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

Esophgatist?


hillyb6

Recommended Posts

hillyb6 Rookie

ok my 8yr dd had her endoscop and colonoscopy done today and they ruled out crohns

but we wont have the biopsy results back for a few days to a week

they did find grade 4 errosion of her esophgus and some gastrist in her stomach

can that be related to celiacs? or is that seperate issues altogether

another thing i am shocked about is they are testing her for crohns and celiac but as she came to they offered her nothing but glutton

what if she was celiac they had only chex mix, gold fisha nd grammy bears for her to eat arghhhhhhhh

i said she cant have those they make her stomach hurt they were surprised and said well thats all we have

and this is a childrens hospital right before she went in a little 3yrold was having his scope done and had a huge post on his celiac blood panel so i

wonder if they fed him glutton too

:(

http://img.photobucket.com/albums/v378/sba...giphotos1-1.webp


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



Celiac.com Sponsor (A8-M):



Nikki2003 Contributor
ok my 8yr dd had her endoscop and colonoscopy done today and they ruled out crohns

but we wont have the biopsy results back for a few days to a week

they did find grade 4 errosion of her esophgus and some gastrist in her stomach

can that be related to celiacs? or is that seperate issues altogether

another thing i am shocked about is they are testing her for crohns and celiac but as she came to they offered her nothing but glutton

what if she was celiac they had only chex mix, gold fisha nd grammy bears for her to eat arghhhhhhhh

i said she cant have those they make her stomach hurt they were surprised and said well thats all we have

and this is a childrens hospital right before she went in a little 3yrold was having his scope done and had a huge post on his celiac blood panel so i

wonder if they fed him glutton too

:(

http://img.photobucket.com/albums/v378/sba...giphotos1-1.webp

when nicole went in for her scope they found she also has gastritis and esophagitis also she is on prevacid now and doing great with it. When she woke up they just offered her a popsicle because they dont really want them to eat alot or heavy for a while. Maybe they figure since you don't know yet what does it matter. But it does matter especially if it hurts them. Nicole came back celiac even though they couldn't see it before the biopsy results came back.

I hope all goes well for you now on.

Celina

hillyb6 Rookie
when nicole went in for her scope they found she also has gastritis and esophagitis also she is on prevacid now and doing great with it. When she woke up they just offered her a popsicle because they dont really want them to eat alot or heavy for a while. Maybe they figure since you don't know yet what does it matter. But it does matter especially if it hurts them. Nicole came back celiac even though they couldn't see it before the biopsy results came back.

I hope all goes well for you now on.

Celina

hannah been on previcid 30mg since sept its clearly not helping so i guess we try soemthing else now

2kids4me Contributor

My son has duodentitis and is on Nexium...works well.

another thing i am shocked about is they are testing her for crohns and celiac but as she came to they offered her nothing but glutton

We had that experience too at a Childrens hospital - offered a sandwich :blink:

When Kathryn was reovering form her appendectomy - she had nothing to eat for 2 days because she was sick (vomiting) then had surgery...offered her jello the first day and then - get this - her first real food is not rice or soup or someting easy to digest. Kathryn said it almost made her sick looking at it - a huge plate with 2 pieces of chicken, fries (which no one knew if they were cross contaminated), and carrots. Kathryn refused it all because the fries had touched the other food on the plate. She was labeled as "difficult eater"

Any time a hospital stay is involved, I throw in some handy "stand bys" of gluten free products.

Sandy

hillyb6 Rookie

yah well that is basically what they fed hannah too after her surgery was nothing but gluten so wonder she had amigraine and pain but she was on soo much pain meds proably good thing

i am shocked that kids that were in there with pos blood test for celiacs were being offered nothing but gluten now for my dd its unclear but last night she ate chicken nuggets and was sick with in the hour i woudlnt have fed her that but i wasnt home either daddy let her pick what she wanted since she had to endure her testing that day sigh

he is not on the wagon about the gluten free or even gluten light he says he is but then he feed her chicken nuggets and calls to find out where her meds are to help her stomach pains

Guest cassidy

Reflux is one of my main symptoms when I'm glutened. I had surgery for it when I was 10 but it came back. Now that I'm gluten-free I only get reflux if I eat gluten. Even a crumb will make me reflux for about 3 weeks. You may find that after she goes gluten-free the reflux will go away over time.

