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

Got Test Results- Need A "hug"


Guest BERNESES

Recommended Posts

Guest BERNESES

Hi Everyone- This board has been so helpful to me in so many ways since I was told by my primary care doctor that I may have Celiac's. I have had multiple blood tests (including the test for Celiac's which showed a weak positive) a CT scan and an upper GI/ small intestine biopsy. I got the results today- technically, I don't have Celiac's.

However, I had been gluten-free for 9 weeks before the test and was starting to feel much, much, much better in so amny ways. Many of my symptoms resolved, but I ate gluten for 10 days before the test and was sick as a dog- all my old symptoms retturned- even some little ones that I hadn't even noticed as being related to the wheat. According to the doctor, it may have been "mind over matter" although I'm not quite sure exactly how I could conjure up all the things that happened to me ;) I'd have to be a magician.

I said before the biopsy that I didn't need a definitive diagnosis to know that I can't eat gluten, but just when I was starting to feel better after ten days of hell, I accidentally "glutened" myself on Monday and wound up in the ER room last night with all my symptoms back in a fury. I seriously felt like I was going to DIE. They, of course, ran tons of tests, none of which showed anything except constipation (my bowels are quite backed up). I KNOW this is gluten but that was the worst experience I've ever had. I just need some cheerleading right now while I get this stuff out of my system. I feel a little better today but not much. Thanks everyone, Beverly


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



Celiac.com Sponsor (A8-M):



Canadian Karen Community Regular

Hi Beverly,

I think the fact that you have had such a positive response to the gluten free diet would be enough for me to accept the fact that I have Celiac Disease. Remember, when they do biopsies, they take biopsies from various sections but that does not guarantee that if there is damage, they are going to hit the right spots. From what I have read here, there are lots of times a biopsy does not show the damage because damage tends to be sporatic.

I would certainly keep on the gluten free diet. At the very least, even if it not celiac, you could have just an "allergy" to wheat without actually having celiac, which in that case the gluten free diet would be the way to go anyway...... Maybe trying an elimination diet would help you pinpoint which allergy you suffer from......

Sending you cyber hugs to help you get through this and give some support.......

Karen

KaitiUSA Enthusiast

Just because a biopsy shows no damage does not mean you do not have celiac. You may not have damage at this point or you could have sporadic damage and they got a sample from a section that was not damaged. Obviously you have a problem with gluten...my guess is you are either gluten intolerant or celiac. Listen to your body though..it knows best. What blood tests did you have done for celiac? Some are very specific so if they were elevated there has to be something going on.

Guest gliX

Also, if you had a virus during the bioscopy (doesn't have to mean you're sick or feel any symptoms from being sick), then the test wouldn't have shown the right results.

Guest BERNESES

Thanks Everyone- I know that I have Celiac's, I guess I just have to give up on waiting for a doctor to agree. I had pretty much made peace with it after getting such a positive response from the gluten-free diet and the ONLY reason that I even did the biopsy was to hope I'd get a more definitive answer because I know it's genetic and I'm adopted so I wanted to know for the purpose of my own children's sake when I have them. But, now I at least know what to look for in a baby as well thanks to this board and the research I have done.

I had all the blood tests done except for the gene and it was either my IgG or IgA that was a weak positive. It was about a 23 with over 20 being considered a weak positive.

Thank you all for responding. Last night was really scary- it really was the sickest I've ever felt in my entire life. Health to all, Beverly

bigapplekathleen Contributor

HI Beverly,

I am so sorry to hear how sick you are. Have you ever had the genetic test for Celiac Disease? That will give you pretty accurate results even if you're on a gluten-free diet. (95-97% of Celiac patients have the gene, perhaps even higher percentage according to latest studies.)

I see one of the top celiac docs in the world, but know now that I don't have celiac disease. I do, however, have non-celiac gluten intolerance, which means I don't have the gene for celiac, but I do get a lot of symptoms when I consume gluten.

Is it possible that you are gluten intolerant but not celiac? Does your doc know about this possibility? There are other diseases, also, that can get better on a gluten-free diet.

I have hit the point now, though, where I have pretty much given up on doctors' diagnoses - even these top docs - because they are always just looking for more sickness, rather than concentrating on wellness. I know I feel well when I follow a pretty strict PALEO diet and when I don't eat the same foods every day (I am aiming for a 4-day rotation of all foods).

I wish you the best in your recovery...

kathleen

Guest BERNESES

Thanks kathleen- I pretty much know what makes me feel better and it is not eating gluten. I've never had the gene test but I am considering it. Either way- if I have Celiac's or am gluten intolerant- I'm staying away from gluten FOREVER! By the way, what is the PALEO diet with a four day rotation. Thanks for all your support, Beverly


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



Celiac.com Sponsor (A8-M):



FaithInScienceToo Contributor

Beverly -

Just wanted to add my message of support -

MAINLY...keep on listening to your body.

I think you should, though, get the gene testing done, to be know if you can actually have 'Celiac disease,' because without one of the two ID'd genes, you cannot have 'celiac'...

...but also know that even if you don't have one of the 2 genes, gluten-intolerance can still cause great bodily distress, and being gluten-intolerant isn't 'less disconcerting' than having celiac disease...some people who are celiacs are less sick then some people who are severely gluten-intolerant...there is a wide range of variability in both 'illnesses'...having one does not trump the other, or qualify a person for more empathy...

I would bet that severe gluten-intolerance alone will one day be linked to many serious disorders, just like celiac diesase is...

Enterolab offers testing for both gluten intolerance and genetic testing (via cheek swabs)...I would recommend that you get those tests...but, you don't 'need' to...If you do, however, it will give you more scientific info about your body to have on hand, to be able to help you understand both current and future research findings/reports...

Only you know how you feel, though, and only you can do for you what you need to do to feel your best and protect your health.

Best wishes for improved health to you, Gina

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.