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Newly Diagnosed And Starving...help Please


valeriek

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valeriek Apprentice

I was just diagnosed and I am lost. I cant even figure out how to use this site. I hope someone will get my message and help me. I am going to put up my email address because I dont understand how to see if any one responds to me. Any way what can I eat. I have been eating raw spinach for a week and I am starving. ok my email is

chrisvalk@nc.rr.com.....if someone could help me figure out this site I would be so grateful. :(


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Lisa Mentor

Valerie, so glad that you found us. ;)

Lisa

nikki-uk Enthusiast
I was just diagnosed and I am lost. I cant even figure out how to use this site. I hope someone will get my message and help me. I am going to put up my email address because I dont understand how to see if any one responds to me. Any way what can I eat. I have been eating raw spinach for a week and I am starving. ok my email is

Hi Valerie and welcome :)

Looks like you posted this message ok so your doing something right!!

It can feel terribly overwhelming at first,....but take heart!...it does get easier with time.

It's easier to keep things plain at first.

Plain meats, potatoes, veg, fruit and rice are all good starting points.

A key thing to staying gluten-free is to always read the ingredients, but suprisingly this will become second nature to you!!

I'm afraid as I'm in the UK I can't help with any lists of OK items (I'm sure someone will point you in the right direction)

Your knowledge of what's ok will build up gradually...until you find yourself AN EXPERT!! :D

You'll also become more adventurous with your cooking (plenty of recipes on here!)

Please, ask any questions you need to....there's a wealth of knowledge here

Good luck :)

blueeyedmanda Community Regular

Hi Valerie!

It is very overwhelming in the begining-but it gets much better. This board is such a great resource. Not only have I found the knowledge to start a new life but I found an amazing support group who are always here to help me.

I hope this helps a little. :)

elye Community Regular

Hi, Valerie!

Yes, it is overwhelming at first......I remember those days very well, and I am also a type one diabetic, so I went from one restrictive diet to the inclusion of another - -thought I could never do it. But Nikki is right....it absolutely gets easier. And again as Nik said, plain, unprocessed foods at first: meats, fruit and vegetables, rice, corn......when you step back a bit, there really is a lot of choice!

So glad you've found us here. This is a terrific site with SO many voices of wisdom and support. Ask any question - -there will always be someone here who can answer it! :)

ravenwoodglass Mentor
I was just diagnosed and I am lost. I cant even figure out how to use this site. I hope someone will get my message and help me. I am going to put up my email address because I dont understand how to see if any one responds to me. Any way what can I eat. I have been eating raw spinach for a week and I am starving. ok my email is

chrisvalk@nc.rr.com.....if someone could help me figure out this site I would be so grateful. :(

I am glad you found us. As mentioned fresh fruit and veggies, single ingredient frozen, plain rice, white or wild, fresh meats, chicken and fish, beans etc are all safe.

Some quick prepared foods that are safe are:

Dinty Moore Beef Stew (says it right on the can), Hormel makes some prepared roasts, beef and pork that are safe, they also say gluten free make sure they are the AuJus. Hormel also makes some luncheon meat that comes in a brown package, those are also marked gluten free. Rice Chex is gluten free and will say so on the box. This is a new formula so make sure your market does not carry the older ones. Most cereals are off limits because of the barley malt or added wheat starch.

Delmonte veggies and fruits are all gluten free. They also have some pasta sauces that are safe. I believe it is the meat flavor that are not.

If you live in an area that has a Wegmans market they label all their gluten free stuff so that makes it easy to shop.

Thai Kitchen rice noodles are safe, I love them. They also make some 'kits' that are gluten free, just make sure it says so on the box.

I hope this helps a bit.

RiceGuy Collaborator

Fortunately, most foods do not naturally contain gluten. Processed foods however, are a different story. As others have stated, you'll get the hang of it, and you've come to the right place for help!

Here is a list of many delicious gluten-free recipes:

https://www.celiac.com/categories/Gluten%252dFree-Recipes/


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Darn210 Enthusiast

Hi Valerie, welcome to the board . . . there are lots of caring people here with a lot of good information to share.

Here is a site that I found helpful

Open Original Shared Link

This is a list of companies that do not hide gluten ingredients in their labeling. By law, wheat has to be called out on the ingredient list. However, rye, barley and oats do not (when lumped into something like "natural flavors"). This list of companies will list rye, barley and oats so you can just read the ingredient list to determine if gluten is in the ingredients.

