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

Need Input


deb

Recommended Posts

deb Apprentice

I don


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



Celiac.com Sponsor (A8-M):



burdee Enthusiast

Hey Deb:

Don't settle for the "IBS" label. That's a doctor copout. Someone on this board renamed that label "IDK" or "I don't know" which is what doctors SHOULD say rather than using a disease sounding acronym to hide their ignorance. I prefer to translate IBS as "I'm being squeezed", because that's exactly how my intestines feel when I'm suffering celiac relapse (gluten slip) pain. Your abdominal symptoms and pain sound SOOOO much like mine pre gluten-free diet. If I sound a little angry about the IBS diagnosis, that's because my doctor told me "IBS" 7 years ago to explain my excruciating pain and recommended the IBS diet which included more 'whole wheat products' to resolve constipation. Obviously the wheat just exacerbated the pains which my doctor didn't recognize as celiac. Either get a second opinion from a doctor who will consider the possibility that you have celiac disease or try the gluten free diet to see whether that reduces your symptoms. ;)

BURDEE

Guest jhmom

Hi Deb and welcome to the board!

Your story sounds all too familiar, I suffered with abdominal pain, diarrhea, etc for over a year only to be told I had IBS or the I don't know dx. I believe my Gastro doc is a good one and he even stated to me that sometimes it takes time for a disease to show up in the blood but time was something I didn't have.

I agree with Burdee you can try the gluten-free for a couple of months to see if you show an improvement OR you can order a stool panel test from Open Original Shared Link which is more sensitive than blood, more accurate and you do not have to be on gluten for it to be accurate.

Enterolab is the way I was dx and it was well worth the money I spent. I know some people on this board do not accept Enterolab and think it's not on the up and up but I will tell you from experience that he is for real, the test ARE accurate and I trust him 100%!!! In the beginning I was skeptical and thought "maybe this is not what is wrong with me, maybe its something else, maybe I can eat wheat/gluten" I was WRONG, I have had a few "cross contaminations accidents" and I know for sure that I have a problem with it, so an improvement on the diet is a test in itself!

Good luck and take care!

Guest gillian502

I agree not to accept the IBS diagnosis until every other avenue has been exhausted. Before my dr. discovered my Celiac and my Colitis, he thought I may have IBS, and all I could think was, "yeah, someone's full of BS, but it's not I..." ;)

deb Apprentice

Hey Thanks for responding guys. I feel better now that I know someone is listening to me. My GP's nurse told me "why don't you just go on a gluten-free diet" The only thing is I really want to know if this is what is wrong. It is my understanding the small bowel biopsy would be inaccruate if I was on the diet. The GI said in his notes to my family doc (which gave me a copy of the consult) that if the BE did not reproduce my pain than he wanted to look at doing asmall bowel series. Is that the same as the biopsy to show celic?? any way the BE was only degrading & uncomfortable. not the same pain in any way shape or form. again thanks for listening. Deb

gf4life Enthusiast

Hi Deb,

The small bowel series is a series of x-rays. It will not show Celiac. The stomach scope they did before is what they do for the biopsy. They need to take tissue samples from your small intestines. It doesn't sound like they did that during the previous scope. Mine didn't either and I had to do it again to get the biopsies, which ended up being negative, since I had gone gluten free prior to the biopsy. I recommend that you do NOT go gluten free before they are finished testing. Even a few weeks being gluten free can mess up your future results.

If you want solid results for your own benefit I recommend Enterolab. Most GI doctors will not accept the results for a diagnosis, but it will help you decide if you need to be gluten free for the rest of your life.

