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nickra

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nickra Rookie

Hi

I was diagnosed 2 days ago and I am so lost and confused.

I've given the contents of my food cupboard to my house mates and now they think I am mad.

I have decided not to tell anyone about my celiac disease. House mates know and my parents, but i don't want to tell anyone else. Not because I am embarassed or anything, I just can't be bothered to explain it to people. I can't even explain it myself yet - I'm just not ready to tell anyone.

Has anyone else kept their celiac disease a secret? Just wondered if it is possible?

Thanks


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joemoe003 Apprentice

Well i dont know if it is possible to keep it a secret but i know how much trouble it in explaining it to everyone what it is and everything else. i dont know if i would be any help but if you want to you can email me or instant message me at pippigirl32@hotmail.com (thats my msn im) cjtsm@aol.com (my email). i have done lots of research on it and would love to help you. So feel free to im me any time.

Joe Moe

nickra Rookie

Hi,

Thanks for that - will hopefully have a chat with you on msn sometime - I would really appreciate some advice!

Cheers

Newbie Rookie

Hi Nickra, welcome to the board. You know, I've been gluten free for almost 3

months, and I'm still trying to keep it a secret. Same reason like you... I'm not embarassed, I just don't think a lot of people understand what it's really like

unless they're going through it. The people who know are my immediate family and a couple of friends. That's it. And I'm doing my best to keep it that way, but

it's hard. Especially when they keep offering food and you keep turning it down and won't even have just a small bit. I sometimes just say, no thanks, I don't feel good after I eat bread and stuff like that. And that works most of the time. It's a challenge to keep it a secret, but do what you feel until you're ready to tell others.

Good luck and keep asking questions! :)

Laura Apprentice

I told my friends, especially because I often stay over with a lot of them and you really can't stay at someone's house and not tell them. I thought I wouldn't tell, like, strangers about it, though. But I pretty quickly decided that I'd rather not have people like waiters and stuff think that I was on Atkins when I asked for no bread. I think you just have to make a choice. People are going to think something if they're around when you eat, so you just have to decide what it is that you want them to think -- that you're on a diet, that you're just plain weird, that you have celiac disease.

hapi2bgf Contributor

I can't say I wanted to keep it a secret, but then again with my Mom there is no way to keep ANYTHING a secret for very long. I was so sick for so long I was thrilled to have an answer that did not involve chemotherapy or worse. I am an extremely private person and I have found that by explaining the celiac disease to friends and family I actually have less to worry about when I eat with them. They all understand the very basics of a gluten-free meal and understand cross-contamination issues. And workers take my questions and requests much more seriously when I mention I have food allergies (I know it is not technically an allergy, but the word allergy equals lawsuit which makes them respond ).

In my opinion, the first few months are the hardest because the part about figuring out which foods you can actually eat is absolutely mind boggling to put it mildly. But it does get easier. I was biopsy diagnosed in Oct 2003. I still have mistakes but it gets easier. I made lists of staple foods, drinks (alcoholic), and restaurants that I know are gluten-free and I can eat at safely.

nickra Rookie

Thanks everyone for the advice.

I think it was one of my house mates responses that put me off - i was feeling really down having only just been told i had celiac disease that day and he basically told me that doctors are full of rubbish and not to take any notice. - but he has no idea of the suffering i have been going through to make me go to the doc in the first place

when the doc first told me i was so relieved to actually have something diagnosed, ive struggled for so long with no real explanation - to have this immediatly pulled apart by a friend was difficult when all i really wanted was someone to tell me everything would be ok.

im feeling more positive today :rolleyes: but one thing i am not sure about is sticking to the gluten-free diet before i have my biopsy - i have had a positive blood test result but i am waiting for the hospital appointment now, but i dont want to continue damaging myself before i have the test. do most people wait until they have the biospy before starting the diet - my doctor didnt tell me to wait???

thanks again everyone


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Guest aramgard

As usual your doctor does not know much about Celiac. Please do not go on a gluten free diet until after your biopsy, it will skew the results. And ask the doctor who gives your the endoscopy to take a lot of biopsies, because Celiac is often missed because there can be spotty damage to your jejunum. Also, even if (and I do say if) the biopsies are not positive. Most of us Celiacs would suggest you try a gluten free diet for at least several months. Also the first month or so stay dairy free, often the digestive system in Celiacs cannot handle dairy. But when the villi begin to heal, you may again be able to consume dairy. Don't allow anyone to deter you from a proper diagnosis, friend or not. You are entitled to feel better and your health is the most important thing in your life. Believe me, I am the poster child for misdiagnoses. I started showing symptoms, dermatitis herpetiformis, when I was 14. And after many, many years of health problems was finally diagnosed at age 67, three years ago. If the dermatologist had put me on the wheat free diet, forever, that he suggested for three weeks, I would probably have a much healthier immune system. So-o-o, make your health your priority. Learn about Celiac. Read the celiac.com website carefully. Go to the GIG website and read that one. I hope your quest reveals the problem and you can lead a health life from now on. Shirley

nickra Rookie

Thanks for your advice Shirley,

My doctor was quite honest with me and said she didnt know much about it - in fact she said i was the first person she has had come back positive from the blood test. so i will give her a ring on monday and tell her i dont want to affect the biopsy by going gluten free too soon.

