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Any Celiac Teens Out There?


kellyisfresh

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breeeebreeee Newbie

Hi kelly! I just got diagnosed with Celaic disease late last year and I'm turning 16. I find the diet difficult and all my friend's seem to get anoyed with my special diet needs!

But, some even go out of their way to buy me little snacks and I met a fellow celiac this year at school:)

-Bree


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  • Replies 77
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SusieQ Rookie

Hi! Im 14 and I've had it like 8 months now.. it sucks! But its great to know there are others out there...!! Whats up??:)

hey im 13 and i don't know anyone around my age that has it. i have been diagnosed for 2, almost 3 weeks now. :)

  • 2 weeks later...
123bree Newbie

hey my name is mikaela and i am almost sixteen too!! i started getting sick when i was eight then after three years of tests i found out i have celiac. i never really liked baked goods so it wasen't very hard to go off gluten. i am getting fed up with having to read all the lables on the packages though. but my friends have been really good and always have something gluten free in the cupboard for me. do you know of a good bread company cuz i am having a hard time finding good gluten-free bread??

The best one i found is UDI's gluten free bread and they have other products to that are the best lol

gibberish093 Rookie

I'm 19, been diagnosed for a year now :) Anybody in BC, Canada? I'd really like to meet some Celiacs, I feel so alone..

I live in BC, Canada (haha where else :P). I am 17 - almost 18 mind you. And I have just been diagnosed 3 weeks ago with celiac. I also feel quite alone because I know no one my age, or around my age with this disease. I would love to meet people or just talk with people closer to my age with it. :)

gibberish093 Rookie

I am Cherie. Been celiac for about 3 years now. Self diagnosed 4 weeks ago, been on the gluten free ever since and I have never felt better! I am turning 18 this December and I live in BC, Canada. I am so happy that I have found other teens that I can talk to about this because the only other person I know who has celiac is my step-grandma and she isn't exactly going be going through the same situations as me. Anyone in BC or around it out there?? :) Feel free to message me, I am happy to meet new people :D

  • 4 weeks later...
Sammmmmy Newbie

Where in CT?

gibberish093 Rookie

CT??


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BakingQueen Newbie

Hi I'm 15 and I'm from Canada. I've been diagnosed for 4 years now, and I still sometimes have difficulty explaining it all to friends.

janineisaceliac Newbie

Hey! I'm Janine, I'm 16, and I've been diagnosed for about 11 1/2 years now. I live in Northern California, so if there's anyone in the area, contact me!

  • 3 weeks later...
Katah Newbie

Rebecca, 19. I self-diagnosed in Feb via diet change. No doctor could help so I just started looking myself. I live in Barrie, ON during the summer months, and in St. John's NL for the school year. Anyone in either province??

Hey, I live in Barrie too! I am 16 and have been gluten free for about 5 months now!

  • 1 month later...
Hadrian Newbie

Hi! I'm Dolan (random Irish last name that my parents decided was a good first name xD). I'm a 15 year old guy from Florida and I've been diagnosed when I was around 6 or 7 I believe.

  • 2 weeks later...
allergyprone Contributor

hi i'm Nicole i'm 18 and i just started college :mellow: in a different state i've met another student with celiacs (the 1st i ever met) but it is hard being in a different place and having to fend for my self and maintain a gluten-free diet (even if i am cooking all my own food) anyone out there in richmond kentucky id love to find out all the secrite gluten-free spots and stores

  • 2 weeks later...
Katie H Newbie

Hello, I'm Katie. I'm 17 and I've only been diagnosed with Celiac for about 3-4 months now. Still challenging and frustrating, but it's getting better! :)

DanPatch Rookie

Hey!

I'm in Ontario, and was diagnosed in May-ish of this year...

This disease seems to be growing by leaps and bounds...this will likely mean that it will improve for us celiacs :) , but really, what is the world coming to?! :blink:

Anyone else have suggestions on how to handle "may contain" foods? (chocolate :rolleyes: ). I'm still newly diagnosed, and my symptoms haven't really relieved themselves yet, so I'm not really sure.

