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

Hello Fellow Celiacs


Gf Princess182

Recommended Posts

Gf Princess182 Rookie

Hello everyone,

Well I am new to the site, but I have been gluten free for 2-3 years. It almost seems yesterday that I went gluten-free. I was wondering how everyone else found out they were a Celiac. Anyone want to share stories? Also I was curious how everyone else handled the news.


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



Celiac.com Sponsor (A8-M):



Mateto Enthusiast

Hello everyone,

Well I am new to the site, but I have been gluten free for 2-3 years. It almost seems yesterday that I went gluten-free. I was wondering how everyone else found out they were a Celiac. Anyone want to share stories? Also I was curious how everyone else handled the news.

Not from a doctor I can assure you :P

When I figured it out, my doctor had merely suggested it and left it at that. I joined this forum then, and got smart!

Lisa Mentor

Welcome Princess! I was home bound for several months and was scheduled to see a GI, who diagnosed me through endoscopy. It was a relief to find Celiac and not the dreaded "cancer" word.

I came home and did a search and found this place. I've settled in. ;)

Gf Princess182 Rookie

Not from a doctor I can assure you :P

When I figured it out, my doctor had merely suggested it and left it at that. I joined this forum then, and got smart!

Well it's good that you found out. My test came up negative but I was already gluten free. I tried to go back and ended up facing dire consequences. My mom also ended up going on the gluten free diet to be nice and she decided to cheat on the diet. She ended up with a pretty nasty rash.

Gf Princess182 Rookie

Welcome Princess! I was home bound for several months and was scheduled to see a GI, who diagnosed me through endoscopy. It was a relief to find Celiac and not the dreaded "cancer" word.

I came home and did a search and found this place. I've settled in. ;)

Thank you for the welcome Lisa. How are you coping with being a celiac? I know that even though I've been gluten free for 3 years it's still really hard.

TEDDYbear777 Newbie

I was very very sick Ended up going through the ropes with doctors and Tests, Can't say I enjoyed cameras going in both ends at 18 but it's finally over and I'm getting better! =)

Lisa Mentor

Thank you for the welcome Lisa. How are you coping with being a celiac? I know that even though I've been gluten free for 3 years it's still really hard.

I generally don't have a problem day to day. I can always find "something" in a restaurant to eat.

Do you work or are you at home?


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



Celiac.com Sponsor (A8-M):



Gf Princess182 Rookie

I generally don't have a problem day to day. I can always find "something" in a restaurant to eat.

Do you work or are you at home?

I don't work yet. I just recently moved so I'm looking at getting a job. I can only work part time though, a full time job wears me down really fast.

Gf Princess182 Rookie

I was very very sick Ended up going through the ropes with doctors and Tests, Can't say I enjoyed cameras going in both ends at 18 but it's finally over and I'm getting better! =)

I know what you mean, I had the endoscopy done and I cant say I enjoyed it either. It's good you are getting better though.

  • 3 weeks later...
Charli61 Apprentice

Hello everyone,

Well I am new to the site, but I have been gluten free for 2-3 years. It almost seems yesterday that I went gluten-free. I was wondering how everyone else found out they were a Celiac. Anyone want to share stories? Also I was curious how everyone else handled the news.

My 80 year old Mum got tested, and then when I investigated Celiac for her, it turns out I had most of the symptoms for DH myself :( So, got tested and the rest as they say is history!

  • 2 weeks later...
NickMcKinnis Rookie

Hello Princess,

I am also new to the site, and have been gluten free for about the same amount of time. For me diagnosis was an extremely drawn out process. I first started showing symptoms of celiac disease when I was in the first grade. I would often feel sick at school and get sent home. However when I went to the doctor, they were never able to land a diagnosis either pointing to anything but celiac. My doctors would come up with things as silly as seasonal allergies or say that I was making it up. I was always very smart when it came to school and so I was always able to keep up until I moved to Cleveland where they have a maximum amount of days you were allowed to miss. So, I took my G.E.D.

Just before I took my G.E.D. and I went to the doctor for problems with diarrhea and my regular doctor had taken off for the weekend forgetting our appointment. I instead saw his partner who made the connection and ordered the blood test which came back positive.

