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

Tournament Dinner - What Should I Do?


Hummingbird4

Recommended Posts

Hummingbird4 Explorer

I've been gluten-free for about 3 months now. In a couple of weeks, I will be playing in a tennis tournament at my health club. There is a "Champagne Ball" dinner on the last night of the tournament. I would really like to go (there is music and dancing afterward). I haven't seen any kind of menu posted, and I don't know who will be catering it. If you were me, what would you do? Contact the person in charge of the tournament to find out who's catering - and then contact them? Or just skip eating the meal? I'm not big on drawing attention to myself, but if I have a special meal or no meal at all, it will be obvious to anyone at my table.

And can I just whine for a second that having Celiac Disease sucks? I know, I know, it could be worse. But it's really no fun in social situations.


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



Celiac.com Sponsor (A8-M):



mushroom Proficient
I've been gluten-free for about 3 months now. In a couple of weeks, I will be playing in a tennis tournament at my health club. There is a "Champagne Ball" dinner on the last night of the tournament. I would really like to go (there is music and dancing afterward). I haven't seen any kind of menu posted, and I don't know who will be catering it. If you were me, what would you do? Contact the person in charge of the tournament to find out who's catering - and then contact them? Or just skip eating the meal? I'm not big on drawing attention to myself, but if I have a special meal or no meal at all, it will be obvious to anyone at my table.

And can I just whine for a second that having Celiac Disease sucks? I know, I know, it could be worse. But it's really no fun in social situations.

Hello Hummingbird:

I am dealing with the same issues this weekend; 75th jubilee of my one-room country primary school. It is a big deal weekend party, barbecue on Friday night, ceremonies and the good ole Kiwi afternoon tea on Saturday afternoon, dinner dance on Saturday night. At least I have company--my sister is staying with us and my husband is also gluten-free, so there are three of us. I have been trying to get the name of the caterer for some time; they wouldn't let me talk to him but I did find out what they are serving, so we know what we can eat and what we have to take--roast beef with gravy on the side, check for the beef; a leg off ham, pass, although it could be okay; parsley buttered potatoes, check; minted green peas (pass, mint sauce usually made with malt vinegar here); fruit salad, check; pavlova (meringue with cream and strawberries on top, check; all the salads are pre-dressed, including the green (pass). For the barbecue (catered by the local community), we will take our own pre-barbecued meat wrapped in foil and have them reheat it on the grill, and our own salad and dressing. Don't know what else they are serving. For both meals we will take our own bread rolls. I know I am lucky; with three of us it's not so bad as being the only one and potentially feeling like a pimple, but even if it were only me I would have done the same thing. This is my first catered eating experience since going gluten-free. I admit it is a pain in the patuti, but don't let it get you down.

I would definitely try to talk to the caterer. Then you can supplement as necessary. Explain to the caterer just as you would to the waiter or chef or manager of a restaurant. Good luck and just act normally when you are there and fob off any potential questions about what you are eating and why with the most minimal of information, if any. And do have a good time!

kbtoyssni Contributor

I would contact the caterer. Many fancy caterers can accommodate a gluten-free diet.

ShayFL Enthusiast

I would contact the caterer too and see what they can do. Have a lara bar or something in your little purse just in case. I am probably not the best to ask because I no longer care what ANYONE thinks. If they dont ask and stare, I just smile. If they ask I tell them. And I go about my business. :)

kenlove Rising Star

Yes by all means contact the caterer/chef to make sure you have something you can enjoy.

Its a chance for you to educate some of the people you sit with when they bring you out a special meal that is usually (hopefully) much better than what others are served. Yeah Celiac sucks but at least you know your eating healthy ..

ken

I've been gluten-free for about 3 months now. In a couple of weeks, I will be playing in a tennis tournament at my health club. There is a "Champagne Ball" dinner on the last night of the tournament. I would really like to go (there is music and dancing afterward). I haven't seen any kind of menu posted, and I don't know who will be catering it. If you were me, what would you do? Contact the person in charge of the tournament to find out who's catering - and then contact them? Or just skip eating the meal? I'm not big on drawing attention to myself, but if I have a special meal or no meal at all, it will be obvious to anyone at my table.

