Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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 Celiac.com!
    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

Link to comment
Share on other sites

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

Link to comment
Share on other sites
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.

Link to comment
Share on other sites
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

Link to comment
Share on other sites
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

Link to comment
Share on other sites
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

Link to comment
Share on other sites
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.

Link to comment
Share on other sites

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!

Link to comment
Share on other sites

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. - Scott Adams replied to Nacina's topic in Related Issues & Disorders
      1

      14 year old with Celiac & EOE still suffering...

    2. - Nacina posted a topic in Related Issues & Disorders
      1

      14 year old with Celiac & EOE still suffering...

    3. - trents replied to Fluka66's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Waiting for urgent referral.

    4. - Fluka66 replied to Fluka66's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Waiting for urgent referral.

    5. - Moodiefoodie replied to Moodiefoodie's topic in Related Issues & Disorders
      9

      Joint swelling when ill even on gluten-free diet


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,066
    • Most Online (within 30 mins)
      7,748

    Danyelhack
    Newest Member
    Danyelhack
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      It sounds like you've been through a lot with your son's health journey, and it's understandable that you're seeking answers and solutions. Given the complexity of his symptoms and medical history, it might be beneficial to explore a few avenues: Encourage your son to keep a detailed journal of his symptoms, including when they occur, their severity, any triggers or patterns, and how they impact his daily life. This information can be valuable during medical consultations and may help identify correlations or trends. Consider seeking opinions from specialized medical centers or academic hospitals that have multidisciplinary teams specializing in gastrointestinal disorders, especially those related to Celiac disease and Eosinophilic Esophagitis (EOE). These centers often have experts who deal with complex cases and can offer a comprehensive evaluation. Since you've already explored alternative medicine with a nutrition response doctor and a gut detox diet, you may want to consider consulting a functional medicine practitioner. They take a holistic approach to health, looking at underlying causes and imbalances that may contribute to symptoms. Given his low vitamin D levels and other nutritional markers, a thorough nutritional assessment by a registered dietitian or nutritionist specializing in gastrointestinal health could provide insights into any deficiencies or dietary adjustments that might help alleviate symptoms. In addition to routine tests, consider asking about more specialized tests that may not be part of standard screenings. These could include comprehensive stool analyses, food intolerance testing, allergy panels, or advanced imaging studies to assess gut health.
    • Nacina
      Hello, I am a 45 year old mom, who was diagnosed at 29 with Celiac. My now 14 year old son was diagnosed just before his 4th birthday. Needless to say, we are old pros with the diet. He was experiencing some issues, overall health took a major plummet a year ago, and through a bit of work, was diagnosed with EOE. Tried diet alone, but his follow up endoscopy didn't show the improvements his DR. wanted to see, so I tried the medication. (Steroid). He became extremely backed up, and they had him taking Miralax daily. His health plummeted. He is a straight A honor's 8th grader who plays club soccer very competitively. His health continued to decline and at 13 had a colonoscopy and another upper gi. (He was still compacted even with the prep). I finally pulled him off all meds and mira lax, after reading much negative literature online, and put him on a gut detox diet and took him to a nutrition response dr. Finally things have improved. However...over a year later and he is having relapse stomach pain, debilitating stomach pain. Missing a day of school a week, to three this week. This is where we downward spiral with him. He says it doesn't feel the same as when he has gotten backed up before. He is eating prunes, taking his supplements, drinking water...all of the things. Yet, he is feeling horrible. Pain is abdomen, headache, lethargy, diarrhea . He is on a strict gluten dairy, egg free diet. He has adapted well in regards to diet. But I feel like we are missing something here. He is too active, too outgoing to be feeling sick all of the time. His Bilirubin is constantly high. His white blood count always runs slightly low. His vitamin D was very low last time he ran tests, (last month) when he was sick for a week. His celiac markers show negative, so it isn't that. His last endoscopy showed no Eosinaphils in his esophagus.  I have taken him to multiple Ped. Gastro specialists. They run tests, and we get zero answers. I meticulously go through labs, hoping to make some sense and maybe catch something. Any thoughts or ideas would greatly be appreciated. 