It is crazy that hospitals offer food that you can't eat. I told my doctor that I suspected celiac and went gluten-free. They sent me in for a test where they watch you swallow a bagel and marshmallow. I brought my own gluten-free bagel because they would have expected me to eat a gluten filled bagel if I hadn't. I'm pregnant and decided that I'm bringing my food from home for when I'm in the hospital. Too many people here had horror stories about what the hospitals fed them.

Good luck and hope she feels better!

Guest aparde

Hi! I am so sorry for this. I am sure she feels aweful!! Reflux has taken a tole on our lives! My son who is 12 months has horrible reflux that has caused breathing problems, laryangomalatia, unalbe to swallow foods, pnuemonias, apnea spells, severe esophagitis... ya he has had it bad.

My daughter has celiac and so they will be testing him for that but they haven't done it yet. I am only nursing him and they are talking about a feeding tube right now. I didn't really know until recently that gluten went through breast milk and I have had a hard time with my digestive system since he was born. I have gone off gluten for about a week now but no change yet. Maybe he will turn around.

I hope she feels better soon!!!


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



Celiac.com Sponsor (A8-M):



Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - trents replied to catsrlife's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Patiently Waiting to See Results

    2. - trents replied to Leeloff's topic in Gluten-Free Foods, Products, Shopping & Medications
      75

      How Come Gluten Didnt Bother Me In Italy

    3. - Gigi2025 replied to Leeloff's topic in Gluten-Free Foods, Products, Shopping & Medications
      75

      How Come Gluten Didnt Bother Me In Italy

    4. - Rejoicephd replied to JulieRe's topic in Related Issues & Disorders
      7

      Oral thrush question

    5. - catsrlife posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Patiently Waiting to See Results


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,897
    • Most Online (within 30 mins)
      7,748