And can I just whine for a second that having Celiac Disease sucks? I know, I know, it could be worse. But it's really no fun in social situations.

DarkIvy Explorer

I third, or fourth the suggestion to contact the caterer.

Worst case scenario, they won't be able to do anything at all. Bring your own sack dinner! I know it sounds kind of attention drawing, but sometimes it happens. If you really want to go, find a way to go and make it enjoyable for yourself.

When people I don't know very well ask me why I'm eating different food, or not eating at all, I just explain that I have celiac disease and the tiniest accidental crumb of bread in my food will make me sick. Some people are surprisingly knowledgeable about it and curious, others will ask questions. I make it simple... I just say "I can't eat wheat, barley, rye or oats." When people ask about bread and pasta, I make a general statement about how there's gluten free bread and pasta usually made from rice. I say the rice bit right away, because in my experience if you just say there is gluten-free bread or pasta, people's next question is "what is it MADE out of??"

At first, celiac really ruined my social scene. I'm in college, so eating together is social time, whether it's at a dorm, restaurant, pizza place, or whatever else. I know how you feel, it can be so rough to adjust to not just eating whatever it is everyone else eats, but I've found that it's not a big deal once you start to figure it out. With closer friends, it's always easy to suggest a safe restaurant, and no one minds when I give my lengthy schpiel to the waiter. If they're really set on a restaurant I can't eat at, or ordering pizza, I either eat before, or bring along my own safe food. Last year, I'd just make a stop at Jimmy John's for an unwhich (the location by me is surprisingly careful about gluten-free food) and then joined my friends at the pizza parlor where my friends were eating. It was no big deal for anyone and I figured if the employees got upset, I could just make some comment about how I can't eat wheat, no big deal.

The hardest situations to get around are the ones in which you've got no control over the food. Example, a big family/friends gathering at a humungous Chinese food buffet.... especially when you go with your boyfriend's family, and only a few of the people there know what's going on with your food situation. Not only do I stick out like a sore thumb because I'm the only one who doesn't look or speak Chinese, I stick out because I can't eat what everyone else eats. It's borderline rude, and I always worry people will assume I'm stuck up and just don't like the food. The thing is, it's about health, and ultimately I don't care what these random people think of me. If anyone asks, I just explain that I can't have wheat, wheat is in soy sauce, soy sauce is in everything. Usually that takes care of it, or his family will explain (in Chinese, haha) that I've got a disease, bla bla. I'm already the odd one out, so while it can be uncomfortable, I'm really not willing to compromise my health to feel a touch more "normal".

Frankly, even if the caterers can make you something, it's likely to be somewhat different than what everyone else is eating, and people will still ask questions. I know this has happened to me before on various occasions, such as airplane rides, sorority events catered by sandwich or burrito places, etc. I definitely understand the desire to blend in and feel "normal", but my normal just happens to include bringing my own food to these types of things and answering a lot of questions. It's not the end of the world, and it's definitely better than being stuck at home all the time!

Gemini Experienced
I would contact the caterer too and see what they can do. Have a lara bar or something in your little purse just in case. I am probably not the best to ask because I no longer care what ANYONE thinks. If they dont ask and stare, I just smile. If they ask I tell them. And I go about my business. :)

What an excellent attitude! I agree, I just don't give a hoot what ANYONE thinks either and it's really the way to go. The funniest part of having celiac disease is that it bothers most people WAY more if you sit there and don't eat anything as opposed to it bothering me. I had a birthday dinner this past week-end and I couldn't have any of the appetizers, bread, or the second course they offered. Everyone else was stuffing their faces while I drank wine and talked. The main course was gluten-free so I ate some of that but people were getting a little nervous because I sat there and didn't eat what I couldn't. What I don't understand is later on, all the women were complaining about how full they were and how the meal killed their weight loss plan for the week-end. I got blank stares when I commented on how good I felt and how "un-full" I was! Sometimes being Celiac is not so bad because it's a great excuse for not over eating and a great way to watch your weight! By the way, all the women that felt like they were ready to explode ate enough bread that night to choke a horse. I'm so glad I'm done with that behavior!


