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

Cyrex Labs--Do I Really Have A Gluten Intolerance?


nostalgic

Recommended Posts

nostalgic Rookie

Hello everyone, I hope you'll bear with me because this may be a long post.  Feel free to skim, I just want to make sure I provide enough information.

 

I have had health problems since I was around 16 (I am now 21).  I first started off with gastrointestinal symptoms, chronic nausea and heartburn/indigestion.  I also have what they like to call IBS---my bowels alternate between constipation and diarrhea but are never truly "normal" although there is a "normal" for me. My heartburn is pretty well controlled by Nexium now. I also developed hyperthyroidism around this time, but that was deemed to be transient and I have not had any problems since.  When I got to college, my health got a bit crazy.  I got diagnosed with pernicious anemia (autoimmune B-12 deficiency), endometriosis, adenomyosis, and interstitial cystitis.  I also have some form of tachycardia which is now controlled by a beta blocker.  I also have had lifelong allergies, eczema, and bad acne since puberty that has not really let up.  

Anyway, after my 2nd laparoscopy for endo within a year, my menstrual pain had decreased substantially but I was still having other pretty severe symptoms during my period, mainly horrific nausea, loss of appetite and severe fatigue.  I went to see an acupuncturist because I had reached the point where I was desperate and willing to try anything...  Anyway, my naturopath told me all about gluten intolerance, how I might have it and that would explain all the autoimmune issues blah blah blah.  He convinced me to order Cyrex labs, and the results came back that I am "gluten intolerant".  I gave up gluten a little over a month ago, and am careful to avoid cross-contamination, do everything I can.

 

I haven't seen an improvement, but I realize this could take time.  So I didn't really think anything of it.  But now I'm reading a lot that Cyrex labs is probably scammish.  So, do I have gluten intolerance or not?  Feel free to ask any questions... I am very confused and don't know what to do.


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



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

I don't know much about Cyrex either, but I have heard some conflicting reports about their high positive rate too. Since you have not had relief of your symptoms, going back on gluten to get blood tests done should not be too uncomfortable....hopefully. That is if you decide to do further testing. The blood tests to request from a doctor are:

Ttg IgA and ttg IgG

EMA IgA

DGP IgG and DGP IgA

Total serum IgA

AGA IgG and AGA IgA

If you decide to stay gluten-free and not test now, you are correct that you should probably give the gluten-free diet more time. Most people recommend 3-6 months.

My "C" did not improve until my hypothyroidism was being treated. Some of your symptoms sound like thyroid problems (they often re-occur) . If you want to get it checked, I would recommend requesting:

TPO antibodies - should be very low

Free T4 and Free T3 - should be in the 50-75% range of your labs normal reference ranges

TSH - should be near a 1

Get copies of all of your labs and research your results. Some doctors do not read or understand labs very well so the patient needs to look out for herself.

Best wishes. I hope you feel better soon!

EmiPark210 Contributor

If you don't trust the labs that did your testing you could go back on gluten for about 12 weeks and get a test done through your PCP or a local hospital. But if you can get a copy of your actual lab results with the types of tests done and post them here, we can help you interpret them. 

 

As to menstrual related issues, I was having the same thing when I was 16-18. I also have an IBS diagnosis that I think is still valid (different symptoms than when glutened) and as much as I've seen other people have issues with it, because my constipation/diarrhea cycle was synced up with my menstrual cycle I talked to my gyno about going on hormonal birth control and that helped straighten those issues out except when I would eat gluten. So we decided that was a hormonal issue. Every body is different so it might be helpful for when you're trying to figure things out to keep a food and symptom journal so it's easier to track what causes what and to notice patterns. 

nostalgic Rookie

I left out some info from my original post but didn't get a chance to edit it.

When I first developed GI symptoms back in 2009, I had the celiac panel done probably at least once (I have now had it done probably five times -_-).  I had an endoscopy not specifically for celiac, that is when I got diagnosed with GERD.  My gastroenterologist did a biopsy for celiac which was negative, although apparently I had flattened mucosa that made him suspicous.  I get my thyroid tested pretty often because of my history.  I have always had good results and even see an endocrinologist occasionally.  I agree that it is probably hormonal for a lot of it.

 

I have been on every type of birth control imaginable: minipill, low dose, normal oral contraceptive, the ring, Mirena, you name it, I've tried it.  All of them have horrific side effects for me, I simply cannot tolerate birth control.  It is not an option.  Instead I have had the two surgeries (one from a top surgeon in Atlanta) which helped a bit with the pain, and I take other medication like Zofran during my actual period and just lay low...

kareng Grand Master

Open Original Shared Link

GottaSki Mentor

Open Original Shared Link

 

I agree.

