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

Family Get Togethers


Firegirl43

Recommended Posts

Firegirl43 Contributor

It is getting to the point that I really hate family get togethers,. Thanksgiving we all went to my cousins house, I had my own food, But I felt like I stuck out. My food had to be microwaved and was on a seperate plate from everyone else. Everyone there kept makeing a big deal about it, asking me well well cant you have some of the cheese( which was covered in bread crumbs) or the fruit . I dont think anyone really understands, I mean a few people try but I know some of my family think that I am gluten-free by choice. To be honest I really dont care if I go to another family thing. All I do is feel way too diffrent ( I know thats not a bad thing) way too segregated. :(


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



Celiac.com Sponsor (A8-M):



MaryJones2 Enthusiast

I do know how you feel. I've been at this a few years and have a very large family that gets together a few times a year. I bring my own food too and prefer to do so. I am just there to have a good time and enjoy the company but occasionally the conversation turns to my diet or my food and before I (or my husband) can successfully change the subject someone makes some offhanded comment. I try to take it all in stride but sometimes it's a little difficult.

Tamradee Newbie

Hi, I avoided Thanksgiving all together this year. I get sick just smelling other people's food ;) . Of course, I proceeded to make an entire feast for my family - I have to avoid gluten, sulfites and msg - that was 100% safe for me and my daughter (and the whole family) to eat. It's not THAT difficult - I just wish that the rest of the family would make an effort!!!

I will do Christmas with the extended family this year - but will bring lots of goodies for me & my daughter so that we are not tempted to *try* something and be sick for the entire day. Of course, I'm sure we'll be sick anyway - it just seems unavoidable. Inevitably someone will attempt to talk me into trying something and I'll suffer from temporary amnesia and not remember all the things I can't eat and I'll cave in, eat and commence suffering!!!!!

sickchick Community Regular

You know what I do?

I eat @ my apartment then I go and run around and visit my family.

I find it works for me.

Be well and BE PATIENT WITH YOURSELF B)

lovelove

Lori T. Newbie
It is getting to the point that I really hate family get togethers,. Thanksgiving we all went to my cousins house, I had my own food, But I felt like I stuck out. My food had to be microwaved and was on a seperate plate from everyone else. Everyone there kept makeing a big deal about it, asking me well well cant you have some of the cheese( which was covered in bread crumbs) or the fruit . I dont think anyone really understands, I mean a few people try but I know some of my family think that I am gluten-free by choice. To be honest I really dont care if I go to another family thing. All I do is feel way too diffrent ( I know thats not a bad thing) way too segregated. :(

know how you feel. Diagnosed X2 yrs and still get question after question, which is not so bad, but then I get the ever helpful "but I am sure a little taste won't kill you". Oh, yeah, it will!! At least it will feel that way. Usually understanding family members who just choose to ignore my problems for theirs, become the ever knowledgable ones during times with friends and outside guests around. I get "she can't try that. She's on that gluten diet thing" or "She has some kind of an allergy.What is it that you can't eat Lori??" Explanations turn into people staring blankly at me. I feel like just saying I am Gluten intolerant should do it but then they persue the issue and I further explain. Then they slowly start to walk away like I am a leper. And I know what you mean about the food. I always bring my own food for small gatherings or a dish I know I can eat but that anyone else could too. Now that everyone knows, the first thing I get asked at a party is "Is that one of those Gluten Free things that you made?". If I say "Yes", they hesitate and will not try it. Have even brought standard Spinach Dip_

Spinach,Artichokes,cream cheese, mayo, parmesan and pepper and bake it-and no one would try it thinking I guess that it will taste funny. Even after I tell how simple/normal the recipe is. People are funny. If it were them, maybe they would not want anyone to know and keep it inside. I feel as if I need to connect with other people. Food issues are just one piece of who I am. I just refuse to sit in the corner. Even though I feel like the only human who is gluten-free sometimes, I still refuse to let others ignorance dictate my social life. REAL friends don't stare, make comments or leave you out of the loop. One thing about gluten-free life, you find out who the REAL friends are!!!