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



Celiac.com Sponsor (A8-M):



Ellie11 Newbie

Hi! i found out i couldnt eat gluten less than a year ago so im still getting used to it. i have found it really hard adjusting in social situations, especially dealing with comments from some of my (previously) closest friends who seemed to think i was doing this on purpose and practially demanded a doctors certificate as proof. Anyway, i definately get what you all mean about the wierd looks you get when you only eat the fruit platter at a catered lunch full of yummy looking bagettes and wraps!

i've found the best thing to do when your going to have to take your own food is to make sure it still looks like a nice substantial meal so people don't think your skipping a meal or aren't eating cuz your anorexic or something (a big problem when your a 18 year old girl who lost heaps of weight pre-diagnosis). So when i take my own food a make sure its not just a little salad but make a nice rice or quinoa or buckwheat dish i can either have hot or cold. I find that most places (even if they don't have gluten free food) are happy to re-heat your own food for you - but make sure you have it properly covered or in a sealed container so it can't get contaminated.

but in saying that, first try you hardest to get in contact with the caterer, ive always had heaps of help when ive asked. Just be really sweet and polite and people tend to feel sorry for u ;)

i hope u enjoy ur dinner! xx

Gemini Experienced
but in saying that, first try you hardest to get in contact with the caterer, ive always had heaps of help when ive asked. Just be really sweet and polite and people tend to feel sorry for u ;

Ellie...it sounds like you have done a marvelous job handling social situations that revolve around food and I commend you for doing what I try to do.....when I do bring my own food, I always make sure to have something better than what the gluten eaters have so they get a different perspective of the gluten-free diet. The only comment you made that made my 49 year old spine cringe was the above remark. Sorry, can't help it but I never want people to feel sorry for me. I get enough of that already and there is no need to feel sorry for me, even when trying to get some food to eat or something re-heated. I actually feel sorry for people who don't know what the heck is in the food they eat! I get your point and it's always good to be polite when asking for assistance but not to the point where they act like your disabled or something.

I'm not trying to be critical but I guess my age is showing! :P

Hummingbird4 Explorer

Thanks everyone for your suggestions. I will contact the caterer and see what information I can get from them. If there is nothing for me to eat, I'll bring some food of my own. And drink champagne. ;)

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. - suek54 replied to suek54's topic in Dermatitis Herpetiformis
      5

      Awaiting dermatitis herpetiformis confirmation following biopsy

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

      how much gluten do I need to eat before blood tests?

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

      how much gluten do I need to eat before blood tests?

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

      how much gluten do I need to eat before blood tests?

    5. - catnapt posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      how much gluten do I need to eat before blood tests?

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

    • Total Members
      133,257
    • Most Online (within 30 mins)
      7,748

    KariNoMoreGluten
    Newest Member
    KariNoMoreGluten
    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

