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

Craving Sweets...


Guest imsohungry

Recommended Posts

Guest imsohungry

Hey everybody,

I've been reading a lot of these posts and noticing a common theme in many of them... SWEETS, SUGAR, and CHOCOLATE! :)

O.K.

Here is my issue. Most days I crave sweets very often, and I stay fatigued. I literally want to gag if I smell "real food," but show me a candy bar, and my mouth waters.

I've gotten where I hate to eat. I only really like bread and sugar and milk, but I am ALWAYS tired and have muscle/joint aches, constipation, dermatitis, and headaches. I usually feel worse after I eat. My husband says that he finds it hard to believe that I feel better if I skip lunch, but honestly, as soon as I eat, I feel icky again. The most frusterating thing is that I can't relate it just to gluten.

I'm not hypoglycemic (according to bloodwork). How do I know if I am lactose or yeast intolerant? Or could I be sugar-intolerant? How do I know? I am willing to cut things from my diet, but I am just so confused! :blink:

This morning, I had 3 pieces of bacon, a bowl of grits, and orange juice for breakfast (which I thought was a good breakfast)...but I immediately got so tired that I could hardly stay awake and my head started aching! UGGGGHHH! I could just cry. :(

I'm trying so hard to feel better. Oh, well. Any suggestions??? Hope to hear from somebody soon.

Much hugs. -Julie :)


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



Celiac.com Sponsor (A8-M):



Deby Apprentice

Julie,

I can't be any help except to say that I share a lot of your same symptoms. I don't feel bad after eating though, at least not all of the time. But I DO CRAVE SUGAR!

My sister went on a sugar purge. It seemed like an awful diet, but it only lasted a month. This was supposed to stop some process, firmintation maybe ~

She complained the whole time going through it and she doesn't have celiac disease. I'm already soooo restricted, I can't imagine restricting another thing. I'm about ready to ask my doc for a pep pill!!

LynnR Explorer

For me - my problems are chocolate . . . candy bars, cake, hot cocoa, etc. I could never get enough of it. In the past, I would even have chocolate bars in the morning. If I saw them, I had to have them. I knew that I had to do something about this. So I got them all out of the house which was very difficult for me to do. But at the same time, it helped me out greatly.

Now when I have something with chocolate it in i.e. ice cream or occasionally cake I no longer crave it. Even my cravings for sweets are entirely gone. I do eat cookies & ice cream on a daily basis because I want it not because I crave it. It tastes so much better to me now too.

sunflower Newbie

Hi guys,

I can relate - I have the same problem. Have you ever considered yeast (Candida) overgrowth as the reason of craving sweets?

There are threads about it on this site:

Open Original Shared Link

and

Open Original Shared Link

Guest imsohungry

Thank you so much for the feedback (and links...I looked at them) :)

Gosh, this is so frustrating. I wish I knew the answer! I feel like, after all of these years, I am "on-to-something" with the gluten and food intolerance problems. I just need to keep researching!

I took a nap this morning at work. I didn't have a choice; I was awake one minute and then so sleepy that I couldn't sit up the next minute. The only thing that I had eaten this morning before it occurred was gluten-free rice milk over gluten-free rice cereal.

What is wrong with me??????? I know that I also have lupus and epilepsy, and I am on medication for both. I don't consider myself a hypochondriac; in fact, I rarely complain, and my work often doesn't know when I have had a week full of seizures...because I come in to the office anyway (what good would it do to complain about it...seizures are a fact of life for me). :rolleyes:

Thanks for letting me vent. I am learning and trying and frustrated. You all are great!

Hugs and blessings. -Julie

Maggie1956 Rookie

Wow, I'm finding out that a lot of what I thought was just MY problems, are really common for a lot of coeliacs.

I crave sugary food something chronic. I can't eat proper chocolate because of migraines. I've assumed I'm allergic to it. But if I get anywhere near white chocolate, I eat the lot in one sitting. It seems like a real addiction...is it maybe? :unsure:

Actually anything sweet is a real temptation, but I am beginning to think that I feel aweful afterwards from having it.

