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

Newbie - Frustrated


SillyHats

Recommended Posts

SillyHats Newbie

Hello! I was diagnosed with Celiac about a month ago. After a brief mourning period, I pulled myself up by the bootstraps and decided I can handle anything! That's very easy to do when I'm at home and able to cook whatever I want with a few modifications. Not so easy to do when I'm not home. I have been glutened by three restaurants in the past 2 weeks. I do my best to meekly ask for something that doesn't contain any gluten, but due to my inability to quickly and easily explain exactly what I need, I seem to always end up anywhere from a little uncomfortable to up all night running to the bathroom. I guess I need to learn to order better. I will gladly accept any advice on how to be a good customer and still get a meal that is safe for me. I already have tipping a lot extra down to a science, but that doesn't do me much good when the tipping occurs and I still end up glutened.

Also, I was surprised to learn that I have two "friends" who get annoyed anytime they hear me say something about Celiac or any food allergy, whether or not I am addressing them. One of them says he doesn't believe in food allergies and the other says people with food allergies are annoying and he hates dealing with them in the restaurant business. I don't know what to do with those two "friends." We run in mutual circles, so avoiding them is not possible. Should I learn to accept and live with people who treat me like I have a made-up illness and have no respect for what I'm going through? I feel like having an allergy might be easier because I can prove it by going into Anaphylactic Shock in front of these friends and dying, thereby proving that it isn't made up. How do you deal with people who don't take you seriously because they can't physically see what you're going through?

Thanks!


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



Celiac.com Sponsor (A8-M):



Cujy Apprentice

If all you can do is ignore them then so be it...we all here know that you arn't lying or making things up!!!! When my husband first was told that I "maybe" had ciliac, he said its a term used by doctors for every ailment known to man...well now that I have two confirmation tests under my belt he believes it. Doctors are quick to blame every symptom now on my celiac and that is hard to deal with, but Joe Blow public just won't get it. If you can explain it, if they are worth it, if not, just let them be. Stick to your guns and do what you need to to make yourself feel better.

As far as the restaurant thing, let me know if you get any good advice, I havn't travelled that road yet, as Im still a baby to the diet.

All the best with your quest to feel better, and Im sure alot of people here will tell you to forget about those NOT friends!!! Maybe the restaurant guy feels pressured to have more gluten free meals available in his line of business!!!! Right on!

heatherjane Contributor

The trick to restaurants is to plan ahead. You have to do some kind of research before you go: check online for gluten free menus, email or call the manager on off-hours and ask about their prep practices, go to places that have proven themselves trustworthy with other celiacs. If researching ahead of time isn't possible, you need to be willing to ask questions of the waitstaff even if it makes the situation a little uncomfortable. Make sure they know that you need to have your meal prepared with proper precautions to avoid cross-contamination (e.g. changed gloves, clean cooking area, no contact with gluten items). You have to be very specific. If they seem clueless, the best route is not to eat. Because situations like this can happen, make sure you have snacks on hand so you don't starve...or eat beforehand and get a drink while you're there so you don't feel completely out of place.

Triumph Dining makes good "allergy" cards that you can hand to the server which really saves you a lot of work in having to explain. They have them for different cuisines and in different languages. They've saved my rear so many times!

As for the people who don't get it. The best thing to do is politely disagree/explain, drop the subject, and carry on as usual. It's hard, but you're going to come across people like that, unfortunately. The good thing is that more and more people are becoming aware of this disease, so the rude ones are becoming fewer and farther between. Just try not to let them get to you, and surround yourself with supportive people.

Hang in there!

SillyHats Newbie

Thanks, ladies!!! Great advice!

quincy Contributor

Thanks, ladies!!! Great advice!

I am 2 years into being gluten-free and I STILL have the dining out problem. I just don't trust anyone when they say they are being careful because in reality they are NOT a gluten-free kitchen. I feel safe in a PF changs because they have been doing gluten-free for a long time. I don't really have any answers about this except to speak up no matter what. I was glutened alot when I first got dx'd too.

my concern is that I am less sensitive now so if my body doesnt tell me right away that I ingested gluten, does that mean that I didn't ingest it? CC is a bad thing for us.

WendyLee Rookie

Hello! I was diagnosed with Celiac about a month ago. After a brief mourning period, I pulled myself up by the bootstraps and decided I can handle anything! That's very easy to do when I'm at home and able to cook whatever I want with a few modifications. Not so easy to do when I'm not home. I have been glutened by three restaurants in the past 2 weeks. I do my best to meekly ask for something that doesn't contain any gluten, but due to my inability to quickly and easily explain exactly what I need, I seem to always end up anywhere from a little uncomfortable to up all night running to the bathroom. I guess I need to learn to order better. I will gladly accept any advice on how to be a good customer and still get a meal that is safe for me. I already have tipping a lot extra down to a science, but that doesn't do me much good when the tipping occurs and I still end up glutened.

Also, I was surprised to learn that I have two "friends" who get annoyed anytime they hear me say something about Celiac or any food allergy, whether or not I am addressing them. One of them says he doesn't believe in food allergies and the other says people with food allergies are annoying and he hates dealing with them in the restaurant business. I don't know what to do with those two "friends." We run in mutual circles, so avoiding them is not possible. Should I learn to accept and live with people who treat me like I have a made-up illness and have no respect for what I'm going through? I feel like having an allergy might be easier because I can prove it by going into Anaphylactic Shock in front of these friends and dying, thereby proving that it isn't made up. How do you deal with people who don't take you seriously because they can't physically see what you're going through?