Afterwards, I lived in a state of depressed denial for a few years. My life changed slowly for the better despite the constant glutening and at some point I realized I had something to lose so after a while of feeling sorry for myself and seeing my symptoms grow even worse, I decided that enough was enough and haven't looked back ever since. I still make mistakes but my symptoms seem to be better now. Sometimes I'm not sure though if I have an accurate frame of reference of what symptom free is as I have been living with the symptoms for so long.

Sorry for the essay, It was the first time I have really told the story so openly.

jeanzdyn Apprentice

Welcome to the forum.

For a few reasons I decided to have a colonoscopy. The GI also did an endoscopy. Biopsy with both procedures of course. They also did a blood test. The result was a diagnosis, but how they verbalized that was "we think that maybe you have celiac disease".

I was not surprised by the diagnosis. I had experimented with a rotation diet where I did not eat any bread or pasta for 3 days, and on the 4 day I ate whatever I wanted. So, 3 days off and 1 day on. That relieved my main symptom that was bothering me which was severe, burning itching of the skin. (no rash, no eruptions, no scaly skin, no visible evidence of the itching)

So, I was diagnosed by a gastroenterologist, but I was on my way to figuring it out for myself (after many years of symptoms).

I was never terribly ill, never hospitalized, and for that I am very thankful.

Gf Princess182 Rookie

Hello Princess,

I am also new to the site, and have been gluten free for about the same amount of time. For me diagnosis was an extremely drawn out process. I first started showing symptoms of celiac disease when I was in the first grade. I would often feel sick at school and get sent home. However when I went to the doctor, they were never able to land a diagnosis either pointing to anything but celiac. My doctors would come up with things as silly as seasonal allergies or say that I was making it up. I was always very smart when it came to school and so I was always able to keep up until I moved to Cleveland where they have a maximum amount of days you were allowed to miss. So, I took my G.E.D.

Just before I took my G.E.D. and I went to the doctor for problems with diarrhea and my regular doctor had taken off for the weekend forgetting our appointment. I instead saw his partner who made the connection and ordered the blood test which came back positive.

Afterwards, I lived in a state of depressed denial for a few years. My life changed slowly for the better despite the constant glutening and at some point I realized I had something to lose so after a while of feeling sorry for myself and seeing my symptoms grow even worse, I decided that enough was enough and haven't looked back ever since. I still make mistakes but my symptoms seem to be better now. Sometimes I'm not sure though if I have an accurate frame of reference of what symptom free is as I have been living with the symptoms for so long.

Sorry for the essay, It was the first time I have really told the story so openly.

Thank you so much for your story. I am so glad that you shared. When I found out that I might have Celiac I too went through a state of depression. It's shameful to say this, but I felt like a prisoner in my own body. Once I figured out how to eat and got a doctor that cared I started getting better.

It was really hard having to explain things to people so I stopped seeing friends, dating, and going out. It's really hard being Celiac...no one knows what it is, no one understands it, and people think you're weird or contagious. After I realized I was missing out on my life I slowly began to start going out again. It's been 2-3 years since then and now I realize that it was worth missing out on life. I now tell everyone I know about Celiac and try to raise awareness.

I've lived in Oklahoma my entire life and moved away for the first time in my life (to Illinois); I was stunned to find so many gluten free options. Where I live in Oklahoma theres scarcely any gluten free food. I just moved back to Oklahoma and now they are starting to carry more Gluten free foods. Awareness is being raised and that just makes it so much easier on new celiacs. I am glad to hear that you are getting better and that you are able to openly tell the story. That's only the first step, it'll keep getting so much easier with time.

Sorry for the book I wrote lol

Gf Princess182 Rookie

Welcome to the forum.

For a few reasons I decided to have a colonoscopy. The GI also did an endoscopy. Biopsy with both procedures of course. They also did a blood test. The result was a diagnosis, but how they verbalized that was "we think that maybe you have celiac disease".

I was not surprised by the diagnosis. I had experimented with a rotation diet where I did not eat any bread or pasta for 3 days, and on the 4 day I ate whatever I wanted. So, 3 days off and 1 day on. That relieved my main symptom that was bothering me which was severe, burning itching of the skin. (no rash, no eruptions, no scaly skin, no visible evidence of the itching)

So, I was diagnosed by a gastroenterologist, but I was on my way to figuring it out for myself (after many years of symptoms).

