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

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
      132,563
    • Most Online (within 30 mins)
      7,748

    Bob Madden
    Newest Member
    Bob Madden
    Joined

  • Celiac.com Sponsor (A20):



  • Celiac.com Sponsor (A22):




  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • Scott Adams
      Oats naturally contain a protein called avenin, which is similar to the gluten proteins found in wheat, barley, and rye. While avenin is generally considered safe for most people with celiac disease, some individuals, around 5-10% of celiacs, may also have sensitivity to avenin, leading to symptoms similar to gluten exposure. You may fall into this category, and eliminating them is the best way to figure this out. Some people substitute gluten-free quinoa flakes for oats if they want a hot cereal substitute. If you are interested in summaries of scientific publications on the topic of oats and celiac disease, we have an entire category dedicated to it which is here: https://www.celiac.com/celiac-disease/oats-and-celiac-disease-are-they-gluten-free/   
    • knitty kitty
    • knitty kitty
      Hi, @Ginger38, I've had shingles in the past.  I understand how miserable you're feeling.   Not only do i have the chickenpox virus lurking about, I also have the cold sore virus that occasionally flares with a huge cold sore on my lip when stressed or exposed to gluten.  The virus lives dormant in the nerves on the left side of my face.  It causes Bell's Palsy (resulting in drooling).  The cold sore virus is also in my eye.  My eye swells up and my vision is diminished permanently whenever I have a flare, so it's of the utmost importance to keep flares away and treat them immediately if they do happen so I don't lose any more vision.   I take the amino acid supplement L-Lysine.  Lysine messes with the replication of viruses, which helps the body fight them off.   I haven't had an outbreak for several years until this year when exceptionally stressed and contaminated, it flared up again. Lysine has been shown to be beneficial in suppression of viruses like the cold sore virus (a herpetic virus), the chickenpox virus (also a herpetic virus), as well as the HIV virus, and even the Covid virus.   I also take additional Thiamine in the form TTFD (tetrahydrofurfuryl disulfide) because Thiamine has antiviral properties as well.   For pain, a combination of Thiamine (like TTFD or Benfotiamine or Thiamine Hydrochloride), with B12 Cobalamine, and Pyridoxine B6 have been shown to have analgesic properties which relieve pain and neuropathy.    The combination of Thiamine B1, Pyridoxine B6 and Cobalamine B12 really does work to relieve pain.  I take it for back pain from crushed vertebrae in my back.  This combination also works on other pain and neuropathy.   I usually buy a supplement that combines all three and also Riboflavin B2 called EXPLUS online.  However, it's made in Japan and the price with the tariffs added makes it really expensive now.  But the combination of Thiamine B1, Pyridoxine B6 and B12 Cobalamine (and Riboflavin B2) still work even if taken separately.   I can't take Tylenol or ibuprofen because of stomach upsets.  But I can take the vitamin combination without side effects.  However, you can take the three vitamins at the same time as other pain relievers for added benefit.  The vitamins help other pain relievers work better. I hope you will try it.  Hopeful you'll feel better quickly. Interesting Reading: Thiamine, cobalamin, locally injected alone or combination for herpetic itching: a single-center randomized controlled trial https://pubmed.ncbi.nlm.nih.gov/23887347/ Mechanisms of action of vitamin B1 (thiamine), B6 (pyridoxine), and B12 (cobalamin) in pain: a narrative review https://pubmed.ncbi.nlm.nih.gov/35156556/ Analgesic and analgesia-potentiating action of B vitamins https://pubmed.ncbi.nlm.nih.gov/12799982/ A Narrative Review of Alternative Symptomatic Treatments for Herpes Simplex Virus https://pmc.ncbi.nlm.nih.gov/articles/PMC10301284/
    • Mari
      I think, after reading this, that you areso traumatized by not being able yo understand what your medical advisors have been  what medical conditions are that you would like to find a group of people who also feel traumatized who would agree with you and also support you. You are on a crusade much as the way the US Cabinet  official, the Health Director of our nation is in trying to change what he considers outdated and incorrect health advisories. He does not have the education, background or experience to be in the position he occupies and is not making beneficial decisions. That man suffered a terrible trauma early in his life when his father was assonated. We see now how he developed and worked himself into a powerful position.  Unless you are willing to take some advice or  are willing to use a few of the known methods of starting on a path to better health then not many of us on this Celiac Forum will be able to join you in a continuing series of complaints about medical advisors.    I am almost 90 years old. I am strictly gluten free. I use 2 herbs to help me stay as clear minded as possible. You are not wrong in complaining about medical practitioners. You might be more effective with a clearer mind, less anger and a more comfortable life if you would just try some of the suggestions offered by our fellow celiac volunteers.  
    • Jmartes71
      Thus has got to STOP , medical bit believing us! I literally went through 31 years thinking it was just a food allergy as its downplayed by medical if THEY weren't the ones who diagnosed us! Im positive for HLA-DQ2 which is first celiac patient per Iran and Turkey. Here in the States especially in Cali its why do you feel that way? Why do you think your celiac? Your not eating gluten so its something else.Medical caused me depression. I thought I was safe with my former pcp for 25 years considering i thought everything I went through and going through will be available when I get fired again for health. Health not write-ups my health always come back when you're better.Im not and being tossed away at no fault to my own other than shitty genes.I was denied disability because person said he didn't know how to classify me! I said Im celiac, i have ibs, hernia, sciatica, high blood pressure, in constant pain have skin and eye issues and menopause intensified everything. With that my celiac nightmare began to reprove my disregarded disease to a bunch of clowns who think they are my careteam when they said I didn't have...I feel Im still breathing so I can fight this so no body else has to deal with this nightmare. Starting over with " new care team" and waisting more time on why I think I am when diagnosed in 1994 before food eliminated from my diet. P.s everything i went through I did write to medical board, so pretty sure I will continue to have a hard time.
×
×
  • 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.