Thanks!

I can't help with the dining out issue mainly because we don't dine out. But with your two 'friends' try explaining to them as someone else on the internet explained it. Gluten is POISON to you and being glutenated is the same as suffering food poisoning. They wouldn't knowingly eat anything that would poison them and neither do you.

krysty Newbie

Thank you so much for information.


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



Celiac.com Sponsor (A8-M):



Annie82 Newbie

I was diagnosed less than a month ago and I am so uncomfortable trying to explain Celiac because cross-contamination automatically makes you sound like you have OCD even though it's completely valid. I hate thinking (worrying) about it all the time because I feel so sick and feeling like everyone is sick of hearing about it. Yuck. I'm glad you posted about this. I feel less alone.

aliceintown Newbie

It's really hard, as I was only recently diagnosed and not only do I have to stay from all the foods I used to love, I now get sick at the slightest bit of contamination. Not fun.

Perhaps you should ask your friends if they've been checked out. ;) Just a thought. :o

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Rogol72 replied to klmgarland's topic in Dermatitis Herpetiformis
      3

      Help I’m cross contaminating myself,

    2. - ShariW commented on Scott Adams's article in Frequently Asked Questions About Celiac Disease
      4

      What are Celiac Disease Symptoms?

    3. - klmgarland replied to klmgarland's topic in Dermatitis Herpetiformis
      3

      Help I’m cross contaminating myself,

    4. - Scott Adams replied to klmgarland's topic in Dermatitis Herpetiformis
      3

      Help I’m cross contaminating myself,

    5. - Scott Adams replied to Jmartes71's topic in Coping with Celiac Disease
      1

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,909
    • Most Online (within 30 mins)
      7,748

    Hmart
    Newest Member
    Hmart
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Rogol72
      @klmgarland, My dermatitis herpetiformis didn't clear up until I became meticulous about cross contamination. I cut out gluten-free oats and all gluten-free foods, dairy and gluten-free rice. Additionally, getting the right amount of protein for my body weight helped significantly in my body's healing process ... along with supplementing with enough of all the vitamins and minerals ... especially Zinc and Magnesium. I went from 70kg to 82kg in a year. Protein with each meal 3 times daily, especially eggs at breakfast made the difference. I'm not sure whether iodine was a problem for me, but I can tolerate iodine no problem now. I'm off Dapsone and feel great. Not a sign of an itch. So there is hope. I'm not advocating for the use of Dapsone, but it can bring a huge amount of relief despite it's effect on red blood cells. The itch is so distracting and debilitating. I tried many times to get off it, it wasn't until I implemented the changes above and was consistent that I got off it. Dermatitis Herpetiformis is horrible, I wouldn't wish it on anyone.  
    • klmgarland
      Thank you so very much Scott.  Just having someone understand my situation is so very helpful.  If I have one more family member ask me how my little itchy skin thing is going and can't you just take a pill and it will go away and just a little bit of gluten can't hurt you!!!! I think I will scream!!
    • Scott Adams
      It is difficult to do the detective work of tracking down hidden sources of cross-contamination. The scenarios you described—the kiss, the dish towel, the toaster, the grandbaby's fingers—are all classic ways those with dermatitis herpetiformis might get glutened, and it's a brutal learning curve that the medical world rarely prepares you for. It is difficult to have to deal with such hyper-vigilance. The fact that you have made your entire home environment, from makeup to cleaners, gluten-free is a big achievement, but it's clear the external world and shared spaces remain a minefield. Considering Dapsone is a logical and often necessary step for many with DH to break the cycle of itching and allow the skin to heal while you continue your detective work; it is a powerful tool to give you back your quality of life and sleep. You are not failing; you are fighting an incredibly steep battle. For a more specific direction, connecting with a dedicated celiac support group (online or locally) can be invaluable, as members exchange the most current, real-world tips for avoiding cross-contamination that you simply won't find in a pamphlet. You have already done the hardest part by getting a correct diagnosis. Now, the community can help you navigate the rest. If you have DH you will likely also want to avoid iodine, which is common in seafoods and dairy products, as it can exacerbate symptoms in some people. This article may also be helpful as it offers various ways to relieve the itch:  
    • Scott Adams
      It's very frustrating to be dismissed by medical professionals, especially when you are the one living with the reality of your condition every day. Having to be your own advocate and "fight" for a doctor who will listen is an exhausting burden that no one should have to carry. While that 1998 brochure is a crucial piece of your personal history, it's infuriating that the medical system often requires more contemporary, formal documentation to take a condition seriously. It's a common and deeply unfair situation for those who were diagnosed decades ago, before current record-keeping and testing were standard. You are not alone in this struggle.
    • Scott Adams
      Methylprednisolone is sometimes prescribed for significant inflammation of the stomach and intestines, particularly for conditions like Crohn's disease, certain types of severe colitis, or autoimmune-related gastrointestinal inflammation. As a corticosteroid, it works by powerfully and quickly suppressing the immune system's inflammatory response. For many people, it can be very effective at reducing inflammation and providing rapid relief from symptoms like pain, diarrhea, and bleeding, often serving as a short-term "rescue" treatment to bring a severe flare under control. However, experiences can vary, and its effectiveness depends heavily on the specific cause of the inflammation. It's also important to be aware that while it can work well, it comes with potential side effects, especially with longer-term use, so it's typically used for the shortest duration possible under close medical supervision. It's always best to discuss the potential benefits and risks specific to your situation with your gastroenterologist.
×
×
  • 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.