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

New


nicoleee

Recommended Posts

nicoleee Newbie

I was just diagnosed with Celiac. I have been reading a lot online about it and some of the things I read make me nervous. It was only confirmed 2 days ago and I have only been Gluten free for 2 days. When I first found out my mind went straight to a list of foods I couldn't eat and it seems that over the past 2 days that is all I have come across. I actually feel that I might be depressed about it. That probably sounds very dramatic, but it's as if it is all still sinking in. My family has been pretty good about it, we went to the store tonight to buy all Gluten-free foods and I hated it. Everything I wanted seemed to have Gluten in it. I know things could be worse and everyone seems to keep telling me that, but I feel like no one really understands.

I also tend to eat out a lot, so if anyone has any recommendations because I am finding it extremely hard to eat out and I guess narrowing down the amount of times I eat out will help, but I was wondering if anyone had any suggestions.

Thanks,

nicoleee


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



Celiac.com Sponsor (A8-M):



Lux Explorer
I was just diagnosed with Celiac. I have been reading a lot online about it and some of the things I read make me nervous. It was only confirmed 2 days ago and I have only been Gluten free for 2 days. When I first found out my mind went straight to a list of foods I couldn't eat and it seems that over the past 2 days that is all I have come across. I actually feel that I might be depressed about it. That probably sounds very dramatic, but it's as if it is all still sinking in. My family has been pretty good about it, we went to the store tonight to buy all Gluten-free foods and I hated it. Everything I wanted seemed to have Gluten in it. I know things could be worse and everyone seems to keep telling me that, but I feel like no one really understands.

I also tend to eat out a lot, so if anyone has any recommendations because I am finding it extremely hard to eat out and I guess narrowing down the amount of times I eat out will help, but I was wondering if anyone had any suggestions.

Thanks,

nicoleee

Hey hun,

I know it can seem overwhelming at the beginning - but, honestly, as so many other people on this forum will tell you, it gets better.

I began a gluten/wheat free diet 9 days ago and today I have also begun eliminating both soy and dairy. What is most frustrating for me is when I accidentally eat something that contains "hidden" gluten (happened to me last week) and feeling as if I have to start over. But it's all a learning curve. I like to think of it as a kind of adventure; it can be kind of fun to experiment with the foods you CAN eat (and believe me, there are more than you would at first imagine) and create all sorts of weird and wonderful things...

It's so normal to mourn that previous way of life, wherein you could eat whatever you wanted without feeling sick. But if you focus on the notion of becoming healthy and feeling good, it becomes a lot easier. I promise.

As for eating out, where do you ordinarily go, and where do you live? I think this is probably the hardest part of the whole thing for me, but there are ways of dealing with it - you just have to be really, really careful.

xx

nicoleee Newbie
Hey hun,

I know it can seem overwhelming at the beginning - but, honestly, as so many other people on this forum will tell you, it gets better.

I began a gluten/wheat free diet 9 days ago and today I have also begun eliminating both soy and dairy. What is most frustrating for me is when I accidentally eat something that contains "hidden" gluten (happened to me last week) and feeling as if I have to start over. But it's all a learning curve. I like to think of it as a kind of adventure; it can be kind of fun to experiment with the foods you CAN eat (and believe me, there are more than you would at first imagine) and create all sorts of weird and wonderful things...

It's so normal to mourn that previous way of life, wherein you could eat whatever you wanted without feeling sick. But if you focus on the notion of becoming healthy and feeling good, it becomes a lot easier. I promise.

As for eating out, where do you ordinarily go, and where do you live? I think this is probably the hardest part of the whole thing for me, but there are ways of dealing with it - you just have to be really, really careful.

xx

Hey,

Thanks for getting back to me! Why did you begin eliminating soy and dairy, because you had to? or just because it was something you chose to do. And I am afraid of eating "hidden" gluten, I check and re-check everything I eat before I eat it. I guess it is something I will get used to, I keep hearing that before I know it, it will be normal to me, so I guess I just have to wait and see with that.

When I go out, I normally go to Italian restaurants or pizzaria's, which I get salads from there, or American restaurants, which I realize I can get steak or a burger without bread, but I just feel like I am going to get sick of these foods. I live in Westchester County in New York.

