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

Glutened By Colgate Wisps?


aquaholical

Recommended Posts

aquaholical Apprentice

So I've been attempting to do an elimination diet for over a month but I've had a couple of setbacks with glutenings. Quinoa got me the first time and it lasted about a week, which has been typical glutening duration for me. But right after I started feeling decent from that I slipped and used a Colgate Wisp (little disposable toothbrushes) and it got me BAD. Has anyone else been glutened by them? (I know it couldn't have been anything else I had that day because of the elim diet-only eating sweet potatoes and veggies, basically.) This is day 12 of the glutening and my tummy is not letting up one bit. :/


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



Celiac.com Sponsor (A8-M):



Adalaide Mentor

Glutenfreeda mentioned at one point that these were gluten free. Not that I am saying every gluten free blogger in the universe is always 100% right but so far in my personal experience with this one I haven't been led astray. The celiacsociety website also lists Colgate as 100% gluten free, meaning all of their products. Since a quick call could clear this up, I'd recommend a call to the company. (800-468-6502)

aquaholical Apprentice

yeah, I was originally assuming it couldn't have been the wisp because I know Colgate toothpaste is gluten free. But that's the only thing out of the ordinary I had that day/week. That same day (thanks, food diary) I did make a mock pesto out of pine nuts and basil, so I'm definitely going home and double checking those pine nuts. Aside from that I suppose it could still be a continuation of the AWFUL glutening I got with quinoa on July 8. (?) I've just been assuming it was a whole new glutening because it's been so long and I had a couple days of very minimal symptoms.

I know everyone's different, but is there sometimes an ebb and flow like that when you've been glutened? All the times I have been before I feel like total crud for 4-5 days, then it lightens up for a couple days and finally passes. If it's a really bad glutening could it be spread out over a month with symptoms fluctuating between better and worse? Or do you think it's more likely that I'm unknowingly continually ingesting something contaminated? (looking through my food diary I think the pine nuts are about the only thing that could be, though.)

Howlin-Radio Newbie

Are you eating dairy? Proteins are cross-reactive. In addition, lactose intolerance in a common symptom if your villi are destroyed.

aquaholical Apprentice

no dairy, no soy--react to both.

aquaholical Apprentice

Okay, yall. Finally had a chance to call Colgate. They said the Wisps do not contain soy but they can not verify that their ingredients do not come in contact with gluten. They were incredibly friendly and sent me a bunch of full price coupons for toothpaste. :)

AND the pine nuts I used in dinner that night (Fischer) are also apparently manufactured in a facility that also processes wheat. BOO. The woman I spoke to here assured me that the machines were washed thoroughly before and after use but I explained that I am unfortunately one of those uber sensitive celiacs and that it doesn't really matter how well anything is washed. I can't even eat out at restaurants, AT ALL without getting sick.

So sounds like I could have been double-hit, mystery kinda solved.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,543
    • Most Online (within 30 mins)
      7,748

    yfuvhg
    Newest Member
    yfuvhg
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.