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

Tattoos & Sun Screen

L.A.

By L.A.
in Coping with Celiac Disease

Recommended Posts

L.A. Contributor
L.A.
Posted

Hi: I have a new tattoo and need to keep it protected with sun screen--anyone know which brands are gluten free? Thanks, L.A.

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

Celiac.com Sponsor (A8-M):


Guest jokamo
Guest jokamo
Posted

L.A.,

I have no idea but I would also like to know.

Jokamo

aaascr Apprentice
aaascr
Posted

I know there are some mainstream products that are okay -

but I use badger sunscreen due to all of my other allergies:

Open Original Shared Link. It was okay on my tattoo as well.

JennyC Enthusiast
JennyC
Posted

Coppertone and Banana Boat SUNBLOCKS are gluten free. The tanning lotions may have gluten. I called Banana Boat yesterday and Coppertone was on the Clan Thompson software.

Hope this helps.

L.A. Contributor
L.A.
Posted
  • Author
Coppertone and Banana Boat SUNBLOCKS are gluten free. The tanning lotions may have gluten. I called Banana Boat yesterday and Coppertone was on the Clan Thompson software.

Hope this helps.

My "dragonfly" thanks all of you. We should start a new thread about tattoos and what people have--not really a gluten-free topic but may be interesting. Regards, L.A.

kbtoyssni Contributor
kbtoyssni
Posted

I use Target-brand sunscreen.

Guest jokamo
Guest jokamo
Posted

What about NO-AD sunscreen. It comes in a larger bottle for a decent price, because of my lupus, I use alot!

jokamo

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

Celiac.com Sponsor (A8-M):


Guest j_mommy
Guest j_mommy
Posted

L>A......I have four and working on getting a 5th.

I have: Flowers under my Right ankle, four leaf clovers on the side of my left leg, Kokkepelli on my Right shoulder and the breast cancer pink ribbon above my Right bum!LOL

L.A. Contributor
L.A.
Posted
  • Author
L>A......I have four and working on getting a 5th.

I have: Flowers under my Right ankle, four leaf clovers on the side of my left leg, Kokkepelli on my Right shoulder and the breast cancer pink ribbon above my Right bum!LOL

:P I have 4 and I'm getting my fifth on Thursday--poor hubby just shakes his head :lol: I have a dragonfly on my right upper chest, an elfish script on my wrist, mine and my daughter's astrological signs on my left leg and a sun behind a cloud on my right side knee. Thursday's tattoo is the symbol for love, life & loyalty. My daughters are getting the same thing. L.A.

kerrih Rookie
kerrih
Posted
Hi: I have a new tattoo and need to keep it protected with sun screen--anyone know which brands are gluten free? Thanks, L.A.
kerrih Rookie
kerrih
Posted

I have been in contact with an expert on Celiac from the University of Utah and he states that if you are not ingesting the product, then you need not worry about it being gluten free. I have been trying to research lipstick because I still have symptoms occasionally and am trying to find the exposure.

Guhlia Rising Star
Guhlia
Posted
I have been in contact with an expert on Celiac from the University of Utah and he states that if you are not ingesting the product, then you need not worry about it being gluten free. I have been trying to research lipstick because I still have symptoms occasionally and am trying to find the exposure.

It is virtually impossible to not touch your mouth after rubbing your arm (sunscreen or lotion), scratching your face (makeup), washing your hair (shampoo), touching your hair (shampoo, styling products). This means that you are likely ingesting small amounts of gluten if your body products have gluten in them. Even if you don't get any symptoms, it doesn't mean that you're not damaging your insides. Is it really worth the risk?

Jo.R Contributor
Jo.R
Posted
My "dragonfly" thanks all of you. We should start a new thread about tattoos and what people have--not really a gluten-free topic but may be interesting. Regards, L.A.

It would be fun to have our tattoos as our avatar.

jerseygrl Explorer
jerseygrl
Posted

Since you all are talking about sunscreen... I have a question too.

My 6yo DD has Celiac. No skin outbreaks, no abdominal pain when glutened, mostly neurological issues

Do we need to be selective with sunscreen, shampoos, lotions, etc, when skin reactions have not been an issue?

Guhlia Rising Star
Guhlia
Posted

Yes, you really need to be careful about things applied to the skin... Read my post below.