I was never terribly ill, never hospitalized, and for that I am very thankful.

Thank you so much for sharing. I like to hear how other people have diagnosed and how they are dealing with it afterwards. I am glad you found out though.

NickMcKinnis Rookie

Thank you so much for your story. I am so glad that you shared. When I found out that I might have Celiac I too went through a state of depression. It's shameful to say this, but I felt like a prisoner in my own body. Once I figured out how to eat and got a doctor that cared I started getting better.

It was really hard having to explain things to people so I stopped seeing friends, dating, and going out. It's really hard being Celiac...no one knows what it is, no one understands it, and people think you're weird or contagious. After I realized I was missing out on my life I slowly began to start going out again. It's been 2-3 years since then and now I realize that it was worth missing out on life. I now tell everyone I know about Celiac and try to raise awareness.

I've lived in Oklahoma my entire life and moved away for the first time in my life (to Illinois); I was stunned to find so many gluten free options. Where I live in Oklahoma theres scarcely any gluten free food. I just moved back to Oklahoma and now they are starting to carry more Gluten free foods. Awareness is being raised and that just makes it so much easier on new celiacs. I am glad to hear that you are getting better and that you are able to openly tell the story. That's only the first step, it'll keep getting so much easier with time.

Sorry for the book I wrote lol

I know exactly what exactly what you mean. Social events are definitely hard, and dating is nearly impossible without a disclaimer. My last serious girlfriend was one of my main motivators to go gluten free, she was very encouraging but still didn't take the time to know all the little details. ( I remember her once trying to use hand sanitizer after eating some bread) One thing I would suggest is find yourself a vegan! They understand all the concepts of celiac disease and many resturaunts that offer vegan food also offer gluten free (at least in my area). Glad to hear you are in an area where more options are available. I moved to Cleveland from an extremely small town in Arkansas and had to drive 45 minutes for anything gluten free so I can definitely relate. Here, I even have different stores to pick from and a few resturaunts that I feel comfortable going to.

Going back to social events, would you say your friends understand your disease and how it affects your ability to enjoy yourself in social situations? Sometimes I think mine get it, and other times it's like explaining the disease all over again.

Looks like between the two of us we are going to have the next great american novel... I wish we were getting paid by the word haha

Gf Princess182 Rookie

I know exactly what exactly what you mean. Social events are definitely hard, and dating is nearly impossible without a disclaimer. My last serious girlfriend was one of my main motivators to go gluten free, she was very encouraging but still didn't take the time to know all the little details. ( I remember her once trying to use hand sanitizer after eating some bread) One thing I would suggest is find yourself a vegan! They understand all the concepts of celiac disease and many resturaunts that offer vegan food also offer gluten free (at least in my area). Glad to hear you are in an area where more options are available. I moved to Cleveland from an extremely small town in Arkansas and had to drive 45 minutes for anything gluten free so I can definitely relate. Here, I even have different stores to pick from and a few resturaunts that I feel comfortable going to.

Going back to social events, would you say your friends understand your disease and how it affects your ability to enjoy yourself in social situations? Sometimes I think mine get it, and other times it's like explaining the disease all over again.

Looks like between the two of us we are going to have the next great american novel... I wish we were getting paid by the word haha

I actually just moved back to Oklahoma like 2 weeks ago....sadly. I really don't like to socialize because it's so hard, but if I do I usually eat before attending. Usually before dating someone I tell them flat out and upfront about it, and if they even flinch I wont even consider dating them. When I first found out that I had it I was engaged, and once he found out he decided it "was too much trouble and not worth his time". Where I live there are absolutely no restaurants that are gluten free, not many stores carry the foods here, and theres no vegetarian places around here. I don't even think I've ever met a vegan in my entire life.

I would say that absolutely no one understands and everytime I go to a social event I feel completely out of place. I don't ever really enjoy myself. The nicest thing someone has done for me was at a birthday party, they knew I couldn't eat the cake so they bought me a bowl of fruit to eat instead. I usually eat before I leave the house to ensure I dont get cross contaminated or worse.