Thanks for all the advice, I guess it was better to hear it from someone who has to eat gluten free too!

x1x-Stargirl-x1x Apprentice
I was just diagnosed with Celiac. I have been reading a lot online about it and some of the things I read make me nervous. It was only confirmed 2 days ago and I have only been Gluten free for 2 days. When I first found out my mind went straight to a list of foods I couldn't eat and it seems that over the past 2 days that is all I have come across. I actually feel that I might be depressed about it. That probably sounds very dramatic, but it's as if it is all still sinking in. My family has been pretty good about it, we went to the store tonight to buy all Gluten-free foods and I hated it. Everything I wanted seemed to have Gluten in it. I know things could be worse and everyone seems to keep telling me that, but I feel like no one really understands.

I also tend to eat out a lot, so if anyone has any recommendations because I am finding it extremely hard to eat out and I guess narrowing down the amount of times I eat out will help, but I was wondering if anyone had any suggestions.

Thanks,

nicoleee

well.. just like the other person i got rid of dairy and soy too. well, also because i have hallucinations, and the milk mainly triggers my hallucinations, but i find that in other people getting rid of milk can help alot.

and it's normal to be deprressed over it. and you're not taking a long time to get over it, my god, i've been diagnosed for several years and i'm STILL getting over it. (it's addicting!). And, yeah, it can be worse, but don't listen to them. it kinda makes you feel bad that it 'could be worse' right? well, yeah, it can but you gotta first deal with your situation and feel sorry for yourself before you can realize that that it could be worse. that its, as long as the feeling sorry for yourself doesn't take years and years :)

you can pity yourself, just not for too long. and sometimes rough times will show who your real supporters and friends are. trust me, i know that VERY much!! it's okay. be strong. it's hard, and you'll make MANY MANY MANY mistakes. you'll accidentally eat gluten, or you might just sort of crave gluten and eat it on purpose, but as long as you TRY your very hardest, you're becomeing a better person. :) and don't listen when other people say 'if you were trying your very hardest you wouldn't be doing it" because that's not true. this is true - "if you are trying your very hardest, then you will still make mistakes, but over time you will make less mistakes " and 'over time' may be a couple years. trust me! i know!

Gurlie, feel free to PM me. i don't have any1 to talk to and i'd be happy to talk to youz!

.::STARGIRL::.

caiticakes Newbie

I've been doing this for over a month and i'm still having those cravings. It doesnt really phsyically effect me, but when i eat gluten it makes me depressed and angry like all the time. But when i accidently have something it doesnt seem to effect me anymore and i just wish i could go back to how i used to be where i could eat normally. Idk its just so hard i hate everything about ittttttttttt. Thats why I joined this group, I know over time if i continue eating gluten i'll get really sick which is why i'm trying to get over my cravings. any suggestions..?

Katester Enthusiast

If you get pain from eating foods with gluten, isn't it enough to know that by not eating gluten you're allowing yourself to feel better? I think it's worth it to go that extra step and not eat gluten if you're saving yourself from a lot of pain. I get very sick when I eat gluten. Yeah, I miss pizza and stuff but I've found ways to go around it. Brown rice pasta, etc. Try new recipes and dishes at restaurants. It's all just a learning experience. :)

kbtoyssni Contributor

Welcome! There is a huge learning curve to this diet, and the list of foods you can't eat is extremely overwhelming at first. But keep reading this board and keep reading labels, and in a few months you'll be a pro.

Eating out can also be tricky until you get the hang of it. Try mexican (substituting corn tortillas) or thai (with rice noodles). American food can work pretty well - I usually order a salad or a grilled chicken breast with swiss cheese and pickle/lettuce/tomato and a baked potato or veggies. Grilled fish is good, too. Breakfast style food works well - try omelettes and hash browns (hash browns are ok about 50% of the time). Don't worry about digging through the menu - for american and breakfast food I usually know exactly what I want and ask for that rather than trying to pick something on the menu and have them do substitutions. When I order salads, I often say "salad with no cro


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



Celiac.com Sponsor (A8-M):



caiticakes Newbie
I was just diagnosed with Celiac. I have been reading a lot online about it and some of the things I read make me nervous. It was only confirmed 2 days ago and I have only been Gluten free for 2 days. When I first found out my mind went straight to a list of foods I couldn't eat and it seems that over the past 2 days that is all I have come across. I actually feel that I might be depressed about it. That probably sounds very dramatic, but it's as if it is all still sinking in. My family has been pretty good about it, we went to the store tonight to buy all Gluten-free foods and I hated it. Everything I wanted seemed to have Gluten in it. I know things could be worse and everyone seems to keep telling me that, but I feel like no one really understands.

