Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Temporary Tattoos


123glldd

Recommended Posts

123glldd Collaborator

So I have this small book of temporary fairy tattoos. It lists ingredients in the back of the book:

PVA (polyvinyl acetate) CoPlymer, POlyester resin, modified varnish, deoderized petroleum, silicon dioxide, aluminum silicate, iron oxide, FD&C yellow #5 & 6 Aluminum Lake, D&C Red #7 Lake, FD&C Blue #1 Aluminum Lake. ALL COLORS FOLLOW FDA COSMETIC REGULATIONS.

Additional ingredients: Gllutter tattoos may contain cosmetic polyester glutter, glow in the dark tattoos have luminescent zinc sulfide.

Are any of these ingredients a worry?


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Sounds delicious! :blink: We're you going to eat them? Or put them on your lips or fingertips? I wouldn't worry about them.

123glldd Collaborator

hahaha no no not eating them but in case i touch it or my husband touches it at some point and our fingers touch our mouths we just assume make sure heh

psawyer Proficient

No possible gluten source that I can see there. :)

123glldd Collaborator

*Happy dance* I love my fairies! haha

bartfull Rising Star

One of my banjo students gave me some frogs last night. I'm going to wait until Saturday and make the first eight people who show up for the jam session wear them. And if I'm in a particularly "evil" mood, I'm going to tell them that they have to play every song this day in the key of F.

I always joke with my regulars that it is my shop, so they have to "obey" me. :lol: Life is fun when you're feeling good!

  • 7 years later...
tim frances Newbie
On 6/4/2012 at 7:02 PM, kareng said:

Sounds delicious! :blink: We're you going to eat them? Or put them on your lips or fingertips? I wouldn't worry about them.

That's a terribly annoying response as skin is a large and porous organ which means a product with fake dyes and gluten can absorb directly into the blood stream. I wouldn't make a sarcastic judgement call on something you don't seem to know much about and I wouldn't use anything processed on your body if you have a serious gluten allergy. 


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Wow!  I was a smart ass 7 years ago!  And look how young I looked!  ?

 

skin is porous to a point- obviously not everything can pass thru all the layers of the skin.  And gluten proteins are too large for that.  People with Celiac are not a “ gluten allergy”.  I know many people use that term, but it’s not exactly true.  

cyclinglady Grand Master

What Karen said is true!  

Here are the facts based on medical research and not FAKE news:

https://www.mayoclinic.org/diseases-conditions/celiac-disease/expert-answers/celiac-disease/faq-20057879

By the way, the Mayo clinic is one of the leading celiac research centers. 

Here is more:

https://www.beyondceliac.org/celiac-disease/myths/

If you are reacting to wheat on skin, you may have a wheat allergy (IgE response) instead of celiac disease where gluten (wheat, rye or barley proteins) must be swallowed in order to get an autoimmune reaction (body attacks small intestine).  

kareng Grand Master
9 hours ago, cyclinglady said:

What Karen said is true!  

Here are the facts based on medical research and not FAKE news:

https://www.mayoclinic.org/diseases-conditions/celiac-disease/expert-answers/celiac-disease/faq-20057879

By the way, the Mayo clinic is one of the leading celiac research centers. 

Here is more:

https://www.beyondceliac.org/celiac-disease/myths/

If you are reacting to wheat on skin, you may have a wheat allergy (IgE response) instead of celiac disease where gluten (wheat, rye or barley proteins) must be swallowed in order to get an autoimmune reaction (body attacks small intestine).  

I was basing my comments on that section on skin in A&P class and that biology class- I can’t remember the exact name of -on body systems & the one about body chemistry.  Just some random college classes.   And some stuff some Celiac researchers told me.  ?

but Mayo is good too!  ?

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      126,072
    • Most Online (within 30 mins)
      7,748

    Steph4213
    Newest Member
    Steph4213
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.2k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Wheatwacked
      Hello @MHavoc, thank you for your question and welcome to the clinic. First, has the contstipation abated with the GFD? If your are pursuing further diagnostics you must continue to eat gluten. Each lab has their own reference range for their test, but they indicate an H for high.  Typically anything above 11 is considered positive. Mild chronic inflammation (gastritis) can interfere with intrinsic factor for B12 leading to low B12 causing low MCHC (anemia). So what is causing your gastritis?  A high tTG IgA level generally indicates potential gastrointestinal problems most commonly associated with celiac disease.  Although the biopsy is the Gold Standard for diagnosis, not finding damage in the biopsy does not rule out Celiac Disease. It means they did not find damage where they looked.  The small intestine is over 20 feet long. Many here have been blood positive and biopsy negative, it just delays the diagnosis until you have enough damage to find and fit their diagnostic profile. The Ttg-iga is not only sensitive (90%) but highly specific (98%) and won’t show positive until the damage is severe.  It is estimated that 40% of first degree relatives of diagnosed Celiacs have undiagnosed Celiac Disease, so your sister is a big risk factor in whether you have it. Are You Confused About Your Celiac Disease Lab Results?  This article explains it better and is quite readable. Celiac Disease can cause deficient vitamin D.  Low vitamin D compromises the immune system.  Any other symptoms? liver enzymes?  Recent cold or flue? Celiac Disease and the malabsorption it causes through vitamin and mineral deficiencies can elicit symptoms not usually associated with Celiac Disease. Case in point maybe your gastritis and anemia.  
    • MHavoc
      As with most of the people that come here, I have questions and need perspective/info from this wonderful community.  Some background, started having severe constipation that would not abate even with softners (not really fun to talk about), so I was able to finally get in to see my primary and she scheduled some blood work.  One of things she wanted to test for is Celiac Disease due to my sister having celiac disease since a young child. Here are my test results: MCHC = 31.4 so considered slightly low TISSUE TRANSGLUTAMINASE AB, IGA = 78.8 H So with that result, I was scheduled for an endoscope for confirmation of celiac disease, but I am very confused with the results: Diagnosis 1. Duodenum, biopsy: -No pathologic alteration. 2. Stomach, biopsy: -Mild chronic inflammation with reactive epithelial change -H. pylori not identified on immunostained section. -No intestinal metaplasia or dysplasia I am now scheduled to meet with a GI Specialist from the Celiac team, but that won't be until after the New Year.  I would appreciate thoughts about the biopsy report to understand whether it confirms the celiac disease as was indicated by the blood test results. I have been gluten free for two weeks and it is a very difficult adjustment for me as an older 50+ person.
    • Vozzyv
      Anyone else have intermittent left ear ringing and outer right ear pain? Both seem to happen in the evenings. 
    • cristiana
      If your son eventually becomes very symptomatic, that in itself will help keep him on the diet.  I had a friend who was diagnosed roughly the same time as me and she used to tell me a lot that she could get away with eating certain gluten containing foods.  (Not a good thing to do, but she did all the same).  In time she was unable to tolerate them anymore,  and is now very strict with her diet.   The football situation with the candy:   here in the UK at least, a lot of mainstream chocolate bars and sweets don't actually contain gluten (Bounty Bar, Snickers, Cadbury's Whirl, Crunchie etc) and you may find that that is the case where you live.      
    • jjiillee
      Her appointment ended up getting canceled for today. So now we have to wait until Dec 3.
×
×
  • Create New...