 

If you don't already have the best tests for accurate diagnosis - let me know.

nostalgic Rookie

Thanks, I had read what they said about Enterolabs/Cyrex, and that is what made me worried.  I guess I will give it more time, see if I see any improvement after a long period of time (at least 6 months) and pay attention to whether or not I ever experience "glutening" symptoms.

I think I've had all the proper testing done, like I said, I've had a biopsy and what I assume to be the standard bloodwork around 4-5 times.


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



Celiac.com Sponsor (A8-M):



Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - catnapt posted a topic in Related Issues & Disorders
      0

      anyone here diagnosed with a PARAthyroid disorder? (NOT the thyroid) the calcium controlling glands

    2. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      how much gluten do I need to eat before blood tests?

    3. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      Curious question

    4. - Amy Barnett posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Question

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,322
    • Most Online (within 30 mins)
      7,748

    avery144
    Newest Member
    avery144
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • catnapt
      learned I had a high PTH level in 2022 suspected to be due to low vit D  got my vit D level up a bit but still have high PTH   I am 70 yrs old (today in fact) I am looking for someone who also has hyperparathyroidism that might be caused by malabsorption    
    • catnapt
      I am on day 13 of eating gluten  and have decided to have the celiac panel done tomorrow instead of Wed. (and instead of extending it a few more weeks) because I am SO incredibly sick. I have almost no appetite and am not able to consume the required daily intake of calcium to try to keep up with the loss of calcium from the high parathyroid hormone and/or the renal calcium leak.    I have spent the past 15 years working hard to improve my health. I lost 50lbs, got off handfuls of medications, lowered my cholesterol to enviable levels, and in spite of having end stage osteoarthritis in both knees, with a good diet and keeping active I have NO pain in those joints- til now.  Almost all of my joints hurt now I feel like someone has repeatedly punched me all over my torso- even my ribs hurt- I have nausea, gas, bloating, headache, mood swings, irritability, horrid flatulence (afraid to leave the house or be in any enclosed spaces with other people- the smell would knock them off their feet) I was so sure that I wanted a firm diagnosis but now- I'm asking myself is THIS worth it? esp over the past 2 yrs I have been feeling better and better the more I adjusted my diet to exclude highly refined grains and processed foods. I didn't purposely avoid gluten, but it just happened that not eating gluten has made me feel better.   I don't know what I would have to gain by getting a definitive diagnosis. I think possibly the only advantage to a DX would be that I could insist on gluten-free foods in settings where I am unable to have access to foods of my choice (hospital, rehab, nursing home)  and maybe having a medical reason to see a dietician?   please let me know if it's reasonable to just go back to the way I was eating.  Actually I do plan to buy certified gluten-free oats as that is the only grain I consume (and really like) so there will be some minor tweaks I hope and pray that I heal quickly from any possible damage that may have been done from 13 days of eating gluten.    
    • Jmartes71
      So I've been dealing with chasing the name celiac because of my body actively dealing with health issues related to celiac though not eating. Diagnosed in 1994 before foods eliminated from diet. After 25 years with former pcp I googled celiac specialist and she wasn't because of what ive been through. I wanted my results to be sent to my pcp but nothing was sent.I have email copies.I did one zoom call with np with team member from celiac specialist in Nov 2025 and she asked me why I wanted to know why I wanted the celiac diagnosis so bad, I sad I don't, its my life and I need revalidaion because its affecting me.KB stated well it shows you are.I asked then why am I going through all this.I was labeled unruly. Its been a celiac circus and medical has caused anxiety and depression no fault to my own other than being born with bad genetics. How is it legal for medical professionals to gaslight patients that are with an ailment coming for help to be downplayed? KB put in my records that she personally spent 120min with me and I think the zoom call was discussing celiac 80 min ONE ZOOM call.SHE is responsible for not explaining to my pcp about celiac disease am I right?
    • Amy Barnett
      What is the best liquid multivitamin for celiac disease?
    • Jmartes71
      I've noticed with my age and menopause my smell for bread gives me severe migraines and I know this.Its alarming that there are all these fabulous bakeries, sandwich places pizza places popping up in confined areas.Just the other day I suffered a migraine after I got done with my mri when a guy with a brown paper bag walk in front of me and I smelled that fresh dough bread with tuna, I got a migraine when we got home.I hate im that sensitive. Its alarming these places are popping up in airports as well.I just saw on the news that the airport ( can't remember which  one)was going to have a fabulous smelling bakery. Not for sensitive celiacs, this can alter their health during their travel which isn't safe. More awareness really NEEDS to be promoted, so much more than just a food consumption!FYI I did write to Stanislaus to let them know my thoughts on the medical field not knowing much about celiac and how it affects one.I also did message my gi the 3 specialist names that was given on previous post on questions on celiac. I pray its not on deaf door.
×
×
  • 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.