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

Sort Of Confused And My Story..and Question.


Matt007b

Recommended Posts

Matt007b Rookie

Hello Matthew here.. :)

I came down with a UTI back in the fall of 2005, had an allergic reaction to it that antibiotic I was put on (flagyl) sent me to the ER room with severe nausea and dehydration..then after months of antibiotics trying to clear this infection I was nauseated..sick since then. It was 2 weeks before my flight instructor checkride :(

Anyway, i've had it all..ct scans/mri's/colonscopies..endoscopes..blood tests..

Only postivie consitant test was white blood cells in the stool with no culture (meaning inflammation somewhere) and slight gastritis...with low potassium levels which i'm taking potassium pills now. No effect.

My current symptoms are, nausea..sometimes heavy to the point where I have to lay down, abdominal pain..constipation, sweaty palms, insominia, anxiety attacks.. haven't worked in 8 months and i'm super super poor now with zero insurance (all my savings on testing for what the problem was..)

Soooo over the years I did 3 blood tests, testing for celiac.. not sure how accurate they were but i'm not sure if I ever got properly tested but they all came back negative. Did biopsies in my 2 endoscopes but again not sure if they were looking for it...they were just looking for anything to show up..

I got another opinion from a GI specialist and he suggested it's probably some form of malabsorbtion caused by food allergy of some kind. I went off lactose a few weeks ago and noticed some improvement with my nausea but also noticed that's a side effect of celiac/gluten.. So I went to an allergist and we found I was slightly allergic to oats but the doctor said I could either order ANOTHER celiac panel test ($$$$) or just go gluten free for a few months and see what happens.

So since i'm broke..i'm going gluten free..day 5 now and I know this is going to take time, if this is what it is..I have noticed some improvement in my IBS issues already and since going lactose free (wasn't lactose intolerant before getting sick..) my nausea levels are dropping but still are there..still sick but I'm crossing my fingers.

My question is: I don't want to waste months and screw up.. a few days ago I thought to myself "ok I should take some fiber..maybe that'll help my IBS symptoms" and I took benefiber which was listed 'gluten free'...about an hour after taking that I was in my bed with severe nausea and the next day full of IBS constipation..dark urine..I noticed the ingredient "wheat dextrin" was in it...aren't we supposed to avoid that??

Second and more important question..i've read that some people are just wheat intolerant instead of celiac's...isn't it the exact same diet? I'm avoiding everything gluten right now and I can tell you i've been gluten free for at least a few days now so far. But I don't want to starve myself just to find out that wheat intolerance diets are more strict or the other way around.. can anyone give me advice on the diet?

Thanks,

Matthew

*thanks in advance i know that was a book sorry.. trying to figure out the difference between wheat intolerance and celiac and the difference between diets..I don't want to screw up I need to get back to work asap...yikes....credit cards pilling up on me :o:(:P


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



Celiac.com Sponsor (A8-M):



The Fluffy Assassin Enthusiast
trying to figure out the difference between wheat intolerance and celiac and the difference between diets..

Welcome Matthew,

Actually there are three different possibilities (revolving around wheat): wheat allergy, gluten intolerance, and celiac sprue. The latter two require the same gluten free diet: no wheat, no barley, no barley malt and possibly no oats. Wheat allergy is just what it sounds like, and so the dietary approach is just to cut out wheat. As you clearly can't afford additional medical expenses, you might want to start out by cutting out wheat and see if that makes a difference. If after a week or two you're still feeling bad, cut out the barley and barley malt. A year and a half ago when I started, this basically meant giving up breakfast cereals and beer, but these days both are available gluten free. Really, gluten free living isn't that hard, and if you're flat broke you'll save a lot of money. Eat in, meat, eggs, fresh vegetables, fresh fruits, potatoes, rice, corn. After a couple of weeks gluten free, you should either start feeling a lot better or start looking for something else.

(By the way, Lact-Aid takes care of lactose intolerance completely. If you take one and still have trouble with dairy, this might indicate that you are sensitive to casein.)

Regardless, good luck to you, and again welcome.