    Sgp
    Newest Member
    Sgp
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Welcome to the forum, @catsrlife! Celiac disease can be diagnosed without committing to a full-blown "gluten challenge" if you get a skin biopsy done during an active outbreak of dermatitis herpetiformis, assuming that is what is causing the rash. There is no other known cause for dermatitis herpetiformis so it is definitive for celiac disease. You would need to find a dermatologist who is familiar with doing the biopsy correctly, however. The samples need to be taken next to the pustules, not on them . . . a mistake many dermatologists make when biopsying for dermatitis herpetiformis. 
    • trents
      You state in an earlier post that you don't have celiac disease. Here in this post you state you will "be doing another test". What will this test be looking for? What kind of celiac disease testing have you had done? If you have used a Entero Labs it sounds like you have had stool testing done for celiac disease which is not widely accepted as a valid celiac disease diagnostic testing method. Have you had blood antibody testing for celiac disease done and do you realize that for antibody testing to be valid you must have been eating generous amounts of gluten for a period of weeks/months? 
    • Gigi2025
      No, I've not been diagnosed as celiac.  Despite Entero Labs being relocated to Switzerland/Greece, I'll be doing another test. After eating wheat products in Greece for 4 weeks, there wasn't any reaction.  However, avoiding it here in the states.   Thanks everyone for your responses.  
    • Rejoicephd
      Thank you @JulieRe so much for sharing this extra information. I'm so glad to hear you're feeling better and I hope it keeps moving in that direction. I feel I'm having so many lightbulb moments on this forum just interacting with others who have this condition. I also was diagnosed with gastric reflux maybe about 10 years ago. I was prescribed ranitidine for it several years back, which was working to reduce my gastric reflux symptoms but then the FDA took ranitidine off the shelves so I stopped taking it. I had a lot of ups and downs healthwise in and around that time (I suddenly gained 20 pounds, blood pressure went up, depression got worse, and I was diagnosed with OSA). At the time I attributed my change in symptoms to me taking on a new stressful job and didn't think much else about it. They did give me a replacement gastric reflux drug since ranitidine was off the shelves, but when I went on the CPAP for my OSA, the CPAP seemed to correct the gastric reflux problem so I haven't been on any gastric reflux drug treatment for years although I still do have to use a CPAP for my OSA. Anyway that's a long story but just to say… I always feel like I've had a sensitive stomach and had migraines my whole life (which I'm now attributing to having celiac and not knowing it) but I feel my health took a turn for much worse around 2019-2020 (and this decline started before I caught covid for the first time). So I am now wondering based on what you said, if that ranitidine i took could have contributed to the yeast overgrowth, and that the problem has just been worsening ever since. I have distinctly felt that I am dealing with something more than just stress and battling a more fundamental disease process here. I've basically been in and out of different doctor specialties for the past 5 years trying to figure out what's wrong with me. Finally being diagnosed with celiac one year ago, I thought I finally had THE answer but now as I'm still sick, I think it's one of a few answers and that maybe yeast overgrowth is another answer. For me as well, my vitamin deficiencies have persisted even after I went gluten-free (and my TTG antibody levels came down to measurably below the detectable limit on my last blood test). So this issue of not absorbing vitamins well is also something our cases have in common. I'm now working with a nutritionist and taking lots of vitamins and supplements to try and remedy that issue. I hope that you continue to see improvements in working with your naturopath on this. Keep us posted!
    • catsrlife
      Back at the end of July I got this rash on both of my forearms. It started on my right and continued to the left. It was on the top and side. The rash has bumps that would pop with clear liquid if scratched. They would almost crystalize and scab up. They reminded me of chicken pox. They would scab for weeks and not heal much at all except for the blood clotting. If the scab was scratched off, it would bleed and bleed until it scabbed up again. The skin has lost its pigment where the scabs are. I figured it was probably either the plant I had trimmed around the 15th or some reaction to the magnesium complex I was taking or an allergic reaction to the asthma meds I was on. I stopped the asthma meds and the magnesium. The rash seemed to get better but when I took the asthma meds it flared up again so I went to the urgent care as my doctor was unavailable. The UC doctor said it probably wasn't the meds and asked about my diet. I said I was strict keto. I usually am, but there is a story around this. I feel amazing on keto. When I eat sugar, wheat, and starchy veggies I feel horrible. Blood sugar goes up, IBS type symptoms, brain fog, etc. But I have a horrible addiction to carbs so I blow it sometimes and after Mom died in 2023, I fell off the wagon. No rashes, just weight gain. I finally went back on keto and then around that time had a piece of pizza (or so, it's hard to stop the carb rush.) So I was strict keto, off and on. She ignored that and prescribed some allergy meds. It didn't go away.  What was happening by then was that the rash was now on my upper elbows, both of them, on the back of my arms. It starts with a very itchy bump, spreads around it and sometimes just burns like crazy and other times just itches. Then it started on the sides of my knees on the oustide, a little bit down the sides of the calves. It's not as bad there as it is on my arms even though it comes and goes (and so does wheat in my diet.) I then got three tiny blisters on each hand, 3 on the insdie of my index finger on the right hand and 3 on the inside of middle finger of my left hand. There is still a little scab there even though it was two weeks ago. No more have appeared on the fingers. But right now the back of the arms above my elbows are starting to itch. At some point I started to think mites from the possum that was sneaking into our house but it's been 3 months and they would be dead already. It wouldn't be from humans because I don't go near any humans although I did take an Uber to the doctor and the bus back. Plus, it's symmetrical. It starts on one side and is almost identical on the other.  I did my DNA with Ancestry and MyHeritage. I don't have the HLA-DQ2 or HLA-DQ8. I do have HLA-DQ2.2. I took the blood test but it was negative. Then again, I don't eat wheat every day. I rarely eat it except for lately when I've been preparing for the blood test if I have to take it again. I don't like to. It makes my joints hurt, gives me brain fog, stomach problems, I sleep in the middle of the day, etc. I have a doctor appointment tomorrow. I hope that she will be more serious about this than the UC doctor was.  So I have no idea. With my luck they'll magically disappear before the doctor appointment. That's what happens with everything.
×
×
  • 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.