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

Symptoms Changing?


GlutenFreeAustinite

Recommended Posts

GlutenFreeAustinite Contributor

I have been living gluten-free for just over a year and a half, with the assistance of my best friend, who is also gluten-free. After suffering from daily migraines for a year, and gastritis (inflammation of the stomach lining) since middle school, I was desperate for something to work. So I eliminated gluten, as well as dairy.

Fast forward a year and a half. I have never been diagnosed, but I still remain on the diet, as I know celiac is finicky. I have added dairy back in, as I seem to be able to tolerate it now, but have eliminated soy (dx'ed Fall 2011). I began seeing an allergist who claimed to specialize in food allergies. Little did I know she was a recent med school graduate and had little experience with people who don't present typical symptoms. Example: she doesn't believe I truly have an allergy to soy, because "anyone would test positive with a food panel scratch test." Also, because I don't present typical symptoms (ie, true anaphylaxis), but instead have a quick-onset "throat clogging" (still able to breathe and everything, but tight) for my soy allergy, I don't really need to stop eating it or carry an Epi-Pen.

She also doesn't think I have celiac disease. She doesn't doubt, or so she says, that I may have a problem with gluten. But because my symptoms (migraines) prior to going gluten-free were atypical, she doesn't think it's celiac. To prove this, she ordered a blood test. The test came back negative, which I expected, because I hadn't been eating gluten for 18 months at that point. When I pointed this out, she didn't believe me, but agreed to check with a gastroenterologist, who said the same thing: I need to be eating gluten for at least a month before I can be tested.

Lately, I'm not even sure what my symptoms are. I test myself periodically, and always regret it afterwards. Perhaps it's because I lack a diagnosis, but I seek to challenge my symptoms. The first time I ate a small piece of bread: mild stomachache that lasted two days, and a slight headache. Second time, with another piece of bread: sinus drainage, stomachache that lasted three days. Third time with two small spoonfuls of honey mustard that for some reason included wheat flour: almost instantaneous stomachache that has lasted nearly five days and now seems to be exacerbated by food and exercise, a severe migraine that lasted two days, and intense brain fog. All of this accompanied by alternating diarrhea and constipation. (sorry about the details, guys!)

So, to conclude this little rant: what do I do? what tests do y'all recommend? Should I change allergists? (and on that note, should I carry an Epi-Pen for my little soy debacle?)

Thanks everyone. :-)


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



Celiac.com Sponsor (A8-M):



Skylark Collaborator

I think you need a different allergist. I had a reaction like you describe to shellfish. My Dr. told me to avoid eating it because of the risk of sensitizing worse. Happily, it eventually went away.

My gluten symptoms shift and change but I never like them!

eatmeat4good Enthusiast

If you want to continue exploring this with someone else...get a new allergist or nutritionist or naturopathic helper. She isn't helping you. You probably are doing your own research successfully by eliminating and observing reactions. For what it's worth, I believe you are Celiac even if she doesn't. Do you? If you do, then stay gluten free and be really strict. If you don't, then start eating it for at least 3 months and then get tested...but it could still be negative.

I know it can be frustrating dealing with food intolerances. Mine are iodine, gluten, salicylates, soy, preservatives, and dairy. Ugh. But no Dr. or allergist or dermatologist ever helped me figure them out. They are happy to write them in the chart once they are identified however. That is all I need them to do. I think you are your own best detective. But if you want an assistant...I think you need another one.

Migraines were one of my worst symptoms. I was increasingly ill for years until I found Celiac. She is misinformed to say the least.

My Grain Headaches are gone now.

I hope you can figure this out but for sure stay off of soy as long as you are reacting like that.

mushroom Proficient

Most doctors who don't specialize in celiac are unaware of neurological symptoms from gluten. :(

rosetapper23 Explorer

Geez...your symptoms sound very much like mine when I get glutened--I think you may very well celiac. With regard to the soy, I also am intolerant of it. I'm feeling lousy right now because I felt sick after eating a tasty chicken dish I've made dozens of times in the past. I kept going over the ingredients in my mind and wondering what could have made me sick. Would you believe that it was the chopped garlic?? I suddenly realized that the only ingredient that wasn't "fresh" was the new jar of chopped garlic I'd bought (I usually crush/chop my own garlic, but my garlic press recently broke). Anyway, when I read the ingredients, I was shocked! It contains soybean oil! What's THAT all about? They seem to sneak soybean oil into everything these days (mayo, tuna, etc.), but I'd never suspected chopped garlic.

mushroom Proficient

Oh sheesh, do you mean I have to check my garlic for soy now? :angry:

GlutenFreeAustinite Contributor

Thanks everyone for the support--I've been thinking I should change allergists for a while now, just haven't really gotten to it. She thinks I'm sensitive, possibly, but NOT celiac, so I don't really know what I am, but I suppose that doesn't really matter.

I've actually been thinking celiac has plagued my family for some time. My maternal grandmother had questionable fibromyalgia, Type 1 diabetes, Crohn's disease, osteoporosis, and I'm pretty sure there were some other fun diseases in there too. She was tested for celiac, but that was back in the early 1990s, and I'm sure testing was not the same. I myself was diagnosed with gastritis in middle school.

I'm definitely not going to be "testing" myself independently any time soon--I'm just going to wait and eat safely until I am ordered to eat it for the test.

Soy wise--wow. I know soy's one of the 8 major allergens, but I didn't realize how many people were allergic to it! Soybean oil and soy lecithin don't bother me, thankfully, but insert the word 'protein' and I'm a goner.


