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

Bringing Your Own Items To Restaurants?


hiphobokenmama

Recommended Posts

hiphobokenmama Newbie

i just read somewhere that someone has to bring their own salt and butter to restaurants...salad dressing, i undertand, but what's wrong with salt and butter? this is the first i've heard of it so i'm concerned. my 3 year old was just diagnosed with celiac and we haven't eaten anywhere except McDs since then... but what's the deal?


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



Celiac.com Sponsor (A8-M):



angel-jd1 Community Regular

I know I have seen a saltine cracker in some shakers in Mom and pop type places. It helps absorb moisture. I dont' take my own salt and pepper to places. For me, those things are not that necessary.

-Jessica :rolleyes:

Guest gfinnebraska

I have brought my own butter, sour cream and salad dressing. I never thought of the salt issue... hmmm... now I will make sure I check! Living in a small town, we eat at a lot of "mom and pop" type cafe's.

lovegrov Collaborator

If a restaurant puts something in a salt shaker to absorb moisture it will probably be rice, not a cracker. Personally, I see no reason at all to carry salt or butter to a restaurant. I have yet to see a real butter that has gluten, and I don't think I've ever seen a margarine with it, either.

richard

KaitiUSA Enthusiast

Alot of places that I have been to they have little packets of salt and butter. I haven't been out to eat alot since being diagnosed though but I wouldn't find it a concern. I still check the ingredients on the mini butters though.

plantime Contributor

Every place I go uses packets to avoid contamination with anything else. The salt shakers that are used by the cooks didn't have anything else in them because they used up the salt long before moisture was able to set in. The only place that did have something with the salt had mixed in pepper.

angel-jd1 Community Regular
If a restaurant puts something in a salt shaker to absorb moisture it will probably be rice, not a cracker

I have seen crackers in shakers before.

-Jessica :rolleyes:


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



Celiac.com Sponsor (A8-M):



skbird Contributor

My mom used to always do that! And in the sugar shaker, too. Rice would have gotten through the top for the sugar.

I hadn't thought about that.

Do restaurant butter-ish things sometimes have gluten in them? I have been avoiding anything that they might dip meat in first.

Stephanie

cdford Contributor

I always avoid using the pepper out unless they have a grinder available, but I had not thought to check the salt shaker. I do take butter with me to certain restaurants if they use margarines instead of butter because I react to soy and I have yet to find a margarine without soy in it. Thus far I have not run into any problems once I show them my restaurant card (every so often I have to explain the visit to the hospital problem if I get into something...that usually gets cooperation if nothing else does).

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - trents replied to Paulaannefthimiou's topic in Gluten-Free Foods, Products, Shopping & Medications
      1

      Bob red mill gluten free oats

    2. - trents replied to jenniber's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      10

      Disaccharide deficient, confusing biopsy results, no blood test

    3. - Paulaannefthimiou posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      1

      Bob red mill gluten free oats

    4. - jenniber replied to jenniber's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      10

      Disaccharide deficient, confusing biopsy results, no blood test

    5. - trents replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      High TTG-IgG and Normal TTG-IgA

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

    • Total Members
      132,848
    • Most Online (within 30 mins)
      7,748

    L.Garcia24
    Newest Member
    L.Garcia24
    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

    • trents
      Not necessarily. The "Gluten Free" label means not more than 20ppm of gluten in the product which is often not enough for super sensitive celiacs. You would need to be looking for "Certified Gluten Free" (GFCO endorsed) which means no more than 10ppm of gluten. Having said that, "Gluten Free" doesn't mean that there will necessarily be more gluten than "Certified Gluten" in any given batch run. It just means there could be. 
    • trents
      I think it is wise to seek a second opinion from a GI doc and to go on a gluten free diet in the meantime. The GI doc may look at all the evidence, including the biopsy report, and conclude you don't need anything else to reach a dx of celiac disease and so, there would be no need for a gluten challenge. But if the GI doc does want to do more testing, you can worry about the gluten challenge at that time. But between now and the time of the appointment, if your symptoms improve on a gluten free diet, that is more evidence. Just keep in mind that if a gluten challenge is called for, the bare minimum challenge length is two weeks of the daily consumption of at least 10g of gluten, which is about the amount found in 4-6 slices of wheat bread. But, I would count on giving it four weeks to be sure.
    • Paulaannefthimiou
      Are Bobresmill gluten free oats ok for sensitive celiacs?
    • jenniber
      thank you both for the insights. i agree, im going to back off on dairy and try sucraid. thanks for the tip about protein powder, i will look for whey protein powder/drinks!   i don’t understand why my doctor refused to order it either. so i’ve decided i’m not going to her again, and i’m going to get a second opinion with a GI recommended to me by someone with celiac. unfortunately my first appointment isn’t until February 17th. do you think i should go gluten free now or wait until after i meet with the new doctor? i’m torn about what i should do, i dont know if she is going to want to repeat the endoscopy, and i know ill have to be eating gluten to have a positive biopsy. i could always do the gluten challenge on the other hand if she does want to repeat the biopsy.    thanks again, i appreciate the support here. i’ve learned a lot from these boards. i dont know anyone in real life with celiac.
    • trents
      Let me suggest an adjustment to your terminology. "Celiac disease" and "gluten intolerance" are the same. The other gluten disorder you refer to is NCGS (Non Celiac Gluten Sensitivity) which is often referred to as being "gluten sensitive". Having said that, the reality is there is still much inconsistency in how people use these terms. Since celiac disease does damage to the small bowel lining it often results in nutritional deficiencies such as anemia. NCGS does not damage the small bowel lining so your history of anemia may suggest you have celiac disease as opposed to NCGS. But either way, a gluten-free diet is in order. NCGS can cause bodily damage in other ways, particularly to neurological systems.
×
×
  • 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.