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

Feeling Dizzy


monkeypuss

Recommended Posts

monkeypuss Rookie

just wondered if feeling really dizzy and like you're gonna pass out is normal when glutened? i havent read a great deal about dizzyness related to it, but since i've been ill i've been like this alot, i thought it was from not being able to eat much, which some of the time it probably is, but even when i've eaten, and often sugary stuff, i still get like it..i've fainted quite a lot too :/


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



Celiac.com Sponsor (A8-M):



fedora Enthusiast

Being dizzy wasn't a main symptom from being gluttened for me although at times I got lightheaded and weak. Being dizzy is a main symptom from years of being poisoned though. I have had anemia on and off for years. Also I had low blood pressure. After a few months of being off gluten my blood pressure went up to a more normal level. It went down the other day but that was from a extreme weather change where the temperature went up to the high 90s. yuck.

veggienft Rookie

I got, or recognized I had, celiac after about 25 years fighting candidiasis. Here is a Lancet article showing that candidiasis and celiac are essentially the same disease .........at least for many people:

Open Original Shared Link

Yes, for all of my 25 year fight, dizziness was and is one of my strongest symptoms. There are probably many reasons. They include:

* Elevated blood sugar, both from the stomach contents emptying into the blood, and from pancreas attack

* Elevated blood ammonia levels from liver protein overload

* Combination of this ammonia with ingested oxidants .......ammonium chloride, a bad toxin

* Confused heart electrical impulses due to heart nerve attack and random calcium redeposition

* Nerve attack from the above chemicals combined with gliadin/cassein exorphin attack

Instead of eliminating one food at a time, go to a very strict exclusion diet. Then you can test foods by adding them back.

Candida albicans lives on the gut mucous membranes, thrives on sugar, and survives the oxidants which kill off competing beneficial gut bacteria.

Stop ingesting chlorinated water and foods with dyes. Stop ingesting sweets, including fruit. Stop ingesting glutenous grains. Stop ingesting milk, and cheeses containing raw milk. Those would include "American cheese", cream cheese, and sour cream. Stop eating glutenous grains and beans.

It might be easier to concentrate on what you can eat, and not what you can't eat. Get your protein from cooked meat, fish, fowl, and aged cheese. Get your carbs from rice, potatoes and corn. Eat lots of green veggies. Don't eat anything else until you improve.

However, improvement should be rapid. After a few months, then you can test one food at a time.

Oh .......don't lick envelopes or stamps.

Start eating probiotics, like plain live yogurt. Start taking reasonably large supplements of vitamin C and B complex.

..

KristaleeJane Contributor

Can a regular family doctor test and/or diagnose candida overgrowth in celiac patients? How is this normally treated?

veggienft Rookie
Can a regular family doctor test and/or diagnose candida overgrowth in celiac patients? How is this normally treated?

It can be tough finding a doctor who recognizes celiac as a disease, let alone finding one who recognizes the multitude of autoimmune connections or the un-reliability of celiac tests.

Medicine is driven by patient complaints. If a patient sees a doctor, and complains of a sore swolen tongue, oral thrush, anal or vaginal itch or rash, athlete's foot, eye inflamation...... then yes, most doctors would probably look into candida overgrowth. As most patients expect, though, most doctors deal in the known, the provable, or patient-obvious diagnoses. It results in the treatment of symptoms, and not the treatment of diseases.

Most doctors treat candidiasis with anti-fungal medications. Somewhat fewer doctors are willing to recommend an anti-candida diet. And without the diet candidiasis almost always returns.

As shown over and over again in these pages, most people are forced to self-diagnose their internal celiac symptoms via diet. I'm sure it's the same for most candidiasis patients. It certainly was for me.

Start with a model, and design a diet. If the diet works then stay on it. If you need a name for that, then call it celiac ........or candidiasis ......or both.

P.S. I can also eat cooked chicken egg.

..

GlutenGalAZ Enthusiast

I got dizzy a lot while I was still eating gluten (before I knew anything about gluten) but the thing was I am not sure if it was from the gluten or from my medicine I was taking for my pulse and then switch to a different one.

I have noticed though after being on the gluten free diet that I am not getting dizzy as much. Sometimes around "that time of the month" I get a little dizzy.

I bring cut up apples with peanut butter with me to work so if I get hungry I can snack on that (like an energy boost). I make sure I always have snacks with me at work so I don't get weak or dizzy feeling.

