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

Newly Diagnosed


Bellanovia

Recommended Posts

Bellanovia Newbie

On January 5th I had the upper GI biopsy performed and in February 7th was diagnosed. I won't lie, the Dr was rushed and didn't explain anything. The biopsy was somewhat inconclusive? I have no idea in what way. But with my symptoms and family history he was more then confident in the diagnosis ( not to mention I unintentionally started eliminating gluten high products by just eating more fresh). I have been left on my own to make sense of this. I am discouraged, frustrated and starting to feel very depressed. I went to a bakery that advertises themselves as gluten free..and the only gluten free products were frozen pre packaged items my bread selection was brown rice bread..and brown rice bread. I have been substituting some glistens that i Was eating easily. But I am still eating it. The switch is slow..and it feels like it will never fully happen. Not only do I need to stop eating it..but I have to eliminate cross contamination threats at home. My sister has been a great help..but I still feel totally consumed and overwhelmed. It doesn't help that my kids are suddenly 150 times more needy and I'm pregnant and my husband is out of commission from a surgery :( I wish my dr had been some help. I'm so hungry. But I don't know what to eat. And when I do eat anything with gluten I am in pain almost immediately. So I am confident in the diagnosis. Unfortunately annoying family members keep saying things like, " I was surprised you were diagnosed. You weren't nearly as bad as your sister". And I just want to cry. My sister was so much worse off then me yes..she was totally malnourished, and her body was shutting down. She was 80 pounds overweight, tired, sick, rashy. Since switching he is a different person. I had more IBS symptoms that I hve been making excuses for all my life. 15 plus bowel movements a day..that are emergencies everytime. Extreme stomach pain and cramping. And terribly sensitive skin. I just didn't tell anyone. So now they all seem to think (minus my sister) that I must not have it as bad. And until they have to run into a store carrying two fifty pound kid to use a dirty public washroom they just don't have the right to judge. I hope I am one of the few who can tolerate it in small amounts. But even now one piece of toast sends me into an attack.

Sorry this is so long winded.

I finally bought myself my own peanut butter and margarine. And my husband asked what I was going to put it on and I started bawling because I have no idea :( I don't know how to make bread ..or how to buy crackers. I am totally lost and drowning.

And I feel really dumb for bein this emotional about food. I am very fortunate it isn't serious


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



Celiac.com Sponsor (A8-M):



dhd2000 Newbie

It is emotional, it's really mourning the way things used to be! And if you're pregnant, you have double the emotions going on. So give yourself a break. There's a learning curve and you'll make mistakes early on, that's ok. But you really do have to stop eating things like regular toast for your protection and your baby's protection. Stock your pantry/fridge with easy access items so that you can find something when you're hungry. Here are some easy ideas:

Rice chex

Snyder's Gluten free pretzels

Yogurt and cheese sticks

celery/carrots/cucumbers and ranch dressing

corn chips and salsa

Breyer's ice cream (most flavors)

Hormel chili with cut up hot dogs

van's or Trader Joe's gluten free waffles

Rice

Beans

frozen vegetables

meat - use your own seasonings

gluten free pasta

pop corn

rice cakes

boar's head or homel lunch meats

fruit!!!

loads of gluten free cookies available these days - I like Trader Joe's chocolate chip the best.

Try and find some things that you like and know that you won't have a lot of variety for awhile.

Hang in there, it does get easier!!!

Dee in NC

Simona19 Collaborator

First thing first: Welcome here!

I understand your situation -There is nothing to eat! Everything is made with gluten!- because I lived through it. I was lost at the beginning too. I couldn't even picture myself to make gluten free pancakes.

Now? Year and half later I'm cooking and baking without gluten and milk.

From the beginning eat gluten free things that you have been always eating.

Something like: grilled, baked chicken, fish, pork, beef, vegetable, spaghetti (just substitute pasta), mashed, cooked, baked potatoes, rice, fruit, cheese, hot-dogs, etc.

For breakfast, lunch: cereals, scramble eggs, sunny side or hard boiled eggs, egg salad, fruit, tuna fish salad, fresh salad with grilled chicken etc.

I will give you one important advice: Don't buy things that you never used before going gluten free. You wouldn't like them. It will just be a waste of time and money. I didn't listen and for a wail I was stuck with pantry full of things that didn't taste good. It took me long time to get rid of them.

