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

Vitiligo


Dixiebell

Recommended Posts

Dixiebell Contributor

I am pretty sure my son has vitiligo. He has not be diagnosed as of yet. His ped said to keep an eye on it. I am curious to see if any of your children have had these problems as well. He is 9 and is still wetting the bed once or twice a week. I wake him up at 2am every night to go and sometimes he will already be wet. We also have limited his fluid intake in the evenings. His eyesight has gotten worse over the past year. His Rx for glasses almost doubled. The eye doc. was very surprised. Since being gluten-free he still sometimes says his stomach hurts. What I would like to know is, do any of you think we should have him tested for diabetes or maybe something else or nothing? What are your experiences? Thank you.


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



Celiac.com Sponsor (A8-M):



mommida Enthusiast

Our experience backs up the statistics. Getting diagnosed with one auto-immune disease is an open doorway to more auto-immune disease.

If there are symptoms then go for a diagnoses. There may be medication, diet changes, or other things to alleviate symptoms, but you won't know without a diagnoses.

For vitiligo, I believe there is an immuno-suppressing skin lotion that can be used. Depending on the areas of skin that have lightened, use of sun screen may be needed.

Good luck and God bless!

Arwen2k3 Newbie

Our son has vitiligo. It was the driving force behind my discovering he has celiac (two weeks ago)! He is 4 and for a year I was watching this weird white patch on his tummy. It then spread to his groin area. This summer when he got out in the sun, the sun darkened his skin and more spots showed up on his feet, hands elbows and knees. He also started to get white eyelashes.

I have read that over time on a gluten free diet the vitiligo patches subside. I am hoping, because it seems that there really isn't that effective of a treatment for it.

Through this experience, I have learned never ever to doubt my intuition with my children's health. You sound like you are concerned and have some ideas. I think you should pursue what you think may be going on. It doesn't hurt to see if there are medical reasons behind what is happening, especially when they are so at risk health-wise.

Does he have excessive thirst? Have you reviewed any symptoms lists of childhood diabetes? It's good to be aware so as not to blame everything on the celiac when there may be something else going on. Good luck to you!

Dixiebell Contributor

I talked to his ped. on monday and he wanted me to send him a picture of his spots so he could see if it looked like vitiligo. Of course he couldn't tell in the pics. So I am having him sit in the sun for 20 min after school so they will be more visible when we go back in a few days.(son is light skinned but tans very well) His ped. said he could also get a urine sample and I am going to push for some blood tests also. I don't remember seeing the spots until mid summer break and I really didn't think much of them until I started reading online about the bedwetting possibly being connected to diabetes and then the connection of diabetes and vitiligo. I had an ah-ha moment. I am just so glad that his ped. is listening to my concerns and not poo-pooing me. His thirst is worse at times but not excessive. I have thought it was because of living in the hot south. Thank you.

kareng Grand Master

I'm not discounting the fact that he has something wrong causeing the bed wetting. I'm just offering something that helped my boys. These are exercises to make his bladder bigger and the muscles stronger. Its hard to do during the school day because you have to go to the bathroom at set times. When you feel like you need to pee, wait. You'll have to see if its 10 more minutes or 30.

When you go, start and stop peeing. hold for whatever he can (count of 10?) then pee and hold again.

I saw info that the best time to wake the kids up to pee is about 2 hours after they go to sleep. Has to do with sleep cycles.

I found tht it really isn't as unusual for a boy before the age of 12 to wet the bed at night. Alot of moms won't admit it so you & your kid think they are the only one.

Good luck. Just thought he might like to have something he can do and not feel hopeless. This may take a couple of months. One of my boys just grew a bunch and suddenly, no more problems. The other did this for 2 months before it helped. I noticed that when they peed, they never peed a lot (listen outside door). Now I worry they will flood the toliet!

Dixiebell Contributor

Thank you. I will try to get him to do that when he needs to go.

scarlett77 Apprentice

Wow I learn something new everyday...I had no idea that vitiligo was a possible sign that you have an auto-immune disorder. My celiac son has a patch on his upper thigh since he was about 4-6 months old. It has never moved or grown though.


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



Celiac.com Sponsor (A8-M):



Arwen2k3 Newbie

Scarlett77~ My sons patches don't move either. He has the same patches, but he just has gotten more. It started with just one on his tummy. It looks like I put sunscreen only there. Same texture as the rest of his skin, except there is no pigment there. More and more spots appeared. Often, you can find symmetrical patchiness. Meaning, if there are three on the hand you could find three in the same pattern on the other hand. With my son I don't see a pattern, but he always has them on both limbs in the same areas, not just one hand or one foot etc. He is fair skinned so it is not as noticeable as it is for others. But, over time patches can resolve or lesson and then appear somewhere else later.

THernandez Newbie

Oh my gosh, I had no idea! My daughter has had some patches on her face that seem to come and go and I even told my husband that it looked like vitilago, but then it went away. It seems like every day I hear about more connections between celiac and other disorders.

Roda Rising Star

I would definately ask the ped to check him for diabetes. Better safe than sorry. Hope you find some answers soon.

Dixiebell Contributor

We saw his ped today and he said they didn't find anything with his urine sample. He did use a black light to look at his skin and he thinks it is tinea versacolor. I don't think that's it. It still looks more like vitiligo to me. It's smooth no scaling and the patches are larger and not spotty like the tinea. As for the bedwetting, he thinks we should see a urologist in the near future. My son told me that he needed to go to the bathroom today at school and the teacher told him since he had just gone a little earlier that he could not go again. Well guess what? He did it in his pants! His doc was not happy with that at all and wrote a note right then for the school.

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

      My only proof

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

      My only proof

    3. - marion wheaton posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Are Lindt chocolate balls gluten free?

    4. - Dorothy O. commented on Scott Adams's article in Latest Research
      7

      Study Estimates the Costs of Delayed Celiac Disease Diagnosis (+Video)

    5. - JoJo0611 replied to JoJo0611's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      CT with contrast.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,402
    • Most Online (within 30 mins)
      7,748

    alanhlam
    Newest Member
    alanhlam
    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

    • 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.
    • JoJo0611
      I didn’t know there were different types of CT. I’m not sure which I had. It just said CT scan with contrast. 
    • Scott Adams
×
×
  • 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.