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

Help Sorting Things Out


Kerryloves2travel

Recommended Posts

Kerryloves2travel Newbie

HI~

I'm new here and have had undiagnosed issues for years - last 5 have been a whirlwind of "I've never seen that before" symptoms. Father & his sister had type 1 diabetes & died at 43, so naturally I am terrified of that diagnosis. Sister has discoid lupus, bro now Type 2 ? diabetes with horrible neropathy & nerve damage. Niece has psoriasis.

Latley docs blame mine on menopause, but I keep telling them thers is something autoimmune going on. Have a bit of osteo arthritis in knee, but fluid drainage & yoga has helped that. Been very active all my life.

My symptoms include "traveling" joint pain, fatigue, dry mouth, inflammation, weird rash on trunk of body & side of face, accompanied with extreme fatigue & gut ache- this typically lasts 4-5 days and is gone. By time I get to doc, rash is gone. Finally saw dermatologist that said she had never seen anything like it! Did all types of Lyme disease testing, mercury poisoning, etc. Next step is to do skin biopsy when comes back-

Supporting my brother I went with him to wonderful clinic 4 hours away. I have had burning feet & pin & needles & edema. Neurologist there did test & said I had some nerve damage. Ordered blood work & found very low in B12.

Did research & found joint pain, nerve damage sign of low B12. Eat plenty in diet, so not absorbing it.

Started weekly shots. Good news blood sugar was excellent! Follow up w doc here ..tested for iron, anemia, etc . no problems. But celiac disease test showed:

TTG AB, Iga 1.3 Under 7 neg.

Gliadin DGP AB iga 14. 4 over 7-10 positive Flag H

Iga 607 standard 87-474. Flag H

Is 1st test the standard talked about? Doc said she had never seen such a high Iga number in 16 years of practice.

I have NO gut or bowel issues. In fact, I seem to have a strong stomach compared to most of my friends.

Can anyone help decipher this?

Referred to GI and wants me to do colonscopy (why no endoscopy?) which insurance doesn't pay...goes to deductible which is very high ( so are our premiums- but I bet most of you know this problem already!)

Waiting as my son has had stomach problems, on and off for 2 years. Started in college & stress totally adds to his issues. He is scheduled for endoscopy this week.

Meanwhile, I will try gluten free diet. Couldn't hurt, right?

Any info or comments would sure help....

Thanks.


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



Celiac.com Sponsor (A8-M):



IrishHeart Veteran

Stay on gluten and have a celiac biopsy done!!

Celiac is NOT diagnosed via colonoscopy or just an endoscopy alone.

You need the biopsy done. Your Doctor should know this.

If your derma knows how to do a proper biopsy for Dermatitis herpetiformis, the skin form of celiac disease, she can DX you from that. (If indeed, your rash is DH)

It does not matter if you have no gastro symptoms. Many people have no gastro issues ---but tons of autoimmune problems and vitamin deficiencies--- and when biopsied, show total villous atrophy.

You can have Silent Celiac.

Read about the disease a bit more. To me, all those symptoms you have add up.

Your celiac panel seems incomplete, as far as I know, but someone else can weigh in here with better knowledge.

I am sero-negative, so my test results meant nothing and I confess, I am not very well-versed in interpreting them.

Even if you are NEG on testing, a gluten-free diet will tell you if it's an issue.

Takala Enthusiast

Insist on getting an endoscopy biopsy, NOT a colonoscopy. The endoscopy looks at damage in the stomach/small intestine and is the next step after (positive) blood tests. Stay on gluten until this is done. Refuse the colonoscopy if the GI doc claims that must be done "first" in the sequence. Insist on being referred to non- crooked GI immediately if they do not cooperate. (threaten to turn them in to your state medical board if they persist in doing tests which are irrelevant.) Work with dermatologist to get biopsy done on next skin outbreak, which is also way to get official celiac diagnosis.

Insurances typically will pay for baseline colonoscopy around age 50 and most GI docs see this as a real cash cow- you go to them for anything, and they will try to schedule you for one of these instead of what you came to them for.

Digital cameras are very handy for documenting rashes.

Get all copies of tests, in writing.

PM Skylark if she does not show up here soon.

Cara in Boston Enthusiast

Just wanted to repeat: KEEP EATING GLUTEN until your testing is done. Even a short time gluten free can change test results.

