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

Friends & Food


Brigit

Recommended Posts

Brigit Apprentice

We were invited for supper last night, to a friend who has been very aware of my last 6 week journey with gluten, so I thought she'd be fine with regards to what to cook, as she went dairy and wheat free while breastfeeding her baby. I arrive to see that she's made spaghetti bolognese, a beautiful looking loaf of bread, small green salad and cake for dessert.

Then you just feel silly. Saying sorry I can't eat that. People honestly think it's just a phase, or a picky diet.

Sad & frustrating!


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



Celiac.com Sponsor (A8-M):



Loey Rising Star

We were invited for supper last night, to a friend who has been very aware of my last 6 week journey with gluten, so I thought she'd be fine with regards to what to cook, as she went dairy and wheat free while breastfeeding her baby. I arrive to see that she's made spaghetti bolognese, a beautiful looking loaf of bread, small green salad and cake for dessert.

Then you just feel silly. Saying sorry I can't eat that. People honestly think it's just a phase, or a picky diet.

Sad & frustrating!

Hi Brigit,

I'm sorry you were so frustrated. I find that the longer I'm on the diet, the more people around me pick up on what foods I can eat. I usually have people over to my house for dinner because it just makes it easier. Hang in there and remember that you're not alone. Feel free to PM if you need to vent.

Loey

ravenwoodglass Mentor

That's why it is always a good idea to bring a bit of food with you or eat before you go. It is also a good idea to ask what is being served when you get the invite so you can be best prepared. That must have been quite disappointing for you but hopefully you were able to enjoy the company and conversation.

luvs2eat Collaborator

A fad?? Just being picky?? I'd invite them to stay w/ me for a day or 2 after eating gluten. That would make it crystal clear!!

Brigit Apprentice

A fad?? Just being picky?? I'd invite them to stay w/ me for a day or 2 after eating gluten. That would make it crystal clear!!

he he - yeah exactly!

Thankfully my husband understands, so I'm not 'in this' alone and he was really cool about it all last night. That helped.

IrishHeart Veteran

Sorry, sweetie.

Have you told her you have celiac and you must maintain a lifelong avoidance of gluten to keep you healthy? She may need to be educated a bit.

My family and friends have been educated, but sadly, they still don't grasp it entirely.

In time, I hope they will.

hnybny91 Rookie

I am sorry to say this but if she was very aware and still made all of that food she doesn't sound like much of a friend at all :(


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



Celiac.com Sponsor (A8-M):



IrishHeart Veteran

I am sorry to say this but if she was very aware and still made all of that food she doesn't sound like much of a friend at all :(

I was hesitant to say this, too...but...DOES she know you are a celiac, Brigit? If so, then, yes, what was she thinking?????? :blink::o :o

lynnelise Apprentice

Wow, I think that would have really hurt my feelings! You just don't expect that from friends who know the issues you are dealing with! I hope she just had a serious memory lapse and wasn't being intentionally malicious! I'm sorry you were put in such an awkward situation! :(

Marilyn R Community Regular

We were invited for supper last night, to a friend who has been very aware of my last 6 week journey with gluten, so I thought she'd be fine with regards to what to cook, as she went dairy and wheat free while breastfeeding her baby. I arrive to see that she's made spaghetti bolognese, a beautiful looking loaf of bread, small green salad and cake for dessert.

Then you just feel silly. Saying sorry I can't eat that. People honestly think it's just a phase, or a picky diet.

Sad & frustrating!

Oh Bridget, I'm so sad that your friend did that! What's so frustrating is that if you were a vegetarian, she probably would have made you a separate dish of spagetti with marinara sauce.

People "get" vegetarian. They understand kosher or kosher style. gluten-free is really tough for them to comprehend, especially with CC issues. And our diet isn't a choice.

It you were able to extract yourself from that situation with any grace whatsoever, you deserve stand up applause. :)

Brigit Apprentice

Hi all,

Thanks for your support and advise!

