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 Our Content
    eNewsletter
    Donate

Emotions Following Thanksgiving


Scout1996

Recommended Posts

Scout1996 Newbie

Hi Celiac community! 

I am new here. Thanksgiving weekend made me realize I am desperately needing to connect with other folks with Celiac! 

My name is Scout. I am 25 and over the weekend, I had my first Thanksgiving with my fiance's family. I feel VERY LUCKY that they were willing to prepare an entirely gluten-free meal, use new kitchen utensils and cutting boards, etc. But I couldn't help but feel horrible the entire weekend. I feel guilty that I caused them to have to do these things and take these precautions, and I also felt incredibly singled out all weekend. I know it was well-intentioned, but all weekend everyone was talking about celiac, people they knew with celiac, and my celiac. It was like I could not get a break from hearing about the thing that brings me so much suffering. I'm feeling very drained today from it all. I just wish I did not have to deal with celiac AT ALL. My fiance and I have a strictly gluten-free house, and we have decided to not even speak of gluten or celiac all week so I can recover. 

How do you all deal with emotions related to feeling singled out/like an inconvenience? 

I've been diagnosed for four years now, but sometimes it seems like this thing never gets easier. 


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



Celiac.com Sponsor (A8-M):



Scott Adams Grand Master

Welcome to the forum! 

We have a PhD who has written extensively about this topic for Celiac.com, and you can find her articles here:

I think you are very lucky that they're willing to go out of their way for you, and seem to understand why it's necessary. I also know just how you feel, and probably every celiac does...most of the time you probably don't want people to make a fuss because of you, and it's easy to feel guilty when they do, and it creates more hassle for them.

Above all I think it's important to be thankful for such people, and it might be a good idea to write them an old-fashioned thank you card to let them know how much you appreciate their consideration. Perhaps you can even one day host them?

trents Grand Master

Yes, as Scott said, hosting your fiance's family would be a goodwill gesture and would eliminate the hassle for them. You might even consider cooking some non-gluten dishes just for them if you can do so safely.

RMJ Mentor

It is great that your future in-laws took such good care of you.  We get too many posts here from people whose families don’t believe their celiac diagnosis, try to get them to eat “just a little gluten,” etc.

This was probably all very new for your fiance’s family.  I would guess that next time they serve you gluten free food they won’t talk about it as much, and soon it will be routine for them.

trents Grand Master

Yes, RMJ is spot on. People adjust to a new reality over time and it becomes the norm. Your future in-laws seem to be sensitive, quality people. But be prepared for the fact that not everyone in your social circle will react so graciously. So, it's a good idea to think ahead of some scenarios that might develop and to be prepared with a gracious response. There's usually a weird uncle Alvin in every family who is kind of a jerk and will not accept the medical reality of your condition.

Scout1996 Newbie

Thank you all for your kind responses. I really do appreciate and feel very lucky to have these folks as my new extended family! They are great. I am hoping it becomes routine for them soon enough, as it has for my fiancé. We sometimes even just forget we're a gluten-free household since we're both so used to eating this way. 

It is definitely hard to not feel like a hassle/inconvenience. I usually just bring granola bars in my purse to social situations and eat those to avoid making people do a whole thing for me. I'm working really hard on asserting myself and not feeling so bad about requesting my condition be accommodated, because as Trents said above, it's a medical reality.

 

AlwaysLearning Collaborator

OMG. Marry your fiancé as quickly as possible! What a great family that they are willing to try something new to help others be included! 

I wouldn't worry too much about the next time. The novelty of your celiac disease will wear off and it won't be talked about so much. And you can make a plan with the cook to only worry about making a few dishes gluten free while others are not and you simply don't eat them. Like stuffing would be great to make gluten free because stuffing could also contaminate the bird if it is stuffed. (For traditional stuffing, I would use gluten free French bread as a base though you'd likely have to make it yourself. If you don't stuff the bird or are eating ham instead of turkey, corn bread stuffing should already be gluten free.)

