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

Is A Scope Neccesary?


Guest shai

Recommended Posts

Guest shai

I have had food allergies for years now with reactions such as hives, asthma, and eczema, as well as swelling after meals. I noticed that whenever I would eat starchy foods I would lose weight. When I was pregnant I started getting the diarreah every day, all day. It continued for months after having the baby last June. I went to the doctor in August and told her my symptoms and she did the gluten intolerance blood test and it came back positive for the antibodies. I started the diet and in about a month I saw a big improvement in my symptoms. ALong with the diarreah I had an itchy bum <_< blistery, eczema-like skin problems, and the asthma problems and a sore throat after eating wheat. It almost sounds like I am also allergic to wheat. is that pretty common? Or is an anaphelectic reaction typical with gluten intolerance?

Also, my sons GI specialist told me the only way to know for sure is to get a scope up my butt. I don't want to have to do that. Is it the only way to know for sure, or is the blood test pretty conclusive? My doctor said that only people with celiacs produce the antibodies against gluten, and that along with the symptoms a scope shouldn't be necessary. WHat do you all think.

I'd also like to mention that my sister has all the same symptoms as me, but her blood test came back negative. Should she have the scope too? Thanks!

Shai


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



Celiac.com Sponsor (A8-M):



tom Contributor

I think most of the scoping is down the esophagus.

It's an Upper Endoscopy.

Open Original Shared Link

Re: your sister's negative blood test. Earlier this year, a Columbia U study found an astounding percentage of false negatives in the classic celiac blood (serological) test.

https://www.celiac.com/st_prod.html?p_prodid=1023

They started w/ 115 biopsy-proven adult celiacs, and put them in 2 groups - total villous atrophy and partial.

Only 77% of the group w/ TOTAL atrophy tested positive !

And only a third of the partials.

That means a LOT of celiacs have had a doctor say "the blood test says u don't have celiac disease" when the truth may be they've gotten as far as TOTAL villous atrophy.

If i weren't already diagnosed, i think i'd want the genetic HLA-typing to be sure whether DQ2 and/or DQ8 are there.

[edited typo 12-7]

bigapplekathleen Contributor

The scope is done by "upper endoscopy." Check out the WEbMD info about that procedure.

I had one done yesterday. IT was quick and painless, but I was groggy the rest of the day due to the sedative.

good luck!

judy05 Apprentice

I urge you to have the scope. I'm so glad my GI doc insisted upon it.

I tested neg for celiac, my villi were not damaged but they found

Barrett's Ring around the esophagus. It is caused by a weak

sphincter and the acid "backs up" (reflux) and splashes up into

the esophagus. In time this could turn to cancer so I

have to be scoped yearly. I urge anyone with acid reflux or

gerd to have this done.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,855
    • Most Online (within 30 mins)
      7,748

    Tara M
    Newest Member
    Tara M
    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

    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
    • Francis M
      Thanks. Since the back and forth and promises of review and general stalling went on for more than six months, the credit company will no longer investigate. They have a cutoff of maybe six months.
    • Scott Adams
      Is this the same restaurant? https://www.facebook.com/TheHappyTartFallsChurch/ Is it too late to take this up with your credit card company? Normally you have a few months to do a chargeback with them. It seems very odd that they are taking this approach with someone who is likely to be a regular customer--not a good business-minded way of handling things!
    • Scott Adams
      Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: The most common nutrient deficiencies associated with celiac disease that may lead to testing for the condition include iron, vitamin D, folate (vitamin B9), vitamin B12, calcium, zinc, and magnesium.  Unfortunately many doctors, including my own doctor at the time, don't do extensive follow up testing for a broad range of nutrient deficiencies, nor recommend that those just diagnosed with celiac disease take a broad spectrum vitamin/mineral supplement, which would greatly benefit most, if not all, newly diagnosed celiacs. Because of this it took me decades to overcome a few long-standing issues I had that were associated with gluten ataxia, for example numbness and tingling in my feet, and muscle knots--especially in my shoulders an neck. Only long term extensive supplementation has helped me to resolve these issues.        
×
×
  • 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.