So what I've just done took a lot of guts, but I emailed a bunch of my friends and people I work with and explained word for word what was going on with me and what Celiac Disease meant. I hope it makes things easier into the future. I don't expect understanding from strangers or new friends, but from old friends and family, I really need support and understanding. So hoping the email makes sense to them. I also had to write it, as I'm struggling to want to be around people at the moment, and am wanting to 'run and hide' to a place where this isn't happening to me. So now that I've been honest with my friends, maybe I will be calmer about managing and coping around them in social gatherings.

So here's hoping for easier times! :)

ciavyn Contributor

Brigit -- just a few thoughts...

1. My best friend thought I was a little loopy, but as is her nature, she trusts me to do what is best for me. As it works out, she also may have Celiac's disease, and my willingness the last year and a half to face some discomfort around others has encouraged her to make the switch. She is feeling 100% better, but as frustrated as I was when I first started. So I can help her, because we've been very open about my struggle.

2. Your friends and coworkers also have issues. Some of them you don't know, because they are too embarrassed to share them. So you being willing to be open is giving them the freedom and permission to do the same. That is a gift, and I applaud you for it.

3. Be social -- bring your own dish to add to the event, along with your own plate of it for yourself (to avoid cross contamination but also to ensure you have it made exactly the way YOU want it.) If it's a restaurant, learn some standbys and you'll be fine. A well-questioned and educated server will get you a burger, fish or chicken with nothing on it, and a plate of fries (if safe) or vegetable happily. Just tip them well, show your gratitude, and believe you me, I would have done anything for a good customer when I was a waitress, just for some appreciation.

4. Hang in there. It gets easier, I swear. I'm very social, and love hanging out with folks. It just is a learning curve, and it's hard to be patient when the risk is getting ill.

Best, Ci :)

kellynolan82 Explorer

I really have a lot of time for your patience, Brigit! It is a real virtue and I feel that we need to be open (not whinging) but not guilty and/or worried about what others think too overly.

I always say to 'do your best and let others do or say whatever'.

All the best :)

IrishHeart Veteran

Hi all,

Thanks for your support and advise!

So what I've just done took a lot of guts, but I emailed a bunch of my friends and people I work with and explained word for word what was going on with me and what Celiac Disease meant. I hope it makes things easier into the future. I don't expect understanding from strangers or new friends, but from old friends and family, I really need support and understanding. So hoping the email makes sense to them. I also had to write it, as I'm struggling to want to be around people at the moment, and am wanting to 'run and hide' to a place where this isn't happening to me. So now that I've been honest with my friends, maybe I will be calmer about managing and coping around them in social gatherings.

So here's hoping for easier times! :)

Good for you, Kiddo!

I want you to know that I have informed all of my family and friends, too, right from the beginning....and they still "don't get it" but they try. Some do. Some have taken to ignoring me. It hurts my feelings, but so be it.

You just keep taking care of YOU right now.

One thing most of us forget is...this is a disease of malnutrition. It takes time for the body to recover and it affects us emotionally as well as physically.

It made me "not me" for a long time. I was unrecognizable, even to myself....and that is slowly reversing. If not for my devoted husband, who is my best friend, I do not know what would have become of me. He says I'm a fighter and could have done it solo, but we both know that is not true.

I would like my friends and family to be more supportive, but I think they are bewildered by it all and because I was ill for so long, they are tired of hearing about it. (Some of my family is not listening to me anyway because I tell them they probably have gluten issues, too and they don't want to hear it. Heads are in the sand!!)

They just want me to "be me" again. When I am more recovered, I will try educating them further. In time, all will resolve itself.

With education, perhaps your friends will be more understanding of you as well.

It is a good that you have a loving spouse. Hang in there, honey...you're doing a great job coping with this whole thing, from what I can tell!! ;)

  • 3 weeks later...
hammergirl Newbie

This is just so sad. I know I often feel the same way, that if you tell someone how you need your food prepared in order to avoid extremely painful consequences in a few hours, but they look at you like you're just being high-maintenance, picky, or whiny. I get that a lot from the servers at restaurants. I've had to send food back numerous times due to their ignoring or forgetting my explicit 'do NOT put crutons on my salad please'.

