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

Work Conferences With Meal Provided....


Renaye

Recommended Posts

Renaye Contributor

My immediate boss and co workers know of my many health troubles but corporate doesn't and I plan on keeping it that way. I have to go to a conference where they serve lunch with a guest speaker and then have break out sessions. I am doomed. I know I can try to call and find out who is catering, I can hide and eat in the bathroom or just look at my plate of food......

I am just dreading when this day comes.

Renaye


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



Celiac.com Sponsor (A8-M):



psawyer Proficient

Special dietary needs are common, and just about every caterer can accommodate them--provided they know in advance. Celiac disease is nothing to be ashamed of. I don't understand why you want to keep it secret.

Marilyn R Community Regular

One of the top exec's at the company I formerly worked with used to call the hotel/caterer ahead of time and ask for peaches and cottage cheese for her lunch.  Everyone just figured she was sick of rubber chicken and overcooked veggies.

Renaye Contributor

I also have sjogren's and I get extremely tired and don't want anyone at work to believe that I am not capable of doing my job. It is really not the eating part. I just worry that I may not make it to retirement.

Renaye

Kassia Newbie

I agree with those who suggest contacting the caterer in advance -- chances are they're already doing special meals for other people (diabetics, vegetarians). At least you'll be able to know what's on the menu in advance, and make plans accordingly. I attend a lot of conferences, and find my meal strategies depend on the type of event and what's being served. Since it won't be possible for you to slip out and grab a meal somewhere else, knowing what's on the menu seems like the best place to start. You can supplement with foods you've brought yourself after that.

IrishHeart Veteran

Special dietary needs are common, and just about every caterer can accommodate them--provided they know in advance. Celiac disease is nothing to be ashamed of. I don't understand why you want to keep it secret.

 

EXACTLY what HE said.

 

I just tell people "I have celiac disease and I need to be gluten free. "Watcha got I can eat?" with an  ingratiating smile. :)

I have been to weddings, funerals, and meetings and no one has ever made me sick. Most people want to help!

CALL the caterer.

 

Hon, if you have Celiac, this is for the rest of your life. Get used to being a bit assertive, a bit humorous and NOT AT ALL ashamed.

 

I also own a Koolatron cooler and bring food with me in my car everywhere I go.

 

This is not a big deal, honest. Do not let one single meal get you down or make you crazy. if nothing else, bring fruit, yogurt, some JIF PB cups and gluten-free crackers and  just dip away. Honestly, it's not a big deal.

 

if you simply cannot do any of these things for whatever reason, well, I have skipped lunch and nothing bad has ever happened.

Just drink water so you do not dehydrate..

Nikki2777 Community Regular

I did this and called the caterer ahead of time.  They had a plate ready for me.  If you want to be discreet, tell them you'll make yourself known to them when you arrive (get there a little early) and that way they can get you your plate quietly.  Worked very well for me.  

 

Other times, I've just put a Kind bar or two in my bag, taken a plate of food and smushed it around so it looks like I tried it.  Then ate my Kind bar when we got back to our seats.

 

There's almost always a plate of fruit, too, in my experience - just try to get to it early so you can avoid contamination.

 

Good luck.  


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



Celiac.com Sponsor (A8-M):



Gemini Experienced

I also have sjogren's and I get extremely tired and don't want anyone at work to believe that I am not capable of doing my job. It is really not the eating part. I just worry that I may not make it to retirement.

Renaye

Renaye....I have Celiac, Sjogren's, Reynaud's and Hashi's thyroid disease so I understand your concern about fatigue and the fear of having people think you are a "sickie" and may not be able to last in your job.  I have a very demanding job, particularily this past month.  I have been doing lots of overtime to meet a deadline before I head off on vacation at the end of the month.  It's insane here right now but I have been gluten-free for 8 years and, although I do not like working 12 hour days right now, I can do it without too much wear and tear. Not to say I am not tired by Friday but I am managing well enough.

 

I do not know how long you have been gluten-free but it will get better with time and you should be able to make it to retirement even with these AI problems.  Think positive and stick to the diet religiously and it will pay off.  I would not eat the food prepared by the caterer unless they can really assure you the food will be safe and they take it seriously.  Otherwise, bring a yummy lunch with you and do not worry one bit about eating something different in front of anyone.  This is not high school and you should never be afraid to do this.  Just tell them you have food intolerances and prefer to bring your own food...end of discussion.  You have nothing to be ashamed of.

 

Hang in there....you will be fine!  :)

Celtic Queen Explorer

I second calling ahead to the caterer.  I have done this twice recently.  The first was for an awards presentation for a friend of mine.  The event was held at a hotel ballroom that is used to handling a lot of conventions and meetings.  It was no problem at all.  I didn't realize that my friend had also called to get me a gluten free meal (yes, she is an awesome friend!) and so we both ended up eating gluten-free.  Her husband had the regular meal and they both decided the gluten-free meal (which was salmon) tasted much better than the regular chicken.  There was a sign by my plate marking it as a special meal and we got served first.