It can seem over-whelming at first, but you'll be surprised at how quickly you come up to speed.

valeriek Apprentice

ok I think I might have it figured out. But why last week when diagnosed I was like ....no big deal. Now I am sitting here crying like a baby. What is wrong with me? I am so hungry but when I try to eat I feel sick. I got mashed potatoes, green beans and corn from Boston Market and I tried to eat but felt sick. I really feel weird and dizzy and emotional. Thanks for all your help

Darn210 Enthusiast
ok I think I might have it figured out. But why last week when diagnosed I was like ....no big deal. Now I am sitting here crying like a baby. What is wrong with me? I am so hungry but when I try to eat I feel sick. I got mashed potatoes, green beans and corn from Boston Market and I tried to eat but felt sick. I really feel weird and dizzy and emotional. Thanks for all your help

Because you are in shock and you are mourning your "lost food" . . . it's a big deal and it's OK to be emotional - it will pass. My daughter was 6 when she was diagnosed and she didn't truly understand the ramifications . . . so being the good mother I am, I cried for her . . . I cried because she wasn't ever going to get to eat cheesecake and she didn't even like cheesecake :huh: and now that we are coming up to two years into this . . . it's pretty much "hell yes she can have cheesecake, I just have to make a little bit different crust!!!" . . . and by the way, she still is not interested in cheesecake :lol:

Mtndog Collaborator
ok I think I might have it figured out. But why last week when diagnosed I was like ....no big deal. Now I am sitting here crying like a baby. What is wrong with me? I am so hungry but when I try to eat I feel sick. I got mashed potatoes, green beans and corn from Boston Market and I tried to eat but felt sick. I really feel weird and dizzy and emotional. Thanks for all your help

Hi Valerie- Wecome and (((((HUGS))))

It's really tough at first. The first month I lived on peanut butter. It's probably the reality sinking in that you have a disease that won't go away- a lot to swallow since we can't swallow a pill and make it all go away. It's a lot to process.

Some suggestions that others have given you.

1. While you're healing, eat mellow. Make your own potatoes, rice, veggies and meat when you have the energy. Keep it plain so you don't have to worry about gluten. You could make a grilled chicken and rice with a veggie you like and just use some salt and butter.

2. Veggies, fruits, meats are all naturally gluten-free.

3. Eat frequentl, small meals because chances are your body needs t heal, recover and get nutrients.

4. Get outside and get some fresh air- if you feel up to it go for a walk. No matter what- do something nice for yourself EVERY day- a bath, a walk, buy yourself some flowers, a nice candle. And breathe!

5. Depending on where you live and when you're up to it- go to a Whole Foods, health food store and look at the gluten-free options- you will be cheered immediately.

Remember- you only have to do this one day at a time-heck, one meal at a time!!!!! And we ARE here! PM me or email me through the board ANY time. Best, Beverly

Darn210 Enthusiast
ok I think I might have it figured out. But why last week when diagnosed I was like ....no big deal. Now I am sitting here crying like a baby. What is wrong with me? I am so hungry but when I try to eat I feel sick. I got mashed potatoes, green beans and corn from Boston Market and I tried to eat but felt sick. I really feel weird and dizzy and emotional. Thanks for all your help

As far as feeling sick after eating at Boston Market . . . there is always the possibility of cross-contamination (called cc on this site) at restaurants. There is also a chance that you may be reacting to dairy. Many celiacs may have problems with dairy (lactose intolerance) . . . for most it is a short term problem until their intestines heal. If you notice problems when eating dairy, you may try a lactaid tablet or you may want to avoid dairy for a couple of months. The symptoms can be similar.

Durntootinnoglutin Rookie
ok I think I might have it figured out. But why last week when diagnosed I was like ....no big deal. Now I am sitting here crying like a baby. What is wrong with me? I am so hungry but when I try to eat I feel sick. I got mashed potatoes, green beans and corn from Boston Market and I tried to eat but felt sick. I really feel weird and dizzy and emotional. Thanks for all your help

Val....food is a deeply emotional factor, it's the stuff we are utterly dependant upon for life. To find there is something out of whack with the way your body can use it does make an emotional impact. Mostly it's fear. Fear of a great change or even dealing with the question if the quality of life will be so changed it won't be enjoyable anymore.

You CAN change, you CAN adjust, you CAN empower yourself, and you CAN enjoy living with it. Become a food warrior by educating yourself. This is a good place to do it.

