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

Health And Beauty Aids For Kids...


africanqueen99

Recommended Posts

africanqueen99 Contributor

Just wondering what you all use for your celiac kids.

 

Shampoo and conditioner

Body wash/soap

Lotion

Chapstick/Lip Goo - we are using eos and it's working ok (my oldest had "celiac lips" for years before DX and now I realize it's because our lip goo was just poisoning her over and over.  UGH!!)

 

We are going camping with the Girl Scouts soon and I'm going to need sunscreen and bug spray.

 

In the past we've always leaned toward the more natural ingredients, but I'm willing to push that aside, for now, while the girls still heal

 

Thanks.


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

We use Suave or Kirkland (Costco brand) shampoos and conditioners.  Dove soap (no body washes) and Cerave as a lotion.  Though J & J Baby lotion has a new "natural product" that lists all ingredients and their sources.  We use Eos too.  

 

Banana Boat is our favorite sunscreen.  I use the baby sunscreen for my face as it does not run into my eyes on bike rides.  

 

Haven't looked into bug spray.  We use whatever's at my parent's house and I make sure my husband and I wash our hands after applying.  No bugs where we live!  

 

We are Girl Scouts too!  Our troop does accommodate me (gluten-free) and a girl with peanut and milk allergies.  Not all troops are so careful as it depends on the leaders who are volunteers.  We have lots of fun camping!  

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,122
    • Most Online (within 30 mins)
      7,748

    jenr8er
    Newest Member
    jenr8er
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • trents
      Sorry, I think I got you mixed up with another poster.
    • rei.b
      I hadn't been eating gluten free before having the antibody test done. I started eating gluten free after having the test done because the gastro PA told me to eat gluten-free for 6 months. I'm now 3 months in.
    • trents
      I tend to agree with RMJ. Your doc took the reasonable and practical approach to diagnosis. All things considered, it was the right way to go. However, if you have first degree relatives that show signs of possible celiac disease, urge them to get formally tested before they start the gluten free diet.
    • RMJ
      It sounds like you have a very reasonable GI doctor, who diagnosed you based on family history and symptoms after eating gluten. I would consider you lucky! The other option would be to make yourself very sick by doing weeks of a gluten challenge prior to an endoscopy.
    • captaincrab55
      Hi Colleen H,   I suffered with the pins and needles/burning feeling in my legs and feet for at least  6 years until my Nephrologist figured out that I had to go on a low salt diet.  He said my kidneys weren't strong enough to remove the salt.  The simple fix was a diuretic, but that med leaves the uric acid behind, so that wasn't an option.  On the bright side the low salt diet lowered my BP over 20 points and and the pins and needles/burning feeling went away.  Good Luck and hope this helps.  
×
×
  • 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.