 

The second event was a company meeting.  I called and they said they were doing a buffet and couldn't accomodate my diet.  This was in a local community center that had just opened, so they had much less experience catering than the hotel did.  I just stopped by Wendy's on the way to the meeting and grabbed a salad and baked potato.

 

I think so many people are on different diets now for varying reasons - vegetarian, vegan, gluten free, corn free, paleo, etc., that it's not a big deal.  If anyone asks why you're eating something different, just say "I'm on a restricted diet."  Beyond that it's none of their business. 

Renaye Contributor

Thanks for the support. I have several weeks before the confernece so I will ask about the catering.

Gemini - I have been gluten-free since May 2011. Not sure how much it has really helped as I started plaquenil for fatigue at the same time. I am still constipated but won't ever go back to a regular diet for fear of getting something worse than sjogren's.

Thanks again,

Renaye

Gemini Experienced

Renaye......have you had your vitamin/mineral levels checked, especially iron and ferretin, plus your thyroid?  Please exhaust all other possibilities for your fatigue before resorting to meds.  I understand the fatigue but I obviously am not as bad as you are suffering right now because I can do a normal day and go to the gym and not be dragging.  Ok...I am dragging a bit today but its over work related. It's been a longgggggggggg week for me.  I have also been gluten-free for much longer than you have so please be patient with this.  I am sure things will improve over time but am sorry you feel so tired.  I have been there, done that and it is not easy to deal with if you are a working girl.  My Sjogren's was horrible at diagnosis of Celiac but it has gotten much, much easier to deal with and also symptom wise.  There is no doubt about it though...Sjogren's is a b_itch!  :angry:

Renaye Contributor

Gemini

Yes I have had my iron, ferretin and thyroid checked. My bloodwork is all normal except a +ana, low vitamin D and I also have osteopenia. So I take vitamin D and calcium. Even my celiac bloodwork is messed up and really not sure since I had a negative biopsy. My gastro resigned suddenly so I am looking for a new one. Hopefully he will have some answers for me. So I assume that you are not on plaquenil? I have sicca and they are really not sure what it will develop into but my grandfather died suddenly with lung complications and swollen sausage like hands so odds are I have something going on....

Renaye

Gemini Experienced

So we are much the same.  :)   I have a positive ANA and RF and they are not a little high but up there. They have come down slowly but recent blood work shows a spike in RF BUT I have no symptoms of anything arthritis. I guess it could be classified as sicca also because I have no arthritis symptoms but my doctor calls it Sjogren's.  My blood work for Sjogren's was positive.

 

I have osteopenia in my hip and osteoporosis in my spine that I have stabilized through weight training, in a gym with a personal trainer who is not shy about making the exercises hard.  It's brutal but I love it.  I am now playing with my thyroid dose to try and lower it to aid in bone regeneration.  It challenging for us older ladies.

 

One added word of unasked for advice......start taking Vitamin K2 with your calcium.  Usually around 80mcg per day should start you off well.  K2 directs calcium into the bone because it doesn't always end up in the bone. There have been recent studies from Europe showing this benefit and many people are deficient today for the K's.  Doctors, many female, are starting to recommend this vitamin to aid in bone development.  I take it myself so we'll see what happens.

 

No, I am not on Plaquenil.  My symptoms, or lack of, keep me away form anything more than Restasis for my eyes. My niece takes Plaquenil for lupus (she is in denial she has Celiac) and there are side effects.  I am stubborn and will not take anything unless I am dying. So far, I feel pretty good and can do a demanding day without collapsing.  My blood work is a bit scary but until I start to disintigrate, I am not worrying about it.  Keep moving, exercise and try and stay positive. It really helps. It just took me awhile to get there.

 

You say your Celiac blood work is messed up?  In what way?  Keep with the diet because I have read that those with Sjogren's should also be gluten free, even if they do not have celiac and it's all about genetics and how they play out.  I will look for the article that explained this. All I know is that my extreme dry eye and mouth improved after being gluten-free for awhile.  It's comfortable to deal with now and I was miserable pre-diagnosis of Celiac.

 

Gotta run but I will look for that article....... :D

Renaye Contributor

Gemini

Thanks for your kindness. I will look into the vitam k2. I am just walking and jumping rope for my osteo. I see the rhuemmy doc next month and will ask him to see if my effort is paying off. Trainer, huh....I am impressed!! I have very mild joint pain in my hands, wrists and my feet but very tolerable since plaquenil. I am very thankful that I found someone to treat me as I am a teacher and have two boys still at home. I believe the plaquenil has helped especially with the fatigue.

