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Newbie With Questions, Please ?


Nanjee

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Nanjee Rookie

Hello everyone. I am so glad to have found this forum !! Lots of questions - I hope I am not making a pest of myself :+)

I have had "IBS" for 20 years, but usually had it pretty much under control. I also have Fibromyalgia, but that ws always very much under control as well - it really didn't alter my life that much, except for an occassional flare. About 3-/12 years ago, I began to have diarrhea only, and severe stomach "spasms" or cramps. I put it off as my IBS in a huge flare.

Now, 3 years later, I am searching for what in heavens name is wrong with my upper intestines!!! I had the blood work done for Celiac - it was negative. Had an upper an lower scope done - Gasto said everything was fine - kind of dismissed me as "only IBS".

I am SO weak. I don't know what to eat !!! Last night I had a slice of French bread - I woke up at 3am with spasms in my upper intestines - and oodles of gas.

So today it is back to bananas and tea.

My question - if I am gluten intolerant - can this also lead to vitamin deficiencies ?

I have really wondered about Vitamin B12 - I am cold ALL the time - severe headaches daily - feel like I am in a fog. Severe muscle pain, dizzy and a very fast heart rate when I am up. I am so exhausted - I spend so much time lying down. This is NOT me !!! I was a go getter, and I don't know which way to turn anymore. Have any of you had anemia type symptoms before going gluten free ?

I was thinking of using the lab that tests your stool sample - to see what concluson they could come up with. My internist said if the blood work was negative- then I am not gluten sensitive.

If this sounds familiar to any of you - I would sure appreciated your input and comments. I hope to get to know you all a little better !!

Thanks so much for taking the time to read my post :+)

Nanjee


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kabowman Explorer

What worked wonders for me was an elimination diet and a 4 week food diary with notes on symptoms and what you thought it was tied to...(gas, dh, bloating, fever, joint pain, lethargy, etc.) EVERYTHING! I started with plain meat, salt, pepper, & garlic...only. Plain fruits and veggies. celiac disease was rulled out - I had already been gluten-free for several months and refused to go back on for testing so I either have it or I don't; either way, I still can't have gluten.

I went through the IBS, all kinds of blood tests, EDG, Colonoscopy, etc. without any real progress or DX; still lots of pain, no energy, etc. for YEARS. I discovered my lactose/casein intolerance about 5+ years ago, I finally admitted that there was more and started the elimination. After about 3 months, I started the diary and that REALLY helped.

Now, for the first time in YEARS, I actually feel like my old self again. Most of my symptoms, including the joint pain and persisting low-grade fever are finally gone! Wow, I have energy. However, the list of foods I cannot eat is HUGE, but I feel great and I (and my whole family) are eating healthier than ever before:

-Lactose/Casein

-Gluten

-Soy Beans

-MSG

-Yeast

-Corn

-Vinegar

-Peanuts

-Almonds

-Garbonzo Beans

-Wine

I hardly miss those foods...if I forget, I just remember back to the last mistake (they changed an ingredient and I neglected to double check) that left me on the couch for a full day and in pain for the next 3 days.

I take multi-vitamin that is gluten/lactose/corn/yeast/soy free and 1000 MG of calcium per day. Per my doc, I also take B Complex Complete & C daily. I have always worried about getting enough vitamins. Just make sure that they are not making you sick too!!!!! Most contain some starch and my GI doc suggested I suppliment my Nexium with Priolosec - however, after the second time of getting sick, I read the ingredients! Starch!!!! I now read ALL meds ingredients.

Good luck and don't be discouraged!!!! It is for the best.

-Kate

burdee Enthusiast

I would highly recommend the Enterolab stool tests which also tests milk sensitivity (casein antibodies) even AFTER you have gone gluten-free for several months. From what I understand, blood tests can only detect gluten antibodies which have LEAKED from the small intestines into the blood stream. So those tests require that you've been sick with celiac disease long enough to develop a 'leaky gut'. E-Lab tests STOOL samples which would more logically have antibodies created in the INTESTINES.

If you have symptoms which are alleviated by abstaining from gluten, you most likely have gluten intolerance, symptomatic of celiac disease. I believe about 44% of celiacs are MISdiagnosed with the IBS label which is not a disease, but rather a catch all category for symptoms for which doctors don't understand and can't 'cure'. Like the average celiac in this country who is stalled from a celiac disease diagnosis for 11 years, I was misdiagnosed for 10 years with the IBS label.

Anemia, stomach cramps, diarrhea, fatigue, fibromyalgia pain, headaches and fogginess are ALL celiac disease symptoms. However living on tea (with caffeine) and bananas (high glycemic) can influence reactive hypoglycemic (low blood sugar) symptoms of dizziness, fogginess and faintness. I recommend you start substituting Gluten free foods for gluten containing foods you normally eat so you can avoid gluten. Then contact Enterolab for stool tests, if you want a diagnosis, so you don't ever have to consume gluten again.

BURDEE

Nanjee Rookie

Thanks so very, very much for your replies !!! I right now am going to have my hubbie get me some gluten free bread, and maybe some pasta - oh how I long for pasta !!! And some crackers - maybe ?

The Tea I am drinking is herbal tea - fennel tea or spearmint leaves - never caffiene for me !!!

I just keep getting weaker, and have hit a wall. I look back to 3 1/2years ago - I am a professional person !!! Now it is SO exhausting to just get washed up for the day.

