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

I'm Really Over All The Insensitive Comments, 6Yr gluten-free


sunnyfla

Recommended Posts

sunnyfla Newbie

I've been gluten free for at least 6 years and at first it was REALLY hard, not so much missing the food as odd at that sounds (I think not being so sick made giving it all up easier, maybe if I hadn't it would have been different).  I was more depressed and upset because I was excluded from so many social things or at the end of snide comments. 

 

I remember one time someone who I thought was a friend saying oh just have a diet coke if you really want to come along for dinner with us. 

You know what happens when you do that, everyone stares at you and tries to give you just one bite and you get to forever explain that you can't, so then the next time oh gee sorry we forgot to let you know we were going out...

 

Eating out is so hit or miss,  I know you all understand but it is so hard for others to get it because I don't break out in welts like a peanut allergy, although I will react to flour in the air with red itchy blotchy skin so now I carry an epipen.

 

So this last week, someone who has been a friend for over 20 years and recently moved here had me in tears over the way I handled explaining needing food gluten free.  The server asked what would happen and I said I would spend a lot of time in the bathroom later and be very sick with headaches and body aches.  So the next day she told me, at all places the dinner table, that discussing that while I was out was inappropriate conversation for mealtime.  Mind you she is the sort that nothing is beyond discussion so I was shocked and hurt, especially given I did not go into any sort of graphic details.  She also glutened me about a year ago so she knows what just a tiny bit will do to me so I was just dumbfounded and hurt over this most recent thing. 

 

Normally I would just quietly explain and if I got sick not say or do anything and then one day I met this tiny girl who looked about 4 who was actually 8 and I found out she almost died from undiagnosed celiac disease.  From that point on I've been more vocal about not safe restaurant meals when we do eat out, not just for me but for everyone else and especially her to be safe. 

 

I had another episode on Sunday where they screwed up my brunch omelet at Bonefish grill and I ended up waiting for a hastily fixed meal while my family ate and were almost done by the time I could eat.  The worst was the treatment by the staff. 

 

I came home and had a pity party, why does it have to be so hard?

 

 

 


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



Celiac.com Sponsor (A8-M):



qlwmdw Newbie

I've been gluten free for at least 6 years and at first it was REALLY hard, not so much missing the food as odd at that sounds (I think not being so sick made giving it all up easier, maybe if I hadn't it would have been different).  I was more depressed and upset because I was excluded from so many social things or at the end of snide comments. 

 

I remember one time someone who I thought was a friend saying oh just have a diet coke if you really want to come along for dinner with us. 

You know what happens when you do that, everyone stares at you and tries to give you just one bite and you get to forever explain that you can't, so then the next time oh gee sorry we forgot to let you know we were going out...

 

Eating out is so hit or miss,  I know you all understand but it is so hard for others to get it because I don't break out in welts like a peanut allergy, although I will react to flour in the air with red itchy blotchy skin so now I carry an epipen.

 

So this last week, someone who has been a friend for over 20 years and recently moved here had me in tears over the way I handled explaining needing food gluten free.  The server asked what would happen and I said I would spend a lot of time in the bathroom later and be very sick with headaches and body aches.  So the next day she told me, at all places the dinner table, that discussing that while I was out was inappropriate conversation for mealtime.  Mind you she is the sort that nothing is beyond discussion so I was shocked and hurt, especially given I did not go into any sort of graphic details.  She also glutened me about a year ago so she knows what just a tiny bit will do to me so I was just dumbfounded and hurt over this most recent thing. 

 

Normally I would just quietly explain and if I got sick not say or do anything and then one day I met this tiny girl who looked about 4 who was actually 8 and I found out she almost died from undiagnosed celiac disease.  From that point on I've been more vocal about not safe restaurant meals when we do eat out, not just for me but for everyone else and especially her to be safe. 

 

I had another episode on Sunday where they screwed up my brunch omelet at Bonefish grill and I ended up waiting for a hastily fixed meal while my family ate and were almost done by the time I could eat.  The worst was the treatment by the staff. 

 

I came home and had a pity party, why does it have to be so hard?

