Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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 Celiac.com!
    eNewsletter
    Donate

Help With Celiac-Like Symptoms But 2 Negative Blood Tests


dzaz

Recommended Posts

dzaz Newbie

I'm hoping I can get some input for what's been going on with me, and thanks in advance.

Over the past 5 years, I've had pretty normal health but perhaps every 14 months I'll get: abdominal distention, incredible gas, stools become very loose and rancid, and exhaustion. The bouts last for between 1 to 2 months and seem to resolve on their own with no diet change or meds. Last bout was 2006 and after lots of testing, they decided I had caught a parasite in the Caribbean, treated it, symptoms went away.

Same thing happened a month ago but this time after about 2 weeks of the symptoms I got a sudden sharp pain in lower right-side abdomen (like an ovarian cyst bursting); doctor checked for appendicitis (nope) but CT showed small bowel malapsorption and bile duct dilation. 2 Celiac blood tests came beck negative. Doctor said try going off gluten and dairy; I did and felt better within days.

Saw doctor yesterday; he said to add dairy back in and see how it goes and wants a MRI for "interesting" CT results of bowel and bile duct.

He said if dairy goes okay, to try gluten and if that doesn't go okay, to do the endoscopy. My question is what's the reasoning behind the endoscopy? If the gluten hurt, the gluten hurt, right? Would the endoscopy give results that would results in some sort of treatment (medication, surgery) or is it just more information? (FWIW I had a yogurt last night and my stars, that was a mistake).

I understand the blood test results can be non-conclusive and I'm fine with staying gluten and dairy free if I feel better, but my questions are: the small bowel and bile duct irregularities: are those Celiac markers or something else? And is there any point to adding gluten back and and getting the endoscopy?

Thanks for all responses; the internet can be a little overwhelming.

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



GlutenFreeManna Rising Star

Welcome! The Endoscopy gives more information about how much damage you have. However it's not always conclusive either. The damage could be patchy and if they don't take enough samples from the right places then they may miss it. The question you need to ask yourself is if you need to have a doctor diagnosis to stick to the diet or to convince other people in your life you need to stick to the diet. If you can do the diet without cheating and feel good then you should just do that. There's no surgery or medication for celiac disease/gluten intolerance. The diet is the only treatment at this time. You may need to take additional vitamins and will want to watch for other auto-immune diseases.

Link to comment
Share on other sites
dzaz Newbie

Thanks; this is exactly what I was wondering about the endoscopy.

I'm still confused about the dilated bile duct and small bowel malabsorption. Celiac-type of thing or not?

Thanks again!

Link to comment
Share on other sites
Kay DH Apprentice

Small bowel malabsorption is a characteristic of celiac disease. With celiac, it results from damage to the villi in the duodenum (just south of the stomach). These villi, like little fingers, absorb nutrients. A person's immune system attacks the villi and damaged villi cannot absorb nutrients. If you do have an endocopy, make sure the doctor has you on 4+ slices of bread/day for at least 4 weeks and takes multiple samples for biopsy. Regarding bile ducts, celiac can affect multiple organs. A family member, for example, had to have the gallbladder removed this year (she's going gluten free now).

Link to comment
Share on other sites
star25 Newbie

hi im new here ive also had abdominal issues mine started 8months ago

after a kidney infection ever since suffered non stop uti (but no symptoms till

it reaches kidneys).....then started getting right side abdo pain lower/upper

then moved to left side,started getting tenderness then suddenly hit with

weight gain of 3stone no reason took me months to get the doctor to take

me seriously and my blood tests always showed high wwc and crp,,finally seen

a gastro who ordered ct scan and upper endoscopy/gastroscopy.....

before this started getting very loud gas and my intestines makes alot of noise

i sometimes get headaches and get the most awlful side and back pain...

they tested me for thryoid--neg the usaul testing then celiacs which came

back neg,i get constapiated and odd diarrea,loose and fatty stools sometimes...

i thought it was gallbladder as i found things like pastry's,choc,gravey etc made

pain worsen...i even look pregnant but im not.....ct scan showed i had swollon lymth nodes taking it in my small bowels like i said bloods showed nothing

but inflammation im waiting on 2 biopsys taken last week from gastroscopy

one for h-polri and one for celiacs they decided to take one for celiacs

as the test showed i had multi erosions (non ulcer)....i think my problems

are linked to the uti's aswell so been researching myself wether celiacs and utis are related etc..........however i think its worth having the camera since

it can look inside.......good luck

Link to comment
Share on other sites
Skylark Collaborator

Thanks; this is exactly what I was wondering about the endoscopy.

I'm still confused about the dilated bile duct and small bowel malabsorption. Celiac-type of thing or not?

Thanks again!

A doctor cannot see the celiac villous damage on CT. The damage is microscopic. Malabsorption can be celiac, but also Crohn's or microsocopic colitis. I've noticed a lot of people on this board have gall bladder and bile duct problems, so that is consistent with celiac. With the endoscopy, your doctor would take a biopsy and look for the celiac damage and rule out other problems.

There is no treatment for celiac other than the gluten-free diet, so if gluten hurts you pretty much have the answer you need. Your doctor is probably trying to be conservative and make sure you don't have other things going on.

