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

Completely New To Gluten Free Diet


alexschatzi

Recommended Posts

alexschatzi Rookie

I don't even know where to start. I just got my diagnoses from my Natruopath on my food sensitivity to Gluten. What do you eat. I am not even sure what Gluten means. Just slightly overwhelmed. I bought a few products at the health food store. What about lunch meats, tomato sauce, fish, dairy etc. What do you cook? Any wine alowed? I am supposed to stay away from sugar as well because of the candida. Any tips will be appreciated!


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



Celiac.com Sponsor (A8-M):



dlp252 Apprentice

Hi, it's a little overwhelming at first but you'll get the hang of it very quickly. I can do the basics...

Gluten = the protein in wheat, oats, rye and barley and anything made with those products. Gluten also can be found in other grains but it is a different kind of gluten.

You'll unfortunately have to read labels because all of those things can be used in other things. Soy sauce comes to mind. Who'd a thunk that wheat would be in soy sauce, but it's there in some brands...but there are also some without.

Tinkyada makes a VERY good brown rice pasta and really, I like every bit as much as "regular" pasta, and I'm part Italian, lol. They sell this brands in some of the major supermarkets now too.

Rice and brown rice are naturally gluten free as are potatoes, fruits, veggies...

Be careful on some lunch meats...I don' t have a list offhand, but there can be some natural flavorings added which could contain gluten...gosh, why can't I remember the name of the brands that are okay, lol.

Basically you have to look at things like tomatoe sauce to be sure that the "flavorings" aren't wheat.

I don't like wine so can't help with that...

Okay, brain fog is setting in, hope that helped a little.

Pilgrim South Rookie
I don't even know where to start. I just got my diagnoses from my Natruopath on my food sensitivity to Gluten. What do you eat. I am not even sure what Gluten means. Just slightly overwhelmed. I bought a few products at the health food store. What about lunch meats, tomato sauce, fish, dairy etc. What do you cook? Any wine alowed? I am supposed to stay away from sugar as well because of the candida. Any tips will be appreciated!

Its really not that bad, once you get the hang of it, it will become natural. First, wine is a sugar, so I would guess you will need to keep away from it for a while. Lunch meats, unless they are from places like Whole Foods, will have nitrates, which are carcinagenic and can contain all sorts of things. Gluten would be wheat, oats, barley, and rye. There are gluten free lists of do's and don'ts in various places, including Clan Thompson's great food/drug lists. You can get them in paper form or downloadable searchable forms. There are tons of celiac web sites with oodles of information, just google gluten free or celiac and you will have hours and hours of helps and fun. There are tremendous cookbooks, Carol Fensters are my favorite. Bob's Red mill is great...here is where their gluten free foods are listed Open Original Shared Link

They have tons of recipes and you can search for gluten free ones. There are several, actually "many" places on the internet to order gluten free foods, just google gluten free foods and see what wonderful things come up!

I cook normal with normal fresh meats and veg's. I adapt my old favorite recipes to make them gluten free, even chocolate chip cookies. There are many "packaged" gluten free cakes, cookies, breads etc. and etc. and there are more being created all the time! Where I love Whild Oats actually has more gluten free selections, and I think its because Whole Foods bakes their own gluten free things. They have dairy that our family can't have so we can't buy their things. I just ordered 100 #'s of 4 different gluten free flours and mixes because we eat tons of gluten-free waffles, breads and baked goods. You can buy things in small packages or in larger quantities like the 25# bags of mix and flours like I did. There is even a Dummies book for gluten free living! Open Original Shared Link .com/Living-Gluten-Free-D...s/dp/0471773832

I hope this helps a little and just know you are probably going to feel so much better once you get the hang of it! This list is super helpful and they are only a click away! Happy gluten-free living!

TinkerbellSwt Collaborator

Hormel Natural Lunch meats that are sold in the regular grocery store in the dairy sections usually are gluten free, always double check.. these do say gluten free on the back. Oscar Mayer beef bologna is gluten free also. There are a lot of foods out there that are just naturally gluten free.. you will have to become an avid label reader, it takes time to get used to.. but in the long run it is the safest bet.

Welcome to the board, ask any questions you need answered. There are no stupid questions. The only stupid ones are the ones not asked. There are many great recipes on this site, particularly Carrie's and tarnalberrys.. they have lots of good stuff, as do many others.

Please just reach out for the help. The people on this board are great and have been life savers!

Welcome!! :)

Gamecreature Rookie

First of all, don't panic.