You can check these posts to get some ideas what to eat (some of them are easy to make):http://www.celiac.com/forums/topic/81858-whats-for-breakfast-today/

https://www.celiac.com/forums/topic/87765-what-did-you-have-for-lunch-today/

https://www.celiac.com/forums/topic/75238-what-are-you-cooking-tonight/

I left out bread because that is the one thing that you can't replace, but you can come close to real thing. If you are in the USA, go to Whole food, Wegmans, or Trades Joe's where you can find bigger selection of gluten free breads, bagels, muffins, or buns.

If you can't, then check this:

https://www.celiac.com/forums/topic/85650-gluten-free-sandwich-bread/page__p__735949__fromsearch__1#entry735949

https://www.celiac.com/forums/topic/84873-simonas-braided-challah/page__p__729391__fromsearch__1#entry729391 .

https://www.celiac.com/forums/topic/85686-gluten-and-casein-free-hamburger-buns/page__p__736212__fromsearch__1#entry736212

Or just write what you are looking for in search engine and many recipes will pop up.

Bubba's Mom Enthusiast

On January 5th I had the upper GI biopsy performed and in February 7th was diagnosed. I won't lie, the Dr was rushed and didn't explain anything. The biopsy was somewhat inconclusive? I have no idea in what way. But with my symptoms and family history he was more then confident in the diagnosis ( not to mention I unintentionally started eliminating gluten high products by just eating more fresh). I have been left on my own to make sense of this. I am discouraged, frustrated and starting to feel very depressed. I went to a bakery that advertises themselves as gluten free..and the only gluten free products were frozen pre packaged items my bread selection was brown rice bread..and brown rice bread. I have been substituting some glistens that i Was eating easily. But I am still eating it. The switch is slow..and it feels like it will never fully happen. Not only do I need to stop eating it..but I have to eliminate cross contamination threats at home. My sister has been a great help..but I still feel totally consumed and overwhelmed. It doesn't help that my kids are suddenly 150 times more needy and I'm pregnant and my husband is out of commission from a surgery :( I wish my dr had been some help. I'm so hungry. But I don't know what to eat. And when I do eat anything with gluten I am in pain almost immediately. So I am confident in the diagnosis. Unfortunately annoying family members keep saying things like, " I was surprised you were diagnosed. You weren't nearly as bad as your sister". And I just want to cry. My sister was so much worse off then me yes..she was totally malnourished, and her body was shutting down. She was 80 pounds overweight, tired, sick, rashy. Since switching he is a different person. I had more IBS symptoms that I hve been making excuses for all my life. 15 plus bowel movements a day..that are emergencies everytime. Extreme stomach pain and cramping. And terribly sensitive skin. I just didn't tell anyone. So now they all seem to think (minus my sister) that I must not have it as bad. And until they have to run into a store carrying two fifty pound kid to use a dirty public washroom they just don't have the right to judge. I hope I am one of the few who can tolerate it in small amounts. But even now one piece of toast sends me into an attack.

Sorry this is so long winded.

I finally bought myself my own peanut butter and margarine. And my husband asked what I was going to put it on and I started bawling because I have no idea :( I don't know how to make bread ..or how to buy crackers. I am totally lost and drowning.

And I feel really dumb for bein this emotional about food. I am very fortunate it isn't serious

I completely understand your frustration! When I was DXed I was told "you have Celiac disease. Don't eat gluten. Look it up on the internet." Not even a sheet of paper telling me what gluten was..or the other names it goes by. We're told we have this serious condition..but we're on our own in treating it.

Your sister being Dxed before you is a blessing AND a curse..IMO. On the one hand, she may be able to answer some of your questions and give support, and on the other..you're being compared to her and feel that others may not be taking your Dx as being as serious? It's a serious disease, which is life changing. You're going to have times where you mourn the loss of foods you enjoyed.

Please don't eat gluten! :o You must be sure to remove all traces of it in your diet so your system can heal.

Try to stick to a mostly whole foods diet with plenty of fruits and veggies. Look for gluten free waffles(Van's) to put your peanut butter or margarine on. Be sure to get yourself a toaster dedicated to gluten-free.

King Arthur's gluten free flour is usually pretty easy to find in the regular flour aisle of the market. They have a bread recipe on the package that's easy and pretty good.