ang1e0251 Contributor

I think if we want to be social, we just have to put up with the ignorance and cut non-celiacs some slack. After all, I have a friend 15 yrs celiac and I thought I knew the basics. What I knew could fit on the head of a pin compared to what I've learned this past year while I was on the diet. And there is so much more to learn! We really can't expect those who have never had this disease to know where we're coming from. You wouldn't be angry at a child who asked a question about a subject that they knew nothing about. Don't expect others to know about your condition.

I do wish my family had higher standards and tried harder to educate themselves but I see that most families written about on the forum are just like mine. My sister is diabetic and if I'm with her I just ask her my diabetic q's. I'm sure she feels the same with me. It's just easier to ask me. I don't want to feel like an outsider or frustrated with my family over this. I have chosen to let it go and take care of myself.

I can't tell you how to feel but I will say that I found it incredibally liberating and a big load off my shoulders when I chose not to fault others for what they don't know. I refuse to lose my family and friends to this disease!

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. - Scott Adams replied to MauraBue's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Have Tru Joy Sweets Choco Chews been discontinued??

    2. - Jmartes71 replied to chrish42's topic in Doctors
      7

      Doctors and Celiac.com

    3. - Wheatwacked replied to MauraBue's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Have Tru Joy Sweets Choco Chews been discontinued??

    4. - Theresa2407 replied to chrish42's topic in Doctors
      7

      Doctors and Celiac.com

    5. - Scott Adams replied to MauraBue's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Have Tru Joy Sweets Choco Chews been discontinued??

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

    • Total Members
      133,266
    • Most Online (within 30 mins)
      7,748

    Barbara lynn
    Newest Member
    Barbara lynn
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Scott Adams
      But M&M's contain milk, and would not be at all like a Tootsie Roll.
    • Jmartes71
      I appreciate you validating me because medical is an issue and it's not ok at all they they do this. Some days I just want to call the news media and just call out these doctors especially when they are supposed to be specialist Downplaying when gluten-free when they should know gluten-free is false negative. Now dealing with other issues and still crickets for disability because I show no signs of celiac BECAUSE IM GLUTENFREE! Actively dealing with sibo and skin issues.Depression is the key because thats all they know, im depressed because medical has caused it because of my celiac and related issues. I should have never ever been employed as a bus driver.After 3 years still healing and ZERO income desperately trying to get better but no careteam for celiac other than stay away frim wheat! Now im having care because my head is affected either ms or meningioma in go in tomorrow again for more scans.I know im slowly dying and im looking like a disability chaser
    • Wheatwacked
      M&M Peanuts. About the same calories and sugar while M&M Peanuts have fiber, potassium, iron and protein that Tootsie Rolls ("We are currently producing more than 50 million Tootsie Rolls each day.") don't. Click the links to compare nutritional values.  Both are made with sugar, not high fructose corn syrup.  I use them as a gluten free substitute for a peanut butter sandwich.  Try her on grass fed, pasture fed milk. While I get heartburn at night from commercial dairy milk, I do not from 'grassmilk'.     
    • Theresa2407
      I see it everyday on my feeds.  They go out and buy gluten-free processed products and wonder why they can't heal their guts.  I don't think they take it as a serious immune disease. They pick up things off the internet which is so far out in left field.  Some days I would just like to scream.  So much better when we had support groups and being able to teach them properly. I just had an EMA blood test because I haven't had one since my Doctor moved away.  Got test results today, doctor ordered a D3 vitamin test.  Now you know what  type of doctors we have.  Now I will have to pay for this test because she just tested my D3 end of December, and still have no idea about my EMA.    
    • Scott Adams
      Some of the Cocomels are gluten and dairy-free: https://cocomels.com/collections/shop-page
×
×
  • 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.