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

Mild Case Of Celiac Disease


GF ME

Recommended Posts

GF ME Newbie

I had my endocopy on 7/12. It was confirmed that I had a mild case of celiac/sprue and that I should stick to the gluten free diet. The only thing that I really changed is not eating pasta, bread and the obvious gluten-free products. I watch how I prepare stuff, but I enjoy going out. But does anyone know how strick I really have to be with this if I only have a mild case?

I still use the same shampoo, toothpaste, lotion, etc. Am I not healing at all if I don't follow this diet to a 'T'?

This is very confusing to me. I feel better and I am not getting glutened hardly at all.

Can anyone shed some light on this or should I see a dietician or a support group?

Thanks!

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



swittenauer Enthusiast

I've never heard of a mild case. I thought you either had it or didn't have it. I would recommend being 100% gluten free.

Link to comment
Share on other sites
CarlaB Enthusiast

It's really not accurate for them to have told you "mild case" of celiac. You either have it or you don't! Mild can only refer to the level of damage you have. If it's only a mild level of damage, you are very lucky that it didn't take very long and a lot more damage to discover the celiac! You need to be entirely gluten-free because the mild damage can get worse and certainly won't get better if you still consume gluten.

Welcome to the board.

Link to comment
Share on other sites
beaglemania Rookie

I'm like you I only have a mild case, my only serious effect I've gotten from Celiac Disease is osteoporosis. I've stuck with all my regular toothpastes and shampoos and I feel fine. The best gluten-free pasta is BiAglut go to glutensolutions.com I love it!! Tastes like regular pasta. No way to reheat gluten-free pasta's though. For bagels, english muffins, all bread products go to glutino.com. Awesome poppy seed and plain bagels and breads!!

Don't eat anything with gluten though still. If you go out to eat beware of sauces and croutons on salads and dedicated fryers for french fries.

Link to comment
Share on other sites
2kids4me Contributor

I also have never heard ofa mild case of celiac - its kinda like being "a little pregnant".

My kid's GI doc refered to the changes on my daughters biopsy as mild to moderate but followed that by ...conclusive evidence of celiac disease. The biopsy had patchy areas... My son's biopys was severe with subtotal villous atrophy on all biopsies taken from the duodenum. Symptom wise - mydaughter had more serious outward signs and my son had mild stomach aches and joint pain (+ bed wetting that stopped after going gluten-free).

You cannot rely on outward symptoms - celiac is celiac just like pregnant is pregnant.

Link to comment
Share on other sites
Guest southgoingzax

All true. Some people may have a different level of sensitivity - i.e. a tiny bit of gluten makes them sick, while other people can even drink a beer without noticing any ill effects. That being said, just because you don't NOTICE any symptoms doesn't mean no harm is done. The very best thing for your health is to be completely gluten-free - otherwise, your "mild" celiac could turn into a laundry list of associated illnesses and conditions (chronic joint pain, headaches, brain fog, numb or weak legs and arms, thyroid issues, diabetes, cancer, depression, vitamin deficiencies, etc., etc).

It is your choice, but maybe you should do a little more research into the matter before making a decision, good luck,

zax

Link to comment
Share on other sites
GF ME Newbie

Thanks for all your responses. That makes so much more sense. I will look into getting a dietician. Does anyone know of any in Southern New Jersey/Philadelphia area?

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



BBadgero Newbie

I agree with everyone - have it or not. But the true test is not getting tagged. One question - how often does it take some of you to notice you "totally ate gluten"? Sometimes for me it is within the hour - but could be in my head sometimes too? A little help from the "veterans"?

Also, anyone have a forum yet on here to address specific foods? I have done some research on certain medicines (Tylenol, Allegra, and Tagament) that have been confirmed gluten-free. If there is a forum on here where that can be shared - I can't find it yet.... :blink:

Link to comment
Share on other sites
Lisa Mentor

Delfi Forums has a Gluten Free Product list which is very helpful in the beginning.

Nini on this site has a beginners list of just about everything. PM her and she will send it on.

Lisa

Link to comment
Share on other sites
2kids4me Contributor
I agree with everyone - have it or not. But the true test is not getting tagged. One question - how often does it take some of you to notice you "totally ate gluten"? Sometimes for me it is within the hour - but could be in my head sometimes too? A little help from the "veterans"?

I can only answer for my daughter - she will get a migraine/stoamch ache wuthin 1 -2 hrs after exposure. Once it was inhaled gluten (playing in an empty grain bin with cousins on a farm) - she got a headache within an hour and felt crappy (fatigue, headcahe, tummy ache) for the next 24 hours

Link to comment
Share on other sites
maggee Newbie
Thanks for all your responses. That makes so much more sense. I will look into getting a dietician. Does anyone know of any in Southern New Jersey/Philadelphia area?