Julie, I know what you mean when you say you're always falling asleep. I am constantly really exhausted too.

I have celiac disease, CF (ME) and am hypothoid. It is so strange to actually have the diagnosis now. I've felt sick for a lot of years and wondered why. :huh:

I am at the end of my first day gluten-free, and although I feel as bad as I did yesterday, I guess it will improve over time.

Thanks for all the messages on the boards. I've been trying to take it all in.

Hang in there Julie. :)

Maggie

Mballerina Explorer

I have the same thing, real food makes me gag but sweets are great. My thinking is that my digestive system is so raw and unable to break things down that i start to crave food that is digested really easily which is sweets and simple sugars. I really really believe this because even if i want an apples or a piece of meat i can't swallow it.


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



Celiac.com Sponsor (A8-M):



dbuhl79 Contributor

Well, the odd thing since all my problems started, I hardly crave sweets. In fact my appetite, is ridiculously small.

But, looking at what a lot of you say you're drawn to or eat more frequently, simple sugars, candy, chocolate. I'm wondering if all of you are eating enough of a balance of carbs and proteins? I ask this really from the prospective as a former marathon runner etc.. I tried atkins ages ago and it was extremely difficult for me to carry on a day, particularly exercising etc. w/o the carbs I was accustomed to.

Maybe take a food log of what you've been eating for awhile, and reflect back on it in 2 weeks, noting when you feel the most fatigued etc. You might find some interesting connections to the foods your eating. I know sugar can give me a great intial buzz get up and go, but I crash hard afterwards. Making me want to do things like, nap at work too.

Good luck, I hope..some of this shed some light for some one!!

jaimek Enthusiast

I too am complete opposite. I have been gluten-free for about 10 months now and recently I have not craved sweets at all. I used to have to have dessert after dinner every night and now I don't even think about dessert. Very strange.....

YankeeDB Contributor

imsohungry, I'm wondering if you have other food allergies, such as corn? (Thinking about the grits you had for breakfast?)

I did the York Labs allergies test (expensive but so worth it) and discovered I need to avoid: milk, yeast, eggs, soy, cashew, sunflower seeds and pears. Truly, if I avoid all these, I feel infinitely better.

I think enterolab is coming out soon with comprehensive food allergy tests too--I'd recommend them as well.

I did an experiment 2 days ago and had some salad dressing with vinegar in it (most vinegar has yeast) and am still feeling sluggish as a result. On the other hand, I've had days of literally dancing around in joy from the energy I've gleaned after years and years of fatigue.

Regarding the sweet tooth, I have a bit of that and recently discovered stevia, a natural sweetener without the energy-sapping properties of refined sugar.

Good luck!

Guest imsohungry

You all have such great (and varying) input! Which is exactly what I need as I am trying to examine this whole situation! :)

YankeeDB-

I hadn't considered a corn intolerance. My brother is allergic to any kind of fish, nuts, and, of all things, rice. He had one of those "prick tests" done at the allergist...he goes into anaphalactic shock (sp?) if he eats these foods. If he is allergic to rice, I suppose I could be allergic/intolerant to corn! :rolleyes: Definitely, something to think about.

Tiffany,

It is interesting to hear that you sometimes have the same "gag" feeling toward "real" food as I do. I try to eat anyway, but sometimes I can't make myself...I'll literally heave when I force myself to eat when I get like that. :unsure: It just isn't worth it. :blink:

Maggie,

Hang in there! You will feel better and better as time progresses. Thank you for your kind words. :) and Welcome to the forums!

Dana,

What you said about protein makes sense. I am actually trying to start a food diary (I even started a thread about it) ;) Although I do not like most high-protein foods, I make sure I eat some protein. I try to eat a balanced/healthy breakfast. gluten-free granola cereal/milk, bacon/OJ/grits, etc. But it seems like no matter how hard I try I always hit bottom energy by mid-morning (9-11 am). However, I am going to document EXACTLY what I eat in hopes of catching something I've previously overlooked.

