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 & 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.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Haugeabs replied to Jane02's topic in Gluten-Free Foods, Products, Shopping & Medications
      23

      Desperately need a vitamin D supplement. I've reacted to most brands I've tried.

    2. - trents replied to xxnonamexx's topic in Gluten-Free Foods, Products, Shopping & Medications
      7

      FDA looking for input on Celiac Gluten sensitivity labeling PLEASE READ and submit your suggestions

    3. - Wheatwacked replied to Heatherisle's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      34

      Blood results

    4. - Known1 replied to xxnonamexx's topic in Gluten-Free Foods, Products, Shopping & Medications
      7

      FDA looking for input on Celiac Gluten sensitivity labeling PLEASE READ and submit your suggestions

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,414
    • Most Online (within 30 mins)
      7,748

    Donna Shields
    Newest Member
    Donna Shields
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Haugeabs
      For my Vit D3 deficiency it was recommended to take with Vit K2 (MK7) with the Vit D. The Vit K2 helps absorption of Vit D3. Fat also helps with absorption. I take Micro Ingredients Vit D3 5000 IU with Vit K2 100 micrograms (as menaquinone:MK-7). Comes in soft gels with coconut oil.  Gluten free but not certified gluten free. Soy free, GMO free.   
    • trents
      @Known1, I submitted the following comment along with my contact information: "I have noticed that many food companies voluntarily include information in their ingredient/allergen label section when the product is made in an environment where cross contamination with any of the nine major allergens recognized by the FDA may also be likely. Even though celiac disease and gluten sensitivity are, technically speaking, not allergic responses, it would seem, nonetheless, appropriate to include "gluten" in that list for the present purpose. That would insure that food companies would be consistent with including this information in labeling. Best estimates are that 1% of the general population, many undiagnosed of course, have celiac disease and more than that are gluten sensitive."
    • Wheatwacked
    • Wheatwacked
      Celiac Disease causes more vitamin D deficiency than the general population because of limited UV sunlight in the winter and the little available from food is not absorbed well in the damaged small intestine.  Taking 10,000 IU a day (250 mcg) a day broke my depression. Taking it for eleven years.  Doctor recently said to not stop.  My 25(OH)D is around 200 nmol/L (80 ng/ml) but it took about six years to get there.  Increasing vitamin D also increases absorption of Calcium. A good start is 100-gram (3.5-ounce) serving of salmon,  vitamin D from 7.5 to 25 mcg (300 to 1,000 IU) but it is going to take additional vitamin D supplement to be effective.  More importantly salmon has an omega-6 to omega-3 ratio 1:10 anti-inflammatory compared to the 15:1 infammatory ratio of the typical Western diet. Vitamin D and Depression: Where is all the Sunshine?
    • Known1
      Thank you for sharing your thoughts.  I respectfully disagree.  You cherry picked a small section from the page.  I will do the same below: The agency is seeking information on adverse reactions due to “ingredients of interest” (i.e., non-wheat gluten containing grains (GCGs) which are rye and barley, and oats due to cross-contact with GCGs) and on labeling issues or concerns with identifying these “ingredients of interest” on packaged food products in the U.S. “People with celiac disease or gluten sensitives have had to tiptoe around food, and are often forced to guess about their food options,” said FDA Commissioner Marty Makary, M.D., M.P.H. “We encourage all stakeholders to share their experiences and data to help us develop policies that will better protect Americans and support healthy food choices.” --- end quote Anyone with celiac disease is clearly a stakeholder.  The FDA is encouraging us to share our experiences along with any data to help develop future "policies that will better protect Americans and support healthy food choices".  I see this as our chance to speak up or forever hold our peace.  Like those that do not participate in elections, they are not allowed to complain.  The way I see it, if we do not participate in this request for public comment/feedback, then we should also not complain when we get ill from something labeled gluten-free. Have a blessed day ahead, Known1
×
×
  • 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.