Februaryrich Rookie

I wish I could go to the cafeteria and shout: ANY CELIACS IN THE PLACE?

Februaryrich Rookie

hey hey

i'm 15 and i've had celiac for almost

my names Anthony and i live in QC Canada... anyone else pleaseee contact me

Anthony! I'm also from QC Canada, we should hang out lol

  • 1 year later...
CeliacEllie Newbie

I was born with celiac disease, but just discovered I had it last week, I'm 15 years old. It's so hard going Gluten-Free... I'm never full, almost always hungry, I've lost a lot of weight already, and when the class/my friends eat something I can't it's torture! I'm having the worst time getting used to this and I'm not even feeling better yet, it's going to take awhile. I really hate this, but it'll be worth it in the end.

  • 3 months later...
DerpTyler Newbie

I'm 18, been diagnosed for 7 years. I go to college in Bc Canada, and iv never met another celiac at my school :P

  • 1 month later...
Stern Newbie

Hi there!

 

I've been gluten-free for a good... Nearly two years now (With a summer off for a pointless blood test, worst summer ever. >:- | ) I'm in Northern California, I'd love to talk to anyone else around here that's working through Celiac's! x_X Or any other food allergies, don't get me started on my list, no fun. X- P

  • 1 month later...
JetLockheart Newbie

I'm 20, I've reacted since I was old enough to eat solid food, but  I've never been truly diagnosed with celiac. At the age of 2 or 3 I was put on a gluten free diet( among other things) for 2 years and that fixed everything for me. Unfortunately I can't afford to be gluten free and its really messing with my college studies.

  • 1 month later...
soccerchic383 Newbie

Hey guys. Don't know if this thread is dying but I wanted to introduce myself. I'm Casey (girl) about to turn 18 and I was diagnosed with celiacs about a month ago and enduring that lovely (awful) healing period. I live in northern Cali and I'd love to talk to some other teens with celiacs!!

  • 4 months later...
arfellman Newbie

Hey my names kimberlie . I've been a celiac for almost a year now . I live in cali . Contact me smile.gif I need some celiac friends. I know of only one other celiac Wich is my best friends Grammy .

Where in Cali? I live in Ukiah (North California)

  • 4 months later...
djsimendinger Newbie

Hey I'm Dana, I'm 20 and I think I was diagnosed 2 years ago. Glad to meet others who have celiac/can't eat gluten!

  • 1 month later...
gerbilgirl Rookie

I'm a college student.  I'm still in the process of a diagnosis but I definitely have a gluten sensitivity as well as sensitivity to oats even if they are certified gluten free.  I have other allergies as well.  Been eating gluten-free for about a year but lately I seem to be becoming more sensitive, used to be able to eat a small amount of gluten every so often (such as some teriyaki sauce) but now that just doesn't cut it.  Cross-contamination is also becoming an issue.    

  • 1 year later...
LaurenIsSilly Newbie

Hi! I'm Lauren from Seattle, I am 18 and I have DH Celiac Disease as well as hypothyroidism. It took me about two years to finally diagnose my disease because I never had any stomach issues, instead my Celiac disease presents as a horrible rash all over my body and face. It has been really hard having to go to high school with such a physically different disease and have had to be home schooled this year. I recently missed my senior prom, and am missing graduation this weekend because of how I look. I wish I could be more confident in how I look, but it's really hard seeing yourself as anything other than how you looked with a raging rash all over. Dating and any type of relationship have been hard to make because I rarely leave the house due to how I look. I hope to hear from some other teens dealing with a similar situation because so far I don't know anyone else like me.