Doctors just look at you - "must be IBS and chronic fatigue". AARRGGGHHHH !!!!

I will go ahead with the testing from Entero labs.

Thanks again for listening - it has meant a lot :+)

Nanjee

cdevane Rookie

Okay, I have read a lot hear and tried to understand it all, but I do have some questions.

Burdee, you amongst others have mentioned the Entero Lab tests. How do I go about finding more information about that?

I have been gluten-free (with some slips...still learning) for about three weeks and have noticed 70% of my "IBS" symptoms have disappeared. My Celiac blood test came back negative, as did the stool test that checks for malabsorbtion. But I am convinced there is some sort of connection. I know the easy answer would be just to remain gluten free if its working, but I honestly don't think I have that type of long term will power!

What sorts of other things are automatically eiliminated when you go gluten-free, besides wheat? And can that be tested for as a seperate allergen.

I would appreciate any input as I am convinced that my doctor's are not very knowledgable about this area and I am hesitant to do the big expensive tests (endoscopy, colonoscopy) if they are not really necessary.

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    • catnapt
      so do you have celiac or not? 🤔 why are your vision issues undiagnosed? 😢 what does your ophthalmologist say?  do you have a serious vit A deficiency? what do you take for it? how long have you had celiac disease and how long did  it take to get a diagnosis?   if you are legally blind there are adaptive devices that will help you. I have vision difficulties as well but did not qualify (at least not yet)   do you have a vit A deficiency? why are you undiagnosed? what does your ophthalmologist say? I have a retinal specialist and he tells me my eye condition can not be fixed- until/unless it gets to the point of where surgery is safer since the surgery can leave me actually blind... so you want to wait til it gets really bad 🤪     I hope you find what works for you.    PS   the medication I started at the same time as the gluten challenge is obvious from the condition it's trying to treat. you can google it 😉 it is not an for any auto immune condition.   
    • knitty kitty
      @catnapt,  I apologize.  Obviously I've confused you with someone else.  I have vision problems due to undiagnosed Celiac complications.  Being legally blind, y'all look the same from here.   You still have not said which new medication you started taking.  Parathyroid disorders can affect antibody production.  Bone Loss Correlated with Parathyroid Hormone Levels in Adult Celiac Patients https://pubmed.ncbi.nlm.nih.gov/36619734/ Effect of vitamin B1 supplementation on bone turnover markers in adults: an exploratory single-arm pilot study https://pmc.ncbi.nlm.nih.gov/articles/PMC12075007/
    • catnapt
      during the gluten challenge I did not consume any wheat germ   the wheat germ is TOASTED - it's the only way it is sold now afiak doesn't matter I consume vast amounts of lectin containing foods PROPERLY prepared and have for well over a decade. They do not bother me in the least.    no anemia however the endo who ordered the celiac panel is the one who suggested the 2 week gluten challenge of eating at least 2 slices of bread per day or a serving of pasta- ALSO put me on a new drug at the same time (not a good idea)  I ate 4 slices because they were thin, or 2 English muffins, and just once some lasagna that someone else made since I stopped eating wheat pasta years ago. The English muffins caused some of the worst symptoms but that pc of lasagna almost killed me ( not literally but the pain was extreme) during those 12 days there were at least 3 times I considered going to Urgent Care.   This entire process was a waste of time TBH due to being on that new drug at the exact same time. it is impossible to tell if the drug I am taking for the possible renal calcium leak is working or not- given the dramatic response to the gluten challenge and resulting nausea (no vomiting) and eventually a loss of appetite and lower intake of foods so now I have a dangerously low potassium level   I don't have a simple case of celiac or no- I have an extremely complicated case with multiple variables I am seeing an endocrinologist for a problem with the calcium sensing glands - that system is very complicated and she has been unable to give me a firm diagnosis after many tests with confusing and often alarming results. She also appears to be inexperienced and unsure of herself. but I don't have the luxury of finding a new endo due to multiple issues of insurance, lack of drs in my area, money and transportation. so I'm stuck with her At least she hasn't given up    in any case I can assure you that lectins are not and never were the problem. I know they are a favorite villain in some circles to point to, but I have ZERO symptoms from my NORMAL diet which DOES NOT contain gluten. The longer I went without bread or foods with wheat like raisin bran cereal, the better I have felt. my body had been telling me for several years that wheat was the problem- or maybe specifically gluten, that remains to be seen- and stopping eating it was the best thing I could have done   I almost had unnecessary MAJOR SURGERY due to joint pain that I ONLY have if I am eating bread or related products I assumed it was the refined grains - never really suspected gluten but it does not matter I won't put that poison in my body ever again not that it is literally poison but it is def toxic to me        
    • knitty kitty
      @catnapt,  I'm sorry you're having such a rough time.   How much wheat germ and how much gluten were you eating? Lectins in beans can be broken down by pressure cooking them.  Do you pressure cook your beans?  Were you pressure cooking your wheat germ? What drugs are you taking?  Some immunosuppressive drugs affect IgA production.  Do you have anemia?
    • catnapt
      oops my gluten challenge was only 12 days It started Jan 21s and ended Feb 1st   worst 12 days of my life   Does not help that I also started on a thiazide-like drug for rule in/out renal calcium leak at the exact same time No clue if that could have been symptoms worse 🤔
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