And you can make a plan for bringing food with you. For instance, I normally bring a bunch of appetizers to family gatherings so that I can munch before the meal along with everyone else and no one even notices that everything I bring is gluten free. Fruit, veggies, artisan salami, nut-based crackers, cheeses, shrimp ... all gluten free.

My hosts wouldn't even dream of trying to cook gluten free so what I normally do is to make and bring a meal that is really similar to what I expect will be served. When dinner is out of the kitchen and on the table, I quick, slip a plate into the microwave and then eat with everyone else. (For weddings, I bring a small cooler that is slyly slid under the table. When everyone else is served, I just miraculously produce my salad or whatever cold dish I can make and bring.) Just don't forget to bring a dessert for yourself and be willing to share your food with others.


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



Celiac.com Sponsor (A8-M):



EmmaW Newbie

Hi Scout,

It gets easier. But truthfully travel and holiday celebrations are the hardest. We all want to just feel normal. It was very nice of them to accommodate you. Maybe they went a little overboard. I usually tell my friends and family that I don't have an expectation that every single item is gluten free. I just like to make sure that what is gluten free is prepared safely. As long as I have some food to eat, its all good.

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      126,112
    • Most Online (within 30 mins)
      7,748

    cam4180
    Newest Member
    cam4180
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.2k

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)

    • There are no registered users currently online

  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • StaciField
      There’s a Cosco in Auckland in New Zealand. It’s a bit away from where I live but it’s worth the travel for me. Very appreciative of your advice.
    • Wheatwacked
      It seems you have proven that you cannot eat gluten.  You've done what your doctors have not been able to do in 40 years. That's your low vitamin D, a common symptom with Celiac Disease.  Zinc is also a common defiency.  Its an antiviral.  that's why zinc gluconate lozenges work against airborne viruses.  Vitamin D and the Immune System+ Toe cramps, I find 250 mg of Thiamine helps.   When I started GFD I counted 19 symptoms going back to childhood that improved with Gluten Free Diet and vitamin D. I still take 10,000 IU a day to maintain 80 ng/ml and get it tested 4 times a year. Highest was 93 ng/ml and that was at end of summer.  Any excess is stored in fat or excreted through bile.   The western diet is deficient in many nutrients including choline and iodine.  Thats why processed foods are fortified.  Celiac Disease causes malabsorption of vitamins and minerals from the small intestine damage.  GFD stops the damage, but you will still have symptoms of deficiency until you get your vitamins repleted to normal.  Try to reduce your omega 6:3 ratio.  The Standard American Diet is 14:1 or greater.  Healthy is 3:1.  Wheat flour is 22:1.  Potatoes are 3:1 while sweet potatoes are 14:1.  So those sweet potatos that everyone says is better than Russet: they are increasing your inflammation levels.   
    • Scott Adams
      My mother also has celiac disease, and one of her symptoms for many years before her diagnosis was TMJ. I believe it took her many years on a gluten-free diet before this issue went away.
    • Jeff Platt
      Ear pain and ringing your entire life may or may not be TMJ related but could be something else. A good TMJ exam would be helpful to rule that out as a potential cause from a dentist who treats that. I have teens as well as adults of all ages who suffer from TMJ issues so it’s not a certain age when it shows up.   
    • cristiana
      Not sure if related to coeliac disease but my ear ringing  has stepped up a notch since diagnosis.  Even since a child silence really hurts my ears - there is always a really loud noise if there is no other noise in a quiet room - but my brain has learned to filter it out.  Since diagnosis in my forties I also get a metallic ringing in my ears, sometimes just one, sometimes both.  But it comes and goes.   My sister also suffers now, we are both in our fifties, but she is not a coeliac, so for all I know it could just be an age thing.  I do get occasional stabbing pain in my ears but that has been all my life, and I do appear to be vulnerable to outer ear infections too.  So not a particularly helpful reply here, but I suppose what I am trying to say is it might be related but then again it could just be one of those things.   I think in the UK where I live doctors like you to report if you get tinnitus in just the one ear.  I reported mine but no cause was found.  Most of the time it is nothing but sometimes it can have a cause that can be treated, so perhaps worth reporting to your GP.  
×
×
  • Create New...