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

Egd / How Many Have Been Diag With Candida Besides Celiac Or Gluten Intolerance


skurtz

Recommended Posts

skurtz Explorer

Son had egd done today would like to know how many people have celiac or gluten intol & Candida??

Actual Candida found by a EDG ?


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



Celiac.com Sponsor (A8-M):



  • Replies 51
  • Created
  • Last Reply
Rachel--24 Collaborator

The 3 things I've been diagnosed with so far are gluten intolerance, candida, and c-diff infection. Candida is often seen with gluten intolerance. In my case I've been gluten free for several months so candida is more likely due to the bacteria infection and the unhealthy state of my digestive tract. My candida was found in a stool test.

skurtz Explorer

son had egd done today along with blood work, Dr. came out explained everything that was don said they took 5 biopsy he also brought pictures out & explained what was on them. He said he saw about 6 patches & beleives they are candida but wont know for sure until test results are in. He asked if hes been on any antibiotics recently , i told him no its been prob a couple of years. Anyhow Rachel I thought you had celiac?

Tommorrow my son is going right back on gluten free & hes looking forward to it. He's 11 yrs old 2 years ago we did the yeast free diet because I suspected candida because of this rash he would get. His Peditrician wouldnt test him he would just give him steroid creme & tell me not to feed him it. I used the creme maybe 2 times because it would come bk as soon as you stopped the cream. I didnt notice much difference in him or myself on the yeast free diet he said he feels way better on the gluten free I myself feel way better on the gluten free. My son also has Aspergers. go figure Dr always said he had add & every year I would take him in for yearly check up he would ask if i was ready for ritalin? When asperger diagnosis came bk & Specialist ruled out ADD Dr said it was a wrong diag. I do agree that there are some drs that shouldnt be drs but there are def some good ones. thanks for letting me vent.

chrissy Collaborator

my daughter was diagnosed with a fungal infection in her esophagus when she had an EDG----but this was before we suspected she had celiac. you could see little white patches all over in the picture he brought me.

christine

Rachel--24 Collaborator
Anyhow Rachel I thought you had celiac?

I never got diagnosed with Celiac. I went on the diet before taking my bloodtests because I didnt know any better and the doctor told me it wouldnt affect tests. He didnt know much about Celiac or testing. I was negative so went back to normal diet and a few months later I had lost 25 lbs. and was very sick. I thought I was dying so I put myself back on a restricted diet and started to get better. I had a biopsy 6 months later. I wasnt expecting the biopsy to show anything after 6 months on the diet and it didnt. I wanted an answer so did stool testing through Enterolab because I didnt have to go back on gluten for that test. It came back positive but the test cant diagnose Celiac it can only tell if I have immune response to gluten. So I'll never know if its Celiac or Gluten Intolerance...doctors just told me to stay on the diet regardless because that is the only treatment for both.

If your son is having a problem with Candida he should avoid sugar. Sugar feeds candida. Also probiotics of some kind may help. Plain yogurt may help if he can have dairy.

slpinsd Contributor

I'm in for the candida, as well. Don't know if it's due to Gluten Intol (not diagnosed Celiac, either), or H. Pylori. however, h pylori treatment is done and i'm still symptomatic.

rachel- i have a ques. enterolab gives you antitransglutaminase antibodies, right? i know in blood tests, these the antibodies that are more indicative to celiac tissue damage anyway, so you could assume that it IS more indicative of celiac, if yours were positive? (even though a biopsy is supposedly still the gold standard)

munchkinette Collaborator

What is candida? You don't mean the yeast, do you? In the GI tract? I keep reading about probiotics, but I'm wondering how good they are. I started taking the Trader Joe's acidophilus pills because I'm on antibiotics, but I'm not sure how useful they are.


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



Celiac.com Sponsor (A8-M):



penguin Community Regular

yogurt is one of the things that my mom has always shoved down my throat when I had a stomach problem to replace the good bacteria. Now grown, I see that my body likes the good bacteria and I like to give them a home in my war torn digestive tract :D

That's the only thing I do, probiotically, because I'm afraid of any vitamin like pills :blink:

Rachel--24 Collaborator
rachel- i have a ques. enterolab gives you antitransglutaminase antibodies, right? i know in blood tests, these the antibodies that are more indicative to celiac tissue damage anyway, so you could assume that it IS more indicative of celiac, if yours were positive? (even though a biopsy is supposedly still the gold standard)