I also tend to eat out a lot, so if anyone has any recommendations because I am finding it extremely hard to eat out and I guess narrowing down the amount of times I eat out will help, but I was wondering if anyone had any suggestions.

Thanks,

nicoleee

about eating out though. some chains have gluten free menus. the ones that don't; if you ask to talk to a manager they will usually be more than happy to accomodate you and will work with you to find things on the menu you can eat. in non-chain resteraunts its easier because you can work off the menu and mix and match things together. usually plain foods are the way to go, e.g. salads, plain veggies, grilled chicken or fish. its best to have the grill cleaned off if possible.

hope that was some help.

nikky Contributor

i know what you mean, its amazing how many things they slip gluten into, but have faith there are some really good alternatives out there. the thing with coeliac disease is we are in controll of our own health, sure our family can help us but they cant watch over us 24/7 (although i know my pearents would probably like to). keep going and dont give in, ive been on the diet for 2 months and already its just become part of my life, its like ive never known any different. for futher support from people our age check out www.celiacteens.com, its really helpful and everyone there knows exactly what we are going through

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,148
    • Most Online (within 30 mins)
      7,748

    LCookies
    Newest Member
    LCookies
    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
      In case you decide to go the route of a gluten challenge for a celiac disease blood test or biopsy: 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:    
    • Wheatwacked
      Kosher salt is not usually iodized. Shortly after starting GFD in 2014, I realized I wasn't getting enough iodine.  Growing up in the 50's and 60's we ate bread that used iodine as a dough modifier so each slice had about 100 mcg of iodine.  A sandwich and glass of milk supplied 300 mcg a day.  In the 70's they stopped using iodine as a conditioner in the US.  Then everyone got scared of milk.  The US intake of iodine dropped 50% since 1974.  Prescriptions of Thyroxine for hypothyroid disease doubled in the same period.  I tried using iodized salt and seaweed and took an expensive thyroid supplement but it wasn't enough.  In 2014 I had a sebaceous cyst (third eye blind).  The previous 6 cysts on my face had all drained and healed with no problem back in the 1990,s.  One on my check had sugically removed. They are genetic from my mom and my brother and son also get them in the same places.  This one I did not have surgery for because I wanted a bellweather to moniter healing.  It did not start healing until I started until 10 years when I started taking 600 mcg of Liquid Iodine a year ago Nov 2023. Lot's of comment about how it was offputting and maybe cancer, it was deep, down to the bone, but I can be obstenant.  Now it is scabbing over and healing normally.  Vision is returning to my right eye (glucoma), musle tone in my chest was the first sign of improvement.  For healing, iodine breaks down defective and aging cells to make room for new growth. I take Liquid Iodine drops from Pipingrock.com but there is also Strong Iodine and Lugols Solution. 50 mcg/drop a dropper full is 12 drops, 600 mcg.,  usually I put it in a can of Red Bull, My brother, son and his family also started taking it. https://www.pipingrock.com/iodine/liquid-iodine-2-fl-oz-59-ml-dropper-bottle-14690 390 drops for $8.  They ship internationally if you can't find it locally. It the US the Safe Tolerable Upper Limit is 1000 mcg a day.  In Japan it is 3000 mcg a day.  The Japanese traditional diet has 50% less breast cancer, nicer hair, skin and nails, and in the 80's the US educational system dropped down comared to the rest of the world while Japanese kids moved up to the top.  Low iodine affects brain fog. According to most education rankings, Japan generally has a higher education rating than the United States, with Japan often ranking within the top 10 globally while the US usually places slightly lower.  In the 1960s, the United States was near the top of the world for education, especially for young people.  About why iodine was removed from medicint: The Wolff-Chaikoff Effect: Crying Wolf? About why over 40% of us are vitamin D deficient: Mayo Proceedings,  Vitamin D Is Not as Toxic as Was Once Thought:  
    • trents
      Current "gluten challenge" recommendations are the daily consumption of at least 10g of gluten (about the amount found in 4-6 slices of wheat bread) daily leading up to the day of the biopsy.
    • Bebee
      Thank you for your input!  I would really like to know if I have celiac disease because you need make sure you are not getting any cross contamination due to cancer concerns.  I guess I need to start with a knowledgeable Gastroenterologist. Thank you again!
    • trents
×
×
  • Create New...