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.


  • 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.