It is virtually impossible to not touch your mouth after rubbing your arm (sunscreen or lotion), scratching your face (makeup), washing your hair (shampoo), touching your hair (shampoo, styling products). This means that you are likely ingesting small amounts of gluten if your body products have gluten in them. Even if you don't get any symptoms, it doesn't mean that you're not damaging your insides. Is it really worth the risk?
debmidge Rising Star
debmidge
Posted

another point as to why it's best to use gluten-free lotion:

most people apply lotion with their hands....when you are at beach or pool you don't apply it and then rinse your hands off. You want the lotion on your hands to prevent burn/sun damage. Children will often put hands in mouth, and people will then grab something to eat. It'll get transfered into mouth unless you deliberately rinse or wash it off.

L.A. Contributor
L.A.
Posted
  • Author

I make sure everything is gluten-free...shampoo, lipsticks, sun screen, soap, body lotions and even my household cleaning supplies. If I touch it, there's a chance it could end up in my mouth--especially soap and shampoo. L.A.

little d Enthusiast
little d
Posted

Because of my Keratosis Poilaris I can't use a lot of lotions and sunscreen's it gets worse, but I can use banana boat sunscreen with no problem.

Donna

Archived

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

Go to topic listing
  • Celiac.com Sponsor (A19):


  • Member Statistics

    • Total Members
      128,311
    • Most Online (within 30 mins)
      7,748
    SWilson
    Newest Member
    SWilson
    Joined
  • Celiac.com Sponsor (A20):

  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.8k
  • Celiac.com Sponsor (A22):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • trents
      SkinSafe

      By trents · Posted

      Welcome to the forum, Linda! Many on this forum can sympathize with you. It can be extremely difficult to get reliable information about gluten when it comes to meds, supplements and oral hygiene products. This is especially true since so much of this stuff is generic and comes from over seas. I will deflect with regard to your question about meds and oral products but take you in another direction. Have you tried a low iodine diet. Iodine is known to exacerbate dermatitis herpetiformis and some find that a low iodine diet helps reduce the number of outbreaks. By the way, have you had your celiac antibodies retested recently? If they are elevated that might be a clue that you are getting gluten in your oral hygiene products or meds.
    • Itsabit
      SkinSafe

      By Itsabit · Posted

      Hi. I’m 70 years old, and a 22 year survivor of head and neck cancer treated with chemo-radiation, which resulted in non-existent submandibular salivary glands and extreme dry mouth and altered oral mucosa. I have been using dry mouth toothpaste, Rx oral dentrifices and moisturizers for years.  I’ve recently been diagnosed with severe celiac dermatitis herpetiformis. I was being treated with oral Dapsone, but it was not effective and I developed some serious side effects. So, the medication was stopped and I was started on Doxycycline (another antibiotic) for inflammation. I’ve been using Rx Betamethasone steroid ointment with little to no effect. I have tried every oral and topical antihistamine treatment available OTC. None have touched this horrible relentless itching. That is my history.  Now to my question. Does anybody know about gluten free toothpastes and mouth moisturizers? I ask because a very common dry mouth brand stated to me that they were indeed gluten free. But as I am not getting any better with my dermatitis herpetiformis, I was wondering if I was getting glutenized some way other than diet as  I have been following a strict clean gluten free diet, but I am not seeing any improvement at all. So, I started looking up the toothpastes and moisturizer ingredients individually and nine (9) of the eleven (11) or so listed showed up as   containing gluten or that may have gluten! Am I getting glutenized orally by these products?  As an aside, I checked on my favorite lavender scented baby lotion which is supposed to be gluten free, but many of those ingredients when investigated separately, show they  do contain or may contain gluten as well. I stopped using the lotion. But I cannot forgo my dental care. I was unable to get any information from the manufacturer of my current brand of chewable multivitamins either. They told me to check with my doctor. If THEY don’t know what’s in their product, how do they think a PCP will?  In light of all this, I am confused and angry that I might keep getting contaminated with gluten through products I am using that are supposedly gluten safe. *I should also state that I have a nickel allergy since I was about 12-13 years old. And I developed a contact allergy to latex (gloves) when I was a student nurse at 19 years old.  I know and I’m sorry that this is so lengthy. I’m trying to do everything I can to combat this condition, and I’m feeling very confused, anxious and angry about not getting adequate information as I try to educate and advocate for myself. I’m hoping someone here is more knowledgeable than me of how to navigate through all of this. Can anyone offer any advice?  Thank you for your time.  Respectfully,  Linda
    • trents
      I’m terrified it’s too late for me😭

