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

pretty in paleo

Recommended Posts

pretty in paleo Apprentice

Well I'm sure I'm not the only one. But its so awkward when someone reacts to my gluten free status by purchasing food for me. And most of the time its not even gluten free (they thought it was). Or its got a ton of other crap that would give me indigestion. Then I feel kinda bad and offer to pay them back, and remind them that gluten is just one of many foods I avoid. Did anyone else go thru this situation??


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



Celiac.com Sponsor (A8-M):



deb445 Rookie

Oh, you are not alone. I find that there is sometimes even an uncomfortable tension - these poor well meaning friends and family feel that they've gone out of their way to accomodate, and then I break the news that while I'm grateful, I can't eat it. I know my wonderful Mother in Law has been a little miffed at times, and I feel bad (I bring this one myself - she doesn't make me feel bad) almost to the point of eating it just so she won't feel tense at having gone to the effort and expense.

Tricky.

And then there are the kind people who bring "gluten-free" food to a pot luck, but I've been paranoid that it may be contaminated. They just want to please, I know.

pretty in paleo Apprentice

Yeah there are people in my family that give me a hard time in this situation. Like my aunt, she insisted on stopping by a gluten free bakery despite me saying most of that stuff is made with oats, which make my throat swell. Surprise, surprise, she got upset that nobody ate it.

Oh, you are not alone. I find that there is sometimes even an uncomfortable tension - these poor well meaning friends and family feel that they've gone out of their way to accomodate, and then I break the news that while I'm grateful, I can't eat it. I know my wonderful Mother in Law has been a little miffed at times, and I feel bad (I bring this one myself - she doesn't make me feel bad) almost to the point of eating it just so she won't feel tense at having gone to the effort and expense.

Tricky.

And then there are the kind people who bring "gluten-free" food to a pot luck, but I've been paranoid that it may be contaminated. They just want to please, I know.

cap6 Enthusiast

My response is just to say thanks, i appreciate the thought but I have had to make it a rule to only eat things prepared in my own kitchem/not at anyone elses kitchen....

Greebo115 Rookie

I always say that I have celiac disease and so many allergies or intolerances that it's impossible to buy ANYTHING ready-made and that I only eat food that I've made myself. Then, depending on the person, I might add: to save you the hassle of ringing an ambulance when I puke on the carpet, stop breathing and go unconscious.

That usually does the trick (even if not completely true). I had a moment at a knit'n'natter group where a new member tried to pressure me into eating just one piece or shortbteaf and all the existing memebers almost shouted "NO! She'll get really ill" - I think it pays to get in there first, before the situation arises.

With my best friend, I have explained thoroughly, and she has seen a couple of my mistakes, so she understands, but I always make sure she sees me eating my food before we go into any place to 'eat'. That way, she doesn't feel bad when I order coffee but she wants to get some food. There's nothing like thinking there's a starving person watching you eat, to put you off your food or provoke a 'can you eat this? or this? or this?' situation..

TheHeartRN Newbie

I have just been diagnosed with Celiac and I am so afraid of this....

pretty in paleo Apprentice

That reminds me of another habit I've acquired, which is when there is a social event that may last all day, make sure the host is very clear on why you only bring your own food. I'm going to a baby shower and the host is cooking everything. Honestly I'm worried since she seems clueless about wheat (offered me brownies after I explained I was allergic to wheat, dairy!!)

I always say that I have celiac disease and so many allergies or intolerances that it's impossible to buy ANYTHING ready-made and that I only eat food that I've made myself. Then, depending on the person, I might add: to save you the hassle of ringing an ambulance when I puke on the carpet, stop breathing and go unconscious.

That usually does the trick (even if not completely true). I had a moment at a knit'n'natter group where a new member tried to pressure me into eating just one piece or shortbteaf and all the existing memebers almost shouted "NO! She'll get really ill" - I think it pays to get in there first, before the situation arises.

With my best friend, I have explained thoroughly, and she has seen a couple of my mistakes, so she understands, but I always make sure she sees me eating my food before we go into any place to 'eat'. That way, she doesn't feel bad when I order coffee but she wants to get some food. There's nothing like thinking there's a starving person watching you eat, to put you off your food or provoke a 'can you eat this? or this? or this?' situation..


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



Celiac.com Sponsor (A8-M):



GottaSki Mentor

Welcome HeartRN!

 

Good news is you have been diagnosed when awareness is on the rise -- bad news is you have to be responsible for everything that goes in your mouth. 

 

More GOOD news -- it really does get easier, although the learning curve is tough.

 

Make sure you read the "newbie 101" thread -- loads of good intel there.