The basic rule of thumb is that the closer you get to food in its natural state (fresh, unprocessed) the less likely it is to be contaminated with gluten. Fresh fruit and veggies are perfectly safe to eat. Some folks have a reaction to dairy until their intestine heals, so keep an eye out for that. Avoid contamination - keep an eye out for bread or wheat coming in contact with your food - you can't just eat around it or pick it off. The same goes for old cookware that might have particles of gluten (especially pasta) stuck in cracks and crevases.

One of the regulars here has put together a good package of materials that you can download - check it out here:

Open Original Shared Link (scroll down)

Good luck.

alexschatzi Rookie

Thank you all so much for your helpful insights. I will do some research on the sights and products you all recommended. Its great to know that there are people out there that are in the same boat. Thanks again everybody!!!!

Aerin328 Apprentice

Yes, first step is not to panic! Just take one step at a time. There are many great "newbie" directed posts on this forum (you can search for them) which go over all the basics of starting up in considerable detail. As you inevitably have questions you can always turn to this forum, there are so many great people here who are willing to help any time. Also, know that you are not alone - there are millions going gluten-free in the US alone and the number is growing.

And welcome to the forum!

Christian


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



Celiac.com Sponsor (A8-M):



happygirl Collaborator

Alex,

Welcome to the gluten free world and the forum. This will definitely be the best place for you!

I highly recommend reading the information on celiac.com, including the lists https://www.celiac.com/st_main.html?p_catid=12

www.celiaccenter.org has great information. Dr. Fasano is one of the leading researchers in Celiac and is at the Univ. of Maryland at Baltimore (it is his celiac center that hosts that link)

I highly recommend getting and reading Dr. Peter Green's "Celiac Disease: A Hidden Epidemic" It is a great, very thorough book that will give you a great foundation for learning about celiac disease. You can order on amazon and some book stores have it, or can order it for you. I wish I had this book when I was diagnosed...it would have all made so much sense.

Tinkyada rice pastas are the best gluten free noodle. They come in all shapes/forms. You can find them in some grocery stores, health food stores, and online.

Amy's frozen foods makes some gluten free frozen products.

I'm not always on and posting, so feel free to PM me if you have any questions. This is so overwhelming, but we really want to help you in any way possible. No question is too off limits...and we mean that. We all started somewhere and all had our day of diagnosis where our head was spinning...so let us know what we can do!

Laura

Rusla Enthusiast

Welcome to the forum. Being gluten-free is not bad and if more restaurants will get on board with it, it will become easier. The biggest problem you or any of us will have is accidental glutenings and being glutened by others.

Guhlia Rising Star

I don't have much to add. The others have given you some pretty good advice. I just wanted to pop my head in and say welcome.

tarnalberry Community Regular

Gluten is the protein is wheat, barley, rye, and oats. So, you need to avoid those grains, and any ingredients that come from those grains. The easiest thing to do is to stick to whole, natural foods - produce, non-gluten grains, meats, and dairy. Take a look around the site and look at the safe/unsafe list, and the newbie kit (nini's, I believe?).

It's a big learning curve, and don't feel alone or odd for feeling overwhelmed - that's a VERY common, dare I say universal, response. It'll take time to get past the learning curve and figure out what to eat, how to avoid contamination in the home, how to eat out, and how to deal with friends and family. But in a few months, you will have a lot more knowledge and experience. It doesn't help a lot to know that now, but know that it will be better.

almostnrn Explorer

If you haven't found it already there is a great string running in Gluten free foods, products section. Its everyone's favorite foods and man I wish I had found that when I was first diagnosed. Good luck!

Guest nini

Welcome, I see someone already posted the link for my webpage so that you can download the newbie survival kit. It's just a bunch of files I wish I'd had when I was first diagnosed.

The best piece of advice anyone ever gave me was to focus on what foods you CAN have, not on what you can't.

Also, if you post where you live (city?) then hopefully someone near you can point you in the direction of local sources of good gluten-free foods.

Initially stick with foods that are naturally gluten free and don't go crazy buying specialty products, wait until you've healed a bit and then ask around for most people's favorites (or you can do a search on this forum).

As far as the candida issue goes, IF you have a problem with candida you may want to avoid sugars and yeasts as well until you get better. I personally just used a product called Candida Cleanse. (I wasn't willing to give up my sugar and yeast as well as the gluten!)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,963
    • Most Online (within 30 mins)
      7,748

    AlissaW
    Newest Member
    AlissaW
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.