Don't let this thing lick you when it is really a matter of adjustment, letting go of what harms you and replacing it with what is good for you.

If you can, talk yourself into gratitude, think, you have been diagnosed, you now have the means to better your condition then what it was before diagnosis.

There is a plethora of food out there awaiting you, and the creative combinations you can make of it, and the self reliance you will develope by taking charge of your own well being.

A pep talk? You betcha....am thinking a good many of the people here have suffered in varying degrees what you are feeling right now. I know i did. Don't just hang in there, start taking charge.

In the meantime a big thought hug to you.

Judyin Philly Enthusiast

WELCOME VALERIE

I see you found out how to work the forum and find your new 'helpers'

We've all been where and you are and I promise it does get easier with time and we're here to help.

I dito all others said.

My first piece of advice is try to cook simple at home and don't eat out until you have a least a few weeks under your belt.

My advice is 'keep it simple the first week or 2' with just simple meat, fish, vegs and fruits and try to not have dairy those first weeks

i know others have said this but if I'd done this in the beginning of my 3 1/2 years being here, i could have found out the things that really agreed with me and those that didn't.

hang in there.

that list of good companies is really helpful i think

Judy

mamaw Community Regular

Hi I just sent you a private e-mail to your addy.. Let me know if you receive it.

blessings

GF-Noob Newbie

Valerie...I was diagnosed last week.....we can be celiac buddies!

When I got the call from my doctor I:

1) Cussed....a lot. hahaha...it was obscene.

2) Started thinking of all the things I couldn't eat

3) Cried

I starved for about a day. Then I went to a natural food store and bought myself some gluten free snacks. And then I figured out what yummy things I can still eat (Heellloo chocoloate covered strawberries!)

I picked up some books about the disease and my diet...trying to learn as much as possible.

I'm stilled pissed though. hahaha. Especially when people say "It could be worse! At least you just have to change your diet!"

I want to punch them.....they can eat all the asiago bagels they want!!! They'd be crying too if they were in the same place.

Anyway....you are NOT alone. Let me know if you ever want to talk....maybe we can trade tips about what food is good and what sucks...etc.

*hugs* :)

DakotaRN Newbie

I very new at this too but once you get past the anger etc. , you will find there are a lot of wonder ful recipes available. I thought that I wouldn't be able to ever eat my favorite foods. That isn't true the recipes may be different but the end product is very good. I have tried recipes from this site and have really liked them.

Just take one day at a time. The support here is wonderful. Hang in there.

valeriek Apprentice
Valerie...I was diagnosed last week.....we can be celiac buddies!

When I got the call from my doctor I:

1) Cussed....a lot. hahaha...it was obscene.

2) Started thinking of all the things I couldn't eat

3) Cried

Hey Celiac Buddy

Wow you were just diagnosed last week like me. I know this really sucks. Believe me I cussed so much I think jesus came down and slapped my ass. Oh well. So where are you from. I live in Raleigh. I dont know how to add you as a friend. I can hardly figure out this website. So what do you eat now? I got some rice chex....yeh. They are actually good. Thanks for writing me.

I starved for about a day. Then I went to a natural food store and bought myself some gluten free snacks. And then I figured out what yummy things I can still eat (Heellloo chocoloate covered strawberries!)

I picked up some books about the disease and my diet...trying to learn as much as possible.

I'm stilled pissed though. hahaha. Especially when people say "It could be worse! At least you just have to change your diet!"

I want to punch them.....they can eat all the asiago bagels they want!!! They'd be crying too if they were in the same place.

Anyway....you are NOT alone. Let me know if you ever want to talk....maybe we can trade tips about what food is good and what sucks...etc.

*hugs* :)

GF-Noob Newbie

I'm from Chicago. I actually used to live in Atlanta and visited Raleigh before.

My george forman grill has been a life saver. I cook a few chicken breasts at a time with different seasonings. I cut it up and eat it in a salad (baby spinach with vinagerette) or maybe some rice. I let myself splurge on gluten free cookies too. I've spent time at the store just finding things I CAN eat and figuring out ways to still eat yummy stuff.

I had a company party today at my favorite pizza place...it was torture!!!! I was so tempted...but nothing could make me eat gluten knowing how awful it will make me feel.

I hope you are doing okay over there *hugs* You do have a trader joe's in chapel hill....they have some great gluten free stuff. They even have a list they can give you of all the food that is gluten free. Their trail mix is really good.

UnhappyCoeliac Enthusiast

Hello

Your staving because spinach isnt giving you enough calories.