    • suek54
      Thank you all for your advice and the dermatitis herpetiformis article. The latter made me realise I had stopped taking my antihistamine, which I will restart today. The Dapsone has cleared the rash entirely but I still get quite a bit itching, absolutely nothing to see though. I know its notoriously hard to clear and its still relatively early days for me.  The iodine issue is very interesting. I do eat quite a bit of salt because I have Addison's disease and sodium retention is an issue. I also have autoimmune hypothyroidism, not sure how a low iodine diet would play into that? Because of my Addison's I am totally steroid dependent, I take steroids 4 x daily and cannot mount any defence against inflammation. I need to increase my meds for that. Now that I know what is wrong I can do just that if Im having a bad day. Life is very sweet, just so damn complicated sometimes! Hey ho, onwards. Thank you again for your advice.  
    • trents
      So, essentially all of the nutrition in the food we eat is absorbed through the villous lining of the small bowel. This is the section of the intestinal track that is damaged by celiac disease. This villous lining is composed of billions of finger-like projections that create a huge amount of surface area for absorbing nutrients. For the celiac person, when gluten is consumed, it triggers an autoimmune reaction in this area which, of course, generates inflammation. The antibodies connected with this inflammation is what the celiac blood tests are designed to detect but this inflammation, over time, wears down the finger-like projections of the villous lining. Of course, when this proceeds for an extended period of time, greatly reduces the absorption efficiency of the villous lining and often results in many and various nutrient deficiency-related health issues. Classic examples would be osteoporosis and iron deficiency. But there are many more. Low D3 levels is a well-known celiac-caused nutritional deficiency. So is low B12. All the B vitamins in fact. Magnesium, zinc, etc.  Celiac disease can also cause liver inflammation. You mention elevated ALP levels. Elevated liver enzymes over a period of 13 years was what led to my celiac diagnosis. Within three months of going gluten free my liver enzymes normalized. I had elevated AST and ALT. The development of sensitivities to other food proteins is very common in the celiac population. Most common cross reactive foods are dairy and oats but eggs, soy and corn are also relatively common offenders. Lactose intolerance is also common in the celiac population because of damage to the SB lining.  Eggs when they are scrambled or fried give me a gut ache. But when I poach them, they do not. The steam and heat of poaching causes a hydrolysis process that alters the protein in the egg. They don't bother me in baked goods either so I assume the same process is at work. I bought a plastic poacher on Amazon to make poaching very easy. All this to say that many of the issues you describe could be caused by celiac disease. 
    • catnapt
      thank you so much for your detailed and extremely helpful reply!! I can say with absolute certainty that the less gluten containing products I've eaten over the past several years, the better I've felt.   I wasn't avoiding gluten, I was avoiding refined grains (and most processed foods) as well as anything that made me feel bad when I ate it. It's the same reason I gave up dairy and eggs- they make me feel ill.  I do have a bit of a sugar addiction lol so a lot of times I wasn't sure if it was the refined grains that I was eating - or the sugar. So from time to time I might have a cookie or something but I've learned how to make wonderful cookies and golden brownies with BEANS!! and no refined sugar - I use date paste instead. Pizza made me so ill- but I thought it was probably the cheese. I gave up pizza and haven't missed it. the one time I tried a slice I felt so bad I knew I'd never touch it again. I stopped eating wheat pasta at least 3 yrs ago- just didn't feel well after eating it. I tried chick pea pasta and a few others and discovered I like the brown rice pasta. I still don't eat a lot of pasta but it's nice for a change when I want something easy. TBH over the years I've wondered sometimes if I might be gluten intolerant but really believed it was not possible for me to have celiac disease. NOW I need to know for sure- because I'm in the middle of a long process of trying to find out why I have a high parathyroid level (NOT the thyroid- but rather the 4 glands that control the calcium balance in your body) I have had a hard time getting my vit D level up, my serum calcium has run on the low side of normal for many years... and now I am losing calcium from my bones and excreting it in my urine (some sort of renal calcium leak) Also have a high ALP since 2014. And now rapidly worsening bone density.  I still do not have a firm diagnosis. Could be secondary HPT (but secondary to what? we need to know) It could be early primary HPT. I am spilling calcium in my urine but is that caused by the high parathyroid hormone or is it the reason my PTH is high>? there are multiple feedback loops for this condition.    