Matt007b Rookie
Welcome Matthew,

Actually there are three different possibilities (revolving around wheat): wheat allergy, gluten intolerance, and celiac sprue. The latter two require the same gluten free diet: no wheat, no barley, no barley malt and possibly no oats. Wheat allergy is just what it sounds like, and so the dietary approach is just to cut out wheat. As you clearly can't afford additional medical expenses, you might want to start out by cutting out wheat and see if that makes a difference. If after a week or two you're still feeling bad, cut out the barley and barley malt. A year and a half ago when I started, this basically meant giving up breakfast cereals and beer, but these days both are available gluten free. Really, gluten free living isn't that hard, and if you're flat broke you'll save a lot of money. Eat in, meat, eggs, fresh vegetables, fresh fruits, potatoes, rice, corn. After a couple of weeks gluten free, you should either start feeling a lot better or start looking for something else.

(By the way, Lact-Aid takes care of lactose intolerance completely. If you take one and still have trouble with dairy, this might indicate that you are sensitive to casein.)

Regardless, good luck to you, and again welcome.

ooo great ideas thanks fluffy! :) especially about the dairy. I've been totally dairy free over 2 weeks now and it has helped. I have been meaning to buy lactaid and i'm doing probiotics (gluten/dairy free threelac) but that's a great idea about casein. I've been wondering about that one... yeah i'm convinced it's some form of malabsorption caused by a food intolerance with my heavy nausea waves that hit after eating, the anxiety..the total IBS mess, sweaty hands..forgot to mention tingling/cold feet hands.... now what it is I don't know but it's got to be one of them. I've been tested like I said 3 times for celiac..and 2 endoscopes...if I had money i'd just call my gi and ask for a breath test for fructose to eliminate that because i'm even thinking of going fructose low/free for a few weeks..then go wheat...gluten..like you said. Wish I could sleep...and work!

Yeah i've lost 10 pounds already on this gluten free diet (now 165lbs..feel week..tired..hungry but hey it's quite the trimming diet i'll admit) and i'm not losing it on purpose so yeah it sure is cheap living on this diet. Just miss making a sandwich or grabbing whatever I wanted at the local 7-11..

Thank you that helped greatly that's a good idea. I've heard of wheat intolerance (or non-celiac) and I have a bad hunch I'm one of them but I didn't know there where 3 types...I swear doctors just don't have the time to explain these things and I regret letting them talk me into all the mass ct scans/mri's *sigh* or else I wouldn't be stressing about money/work....

anyway.. thank you very much good info.

The Fluffy Assassin Enthusiast
forgot to mention tingling/cold feet hands....

Just miss making a sandwich or grabbing whatever I wanted at the local 7-11..

By tingling, do you mean pins-and-needles? If so, that's the classic sign of B12 depletion, which is in turn a classic sign of celiac sprue. (Or you might be Spiderman, I don't know.:))

As to sandwiches, go get soft corn tortillas and make wraps. They're cheap, they're wonderful, they're versatile and they're gluten free. I truly have completely forgotten to miss bread. I get mine at Aldi, but they're in every store, even here in BFE.

Foxfire62 Newbie

Did they do a full blood panel to test for celiac disease? Did they biopsy the small intestines to look for villi atrophy? If yes, and nothing was conclusive, you could have Crohn's disease, ulcerative colitis, celiac disease, MS, or an intolerance. Probably the best thing to do is stay away from all things gluten, including anything made from wheat, barley or rye, and to play it safe, also stay away from oats.

It would take a little time to get better, but you will. Also, should you have celiac disease, you may become intolerant to some if not all the major allergens (lactose, soy, eggs, fish, peanuts, etc.). You might want to lay off those for awhile and reintroduce them in your system slowly and see if you have any reactions. Also, you always have to check your meds/vitamins to ensure there are no allergens (including wheat, barley, rye or oats) in the product. Check your make-up, lotions and shampoos as well. Don't lick stamps, and wash your hands thoroughly after touching glue-based products. Keep a clean kitchen to ensure less chance of cross-contamination. Better safe than sorry. Stay away from restaurants until you are your old self or close to it. Also, cook from scratch and ensure meat products do not contain any hormone injections that could be a hidden source of gluten. Lastly, as you start healing, you might find your intestines still cannot process meat products (I believe I just figured that one out myself for me). If so, you might want to do a salad/veggie/fruit diet for a few days and see how you do. Reintroduce everything slowly after you found start feeling a lot better. But most likely, you should do fine...I suffer from constipation, so you might not have this problem.

Above all, keep a food journal!!! I did not listen to my husband and only sporadically kept one. Had I kept one initially and kept at it, I would have found out my problem a lot sooner than I did.

