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

Friends Who Don't Get It


QuirkyVeganGirl

Recommended Posts

QuirkyVeganGirl Newbie

Hi! I'm new to the forum. It seems odd to come to strangers for such personal problems, but aside from the love and support form my husband, I'm not getting much feed back. So here I am! :)

 

I've been gluten free for about five months now, aside from multiple accidental glutenings. My husband (not gluten free) and I have ironed out the kinks in our own kitchen, and I finally feel safe when I cook and eat in my own home. The problem arises when my dear friends want to cook or bake for me. My one friend is studying to be a nutritionist, so she feels pretty confident in her philosophies about gluten free eating and other food intolerance issues. And my other friend claims to be gluten sensitive herself (hasn't been tested), however she frequently indulges in foods containing gluten. Whenever I try to explain my situation and how severe my sensitivity is, I feel shot down by them because of their pre-existing notions about gluten sensitivity. Even one crumb can send me into a tailspin of symptoms for days on end! 

 

I have been glutened twice by my sweet nutritionist friend who has gone out of her way to prepare gluten free foods for me. Once was because she was eating gluteney brownies with one hand while preparing my food. And another time was because she used uncertified quick oats in cookies. She said she checked the label and wheat wasn't listed, but that doesn't rule out cross contamination. And my body, as we speak, is arguing her point to the contrary!

 

Both friends believe that the terms Celiac and Non-Celiac refer to the severity of symptoms. In their mind, only Celiacs experience such severe symptoms. 

 

I have a degree in English/Lit, so I'm a person who has learned to research extensively (and secretly enjoy it). I've read hundreds of articles and books on the subject of Celiac and Non-Celiac Gluten Sensitivity. How can I explain these issues to them without alienating them or rejecting their offers of kindness? I love my friends so dearly, and as an introvert with only a few close friends, I'd hate to lose them over something so trivial.

 

Because I don't have Celiac disease, I don't have to worry about the increased risk of intestinal damage, cancer, etc. when I accidentally eat gluten, but even still. Is it worth the ten days of misery not to hurt someone's feelings?


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

You sound like you might have Celiac disease. And it sounds like you were never tested for celiac, so you could have it. Would explain your severe reactions. Maybe you should just tell them you have Celiac and you have been advised to not eat food prepared by others?

BlessedMommy Rising Star

It's tough, but if you know that they can't prepare safe food, I would stick to providing your own food. Either that, or stand in their kitchen and supervise them while they make it.

 

Just explain to them that you get so sick from small amounts that you just can't take the chance.

BlessedMommy Rising Star

Also, due to the small amount of information that is actually available on NCGS, we don't really know what long term health ramifications there are from NCGS people eating small amounts of gluten. 

Jmg Mentor

They sound like good friends. I'll bet if they could just read your post above that would get you 90% of the way there.  

Adalaide Mentor

Also, due to the small amount of information that is actually available on NCGS, we don't really know what long term health ramifications there are from NCGS people eating small amounts of gluten. 

 

This is exactly what I was going to point out. No one knows what your increased health risks are if you have NCGS so it is important to treat it as seriously as celiac.

 

I tell my well meaning friends that even though they're well meaning and thoughtful, I simply do not, ever, under any circumstances, no matter what, PERIOD, eat food that someone else has prepared for me in their own kitchen. It sounds like you need to put your foot down with a rule like this. If they don't understand that things like oats aren't a safe food, their baking pans aren't safe, baking gluten-free foods while eating brownies isn't safe then they're endangering your health and frankly if someone who is a nutritionist is doing this they could be endangering the health of many others through their counseling. Put your foot down and stop ever putting food in your mouth from them if you want to be well. Frankly, if that offends them so greatly the refuse to be friends with you any longer then what kinds of friends are/were they?

QuirkyVeganGirl Newbie

Thank you for the great responses!

And yes, they truly are good friends.

Also thank you for pointing out how young the research is on NCGS. I often forget that there is still a lot we don't know about it, which is a hard truth to accept when you don't feel well and are so desperate for answers.


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



Celiac.com Sponsor (A8-M):



BethM55 Enthusiast

I just started reading Gluten Freedom, a book by Alessio Fasang, MD.  The book has been available since the end of April, 2014.  It has excellent information about celiac and NCGS.  Might be a good resource for you, and to share with your friends.  Perhaps if they understand the science behind the illnesses they might understand your needs better.

QuirkyVeganGirl Newbie

Thanks Beth! I'll check it out!

CathyO Rookie

I'm newly diagnosed, also.

 

What I've told friends is this:  For right now, until I have everything under control and feel comfortable, I'm just going to have to stick to eating only foods I prepare for myself.  I'd love to come to their house and have dinner, and my husband would be happy to eat what they prepare .... rather than have them go to a big fuss and worry about me getting sick, I will just bring my own food .... and we can have the joy of spending time together while not worrying.

 

Good friends have said "Sounds like a great idea!"

Not-so-good friends have said "You're being ridiculous."

My response to the not-so-good friends is along the lines of "I'd rather be ridiculous than be in and ambulance, again, and in the cardiac unit of the hospital for three days. So, I'll just be ridiculous, and we'll pass on the dinner invite for now."

 

At my age, I can appear ridiculous and don't really care what they think.  I want to be alive and enjoy all these grandkids !!!

 

QuirkyVeganGirl Newbie

Thanks, Cathy!

I think I'm going to have to start saying that to people too.

BlessedMommy Rising Star

I'm newly diagnosed, also.