Link to comment
Share on other sites

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,074
    • Most Online (within 30 mins)
      7,748

    Robert Noah
    Newest Member
    Robert Noah
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Nacina
      Well, that's a big question. When he was seeing the nutrition response testing dr. that changed each time we went in. He hasn't been seeing him regularly for theist ten months. When he had a horribly week in March I started him back on the 4 that were suggested to keep him on. Those are: Standard Process Chlorophyll Complex gluten-free, SP A-F Betafood gluten-free, SP Tuna Omega-3 Oil gluten-free, And Advanced Amino Formula. He also takes a one a day from a company called Forvia (multivitamin and mineral) and Probiotic . Recently he had to start Vitamin D as well as he was deficient.  
    • Fluka66
      Thank you again for your reply and comments which I have read carefully as I appreciate any input at this stage. I'm tending to listen to what my body wants me to do, having been in agony for many years any respite has been welcome and avoiding all wheat and lactose has thankfully brought this.  When in pain before I was seen by a number of gynacologists as I had 22 fibroids and had an operation 13 years ago to shrink them . However the pain remained and intensified to the point over the years where I began passing out. I was in and out of a&e during covid when waiting rooms where empty. My present diet is the only thing that's given me any hope for the future. As I say I had never heard of celiac disease before starting so I guess had this not come up in a conversation I would just have carried on. It was the swollen lymph node that sent me to a boots pharmacist who immediately sent me to a&e where a Dr asked questions prescribed antibiotics and then back to my GP. I'm now waiting for my hospital appointment . Hope this answers your question. I found out more about the disease because I googled something I wouldn't normally do, it did shed light on the disease but I also read some things that this disease can do. On good days I actually hope I haven't got this but on further investigation my mother's side of the family all Celtic have had various problems 're stomach pain my poor grandmother cried in pain as did her sister whilst two of her brother's survived WW2 but died from ulcers put down to stress of fighting.  Wishing you well with your recovery.  Many thanks  
    • knitty kitty
      Welcome to the forum, @Nacina, What supplements is your son taking?
    • knitty kitty
      @BluegrassCeliac, I'm agreeing.  It's a good thing taking magnesium. And B vitamins. Magnesium and Thiamine work together.  If you supplement the B vitamins which include Thiamine, but don't have sufficient magnesium, Thiamine won't work well.  If you take Magnesium, but not Thiamine, magnesium won't work as well by itself. Hydrochlorothiazide HCTZ is a sulfonamide drug, a sulfa drug.  So are proton pump inhibitors PPIs, and SSRIs. High dose Thiamine is used to resolve cytokine storms.  High dose Thiamine was used in patients having cytokine storms in Covid infections.  Magnesium supplementation also improves cytokine storms, and was also used during Covid. How's your Vitamin D? References: Thiamine and magnesium deficiencies: keys to disease https://pubmed.ncbi.nlm.nih.gov/25542071/ Hiding in Plain Sight: Modern Thiamine Deficiency https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533683/ The Effect of a High-Dose Vitamin B Multivitamin Supplement on the Relationship between Brain Metabolism and Blood Biomarkers of Oxidative Stress: A Randomized Control Trial https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316433/ High‐dose Vitamin B6 supplementation reduces anxiety and strengthens visual surround suppression https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9787829/ Repurposing Treatment of Wernicke-Korsakoff Syndrome for Th-17 Cell Immune Storm Syndrome and Neurological Symptoms in COVID-19: Thiamine Efficacy and Safety, In-Vitro Evidence and Pharmacokinetic Profile https://pubmed.ncbi.nlm.nih.gov/33737877/ Higher Intake of Dietary Magnesium Is Inversely Associated With COVID-19 Severity and Symptoms in Hospitalized Patients: A Cross-Sectional Study https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132593/ Magnesium and Vitamin D Deficiency as a Potential Cause of Immune Dysfunction, Cytokine Storm and Disseminated Intravascular Coagulation in covid-19 patients https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7861592/ Sulfonamide Hypersensitivity https://pubmed.ncbi.nlm.nih.gov/31495421/
    • BluegrassCeliac
      Hi,   Not saying Thiamine (B1) couldn't be an issue as well, but Mg was definitely the cause of my problems. It's the only thing that worked. I supplemented with B vitamins, but that didn't change anything, in fact they made me sick. Mg stopped all my muscle pain (HCTZ) within a few months and fixed all the intestinal problems HCTZ caused as well. Mom has an allergy to some sulfa drugs (IgG Celiac too), but I don't think I've ever taken them. Mg boosted my energy as well. It solved a lot of problems. I take 1000mg MgO a day with no problems. I boost absorption with Vitamin D. Some people can't take MgO,  like mom, she takes Mg Glycinate. It's one of those things that someone has try and find the right form for themselves. Everyone's different. Mg deficiency can cause anxiety and is a treatment for it. A pharmacist gave me a list of drugs years ago that cause Mg deficiency: PPIs, H2 bockers, HCTZ, some beta blockers (metoprolol which I've taken -- horrible side effects), some anti-anxiety meds too were on it. I posted because I saw he was an IgG celiac. He's the first one I've seen in 20 years, other than my family. We're rare. All the celiacs I've met are IgA. Finding healthcare is a nightmare. Just trying to help. B  
×
×
  • Create New...