God bless,

Mariann

deb Apprentice

Thanks Mariann for the info. you are right I did not have samples of my small bowel. the stomach scope was done by a general surgen and he told me he does not feel quified to go that far down. He just went past the stomach a little way. I saw him for a consult on my gallbladder. I really liked the fact he sugested I just wait and see since I didn't have any GB findings. I really respect him for not just wanting to cut on me. I hope I can find out what for sure the GI wants to do next. I agree that xrays won't show what I am wanting to confirm. Is the Entrolab just stool test or do they do blood and stool? Thans anagin for the help. Deb :)


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



Celiac.com Sponsor (A8-M):



Tasha2004 Contributor

Could it also be fibromyalgia or thyroid trouble?

these things all run so much together/.

deb Apprentice

HI Tasha,

No its not fibromyaliga, I do not have the trigger points. And my thyroid has always been in the low normal range, but still normal. I have a lot of the symptoms of hypothroidism, but have not gained any weight. you know really dry itchy skin, facial hair growth, tiredness, etc. That has been going on for almost 18 years. every year at the health fair I have blood drawn and it showes all sorts of different results. nothing serious, except my chol. thats been up and down for years & years. Took lipator for 2 years and then the new dr I got took me off of it. chol went back up , so now he wants me to take omega 3. plus the fiber thing and excersize

Tasha2004 Contributor

OK, then maybe the others are right and you should try Enterolab?

I do hope you figure it out soon!

deb Apprentice

Well I checked with the DR yesterday and today and still can't get an answer to what results were for my BE. I am so frustrated I don't know what to do. :unsure: I'm interested to know how many of you have had luck with your doc's and the Enterolab results???? Also does anyone know about insurance and the Lab. any input is apperciated. Thanks Deb

gf4life Enthusiast

Hi Deb,

Sorry I didn't get right back to you, but Enterolab does stool tests and a cheek swab gene test. They do NOT do blood tests.

As for the insurance issue, some people have gotten reimbursed by their insurance company, but it varies with the different insurance companies.

I have had luck with some of my children's doctors accepting the results: neurologist, rheumotologist/immunologist, ENT, and physicians assistant at our primary care office.

The doctors I've had that have NOT accepted it are my own GI, the pediatrician at our primary care office. My children's ped. GI didn't accept the results for diagnositic purposes, but he was willing to keep his mind open and follow their progress on the diet. That is a start at least.

I never could get any answers about any of my tests including the BE, except they were "fine". Everything was normal, I just felt sick everyday of my life for no apparent reason! Well it is pretty apparent to me, since if I get even a tiny bit of gluten in my diet I get sick again for a few weeks. I am so glad that I feel better on the gluten-free diet. :D

God bless,

Mariann

deb Apprentice

Hey Mariann thanks for responding. I was talking to a co worker today and she ask me why I don't just go gluten-free. I just need to know , I think so if I am I can have my children tested also. I fell like I owe It to them. I guess I'm worried that if I do go gluten-free and I fell better I won't be sure If it isn't because I want it to work or I really have Celaic. I am starting to think the Dr's Think it's all in my head. Oh well I'm starting to sound like a real head case. Thanks again. Deb :blink:

gf4life Enthusiast

Deb,

I felt the same as you. I had to have something in writing in front of me to prove to me that I really had a problem with gluten. I knew I would never be able to stay gluten free forever without it. I would start feeling better and then convince myself that it was "all in my head" and go back on gluten occasionally. I didn't want to play those kinds of mind games with myself! Also I wanted to be sure before testing my kids. I am so thankful for Enterolab and Dr. Fine, without them I never would have been secure enough with my self diagnosis to go gluten-free for life!!

And I got the "why don't you just go gluten-free?" thing a lot. But it just wasn't that simple for me... :rolleyes:

God bless,

Mariann

deb Apprentice

Got the results from my BE. It showed I have polyps and some sort of a pouch in the upper right part of the colon. :( Still these areas are not where I am having problems. I,m not sure if I should post a new topic or just keep adding to the original. :unsure: Any way has anyone else had a colon problem, polyps etc. along with their celiac disease?? have not heard from the GI, but I guess now I will have to have a colonoscopy. Any replies are appreciated. Thanks Deb

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.