You are also starving because alot of gluten free food is not high in fibre or in calories (Vegetables may be good for you but they dont fill an active persons stomach)

What I have learn t is you cannot get by being coeliac without

-gluten free pasta

-gluten free bread

These are the sort of foods that keep you fool. I have one or the other everyday. So gluten free carbs will stop the hunger and no you wont put on weight, if your hungry there is already a defict of calories!

I also have a gluten free burger with the lot twice a week refueling :) egg, meat, lettuce, Gluten-Free bun = win

ranger Enthusiast
I was just diagnosed and I am lost. I cant even figure out how to use this site. I hope someone will get my message and help me. I am going to put up my email address because I dont understand how to see if any one responds to me. Any way what can I eat. I have been eating raw spinach for a week and I am starving. ok my email is

chrisvalk@nc.rr.com.....if someone could help me figure out this site I would be so grateful. :(

dear val, Im pretty new to this, too. Best advice is to keep it simple at first. Do you have time to cook? Early on, I bought bread,pizza crust, ect. They were really bad! And, even though I was a good cook, my first attemps at gluten-free baking were really bad! The gluten-free flours just didnt act like flour. It took me a few attemps, but finally I was able to make good quality gluten-free food. My dh is not celiac and eats the same things I do, and is very happy with it. In fact, most of the time, he doesnt realize that we're eating gluten-free. I get a lot of recipes on-line, some from cookbooks, and some are just old recipes I've always used, but tweaked. I know it looks awful right now, but I can tell you that I eat very good, very often, and very varied. I dont't miss gluten at all. And I don't miss running to the bathroom all day, either! Hang in ther, Susan

Robin63 Newbie
:rolleyes: Hey there, I hope you are doing okay. I also was just diagnoised with Celiac in Oct.08. It has been a hard 4 months, learning all of the do's and don't's . My Doctor was absolutely no help whatsoever. I had battled stomach issues since I was 6yrs old and anemic most of my life. I had been diagnoised with everything from IBS to Diverticulosis to Colitis. I went to a gastro. doctor about 9yrs ago and ended up having my gallbladder out. It was diseased and only 10% functioning. I thought that would be the end of the stomach issues and pain. Not true. It only got worse. For about 4 years now it got almost intolerable. I started researching my symptoms, and found that Celiac and gluten intolerence kept coming up. I figured its only a diet modification and so I semi=tried it. I did give in and go back to the Gastro. Doctor and told him what I had done. He ordered the blood test even though he knew I had gone off of most gluten. It came back neg. as well as the endoscopy biopsy. He suggested I go on a Completely Gluten Free Diet. This has been a whole new world of pain free, bloat free, mostly symptom free for me. I am 45yrs old and have lived with this almost all of my life. As a child they ran so many test and found nothing. I was skinny and had stomach aches that hurt so bad. I have felt very blessed to have had a diagnosises after all these year. It is very tough but very worth it. Eating out is not very safe, but I take my chances on occasions. The true diagnosises was the skin outbreaks. It did not show in my blood work, but I have DH and that proves enough to me. I also am almost symptom free and that is to me another positive. The diagnosised is very hard but the trial of the diet is 100%. IT IS A DIET YOU CANNOT CHEAT ON> I was just visiting your area and just got back today. I have a brother that lives in Raleigh. I am about 2 1/2 hours away. He lives on Pat's Branch Drive. Get some gluten free pasta and bread. Find a health food store that has gluten free foods. I just found in Roanoke today at one of the Health Food stores, Corn Dogs and Breaded Chicken Strips. Kroger has a good Gluten Free Section. Hope this helps. Robin