It could be from not eating that much. When I first started on the diet I was still figuring out what I could eat/what was safe so I was getting dizzy/icky feeling from not eating that much. There are a lot of foods at the normal store (not just health food stores) that are gluten free (just have to read the label). I am not sure about the UK how label laws are there but I do majority of my shopping just at the normal grocery store and buy things like gluten free mixes and gluten free pretzels at the health food store.

Hope you feel better :)

ShayFL Enthusiast

It is one of my biggest complaints. I hate it.


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



Celiac.com Sponsor (A8-M):



TheMinsterman Newbie

Define dizzy, do you mean spinning vertigo? The type of dizziness is a key step to discovering the source.

I've had inner ear fluid issues since getting ill in February (constantly everyday and is continuing as I type).

msmini14 Enthusiast

What kind of diet does one adhere to if they think they have candiden? I think I might have that problem, I should go to the doctor but I will get in trouble if I miss anymore work. My boyfriend laughed at me when I told him I am having problems. So, I need to stay gluten-free and stop eating carbs and sugar for Candiden?

ShayFL Enthusiast

Yeast aggravate Candida. Some cannot even tolerate fruit sugar.

Open Original Shared Link

I have tested negative for it via blood, saliva and fecal. I am so glad I did. I would hate to try to follow that diet if I did not need to.

  • 7 years later...
T.Adams Newbie
On 5/22/2008 at 6:48 AM, monkeypuss said:

just wondered if feeling really dizzy and like you're gonna pass out is normal when glutened? i havent read a great deal about dizzyness related to it, but since i've been ill i've been like this alot, i thought it was from not being able to eat much, which some of the time it probably is, but even when i've eaten, and often sugary stuff, i still get like it..i've fainted quite a lot too :/

When I get glutened after a few hours I feel nauseous and dizzy, I get a headache, bloated tummy. And when it's real bad I will get woken up from being asleep with these waves that come over me that feel like I am going to pass out. It really freaks me out when that happens. I hope you feel better soon.

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. - Scott Adams commented on Scott Adams's article in Latest Research
      3

      New "Glowing Bacteria" Pill Could Transform Gut Disease Detection (+Video)

    2. - trents replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      7

      Help understand results

    3. - Jordan Carlson posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      Fruits & Veggies

    4. - wellthatsfun posted a topic in Gluten-Free Recipes & Cooking Tips
      0

      heaps of hope!

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

    • Total Members
      132,997
    • Most Online (within 30 mins)
      7,748

    IwannabHealthy
    Newest Member
    IwannabHealthy
    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