Hang in there! I know that telling those around you will really help out. I truly hope that I have the guts to do this sort of thing when the time comes.

hnybny91 Rookie

This reminds me of the time when I was vegetarian. My MIL told me one Thanksgiving that she had left some of the stuffing out of the bird just for me. I felt so loved until I took my first bite. I said, "This tastes like meat." and she replied, "That's because I put sausage in the stuffing!" UGH!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,203
    • Most Online (within 30 mins)
      7,748

    Barbara 1981
    Newest Member
    Barbara 1981
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.7k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Given your history of a high TTG (167) that decreased to 16 on a gluten-free diet, along with genetic confirmation of celiac disease, it’s likely the negative biopsy is a false negative due to not eating gluten before the endoscopy. Gluten is necessary to trigger the intestinal damage seen in celiac disease, and avoiding it can lead to healing and a normal biopsy despite ongoing immune activity (reflected in your still-elevated TTG). The inflammation observed during the endoscopy (“diffuse moderately erythematous mucosa”) could be residual damage, mild ongoing inflammation, or another condition like peptic duodenitis, but it’s consistent with celiac disease in context. Continued positive blood markers suggest ongoing gluten exposure, possibly from cross-contamination or hidden sources. Strict adherence to a gluten-free diet and follow-up testing are key to managing symptoms and reducing inflammation. Discuss these findings with your doctor to confirm the diagnosis and refine your dietary approach. This article has some detailed information on how to be 100% gluten-free, so it may be helpful (be sure to also read the comments section.):    
    • Scott Adams
      Yes, it sounds like great progress, but what was the time frame between the two endoscopies? 
    • Scott Adams
      Your symptoms—headaches, dizziness, nausea, irregular bowel movements, anemia, and menstrual changes—along with a family history of celiac disease, strongly suggest celiac disease could be the cause. The mild duodenal changes seen in your biopsy are consistent with early or mild celiac disease, though they could also be due to other factors. The improvement in bowel movements after cutting out gluten is a positive sign, but other symptoms like headaches and dizziness may take longer to resolve as your body heals. It’s important to continue a strict gluten-free diet and discuss further testing, such as celiac antibody blood tests or a follow-up biopsy, with your doctor to confirm the diagnosis. Many people experience a gradual improvement in symptoms over weeks to months, so patience and strict adherence to the diet are key. You’re not alone in this process, and support from celiac communities can be very helpful. This article has some detailed information on how to be 100% gluten-free, so it may be helpful (be sure to also read the comments section.):    
    • Scott Adams
      For people with celiac disease and corn intolerance, most salts, including table salt with dextrose, are generally safe in small amounts, as the dextrose is typically highly processed and unlikely to contain problematic corn proteins. However, if you’re highly sensitive, you might consider switching to pure kosher or Himalayan salt, which don’t contain additives. While bringing your own salt to restaurants or avoiding seasoned foods can feel overwhelming, it’s a practical step if you’re concerned. Many people with corn intolerance tolerate trace amounts of dextrose in salt without issues, but individual sensitivity varies. If your current salt isn’t causing symptoms, it’s likely fine to continue using it, especially given your financial constraints and the challenges of managing dietary restrictions. Focus on what works for you and prioritize avoiding larger sources of corn, like cornstarch.
    • Scott Adams
      Your daughter’s ongoing stomach pains two weeks into a gluten-free diet could be due to her body still healing after months of gluten exposure, as recovery from celiac disease can take time. Her inconsistent eating habits and possible eating disorder behaviors may also delay healing. While she’s now eating gluten-free snacks, her limited intake and emotional withdrawal complicate the process. It’s positive that she’s trying, but recovery may take weeks to months. Addressing her depression and mental health is crucial, as celiac disease can impact mood, and proper nutrition may help. Patience and support are key, but if symptoms persist, consult her doctor to rule out accidental gluten exposure or other issues. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal.  
×
×
  • Create New...