Be sure your dietician / nutritionist has experience with celiac. When my son was diagnosed we were referred to a nutritionist. When we met with her she had to go "dig-up" a list of allowable foods on a gluten free diet. Top of the list was a burger king burger - "just remove the bun" :o

By the end of our visit she admitted I already knew more than she did about the diet (and that was only about half of what I should have known at the time).

sorry I don't have a recommendation in your area but I used books as a starting point (Danna Korn - "Wheat Free Worry Free"). And I check out the info here for updates on gluten-free products.

Good Luck.

Link to comment
Share on other sites
JenAnderson Rookie

I was diagnosed with a "mild case" and I can tell you honestly that you have to follow the diet. I tried not to at first and it almost killed me. I still use the toothpaste and shampoos that I usually would have, but I have to be conscious of everything that I injest. I have had severe bone pain, and brain fog, and vitamin deficiencies just having a few crumbs from the butter tub. I don't have DH, and all the other things. All I can tell you is that you need to follow the diet. There will be so much of a difference.

Link to comment
Share on other sites
debmidge Rising Star
All true. Some people may have a different level of sensitivity - i.e. a tiny bit of gluten makes them sick, while other people can even drink a beer without noticing any ill effects. That being said, just because you don't NOTICE any symptoms doesn't mean no harm is done. The very best thing for your health is to be completely gluten-free - otherwise, your "mild" celiac could turn into a laundry list of associated illnesses and conditions (chronic joint pain, headaches, brain fog, numb or weak legs and arms, thyroid issues, diabetes, cancer, depression, vitamin deficiencies, etc., etc).

It is your choice, but maybe you should do a little more research into the matter before making a decision, good luck,

zax

I second this. Did Dr. tell you it's a mild case or is that how you view it as you get little or no known symptoms?

I'd worry about the silent neurological damage, the connection between your eating gluten and arthritis, and the higher chance of cancer. All silent damage of course will not show up until years later and you'll then wish you were 100% gluten-free.

The people on this board offer a wealth of experience and information and I trust their opinions and instincts on Celiac.

Link to comment
Share on other sites
loraleena Contributor

There is no such thing as a mild case. You have it or you don't. Even if you don't feel sick, the tiniest amounts can do hidden damage. You need to be compeletely gluten free.

Link to comment
Share on other sites

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. - BluegrassCeliac replied to lasthope2024's topic in Food Intolerance & Leaky Gut
      7

      This forum might be the last hope I have in my life. Please I beg you

    2. - Scott Adams replied to Nacina's topic in Related Issues & Disorders
      1

      14 year old with Celiac & EOE still suffering...

    3. - Nacina posted a topic in Related Issues & Disorders
      1

      14 year old with Celiac & EOE still suffering...

    4. - trents replied to Fluka66's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Waiting for urgent referral.

    5. - Fluka66 replied to Fluka66's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Waiting for urgent referral.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,068
    • Most Online (within 30 mins)
      7,748