Yes...I had positive tTG...BUT I do not carry either of the main celiac genes. I have genes which cause gluten sensitivity. The doctors say genes do not tell the whole story because a small amount of biopsy proven Celiacs do not carry the main genes. They have not yet determined all genes involved. I'm kind of on the fence. Most days I believe I'm gluten intolerant w/out Celiac. Its not something I think about that much anymore because I need to be on the diet regardless so I guess it doesnt matter. In the beginning I wanted more answers but I've put that to rest. The tTG may be indicative of tissue damage but maybe it doesnt necessarily mean flattened villi. Maybe w/out Celiac genes the villi dont get flattened...therefore technically not Celiac. I dunno...I was always confused about that. :unsure:

skurtz Explorer

My son & I both followed the yeast free diet 2 yrs ago I really didnt see much difference but

when on the gluten free diet in jan for 2 wks noticed a huge difference. We were still having sugar so I guess we will have to wait till the results come bk. I just wanted to know if its poss to have both celiac & candida? I think you can but im not sure

Rachel--24 Collaborator

Yes, its very possible to have candida alongside any disease that weakens the immune system. Its especially common in Celiac because celiac damages the intestines.

danikali Enthusiast

Actually, it's perfect that this thread is up. I'm actually having problems with what I believe is a yeast infection, but it's not like it normally is.

Okay, this is going to get gross.

Well, I know if you have a yeast infection, you can get discharge that is thick and white like cottage cheese or something. Well, I have this, except it is also pink, bloody like. Sometimes, it is brown, but mostly pink. Last week, I had a lot of sugar, A LOT. And that's when it started up again. I'm also very bloated and it won't go away. I'm off of all sugar now, along with all of the other food intolerances I'm dealing with. Since Sunday, all I am eating is fruit, veggies, fish and meat. But this discharge and bloating won't go away. Does anyone know what this could be? I made an apt. with the gyno. for Thursday, but I'm thinking they are just going to give me antibiotics and I feel kind of iffy on that because my immune system is already obviously so weak. I take acidopholis every day though.

Anyway, have any of you ever experienced this kind of discharge? I had it before, but it went away in 2 days. Now I've had this again since Saturday. Could this be a yeast thing, or something more serious?

skurtz Explorer

I have never exper anything like that. You should prob call the Dr.

If anybody is interested there is a product called THREELAC its all natural its listed on one of the autism websites, its for candia problems.

danikali Enthusiast
I have never exper anything like that. You should prob call the Dr.

If anybody is interested there is a product called THREELAC its all natural its listed on one of the autism websites, its for candia problems.

I actually just started taking it on Sunday. I hope it works. Have you tried it?

skurtz Explorer

Yes my son & i took it last year it seemed to help me, but it was to big a fight to get him to take it, so I just cut off all breads, cookies anything yeasty. I finally got rid of the rash in the private area on him by soaking

his feet in tea bags about15 of the in hot water then when it cooled a little,he soaked his feet for 20 min.

he had the rash for a good 3 years but all the drs would give me were cremes with steroids in them. DUH

as soon as you stop them it would come back. Anyhow I really like the taste of the threelac I was like hooked on them. to me they taste like pixie sticks??? I purchased the 1st box for like 48.00 the 2nd box for 37.00 on line of course asked around at a couple of health stores & they never heard of it. I read somewhere you shouldnt take asadouphlis (spelled wrong) becasue your putting to much yeast back in your system?? dont know how true that is but I think the threelac works much better. Also you still have to stay more less on a yeast free diet or it comes bk.. let me know what you think if you want to : my email is 110sad@earthlink.net

penguin Community Regular

I've had that before, but it was just a wierd period, the gyno told me to do a pregnancy test. It was wierd because of a new brand of pills.

If it's a yeast infection, it's a fungal overgrowth and they're not going to give you antibiotics because antibiotics cause yeast infections because the good bacteria that normally keeps the fungal stuff under control gets killed.

Either use monistat or get an rx for diflucan if it's a yeast infection. The gyno will be able to tell you within like, 3 seconds of seeing it if it is yeast or not.

Yogurt (or anything with live cultures in it) helps a lot because it replaces good bacteria in your system. If you're on a no dairy thing, Silk has this new Silk live stuff that is soy yogurt. Acidophilus is one of the cultures that is good for you, and you can get that as a pill I think, but most yogurt has 6-8 live cultures, including the acidophilus.