Many blessings and much hugs to all that have replied!

-Julie B)

dbuhl79 Contributor

Julie,

Glad we all can help some! I just had a thought, you said that you hit a low spot around 9-11.. Perhaps around that time, you can have a small snack on the side, nuts or something that will boost your energy. Just a thought!!! Let us know how it goes!

Maggie1956 Rookie

:o It is like a light has come on in my head since I started reading the posts here!

Recently, I have started gagging on some foods, mainly meat. It is really embarrasing :( when it happens in front of people. Trying to hide the fact that I cannot swallow it, or spit it out is simply aweful.

How do you handle it when in that situation Tiffany? I'm starting to feel like it's just best to stay home.

I'm freaking out a little today, because my husband's work dinner is tonight and I have to go with him. :unsure:

Also, after really trying not to eat anymore gluten, I bought rice crisps yesterday which said they were 'gluten free'. I ate a couple, and immediately started feeling like a vice had been pulled around my stomach.

Then I read the fine print. It has soy sauce in it, doesn't it! :angry:

So, here we go again...I'll start my gluten-free diet afresh from now on. I guess I will learn by experience.

Thanks for the advice and encouragement everyone.

Maggie B)

  • 4 weeks later...
wclemens Newbie

Hi,

I have Celiac and am intolerant of all grains, milk & dairy, egg whites and yeast. I have spent years learning the foods which affect me adversely, and now I never touch any of them, read labels diligently, and always work to remain gluten free.

However, even with eliminating all those foods, I often felt drained or overly tired, just as you are describing. I finally came across the book, The Carbohydrate Addict's Diet, which said that those from families where diabetes is prevalent might have a tendency to eventually develop that disease (my mother had diabetes).

I immediately began following their diet, which involves eating only high-protein, low carbohydrate foods 23 hours a day, with one hour devoted to eating or drinking anything to which you are not intolerant. It sounded too good to be true!

Within a couple of weeks I was feeling good, losing weight, sleeping better, and having no times of letdown fatigue.

It works!

Now I eat chicken, chili burgers, steak, ribs, salmon, tuna, fish, salad, egg yolks, etc. for those 23 hours a day, and indulge in all kinds of treats for my one hour "reward meal" (that's what Richard and Rachel Heller call you one hour meal). They both went from being several hundred pounds of unhealthy flesh to normal weights and healthy lifestyles.

Hope this helps. Welda

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - cristiana replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

    2. - chrisinpa commented on Scott Adams's article in Skin Problems and Celiac Disease
      2

      Celiac Disease and Skin Disorders: Exploring a Genetic Connection

    3. - knitty kitty replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      My journey is it gluten or fiber?

    4. - trents replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

    5. - trents commented on Jefferson Adams's article in Other Diseases and Disorders Associated with Celiac Disease
      6

      Celiac Disease Patients Face Higher Risk of Systemic Lupus

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,692
    • Most Online (within 30 mins)
      7,748

