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

New To This And Don't Know Where To Start...


nickra

Recommended Posts

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


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



Celiac.com Sponsor (A8-M):



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


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



Celiac.com Sponsor (A8-M):



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.

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. - trents replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      how much gluten do I need to eat before blood tests?

    2. - catnapt posted a topic in Related Issues & Disorders
      0

      anyone here diagnosed with a PARAthyroid disorder? (NOT the thyroid) the calcium controlling glands

    3. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      how much gluten do I need to eat before blood tests?

    4. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      Curious question

    5. - Amy Barnett posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Question

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

    • Total Members
      133,322
    • Most Online (within 30 mins)
      7,748

    avery144
    Newest Member
    avery144
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • trents
      Under the circumstances, your decision to have the testing done on day 14 sounds very reasonable. But I think by now you know for certain that you either have celiac disease or NCGS and either way you absolutely need to eliminate gluten from your diet. I don't think you have to have an official diagnosis of celiac disease to leverage gluten free service in hospitals or institutional care and I'm guessing your physician would be willing to grant you a diagnosis of gluten sensitivity (NCGS) even if your celiac testing comes up negative. Also, you need to be aware that oats (even gluten free oats) is a common cross reactor in the celiac community. Oat protein (avenin) is similar to gluten. You might want to look at some other gluten free hot  breakfast cereal alternatives.
    • SilkieFairy
      After the birth of my daughter nearly 6 years ago, my stools changed. They became thin if they happened to be solid (which was rare) but most of the time it was Bristol #6 (very loose and 6-8x a day). I was on various medications and put it down to that. A few years later I went on this strict "fruit and meat" diet where I just ate meat, fruit, and squash vegetables. I noticed my stools were suddenly formed, if a bit narrow. I knew then that the diarrhea was probably food related not medication related. I tried following the fodmap diet but honestly it was just too complicated, I just lived with pooping 8x a day and wondering how I'd ever get and keep a job once my children were in school.  This past December I got my yearly bloodwork and my triglycerides were high. I looked into Dr. William Davis (wheat belly author) and he recommended going off wheat and other grains. This is the first time in my life I was reading labels to make sure there was no wheat. Within 2 weeks, not only were my stools formed and firm but I was only pooping twice a day, beautiful formed Bristol #4.  Dr. Davis allows some legumes, so I went ahead and added red lentils and beans. Nervous that the diarrhea would come back if I had IBS-D. Not only did it not come back, it just made my stools even bigger and beautiful. Still formed just with a lot more width and bulk. I've also been eating a lot of plant food like tofu, mushrooms, bell peppers, hummus etc which I thought was the cause of my diarrhea before and still, my stools are formed. In January I ran a genetics test because I knew you had to have the genes for celiac. The report came back with  DQ 2.2 plus other markers that I guess are necessary in order for it to be possible to have celiac. Apparently DQ 2.2 is the "rarer" kind but based on my report it's genetically possible for me to have celiac.  I know the next step is to bring gluten back so I can get testing but I am just not wanting to do that. After suffering with diarrhea for years I can't bring myself to do it right now. So that is where I am!   
    • catnapt
      learned I had a high PTH level in 2022 suspected to be due to low vit D  got my vit D level up a bit but still have high PTH   I am 70 yrs old (today in fact) I am looking for someone who also has hyperparathyroidism that might be caused by malabsorption    
    • catnapt
      I am on day 13 of eating gluten  and have decided to have the celiac panel done tomorrow instead of Wed. (and instead of extending it a few more weeks) because I am SO incredibly sick. I have almost no appetite and am not able to consume the required daily intake of calcium to try to keep up with the loss of calcium from the high parathyroid hormone and/or the renal calcium leak.    I have spent the past 15 years working hard to improve my health. I lost 50lbs, got off handfuls of medications, lowered my cholesterol to enviable levels, and in spite of having end stage osteoarthritis in both knees, with a good diet and keeping active I have NO pain in those joints- til now.  Almost all of my joints hurt now I feel like someone has repeatedly punched me all over my torso- even my ribs hurt- I have nausea, gas, bloating, headache, mood swings, irritability, horrid flatulence (afraid to leave the house or be in any enclosed spaces with other people- the smell would knock them off their feet) I was so sure that I wanted a firm diagnosis but now- I'm asking myself is THIS worth it? esp over the past 2 yrs I have been feeling better and better the more I adjusted my diet to exclude highly refined grains and processed foods. I didn't purposely avoid gluten, but it just happened that not eating gluten has made me feel better.   I don't know what I would have to gain by getting a definitive diagnosis. I think possibly the only advantage to a DX would be that I could insist on gluten-free foods in settings where I am unable to have access to foods of my choice (hospital, rehab, nursing home)  and maybe having a medical reason to see a dietician?   please let me know if it's reasonable to just go back to the way I was eating.  Actually I do plan to buy certified gluten-free oats as that is the only grain I consume (and really like) so there will be some minor tweaks I hope and pray that I heal quickly from any possible damage that may have been done from 13 days of eating gluten.    
    • Jmartes71
      So I've been dealing with chasing the name celiac because of my body actively dealing with health issues related to celiac though not eating. Diagnosed in 1994 before foods eliminated from diet. After 25 years with former pcp I googled celiac specialist and she wasn't because of what ive been through. I wanted my results to be sent to my pcp but nothing was sent.I have email copies.I did one zoom call with np with team member from celiac specialist in Nov 2025 and she asked me why I wanted to know why I wanted the celiac diagnosis so bad, I sad I don't, its my life and I need revalidaion because its affecting me.KB stated well it shows you are.I asked then why am I going through all this.I was labeled unruly. Its been a celiac circus and medical has caused anxiety and depression no fault to my own other than being born with bad genetics. How is it legal for medical professionals to gaslight patients that are with an ailment coming for help to be downplayed? KB put in my records that she personally spent 120min with me and I think the zoom call was discussing celiac 80 min ONE ZOOM call.SHE is responsible for not explaining to my pcp about celiac disease am I right?
×
×
  • 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.