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    • Theresa2407
      Usually when I digest gluten or wheat I have a 4 hour window before reacting.  If it is immediate it may be an intollerence to another food.  Dairy, Frutose, and bacteria (SIBO) will react with many of the celiac disease symtoms.Has your Doctor ran a  Fructose test which is measuring your Fruit Sugar?  A Hydrogen Beath Test which checks your intestinal bacteria and Dairy?After my biopsy and blood work, these (3) tests were also ran, along with allergy tests, which allery test was sent out of State.  It was a mouth swab. How fast you heal depends on the diet you are following… The following are my personal recommendations to healing. I talk to many newly diagnosed people who start the gluten-free diet with pasta, breads, snacks, and pizza. After a month or so, they do not know why they don’t feel any better and still are sick with their original symptoms: They worry the diet is not working for them. For some there may be other factors involved, but most just aren’t letting their body heal properly. I blame the internet, and misinformation it contains. People want a quick fix, not realizing this is a life long disease. They need a good support group, with people who have been through this and knows what works!  This is what I have found will work for you.                                                                                            First 6 weeks should be:                                                                                                                                 lean meat (beef, pork, chicken, turkey, salmon, sardines, buffalo, deer)                                                   fresh vegetables (steamed or roasted with a little Olive Oil) with 2 cups per day being raw (5 servings; a serving is 1/2 cup)                                                                                                                                      fresh fruit (3 servings; include strawberries, blackberries and blueberries daily)  Makes good shakes with Almond milk.                                                                                                                                        A hand full of almonds daily (pecans and walnuts can be substituted)                                                        brown rice, lentils, Citrucel daily (or the equivalent) Good source of fiber. I use Calm because my body doesn’t absorb Magnesium and I only need to take once in evening.                                                    No dairy of any kind (milk, cheese, yogurt, No breads, No past,  No oats, No pizza, No gluten-free beer, No snacks like cake, biscuits, pies, donuts.                                                                                                Many dietitians will tell you to follow a gluten free diet but you have to heal first. Don’t misunderstand me, dietitians are our friends and help us.                                                                                              10% of people with gluten-free will be intolerant to dairy                                                                                  10% can not tolerate oats                                                                                                                     After the six weeks, you can start to add these foods back into your diet. 1 new food every 4 days; this way you know if you react to this food.                                                                                                  Oats shouldn’t be tried for 1 year after being diagnosed; then start with 1/3 of a cup. Only gluten-free Oats are acceptable.                                                                                                                                              You should have results within 3 days of following a correct healing diet. Bloating should be leaving, migraines should be gone. Might take bowels a little longer to respond. If you start with 5 times a day on the Citrucel and cut back as your bowels return to normal; then use 1 Tbsp. daily. This works if you have constipation or diarrhea.                                                                                                        Meanwhile make sure you have had a Dexa test (bone density) and a blood test to check your vitamin and mineral levels: Zinc, D,K,B,C and iron levels.                                                                                  Don't take supplements while healing as your body is not accepting them and they will flush through your body.                                                                                                                                              Have you had a breath test for Dairy, Fructose, and bacteria overgrowth? Should have done when first diagnosed.                                                                                                                                        How fast you heal depends on the diet you are following… The following are my personal recommendations to healing. I talk to many newly diagnosed people who start the gluten-free diet with pasta, breads, snacks, and pizza. After a month or so, they do not know why they don’t feel any better and still are sick with their original symptoms: They worry the diet is not working for them. For some there may be other factors involved, but most just aren’t letting their body heal properly. I blame the internet, and misinformation it contains. People want a quick fix, not realizing this is a life long disease. They need a good support group, with people who have been through this and knows what works! This is what I have found will work for you. First 6 weeks should be: lean meat (beef, pork, chicken, turkey, salmon, sardines, buffalo, deer) fresh vegetables (steamed or roasted with a little Olive Oil) with 2 cups per day being raw (5 servings; a serving is 1/2 cup) fresh fruit (3 servings; include strawberries, blackberries and blueberries daily) a hand full of almonds daily (pecans and walnuts can be substituted) brown rice lentils Citrucel daily (or the equivalent) Good source of fiber. No dairy of any kind (milk, cheese, yogurt) No breads