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

Yeast Overgrowth (mouth, Vagina, Butt)


julu83

Recommended Posts

julu83 Newbie

I have lived my whole life off and on with vaginal yeast infections, and soreness around the anal area.

Last week, on the back of my tongue, I discover these white bumps. I went to my PCP and when he looked in my mouth, his first reaction was OOOOOOOOOOOO! I do not know what that is! Wow! Could he use a little bedside manners training. Needless to say, he gave me 2 scripts, one for Majic mouthwash and one for Nystatin. Wish I'd have filled the Nystatin 1st! The first script seemed to be doing nothing but numb my mouth and lips. So, after I filled the Nystatin and had taken it for 3 days, the white bumps are leaving very fast. Today, I had a dental cleaning and was told it was indeed a yeast overgrowth. I came home and after doing some research on wikapedia, I'm thinking I might have celiacs disease, because I have a lot of the symptoms.

I'm thinking maybe I need to follow the celiac diet and try a different approach to end this life long Yeast Infection Somewhere syndrome. Has anyone out there in cyber world ever shared any similar, long term, ongoing, chronic Yeast problems? I would appreciate any backfeed!!!!


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



Celiac.com Sponsor (A8-M):



Kim Hopkins Rookie

I can relate to the yeast problems, although mine started after about 5 years of being on the gluten free diet and feeling good. Didn't know what was going on for so long - no doctors did either. I found the work of Dr. Crook (The Yeast Connections & Womens Health). It helped me a lot. I adjusted my diet and took Nystatin. Yeast overgrowth can be attributed to many different things - you might want to learn more about what it's connected to before just going gluten free. Hope this helps!

Kim

julu83 Newbie
I can relate to the yeast problems, although mine started after about 5 years of being on the gluten free diet and feeling good. Didn't know what was going on for so long - no doctors did either. I found the work of Dr. Crook (The Yeast Connections & Womens Health). It helped me a lot. I adjusted my diet and took Nystatin. Yeast overgrowth can be attributed to many different things - you might want to learn more about what it's connected to before just going gluten free. Hope this helps!

Kim

Thanks! So, where do I find this Dr. Crook and the womens yeast connection?

Judy

Kim Hopkins Rookie

I found it on Amazon. He's got other books, too. There is also a website www.yeastconnection.com

Good luck!

Thanks! So, where do I find this Dr. Crook and the womens yeast connection?

Judy

burdee Enthusiast

After treatment for a bladder infection during my 20s, I developed a vaginal yeast infection. My doctor just told me that switching to another antibiotic (for the bladder infection) would eliminate the yeast infection. 40 years ago most docs didn't understand the connection between antibiotic treatment and developing overgrowths from other 'bugs'. (Some modern docs STILL don't get it.) Nobody ever mentioned taking probiotics back then. Fortunately the vaginal yeast symptoms disappeared and I believed the doctor's logic.

However 30 years later when I give a stool test for bacteria, parasites and yeasts, I learned that I had candida overgrowth in my intestines. I had also endured candida symptoms during all those years. By that time I had been diagnosed with celiac and 6 otherfood allergies. So I did NOT want to limit my diet any more to treat candida. I didn't consume a lot of sugary treats, but I did consume fruits, which are often banned from 'anti-candida diets'. So I treated my candida with nystatin AND daily probiotics (to restore normal good bacteria to my gut as the yeast was killed by nystatin). Nystatin was very easy to take (after initial nausea symptoms for about 3 days). So I took nystatin for about 4 months. On the next stool test I had NO candida.

So I suggest you continue to treat your candida with nystatin. You don't need to follow a special resrictive diet, but you DO need to take high dose probiotics to restore your gut health as Nystatin kills off the candida.

SUE

I have lived my whole life off and on with vaginal yeast infections, and soreness around the anal area.

Last week, on the back of my tongue, I discover these white bumps. I went to my PCP and when he looked in my mouth, his first reaction was OOOOOOOOOOOO! I do not know what that is! Wow! Could he use a little bedside manners training. Needless to say, he gave me 2 scripts, one for Majic mouthwash and one for Nystatin. Wish I'd have filled the Nystatin 1st! The first script seemed to be doing nothing but numb my mouth and lips. So, after I filled the Nystatin and had taken it for 3 days, the white bumps are leaving very fast. Today, I had a dental cleaning and was told it was indeed a yeast overgrowth. I came home and after doing some research on wikapedia, I'm thinking I might have celiacs disease, because I have a lot of the symptoms.

I'm thinking maybe I need to follow the celiac diet and try a different approach to end this life long Yeast Infection Somewhere syndrome. Has anyone out there in cyber world ever shared any similar, long term, ongoing, chronic Yeast problems? I would appreciate any backfeed!!!!

mommida Enthusiast

Chronic yeast infections have been linked to Celiac and other auto-immune diseases.

If you are going to get tested for Celiac you have to continue eating gluten until the testing is done.

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. - trents replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?

    2. - BlessedinBoston replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?

    3. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      14

      My only proof

    4. - Jmartes71 replied to Jmartes71's topic in Related Issues & Disorders
      14

      My only proof

    5. - marion wheaton posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,410
    • Most Online (within 30 mins)
      7,748

    Marilyn Gingras
    Newest Member
    Marilyn Gingras
    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
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
    • marion wheaton
      Wondering if anyone knows whether Lindt chocolate balls are gluten free. The Lindt Canadian website says yes but the Lindt USA website says no. The information is a bit confusing.
×
×
  • 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.