not looking forward to cutting out dairy - but it will be so worth it if it makes me feel better!

thanks again to all of you, this forum has been a godsend in my first few days since being dx

nickra

andyc Newbie

I have been gluten-free for over a year - well almost. I don't really tell anyone anything except that I can't eat wheat it is too much to explain. I am sure that I still injest some glutin. Before i went gluten-free I never had any symtoms - now when I have an accident _I get sick -

mario Explorer

andyc;

thats because your body got extra sensitive to gluten and, doesn't want it at all

Guest neRdz

hi i was diag.. last summer and i found out that i had celiac disease ... and found out that i had it for a year ,, now i'm going crazy i'm stok in a smal town called lachute whit no one i know that as celiac disease there is nothing in town that can help me the stores that as special food and stuff are far .. crapy .. since the day that the symptomes started my life turn to be crap ... don't know what to do,, tired of having to eat wierd food that taste like crap... need help ,, i'm 22 years old live in a appartment i have look on the internet for stores and it cost so much no credit card ,, don't no what to eat no more .. don't no what to do no more ,, anyway al stop "b%$@#ing" i just don't know to who to talk about this kind of stuff ....

sorry for my poor spelling i'm french .... :unsure:

DLayman Apprentice

NeDrz,

stick with the basics.. meat fruit and vegetables also cheeses if you can tolerate them. There is alot of variety just among those things if you give it a try! You can do it!!!

Denise

Guest neRdz

yeah i got no problem whit milk (lactose) :D

Laura Apprentice

neRdz,

If you can eat corn, corn tortillas are really helpful. I make cheeseburgers, tuna salad, chicken breast, just all kinds of things, and eat them wrapped in corn tortillas. And obviously there's all kinds of mexican food you can make that way. One of my favorite easy lunches is quesadillas -- I put cheese in a tortilla and microwave it for 45 seconds or so and eat it with lots of salsa so there's even a little vegetables in it.

Plus you can do a lot with potatoes...I'm making hash tonight for dinner.

It's definitely easier to live where there are health-food stores that sell gluten-free foods, but even if you don't, there's a lot you can do with regular food ingredients. It just means you have to cook for yourself more than lots of Americans do. And if you ever visit a town with a health-food store, or even just with a bigger grocery store than you're used to, look around for things to bring back home. I also write lots of requests to my grocery store, and every now and then they actually get something I asked for, like gluten-free toaster waffles.

plantime Contributor

Nerdz, I live in a small town in Kansas, and it takes an hour to get to the nearest decent healthfood store. We are quite poor, just a click above the poverty level, so I don't have much money to spend on "my" food. I just use fruits, veggies, and meats, and fix the meals from scratch. That way, I can hoard what I do get of breads and pastas, so it doesn't cost so much. It is fairly easy to be gluten-free if you shop around the perimeter of the store, do not buy processed foods, and fix everything yourself. Time is a factor, it takes lots of it. I am not sick like I was, so I think it is definitely worth the time!

Guest aramgard

Dessa, If the nearest large town has an Asian market, the next time you are nearby try shopping there for cheap rice flour and tapioca flour, also sometimes they have garbanzo bean flour (also known as chickpea flour). That way you can make some of your own breads, etc. Shirley in San Diego

plantime Contributor

I don't know about an Asian market, but we do have a mexican store. I will have to check them out. Thanks! :D

Rick1254 Newbie

I noticed that these messages are pinned and the one I posted ended up at the very end. Is there a secret to pinning these messages?

Thanks,

Rick

plantime Contributor

Pinning just means that the topic is where it belongs on the board. It is more of a note to the other moderators that it has been checked by one of them. Your post winds up at the end because it is the most recent. Look at the dates and times, and you should see them to be in chronological order.