I completely get where you are coming from.  I have for the most part given up on eating out, it just seems like a pointless exercise to me.  All I do is worry constantly about cross-contamination and not to mention the fact that my work puts me in the back of house of many restaurants; so I get to see things that I wish I hadn't seen.  I have Celiac and it very nearly killed me literally, but even after being gluten free for oh five years now it's still no cake-walk.  It really is depressing... to add insult to injury I also have intolerances to sugar alcohols, preservatives, nuts, milk, carageenan, xanthan gum, the list goes on and on; luckily I'm not dangerously allergic to anything, well yet at least, but it makes eating even at home a massive challenge.  So much to the point that I eat the same thing for breakfast and dinner every single day; I don't even bother with lunch since that makes things worse with the old "Abominable Bowel Syndrome" as I like to call it because after seeing, hearing, and writing IBS out so many times it really just gets old so I try to have some modicum of humor with it.  Sheesh look at my rant, sorry just wanted to let you know you are without a doubt not alone in this wretched misery; I used to tell myself that I don't miss the food, and like you my reasons were very sound in that the food was not worth the punishment; and anyone that says otherwise has never felt the pain and nerve wracking sensations of being "glutened."  However, I do really miss the food, or at least the ability to eat something different or like yourself just able to share the experience with family and friends, because eating is a social occasion.  For some of us though it's a necessary evil.

CK1901 Explorer

Do you have any support organizations in your area? I haven't tried this yet, but I've thought about it. It would be nice to go out and eat with some other folks that really understand. I've kind of given up on my family being nice or competent about it. I have a few friends that will at least tolerate me instead of being outright mean about it. Others have been jerks. Following this kind of diet requires an intense amount of discipline and I try to let knowledge make me feel better instead of worse. Imagine all the other things that we are capable of overcoming and mastering given that we utilize that much discipline as part of just a regular day. 

mommida Enthusiast

It's times like this when you find out who your friends are.

You find out how strong you are.

 

..and you figure out how to keep on going.  Sometimes you need to drop the baggage of crappy relationships.

 

Getting diagnosed can be like a liberation, from getting sick and from sickening people. ;)

mamaw Community Regular

I  think  this  is one aspect  of being  gluten-free  for health  reasons  is so  hard.. We  mostly  don't  appear to be ill or  look  like  we  have a serious  disease....plus  for  the  layperson  who knows  nothing about  health issues  just  can't  wrap  their head  around  a  statement  that  eating  food  could make  us  terribly  ill not  to mention  developing  a  cancer...I  quit  a long  time ago  trying to make  family  &  supposed  to be friends  understand....even some of the  medical community  doesn't  even  understand...

I do go out  to  eat but  always do my homework  first  so  when  with  friends I  know  what  I can order  &  eat  safely..so  no big  scene, I just  state  I'm  gluten-free  please  tell the  chef  &  order  from  what  I decided  before   I  went  into the  restaurant...If  I get a  salad  with  croutons  on it  I just  send  it  back  &  tell them NOT to pick off  the croutons...I  order  very plain  foods, nothing  fancy with  loads  of  sauces, cheese  &  things  that  can  harbor  gluten....For me it is  usually  a  salad NO croutons ,  wild  caught  salmon,,,or  if  I'm at a red robin I do get the burger..I never  order pasta  because  first  it is never cooked  right &  many times  they  cook it in the  wheat  pasta water, never  realizing  that  is  putting  gluten into  our  mouths....

If  I'm  eating breakfast  out  I always ask  about  the  scrambled  eggs  to make  sure  there  is not pancake flour  added to the  scramble....

I always  pick  where to eat  with friends, they give a few places  where they want to go & I say  yes, or no  for me.. Since  they are true friends  they  always go where I can eat  as well...I do  have  other  so called  friends but  I stopped  eating out  with them &  the  stupid  insulting  comments...

A good  support  group  is a wonderful  asset.. Once  you are  there  look  around  &  find  a  non  cheating  ,knowledgeable celiac to  shadow  & learn from..... I know  many celiac  who  have  been gluten-free  for  20  years  but  still don't  understand   or  stay updated on  celiac so  they are  worthless.....

Misinformation  is  worse  than no information  !!!!

hth

Nikki2777 Community Regular

I've never heard of this -- pancake flour gets added to scrambled eggs?  Wow, that's frightening.

 

 

If  I'm  eating breakfast  out  I always ask  about  the  scrambled  eggs  to make  sure  there  is not pancake flour  added to the  scramble....

 

mamaw Community Regular

yes scary for sure! restaurants ( some) add pancake flour to scrambles eggs to make an omelet fluffier... SO always check... I recently found out some places are now doing the same thing with mashed potatoes.....Another thought always ask about mashed potatoes real or boxed to see if they are truly gluten-free....


