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 Celiac.com!
    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!

Link to comment
Share on other sites

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

Link to comment
Share on other sites
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.

Link to comment
Share on other sites
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!!

Link to comment
Share on other sites
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.

Link to comment
Share on other sites
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.

Link to comment
Share on other sites
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 :(

Link to comment
Share on other sites

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

Link to comment
Share on other sites
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! :(

Link to comment
Share on other sites
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. :)

Link to comment
Share on other sites
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! :)

Link to comment
Share on other sites
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 :)

Link to comment
Share on other sites
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 :)

Link to comment
Share on other sites
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!! ;)

Link to comment
Share on other sites
  • 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.

Link to comment
Share on other sites
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!

Link to comment
Share on other sites

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,224
    • Most Online (within 30 mins)
      7,748

    Suzi374
    Newest Member
    Suzi374
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Was a biopsy done when you had your gastroscopy? Concerning your anemia, are you B12 deficient? It's nearly impossible to get sufficient B12 if you are a vegetarian unless you take supplements.
    • Suzi374
      And I’m anaemic, however I’m also female and vegetarian. I had an iron trans a couple of years ago however it’s starting to dwindle and taking supplements doesn’t seem to work. I can’t seem to absorb it. 
    • Suzi374
      Hi, I attended a neurologist appt last Tuesday, which I nearly cancelled, due to ongoing numbness and tingling in toes to mid foot. One of the first things he asked was ‘are you celiac’. I’m not. He thought all reflexes were ok but at the last minute decided on nerve conduction tests which were low normal. He was a little confused as he felt they should be better and tried a new set of probs, all the time, giving me multiple shocks which were not enjoyable lol. Anyway, he’s now ordered tests for myeloma, and all the vitaminy things that so many of you mention on here, also tests looking for autoimmune responses. I already have Hashimotos. Interestingly, to me, but maybe someone out there can relate or knows more than i do, although I was a nurse, but ED not ‘weird symptoms’  nurse. Anyway back to the interesting thing, I took duramine in 2013 to lose weight which caused a massive panic attack when I stopped taking it and half my hair fell out. I only took it for a week but it was horrible and I regret it. It triggered ongoing panic attacks which are horrendous. So I feel like I’m a bit crazy. Then in 2020 I had this sudden onset of horrible pain when trying to eat a cinnamon roll. It continued and I lost around 20 kgs. I had two gastroscopes and a colonoscopy and they were all normal. I scored a barium swallow and CT angiogram. All normal. The pain subsided a little but I was left with reflux and an awful feeling that I couldn’t get air when I ate some foods. This was not anxiety.  The anxiety was separate and I still maintain this. This was something to do with eating. It was like the air was thick but I wasn’t short of breath. I just had the sensation I was, then it triggered anxiety. Anyway, I had other weird things- couldn’t bend knees to shave legs in shower lol. Knees felt stiff and swollen but they weren’t. Knee WOUld swell up randomly but mri showed minimal issues. A bit of a meniscus degeneration but insignificant. Then the buzzing sensations in my head, the feeling like someone was stabbing me with something sharp. So now, I pre empted his tests, although I don’t think I’m celiac because it should have come up on gastroscopy, I’ve gone off gluten. Since Tuesday last week so 9 days. Since then I don’t appear to be as constipated, I realised I got through today without a nap and I’m not tired, maybe it’s just today and not related but I get very tired normally and sleep straight after work often, I can bend my knees and shave my legs lol, the buzzing vibrating has gone from my head, I had to call and ambulance as my heart decided we were off on a run, but we weren’t running and I’ve been a bit twitchy at bed time when trying to sleep, reflux is improving, I did get the weird suffocating feeling a bit when eating today but not as bad normall. Tingling and numbness still present and I felt like it moved up my legs a bit today but I’m a bit jittery. So I don’t know if it’s celiac disease or a gluten intolerance but I think, and it may be wishful thinking because my symptoms do make life a bit challenging, but maybe I’m feeling better. I don’t feel as cloudy. My thinking feels crisper. Like there’s no buzzing and I’m not fighting to break through the cloudiness now. I hope so much that this may help me feel a bit better moving forward. It would be a miracle as I really have struggled to work and parent and keep the house clean and I’m always anxious and exhausted.  If you get this far, please tell me if you you can relate to any of the above. Oh and tonsils out 5 years ago but before that antibiotics multiple times a year, sometimes intramuscular because they were so bad.  Op was meant to take 30 mins, it took 1.5 hours due to size of them. 
    • Peace lily
      Im still not gaining weight I’m on a gluten free diet . And still having issues with constapation started priobiocs figured it would help been over two weeks . I guess it’s going to be a long road for me .
    • Smith-Ronald
      Enlarged lymph nodes in neck and groin with celiac are not uncommon. They can take time to reduce even after going gluten-free. Monitoring is key.
×
×
  • Create New...