Metoo Enthusiast

HI~

I'm new here and have had undiagnosed issues for years - last 5 have been a whirlwind of "I've never seen that before" symptoms. Father & his sister had type 1 diabetes & died at 43, so naturally I am terrified of that diagnosis. Sister has discoid lupus, bro now Type 2 ? diabetes with horrible neropathy & nerve damage. Niece has psoriasis.

Latley docs blame mine on menopause, but I keep telling them thers is something autoimmune going on. Have a bit of osteo arthritis in knee, but fluid drainage & yoga has helped that. Been very active all my life.

My symptoms include "traveling" joint pain, fatigue, dry mouth, inflammation, weird rash on trunk of body & side of face, accompanied with extreme fatigue & gut ache- this typically lasts 4-5 days and is gone. By time I get to doc, rash is gone. Finally saw dermatologist that said she had never seen anything like it! Did all types of Lyme disease testing, mercury poisoning, etc. Next step is to do skin biopsy when comes back-

Supporting my brother I went with him to wonderful clinic 4 hours away. I have had burning feet & pin & needles & edema. Neurologist there did test & said I had some nerve damage. Ordered blood work & found very low in B12.

Did research & found joint pain, nerve damage sign of low B12. Eat plenty in diet, so not absorbing it.

Started weekly shots. Good news blood sugar was excellent! Follow up w doc here ..tested for iron, anemia, etc . no problems. But celiac disease test showed:

TTG AB, Iga 1.3 Under 7 neg.

Gliadin DGP AB iga 14. 4 over 7-10 positive Flag H

Iga 607 standard 87-474. Flag H

Is 1st test the standard talked about? Doc said she had never seen such a high Iga number in 16 years of practice.

I have NO gut or bowel issues. In fact, I seem to have a strong stomach compared to most of my friends.

Can anyone help decipher this?

Referred to GI and wants me to do colonscopy (why no endoscopy?) which insurance doesn't pay...goes to deductible which is very high ( so are our premiums- but I bet most of you know this problem already!)

Waiting as my son has had stomach problems, on and off for 2 years. Started in college & stress totally adds to his issues. He is scheduled for endoscopy this week.

Meanwhile, I will try gluten free diet. Couldn't hurt, right?

Any info or comments would sure help....

Thanks.

I am no expert, but your blood work shows you have celiac. Usually doctors require the endoscope to diagnose you, they won't just rely on bloodwork alone, but endoscopes can have false positives. Your son probably has it too, its genetic.

Do NOT go gluten-free until you are done with testing.

Many people don't have gastrointestinal symptoms, or are fairly symptomless, but there is still internal damage going on.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,972
    • Most Online (within 30 mins)
      7,748

    Hawaiian Snow
    Newest Member
    Hawaiian Snow
    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

    • cristiana
      Interesting, when I suffered for a few months with ectopics I noticed that carbohydrates would cause indigestion and bloating in my stomach, then that would lead to my heart skipping beats, and I could feel it in my throat, it was very unsettling.  My last serious bout of this was after eating a Muller Rice Pudding for breakfast.   I happened to be wearing a 48 hour halter at the time and cardiology picked it up, but they weren't worried about what they saw. There was some British doctor who'd made some videos on the Vagus nerve that I remember watching at the time which made sense of what I was experiencing, there did seem to be some sort of connection.
    • Scott Adams
      Here are summaries of research articles on celiac disease and migraines: https://www.celiac.com/celiac-disease/celiac-disease-amp-related-diseases-and-disorders/migraine-headaches-and-celiac-disease/
    • Yaya
      I asked my cardiologist about stopping vitamins.  He said his tests account for all detectable vitamins from sources other than food.  I only need to stop them for a couple of days.  He has me keep records of meds and vitamins I've ingested over the past 10 days and prior and he does his calculations.   
    • jessysgems
      Reply to treats I try and eat to bring up the glucose. Sometime I get up 3 times a night and eat something. I don't think food is the issue. A lot of the food they say should help doesn't.  Many mornings my level is 59 and I feel sick, sometimes for hours. It has been recommended I go to an Endocrinologist.  
    • Scott Adams
      Welcome to the forum! This article has some detailed information on how to be 100% gluten-free, so it may be helpful (be sure to also read the comments section.):    This article may also be helpful:
×
×
  • 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.