natural sources like food and sunlight.  However, supplementing can help if you're not getting enough.  Some sources say to take D with K2.  You may want to have iodine levels checked.  If you add iodine, make sure to get sufficient selenium for thyroid.  You can get iodine naturally in most seaweed.  Nori may also be one of the few non-animal sources for B12.  Brazil nuts are a good source of selenium and you only need a few a day to meet RDA.  Some brands of nuts specifically say gluten free.  Unfortunately, there are issues with Brazil nut production and they're much harder to find this year. The more you can vary your diet the better.  One study said aim for at least 30 different foods in a week.  You might want to try kiwi fruit.  There were some studies that said eating kiwi improved mood.  It also has a covering which most people don't eat, so that should protect what's inside from contamination. I've limited my diet quite a bit over the years because of migraines, so I know how uncomfortable it can be finding safe foods.  However, I'm afraid limiting diets like that may actually be causing more harm than good.  It's something I'm trying to work on.  I keep trying to expand the number of foods I eat and my recipe repertoire.  I made a list of brands of foods that I've found that are gluten free so I have a guide when I'm shopping.  
    • knitty kitty
      Hello, @Dora77, I agree with you that your doctors aren't very knowledgeable about Celiac Disease.  My doctors didn't recognize nutritional deficiencies either.  I became very deficient in vitamins before I was diagnosed, so having experienced similar, I understand what a difficult time you're having.   Poor absorption of essential nutrients is caused by the damage done to the intestines by Celiac Disease.  The gluten free diet can be low in essential nutrients, so supplementing to boost your absorption is beneficial.  New symptoms can develop or worsen as one becomes more and more deficient.   There's eight essential B vitamins that our bodies cannot make, so they must come from our food and supplements.  These eight B vitamins work together, like instruments in an orchestra.  They need to be supplemented together with essential minerals like magnesium.   Deficiencies in the B vitamins can have overlapping symptoms.  Some symptoms can be traced to specific B vitamins.  OCD can be traced to low Pyridoxine Vitamin B 6.  Yes, I had OCD and washed my hands until my skin cracked and bled.  ADHD symptoms can be traced to low Thiamine Vitamin B 1.  ADHD is something one is born with.  People who are born with ADHD have a metabolic problem with getting sufficient thiamine into their brain cells.  People who develop symptoms of ADHD later in life are more likely to be low in Thiamine.  The same symptoms appear if one is not getting sufficient thiamine from the diet.  Yes, I developed symptoms of ADHD.  These symptoms improved and disappeared after supplementing with Thiamine and the other essential nutrients. I was diagnosed with Type Two Diabetes.  99% of diabetics of both types are deficient in Thiamine because our kidneys don't re-absorb thiamine properly.  Thiamine is needed to make insulin and digestive enzymes in the pancreas.  Poor digestion (floating, undigested stools) can result with insufficient pancreatic enzymes.  The gall bladder (upper right quadrant) needs thiamine to make and release bile which also helps with digestion.  Constipation is also a symptom of Thiamine and magnesium deficiencies.  The thyroid is another organ that uses lots of Thiamine, too.  Low thyroid hormones can be due to insufficient thiamine, selenium, iron, and iodine.  Swelling of hands, face and feet are also symptoms of thiamine insufficiency.   Our bodies use thiamine to make energy so organs and tissues can function.  Thiamine cannot be stored longer than three weeks.  If our stores are not replenished every day, we can run out of Thiamine quickly.  If we do get some thiamine from our diet, symptoms can wax and wane mysteriously, because a twenty percent increase in dietary thiamine causes an eighty percent improvement in brain function and symptoms.  Thiamine interacts with all the other vitamins in some way.  Many other vitamins and their metabolic processes won't work without thiamine.  In Celiac Disease you are apt to be low in all the essential nutrients, not just thiamine, but thiamine deficiency symptoms may appear first. Talk to your dietician about eating a nutritionally dense gluten free diet.  Keep in mind that processed gluten free foods do not contain sufficient vitamins to be useful.  Processed gluten free foods are filled with saturated fats and excess fiber (that could explain your constipation).  Dairy products, milk and cheese can cause problems because Casein, the protein in dairy, causes the same autoimmune reaction that gluten does in some.  Your current restricted diet is dangerous to your health.  I followed the Autoimmune Protocol Diet (Dr. Sarah Ballantyne).  It's a Paleo diet that promotes intestinal healing.   Discuss with your doctors about correcting nutritional deficiencies as soon as possible.   Interesting reading... https://pubmed.ncbi.nlm.nih.gov/34165060/ https://pubmed.ncbi.nlm.nih.gov/21816221/#:~:text=Lipid-soluble thiamin precursors can,and attention deficit%2Fhyperactivity disorder.
×
×
  • Create New...