Oh, and don't have sex! It'll make it worse and your FI can get it too. He probably won't have symptoms, but he'll keep passing it back to you!

danikali Enthusiast

Well thanks for the good information! I knew that you shouldn't have sex because it could make your infection worse, but I didn't know I could pass it onto him with no symptoms only to get it back again!

So more questions I have are:

1. Can a yeast infection give you pink discharge. Its the same texture as a regular yeast infection, it's just pink.

2. Can a yeast infection give you back pain?

2. About threelac: are there any side effects of it? And is it like a normal yeast medication (when it comes to a vaginal yeast infection). Like Monistat 3 will make you have even more discharge for the next one to two days and then it is gone.

3. Are there foods to stay away from besides the obvious: dairy, gluten, sugar, alcohol and caffeine?

Any help I would love! Thanks!

skurtz Explorer

as far as i know there arent any side affects at least we didnt have any.Im not sure if you asked but you take by mouth you put it on your tounge let it sit for awhile & then drink a glass of water.

Rachel--24 Collaborator

Dani,

Check out this link.

Open Original Shared Link

If you have time listen to the show about gluten intolerance and then listen to the show about candida. Very, very, informative. I go to a Biohealth clinic and my doctor is awesome. Well...so far they've been like a huge gift after everything I've gone through with past doctors....but since this isnt the "rant about doctors thread" I wont get into that. :P

My doctor is just like the doctor speaking in these shows. Very knowledgeable and alot of whats being discussed in these programs has alot to do with questions in this thread. Also in my case I'm already diagnosed with gluten intolerance since last year. Now after finding good doctors and getting proper testing I'm diagnosed with Clostridium Difficile and candida. These programs describe how all this takes place just because of a gluten intolerance. You *may* have underlying cause for your symptoms (aside from gluten intolerance)....I would be least worried about candida although you may have that as well. Definately dont eat lots of sugar as that will aggravate the situation.

skurtz Explorer

I would think the blood tests & biopsies that my son had yesterday will show any underlying problems at least i hope so.

Rachel--24 Collaborator
I would think the blood tests & biopsies that my son had yesterday will show any underlying problems at least i hope so.

Sorry Skurtz,

I was replying to Danikali's post but you're right. If you're son has Celiac as an underlying cause for his candida hopefully that will show up in the tests. :)

Rachel--24 Collaborator
3. Are there foods to stay away from besides the obvious: dairy, gluten, sugar, alcohol and caffeine?

Carbs...like potatoes, white rice. Those turn to sugar pretty quickly.

Anyways I did the whole Candida thing for 4 months last year before I found out I had gluten intolerance. I followed the candida diet perfectly and I felt better but after 4 months I started to figure theres more to it....I mean you cant stay on that type of diet forever. I was living on meat, fish and a few vegetables. Since then I'm a FIRM believer that if you've got candida....theres a reason behind it.

i canary Rookie

I was diagnosed with candidia and celiac on the same day. I followed the candidia diet for 2 years and I am finally free of it. Dr. William Crook has a book "The Yeast Connection" that tells you what to eat and not to eat. Basically - don't eat: yeast, sugar, cheese, baking powder, vinegar, fruit juice and put your leftovers in the freezer not the refrigerator.

skurtz Explorer

I read the yeast connection & a few others like sugar buster I dont mean to sound like a broken record I just know that we son & I did way better in just 2 weeks on the gluten free & its more or less sugar free becuaese you have eliminated all of sugar the only thing he had was a koolaid here or there iin is lunch

it some candy here & there His rash never reappeared the one that I know is caused by yeast ( in Privates)

I say I would have to agree with Rachel-24 when looking bk over everything there must be an underlying problem that Im sure we will find out on mon when his test results are bk in. I mean hes either celiac or gluten free intolher either way hes bk on diet.

danikali Enthusiast

Good information!

Well, I am sure my underlying problem is Celiac disease, (possibly casein intolerance?) and I am sure that I have a problem with Candida. I know that when I have sugar (like candy) or any kind of processed foods, I get really bad stomach problems. Then I go back to eating plain whole foods, and I get better. So, I am positive that I've got the leaky gut, etc. So my question is, should I really not have potatos and rice anymore either? And any kind of fruit? I read online about this and some doctors recommended no fruit for the first 3 months and some doctors said it was okay. I had an apple this morning and some celery and carrots about 2 hours later. Neither hurt my stomach at all. I had rice cakes last night, and I didn't think about it, but I blew up like crazy after that and had foul gas again. I also had a potato for lunch yesterday and had problems again. Soooo, I'm thinking (and hoping) that fruit is okay, right? I haven't noticed any problems with it so far........