It's an adjustment, to be sure. We're here for you. If you have any questions..just ask. A lot of our eating has emotions tied to it. It's not unusual to feel emotional about food! :D

Simona19 Collaborator

I found the recipe with the KA flour

https://www.celiac.com/forums/topic/85254-perfect-gluten-free-whitesandwich-bread/ , but the flour is very expensive where I live, so I created the copy cat recipe for people that can

Bellanovia Newbie

I can't even begin to thank you for the suggestions/support/resources. I was in a really bad place yesterday and reading these replies have really helped to motivate me. I am still scared..but I feel a little more confident. We went shopping today and bought some bread yogurts, noodles, and tortilla wraps. The prices are astounding. But my husband is supportive thankfully.

Now..do we all have to go gluten free? We are investing in a new toaster and sterilizing what we do have. But how easily do we cross contaminate. How do we even sterilize? I clean everything with vinegar which I've been told had gluten..and baking soda too? Should I do orange peel cleaners? Or go get chemical cleaners? I was totally gluten free today and it was so nice not having constant pain. Though I still was a little crampy it was nice to have less intensity.

How do I properly clean out my 14 and 29 month olds mouths if they do have gluten. How badly will it hurt me if I forget or miss a spot

Bubba's Mom Enthusiast

Some people find it easiest to have the whole household gluten-free.

Stainless steel pans can be washed well and scrubbed. So can your dishes and glassware. You want to replace anything that's porous, like cutting boards, wooden spoons, plastic storage containers, colanders that are nearly impossible to clean well, toaster and can opener.

If you have any scratched non-stick cookware..toss it, or or keep it ONLY for gluten foods if you'll still be using them. Keep your gluten-free items seperate from anything that gluten will be used with.

Most vinegar is gluten free. Read the label. Vinegar or soda won't really affect how you clean items. They are better for cutting through grease or neutralizing PH. You aren't fighting germs here..it's tiny, miniscule molecules of protein you are trying to get rid of.

If your kids are eating gluten..it's tricky. An adult can brush their teeth well and use a rinse, but kids are different. They don't cooperate as well? Just be very aware of the possibility of their kisses/saliva being a source of CC?

The best way to go IMHO is to try to eat a mainly whole foods diet rich in fruits and veggies, and limit the gluten-free replacement processed foods?

You can bake your own breads and sweets if you want/need them. There are recipes all over. If you make your own it cuts down on the cost, and you know what's in it.


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



Celiac.com Sponsor (A8-M):



kb27 Apprentice

I can't even begin to thank you for the suggestions/support/resources. I was in a really bad place yesterday and reading these replies have really helped to motivate me. I am still scared..but I feel a little more confident. We went shopping today and bought some bread yogurts, noodles, and tortilla wraps. The prices are astounding. But my husband is supportive thankfully.

Now..do we all have to go gluten free? We are investing in a new toaster and sterilizing what we do have. But how easily do we cross contaminate. How do we even sterilize? I clean everything with vinegar which I've been told had gluten..and baking soda too? Should I do orange peel cleaners? Or go get chemical cleaners? I was totally gluten free today and it was so nice not having constant pain. Though I still was a little crampy it was nice to have less intensity.

How do I properly clean out my 14 and 29 month olds mouths if they do have gluten. How badly will it hurt me if I forget or miss a spot

Hi! We're newly gluten-free, too. My son was just diagnosed 2 weeks ago. We decided to switch the whole house gluten-free for now at least until we figure out how to get the hang of this. It has helped me not be paranoid about every little crumb, and now everything in the house is safe for my son to eat. I know everything is gluten-free. I'm experimenting with gluten-free bread, pancakes, pie crust, and other baked goods. Sometimes it works, sometimes it doesn't, but I think I'll get the hang of it eventually. We celebrate our successes, one by one. Overall though, we are eating not so different than we were, but there are a lot less snacky foods. We bought gluten-free pastas, crackers, pretzels, Chex cereal, and sauces. Lots of regular food is fine: Eggs, cheese, beans and rice, fruits, veggies and dips, meats, tacos, and so on.

The de-glutening process involved scrubbing out the kitchen and everything in it, top to bottom. I just used soap and water. Not so fun - my mother-in-law came and helped and we just did it all in one weekend.

