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

How vigilent do we need to be?


MelissaNZ

Recommended Posts

MelissaNZ Apprentice

My daughter has just been diagnosed and her symptoms are relatively minor, in that she doesn’t get major stomach pains etc (just sometimes feels a bit yucky and the odd throw up once very few months), but her main symptoms are she can get constipated and also has low weight and height gain.

 

So how vigilent do we have to be?  Like I know we have to remove gluten from her diet, but do we have to be super careful about cross contamination? Worry about things like gluten in hair products, cooking with different pans etc?  Will tiny amounts cause her on-going damage? It’s difficult because it’s not like she is suddenly ill or has symptoms  when she has some, so we don’t know what’s really going to affect her or how careful we have to be about cross contamination, as her symptoms are something we can't physically see (besides her being tiny).  Is everyone different and some can tolerate tiny amounts? – or does everyone who has Celiacs have to be extremely careful about every little speck of gluten they come across?

 

What about things like a bag of chips that says they just contain potatoes and oil – are they okay?  Or does it specifically have to say gluten-free?

 

Thanks


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



Celiac.com Sponsor (A8-M):



RMJ Mentor

How was she diagnosed?  If she had antibody tests, you can repeat those in 6-12 months to see if they return to normal levels.  If not, you should be more careful.

I had few if any symptoms, but discovered through antibody testing that I am very sensitive to teeny tiny levels of gluten.  One of my antibody levels (Dgp IgA) is still a bit above the normal range.  I find out next week if my villi are damaged (doc decided to do an endoscopy since I was due for my every ten year colonoscopy).  Visual examination said some villi are blunted, just waiting for biopsy results.

MelissaNZ Apprentice

She had blood tests and are waiting on a biopsy.  These were her test results - so I'm guessing they are anti-body tests?:

 

Gliadin peptide - 17.2

tTG IgA AB - 15.4

 IGA - 0.7

Endomysial antidoies - positive.

RMJ Mentor

Yes, those are antibody tests.  The gliadin, tTg and endomysial should be repeated after she has been gluten free for a while (but DON'T go gluten free until the endoscopy/biopsy has been done).   The IgA is a control test.  Different laboratories use different ranges so to compare, the repeat tests should be done by the same lab as the original ones.  And you'll need to find out the reference ranges so you'll know when she is in the normal range.

pschwab Enthusiast

My two year old was just diagnosed a little over three months ago. We have chosen to be extremely careful and overly cautious until we can go in for his follow up and see how much better he has gotten. There are so many different symptoms and some people don't outwardly show much. But that doesn't mean their body isn't being harmed immensely on the inside. In my opinion kids should be the most cautious because their bodies are growing and developing. But we are very new to this, and I am very far from being an expert. I would check with your gi dr. Good luck. I'm sure you will do great since you sound like a concerned parent. :)

squirmingitch Veteran

You need to be worried about cross contamination. Read our Newbie 101 pinned to the top of the Coping Section. It will tell you what you need to change.

Ockero girl Newbie

Hi

my daughter was diagnosed 1.5 years ago at 3.5 years old. She also hadn't grown properly (still looked 18 months old) and hadn't put on any weight for a year. She also had ADHD like symptoms and occasional diarrhea (although I think this was lactose!). 

I was ultra cautious initially, but rewarded when my daughter put on 3kg and grew 5cm in a month. Now she has grown 16cm in 12 months and is in the normal range for both height and weight growth charts. Our whole house is now gluten free and I replaced all chopping boards, non stick pans and anything with cut marks in them such as plastic bowls.

You don't have to buy only products with the specific gluten free labels on. I also buy products that don't label any gluten containing ingredients and don't have the warning statement of may contain gluten (but I live in Europe so the labeling might be different). Also gluten free food is full of sugar and tastes awful IMHO! I make a lot of our snacks and cakes and they don't taste much different to gluten stuff.

I also make sure her toothpaste is gluten free as she sometimes swallows some! I was told sodium laurel sulphate is wheat - can someone confirm this? I don't worry about anything else.

I think my daughter has occasionally had some cross contamination when out, but hasn't reacted to it other than a mild stomach ache. this is something you will find out later specific to your own daughter as some people can be very ill for a long time.

Good luck - you will work it all out. 

 


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



Celiac.com Sponsor (A8-M):



kareng Grand Master
4 hours ago, Ockero girl said:

Hi

my daughter was diagnosed 1.5 years ago at 3.5 years old. She also hadn't grown properly (still looked 18 months old) and hadn't put on any weight for a year. She also had ADHD like symptoms and occasional diarrhea (although I think this was lactose!). 

I was ultra cautious initially, but rewarded when my daughter put on 3kg and grew 5cm in a month. Now she has grown 16cm in 12 months and is in the normal range for both height and weight growth charts. Our whole house is now gluten free and I replaced all chopping boards, non stick pans and anything with cut marks in them such as plastic bowls.