And how long is the typical time period that I must stay on this diet? A year? Does that mean I shouldn't have potatos or rice either for a whole year?

Also, whatelse could be my underlying problem besides the gluten intolerance thing?

I'm getting hungry thinking about all of the foods that I can't eat right now.........

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,391
    • Most Online (within 30 mins)
      7,748

    Salt14
    Newest Member
    Salt14
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
    • Clear2me
      Thanks for the info. I recently moved to CA from Wyoming and in that western region the Costco and Sam's /Walmart Brands have many nuts and more products that are labeled gluten free. I was told it's because those products are packaged and processed  in different  plants. Some plants can be labeled  gluten free because the plant does not also package gluten products and they know that for example the trucks, containers equipment are not used to handle wheat, barely or Rye. The Walmart butter in the western region says gluten free but not here. Most of The Kirkland and Members Mark brands in CA say they are from Vietnam. That's not the case in Wyoming and Colorado. I've spoken to customer service at the stores here in California. They were not helpful. I check labels every time I go to the store. The stores where I am are a Sh*tshow. The Magalopoly grocery chain Vons/Safeway/Albertsons, etc. are the same. Fishers and Planters brands no longer say gluten free. It could be regional. There are nuts with sugar coatings and fruit and nut mixes at the big chains that are labeled gluten free but I don't want the fruit or sugar.  It's so difficult I am considering moving again. I thought it would be easier to find safe food in a more populated area. It's actually worse.  I was undiagnosed for most of my life but not because I didn't try to figure it out. So I have had all the complications possible. I don't have any spare organs left.  No a little gluten will hurt you. The autoimmune process continues to destroy your organs though you may not feel it. If you are getting a little all the time and as much as we try we probably all are and so the damage is happening. Now the FDA has pretty much abandoned celiacs. There are no requirements for labeling for common allergens on medications. All the generic drugs made outside the US are not regulated for common allergens and the FDA is taking the last gluten free porcine Thyroid med, NP Thyroid, off the market in 2026. I was being glutened by a generic levothyroxin. The insurance wouldn't pay for the gluten free brand any longer because the FDA took them all off their approved formulary. So now I am paying $147 out of pocket for NP Thyroid but shortly I will have no safe choice. Other people with allergies should be aware that these foreign generic pharmaceutical producers are using ground shellfish shell as pill coatings and anti-desicants. The FDA knows this but  now just waits for consumers to complain or die. The take over of Wholefoods by Amazon destroyed a very reliable source of good high quality food for people with allergies and for people who wanted good reliably organic food. Bezos thought  he could make a fortune off people who were paying alot for organic and allergen free food by substituting cheap brands from Thailand. He didn't understand who the customers were who were willing to pay more for that food and why. I went from spending hundreds to nothing because Bezo removed every single trusted brand that I was buying. Now they are closing Whole foods stores across the country. In CA, Mill Valley store (closed July 2025) and the National Blvd. store in West Los Angeles (closed October 2025). The Cupertino store will close.  In recent years I have learned to be careful and trust no one. I have been deleberately glutened in a restaurant that was my favorite (a new employee). The Chef owner was not in the kitchen that night. I've had  a metal scouring pad cut up over my food.The chain offered gluten free dishes but it only takes one crazy who thinks you're a problem as a food fadist. Good thing I always look. Good thing they didn't do that to food going to a child with a busy mom.  I give big tips and apologize for having to ask in restaurants but mental illness seem to be rampant. I've learn the hard way.          I don't buy any processed food that doesn't say gluten free.  I am a life long Catholic. I worked for the Church while at college. I don't go to Church anymore because the men at the top decided Jesus is gluten. The special hosts are gluten less not gluten free. No I can't drink wine after people with gluten in their mouth and a variety of deadly germs. I have been abandoned and excluded by my Church/Family.  