    DaciaDH
    Newest Member
    DaciaDH
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • 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  
    • Scott Adams
      It sounds like you've been through a lot with your son's health journey, and it's understandable that you're seeking answers and solutions. Given the complexity of his symptoms and medical history, it might be beneficial to explore a few avenues: Encourage your son to keep a detailed journal of his symptoms, including when they occur, their severity, any triggers or patterns, and how they impact his daily life. This information can be valuable during medical consultations and may help identify correlations or trends. Consider seeking opinions from specialized medical centers or academic hospitals that have multidisciplinary teams specializing in gastrointestinal disorders, especially those related to Celiac disease and Eosinophilic Esophagitis (EOE). These centers often have experts who deal with complex cases and can offer a comprehensive evaluation. Since you've already explored alternative medicine with a nutrition response doctor and a gut detox diet, you may want to consider consulting a functional medicine practitioner. They take a holistic approach to health, looking at underlying causes and imbalances that may contribute to symptoms. Given his low vitamin D levels and other nutritional markers, a thorough nutritional assessment by a registered dietitian or nutritionist specializing in gastrointestinal health could provide insights into any deficiencies or dietary adjustments that might help alleviate symptoms. In addition to routine tests, consider asking about more specialized tests that may not be part of standard screenings. These could include comprehensive stool analyses, food intolerance testing, allergy panels, or advanced imaging studies to assess gut health.
    • Nacina
      Hello, I am a 45 year old mom, who was diagnosed at 29 with Celiac. My now 14 year old son was diagnosed just before his 4th birthday. Needless to say, we are old pros with the diet. He was experiencing some issues, overall health took a major plummet a year ago, and through a bit of work, was diagnosed with EOE. Tried diet alone, but his follow up endoscopy didn't show the improvements his DR. wanted to see, so I tried the medication. (Steroid). He became extremely backed up, and they had him taking Miralax daily. His health plummeted. He is a straight A honor's 8th grader who plays club soccer very competitively. His health continued to decline and at 13 had a colonoscopy and another upper gi. (He was still compacted even with the prep). I finally pulled him off all meds and mira lax, after reading much negative literature online, and put him on a gut detox diet and took him to a nutrition response dr. Finally things have improved. However...over a year later and he is having relapse stomach pain, debilitating stomach pain. Missing a day of school a week, to three this week. This is where we downward spiral with him. He says it doesn't feel the same as when he has gotten backed up before. He is eating prunes, taking his supplements, drinking water...all of the things. Yet, he is feeling horrible. Pain is abdomen, headache, lethargy, diarrhea . He is on a strict gluten dairy, egg free diet. He has adapted well in regards to diet. But I feel like we are missing something here. He is too active, too outgoing to be feeling sick all of the time. His Bilirubin is constantly high. His white blood count always runs slightly low. His vitamin D was very low last time he ran tests, (last month) when he was sick for a week. His celiac markers show negative, so it isn't that. His last endoscopy showed no Eosinaphils in his esophagus.  I have taken him to multiple Ped. Gastro specialists. They run tests, and we get zero answers. I meticulously go through labs, hoping to make some sense and maybe catch something. Any thoughts or ideas would greatly be appreciated. 
    • trents
      But if you have been off of wheat for a period of weeks/months leading up to the testing it will likely turn out to be negative for celiac disease, even if you actually have celiac disease. Given your symptoms when consuming gluten, we certainly understand your reluctance to undergo  the "gluten challenge" before testing but you need to understand that the testing may be a waste of time if you don't. What are you going to do if it is negative for celiac disease? Are you going to go back to merrily eating wheat/barley/rye products while living in pain and destroying your health? You will be in a conundrum. Do I or do I not? And you will likely have a difficult time being consistent with your diet. Celiac disease causes inflammation to the small bowel villous lining when gluten containing grains are consumed. This inflammation produces certain antibodies that can be detected in the blood after they reach a certain level, which takes weeks or months after the onset of the disease. If gluten is stopped or drastically reduced, the inflammation begins to decrease and so do the antibodies. Before long, their low levels are not detectable by testing and the antibody blood tests done for diagnosing celiac disease will be negative. Over time, this inflammation wears down the billions of microscopic, finger-like projections that make up the lining and form the nutrient absorbing layer of the small bowel where all the nutrition in our food is absorbed. As the villi bet worn down, vitamin and mineral deficiencies typically develop because absorption is compromised. An endoscopy with biopsy of the small bowel lining to microscopically examine this damage is usually the second stage of celiac disease diagnosis. However, when people cut out gluten or cut back on it significantly ahead of time before the biopsy is done, the villous lining has already experienced some healing and the microscopic examination may be negative or inconclusive. I'm not trying to tell you what to do I just want you to understand what the consequences of going gluten free ahead of testing are as far as test results go so that you will either not waste your time in having the tests done or will be prepared for negative test results and the impact that will have on your dietary decisions. And, who are these "consultants" you keep talking about and what are their qualifications? You are in the unenviable position that many who joint this forum have found themselves in. Namely, having begun a gluten free diet before getting a proper diagnosis but unwilling to enter into the gluten challenge for valid testing because of the severity of the symptoms it would cause them.
    • Fluka66
      Thank you very much for your reply. I hadn't heard of celiac disease but began to notice a pattern of pain. I've been on the floor more than once with agonising pain but this was always put down to another abdominal problem consequently I've been on a roundabout of backwards and forwards with another consultant for many years. I originally questioned this diagnosis but was assured it was the reason for my pain. Many years later the consultant gave up and I had a new GP. I started to cut out certain food types ,reading packets then really started to cut out wheat and went lactose free. After a month I reintroduced these in one meal and ended screaming in agony the tearing and bloating pain. With this info and a swollen lymph node in my neck I went back to the GP.  I have a referral now . I have also found out that acidic food is causing the terrible pain . My thoughts are this is irritating any ulcers. I'm hoping that after a decade the outlook isn't all bad. My blood test came back with a high marker but I didn't catch what it was. My GP and I have agreed that I won't go back on wheat just for the test due to the pain , my swollen lymph node and blood test results.  Trying to remain calm for the referral and perhaps needed to be more forceful all those years ago but I'm not assertive and consultants can be overwhelming. Many thanks for your reply . Wishing you all the best.
×
×
  • Create New...