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 Disease - Would Love Suggestions Or Advice


momandgirls

Recommended Posts

momandgirls Enthusiast

Hello - I've written before about my daughter and her test results (elevated TTG antibodies, negative endomysial antibodies, no flattening on biopsy but very high leukocytes, positive for CeliaGene and symptomatic for many years and particularly symptomatic when eating foods with high gluten like bread). So, even though the doctor, for whatever reason, is hesitant to diagnose her with Celiac (she keeps saying, "Well, she probably has it"), I've decided to take matters into my own hands and have made the decision to go gluten free for her (she's 11). I guess, since pretty much everything I know about Celiac I've learned from this board, I'm just looking for any advice or suggestions that anyone can give me. We're feeling sort of lost and overwhelmed at this point. What brands of food are the best? Any books that are particularly helpful? Corn and rice are always ok, right? But, then, I know there are other things to watch out for like modified food start - right? Honestly, just about anything you could tell me I'd appreciate. Thanks!


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



Celiac.com Sponsor (A8-M):



tiffjake Enthusiast
Hello - I've written before about my daughter and her test results (elevated TTG antibodies, negative endomysial antibodies, no flattening on biopsy but very high leukocytes, positive for CeliaGene and symptomatic for many years and particularly symptomatic when eating foods with high gluten like bread). So, even though the doctor, for whatever reason, is hesitant to diagnose her with Celiac (she keeps saying, "Well, she probably has it"), I've decided to take matters into my own hands and have made the decision to go gluten free for her (she's 11). I guess, since pretty much everything I know about Celiac I've learned from this board, I'm just looking for any advice or suggestions that anyone can give me. We're feeling sort of lost and overwhelmed at this point. What brands of food are the best? Any books that are particularly helpful? Corn and rice are always ok, right? But, then, I know there are other things to watch out for like modified food start - right? Honestly, just about anything you could tell me I'd appreciate. Thanks!

I would recomend getting a couple of books:

Dangerous Grains (if you like the scientific stuff)

Wheat Free, Worry Free by Danna Korn

And there are some really easy recipes in: Wheat-free, Gluten-free Cookbook for Kids and busy adults by Connie Sarros

I am pretty new to all of this too ( just a couple of months in for me) and I have a general rule to stay away from anything made with flour. (there are different kinds of flours, but when I have called the pizza place to ask if they had a gluten free pizza crust, they said "sure, we don't put that stuff in our pizzas" but they had no idea what I was talking about until I said "really? what kind of flour do you use" and they said "white flour" and I just thought, unless they KNOW, then they don't know the difference between soy flour, bean flour, wheat flour, etc. I even had someone say "we don't use wheat flour, we use white flour"......)

Unless I made it or bought it myself from a gluten-free company, I don't trust it. I stick with meat, veggies, and salads when eating out or at a friends. That might be a good rule of thumb for your daughter. And the "modified food starch" is what you are looking for, in things like salad dressings and canned baked beans and stuff like that. It would be in things that need to be thickened to taste better (according to the companies that make the stuff). The problem is that you don't know if you are getting corn starch or wheat starch (or any of 10 other starches) so unless you call the company and ask, it is better to be safe than sorry. Well, hope that is a good starting place!

momandgirls Enthusiast

Thank you - yes, your information is a great starting place. I'm going to try to get to the bookstore tonight as we're leaving on vacation on Sunday. I know that my local library doesn't have those books so hopefully Barnes and Noble will. I was wondering...what about vinegar? or canned/boxed broth? I'm trying to think of recipes that I was planning on cooking while away and what ingredients now should be subsituted...thanks!

teankerbell Apprentice

Go to Whole foods and get the Organic Chicken Broth. Some vinegars can be contaminated. If you go to Whole Foods website, you can print a list of gluten-free foods. Also, they label their shelves if it is gluten-free. Read the labels carefully, and look for the allergy alert. She should stay away from dairy for now.

