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

Going Crazy!


shoestring

Recommended Posts

shoestring Newbie

i was recently diagnosed with celiac disease. i have been doing research on it and figuring out what i can and cant eat. i see all this talk about cross contamination. i am going crazy, getting depressed, stressed and feel like my mind is wilting away. i dont care about not being able to eat my favorite foods no more, i am just going crazy tring to figure out what has gluten in it. i dont know what to eat besides the few things i found i can eat. i am buggin and dont really know where to start. you can probley tell by my spelling i amnot the smartest man in the world and being knowledged in what contains gluten i am finding to be very difficult. any words would be appreciated..


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



Celiac.com Sponsor (A8-M):



rinne Apprentice

Hi. :)

I know it is overwhelming at first but it will get easier, this is a great place to come with questions.

Many people with celiac have no problem with cross contamination, it is important to pay attention too but don't let it make you crazy.

Eating simple is best, whole foods, unprocessed foods.. Do you cook?

How are you feeling physically? :)

There are lists on this site with gluten free products, take a look around.

maile Newbie

hi shoestring!

actually your spelling is just fine, trust me I've seen way worse and from people not as humble as you.

from what I've read on this wonderful forum the easiest thing to do at the beginning is to keep it simple and pure as you can with the food. Rice, corn, meat, chicken, pork, nuts, veggies and fruit all of these you should be able to eat without worry. It's when you get to processed foods that the deliberating has to come in...to help you may find these useful:

here's a list of Open Original Shared Link, print this out and pin it to your fridge or carry it with you when you shop.

here's a list of Unsafe Foods that you can print and use as well...just make sure you label them carefully B)

This is a great place to find information!

mef Newbie

Hi Shoestring,

You are not alone! It is a difficult dietary transition to go through and many people here have experienced what you are feeling. Research is your best tool. Find the foods that you like and figuring out how to make them gluten free. For example, you can still have meats, vegetables, and fruits. There are numerous gluten free products available as well.

Cross contamination just means that somehow gluten gets into a gluten free food. It's like dropping a cracker on a gluten free soup.

Start small with simple meals. This way if you do make a mistake, it's easier to pinpoint what happened. A great tool is the phone number of the manufacturer located on the back of food products. If you are unsure about a product, just give them a call.

Key words you want to avoid are: Wheat, barley, malt, oats, and rye. You want to be suspect of anything with Natural Flavorings--hidden gluten. The FDA requires Wheat to be listed as an allergen, but the other gluten triggers do not have to be on the label.

Keep working hard! It may not seem like it, but the longer you stay on the diet, the easier it becomes. If you do make a mistake, don't beat yourself up for it. Just get back on track.

Good luck!

i was recently diagnosed with celiac disease. i have been doing research on it and figuring out what i can and cant eat. i see all this talk about cross contamination. i am going crazy, getting depressed, stressed and feel like my mind is wilting away. i dont care about not being able to eat my favorite foods no more, i am just going crazy tring to figure out what has gluten in it. i dont know what to eat besides the few things i found i can eat. i am buggin and dont really know where to start. you can probley tell by my spelling i amnot the smartest man in the world and being knowledged in what contains gluten i am finding to be very difficult. any words would be appreciated..
shoestring Newbie

thanks for the responses. i am feeling pretty good. ive only been on the diet for about two weeks now, i know healing takes time. my problems were that my stomach had alot of acid in it, all day it felt like i had to take a number 2, i was taking number 2s quit a bit through out the day, i lost 12 pds ( im 6ft wieghed 150pds, now weigh 138pds, really cant afford to lose weight) and i can never gaine any wieght. they suspected celiac and i looked it up and it all makes sense.

Also the want me to take an endoscopey/biopsy. i am teraffied of being sedated i was once before and it didnt go to well. is this test totally necassary to find out? i took a blood test and am waiting for results.

iread some were on here about a saliva test. does anyone know anything about that? where do they do the test? how can i find out more info about it?

thanks for your time..

rinne Apprentice

How were you diagnosed?

If by blood work and they have told you have celiac, you have celiac. The biopsy is considered a "gold standard" by doctors as they can, once you have enough damage, see the damage. That's the catch, you have to continue to eat gluten in order for the damage to be seen. :(

Diet is considered by some to be a perfectly legitimate diagnostic tool, if you get well on the diet then what is the need for the biopsy?

There are some who can speak to the plus side of this test. I won't. :)

shoestring Newbie

i talked to a specialist. he says it sounds like celiac. waiting for the blood test and to take the biopsy. i will not be taking the biopsy to scared. this i know will piss the doctor off and am scared he will not want to see me know more.. i picked up the diet myself after looking up some info on it.. how long will it take to fell the effects of the diet? i fell about 5% better after 2 weeks..