No pasta No oats No pizza No gluten-free beer No snacks like cake, biscuits, pies, donuts. Many dietitians will tell you to follow a gluten free diet but you have to heal first. Don’t misunderstand me, dietitians are our friends and help us. 10% of people with gluten-free will be intolerant to dairy 10% can not tolerate oats After the six weeks, you can start to add these foods back into your diet. 1 new food every 4 days; this way you know if you react to this food. Oats shouldn’t be tried for 1 year after being diagnosed; then start with 1/3 of a cup. Only gluten-free Oats are acceptable. You should have results within 3 days of following a correct healing diet. Bloating should be leaving, migraines should be gone. Might take bowels a little longer to respond. If you start with 5 times a day on the Citrucel and cut back as your bowels return to normal; then use 1 Tbsp. daily. This works if you have constipation or diarrhea. Meanwhile make sure you have had a Dexa test (bone density) and a blood test to check your vitamin and mineral levels: Zinc, D,K,B,C and iron levels. Don't take supplements while healing as your body is not accepting them and they will flush through your body. Have you had a breath test for Dairy, Fructose, and bacteria overgrowth? Should have done when first diagnosed. Remember to have a tTg IgA blood test repeated at 6 months then every year after, with another scope done in 3 years. Only way to know if you are healed. I don’t have all the answers; we are learning everyday new ways of doing things, but this is a start! Remember to have a tTg IgA EMA blood test repeated at 6 months then every year after 
    • Wheatwacked
      Marsh 3b is the Gold Standard of diagnosis for Celiac Disease.  Until recently, regardless of antibody tests, positive or negative, you had to have Marsh 3 damage to be awarded the diagnosis of Celiac. As I understand you,  you were having constant symptoms..  Your symptoms improved on GFD, with occassional flare ups. Did your doctor say you do and you are questioning the diagnosis? Regarding your increasing severity when you get glutened it is "normal".  Gluten acts on the Opiod receptors to numb your body.  Some report withdrawal symptoms on GFD.  I was an alcoholic for 30 years, about 1/2 pint of voda a day. Each time I identified a trigger and dealt with it, a new trigger would pop up.  Even a 30 day rehab stint, with a low fat diet (severe pancreatis) during which I rarely had cravings.  Stopped at a Wendys on the way home and the next day I was drinking again.  20 years later, sick as a dog, bedridden on Thanksgiving, after months of reasearch, I realized that gluten free was my Hail Mary.  Back in 1976 my son was diagnosed at weaning by biopsy with Celiac Disease and his doctor suggested my wife and I should also be gluten free because it is genetic.  At 25 years old I felt no gastro problems and promised if I ever did I would try gluten free.  Well, I forgot that promise until I was 63 and my wife 10 years dead.  Three days of gluten and alcohol free, I could no longer tolerate alcohol. Eleven years gluten and alcohol free, with no regrets. Improvement was quick, but always two steps forward and one back.  Over time I found nineteen symptoms that I had been living with for my entire life, that doctors had said, "We don't know why, but that is normal for some people". Celiac Disease causes multiple vitamin and mineral deficiency.  It is an autoimmune disease, meaning your immune system B and T cells create antibodies against ttg(2) in the small intestine in Celiac Disease, and sometimes ttg(3) in skin in Dermatitis Herpetiformus.  'Why' is poorly understood.  In fact, it wasn't even known that wheat, barley and rye gluten was the cause.  Celiac Disease was also called Infantilism, because it was deadly, and believed to only be a childhood disease. So, as part of your recovery you must deal with those deficiencies.  Especially vitamin D because it contols your immune system.  Virtually all newly diagnosed Celiacs have vitamin D deficiency.  There are about 30 vitamin and minerals that are absorbed in the small intestine.  With Marsh 3 damage you may be eating the amount everyone else does, but you are not absorbing them into your system, so you will display symptoms of their deficiency.   As time passes and you replenish your deficiencies you may notice other symptoms improve, some you did not even know were symptoms. Our western diet has many deficiencies built into it.   That is the reason foods with gluten are fortified.  Gluten free processed food are not required to fortify.  Vitamin D, Iodine, choline.  The B vitamins, especially Thiamine (B1) run deficient quickly.  We only store enough thiamine for 2 weeks so the symptoms of Gastrointestinal BeriBeri can come and go quickly.  Magnesium, zinc, etc. each having its own symptoms affecting multiple systems.  High homocystene, an indicator of vascular inflamation can be cause by deficient Choline, folate, B6 and or B12.  Brain fog symptoms by deficient choline, iodine, thiamine B1. Dietary intake of choline and phosphatidylcholine and risk of type 2 diabetes in men: The Kuopio Ischaemic Heart Disease Risk Factor Study  
    • Rogol72
      I cut out the rice because it was affecting my stomach at the time ... not necessarily dermatitis herpetiformis. It was Tilda Basmati Rice, sometimes wholegrain rice. I was willing to do whatever it took to heal. Too much fiber also disagrees with me as I have UC.
    • trents
      But you didn't answer my question. When you consume gluten, is there an identifiable reaction within a short period of time, say a few hours?
    • Scott Adams
      You can still have celiac disease with negative blood test results, although it's not very common:  Clinical and genetic profile of patients with seronegative coeliac disease: the natural history and response to gluten-free diet: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606118/  Seronegative Celiac Disease - A Challenging Case: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441776/  Enteropathies with villous atrophy but negative coeliac serology in adults: current issues: https://pubmed.ncbi.nlm.nih.gov/34764141/   
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