so I will keep eating the bread and some wheat germ that does not seem to bother me too much (it hasn't got enough gluten to use just wheat germ)    but I'm curious- if you don't have a strong reaction to a product- like me and wheat germ- does that mean it's ok to eat or is it still causing harm even if you don't have any obvious symptoms? I guess what you are saying about silent celiac makes it likely that you can have no symptoms and still have the harm... but geez! you'd think they'd come up with a way to test for this that didn't require you to consume something that makes you sick! I worry about the complications I've been reading about- different kinds of cancers etc. also wondering- are there degrees of celiac disease?  is there any correlation between symptoms and the amnt of damage to your intestines? I also need a firm diagnosis because I have an identical twin sister ... so if I have celiac, she has it too- or at least the genetic make up for having it. I did have a VERY major stress to my body in 2014-2016 time frame .. lost 50lbs in a short period of time and had severe symptoms from acute protracted withdrawal off an SSRI drug (that I'd been given an unethically high dose of, by a dr who has since lost his license)  Going off the drug was a good thing and in many ways my health improved dramatically- just losing 50lbs was helpful but I also went  off almost a dozen different medications, totally changed my diet and have been doing pretty well except for the past 3-4 yrs when the symptoms related to the parathyroid issue cropped up. It is likely that I had low vit D for some time and that caused me a lot of symptoms. The endo now tells me that low vit D can be caused by celiac disease so I need to know for sure! thank you for all that great and useful information!!! 
    • trents
      Welcome, @catnapt! The most recent guidelines are the daily consumption of a minimum of 10g of gluten (about the amount found in 4-6 slices of wheat bread) for a minimum of two weeks. But if possible stretching that out even more would enhance the chances of getting valid test results. These guidelines are for those who have been eating gluten free for a significant amount of time. It's called the "gluten challenge".  Yes, you can develop celiac disease at any stage of life. There is a genetic component but also a stress trigger that is needed to activate the celiac genes. About 30-40% of the general population possesses the genetic potential to develop celiac disease but only about 1% of the general population actually develop celiac disease. For most with the potential, the triggering stress event doesn't happen. It can be many things but often it is a viral infection. Having said that, it is also the case that many, many people who eventually are diagnosed with celiac disease probably experienced the actual onset years before. Many celiacs are of the "silent" type, meaning that symptoms are largely missing or very minor and get overlooked until damage to the small bowel lining becomes advanced or they develop iron deficiency anemia or some other medical problem associated with celiac disease. Many, many are never diagnosed or are diagnosed later in life because they did not experience classic symptoms. And many physicians are only looking for classic symptoms. We now know that there are over 200 symptoms/medical problems associated with celiac disease but many docs are only looking for things like boating, gas, diarrhea. I certainly understand your concerns about not wanting to damage your body by taking on a gluten challenge. Your other option is to totally commit to gluten free eating and see if your symptoms improve. It can take two years or more for complete healing of the small bowel lining once going gluten free but usually people experience significant improvement well before then. If their is significant improvement in your symptoms when going seriously gluten free, then you likely have your answer. You would either have celiac disease or NCGS (Non Celiac Gluten Sensitivity).
    • catnapt
      after several years of issues with a para-gland issue, my endo has decided it's a good idea for me to be tested for celiac disease. I am 70 yrs old and stunned to learn that you can get celiac this late in life. I have just gradually stopped eating most foods that contain gluten over the past several years- they just make me feel ill- although I attributed it to other things like bread spiking blood sugar- or to the things I ate *with* the bread or crackers etc   I went to a party in Nov and ate a LOT of a vegan roast made with vital wheat gluten- as well as stuffing, rolls and pie crust... and OMG I was so sick! the pain, the bloating, the gas, the nausea... I didn't think it would ever end (but it did) and I was ready to go the ER but it finally subsided.   I mentioned this to my endo and now she wants me to be tested for celiac after 2 weeks of being on gluten foods. She has kind of flip flopped on how much gluten I should eat, telling me that if the symptoms are severe I can stop. I am eating 2-3 thin slices of bread per day (or english muffins) and wow- it does make me feel awful. But not as bad as when I ate that massive amnt of vital wheat gluten. so I will continue on if I have to... but what bothers me is - if it IS celiac, it seems stupid for lack of a better word, to intentionally cause more damage to my body... but I am also worried, on the other hand, that this is not a long enough challenge to make the blood work results valid.   can you give me any insight into this please?   thank you
×
×
  • 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.