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Rash On Baby's Back?
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Started by nu_to_no_glu,

3 posts in this topic

Posted

My son has not been diagnosed with celiac, but I am working on getting us both diagnosed. He is 20 months old (I guess he's considered a toddler, but he's still my baby) :)

Anyway, he usually has a horrible rash on his toosh and up the back from his toosh that we are used to seeing that I suspect is related to gluten and diarrhea. But, after I gave him a bath tonight I noticed a rash accross the back of his shoulders and neck and a few specs on his tummy. It's not as bad as his butt rash, but I wanted to hear if any mom's with kids had rashy type problems before their kids went gluten free? It looks a lot like a general skin rash, nothing near DH, etc. Can you share with me? I think it'll help when we go to the pediatrician. Also, any other symptoms I might not relate that you noticed in your child besides the failure to thrive, typical symptoms? Thanks so much! Sure wish he could talk to me and tell me how he's feeling!

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Posted

My twin girls who are 9 would always, for at least 2 years, want me to scratch their back constantly. On the top of their backs and down almost half they would have this rash. It was more 'invasive" looking that a typical heat rash and would really itch them. We tried things like changing shampoos, changing soaps, new laundry products but nothing would help. I would put hydrocortisone cream on the rash to help with the itching but that didn't help much. I would have to cut out all the tags on their clothes.

Guess what? They have been gluten free for almost 10 weeks and no more itchy back rash!! It just had to be related to gluten. Their skin is smooth and clear now.

But they still want mom to scratch their backs! :):)

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My little guy had it on the back of his neck and shoulders, down to the middle of his back. He was constantly itching also. We have been gluten free for 5 weeks and his rash is almost completely gone and he doesn't itch it anymore!

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Go To Topic Listing Celiac Disease - Parents of Kids or Babies With Celiac Disease

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    • GFinDC
      Potential Celiac Diagnosis?

      By GFinDC · Posted

      Hi Kasia2016, Yes, celiac disease symptoms can vary widely.  Some people have no symptoms, we call that silent celiac.  Other have difficulty walking (gluten ataxia), skin rashes (dermatitis herpetiformis), and thyroid disease (Hashimoto's thyroiditis).  The list goes on and on.  GI symptoms can vary widely too, from mild symptoms at times to severe symptoms.
    • GFinDC
      Overwhelmed and unable to accept

      By GFinDC · Posted

      Hi egs1707, Welcome to the forum! Irene is right, you should not be gluten-free until all testing is completed.  The celiac disease tests are checking for immune system reactions and damage, and when you go gluten-free that starts to decline.  So the tests may not show the true immune reaction that is going on or the normal damage.  They may not show any damage in fact and you could get a false negative diagnosis.  You body starts healing and out the window go the test results.  Your doctor gets an "F" grade if they told you to go gluten-free now. But you aren't alone in having a doctor who doesn't understand the celiac disease testing process.  Many of them are woefully ignorant of proper testing for celiac disease.  That why the current estimate is somewhere in the range of 85% of celiacs in the USA are undiagnosed.  It doesn't help when doctors screw up the testing themselves.  Or refuse to test people.  Which is also far too common. I was vegetarian for 5 years.  I am not anymore and don't recommend it.  It is hard enough living gluten-free and finding safe food to eat and adequate nutrition for healing a damaged body.  I used to eat a lot of soy products when I Was vegetarian, but now soy makes me physically sick.  We can sometimes develop reactions to foods we eat a lot of while our guts are inflamed IMHO.  Soy is not a healthy food anyway from my reading. I can't do dairy now but may people who start out lactose intolerant end up being able to eat dairy after they have recovered. The best advice I can give is to avoid as much processed food as you can, and eat mostly whole foods you cook yourself at home.  When you do cook, cook big, and freeze the leftovers.  That way you can quickly take a small portion of food out of the freezer and reheat it.  Being celiac it is more important to learn how to cook.  Unless you are wealthy all those gluten-free processed foods add up quick.  Plus gluten-free processed foods often are lacking in fiber and vitamins. You'll want to watch out for vitamin deficiencies also.  Since celiac disease damages the villi in the small intestine, the vitamins and minerals etc are not digested and absorbed well.  So celiacs can be low on vitamin D, calcium,  and one other one I forget.  Vitamin B-12 may be low also ( it is important for nerve health).  Then there are some vitamins that vegetarians tend to have problems getting enough of also to consider. Adjusting to living with celiac disease means adjusting to a new diet and some lifestyle changes.  There's lots of us that make that change every year though, it's not impossible.  You will most likely end up eating better, more nutritious food than many of your peers.  And you will avoid a pletora of additional health concerns that can come along with untreated celiac disease. Learning to cook can be an adventure and you may enjoy it once you start.  you may find your taste in foods changes once you have been gluten-free for a while too. Recovery from celiac disease can take some months.  The immune system is very serious about protecting us and doesn't give up quickly.  Also it always remembers so it will react to even small amounts of gluten.  I live with gluten eaters at home and I do fine.  I just am careful about rinsing dishes off and so forth before using them. There is a Newbie 101 thread at the top of the coping with forum subsection.  It may provide some helpful info.  
    • GFinDC
      Hope for Super Sensitive?

      By GFinDC · Posted

      That's great to hear you are feeling better Nightsky.  I really think when our GI systems are in distress already that it doesn't take much to set off symptoms.  Once I eliminated the other foods that cause me symptoms that helped a lot too.  And added some extra vitamin D to my diet and selenium. Many of us have developed reactions to other foods besides gluten and need to avoid them to keep symptoms at bay.  For me nightshades, carrots, soy, dairy, and celery all cause symptoms.  It took me awhile to figure out all those food culprits, but it made a big difference getting them out of my diet. But we are all individuals, and our bodies react individually.  So you may or may not have additional food intolerances develop. Celiac is one of those life journey things and we learn as we go.  Just keep the bottle of aspirin handy!
    • admin
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    • squirmingitch
      Worcestershire Sauce - Are There Any Gluten-Free Brands?

      By squirmingitch · Posted

      I know that Lea & Perrins Worcestershire Sauce  in the US is gluten free, I also know that in Canada it is NOT. This is a very reliable site: http://www.glutenfreedietitian.com/vinegar/ But it is in the US. I'm agast that the Irish Celiac Society says malt vinegar is gluten free.  I wouldn't use it. No sense taking any chance at all.

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