xoxo ~ Lauren  :D

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    • trents
      So, essentially all of the nutrition in the food we eat is absorbed through the villous lining of the small bowel. This is the section of the intestinal track that is damaged by celiac disease. This villous lining is composed of billions of finger-like projections that create a huge amount of surface area for absorbing nutrients. For the celiac person, when gluten is consumed, it triggers an autoimmune reaction in this area which, of course, generates inflammation. The antibodies connected with this inflammation is what the celiac blood tests are designed to detect but this inflammation, over time, wears down the finger-like projections of the villous lining. Of course, when this proceeds for an extended period of time, greatly reduces the absorption efficiency of the villous lining and often results in many and various nutrient deficiency-related health issues. Classic examples would be osteoporosis and iron deficiency. But there are many more. Low D3 levels is a well-known celiac-caused nutritional deficiency. So is low B12. All the B vitamins in fact. Magnesium, zinc, etc.  Celiac disease can also cause liver inflammation. You mention elevated ALP levels. Elevated liver enzymes over a period of 13 years was what led to my celiac diagnosis. Within three months of going gluten free my liver enzymes normalized. I had elevated AST and ALT. The development of sensitivities to other food proteins is very common in the celiac population. Most common cross reactive foods are dairy and oats but eggs, soy and corn are also relatively common offenders. Lactose intolerance is also common in the celiac population because of damage to the SB lining.  Eggs when they are scrambled or fried give me a gut ache. But when I poach them, they do not. The steam and heat of poaching causes a hydrolysis process that alters the protein in the egg. They don't bother me in baked goods either so I assume the same process is at work. I bought a plastic poacher on Amazon to make poaching very easy. All this to say that many of the issues you describe could be caused by celiac disease. 
    • catnapt
      thank you so much for your detailed and extremely helpful reply!! I can say with absolute certainty that the less gluten containing products I've eaten over the past several years, the better I've felt.   I wasn't avoiding gluten, I was avoiding refined grains (and most processed foods) as well as anything that made me feel bad when I ate it. It's the same reason I gave up dairy and eggs- they make me feel ill.  I do have a bit of a sugar addiction lol so a lot of times I wasn't sure if it was the refined grains that I was eating - or the sugar. So from time to time I might have a cookie or something but I've learned how to make wonderful cookies and golden brownies with BEANS!! and no refined sugar - I use date paste instead. Pizza made me so ill- but I thought it was probably the cheese. I gave up pizza and haven't missed it. the one time I tried a slice I felt so bad I knew I'd never touch it again. I stopped eating wheat pasta at least 3 yrs ago- just didn't feel well after eating it. I tried chick pea pasta and a few others and discovered I like the brown rice pasta. I still don't eat a lot of pasta but it's nice for a change when I want something easy. TBH over the years I've wondered sometimes if I might be gluten intolerant but really believed it was not possible for me to have celiac disease. NOW I need to know for sure- because I'm in the middle of a long process of trying to find out why I have a high parathyroid level (NOT the thyroid- but rather the 4 glands that control the calcium balance in your body) I have had a hard time getting my vit D level up, my serum calcium has run on the low side of normal for many years... and now I am losing calcium from my bones and excreting it in my urine (some sort of renal calcium leak) Also have a high ALP since 2014. And now rapidly worsening bone density.  I still do not have a firm diagnosis. Could be secondary HPT (but secondary to what? we need to know) It could be early primary HPT. I am spilling calcium in my urine but is that caused by the high parathyroid hormone or is it the reason my PTH is high>? there are multiple feedback loops for this condition.    so I will keep eating the bread and some wheat germ that does not seem to bother me too much (it hasn't got enough gluten to use just wheat germ)    but I'm curious- if you don't have a strong reaction to a product- like me and wheat germ- does that mean it's ok to eat or is it still causing harm even if you don't have any obvious symptoms? I guess what you are saying about silent celiac makes it likely that you can have no symptoms and still have the harm... but geez! you'd think they'd come up with a way to test for this that didn't require you to consume something that makes you sick! I worry about the complications I've been reading about- different kinds of cancers etc. also wondering- are there degrees of celiac disease?  