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New To Diet...need Help


Crystalkd

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Crystalkd Contributor

Being so new to the diet and not being able to afford to continue eating the processed stuff I need help figuring out what "the basics" are. I like to cook but I'm not sure what the basics are of what I need to have to make alot of things myself. So far all I know I have is gluten problem. What do I need and what Brands to make things taste as "normal" as possible? I have to admit I'm a little lost.


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lcbannon Apprentice

I am fairly new to this as well, this site has been wonderful. NOGLUGIRL has a basic list I think, best advise I have is to read labels. As far as the pricey health food store stuff I try to stay away from most of this. I find I do not like the taste, i tend to find receipes and make my own and I have stepped outside of what I am used to eating. Overall I would say it has been a good process for me,

Go to your local library and check out some gluten-free cookbooks, find online receipes that are gluten-free.

I use corn tortillas for all kinds of wraps and even to wrap my burgers in. If you have an Asian Market near you the white rice, and other specialty flours are much cheaper there. Hang in there it gets better.

Crystalkd Contributor

We have a big international framers market here. I've been told things are cheap there. I need some pointers on the types and brands of gluten-free baking products and things that don't taste like cardboard. What cheeses can I eat? What are some things that have gluten in them that I might not sspect. I'm getting better at reading labels but it's still confusing and a bit difficult. Trying to carry around 5 pages of what does, doesn't, or may contain gluten makes it even more frustrating! I don't want to have to eat salads all the time or the same old boring dinners. I eat alot of Italian good and like my Cajun food as well. I'm trying to figure out how to eat the things I grew up on and not make myself sick. I'm also not opposed to trying new things. What spices should I stay away from? (brands) I think the Season Salt I have contains some form of gluten. There's so much to keep up with. At this early stage it's mind boggling. I have no doubt I'll get used to it. I know it'll take time.

Guhlia Rising Star

McCormick spices will clearly list gluten so you can season your meats and veggies so they don't always taste the same. There's a huge list of companies that will divulge any gluten, but I cant remember who usually posts the list, I don't have it. :(

For recipe ideas, it might be nice to invest in a few gluten free cookbooks. I recommend anything by Bette Hagman and Incredible Edible Gluten Free Food for Kids (not just for kids) by Shari L. Sanderson. Also, you can check out allrecipes.com for recipe ideas. Many recipes are naturally gluten free. You can use the list of companies that will list gluten to find the ingredients. I wish I could help you more on that one.

Welcome to the forum!

tom Contributor
Trying to carry around 5 pages of what does, doesn't, or may contain gluten makes it even more frustrating!

Boy that brings back memories. I was using a SIXTY page PDF and bought a Palm handheld just to always have the list w/ me.

For pasta, it's Tinkyada all the way. EXCEPT - if there's a Trader Joe's near u, it's a buck less and their house brand is, I believe even from the same factory in Canada. (They like to re-brand as a distributor)

As far as cooking, due to celiac-related complications, I suddenly had to only eat what *I* made but had few cooking skills. Watching the food channel or America's Test Kitchen on PBS will be a great help w/ the processes.

Like, how was *I* supposed to know to season a little every step. I woulda done it all at the beginning or end and it doesn't end up as flavorful.

I've seen some recent talk of asian flours (actually FROM asia) being more susceptible to cross-contamination, so u might want to keep that in mind at the international market.

Lillian Newbie
Being so new to the diet and not being able to afford to continue eating the processed stuff I need help figuring out what "the basics" are. I like to cook but I'm not sure what the basics are of what I need to have to make alot of things myself. So far all I know I have is gluten problem. What do I need and what Brands to make things taste as "normal" as possible? I have to admit I'm a little lost.

Hi Crystal, I've been on the gluten-free diet for about a year and a half now. The best thing to do is to get yourself in to see a nutrionist that specializes in gluten-free diets. Think of all that you can eat, as opposed to what you can't. For starters, any raw vegetabe or fruit is fine. As far as chicken, beef or fish is concerned, anything broiled with olive oil, oregano, garlic, lemon or gluten-free barbcue sauce is fine too. No lunch meats, except the ones that say 'gluten free'. Try to learn to like rice cakes or the tons of crackers that are gluten free instead of bread. I haven't tried a bread that I like yet, but just as well. As soon as you start healing, you'll probably put on some weight because you'll be absorbing nutrients, which you have probably not been absorbing til now. Rice, potatoes and rice pasta are fine too. Be careful with sushi. First of all, California rolls- NO- they have imitation crab meat- all preservatives. But if you like raw tuna sushi, vegetable sushi, or whatever is raw then fine with wheat free soy sauce only- very important. I actually take the wheat free soy sauce with me whenever we go for sushi.

Also it's good to have raw almonds around, fresh peanut butter, and some gluten free snack bars.

You'll do great. Stick to organic stuff whenever possible, no preservatives, prepared foods, or whatever you don't know about. You'll have to learn to be your own advocate- ask questions in restaurants- be careful with salad dressings- tons of them contain wheat- find a gluten-free you like and take with or ask for oil, vinegar and lemon.

It's totally doable. Yah, the food may be more expensive, but there is a solution to this intolerance. My motto is, pay now or pay later. Work on this everyday until is becomes natural. You can do it. Hope this helps!