You don't have to buy only products with the specific gluten free labels on. I also buy products that don't label any gluten containing ingredients and don't have the warning statement of may contain gluten (but I live in Europe so the labeling might be different). Also gluten free food is full of sugar and tastes awful IMHO! I make a lot of our snacks and cakes and they don't taste much different to gluten stuff.

I also make sure her toothpaste is gluten free as she sometimes swallows some! I was told sodium laurel sulphate is wheat - can someone confirm this? I don't worry about anything else.

I think my daughter has occasionally had some cross contamination when out, but hasn't reacted to it other than a mild stomach ache. this is something you will find out later specific to your own daughter as some people can be very ill for a long time.

Good luck - you will work it all out. 

 

I don't think sodium laurel sulphite is ever even made from wheat.  But even if it were, it seems to be one of those chemicals that has none of the proteins left.

But, whether you believe me or not.... I have never seen it listed on any reputable celiac group sites as something to avoid for gluten.

 

Beverage Proficient

Yes you need to read Newbie 101. Yes you need to be super vigilent. Yes even a spec the size of your smallest freckle can cause a problem for her. Even if it does not trigger noticeable symptoms, it does not mean it's not triggering an attack on her intestines!!! 

Yes, donate all non-stick and cast iron cookware and muffin pans and glazed on baking pans to someone else, get rid of wooden spoons, get a new toaster, waffle maker, etc.  Get rid of old cutting boards, wood and plastic.  Get new sponges! Anything previously used to cook something with gluten can hold onto it. Seriously clean all regular pans and utensils you are going to keep, scrub scrub srub. Clean out the fridge, cabinets, and drawers for any crumbs or flour left behind.

I chose to replace all face and hair and body products with gluten free. Started with the obvious of lipstick (I now use Red Apple brand), face, and hair (washes over your face when you rinse), then replaced body lotions after I used the old ones up (too easy to scratch your leg or arm and oops....)

I sincerely and strongly recommend that the whole household be gluten free within the house. No way was I going to cook one pot of something for him and one for me...too easy to use one spoon to stir the wrong thing...added clean up and what was the point anyway...gluten free is better for everyone anyway (read the book The Grain Brain). 

Until my partner was also diagnosed with Celiac's, we tried all meals at home being gluten free except for bread or cracker items for him. But that was kinda stressful on me.  Can I safely use the sponge to wipe up that crumb and then what do I do with the now  contaminated sponge?  I read to have 2 sponges...but what about the crumb that I didn't see that I wiped up with my so-called gluten free sponge?  What if a spec gets on the table mats...so I can't even put my fork on a table mat in case it has a crumb? Too crazy and you just never relax. What if he dipped into the jam and then put it on his toast and then re-dipped??? (caught him doing that even though he was trying to be very very careful...things like that are just too much of a habit). What if he ate that bread and then kissed me??? Ahhhhhhhh! Too much!

As soon as he was diagnosed and we tossed the remaining gluten items, it was a huge sense of relief. So yes, you can manage keeping your daughter's food gluten free through lots of care, but really, it is the mental side of it that was important to me.  So set yourself up for SUCCESS, not failure and paranoia. HOME SHOULD BE A SAFE ZONE!!!

Also...we have pets, so if they are prone to licking you, you might want to consider that. There are lots of grain free pet foods available now...grain isn't so great for a lot of them either.

My latest phase has been to replace all my herbs & spices (they were old anyway). I read that although they are naturally gluten free, outside testing has shown that they can contain some high amounts, possibly from cross contamination in processing or in where they are grown.  Spicely is a good brand that is gluten-free, but I couldn't find it around where I live. I found Morton & Bassett now labels theirs gluten-free, and I can find it at Fred Meyer's (grocery chain in the northwest), or mail order it from their web site. They have specials regularly, just sign up for their newsletter.

I'm sure there will be those who totally disagree with me, but I have been so much happier, much more mentally positive, and this is so much easier to deal with since my home is now totally gluten-free.  A big weight was lifted just by having my safe world at home.  Good luck!

 

 

notme Experienced

just a note:  gluten cannot enter your skin even if you cut yourself, so if you're not eating/drinking/getting it into your mouth, you're good.   it's a skin vs molecule thing.    

Beverage Proficient

Right, but if it's on your skin or your hair and you touch that and then touch something that goes into your mouth or put your hands in your mouth, then you can get glutened. That's why I used up my body lotion, but was really careful about washing hands if I touched my skin ... it was a pain to do and it's much nicer now that all my body products are free of that stinkin' gluten.  And my doctor said to be careful of all products that get into eyes, nose, ears, and of course mouth ... all those parts drain down the throat to the stomach.

 

notme Experienced

o, i see what you mean.  one of the hardest things i had to learn was to stop licking my fingers lolz 

Archived

This topic is now archived and is closed to further replies.