 

What I've told friends is this:  For right now, until I have everything under control and feel comfortable, I'm just going to have to stick to eating only foods I prepare for myself.  I'd love to come to their house and have dinner, and my husband would be happy to eat what they prepare .... rather than have them go to a big fuss and worry about me getting sick, I will just bring my own food .... and we can have the joy of spending time together while not worrying.

 

Good friends have said "Sounds like a great idea!"

Not-so-good friends have said "You're being ridiculous."

My response to the not-so-good friends is along the lines of "I'd rather be ridiculous than be in and ambulance, again, and in the cardiac unit of the hospital for three days. So, I'll just be ridiculous, and we'll pass on the dinner invite for now."

 

At my age, I can appear ridiculous and don't really care what they think.  I want to be alive and enjoy all these grandkids !!!

 

I love it Kathy! Great job sticking up for yourself!

 

I'm not quite as spunky as you, but I'm making progress.

 

A friend is hosting a bridal shower for her daughter and I mentioned that I would be coming. She said, "We'll have wheat free stuff there." I said, "Thanks, but I'll provide my own food, don't worry about me!" My friend said, "Oh it's safer to bring your own, isn't it? I can understand that you'd rather not risk it."  :) 

So I called her later and found out what the menu was so that I could bring something similar. 

NatureChick Rookie

I totally agree with the comment about not knowing what damage NCGI does to the body. They really don't know ... yet. But it sounds as if you take your avoidance of gluten seriously so no need to harp on that.

I feel your pain when it comes to the friends. I have a close friend who also can't eat gluten, but it has actually caused some conflict in our friendship rather than creating an additional bond. He is willing to take a lot more risks when it comes to getting glutened than I am, so when we are out, he expects to be able to go to a restaurant and judges me for not wanting to, while I think he's crazy for not taking it all more seriously. He also gets peeved when I tell him why foods he is still eating are not actually gluten free. 

For the friends, I would explain parts per million, how even a wooden cutting board or a plastic spatula can be a source of cross contamination, or flour dust in the air. I don't think you have to teach them everything, just enough to get them to stop trying so hard and to realize that it really is outside of their control, even with the right ingredients, unless they were willing to replace half of their kitchen utensils and appliances.

But it sounds as if they really do want to try to make your life easier. How about inviting them over to your house once a month to do some gluten-free cooking in a safe kitchen - making it something you can do together? If you also do the grocery shopping beforehand together, you'll have some additional opportunities to talk about hidden sources of gluten. 

If you are going to eat at their houses, can you bring along utensils that are gluten free, like a cutting board, and offer to help prepare something so that you can be certain of what went into it, or set aside a portion for yourself that you know is safe before any gluten ingredients are added?

Also, tell them about how the reaction to gluten can actually become more pronounced and more painful after going gluten-free so that they understand why you aren't willing to take even a calculated risk.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,914
    • Most Online (within 30 mins)
      7,748

    ChrisMary
    Newest Member
    ChrisMary
    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

    • klmgarland
      So I should not eat my gluten free bread?  I will try the vitamins.  Thank you all so very much for your ideas and understanding.  I'm feeling better today and have gathered back my composure!
    • knitty kitty
      Some people prefer eating gluten before bed, then sleeping through the worst symptoms at night.  You might want to try that and see if that makes any difference.   Several slices of toast for breakfast sounds okay.  Just try to work up to the Ten grams of gluten.  Cookies might only have a half of a gram of gluten.  The weight of the whole cookie is not the same as the amount of gluten in it.  So do try to eat bread things with big bubbles, like cinnamon rolls.   Yeah, I'm familiar with the "death warmed over" feeling.  I hope you get the genetic test results quickly.  I despise how we have to make ourselves sick to get a diagnosis.  Hang in there, sweetie, the tribe is supporting you.  
    • Clear2me
      Thank you, a little expensive but glad to have this source. 
    • Xravith
      @knitty kitty  Thank you very much for the advice. I did the exam this morning, my doctor actually suggested me to take something called "Celiac duo test" in which I first do the genetic test and if it's positive, then I'll have to do the antigen blood test. I have to attend 1 month until my results are ready, so I have some weeks to increase the amount of gluten I eat daily. It will be hard because my health is not the best right now, but I also did a blood test to cheek my nutritional deficiencies. The results will arrive on Tuesday, so I can ask my doctor what should I do to control my symptoms and blood levels during this month. For now I'm resting and paying attention to what I eat— at least I don’t look like a vampire who just woke up, like I did yesterday. I'm still scared because is the first time I've felt this sick, but this is the right moment to turn things around for the better.  I realized that if I eat gluten at lunch I cannot finish the day properly, I become severely tired and sometimes my stomach hurts a lot - let's not talk about the bloating that starts later. Do you think is it ok to eat gluten just in the morning, like some cookies and slices of bread for breakfast? 
    • knitty kitty
      I suffer from Dermatitis Herpetiformis, too.  Like @Rogol72, I had to cut out all gluten-free processed foods, dairy, oats, and eggs before my skin cleared up.  I followed the Autoimmune Protocol Diet. I also supplement with the eight essential B vitamins.  (Meat and liver are great sources of B vitamins.)  Low levels of certain B vitamins ( B12, Thiamine, Pyridoxine, and Niacin) can affect the nerves, resulting in itching and tingling.  Niacin especially helps with the itching and healing the blisters.  Tallow Balm helps with the healing, too.  Zinc and Vitamin A also help with skin health.   I've gotten such good results with Niacin and the other vitamins mentioned that I've never had to go on Dapsone.
×
×
  • 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.