Celiac panel from prometheus

DGP IgG +

DGP IgA +

All other levels were negative

HLA typing pattern was not able to be read due to substances in the sample that interfere with the reading. LOL and my insurance didn't pay for it. So much for the genetics part??

Renaye

Gemini Experienced

I had to use a trainer......I had never done weight training and I did not want to hurt myself.   ;)   It really helps to have someone teach you the correct way to do things because, at this point, I want no injuries.  They push you a bit to challenge you and mix up the exercises for added benefit.  I have no choice but to do this as I do not want to take meds for it.  I highly recommend it!

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. - Scott Adams replied to Russ H's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      KAN-101 Treatment for Coeliac Disease

    2. - Scott Adams replied to miguel54b's topic in Related Issues & Disorders
      1

      Body dysmorphia experience

    3. - Scott Adams replied to Colleen H's topic in Related Issues & Disorders
      2

      Heat intolerant... Yikes

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

      Related issues

    5. - knitty kitty replied to Sarah Grace's topic in Related Issues & Disorders
      23

      Headaches / Migraines and Hypoglycaemia


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,149
    • Most Online (within 30 mins)
      7,748

    dvyoung
    Newest Member
    dvyoung
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      I agree that KAN-101 looks promising, and hope the fast track is approved. From our article below: "KAN-101 shows promise as an immune tolerance therapy aiming to retrain the immune system, potentially allowing safe gluten exposure in the future, but more clinical data is needed to confirm long-term effects."  
    • Scott Adams
      Thank you so much for having the courage to share this incredibly vivid and personal experience; it's a powerful reminder of how physical ailments can disrupt our fundamental sense of self. What you're describing sounds less like a purely psychological body dysmorphia and more like a distinct neurological event, likely triggered by the immense physical stress and inflammation that uncontrolled celiac disease can inflict on the entire body, including the nervous system. It makes complete sense that the specific sensory input—the pressure points of your elbows on your knees—created a temporary, distorted body map in your brain, and the fact that it ceased once you adopted a gluten-free diet is a crucial detail. Your intuition to document this is absolutely right; it's not "crazy" but rather a significant anecdotal data point that underscores the mysterious and far-reaching ways gluten can affect individuals. Your theory about sensory triggers from the feet for others is also a thoughtful insight, and sharing this story could indeed be validating for others who have had similar, unexplainable sensory disturbances, helping them feel less alone in their journey.
    • Scott Adams
      The most common nutrient deficiencies associated with celiac disease that may lead to testing for the condition include iron, vitamin D, folate (vitamin B9), vitamin B12, calcium, zinc, and magnesium.  Unfortunately many doctors, including my own doctor at the time, don't do extensive follow up testing for a broad range of nutrient deficiencies, nor recommend that those just diagnosed with celiac disease take a broad spectrum vitamin/mineral supplement, which would greatly benefit most, if not all, newly diagnosed celiacs. Because of this it took me decades to overcome a few long-standing issues I had that were associated with gluten ataxia, for example numbness and tingling in my feet, and muscle knots--especially in my shoulders an neck. Only long term extensive supplementation has helped me to resolve these issues.      
    • Scott Adams
      I am so sorry you are going through this; it sounds incredibly overwhelming and disheartening to be dismissed by the very medical professionals you're turning to for help. It is completely understandable that you feel lost and exhausted, not just from the relentless physical symptoms like the leg pain, stomach issues, and profound fatigue, but from the psychological toll of being told it's "just IBS" or that you need a therapist when you know your body is signaling that something is wrong. While it's true that a normal tTG test can indicate that celiac disease itself is being managed from a dietary perspective, it is a major oversight for your doctors to ignore your other diagnoses like SIBO, a hernia, and Barrett's esophagus, all of which can contribute significantly to the symptoms you describe. You are absolutely right to be seeking a new Primary Care Physician who will listen to your full history, take your Barrett's diagnosis seriously, and help you coordinate a care plan that looks at the whole picture, because your experience is not just in your head—it's in your entire body, and you deserve a medical team that acknowledges that. I had hernia surgery (laparoscopic), and it's not a big deal, so hopefully you can have your new doctor give you some guidance on that.
    • knitty kitty
      Some people have difficulty processing tyrosine.  Cut out the nuts and cheese and see if there's any difference.  Everyone is different. This study shows that tyrosine can affect our brain with detrimental effects as we age. Neuro-Cognitive Effects of Acute Tyrosine Administration on Reactive and Proactive Response Inhibition in Healthy Older Adults https://pmc.ncbi.nlm.nih.gov/articles/PMC6084775/ "In conclusion, we show age-related effects of tyrosine administration especially on proactive, not reactive, response inhibition, accompanied by signal changes in dopamine-rich fronto-striatal brain regions. Specifically, we observed that tyrosine’s effect on brain and cognition became detrimental with increasing age, questioning the cognitive enhancing potential of tyrosine in healthy aging."
×
×
  • 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.