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    • trents
      Welcome to the celiac.com community @EssexMum! First, let me correct some misinformation you have been given. Except in the case of what is known as "refractory" celiac disease, which is very rare, it is not true that the "fingers" will not grow back once a consistently gluten free diet is adopted. Celiac disease is an autoimmune condition whereby the ingestion of gluten triggers an inflammatory process that damages the millions of tiny finger-like projections that make up the lining of the small bowel. We call this the "villous lining". Over time, continued ingestion of gluten on a regular basis results in the wearing down of these fingers which greatly reduces the surface area of this very important membrane. It is where essentially all the nutrition from what we eat is absorbed. So, losing this surface area results in inefficiency in nutrient absorption and often to medical problems related to nutrient deficiencies. Again, if a gluten-free diet is consistently observed, the villous lining of the small bowel should rebound. "We was informed that her body absorbs the gluten rather then rejecting it and that is why she doesn't react to the gluten straight away, it will be a build up and then the pains start. " That sounds like unscientific BS to me. But it does sound like your stepdaughter may have a type of celiac disease we know as "silent" celiac disease, meaning, she is asymptomatic or at least the symptoms are not intense enough to usually notice. She is not completely asymptomatic, however, because you stated was experiencing tummy aches off and on. Cristiana gives some good suggestions about ordering "safe" food for your stepdaughter from restaurant menus in Europe. You must realize that as the step parent who only has her part of the time you have no real control over how cooperative her other set of parents are with regard to your stepdaughter's needs to eat gluten free. It sounds like they don't really understand the seriousness of the matter. This is very common in family settings where other members are ignorant about celiac disease and the damage it can do to body systems. So, they don't take it seriously. The best you can do is make suggestions. Perhaps print out some info about celiac disease from the Internet to send them. Being inconsistent with the gluten free diet keeps the inflammation smoldering and delays or inhibits healing of the villous lining. 
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    • cristiana
      Good evening @EssexMum You are quite right to be concerned about this situation.  Once diagnosed as coeliac, always a coeliac, and the way to heal  is through adopting and sticking to a strict gluten diet. That said... I have travelled twice to France since my diagnosis, firstly in May 2013 and again in August 2019.   My spoken French isn't bad, and whilst there I tried my best to explain my needs to chefs and catering staff, and I read labels very carefully when shopping in supermarkets, but both times I came away with worsening gastric symptoms and pain. Interestingly,  after the second holiday, my annual coeliac review took place the following month and although I'd been very careful to avoid gluten all year, thanks to that August holiday my coeliac antibodies were elevated,  Clearly I hadn't been imagining these symptoms and they must have been caused by gluten sneaking in somehow. When I spoke to my gastroenterologist on my return, who is an excellent doctor, he told me with a smile that this was a very common experience in France among his patients, and not to worry too much about it! In fact, before we went away in May 2013, which was just after I had been formally diagnosed, he told me not to even bother trying to adopt a gluten free diet until I returned, knowing what France was like, but I was feeling so awful at that time I ignored his advice and at least tried to make a start with it. (I ought to say - both these visits were some time ago, so perhaps things are a lot better there now.) So what to do?  I would say at least try to explain to catering staff the situation - they should be able to rustle up a plate of cheese, boiled eggs, tuna, salad and fruit, and if things like crackers and gluten-free pot noodle or oats can be packed in the UK, those can be produced at mealtimes.    Of course, most larger supermarkets in France do now cater for coeliacs, but when I was last there the the choice wasn't as wide a range as we have in the UK but I think that is partly because the French like to cook from scratch, whereas our gluten-free aisles have quite a lot of dried or pre-baked goods in them/convenience foods, because I think we as a nation tend to use them more. I would be worth doing a bit of research on the internet before the trip, - the words you want are 'sans gluten'.  I've just googled 'sans gluten Disney Paris" and this came up.  I do hope at least some of this is of help. https://www.tripadvisor.co.uk/Restaurants-g2079053-zfz10992-Disneyland_Paris_Ile_de_France.html  Whatever befalls in France, at least your stepdaughter can resume her usual diet on her return. On a related tack, would you be happy to post any positive findings/tips upon her return - it might be of use to others travelling to Disneyland Paris with children in future? Cristiana
    • EssexMum
      Hi, I am after some advice re my step daughter and her Coeliac Disease. She is 9 years old and had a very limited diet before being diagnosed (very fussy and very lenient parents), since being diagnosed it has become hard to find places out that will cater for her, but we manage.  History: She had been having severe tummy pains on and off every few months so had a bunch of tests and eventually was diagnosed with celiac disease a number of months ago. We was told that she is at a very high level and should avoid gluten for the rest of her lift, we was told that the gluten she has been eating has damaged the 'fingers' inside her and they will not replenish. We was informed that her body absorbs the gluten rather then rejecting it and that is why she doesnt react to the gluten straight away, it will be a build up and then the pains start. We was advised that by her not reacting straight away, it did not mean it wasnt harming her inside. We was given literature about buying a separate toaster and cutting board etc to avoid cross contamination and have been checking all food labels etc.  Problem: the issue is the novelty seems to have worn off with her Mum and we are now posed with a situation. They are going on holiday to Disneyland Paris for 3 nights and she phoned the hotel who said they cannot cater for gluten free. She phoned the GP and had a conversation and then told my partner that the GP had said it was fine for her to have gluten for the 3-4 days. He questioned it and she said no its fine, she hasnt had it for months so a few days wont hurt and she exposed to it anyway without knowing so it will be fine and shes not ruining her holiday etc.   My partner could see from the online notes that his ex wife had told the doctor that the child does not follow a strict gluten-free diet anyway - not true. At least not with us! My partner requested a call with the same doctor who told him that it is the mums discretion and that the child should be monitored for reactions - he explained that the issue is she doesnt react straight away. The GP said no its all mums discretion and she knows best. We are going to try to speak to the consultant at the hospital, but I just wanted to gauge some thoughts. It just seems bizarre to me that we can go from being told to avoid gluten for the rest of her life and how harmful it is to her body, to now it being ok for her to have it for a few days. Thanks in advance  
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