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

Gluten-free And Sugar-free


sunflower

Recommended Posts

sunflower Newbie

I've been gluten-free and lactose free for many years, and I think I am not having (major ;) ) problems following the diet. Still, recently I've been trying to go sugar-free and yeast-free and I am finding this next to impossible. I get such horrible cravings for ANYTHING sweet that I think I am addicted to sugar! Help! Anybody has been through this and survived? Any tips?

The reason I am attempting this suicidal diet change is that I suppose I have candida overgrowth in my intestines. From what I read in the Internet, I have typical symptoms - I am going to see a natural medicine specialist about it, since no other doctor seems able (or willing) to help me with this, so hopefully I will have a doctor's diagnosis in about 2 weeks.

I've been trying and failing to go off sugar a few times this year - one month is my biggest success - but it is so hard to stick to this diet. Firstly, it is another dietary restriction on top of gluten and lactose, and I hate restricting my diet further. Then, the way I learned to manage gluten-free and lactose-free diet is by finding substitutes, trying to treat the restrictions (like, "I can't have milk") more like changes ("I can have soy milk instead"). So, I managed the one month without sugar only because I substituted white sugar and processed sweets with lots of fresh fruit, but now I have read that in the anti-candida elimination diet you have to give up all sweet foods, including sweet fruit and dried fruit, and anything baked with white flour and yeast, and I just don't know how to stick to it. After a day or two without any sugar, my craving for something sweet gets so strong that if I don't find some substitute, I break down and eat some chocolate. Any ideas how to deal with it? I know that craving chocolate might mean lack of magnesium, so I could try taking some magnesium pills, but it still leaves the problem of sugar in general.

It is really ridiculous when I stop to think about it. I mean, I don't smoke, but now I think I started to understand what some of my friends were going through when they tried to give up smoking. This is just sugar, it should be easier to give up, shouldn't it?

I'd appreciate any input from people who had similar experience.

I'm sorry for the ranting, I think I'm just feeling too sorry for myself today.

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



tarnalberry Community Regular

First, figure out if you really need to go that strict, or if you can have _some_ fruit each day. (As for soymilk, Unsweetened Silk has something like 2g of sugar, and I like the taste. ;-) )

Link to comment
Share on other sites
whitelacegal Contributor

Sunflower,

I have also been on this gluten-free and candida diet for 8 months and finally gotten over the yeast problems, i couldnt get better until i took all sugar products out of my diet and now that i am better its hard for me to try sugar again, The diet is really hard to stick to( the candida diet) but if you dont stick to it , the yeast will never go away cause that is what happened in my case. good luck

Link to comment
Share on other sites
tammy Community Regular

Hi Sunflower,

Yes I can relate. My biggest tip is to really decide what you can and will do consistently. I have not heard that chocolate cravings may mean a lack of magnesium but find that very intriguing. I will say that I have increased my magnesium intake for many of my symptoms. Although I continue to battle the urge for carbohydrates, simple and complex, I do relish that fact that I remain gluten-free and semi-casein free since Decemer 2002. At one point I was gluten-free, Casein-Free, Soy-Free, Corn-Free and Sugar-Free. I stopped. I am solely gluten-free, and I reduce all of the other foods. I needed a degree of peace of mind. The very high level of stress that it was creating for me seemed to be pointless.

My greatest tip to you is to find what you will be the most committed to and stick with it!

:D

Link to comment
Share on other sites
kabowman Explorer

I have recently discovered that I am yeast intolerant and have been considering going suger/carb free (are greatly reduced) to see if that will help. However, from what I have read, even once you "cure the yeast intolerance" you still have to watch what you eat for the rest of your life due to possible "flare ups."

So, my question is: is it worth it if you just give up the yeast? Especially if I don't have a lot of the other side-effects a lot of people with this have (i.e., yeast infections). Maybe this is just another intolerance on top of all the rest?

-Kate

Link to comment
Share on other sites
  • 2 weeks later...
sunflower Newbie

Thank you all for your posts and your encouragement! And sorry for my late answer.

