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

HAVING TO DEAL WITH IGNORANCE.Have you given your "gluten-free" food at parties secretly to the dog?


Dedegirl

Recommended Posts

Dedegirl Newbie

I have been on the gluten-free diet for the past 5 years after being very sick for a while until finally diagnosed with celiac.

One of the hardest things that I had to deal with was not when I went on the diet, not the looking for gluten-free products, 

but when I had to persuade some of my friends and relatives , who knew me as a foodie and eat-all person, never on a diet,

that I can no longer have ANYTHING that contains even the slightest amount of gluten! Some thought that I was just being pretentious,

some that I was on a quest for good figure and youth. But the most disturbing was when, after checking the labels of hot dogs at a birthday party 

 someone  told me to just have some and when I get the stomach pain I will know that there was gluten in it! 

It is embarrassing enough to have to refuse  food, to do all the explaining, reading labels, and on top to have to handle 

remarks of ignorant people, who have no idea of the degenerative disease and the tall in can take on the sufferer.

Another type of people are once who say, "Oh, but there is just this little bit of oats in this, they have no gluten, have they..?"

Or "it is only the vinaigrette that has it..!"--and still offer you food, that you know will make you suffer for at least 3-4 days post being nice to the hostess. 

I have had to pretend that I am eating, secretly give it to the dog, or just...chew and discretely spit it out in my napkin!

I have suffered a few times with accepting food that is gluten-free for sure and it was not, and learned my lesson.

I wonder if I should start saying that I have a deadly Gluten allergies, so restaurants and well meaning hostesses should stop offering me this just  little bit of  it in it. 

Because you do not offer just a little bit of a peanut to  someone with peanut allergy. I wonder what should be done to 

make the public more aware of this disease and not to think that if we are not rushed to the emergency room we could just have a little bit!

 


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



Celiac.com Sponsor (A8-M):



Ennis-TX Grand Master

I sometimes debate being a ass about it and eating in dangerous places or poisoning myself to make a point....never done it. But I recall what happened last time I got straight gluten poisoning at a restaurant....I rushed home and it hit me right as I was making it in the door a hour later....lost motor control and dropped to the floor. Bit later started vomiting while unable to move on the floor gut wrenching pain going in and out of it.....was there for 6-8 hours. Fitness monitor got my heart at a avg 36bpm for that time while my friend said they thought I was dead and turned completely white. After I regained motor control it was running to the toilet for the back half of episode, then constipation, brain fog, numbness for the next week or so.... I wear medical dog tags with emergency info incase s$#& happened and never leave my house for a event without someone else to drag my body someplace safe if something happens.

But I wonder, what kind of settlement I could get out of something if I got poisoned by gluten with a so called gluten-free meal at a restaurant....and actually stuck around til I lost motor control.

In all honestly I want to punch those people that claim a little is alright or those people who think it is no big deal......hell I get scared of little kids with cookies, or that guy walking around with a cup of beer at events.....unsure if I am scared how I would react out of fear if they spilled it on me or the stuff getting on me.....bit overly paranoid I know but gluten and the way it effects scares me shitless....I would probably shoot someone if they antiqued me. (Antiquing is the act of throwing a handful of flour on  people)

tessa25 Rising Star

I had food issues long before the celiac thing and I solved the whole explaining why I can't eat something by not explaining at all. I just say I have damaged insides and bring my own food. Although I've never really come across people who would care one way or the other. Maybe it depends on where you live. Maybe people in Colorado are more accepting of others dietary choices.

If I go to a barbecue I can wrap a hot dog in aluminum foil or hamburger in aluminum foil and stick that on their grill. I can bring loaded potato skins or batter dipped chicken wings or shrimp cocktail as a dish to share with everyone. That stuff's a big hit.

xoxorainbowbritexoxo Newbie

I went into a Co-Op/Natural Foods store recently to order a Gluten-Free sandwich, and they rolled their eyes saying, "Is it an allergy or a preference?" I said: "Neither! It's an Autoimmune Disease!"

TexasJen Collaborator

I have some very well meaning friends who try to make me food every time they have us over.  Usually, there is a high chance of CC and so I very sweetly thank them for making the food and then tell them that I just can't eat it due to my illness. I say things like, "I know this diet is crazy! I wish I could eat your food. It looks so good". I draw the line and don't eat anything at the party.  When you are confident in refusing their offer, they will treat it seriously most of the time. (admittedly, since I have a background in the medical world, people treat me a bit better I think than if I didn't).  I usually eat before I go. I keep a drink in my hand and tell them I'm full and I'll get something later if I"m hungry.