    Ali Zaib
    Newest Member
    Ali Zaib
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • cristiana
      I agree, it so often overlooked! I live in the UK and I have often wondered why doctors are so reluctant to at least exclude it - my thoughts are perhaps the particular tests are expensive for the NHS, so therefore saved for people with 'obvious' symptoms.  I was diagnosed in 2013 and was told immediately that my parents, sibling and children should be checked.  My parents' GP to this day has not put forward my father for testing, and my mother was never tested in her lifetime, despite the fact that they both have some interesting symptoms/family history that reflect they might have coeliac disease (Dad - extreme bloating, and his Mum clearly had autoimmune issues, albeit undiagnosed as such; Mum - osteoporosis, anxiety).  I am now my father' legal guardian and suspecting my parents may have forgotten to ask their GP for a test (which is entirely possible!) I put it to his last GP that he ought to be tested.  He looked at Dad's blood results and purely because he was not anemic said he wasn't a coeliac. (This was the same GP who said Dad didn't have dementia, when months before one of his colleagues suspected it and told me Dad must be diagnosed).  Hopefully as the awareness of Coeliac Disease spreads among the general public, people will be able to advocate for themselves.  It is hard because in the UK the NHS is very stretched, but the fallout from not being diagnosed in a timely fashion will only cost the NHS more money. Interestingly, a complete aside, I met someone recently whose son was diagnosed (I think she said he was 8).  At a recent birthday party with 8 guests, 4 boys out of the 8 had received diagnosis of Coeliac Disease, which is an astounding statistic  As far as I know, though, they had all had obvious gastric symptoms leading to their NHS diagnosis.  In my own case I had  acute onset anxiety, hypnopompic hallucinations (vivid hallucinations upon waking),  odd liver function, anxiety, headaches, ulcers and low iron but it wasn't until the gastric symptoms hit me that a GP thought to do coeliac testing, and my numbers were through the roof.  As @trents says, by the grace of God I was diagnosed, and the diet has pretty much dealt with most of those symptoms.  I have much to be grateful for. Cristiana
    • knitty kitty
      @xxnonamexx, There's labeling on those Trubar gluten free high fiber protein bars that say: "Manufactured in a facility that also processes peanuts, milk, soy, fish, WHEAT, sesame, and other tree nuts." You may want to avoid products made in shared facilities.   If you are trying to add more fiber to your diet to ease constipation, considering eating more leafy green vegetables and cruciferous vegetables.  Not only are these high in fiber, they also are good sources of magnesium.  Many newly diagnosed are low in magnesium and B vitamins and suffer with constipation.  Thiamine Vitamin B1 and magnesium work together.  Thiamine in the form Benfotiamine has been shown to improve intestinal health.  Thiamine and magnesium are important to gastrointestinal health and function.  
    • trents
      Welcome to celiac.com @sha1091a! Your experience is a very common one. Celiac disease is one the most underdiagnosed and misdiagnosed medical conditions out there. The reasons are numerous. One key one is that its symptoms mimic so many other diseases. Another is ignorance on the part of the medical community with regard to the range of symptoms that celiac disease can produce. Clinicians often are only looking for classic GI symptoms and are unaware of the many other subsystems in the body that can be damaged before classic GI symptoms manifest, if ever they do. Many celiacs are of the "silent" variety and have few if any GI symptoms while all along, damage is being done to their bodies. In my case, the original symptoms were elevated liver enzymes which I endured for 13 years before I was diagnosed with celiac disease. By the grace of God my liver was not destroyed. It is common for the onset of the disease to happen 10 years before you ever get a diagnosis. Thankfully, that is slowly changing as there has developed more awareness on the part of both the medical community and the public in the past 20 years or so. Blessings!
    • knitty kitty
      @EndlessSummer, You said you had an allergy to trees.  People with Birch Allergy can react to green beans (in the legume family) and other vegetables, as well as some fruits.  Look into Oral Allergy Syndrome which can occur at a higher rate in Celiac Disease.   Switching to a low histamine diet for a while can give your body time to rid itself of the extra histamine the body makes with Celiac disease and histamine consumed in the diet.   Vitamin C and the eight B vitamins are needed to help the body clear histamine.   Have you been checked for nutritional deficiencies?
    • sha1091a
      I found out the age of 68 that I am a celiac. When I was 16, I had my gallbladder removed when I was 24 I was put on a medication because I was told I had fibromyalgia.   going to Doctor’s over many years, not one of them thought to check me out for celiac disease. I am aware that it only started being tested by bloodwork I believe in the late 90s, but still I’m kind of confused why my gallbladder my joint pain flatulent that I complained of constantly was totally ignored. Is it not something that is taught to our medical system? It wasn’t a Doctor Who asked for the test to be done. I asked for it because of something I had read and my test came back positive. My number was quite high.Are there other people out here that had this kind of problems and they were ignored? 
×
×
  • 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.