    • trents
      Actually, it would be more correct to say that the genetic potential to develop celiac disease is passed down from parents to children. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% of the general population actually do. But it is also true that the offspring of those who do have active celiac disease are at a considerably higher risk of developing active celiac disease than those of parents who have the genes but don't develop the disease. Some recent, larger studies put the risk at near 50% for the first degree relatives of those who have active celiac disease.
    • Jordan Carlson
      Hello everyone! Been a while since I posted. The past few moths have been the best by for recovery for myself. I have been the least bloated I have ever been, my constant throat clearing is almost gone, I have stopped almost all medication I was prevously taking (was taking vyvanse for adhd, pristiq for anxiety,fomotadine/blexten for histamine blockers and singulair). Only thing I take now is Tecta. I also no longer get any rashes after eating. Things are going very well. Most success came actually once I upped my B12 daily dose to 5,000 mcg. I do have one thing I am un able to figure out and want to see if anyone else has this issue or has experience working around it. Ever since I was born I have always had a issue getting fruits and veggies down. No matter how hard I tried, it would always result in gagging or throwing up. Always just thought I was a picky eater. Now that my stomach and system has healed enough that I can feel when something is off almost istantly, I notice that after eating most fruits (sometimes I am ok with bananas) and veggies, my stomach instantly starts burning and my heart starts to pound and I get really anxious as if my body doesnt know what to do with what just enetered it. So I am thinking now that this is what probably was going on when I was born and my body started rejecting it before which caused this weird sensory issue with it causing the gagging. Hoping someone has some exprience with this as well because I would love to be able to enjoy a nice fruit smoothie once in a while haha. Thanks everyone!
    • wellthatsfun
      i know i've been rather cynical and sad about being fully diagnosed in june 2025, but my boyfriend has been consistently showing me the wonderful world that is gluten free cooking and baking. in the past couple of days he's made me a gluten free rice paper-wrapped spanakopita "pastry", plus a wonderful mac and cheese bechamel-ish sauce with gluten free pasta (san remo brand if you're in australia/if you can get your hands on it wherever you are).  those meals are notably gluten free, but mainly he's been making me easy gluten free meals - chili mince with white rice and sour cream, chicken soup with homemade stock from the chicken remains, and roast chickens with rice flour gravy and roast veggies. i'm a bit too thankful and grateful lol. how lucky could i possibly be? and, of course, for those who don't have someone to cook for them, it's quite easy to learn to cook for yourself. i've been making a lot of meals for us too. honestly, cooking is pretty darn fun! knowing basic knife skills and sanitary practices are all you really need. experimenting with spices will help you get on track to creating some really flavourful and yummy dishes. coeliac is a pain, but you can use it to your advantage. healthier eating and having fun in the kitchen are major upsides. much luck to all of you! let's be healthy!
    • knitty kitty
      That test is saying that your daughter is not making normal amounts of any IGA antibodies.  She's not making normal amounts of antibodies against gliadin, not against bacteria, not against viruses.  She is deficient in total IGA, so the test for antigliadin antibodies is not valid.  The test was a failure.  The test only works if all different kinds of antibodies were being made.  Your daughter is not making all different kinds of antibodies, so the test results are moot.  Your daughter should have the DGP IgG and TTG IgG tests done.   The tests should be performed while she is still consuming gluten.  Stopping and restarting a gluten containing diet can make her more sick, just like you refuse to eat gluten for testing.  Call the doctor's office, request both the IGG tests. Request to be put on the cancellation list for an appointment sooner.  Ask for genetic testing.   Celiac disease is passed on from parents to children.  You and all seven children should be tested for genes for Celiac disease.  Your parents, your siblings and their children should be tested as well.  Eating gluten is not required for genetic testing because your genes don't change.  Genetic testing is not a diagnosis of Celiac disease.  Just having the genes means there is the potential of developing Celiac disease if the Celiac genes are activated.  Genetic testing helps us decide if the Celiac genes are activated when coupled with physical symptoms, antibody testing, and biopsy examination. It's frustrating when doctors get it wrong and we suffer for it.  Hang in there.  You're a good mom for pursuing this!  
    • knitty kitty
      @hjayne19, So glad you found the information helpful.  I know how difficult my struggle with anxiety has been.  I've been finding things that helped me and sharing that with others makes my journey worthwhile. I like Life Extension Bioactive Complete B Complex.  It contains the easily activated forms of B vitamins needed by people with the MTHFR genetic variation often found with Celiac disease.   Avoid B Complex vitamins if they contain Thiamine Mononitrate if possible.  (Read the ingredients listing.)  Thiamine Mononitrate is the "shelf-stable" form of B 1 that the body can't utilize.  B vitamins breakdown when exposed to heat and light, and over time.  So "shelf-stable" forms won't breakdown sitting on a shelf in a bright store waiting to be bought.  (It's also very cheap.)  Thiamine Mononitrate is so shelf-stable that the body only absorbs about thirty percent of it, and less than that is utilized.  It takes thiamine already in the body to turn Thiamine Mononitrate into an active form.   I take MegaBenfotiamine by Life Extension.  Benfotiamine has been shown to promote intestinal healing, neuropathy, brain function, glycemic control, and athletic performance.   I take TTFD-B1 Max by Maxlife Naturals, Ecological Formulas Allthiamine (TTFD), or Thiamax by EO Nutrition.  Thiamine Tetrahydrofurfuryl Disulfide (TTFD for short) gets into the brain and makes a huge difference with the anxiety and getting the brain off the hamster wheel.  Especially when taken with Magnesium Threonate.   Any form of Thiamine needs Magnesium to make life sustaining enzymes and energy.  I like NeuroMag by Life Extension.  It contains Magnesium Threonate, a form of magnesium that easily crosses the blood brain barrier.  My brain felt like it gave a huge sigh of relief and relaxed when I started taking this and still makes a difference daily.   Other brands of supplements i like are Now Foods, Amazing Formulas, Doctor's Best, Nature's Way, Best Naturals, Thorne, EO Nutrition. Naturewise.  But I do read the ingredients labels all the time just to be sure they are gluten and dairy free. Glad to help with further questions.  
×
×
  • 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.