is there any correlation between symptoms and the amnt of damage to your intestines? I also need a firm diagnosis because I have an identical twin sister ... so if I have celiac, she has it too- or at least the genetic make up for having it. I did have a VERY major stress to my body in 2014-2016 time frame .. lost 50lbs in a short period of time and had severe symptoms from acute protracted withdrawal off an SSRI drug (that I'd been given an unethically high dose of, by a dr who has since lost his license)  Going off the drug was a good thing and in many ways my health improved dramatically- just losing 50lbs was helpful but I also went  off almost a dozen different medications, totally changed my diet and have been doing pretty well except for the past 3-4 yrs when the symptoms related to the parathyroid issue cropped up. It is likely that I had low vit D for some time and that caused me a lot of symptoms. The endo now tells me that low vit D can be caused by celiac disease so I need to know for sure! thank you for all that great and useful information!!! 
    • trents
      Welcome, @catnapt! The most recent guidelines are the daily consumption of a minimum of 10g of gluten (about the amount found in 4-6 slices of wheat bread) for a minimum of two weeks. But if possible stretching that out even more would enhance the chances of getting valid test results. These guidelines are for those who have been eating gluten free for a significant amount of time. It's called the "gluten challenge".  Yes, you can develop celiac disease at any stage of life. There is a genetic component but also a stress trigger that is needed to activate the celiac genes. About 30-40% of the general population possesses the genetic potential to develop celiac disease but only about 1% of the general population actually develop celiac disease. For most with the potential, the triggering stress event doesn't happen. It can be many things but often it is a viral infection. Having said that, it is also the case that many, many people who eventually are diagnosed with celiac disease probably experienced the actual onset years before. Many celiacs are of the "silent" type, meaning that symptoms are largely missing or very minor and get overlooked until damage to the small bowel lining becomes advanced or they develop iron deficiency anemia or some other medical problem associated with celiac disease. Many, many are never diagnosed or are diagnosed later in life because they did not experience classic symptoms. And many physicians are only looking for classic symptoms. We now know that there are over 200 symptoms/medical problems associated with celiac disease but many docs are only looking for things like boating, gas, diarrhea. I certainly understand your concerns about not wanting to damage your body by taking on a gluten challenge. Your other option is to totally commit to gluten free eating and see if your symptoms improve. It can take two years or more for complete healing of the small bowel lining once going gluten free but usually people experience significant improvement well before then. If their is significant improvement in your symptoms when going seriously gluten free, then you likely have your answer. You would either have celiac disease or NCGS (Non Celiac Gluten Sensitivity).
    • catnapt
      after several years of issues with a para-gland issue, my endo has decided it's a good idea for me to be tested for celiac disease. I am 70 yrs old and stunned to learn that you can get celiac this late in life. I have just gradually stopped eating most foods that contain gluten over the past several years- they just make me feel ill- although I attributed it to other things like bread spiking blood sugar- or to the things I ate *with* the bread or crackers etc   I went to a party in Nov and ate a LOT of a vegan roast made with vital wheat gluten- as well as stuffing, rolls and pie crust... and OMG I was so sick! the pain, the bloating, the gas, the nausea... I didn't think it would ever end (but it did) and I was ready to go the ER but it finally subsided.   I mentioned this to my endo and now she wants me to be tested for celiac after 2 weeks of being on gluten foods. She has kind of flip flopped on how much gluten I should eat, telling me that if the symptoms are severe I can stop. I am eating 2-3 thin slices of bread per day (or english muffins) and wow- it does make me feel awful. But not as bad as when I ate that massive amnt of vital wheat gluten. so I will continue on if I have to... but what bothers me is - if it IS celiac, it seems stupid for lack of a better word, to intentionally cause more damage to my body... but I am also worried, on the other hand, that this is not a long enough challenge to make the blood work results valid.   can you give me any insight into this please?   thank you
    • trents
      The biopsy looks for damage to the mucosal lining of the small bowel from the inflammation caused by celiac disease when gluten is ingested. Once you remove gluten from the diet, inflammation subsides and the mucosal lining begins to heal. 
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