Lol maybe the novel will hit the bestsellers list and make millions. Then I would buy my own gluten free company and there would never be any problems again.

deltron80 Rookie

I actually just moved back to Oklahoma like 2 weeks ago....sadly. I really don't like to socialize because it's so hard, but if I do I usually eat before attending. Usually before dating someone I tell them flat out and upfront about it, and if they even flinch I wont even consider dating them. When I first found out that I had it I was engaged, and once he found out he decided it "was too much trouble and not worth his time". Where I live there are absolutely no restaurants that are gluten free, not many stores carry the foods here, and theres no vegetarian places around here. I don't even think I've ever met a vegan in my entire life.

I would say that absolutely no one understands and everytime I go to a social event I feel completely out of place. I don't ever really enjoy myself. The nicest thing someone has done for me was at a birthday party, they knew I couldn't eat the cake so they bought me a bowl of fruit to eat instead. I usually eat before I leave the house to ensure I dont get cross contaminated or worse.

Lol maybe the novel will hit the bestsellers list and make millions. Then I would buy my own gluten free company and there would never be any problems again.

wow sad story :(

welcome to the #1 best celiac forum

Gf Princess182 Rookie

wow sad story :(

welcome to the #1 best celiac forum

Thanks for the welcome :)

No reason to be sad about it, I'm ten billion times healthier.

NickMcKinnis Rookie

I actually just moved back to Oklahoma like 2 weeks ago....sadly. I really don't like to socialize because it's so hard, but if I do I usually eat before attending. Usually before dating someone I tell them flat out and upfront about it, and if they even flinch I wont even consider dating them. When I first found out that I had it I was engaged, and once he found out he decided it "was too much trouble and not worth his time". Where I live there are absolutely no restaurants that are gluten free, not many stores carry the foods here, and theres no vegetarian places around here. I don't even think I've ever met a vegan in my entire life.

I would say that absolutely no one understands and everytime I go to a social event I feel completely out of place. I don't ever really enjoy myself. The nicest thing someone has done for me was at a birthday party, they knew I couldn't eat the cake so they bought me a bowl of fruit to eat instead. I usually eat before I leave the house to ensure I dont get cross contaminated or worse.

Lol maybe the novel will hit the bestsellers list and make millions. Then I would buy my own gluten free company and there would never be any problems again.

I feel ya, I don't attend 90% of the social events in my circle. This has caused a lot of problems for me, as far as keeping friends/social obligation. I am sorry to hear about your ex-fiance, I can relate as I was engaged too and she left me for pretty much the same reason. She knew about it going in but I think that as she thought about the fact that this would be her life, and not just mine. That she wouldn't be able to have the same kinds of experiences as others without the concern of gluten I think that it was too much for her. I am still pretty bitter about it, I feel like I was tricked somehow.

If you get that book deal, don't forget the little people!

Gf Princess182 Rookie

I feel ya, I don't attend 90% of the social events in my circle. This has caused a lot of problems for me, as far as keeping friends/social obligation. I am sorry to hear about your ex-fiance, I can relate as I was engaged too and she left me for pretty much the same reason. She knew about it going in but I think that as she thought about the fact that this would be her life, and not just mine. That she wouldn't be able to have the same kinds of experiences as others without the concern of gluten I think that it was too much for her. I am still pretty bitter about it, I feel like I was tricked somehow.

If you get that book deal, don't forget the little people!

Yeah, it sucks knowing that someone could do such a thing. Just gotta stay positive and eventually there will be someone who understands and someone who doesnt run. I've pretty much forgiven the guy, it doesnt pay to hold a grudge.

pianoland Rookie

Loved reading the stories.

I woke up to a phone call from the doctor saying "Do you want the good news or the bad news first?" The good news was my thyroid and other blood tests were good but the results came back positive for celiac. It was the strangest experience. At first I just wanted to break down but then I realized 1) I don't have to rely on medication 2) my symptoms will finally go away 3) the cure is as simple as changing my diet.

I usually eat before social functions or bring something with me. And you know I'm usually pleasantly surprised that they made something gluten free for me. I really hope you guys don't limit yourself socially because of food. It should never get in the way of living life.

Funny story, one time I tried to dodge a date when a guy asked me to dinner. I was like, well it would be hard because I eat gluten free. I thought he'd be clueless and shy away. He goes, OH well I can take you to -named a couple places-." I was like, err....

Lisa Mentor

Loved reading the stories.