Guest nini

Dana Korn also has a book called something like Kids with Celiac... anyway, I got a copy of that and I let her teachers read it as well as the school nurse. I also have printed letters for school to alert the staff to the dietary restrictions, but I also send her lunch to school. I don't rely on the school to provide her with a gluten free environment. That's not going to happen, so I just do the best I can. I send gluten-free playdough for her class, gluten-free pasta for art projects, safe snacks for birthday parties at school and I keep a supply of gluten-free cupcakes in the freezer to send if she has a birthday party to go to with friends...

It can be challenging, but the rewards are amazing. I was so impressed in the change in my child when she went gluten-free... it's been almost 3 years and she's doing so well with it.

Rachel--24 Collaborator

Barnes and Noble & Borders both have lots of books on gluten-free eating but I had trouble finding books on living with gluten intolerance. I had to order those from Amazon. Wheat Free, Worry Free is a great book and also Dangerous Grains. Dangerous Grains doesnt really deal with the diet itself...it gets more into the "what and why" of gluten intolerance. I love that book.

Have you checked out the safe/forbidden food lists? These lists are very helpful...print them out and keep them for reference.

https://www.celiac.com/st_main.html?p_catid...-25106081771.42

The delphi list is a list of mainstream foods that are gluten-free.

1) Go to the website, Open Original Shared Link

2) Click on "messages" or "start reading"

3) Select the folder "gluten-free Product List"

4) Click on the topic called "Downloadable files word"

5) Of the four options, choose the one in the upper right.

You may need to register (the basic version is free) in which case, just register first, then complete the steps above.

Keep asking questions. This is where I learned everything I needed to know. :)

TCA Contributor

Just so you know, we went back to the Ped. GI last week and he was still hesitant to give our kids an official diagnosis of celiac disease. They didn't have the gold standard of a positive biopsy and an diagnosis can make it harder to get insurance and such. He wants to wait and only give one if we have to have it. He said he knew I would keep them on the gluten-free diet since he knows me really well, but wanted to wait for a diagnosis since that would be with them for life. I don't know yet if I agree or not, but even with all the evidence, drs are still hesitant. go figure.

I sent my food list to you. Hope that helps!


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



Celiac.com Sponsor (A8-M):



ianm Apprentice
...and an diagnosis can make it harder to get insurance and such.

...wait for a diagnosis since that would be with them for life.

I have to agree with the Dr. on this issue. One of the reasons I refuse to get an official diagnosis is because of health insurance. The only thing you can do for celiac is change your diet. I had such a positive response to the dietary change that an official diagnosis would just mess my life up and I really don't need that right now.

tarnalberry Community Regular

The safest way to go is to stick to things that are whole foods and naturally gluten free - produce, beans, gluten-free grains, meats, eggs/dairy. if something comes in a box or a bag, ALWAYS read the label; NEVER assume. if it's prepared/processed in any way, ALWAYS read the label; NEVER assume. (part of the reason for ALWAYS reading the label is that companies DO change their formulas and have been known to add wheat to previously safe products.)

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. - Russ H replied to Charlie1946's topic in Related Issues & Disorders
      15

      Severe severe mouth pain

    2. - cristiana replied to Charlie1946's topic in Related Issues & Disorders
      15

      Severe severe mouth pain

    3. - Scott Adams replied to lmemsm's topic in Gluten-Free Recipes & Cooking Tips
      12

      gluten free cookie recipes

    4. - Florence Lillian replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Fermented foods, Kefir, Kombucha?