Good luck!

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. - jenniber replied to jenniber's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      9

      Disaccharide deficient, confusing biopsy results, no blood test

    2. - trents replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      High TTG-IgG and Normal TTG-IgA

    3. - xxnonamexx replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      32

      My journey is it gluten or fiber?

    4. - xxnonamexx replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      32

      My journey is it gluten or fiber?

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

      High TTG-IgG and Normal TTG-IgA

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

    • Total Members
      132,845
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • jenniber
      thank you both for the insights. i agree, im going to back off on dairy and try sucraid. thanks for the tip about protein powder, i will look for whey protein powder/drinks!   i don’t understand why my doctor refused to order it either. so i’ve decided i’m not going to her again, and i’m going to get a second opinion with a GI recommended to me by someone with celiac. unfortunately my first appointment isn’t until February 17th. do you think i should go gluten free now or wait until after i meet with the new doctor? i’m torn about what i should do, i dont know if she is going to want to repeat the endoscopy, and i know ill have to be eating gluten to have a positive biopsy. i could always do the gluten challenge on the other hand if she does want to repeat the biopsy.    thanks again, i appreciate the support here. i’ve learned a lot from these boards. i dont know anyone in real life with celiac.
    • trents
      Let me suggest an adjustment to your terminology. "Celiac disease" and "gluten intolerance" are the same. The other gluten disorder you refer to is NCGS (Non Celiac Gluten Sensitivity) which is often referred to as being "gluten sensitive". Having said that, the reality is there is still much inconsistency in how people use these terms. Since celiac disease does damage to the small bowel lining it often results in nutritional deficiencies such as anemia. NCGS does not damage the small bowel lining so your history of anemia may suggest you have celiac disease as opposed to NCGS. But either way, a gluten-free diet is in order. NCGS can cause bodily damage in other ways, particularly to neurological systems.
    • xxnonamexx
      I made it through the holiday w/o being glutened. I had my brother cook with gluten-free breadcrumbs and I didn't get sick. I baked cookies with gluten-free flour and had dry ingredients for cookies in ziplock bag. I also made gluten cookies as well and guess I did good washing to avoid CC. My wife also went to a french bakery and bought a gluten-free flourless chocolate cake dedicated gluten-free it was out of this world. 
    • xxnonamexx
      What do you mean it would not allow any celiac to eat gluten again. I think if this helps cross contamination when eating out at a non dedicated gluten-free restaurant this would be nice not to encounter the pains. But is their a daily enzyme to take to help strengthen the digestive system? 
    • SamAlvi
      Hi, thank you for the reply. Unfortunately, no other antibody tests were ordered. I am a 32-year-old male. About two months ago, I ate pancakes and then developed severe diarrhea that lasted the entire day. At night, I became unconscious due to fluid loss and was admitted to the ER, where I received IV fluids. Two days later, I ate bread again and once more developed severe diarrhea. I ended up in the ER again and received IV fluids. In my country, Pakistan, doctors are unfortunately not very thorough, so they treated me for a stomach infection. I visited three or four doctors, including a gastroenterologist, but it seemed like they just wanted to keep me on medications and IV fluids. Eventually, I did some digging myself and started connecting the dots. For years, I’ve had excessive gas buildup and frequent loose stools, but I never paid much attention to it. I also cannot easily digest dairy products. Two years ago, I had a CBC test that showed iron deficiency. My doctor told me to eat more meat and said it was nothing serious. However, for the past five years, I’ve also had severe motion sickness, which I never experienced before. Whenever I get on a bus or in a car, I sometimes lose consciousness for 10–20 seconds and wake up sweaty, and occasionally I feel the need to vomit. After more research on the internet, I came across gluten and celiac disease, so I got two related tests (TTG-IgA & TTG IgG) done along with a stool test and another CBC. The stool test showed weakly positive blood. Ever since eating those pancakes and bread, I’ve had a burning sensation in my gut. My doctor reviewed my tests, he told me to completely stop eating gluten and started me on IV fluids for 20 days, saying that I had severe inflammation in my gut. It has now been two months since I quit gluten, and I’m still not sure whether this is celiac disease or gluten intolerance. I don’t really trust doctors in Pakistan, so I thought I might get some help here.
×
×
  • 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.