I woke up to a phone call from the doctor saying "Do you want the good news or the bad news first?" The good news was my thyroid and other blood tests were good but the results came back positive for celiac. It was the strangest experience. At first I just wanted to break down but then I realized 1) I don't have to rely on medication 2) my symptoms will finally go away 3) the cure is as simple as changing my diet.

I usually eat before social functions or bring something with me. And you know I'm usually pleasantly surprised that they made something gluten free for me. I really hope you guys don't limit yourself socially because of food. It should never get in the way of living life.

Funny story, one time I tried to dodge a date when a guy asked me to dinner. I was like, well it would be hard because I eat gluten free. I thought he'd be clueless and shy away. He goes, OH well I can take you to -named a couple places-." I was like, err....

What a GREAT attitude you have pianoland! You will be just fine on the diet. And welcome to your first day of recovery. Welcome here! :D

pianoland Rookie

Oh that was almost a year ago now! Just was sharing my initial reaction. :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,196
    • Most Online (within 30 mins)
      7,748

    peebo
    Newest Member
    peebo
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Lindquist
      Hi im from northern europe are blood type 0+ have celiac with code K900 on the paper from doctor, have low vitamin D and b12 and folate, zinc, manganese and high copper it say in test. The best food i have eaten for now is LCHF, i tried paleo but i was missing the dairy. And i love the cream in sauces. LCHF is good choice there is no grains in the dishes. It's completly gluten free lifestyle i say. Because i feel good to eat it.
    • WednesdayAddams13
      Hello,   I contacted the makers of Alpine Original Spiced Cider Drink Mix and they sent me this email.....   Subject: [EXTERNAL] Fw: Ref. ID:1335211 Alpine Original Spiced Cider Drink Mix.               On Friday, December 6, 2024, 1:04 PM, Consumer <baking@continentalmills.com> wrote: December 06, 2024   Dear Janie, Thank you for taking the time to contact us regarding our Alpine Original Spiced Cider Drink Mix. We appreciate your interest and are happy to provide you with additional information. This product does not contain gluten. However, it is not manufactured in a gluten free facility. If I can be of further help, please contact me at 1 (800) 457-7744, weekdays 7:00 a.m. to 4:00 p.m. (PT), or visit www.alpinecider.com and select "Contact Us." Sincerely, Kristin Kristin Consumer Relations Specialist Ref # 1335211   I hope this helps everyone.  I am currently looking for a spiced hot apple cider drink and have yet to find one that is not made in a plant that manufactures other gluten products.  It's so frustrating. 
    • trents
      @Rogol72, dermatitis herpetiformis occurs in a minority of celiac patients and if the OP hasn't developed it yet I doubt it will show up in the future. I think it unwise to use a scare tactic that probably won't materialize in the OP's experience. It has a good chance of backfiring and having the opposite effect.
    • Rogol72
      Hi @trents, You're correct. The OP mentioned fatigue and vitamin deficiencies as the only symptoms at the time of diagnosis. Since the family are not taking him/her seriously and find them to be too fussy, I suggested showing them pictures of dermatitis herpetiformis as one of the consequences of not taking the gluten-free diet seriously ... would make life easier for him/her, and the family might begin to take his/her strict gluten-free diet more seriously. A picture says a thousand words and the shock factor of dermatitis herpetiformis blisters might have the desired effect. The OP did say ... "How do you deal with people close to you who just refuse to understand? Are there any resources anyone could recommend for families that are short and easy to read?".  @sillyyak52, It might also help mentioning to your family that Coeliac Disease is genetic and runs in families. Any one of them could develop it in the future if they have the HLA DQ 2.5 gene. Here's a Mayo Clinic study calling for screening of family members of Coeliacs ... https://newsnetwork.mayoclinic.org/discussion/mayo-clinic-minute-celiac-disease-screening-for-family-members/ https://newsnetwork.mayoclinic.org/discussion/mayo-clinic-study-calls-for-screening-of-family-members-of-celiac-disease-patients/ I got glutened a few months ago because I missed the may contains statement on a tub of red pesto. It was my own fault but it happens.
    • peg
      Thank you, Scott!  This is just what I needed.  Appreciate your site very much and all of your time and energy that goes into it! Kind Regards, Peg
×
×
  • Create New...