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

My Story


MJ-S

Recommended Posts

MJ-S Contributor

I've been gathering so much incredible information on this board for the last few months - I just wanted to introduce myself and share my story! I've also been meaning to document everything with a timeline, so hopefully I apologize in advance for TMI. I figure there is no better audience!

March 2010: I started getting sick. It was very sudden (no illness to bring it on, however) with daily nausea, gas, stomach pain/cramps, no D, mild C (I've always had that), a non-itchy rash on my arm, swollen eyelid, and a super white stinky tongue that would come and go.

April 2010: I linked my symptoms to dairy and discontinued it. Symptoms would begin about one day after consuming dairy and last 3-4 days. Immediately after stopping dairy, my eyelid returned to normal and has never resurfaced; initially all other symptoms eased dramatically. Still, I kept getting sick now and then and I drove myself crazy looking for hidden sources of dairy in my diet. My primary doc told me I was lactose intolerant but refused to test for it. I told her I thought I was casein intolerant. She referred me to an allergist who did skin testing, all negative, but didn't know about the casein test.

May - Sept 2010: Symptoms gradually worsened. A few dairy tests (tiny amounts of lactose free milk, goat cheese) put me in bed for days. I was getting new symptoms (daily dizzy spells and angular cheilitis) along with fatigue, and worsening GI symptoms. Constant daily nausea returned. Returned to doc, who tested for Celiac (negative) along with other standard bloodwork. My B12 levels were borderline low. I was referred to GI doc who did nothing (also told me I was lactose intolerant but didn't want to test for it). He did one good thing which was to refer me to a wonderful nutritionist. She, in turn, referred me to a more responsive GI doc AND told me I might be GLUTEN INTOLERANT. I refused to consider that as a viable option at the time.laugh.gif

Oct-Dec 2010: Underwent a battery of tests with new GI doc. Bloodwork (re-tested for celiac, still negative), X-rays, ultrasound, endoscopy, gallbladder. All normal except stomach was found to be red (mild gastritis) and gallbladder was functioning at 88% (doc said that was normal). Folate levels were elevated. I was told to go on FODMAPS diet and take probiotics, along with weekly B12 spray. Continued to get sicker and sicker. New allergist re-skin tested but also refused to do the casein test (said it's unreliable).

Jan 1, 2011: Based on the advice of my nutritionist (note that NONE of the 5 docs I saw suggested this) I decided to try going gluten free. FODMAPS wasn't working and I was desperate. By Christmas I could barely function and everyone was saying how thin I was. I was, however, still consuming low quantities of wheat. I figured it would be easier to eliminate gluten than the entire FODMAPS spectrum. Within days of eliminating gluten I felt SO MUCH better!

Jan-Feb 2011: I improved but still had some gas/pain/brain fog (generally never as bad as it had been). Then I discovered that one of the soymilks I was buying had barley/wheat extract in it. That was a BAD day - I was so discouraged! After that, I got even better. At my follow-up with GI doc, I told him I was gluten intolerant. He said: not possible with negative celiac tests. He told me I had IBS, that I felt better because of wheat (fructose) elimination and sent me on my way. I won't return. Luckily I live in Boston and now know about the Celiac Center.

March 2011: Overall, my energy has returned, my mood is lifted, and GI symptoms have really eased up! The arm rash is almost gone (although not totally). I've had a few more mis-steps. A few weeks ago it was a piece of crabstick at a sushi restaurant - I had pain, extreme fatigue, and brain fog for almost a week. That incident removed a lot of doubt left in my mind. I also found out last week that the Pearl probiotic I've been taking has trace dairy, so I've just discontinued it (beware because the old box says dairy free, but the new box does not, and when I e-mailed the company they confirmed that it's derived from dairy and thus had to change the label). Since last night I've been suffering pretty bad stomach pain because I bought store-made split-pea soup at Whole Foods. The ingredients are a go, but I get nervous anytime it doesn't specifically say Gluten/Dairy Free. It's also one of my first forays in a while into the legume world, so I'm not sure if that's the problem.

So here I am! Happier, less gassy, and usually less pain free! Definitely more energetic, and starting to get a bunch of new favorite foods (the Foods by George english muffins are just sinfully good)! Looking forward to lots of great conversations!


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



Celiac.com Sponsor (A8-M):



kwylee Apprentice

Excellent gluten travel story and so pleased to see it has the promise of a happy ending. I love the part where the doctor tells you that you can't be gluten intolerant. He probably went home, ate a big steaming bowl of "healthy" whole wheat pasta, and one chance out of three, felt bad later but didn't connect the dots. You are so far ahead of the game! Glad you are feeling better.

YoloGx Rookie

Welcome! Your story is not atypical. Most of us have resistance to going on a gluten free diet etc. so ist takes a while before we decide to bite the bullet and do it.

And like the other poster intimated, many doctors aren't aware of severe gluten intolerance without it being celiac. Further, just as an aside, many of the tests for celiac are inadequate. In the future I am betting they will reconsider and improve their approach.

But for you, as it is for many here, its important to know being off gluten (and possible additional allergens or sensitivities from likely leaky gut syndrome) is the main thing to have improved health.

MJ-S Contributor
But for you, as it is for many here, its important to know being off gluten (and possible additional allergens or sensitivities from likely leaky gut syndrome) is the main thing to have improved health.

Yes, that's been key. I've kept a food diary throughout the process; with that and the allergy testing (positive for plums, hazelnuts, sesame - all of which I avoid) I've wanted to be "totally sure". I also hope that maybe one day I'll be able to have dairy again, which I dearly miss (much more than gluten).

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,121
    • Most Online (within 30 mins)
      7,748

    jenr8er
    Newest Member
    jenr8er
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • rei.b
      I hadn't been eating gluten free before having the antibody test done. I started eating gluten free after having the test done because the gastro PA told me to eat gluten-free for 6 months. I'm now 3 months in.
    • trents
      I tend to agree with RMJ. Your doc took the reasonable and practical approach to diagnosis. All things considered, it was the right way to go. However, if you have first degree relatives that show signs of possible celiac disease, urge them to get formally tested before they start the gluten free diet.
    • RMJ
      It sounds like you have a very reasonable GI doctor, who diagnosed you based on family history and symptoms after eating gluten. I would consider you lucky! The other option would be to make yourself very sick by doing weeks of a gluten challenge prior to an endoscopy.
    • captaincrab55
      Hi Colleen H,   I suffered with the pins and needles/burning feeling in my legs and feet for at least  6 years until my Nephrologist figured out that I had to go on a low salt diet.  He said my kidneys weren't strong enough to remove the salt.  The simple fix was a diuretic, but that med leaves the uric acid behind, so that wasn't an option.  On the bright side the low salt diet lowered my BP over 20 points and and the pins and needles/burning feeling went away.  Good Luck and hope this helps.  
    • Colleen H
      Yes this is very frustrating for me ... not sure what to think.  Feels like I'm having reactions to a lot of things  Now applesauce?? I don't understand 😞 
×
×
  • 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.