In the meantime, I've been to the natural medicine specialist, but I'm a bit disappointed and confused. Yes, he agreed this can be either Candida, or some undiscovered allergies, and so he tested me for several allergies and discovered about a dozen or so, including milk, eggs, pork, carrot, oranges and God knows what else. He told me to eliminate them from my diet for a month and then come back for a blood test by which he can define if I have yeast problem and what kind of homeopatic treatment I should have. Only I'm somehow not convinced by the allergy "testing" which consisted of waving a copper rod over me (it was some kind of machine for testing allergies using magnetic waves). OK, some people might believe it, but I need a more solid proof to start an elimination diet as strict as that one. So I'm planning to do some "proper" allergy tests (like blood tests) and see if I get the same results. Well, it seems like it's still a long way to success for me.

Anyway, I noticed one good thing - after severely reducing sugar for the last couple of weeks, the sugar craving is almost gone! Maybe my yeast are dying out ;) Or maybe it's just a matter of getting used to a different diet? I did not manage to cut out sugar completely yet, but I think I made some progress.

Whitelacegal,

Did you take any medicines apart from the diet? Or did you get rid of yeast just by sticking to the diet? The 8 month perspective seems like such a long time, but at least I can hope for a light somewhere at the end of that tunnel... ;)

Also, do you have a list of forbidden products from the yeast diet that you followed? I've seen some candida diets on the Internet, but some are stricter than the others, and I am wondering to what extent I should limit myself?

Kabowman,

In my case, I don't know if I have yeast intolerance, but I do think I have yeast overgrowth, because of frequent yeast infections which can be cured with drugs, but only for some period, and sooner or later they would reappear. I also have the sugar craving, I'm often tired without reason (even though I stick to the gluten-free and milk free diet) and for many years I was often treated with antibiotics. From what I read in the Internet, this seems like the perfect picture for yeast overgrowth.

Tammy,

This is what I decided to start from :) I greatly reduced the sugar, and I feel so much better now. I'm wondering about cutting it off completely, but I guess I need someone more experienced to tell me that this is absolutely what I must do to get rid of the problem.

Tarnalberry,

According to some diets I found on the Internet, the only allowed fruit are the non-sweet ones like grapefruits or kiwis. I don't like either of them very much, so I still continue to eat small amounts of apples, oranges, etc.

Link to comment
Share on other sites
whitelacegal Contributor

Sunflower,

Yes, i was on Sporanox for 4 months and still taking this for the yeast, I basically followed diets that was in the books and didnt eat any sugar products at all, no soda, basically just greens and meats. And i also took alot of supplements but i dont know if they helped or not.

Link to comment
Share on other sites

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

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

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

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

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

      Waiting for urgent referral.

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

      Waiting for urgent referral.

    5. - Moodiefoodie replied to Moodiefoodie's topic in Related Issues & Disorders
      9

      Joint swelling when ill even on gluten-free diet


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,066
    • Most Online (within 30 mins)
      7,748

    Danyelhack
    Newest Member
    Danyelhack
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • 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.
    • Moodiefoodie
      Wow! Fascinating info. Thanks so much! I really appreciate the guidance. @Spacepanther Over the years I have had rheumatologists do full lab work ups on me. They told me they had screened me for arthritis, lupus, and Lyme disease (all negative). In addition to joint pain and stiffness I had swelling in both knees that later moved to my elbow as well.  I also experience stiffness and pain in my neck and shoulders when it flares. I vomited fairly often growing up, but there wasn’t a real pattern to it and I didn’t know it wasn’t normal (thought people caught stomach viruses often).  I don’t usually have stomach symptoms immediately after eating gluten that I notice.  The only other joint condition I know of is fibromyalgia. Good luck! Hope you can get it figured out. I only assumed my joint symptoms were due to the celiac’s because it is under control for the most part on a gluten-free diet.  The rheumatologist also mentioned that some inflammatory/autoimmune diseases can be slow-moving and not detectable until they progress.
×
×
  • Create New...