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.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,855
    • Most Online (within 30 mins)
      7,748

    Tara M
    Newest Member
    Tara M
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
    • Francis M
      Thanks. Since the back and forth and promises of review and general stalling went on for more than six months, the credit company will no longer investigate. They have a cutoff of maybe six months.
×
×
  • 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.