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



Celiac.com Sponsor (A8-M):



rinne Apprentice

So much depends on how long you have been ill, what other conditions you have, whether you are exposed to cross contamination....... feeling better after two weeks is positive. :)

Keep in mind though that some see an initial improvement and then seem to have setbacks which can throw doubt about the diagnosis. Many find that giving up dairy is necessary too, at least until the villi heal.

If you would like to share a little of your health history it might be easier to guess but really that is all it is, a guess. Some resume their lives quickly, some do not.

As for your doctor, well they don't like it when we don't listen to them. :lol: I have a friend, a doctor, that says doctor's are shocked these days at how (my words) rebellious patients are and that this is making the medical profession less appealing to many. :lol: She said that patients sometimes even yell at doctors these days. :o:lol:

i talked to a specialist. he says it sounds like celiac. waiting for the blood test and to take the biopsy. i will not be taking the biopsy to scared. this i know will piss the doctor off and am scared he will not want to see me know more.. i picked up the diet myself after looking up some info on it.. how long will it take to fell the effects of the diet? i fell about 5% better after 2 weeks..
shoestring Newbie

a little history about me - growing up i ate alot of junk food and drank alot of kool aid. my family always had food and lots of junk food. kool aid was my drink of choice, no water just kool aid. after a trip to the dentist and finding out i had 10 cavities i cut out the kool aid and junk food. ive never really been that concerned with my food. was never aware of how bas alot of foods are. i cut out all red meat from my diet. i have been skinny my whole live, could never gain weight. i graduated 10 1/2 yrs ago and still wiegh the same. i have problems with being dizzy after 3 different depressents messing me up and my doc finally listing to me i was found to have sever allergies. allergies to foods included. i do nothing to help my allergies and continue to eat foods i am allergic to. about a yr and a half ago they digenosed me with anxioty. they gave me some pills. about 6 months in to that i noticed i was going number 2 alot. i use to go alot for as long as i can remeber but now i was going alot more. i would eat and have to go to the bathroom imidiatly. i have always had that problem, but just more saver now. i quiet the pills after a while and went through with drawls and all that fun stuff. the stomach pains and trips to the bathroom continued. i went to the doc he said IBS take these pills and sent me on my way. the pills did nothing and i stopped taking them. went back to see him told him pills were not working and i stopped taking them. he got all mad and sent me to a specialist to get a scope put up my butt ( i think he wanted that done to me cause he was mad i stopped taking the ibs pills and refused his orders for me to take them again). but the specialist thinks celiac. my stomach has been really bad for a yr or so. has always been bad but just worse. i now wiegh 138 pds lost 12 pds. cant keep no food in me. it goes in and for the most part right out. sometimes food stays in for awhile not often. i do not feel nauses just stomach pains were it constitly feels like i have to take a number 2.. thats a brief history. sorry its kinda long.. if i left any thing out our you have any more questions feel free to ask.. thanks for your time..

one more mile Contributor

The depression may be part of the food allergies. I was on depression medications for years. But Now that I am gluten free there is actually joy in my life!

I had to cut out all foods and slowly add things back till I found out what was making me ill. Flor the first few months I could not eat rice or potatoes but now seem to have no problem with them. The fewer things in the food the better. when I read a label and their are 10 ingredient I put it back on the shelf. to much of a chance of cross contamination.

I do not eat beef because it makes number 2 hard. but I do eat chicken, and ground pork often. I had cut out most meat from my diet and my blood tests showed that my protein was to low.

It does get easier.

look at this list for ideas on what you can eat.

Open Original Shared Link

( things may be different from brand to brand, some yogurt had wheat in it.)

Many foods have an 800 number you can call. I take my cell phone shopping with me and call if I have a question.

easy understanding of being gluten free

Open Original Shared Link

For a soft number 2 I take some pro-biotics after a big meal a few times a week. PB-8 is gluten free and works well for me. look for big blue lettering. If I did not go number for a day I take them. I find they work much nicer then medications.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - tiffanygosci posted a topic in Coping with Celiac Disease
      0

      New Celiac Mama in My 30s

    2. - knitty kitty replied to klmgarland's topic in Dermatitis Herpetiformis
      8

      Help I’m cross contaminating myself,

    3. - Yaya replied to Jhona's topic in Introduce Yourself / Share Stuff
      29

      Does anyone here also have Afib

    4. - larc replied to Jhona's topic in Introduce Yourself / Share Stuff
      29

      Does anyone here also have Afib

    5. - klmgarland replied to klmgarland's topic in Dermatitis Herpetiformis
      8

      Help I’m cross contaminating myself,


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,919
    • Most Online (within 30 mins)
      7,748