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,196
    • Most Online (within 30 mins)
      7,748

    Marrianne Kraatz
    Newest Member
    Marrianne Kraatz
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Clearly from what you've said the info on Dailymed is much more up to date than the other site, which hasn't been updated since 2017. The fact that some companies might be repackaging drugs does not mean the info on the ingredients is not correct.
    • RMJ
      To evaluate the TTG antibody result we’d need to know the normal range for that lab.  Labs don’t all use the same units.  However, based on any normal ranges that I’ve seen and the listed result being greater than a number rather than a specific number, I’d say yes, that is high! Higher than the range where the test can give a quantitative result. You got good advice not to change your diet yet.  If you went gluten free your intestines would start to heal, confusing any further testing,
    • Bev in Milw
      Scott is correct….Thank you for catching that!      Direct link for info  of fillers.    http://www.glutenfreedrugs.com/Excipients.htm Link is on 2nd page  of www.glutenfreedrugs.com   Site was started by a pharmacist (or 2) maybe 15-20 yrs ago with LAST updated in  2017.  This makes it’s Drug List so old that it’s no longer relevant. Companies & contacts, along with suppliers &  sources would need to be referenced, same amount effort  as starting with current data on DailyMed      That being said, Excipient List is still be relevant since major changes to product labeling occurred prior ’17.           List is the dictionary that sources the ‘foreign-to-us’ terms used on pharmaceutical labels, terms we need to rule out gluten.    Note on DailyMed INFO— When you look for a specific drug on DailyMed, notice that nearly all of companies (brands/labels) are flagged as a ‘Repackager’… This would seem to suggest the actual ‘pills’ are being mass produced by a limited number of wholesaler suppliers (esp for older meds out of  patent protection.).      If so, multiple repackager-get  bulk shipments  from same supplier will all  be selling identical meds —same formula/fillers. Others repackager-could be switching suppliers  frequently based on cost, or runs both gluten-free & non- items on same lines.  No way to know  without contacting company.     While some I know have  searched pharmacies chasing a specific brand, long-term  solution is to find (or teach) pharmacy staff who’s willing help.    When I got 1st Rx ~8 years ago, I went to Walgreens & said I needed gluten-free.  Walked  out when pharmacist said  ‘How am I supposed  to know…’  (ar least he as honest… ). Walmart pharmacists down the block were ‘No problem!’—Once, they wouldn’t release my Rx, still waiting on gluten-free status from a new supplier. Re: Timeliness of DailyMed info?   A serendipitous conversation with cousin in Mi was unexpectedly reassuring.  She works in office of Perrigo, major products of OTC meds (was 1st to add gluten-free labels).  I TOTALLY lucked out when I asked about her job: “TODAY I trained a new full-time employee to make entries to Daily Med.’  Task had grown to hours a day, time she needed for tasks that couldn’t be delegated….We can only hope majorities of companies are as  conscientious!   For the Newbies…. SOLE  purpose of  fillers (possible gluten) in meds is to  hold the active ingredients together in a doseable form.  Drugs  given by injection or as IV are always gluten-free!  (Sometimes drs can do antibiotics w/ one-time injection rather than 7-10 days of  pills .) Liquid meds (typically for kids)—still read labels, but  could be an a simpler option for some products…
    • Ginger38
      So I recently had allergy testing for IGE antibodies in response to foods. My test results came back positive to corn, white potatoes, egg whites. Tomatoes, almonds and peanuts to name a few.  I have had obvious reactions to a few of these - particularly tomatoes and corn- both GI issues. I don’t really understand all this allergy versus celiac stuff. If the food allergies are mild do I have to avoid these foods entirely? I don’t know what I will eat if I can’t  have corn based gluten free products 
    • JForman
      We have four children (7-14 yo), and our 7 year old was diagnosed with NCGS (though all Celiac labs were positive, her scope at 4 years old was negative so docs in the US won't call it celiac). We have started her on a Gluten Free diet after 3 years of major digestive issues and ruling out just about everything under the sun. Our home and kitchen and myself are all gluten-free. But I have not asked my husband/her dad or her other siblings to go completely gluten-free with us. They are at home, but not out of the home. This has led to situations when we are eating out where she has to consistently see others eating things she can't have and she has begun to say "Well, I can't have <fill in the blank>...stupid gluten."  How have you supported your gluten-free kiddos in the mental health space of this journey, especially young ones like her. I know it's hard for me as an adult sometimes to miss out, so I can't imagine being 7 and dealing with it! Any tips or ideas to help with this? 
×
×
  • Create New...