    • trents
      But if you have been off of wheat for a period of weeks/months leading up to the testing it will likely turn out to be negative for celiac disease, even if you actually have celiac disease. Given your symptoms when consuming gluten, we certainly understand your reluctance to undergo  the "gluten challenge" before testing but you need to understand that the testing may be a waste of time if you don't. What are you going to do if it is negative for celiac disease? Are you going to go back to merrily eating wheat/barley/rye products while living in pain and destroying your health? You will be in a conundrum. Do I or do I not? And you will likely have a difficult time being consistent with your diet. Celiac disease causes inflammation to the small bowel villous lining when gluten containing grains are consumed. This inflammation produces certain antibodies that can be detected in the blood after they reach a certain level, which takes weeks or months after the onset of the disease. If gluten is stopped or drastically reduced, the inflammation begins to decrease and so do the antibodies. Before long, their low levels are not detectable by testing and the antibody blood tests done for diagnosing celiac disease will be negative. Over time, this inflammation wears down the billions of microscopic, finger-like projections that make up the lining and form the nutrient absorbing layer of the small bowel where all the nutrition in our food is absorbed. As the villi bet worn down, vitamin and mineral deficiencies typically develop because absorption is compromised. An endoscopy with biopsy of the small bowel lining to microscopically examine this damage is usually the second stage of celiac disease diagnosis. However, when people cut out gluten or cut back on it significantly ahead of time before the biopsy is done, the villous lining has already experienced some healing and the microscopic examination may be negative or inconclusive. I'm not trying to tell you what to do I just want you to understand what the consequences of going gluten free ahead of testing are as far as test results go so that you will either not waste your time in having the tests done or will be prepared for negative test results and the impact that will have on your dietary decisions. And, who are these "consultants" you keep talking about and what are their qualifications? You are in the unenviable position that many who joint this forum have found themselves in. Namely, having begun a gluten free diet before getting a proper diagnosis but unwilling to enter into the gluten challenge for valid testing because of the severity of the symptoms it would cause them.
    • Fluka66
      Thank you very much for your reply. I hadn't heard of celiac disease but began to notice a pattern of pain. I've been on the floor more than once with agonising pain but this was always put down to another abdominal problem consequently I've been on a roundabout of backwards and forwards with another consultant for many years. I originally questioned this diagnosis but was assured it was the reason for my pain. Many years later the consultant gave up and I had a new GP. I started to cut out certain food types ,reading packets then really started to cut out wheat and went lactose free. After a month I reintroduced these in one meal and ended screaming in agony the tearing and bloating pain. With this info and a swollen lymph node in my neck I went back to the GP.  I have a referral now . I have also found out that acidic food is causing the terrible pain . My thoughts are this is irritating any ulcers. I'm hoping that after a decade the outlook isn't all bad. My blood test came back with a high marker but I didn't catch what it was. My GP and I have agreed that I won't go back on wheat just for the test due to the pain , my swollen lymph node and blood test results.  Trying to remain calm for the referral and perhaps needed to be more forceful all those years ago but I'm not assertive and consultants can be overwhelming. Many thanks for your reply . Wishing you all the best.
    • Moodiefoodie
      Wow! Fascinating info. Thanks so much! I really appreciate the guidance. @Spacepanther Over the years I have had rheumatologists do full lab work ups on me. They told me they had screened me for arthritis, lupus, and Lyme disease (all negative). In addition to joint pain and stiffness I had swelling in both knees that later moved to my elbow as well.  I also experience stiffness and pain in my neck and shoulders when it flares. I vomited fairly often growing up, but there wasn’t a real pattern to it and I didn’t know it wasn’t normal (thought people caught stomach viruses often).  I don’t usually have stomach symptoms immediately after eating gluten that I notice.  The only other joint condition I know of is fibromyalgia. Good luck! Hope you can get it figured out. I only assumed my joint symptoms were due to the celiac’s because it is under control for the most part on a gluten-free diet.  The rheumatologist also mentioned that some inflammatory/autoimmune diseases can be slow-moving and not detectable until they progress.
×
×
  • Create New...