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

    • Total Members
      133,050
    • Most Online (within 30 mins)
      7,748

    Rima
    Newest Member
    Rima
    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

    • tiffanygosci
      Hi Cristiana! It's so nice to meet you! Thank you for the kind reply I am glad I live in a time where you can connect with others through the Internet. That is a mercy I am grateful for.
    • knitty kitty
      In the study linked above, the little girl switched to a gluten free diet and gained enough weight that that fat pad was replenished and surgery was not needed.   Here's the full article link... Superior Mesenteric Artery Syndrome in a 6-Year-Old Girl with Final Diagnosis of Celiac Disease https://pmc.ncbi.nlm.nih.gov/articles/PMC6476019/
    • knitty kitty
      Hello, @Jordan Carlson, So glad you're feeling better.   Tecta is a proton pump inhibitor.  PPI's also interfere with the production of the intrinsic factor needed to absorb Vitamin B12.  Increasing the amount of B12 you supplement has helped overcome the lack of intrinsic factor needed to absorb B12. Proton pump inhibitors also reduce the production of digestive juices (stomach acids).  This results in foods not being digested thoroughly.  If foods are not digested sufficiently, the vitamins and other nutrients aren't released from the food, and the body cannot absorb them.  This sets up a vicious cycle. Acid reflux and Gerd are actually symptoms of producing too little stomach acid.  Insufficient stomach acid production is seen with Thiamine and Niacin deficiencies.  PPI's like Tecta also block the transporters that pull Thiamine into cells, preventing absorption of thiamine.  Other symptoms of Thiamine deficiency are difficulty swallowing, gagging, problems with food texture, dysphagia. Other symptoms of Thiamine deficiency are symptoms of ADHD and anxiety.  Vyvanse also blocks thiamine transporters contributing further to Thiamine deficiency.  Pristiq has been shown to work better if thiamine is supplemented at the same time because thiamine is needed to make serotonin.  Doctors don't recognize anxiety and depression and adult onset ADHD as early symptoms of Thiamine deficiency. Stomach acid is needed to digest Vitamin C (ascorbic acid) in fruits and vegetables.  Ascorbic acid left undigested can cause intestinal upsets, anxiety, and heart palpitations.   Yes, a child can be born with nutritional deficiencies if the parents were deficient.  Parents who are thiamine deficient have offspring with fewer thiamine transporters on cell surfaces, making thiamine deficiency easier to develop in the children.  A person can struggle along for years with subclinical vitamin deficiencies.  Been here, done this.  Please consider supplementing with Thiamine in the form TTFD (tetrahydrofurfuryl disulfide) which helps immensely with dysphagia and neurological symptoms like anxiety, depression, and ADHD symptoms.  Benfotiamine helps with improving intestinal health.  A B Complex and NeuroMag (a magnesium supplement), and Vitamin D are needed also.
    • knitty kitty
      @pothosqueen, Welcome to the tribe! You'll want to get checked for nutritional deficiencies and start on supplementation of B vitamins, especially Thiamine Vitamin B 1.   There's some scientific evidence that the fat pad that buffers the aorta which disappears in SMA is caused by deficiency in Thiamine.   In Thiamine deficiency, the body burns its stored fat as a source of fuel.  That fat pad between the aorta and digestive system gets used as fuel, too. Ask for an Erythrocyte Transketolace Activity test to look for thiamine deficiency.  Correction of thiamine deficiency can help restore that fat pad.   Best wishes for your recovery!   Interesting Reading: Superior Mesenteric Artery Syndrome in a 6-Year-Old Girl with Final Diagnosis of Celiac Disease https://pubmed.ncbi.nlm.nih.gov/31089433/#:~:text=Affiliations,tissue and results in SMAS.  
    • trents
      Wow! You're pretty young to have a diagnosis of SMA syndrome. But youth also has its advantages when it comes to healing, without a doubt. You might be surprised to find out how your health improves and how much better you feel once you eliminate gluten from your diet. Celiac disease is an autoimmune disorder that, when gluten is consumed, triggers an attack on the villous lining of the small bowel. This is the section of the intestines where all our nutrition is absorbed. It is made up of billions of tiny finger-like projections that create a tremendous surface area for absorbing nutrients. For the person with celiac disease, unchecked gluten consumption generates inflammation that wears down these fingers and, over time, greatly reduces the nutrient absorbing efficiency of the small bowel lining. This can generate a whole host of other nutrient deficiency related medical problems. We also now know that the autoimmune reaction to gluten is not necessarily limited to the lining of the small bowel such that celiac disease can damage other body systems and organs such as the liver and the joints and cause neurological problems.  It can take around two years for the villous lining to completely heal but most people start feeling better well before then. It's also important to realize that celiac disease can cause intolerance to some other foods whose protein structures are similar to gluten. Chief among them are dairy and oats but also eggs, corn and soy. Just keep that in mind.
×
×
  • 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.