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

Endoscopy today


Jlewisrn

Recommended Posts

Jlewisrn Contributor

I had an endoscopy today and the dr said everything looked good. He took some biopsies but said "you don't have celiac" I cried. Not out of relief but because it's another doctor (and more money) to not know what's wrong with me. This rash is driving me mad. Literally. I could cut out gluten but what if that doesn't work. Then what? Corn, wheat, soy, dairy, foods high in oxalates, salt, cpffee, soda??? Where do I even start? All the dr's know is to prescribe me steroids that don't work. I guess I'll just get doped on on antihistamines. I'm literally getting depressed over this. I was really hoping for answers today. I knew deep down it wouldn't show anything but I was hoping. 


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

DH need to be biospsied on the skin next to a fresh lesion.  Also, Celiac damage is rarely seems by the naked eye - it requires a microscope.

cyclinglady Grand Master

My GI said the same thing, but he warned me that we would have to wait for the pathologist's report.  Guess what?  The report showed moderate to severe patches of intestinal damage.  So, hang in there and just wait for those results.  

GF-Cheetah Cub Contributor

Same here.   Our doctor told us that my daughter does not have celiac right after the endoscopy.   We were overjoyed.   2 weeks later, they called and gave us the test results, and that she does have celiac.

I would wait at least until the actual results before worry about next steps.

Jmg Mentor
4 hours ago, Jlewisrn said:

I could cut out gluten but what if that doesn't work.

What if it does? It did for me despite a negative celiac diagnosis. 

I know you want answers and certainty and you may get them, but if you don't there's still lots you can do to secure the real aim, good health. That's all in the future however and why not cross the bridges when you come to them? 

Gluten-free-01 Enthusiast
6 hours ago, Jlewisrn said:

Not out of relief but because it's another doctor (and more money) to not know what's wrong with me. This rash is driving me mad. 

Please keep in mind that ‘regular’ doctors, unlike doctors of functional medicine, rarely try to find the root causes of their patients’ problems. I had seborrheic dermatitis a few years ago and, as expected, I got a prescription shampoo and a liquid solution and that was it.

I still respect doctors in general, though, because in many health related situations the ‘classical medicine’ approach is the best/saves your life etc. It really depends on the condition. Gluten sensitivity is much more related to the functional medicine approach, in my opininon.

Even though you haven’t been diagnosed as a celiac a gluten-free diet may still help you because you may be non celiac gluten sensitive.

(Sorry if there are any mistakes – not a native English speaker).

Victoria1234 Experienced
1 hour ago, Gluten_free_01 said:

I had seborrheic dermatitis a few years ago and, as expected, I got a prescription shampoo and a liquid solution and that was it.

Did you find something else to help it? I've got sd also and was given a shampoo and cream.


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



Celiac.com Sponsor (A8-M):



squirmingitch Veteran
9 hours ago, Jlewisrn said:

I had an endoscopy today and the dr said everything looked good. He took some biopsies but said "you don't have celiac" I cried. Not out of relief but because it's another doctor (and more money) to not know what's wrong with me. This rash is driving me mad. Literally. I could cut out gluten but what if that doesn't work. Then what? Corn, wheat, soy, dairy, foods high in oxalates, salt, cpffee, soda??? Where do I even start? All the dr's know is to prescribe me steroids that don't work. I guess I'll just get doped on on antihistamines. I'm literally getting depressed over this. I was really hoping for answers today. I knew deep down it wouldn't show anything but I was hoping. 

As has already been stated, the doctor can't tell by a visual. They can in very rare cases when the damage is so complete as to result in total villous atrophy but it's certainly not the norm. The pathology on the biopsies will tell the tale. I hope he took the recommended 6 biopsies. Get a copy of the pathology report when it comes in.

Gluten-free-01 Enthusiast
2 hours ago, Victoria1234 said:

Did you find something else to help it? I've got sd also and was given a shampoo and cream.

No, not really.. It wasn't very severe and eventually went away without any special treatment. The Dr. said it might have been caused by stress.   

Gluten-free-01 Enthusiast

Victoria: I think sd can also be caused by candida so I guess a 'candida diet' could help. No sugar etc. 

Ennis-TX Grand Master
11 hours ago, Jlewisrn said:

I had an endoscopy today and the dr said everything looked good. He took some biopsies but said "you don't have celiac" I cried. Not out of relief but because it's another doctor (and more money) to not know what's wrong with me. This rash is driving me mad. Literally. I could cut out gluten but what if that doesn't work. Then what? Corn, wheat, soy, dairy, foods high in oxalates, salt, cpffee, soda??? Where do I even start? All the dr's know is to prescribe me steroids that don't work. I guess I'll just get doped on on antihistamines. I'm literally getting depressed over this. I was really hoping for answers today. I knew deep down it wouldn't show anything but I was hoping. 

First off again wait for the biopsies to come back in, second NCGS is a real thing and can cause celiac like symptoms but no actual gut damage. If your having DH then those need to tested, Celiacs with DH normally have less intestinal damage but can be more easily diagnosed via skin biopsy taken next to the lesions of the rash.

Wait for testing to be 100% complete then treat this as if you were dia positive for celiac regardless. You will probably feel much better and by the sound of it this could be your cause. Keep a food diary, write down EVERYTHING you eat and how you fix it including seasonings etc. Change up your diet and rotate foods around staying off some seasonings and ingredients for a few days. Record how you feel throughout the day at set intervals. Look for patterns, this is quite enlightening and simplifies matters for other intolerance, and allergy issues.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,857
    • Most Online (within 30 mins)
      7,748

    LowellFrancis
    Newest Member
    LowellFrancis
    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

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • 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    
×
×
  • 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.