    5. - Charlie1946 replied to Charlie1946's topic in Related Issues & Disorders
      15

      Severe severe mouth pain

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

    • Total Members
      132,910
    • Most Online (within 30 mins)
      7,748

    probinson3870
    Newest Member
    probinson3870
    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

    • Russ H
      Hi Charlie, You sound like you have been having a rough time of it. Coeliac disease can cause a multitude of skin, mouth and throat problems. Mouth ulcers and enamel defects are well known but other oral conditions are also more common in people with coeliac disease: burning tongue, inflamed and swollen tongue, difficulty swallowing, redness and crusting in the mouth corners, and dry mouth to name but some. The link below is for paediatric dentistry but it applies to adults too.  Have you had follow up for you coeliac disease to check that your anti-tTG2 antibodies levels have come down? Are you certain that you not being exposed to significant amounts of gluten? Are you taking a PPI for your Barrett's oesophagus? Signs of changes to the tongue can be caused by nutritional deficiencies, particularly iron, B12 and B9 (folate) deficiency. I would make sure to take a good quality multivitamin every day and make sure to take it with vitamin C containing food - orange juice, broccoli, cabbage etc.  Sebaceous hyperplasia is common in older men and I can't find a link to coeliac disease.   Russ.   Oral Manifestations in Pediatric Patients with Coeliac Disease – A Review Article
    • cristiana
      Hi @Charlie1946 You are very welcome.   I agree wholeheartedly with @knitty kitty:  "I wish doctors would check for nutritional deficiencies and gastrointestinal issues before prescribing antidepressants." I had a type of tingling/sometimes pain in my cheek about 2 years after my diagnosis.  I noticed it after standing in cold wind, affecting  me after the event - for example, the evening after standing outside, I would feel either tingling or stabbing pain in my cheek.   I found using a neck roll seemed to help, reducing caffeine, making sure I was well-hydrated, taking B12 and C vitamins and magnesium.  Then when the lockdowns came and I was using a facemask I realised that this pain was almost entirely eliminated by keeping the wind off my face.  I think looking back I was suffering from a type of nerve pain/damage.  At the time read that coeliacs can suffer from nerve damage caused by nutritional deficiencies and inflammation, and there was hope that as bodywide healing took place, following the adoption of a strict gluten free diet and addressing nutritional deficiencies, recovery was possible.   During this time, I used to spend a lot of time outdoors with my then young children, who would be playing in the park, and I'd be sheltering my face with an upturned coat collar, trying to stay our of the cold wind!  It was during this time a number of people with a condition called Trigeminal Neuralgia came up to me and introduced themselves, which looking back was nothing short of miraculous as I live in a pretty sparsely populated rural community and it is quite a rare condition.   I met a number of non-coeliacs who had suffered with this issue  and all bar one found relief in taking medication like amitriptyline which are type of tricyclic anti-depressant.   They were not depressed, here their doctors had prescribed the drugs as pain killers to address nerve pain, hence I mention here.  Nerve pain caused by shingles is often treated with this type of medication in the UK too, so it is definitely worth bearing in mind if standard pain killers like aspirin aren't working. PS  How to make a neck roll with a towel: https://www.painreliefwellness.com.au/2017/10/18/cervical-neck-roll/#:~:text=1.,Very simple. 
    • Scott Adams
      We just added a ton of new recipes here: https://www.celiac.com/celiac-disease/gluten-free-recipes/gluten-free-dessert-recipes-pastries-cakes-cookies-etc/gluten-free-cookie-recipes/
    • Florence Lillian
      I have had celiac for many years and still had terrible digestion. I cook from scratch, never eat anything with gluten ( A Gut that needs special attention seems to affect many who suffer from celiac) .  I made my own Kombucha, it helped my Gut much more than the yogurt I made but I still had issues. Water Kefir did nothing. As a last resort I made MILK Kefir and it has really started healing my Gut. It has been about 2 months now and I am doing so much better. It was trial and error getting the right PH in the Kefir ferment that agreed with my stomach, too little ferment, too much, I finally hit the right one for me. Milk Kefir has the most probiotics than any of the other. I can't find my notes right now but there are at least 30 probiotics in Kefir, Kombucha has about 5-7 and yogurt around 3 if I recall correctly.  I wish you all the best, I know how frustrating this condition can be. 
    • Charlie1946
      @cristiana Hi, thank you so much, I will look into those books for sure! And get bloodwork at my next appointment. I have never been told I have TMJ, but I have seen information on it and the nerve issue while googling this devil plague in my mouth. Thank you so much for the advice!
×
×
  • 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.