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      Welcome to the celiac.com community @EssexMum! First, let me correct some misinformation you have been given. Except in the case of what is known as "refractory" celiac disease, which is very rare, it is not true that the "fingers" will not grow back once a consistently gluten free diet is adopted. Celiac disease is an autoimmune condition whereby the ingestion of gluten triggers an inflammatory process that damages the millions of tiny finger-like projections that make up the lining of the small bowel. We call this the "villous lining". Over time, continued ingestion of gluten on a regular basis results in the wearing down of these fingers which greatly reduces the surface area of this very important membrane. It is where essentially all the nutrition from what we eat is absorbed. So, losing this surface area results in inefficiency in nutrient absorption and often to medical problems related to nutrient deficiencies. Again, if a gluten-free diet is consistently observed, the villous lining of the small bowel should rebound. "We was informed that her body absorbs the gluten rather then rejecting it and that is why she doesn't react to the gluten straight away, it will be a build up and then the pains start. " That sounds like unscientific BS to me. But it does sound like your stepdaughter may have a type of celiac disease we know as "silent" celiac disease, meaning, she is asymptomatic or at least the symptoms are not intense enough to usually notice. She is not completely asymptomatic, however, because you stated was experiencing tummy aches off and on. Cristiana gives some good suggestions about ordering "safe" food for your stepdaughter from restaurant menus in Europe. You must realize that as the step parent who only has her part of the time you have no real control over how cooperative her other set of parents are with regard to your stepdaughter's needs to eat gluten free. It sounds like they don't really understand the seriousness of the matter. This is very common in family settings where other members are ignorant about celiac disease and the damage it can do to body systems. So, they don't take it seriously. The best you can do is make suggestions. Perhaps print out some info about celiac disease from the Internet to send them. Being inconsistent with the gluten free diet keeps the inflammation smoldering and delays or inhibits healing of the villous lining. 
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    • cristiana
      Good evening @EssexMum You are quite right to be concerned about this situation.  Once diagnosed as coeliac, always a coeliac, and the way to heal  is through adopting and sticking to a strict gluten diet. That said... I have travelled twice to France since my diagnosis, firstly in May 2013 and again in August 2019.   My spoken French isn't bad, and whilst there I tried my best to explain my needs to chefs and catering staff, and I read labels very carefully when shopping in supermarkets, but both times I came away with worsening gastric symptoms and pain. Interestingly,  after the second holiday, my annual coeliac review took place the following month and although I'd been very careful to avoid gluten all year, thanks to that August holiday my coeliac antibodies were elevated,  Clearly I hadn't been imagining these symptoms and they must have been caused by gluten sneaking in somehow. When I spoke to my gastroenterologist on my return, who is an excellent doctor, he told me with a smile that this was a very common experience in France among his patients, and not to worry too much about it! In fact, before we went away in May 2013, which was just after I had been formally diagnosed, he told me not to even bother trying to adopt a gluten free diet until I returned, knowing what France was like, but I was feeling so awful at that time I ignored his advice and at least tried to make a start with it. (I ought to say - both these visits were some time ago, so perhaps things are a lot better there now.) So what to do?  I would say at least try to explain to catering staff the situation - they should be able to rustle up a plate of cheese, boiled eggs, tuna, salad and fruit, and if things like crackers and gluten-free pot noodle or oats can be packed in the UK, those can be produced at mealtimes.    Of course, most larger supermarkets in France do now cater for coeliacs, but when I was last there the the choice wasn't as wide a range as we have in the UK but I think that is partly because the French like to cook from scratch, whereas our gluten-free aisles have quite a lot of dried or pre-baked goods in them/convenience foods, because I think we as a nation tend to use them more. I would be worth doing a bit of research on the internet before the trip, - the words you want are 'sans gluten'.  I've just googled 'sans gluten Disney Paris" and this came up.  I do hope at least some of this is of help. https://www.tripadvisor.co.uk/Restaurants-g2079053-zfz10992-Disneyland_Paris_Ile_de_France.html  Whatever befalls in France, at least your stepdaughter can resume her usual diet on her return. On a related tack, would you be happy to post any positive findings/tips upon her return - it might be of use to others travelling to Disneyland Paris with children in future? Cristiana
    • EssexMum
      Hi, I am after some advice re my step daughter and her Coeliac Disease. She is 9 years old and had a very limited diet before being diagnosed (very fussy and very lenient parents), since being diagnosed it has become hard to find places out that will cater for her, but we manage.  History: She had been having severe tummy pains on and off every few months so had a bunch of tests and eventually was diagnosed with celiac disease a number of months ago. We was told that she is at a very high level and should avoid gluten for the rest of her lift, we was told that the gluten she has been eating has damaged the 'fingers' inside her and they will not replenish. We was informed that her body absorbs the gluten rather then rejecting it and that is why she doesnt react to the gluten straight away, it will be a build up and then the pains start. We was advised that by her not reacting straight away, it did not mean it wasnt harming her inside. We was given literature about buying a separate toaster and cutting board etc to avoid cross contamination and have been checking all food labels etc.  Problem: the issue is the novelty seems to have worn off with her Mum and we are now posed with a situation. They are going on holiday to Disneyland Paris for 3 nights and she phoned the hotel who said they cannot cater for gluten free. She phoned the GP and had a conversation and then told my partner that the GP had said it was fine for her to have gluten for the 3-4 days. He questioned it and she said no its fine, she hasnt had it for months so a few days wont hurt and she exposed to it anyway without knowing so it will be fine and shes not ruining her holiday etc.   My partner could see from the online notes that his ex wife had told the doctor that the child does not follow a strict gluten-free diet anyway - not true. At least not with us! My partner requested a call with the same doctor who told him that it is the mums discretion and that the child should be monitored for reactions - he explained that the issue is she doesnt react straight away. The GP said no its all mums discretion and she knows best. We are going to try to speak to the consultant at the hospital, but I just wanted to gauge some thoughts. It just seems bizarre to me that we can go from being told to avoid gluten for the rest of her life and how harmful it is to her body, to now it being ok for her to have it for a few days. Thanks in advance  
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