Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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 Celiac.com!
    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

Link to comment
Share on other sites

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.

Link to comment
Share on other sites
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.

Link to comment
Share on other sites
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

Link to comment
Share on other sites
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.

Link to comment
Share on other sites
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..

Link to comment
Share on other sites
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.  

Link to comment
Share on other sites

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!  :)

Link to comment
Share on other sites
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. 

Link to comment
Share on other sites
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

Link to comment
Share on other sites
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:

Link to comment
Share on other sites
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

Link to comment
Share on other sites
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

Link to comment
Share on other sites
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

Link to comment
Share on other sites
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!

Link to comment
Share on other sites

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,088
    • Most Online (within 30 mins)
      7,748

    Aventine
    Newest Member
    Aventine
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Posterboy
      Nacina, Knitty Kitty has given you good advice. But I would say/add find a Fat Soluble B-1 like Benfotiamine for best results.  The kind found in most Multivitamins have a very low absorption rate. This article shows how taking a Fat Soluble B-1 can effectively help absorption by 6x to7x times. https://www.naturalmedicinejournal.com/journal/thiamine-deficiency-and-diabetic-polyneuropathy quoting from the article.... "The group ingesting benfotiamine had maximum plasma thiamine levels that were 6.7 times higher than the group ingesting thiamine mononitrate.32" Also, frequency is much more important than amount when it comes to B-Vitamin. These are best taken with meals because they provide the fat for better absorption. You will know your B-Vitamin is working properly when your urine becomes bright yellow all the time. This may take two or three months to achieve this.......maybe even longer depending on how low he/you are. The Yellow color is from excess Riboflavin bypassing the Kidneys....... Don't stop them until when 2x a day with meals they start producing a bright yellow urine with in 2 or 3 hours after the ingesting the B-Complex...... You will be able to see the color of your urine change as the hours go by and bounce back up after you take them in the evening. When this happens quickly......you are now bypassing all the Riboflavin that is in the supplement. The body won't absorb more than it needs! This can be taken as a "proxy" for your other B-Vitamin levels (if taken a B-Complex) ...... at least at a quick and dirty level......this will only be so for the B-1 Thiamine levels if you are taking the Fat Soluble forms with the Magnesium as Knitty Kitty mentioned. Magnesium is a Co-Factor is a Co-factor for both Thiamine and Vitamin D and your sons levels won't improve unless he also takes Magnesium with his Thiamine and B-Complex. You will notice his energy levels really pick up.  His sleeping will improve and his muscle cramps will get better from the Magnesium! Here is nice blog post that can help you Thiamine and it's many benefits. I hope this is helpful but it is not medical advice God speed on your son's continued journey I used to be him. There is hope! 2 Tim 2:7 “Consider what I say; and the Lord give thee understanding in all things” this included. Posterboy by the grace of God,  
    • trents
      I'll answer your second question first. The single best antibody test for monitoring celiac blood antibody levels is the tTG-IGA and it is very cost effective. For this reason, it is the most popular and often the only test ordered by physicians when checking for celiac disease. There are some people who actually do have celiac disease who will score negatives on this test anyway because of anomalies in their immune system but your wife is not one of them. So for her, the tTG-IGA should be sufficient. It is highly sensitive and highly specific for celiac disease. If your wife gets serious about eating gluten free and stays on a gluten free diet for the duration, she should experience healing in her villous lining, normalization in her antibody numbers and avoid reaching a celiac health crisis tipping point. I am attaching an article that will provide guidance for getting serious about gluten free living. It really is an advantage if all wheat products are taken out of the house and other household members adopt gluten free eating in order to avoid cross contamination and mistakes.  
    • Anmol
      Thanks this is helpful. Couple of follow -ups- that critical point till it stays silent is age dependent or dependent on continuing to eat gluten. In other words if she is on gluten-free diet can she stay on silent celiac disease forever?    what are the most cost effective yet efficient test to track the inflammation/antibodies and see if gluten-free is working . 
    • trents
      Welcome to the community forum, @Anmol! There are a number of blood antibody tests that can be administered when diagnosing celiac disease and it is normal that not all of them will be positive. Three out of four that were run for you were positive. It looks pretty conclusive that you have celiac disease. Many physicians will only run the tTG-IGA test so I applaud your doctor for being so thorough. Note, the Immunoglobulin A is not a test for celiac disease per se but a measure of total IGA antibody levels in your blood. If this number is low it can cause false negatives in the individual IGA-based celiac antibody tests. There are many celiacs who are asymptomatic when consuming gluten, at least until damage to the villous lining of the small bowel progresses to a certain critical point. I was one of them. We call them "silent" celiacs".  Unfortunately, being asymptomatic does not equate to no damage being done to the villous lining of the small bowel. No, the fact that your wife is asymptomatic should not be viewed as a license to not practice strict gluten free eating. She is damaging her health by doing so and the continuing high antibody test scores are proof of that. The antibodies are produced by inflammation in the small bowel lining and over time this inflammation destroys the villous lining. Continuing to disregard this will catch up to her. While it may be true that a little gluten does less harm to the villous lining than a lot, why would you even want to tolerate any harm at all to it? Being a "silent" celiac is both a blessing and a curse. It's a blessing in the sense of being able to endure some cross contamination in social settings without embarrassing repercussions. It's a curse in that it slows down the learning curve of avoiding foods where gluten is not an obvious ingredient, yet still may be doing damage to the villous lining of the small bowel. GliadinX is helpful to many celiacs in avoiding illness from cross contamination when eating out but it is not effective when consuming larger amounts of gluten. It was never intended for that purpose. Eating out is the number one sabotager of gluten free eating. You have no control of how food is prepared and handled in restaurant kitchens.  
    • knitty kitty
      Forgot one... https://www.hormonesmatter.com/eosinophilic-esophagitis-sugar-thiamine-sensitive/
×
×
  • Create New...