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



Celiac.com Sponsor (A8-M):



BellaBella Rookie

Hi GlutenFreeAustinite,

I'm on my own journey with celiac disease and a gluten free lifestyle, but my 6 year old has life threatening allergies to dairy and peanuts. I am NEVER without an EpiPen. I have read several times that each subsequent exposure to an allergen can cause a worse reaction than the last so it is *possible* that you may experience true anaphylaxis at some point. Knock on wood that will never happen but I would rather carry an EpiPen and never have to use than to need it and not have one. (Even using it unnecessarily is better than using one too late!) They can be quite expensive, even with insurance, but never hesitate to ask your Dr. for a prescription and get it filled ASAP, especially since your reactions make your throat tight already.

Anaphylaxis is the scariest thought for a mother of a child with food allergies. I can handle a split lip, broken arm or stitches but anaphylaxis scares the bejeezus out of me. I wouldn't ever think of being without an EpiPen.

Get one now....just in case.

ETA: My experience is that *most* allergists are relatively unfamiliar with food allergies. And no, you won't always test positive on a skin test, that just happens to be the most reliable test at the moment. Find an allergist that is open to learning more and who stays on top of the research. Steer clear of those who think they know it all because I guarantee they don't. I don't expect every allergist to know everything about food allergies but I certainly appreciate the ones who are open to learning more.

GlutenFreeAustinite Contributor

Bella-Bella,

Thank you. I was actually talking to my mother about this the other day. This is the same allergist who forgot to give me an inhaler after I was diagnosed with asthma, and I'm wondering if this is a similar situation. Regardless, I probably should have one, even if I never ever use it. And I'm sure it''s terribly expensive.

But dairy and peanuts--that's got to be tough. Luckily they label those, but what a pair.

vb10 Newbie

Oh sheesh, do you mean I have to check my garlic for soy now? :angry:

Sorry it is a little off topic... but I have read all food items that you no longer consume "lactose free, soy free" and I have a question for you...

What do you eat? And for how long have you been eating like that?

Looks almost as if you are on Paleo diet.

JonnyD Rookie

I was diagnosed with Celiac as well as Eosinophlic Esophagitis (EE). I've been gluten free for almost a year now. But, I've often experienced the throat clogging from the EE. For EE, your esophagus reacts to an allergen in your diet and flares up for 12 days. I've recently started a food journal to see if I can narrow down what's bothering me. If you do ever get a scope and biopsies (the only way to get a 'true' diagnosis), EE's something to have them check for.

mushroom Proficient

Sorry it is a little off topic... but I have read all food items that you no longer consume "lactose free, soy free" and I have a question for you...

What do you eat? And for how long have you been eating like that?

Looks almost as if you are on Paleo diet.

I am a COOKIE MONSTER :ph34r:

:lol:

Seriously, if you got to the end of sig, I now do tolerate lactose, so dairy is huge for me. Also, you look at the things you can rather than the things you can't - start with the letter A and you 've got asparagus, artichokes, apples, arugula, avocado, apricots, almonds, ahi tuna.... you just have to be a little more creative. And no, I'm not paleo. :) I hope one day to resume eating some of those other things.

BellaBella Rookie

I was diagnosed with Celiac as well as Eosinophlic Esophagitis (EE). I've been gluten free for almost a year now. But, I've often experienced the throat clogging from the EE. For EE, your esophagus reacts to an allergen in your diet and flares up for 12 days. I've recently started a food journal to see if I can narrow down what's bothering me. If you do ever get a scope and biopsies (the only way to get a 'true' diagnosis), EE's something to have them check for.

Funny you should mention that.... My son who's allergic to dairy and peanuts also has EoE. He doesn't have the food impaction part of that though but without meds he vomits up to 6 times a day. We visited his gastro on Monday and she said that the same gene is responsible for Celiac and EoE...that's the first I've heard of that! Send me a PM if you want!

rosetapper23 Explorer

Okay, I admit to being on the paleo/primal diet....and it has helped me a LOT.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,540
    • Most Online (within 30 mins)
      7,748

    Barrie S
    Newest Member
    Barrie S
    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

    • 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.  
    • Celiac50
      That sounds so very likely in my case! I will absolutely ask my doctor on my next bone check coming up in March... Thanks a lot! 
    • trents
      Calcium levels as measured in the blood can be quite deceiving as the body will rob calcium from the bones to meet demands for it by other bodily functions. Also, supplementing with calcium can be counterproductive as it tends to raise gut pH and decrease absorption. More often than not, the problem is poor absorption to begin with rather than deficiency of intake amounts in the diet. Calcium needs an acidic environment to be absorbed. This is why so many people on PPIs develop osteoporosis. The PPIs raise gut pH. And some people have high gut PH for other reasons. Low pH equates to a more acidic environment whereas high pH equates to a more basic (less acidic) environment.
    • Celiac50
      Kind thanks for all this valuable information! Since my Folate was/is low and also my Calcium, there IS a chance I am low in B vitamins... My doctor only measured the first two, oh and Zinc as I has twisted her arm and guess what, that was mega low too. So who knows, until I get myself tested properly, what else I am deficient in... I did a hair mineral test recently and it said to avoid All sources of Calcium. But this is confusing for me as my Ca is so low and I have osteoporosis because of this. It is my Adjusted Ca that is on the higher side and shouldn't be. So am not sure why the mineral test showed high Ca (well, it was medium in the test but relative to my lowish Magnesium, also via hair sample, it was high I was told). But anyway, thanks again for the VitB download, I will look into this most certainly!
    • ElisaAllergiesgluten
      Hello good afternoon, I was wondering if anyone has ever brought their anti-allergy pills? I have been wanting to use their Cetirizine HCI 10mg. They are called HealthA2Z and distributed by Allegiant Health.I’m also Asthmatic and these allergies are terrible for me but I also want to be sure they don’t have any sort of gluten compound.    I have tried calling them but to no avail. Has anyone ever used them? If so, did you had any problems or no problems at all?    thank you
×
×
  • 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.