    SB Willow
    Newest Member
    SB Willow
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • tiffanygosci
      Hello all! My life in the last five years has been crazy. I got married in 2020 at the age of 27, pregnant with our first child almost two months later, gave birth in 2021. We had another baby in April of 2023 and our last baby this March of 2025. I had some issues after my second but nothing ever made me think, "I should see a doctor about this." After having my last baby this year, my body has finally started to find its new rhythm and balance...but things started to feel out of sorts. A lot of symptoms were convoluted with postpartum symptoms, and, to top it all off, my cycle came back about 4m postpartum. I was having reoccurring migraines, nausea, joint pain, numbness in my right arm, hand and fingers, tummy problems, hives. I finally went to my PCP in August just for a wellness check and I brought up my ailments. I'm so thankful for a doctor that listens and is thorough. He ended up running a food allergy panel, an environmental respiratory panel, and a celiac panel. I found out I was allergic to wheat, allergic to about every plant and dust mites, and I did have celiac. I had an endoscopy done on October 3 and my results confirmed celiac in the early stages! I am truly blessed to have an answer to my issues. When I eat gluten, my brain feels like it's on fire and like someone is squeezing it. I can't think straight and I zone out easily. My eyes can't focus. I get a super bad migraine and nausea. I get so tired and irritable and anxious. My body hurts sometimes and my gut gets bloated, gassy, constipated, and ends with bowel movements. All this time I thought I was just having mom brain or feeling the effects of postpartum, sleep deprivation, and the like (which I probably was having and the celiac disease just ramped it up!) I have yet to see a dietician but I've already been eating and shopping gluten-free. My husband and I have been working on turning our kitchen 100% gluten-free (we didn't think this would be so expensive but he assured me that my health is worth all the money in the world). There are still a few things to replace and clean. I'm already getting tired of reading labels. I even replaced some of my personal hygiene care for myself and the kids because they were either made with oats or not labeled gluten-free. I have already started feeling better but have made some mistakes along the way or have gotten contamination thrown into the mix. It's been hard! Today I joked that I got diagnosed at the worst time of the year with all the holidays coming up. I will just need to bring my own food to have and to share. It will be okay but different after years of eating "normally". Today I ordered in person at Chipotle and was trying not to feel self-conscious as the line got long because they were following food-allergy protocols. It's all worth it to be the healthiest version of myself for me and my family. I would be lying if I said I wasn't a little overwhelmed and a little overloaded!  I am thankful for this community and I look forward to learning more from you all. I need the help, that's for sure!
    • knitty kitty
      On the AIP diet, all processed foods are eliminated.  This includes gluten-free bread.  You'll be eating meats and vegetables, mostly.  Meats that are processed, like sausages, sandwich meats, bacons, chicken nuggets, etc., are eliminated as well.  Veggies should be fresh, or frozen without other ingredients like sauces or seasonings.  Nightshade vegetables (eggplant, potatoes, tomatoes, peppers) are excluded.  They contain alkaloids that promote a leaky gut and inflammation.  Dairy and eggs are also eliminated.   I know it sounds really stark, but eating this way really improved my health.  The AIP diet can be low in nutrients, and, with malabsorption, it's important to supplement vitamins and minerals.  
    • Yaya
      Thank you for responding and for prayers.  So sorry for your struggles, I will keep you in mine.  You are so young to have so many struggles, mine are mild by comparison.  I didn't have Celiac Disease (celiac disease) until I had my gallbladder removed 13 years ago; at least nothing I was aware of.  Following surgery: multiple symptoms/oddities appeared including ridges on fingernails, eczema, hair falling out in patches, dry eyes, upset stomach constantly and other weird symptoms that I don't really remember.  Gastro did tests and endoscopy and verified celiac disease. Re heart: I was born with Mitral Valve Prolapse (MVP) and an irregular heartbeat, yet heart was extremely strong.  It was difficult to pick up the irregular heartbeat on the EKG per cardiologist.  I had Covid at 77, recovered in 10 days and 2 weeks later developed long Covid. What the doctors and nurses called the "kickoff to long Covid, was A-fib.  I didn't know what was going on with my heart and had ignored early symptoms as some kind of passing aftereffect stemming from Covid.  I was right about where it came from, but wrong on it being "passing".  I have A-fib as my permanent reminder of Covid and take Flecainide every morning and night and will for the rest of my life to stabilize my heartbeat.   
    • larc
      When I accidentally consume gluten it compromises the well-being of my heart and arteries. Last time I had a significant exposure, about six months ago, I had AFib for about ten days. It came on every day around dinner time. After the ten days or so it went away and hasn't come back.  My cardiologist offered me a collection of pharmaceuticals at the time.  But I passed on them. 
    • klmgarland
      So I should not eat my gluten free bread?  I will try the vitamins.  Thank you all so very much for your ideas and understanding.  I'm feeling better today and have gathered back my composure! Thank you kitty kitty   I am going to look this diet up right away.  And read the paleo diet and really see if I can make this a better situation then it currently is.  
×
×
  • 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.