What I've learned over the last year of having this illness is that if you keep telling people no, they will eventually get it. People are starting to see that I won't eat their food so they are starting to not make any for me. Down side is I feel a bit left out now :(. But I don't feel guilty for them making me food I won't eat.  

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. - Haugeabs replied to Jane02's topic in Gluten-Free Foods, Products, Shopping & Medications
      23

      Desperately need a vitamin D supplement. I've reacted to most brands I've tried.

    2. - trents replied to xxnonamexx's topic in Gluten-Free Foods, Products, Shopping & Medications
      7

      FDA looking for input on Celiac Gluten sensitivity labeling PLEASE READ and submit your suggestions

    3. - Wheatwacked replied to Heatherisle's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      34

      Blood results

    4. - Known1 replied to xxnonamexx's topic in Gluten-Free Foods, Products, Shopping & Medications
      7

      FDA looking for input on Celiac Gluten sensitivity labeling PLEASE READ and submit your suggestions

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

    • Total Members
      133,413
    • Most Online (within 30 mins)
      7,748

    EBeloved
    Newest Member
    EBeloved
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Haugeabs
      For my Vit D3 deficiency it was recommended to take with Vit K2 (MK7) with the Vit D. The Vit K2 helps absorption of Vit D3. Fat also helps with absorption. I take Micro Ingredients Vit D3 5000 IU with Vit K2 100 micrograms (as menaquinone:MK-7). Comes in soft gels with coconut oil.  Gluten free but not certified gluten free. Soy free, GMO free.   
    • trents
      @Known1, I submitted the following comment along with my contact information: "I have noticed that many food companies voluntarily include information in their ingredient/allergen label section when the product is made in an environment where cross contamination with any of the nine major allergens recognized by the FDA may also be likely. Even though celiac disease and gluten sensitivity are, technically speaking, not allergic responses, it would seem, nonetheless, appropriate to include "gluten" in that list for the present purpose. That would insure that food companies would be consistent with including this information in labeling. Best estimates are that 1% of the general population, many undiagnosed of course, have celiac disease and more than that are gluten sensitive."
    • Wheatwacked
    • Wheatwacked
      Celiac Disease causes more vitamin D deficiency than the general population because of limited UV sunlight in the winter and the little available from food is not absorbed well in the damaged small intestine.  Taking 10,000 IU a day (250 mcg) a day broke my depression. Taking it for eleven years.  Doctor recently said to not stop.  My 25(OH)D is around 200 nmol/L (80 ng/ml) but it took about six years to get there.  Increasing vitamin D also increases absorption of Calcium. A good start is 100-gram (3.5-ounce) serving of salmon,  vitamin D from 7.5 to 25 mcg (300 to 1,000 IU) but it is going to take additional vitamin D supplement to be effective.  More importantly salmon has an omega-6 to omega-3 ratio 1:10 anti-inflammatory compared to the 15:1 infammatory ratio of the typical Western diet. Vitamin D and Depression: Where is all the Sunshine?
    • Known1
      Thank you for sharing your thoughts.  I respectfully disagree.  You cherry picked a small section from the page.  I will do the same below: The agency is seeking information on adverse reactions due to “ingredients of interest” (i.e., non-wheat gluten containing grains (GCGs) which are rye and barley, and oats due to cross-contact with GCGs) and on labeling issues or concerns with identifying these “ingredients of interest” on packaged food products in the U.S. “People with celiac disease or gluten sensitives have had to tiptoe around food, and are often forced to guess about their food options,” said FDA Commissioner Marty Makary, M.D., M.P.H. “We encourage all stakeholders to share their experiences and data to help us develop policies that will better protect Americans and support healthy food choices.” --- end quote Anyone with celiac disease is clearly a stakeholder.  The FDA is encouraging us to share our experiences along with any data to help develop future "policies that will better protect Americans and support healthy food choices".  I see this as our chance to speak up or forever hold our peace.  Like those that do not participate in elections, they are not allowed to complain.  The way I see it, if we do not participate in this request for public comment/feedback, then we should also not complain when we get ill from something labeled gluten-free. Have a blessed day ahead, Known1
×
×
  • 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.