      By trents · Posted

      Welcome to the forum, @Cathijean90! I went 13 years from the first laboratory evidence of celiac disease onset before I was diagnosed. But there were symptoms of celiac disease many years before that like a lot of gas. The first laboratory evidence was a rejected Red Cross blood donation because of elevated liver enzymes. They assume you have hepatitis if your liver enzymes are elevated. But I was checked for all varieties of hepatitis and that wasn't it. Liver enzymes continued to slowly creep up for another 13 years and my PCP tested me for a lot of stuff and it was all negative. He ran out of ideas. By that time, iron stores were dropping as was albumin and total protein. Finally, I took it upon myself to schedule an appointment with a GI doc and the first thing he did was test me for celiac disease. I was positive of course. After three months of gluten free eating the liver enzymes were back in normal range. That was back in about 1992. Your story and mine are more typical than not. I think the average time to diagnosis from the onset of symptoms and initial investigation into causes for symptom is about 10 years. Things are improving as there is more general awareness in the medical community about celiac disease than there used to be years ago. The risk of small bowel lymphoma in the celiac population is 4x that of the general population. That's the bad news is.  The good news is, it's still pretty rare as a whole. Yes, absolutely! You can expect substantial healing even after all these years if you begin to observe a strict gluten free diet. Take heart! But I have one question. What exactly did the paperwork from 15 years ago say about your having celiac disease? Was it a test result? Was it an official diagnosis? Can you share the specifics please? If you have any celiac blood antibody test results could you post them, along with the reference ranges for each test? Did you have an endoscopy/biopsy to confirm the blood test results?
    • Cathijean90
      I’m terrified it’s too late for me😭

      By Cathijean90 · Posted

      I’ve just learned that I had been diagnosed with celiac and didn’t even know. I found it on paperwork from 15 years ago. No idea how this was missed by every doctor I’ve seen after the fact. I’m sitting here in tears because I have really awful symptoms that have been pushed off for years onto other medical conditions. My teeth are now ruined from vomiting, I have horrible rashes on my hands, I’ve lost a lot of weight, I’m always in pain, I haven’t had a period in about 8-9 months. I’m so scared. I have children and I saw it can cause cancer, infertility, heart and liver problems😭 I’ve been in my room crying for the last 20minutes praying. This going untreated for so long has me feeling like I’m ruined and it’s going to take me away from my babies. I found this site googling and I don’t know really what has me posting this besides wanting to hear from others that went a long time with symptoms but still didn’t know to quit gluten. I’m quitting today, I won’t touch gluten ever again and I’m making an appointment somewhere to get checked for everything that could be damaged. Is this an automatic sentence for cancer and heart/liver damage after all these symptoms and years? Is there still a good chance that quitting gluten and being proactive from here on out that I’ll be okay? That I could still heal myself and possibly have more children? Has anyone had it left untreated for this amount of time and not had cancer, heart, fertility issues or liver problems that couldn’t be fixed? I’m sure I sound insane but my anxiety is through the roof. I don’t wanna die 😭 I don’t want something taking me from my babies. I’d gladly take anyone’s advice or hear your story of how long you had it before being diagnosed and if you’re still okay? 
    • trents
      diagnostic testing variance

      By trents · Posted

      Genetic testing cannot be used to diagnose celiac disease but it can be used to rule it out and also to establish the potential to develop celiac disease. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% actually develop it. To develop celiac disease when you have the genetic potential also requires some kind of trigger to turn the latent genes "on", as it were. The trigger can be a lot of things and is the big mystery component of the celiac disease puzzle at this point in time with regard to the state of our knowledge.  Your IGA serum score would seem to indicate you are not IGA deficient and your tTG-IGA score looks to be in the normal range but in the future please include the reference ranges for negative vs. positive because different labs used different reference ranges. There is no industry standard.
×
×
  • Create New...