 

Everyone in this thread -- hang in there and ask for help getting through it right here -- it really does speed the process :)

Stern Newbie

I've had this exact thing happen to me as well. x_X I went to the beach for a long weekend with my best friend and her family. I had told them that I would bring my own food (I don't just stay away from gluten, I've tested postitive {and react to} seven more major foods), but they wanted to be nice, and they got an entire bag of gluten-free stuff that I couldn't eat (Usually because of soy). They were pretty nice about it, and they've told me that if I ever come with them again, to give them a list and they'll find more that I can eat when I come with them, but I'm thinking I'll probably just bring my own anyway, since I have it on hand, and it's not the cheapest out there.

 

I can't imagine going through this with someone I didn't know as well as my best friend, just because I know her and her family, and I could see that they started understanding after that (AKA I haven't been offered a gluten cupcake anymore, since my best friend's sister is a baker).

Pegleg84 Collaborator

Yep, while I appreciate the efforts people make. I always insist not to make a fuss over me. I'll take care of myself. Often friends/family will ask if they should make something gluten-free just so I can eat it. If I'm the only one going to something, I say no! Let everyone else enjoy it instead. I'll bring something else.

 

Last thanksgiving my man and I went to his parents for dinner. Of course, the week before, he asks "Mom wants to know what you can eat" Of course, I say don't fuss over me. Of course, being the sweetie that she is, his mom got a gluten-free (no stuffing in it) turkey, made the gravy with corn starch, got me cookies, etc etc. Which was very sweet, but next time I'll be sure to insist they don't do anything special.

I also found the same thing staying at B&B's in England this fall. So accommodating! but almost too accommodating. No, I don't really want this over-processed brownie for breakfast, and you really didn't have to get a whole box of cereal just for me...

My man is also guilty of the "I found this gluten free thing!" problem, only to find out it's go hidden soy or dairy, or made on the same lines, or some other reason why I refuse to touch it. there's still a "gluten removed" beer in my fridge that I'm petrified to touch.

 

So, be thankful for the thoughfulness, but politely decline. If the package hasn't been opened, you could suggest they donate it to a food bank or something?

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,244
    • Most Online (within 30 mins)
      7,748

    Nicky2925NZ
    Newest Member
    Nicky2925NZ
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      No, I would not say this at all. If you were diagnosed with celiac disease and were gluten-free for a while, you could have gone into remission. Everyone's body is different, and some celiacs may be able to get regular contamination and not end up with damaged villi and positive antibody tests, while others who ingest tiny amounts will relapse and have full blown symptoms and flattened villi.  Only a full gluten challenge would reveal where you are at this point. Here is more info about how to do a gluten challenge for a celiac disease blood panel, or for an endoscopy: and this recent study recommends 4-6 slices of wheat bread per day:    
    • Scott Adams
      The most common nutrient deficiencies associated with celiac disease that may lead to testing for the condition include iron, vitamin D, folate (vitamin B9), vitamin B12, calcium, zinc, and magnesium.  Unfortunately many doctors, including my own doctor at the time, don't do extensive follow up testing for a broad range of nutrient deficiencies, nor recommend that those just diagnosed with celiac disease take a broad spectrum vitamin/mineral supplement, which would greatly benefit most, if not all, newly diagnosed celiacs.      
    • Pablohoyasaxa
      Great  post. The skin issue can be intolerable. I have been taking niacinamide for the past month and have improved with respect to the blistering lesions. 
    • knitty kitty
      I've found taking Niacin Vitamin B 3 in the form that causes flushing (nicotinic acid) helps immensely to clear my skin.  The flushing is harmless and goes away the longer Niacin is taken.  The flushing (vasodilation in the skin) helps the body get rid of the tTg 3 IgA antibodies that cause the blisters.  TTg 2 IgA antibodies are found in the blood and are measured in diagnostic testing for Celiac.  People with Dermatitis Herpetiformis make tTg 3 as well as tTg 2 antibodies.  Niacin Vitamin B3 in the non flushing form niacinamide also works without the flushing, but takes a bit longer.   I also avoid foods containing high levels of iodine because iodine activates the tTg 3 IgA antibodies to become more active and make more blisters.  I avoid kelp (nori, seaweed) and crustaceans,  eggs, dairy products, and iodized table salt.   Niacinamide and Nicotinic acid are water soluble and harmless.  I'd much rather take Niacin than Dapsone with scary side effects.  
    • meghanf
      We have a gluten-free household. It's the least stressful option. No one else in my family has Celiac, but they are all extremely supportive. We don't even have Play-doh for this kids.
×
×
  • Create New...