Good luck to you.

Matt007b Rookie
By tingling, do you mean pins-and-needles? If so, that's the classic sign of B12 depletion, which is in turn a classic sign of celiac sprue. (Or you might be Spiderman, I don't know.)

As to sandwiches, go get soft corn tortillas and make wraps. They're cheap, they're wonderful, they're versatile and they're gluten free. I truly have completely forgotten to miss bread. I get mine at Aldi, but they're in every store, even here in BFE

Did they do a full blood panel to test for celiac disease? Did they biopsy the small intestines to look for villi atrophy? If yes, and nothing was conclusive, you could have Crohn's disease, ulcerative colitis, celiac disease, MS, or an intolerance. Probably the best thing to do is stay away from all things gluten, including anything made from wheat, barley or rye, and to play it safe, also stay away from oats.

It would take a little time to get better, but you will. Also, should you have celiac disease, you may become intolerant to some if not all the major allergens (lactose, soy, eggs, fish, peanuts, etc.). You might want to lay off those for awhile and reintroduce them in your system slowly and see if you have any reactions. Also, you always have to check your meds/vitamins to ensure there are no allergens (including wheat, barley, rye or oats) in the product. Check your make-up, lotions and shampoos as well. Don't lick stamps, and wash your hands thoroughly after touching glue-based products. Keep a clean kitchen to ensure less chance of cross-contamination. Better safe than sorry. Stay away from restaurants until you are your old self or close to it. Also, cook from scratch and ensure meat products do not contain any hormone injections that could be a hidden source of gluten. Lastly, as you start healing, you might find your intestines still cannot process meat products (I believe I just figured that one out myself for me). If so, you might want to do a salad/veggie/fruit diet for a few days and see how you do. Reintroduce everything slowly after you found start feeling a lot better. But most likely, you should do fine...I suffer from constipation, so you might not have this problem.

Above all, keep a food journal!!! I did not listen to my husband and only sporadically kept one. Had I kept one initially and kept at it, I would have found out my problem a lot sooner than I did.

Good luck to you.

Yeah if I sit or lay down and read a book with my arms on a table or on my sides holding the book up, my hands get numb...which didn't happen before..now that i'm on this diet they're not doing it anymore so another signs...but yeah I guess you could say my fingers would get tingly..also I read somewhere that asprin really sets off symptoms. Like I had one doctor tell me to take a bunch of asprin thinking it was some airborn allergy and all that did was give me major diareera..so weird things..

I *believe* they did at least the last test I was reffered to a rhumatologist who did a full antibody panel not specifically looking for celiac but it was looking for any inflammation markers, but I know on for sure 3 other blood tests came back negative but I do remember one doctor saying mild hint looking at the numbers "borderline but I don't think so" on celiac... i've had 2 colonoscopies..one upper bowel barium xray (that was fun drinking elmers glue) multiple ct scans and mri's.. doctors have told me it's not UC/chron's/stricture..nothing so they can't see anything wrong. My white blood count is low and constant white blood cells in the stool..with vague abdominal pain in my upper left region, left side..but my pancrease has been totally checked with imagining and blood tests so I have a hunch my small intestine is just inflammed and ticked off and I'm having some spastic colon like symtpoms as well. I'm doing citurucel fiber right now trying to relieve the pain. Even had a camera go up a guys...well..let's just say it felt like a number 2 pencil going up there with a cute nurse in the room=not fun.

On the endoscopes we were looking for anything, not celiac specific...I know they did a few biopsies last endoscope in feb. just to see if we got luck..all it did is drained more money :(

I didn't know that about celiacs becomming intolerant to everything, I heard about diary/lactose :S I've been eating eggs and soy waffles (gluten free/wheat free) but that's not good hopefully that's not a problem as well.. ugh I wish there was an easy way to this like a simple blood test to tell you what is the cause. I have enough funds maybe to last 2 months or I have to sell my only transportation (my car..) so I've got to figure this out. :S I mean it could be fructose as well.. but since I reacted badly to benefiber and not citrucel i'll keep after the wheat/gluten theory I guess.. and tone down on eggs and soy and just go fruits and veggies as much as possible. I'm approaching week 1 on the elimination diet. Thanks for your info you 2. :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,546
    • Most Online (within 30 mins)
      7,748

    KimberlyAnne76
    Newest Member
    KimberlyAnne76
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.