Having nearly died several times, safe food is paramount. If your immune system collapses as mine did, you get sepsis. It can kill you very quickly. I spent 5 days unconscious and had to have my appendix and gall bladder removed because they were necrotic. I was 25. They didn't figure out I had celiac till I was 53. No one will take the time to tell you what can happen when your immune system gets overwhelmed from its constant fighting the gluten and just stops. It is miserable that our food is processed so carelessly. Our food in many aspects is not safe. And the merging of all the grocery chains has made it far worse. Its a disaster. Krogers also recently purchased Vitacost where I was getting the products I could no longer get at Whole Foods. Kroger is eliminating those products from Vitacost just a Bezos did from WF. I am looking for reliable and certified sources for nuts. I have lived the worst consequences of the disease and being exposed unknowingly and maliciously. Once I was diagnosed I learned way more than anyone should have to about the food industry.  I don't do gray areas. And now I dont eat out except very rarely.  I have not eaten fast food for 30 years before the celiac diagnosis. Gluten aside..... It's not food and it's not safe.  No one has got our backs. Sharing safe food sources is one thing we can do to try to be safe.        
    • Mmoc
      Thank you kindly for your response. I have since gotten the other type of bloods done and am awaiting results. 
    • Aretaeus Cappadocia
      I wanted to respond to your post as much for other people who read this later on (I'm not trying to contradict your experience or decisions) > Kirkland Signature Super Extra-Large Peanuts, 2.5 lbs, are labeled "gluten free" in the Calif Costcos I've been in. If they are selling non-gluten-free in your store, I suggest talking to customer service to see if they can get you the gluten-free version (they are tasty) > This past week I bought "Sliced Raw Almonds, Baking Nuts, 5 lbs Item 1495072 Best if used by Jun-10-26 W-261-6-L1A 12:47" at Costco. The package has the standard warning that it was made on machinery that <may> have processed wheat. Based on that alone, I would not eat these. However, I contacted customer service and asked them "are Costco's Sliced Almonds gluten free?" Within a day I got this response:  "This is [xyz] with the Costco Member Service Resolutions Team. I am happy to let you know we got a reply back from our Kirkland Signature team. Here is their response:  This item does not have a risk of cross contamination with gluten, barley or rye." Based on this, I will eat them. Based on experience, I believe they will be fine. Sometimes, for other products, the answer has been "they really do have cross-contamination risk" (eg, Kirkland Signature Dry Roasted Macadamia Nuts, Salted, 1.5 lbs Item 1195303). When they give me that answer I return them for cash. You might reasonably ask, "Why would Costco use that label if they actually are safe?" I can't speak for Costco but I've worked in Corporate America and I've seen this kind of thing first hand and up close. (1) This kind of regulatory label represents risk/cost to the company. What if they are mistaken? In one direction, the cost is loss of maybe 1% of sales (if celiacs don't buy when they would have). In the other direction, the risk is reputational damage and open-ended litigation (bad reviews and celiacs suing them). Expect them to play it safe. (2) There is a team tasked with getting each product out to market quickly and cheaply, and there is also a committee tasked with reviewing the packaging before it is released. If the team chooses the simplest, safest, pre-approved label, this becomes a quick check box. On the other hand, if they choose something else, it has to be carefully scrutinized through a long process. It's more efficient for the team to say there <could> be risk. (3) There is probably some plug and play in production. Some lots of the very same product could be made in a safe facility while others are made in an unsafe facility. Uniform packaging (saying there is risk) for all packages regardless of gluten risk is easier, cheaper, and safer (for Costco). Everything I wrote here is about my Costco experience, but the principles will be true at other vendors, particularly if they have extensive quality control infrastructure. The first hurdle of gluten-free diet is to remove/replace all the labeled gluten ingredients. The second, more difficult hurdle is to remove/replace all the hidden gluten. Each of us have to assess gray zones and make judgement calls knowing there is a penalty for being wrong. One penalty would be getting glutened but the other penalty could be eating an unnecessarily boring or malnourishing diet.
    • trents
      Thanks for the thoughtful reply and links, Wheatwacked. Definitely some food for thought. However, I would point out that your linked articles refer to gliadin in human breast milk, not cow's milk. And although it might seem reasonable to conclude it would work the same way in cows, that is not necessarily the case. Studies seem to indicate otherwise. Studies also indicate the amount of gliadin in human breast milk is miniscule and unlikely to cause reactions:  https://www.glutenfreewatchdog.org/news/gluten-peptides-in-human-breast-milk-implications-for-cows-milk/ I would also point out that Dr. Peter Osborne's doctorate is in chiropractic medicine, though he also has studied and, I believe, holds some sort of certifications in nutritional science. To put it plainly, he is considered by many qualified medical and nutritional professionals to be on the fringe of quackery. But he has a dedicated and rabid following, nonetheless.
×
×
  • 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.