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 Our Content
    eNewsletter
    Donate

Cooking Brown Rice Noodles...Tips?


misslexi

Recommended Posts

misslexi Apprentice

I don't remember this happening the first few times I made brown rice noodles, maybe its a brand issue...but the last several times, with different types, they stick to the bottom! Like crazy, and I don't mean they burn they just stick on good. Not only that but there ends up being this gooey, starchy film over them and I have to rinse them before I can eat them haha.

I add a little bit of vegetable oil like I always do, just like with wheat noodles.

Is there something different I should be doing to get rid of the gooey, and to stop them from sticking so much?


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



Celiac.com Sponsor (A8-M):



purple Community Regular

There are lots of posts on this subject that you could google (Tinkyada). My first thought is use lots of water. I rinse the slime (some don't) :rolleyes: Never had slime with the lasagna noodles. I am sure others will chime in too!

Janessa Rookie

Use more water to avoid the thick starchy film, when you first put the pasta in the water stir it really well and stir more often while it is cooking. I find stirring it really well in the beginning and more often toward the end keeps it from sticking to itself and the pan

VickiLynn Newbie

Use more water to avoid the thick starchy film, when you first put the pasta in the water stir it really well and stir more often while it is cooking. I find stirring it really well in the beginning and more often toward the end keeps it from sticking to itself and the pan

I agree, more water, drop of oil in the water and lots of stirring. Rinsing the pasta is important as well.

celiac-mommy Collaborator

This is what I do:

Make sure your water is at a FULL rolling boil, add pasta, stir well to separate, bring back up to a full boil, decrease heat to a small boil, I only cook for 1/2 the suggested time and then check for doneness. I find that gluten-free pastas cook for less time than the directions state. Drain and rinse.

  • 2 weeks later...
Darissa Contributor

If you can have corn, we love corn pasta much more than rice pasta. We use Mrs. Leepers corn pastas. WE buy them at our local Walmart and at Whole Foods. You can also buy them over the web. IMHO, they hold up much better and taste much better than the rice. We serve them to guest when they come over and they have no idea they are eating a gluten free corn pasta. The kids love them!

Before we found the corn pasta, my brown rice pasta would stick also. I switched over to a nonstick pan, and lowered the heat, and that seemed to help some. Good luck!

CelestialNav Newbie

Tinkyada is a good Rice Pasta. But, I apply the same rule as I do to rice. I put the Rice Pasta into the boiling water, but after stirring it for a bit, I put the lid on the pot and turn off the heat and let it sit for about 6 to 8 minutes. It is usually done to my liking in that time. I drain it in a collandar and serve it with whatever Sauce I've made. I don't rinse it as that washes away nutrients. But, I have found that Thai Kitchen Rice Noodles work much better. Plus, they are easier to find in your Supermarket and easier for your Supermarket to get in for you. Try them, you might like them better and they're not mushy if made per the above directions. ;)


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



Celiac.com Sponsor (A8-M):



Juliebove Rising Star

You're not supposed to add oil with noodles of any kind. I don't know who came up with that idea!

You need to start with a HUGE pot of boiling, salted water. If there's not enough water and it's not boiling, you'll have problems.

I have Rachel Ray's Oval Spaghetti Pot. I use it for all my pasta. I never have trouble.

digmom1014 Enthusiast

You're not supposed to add oil with noodles of any kind. I don't know who came up with that idea!

You need to start with a HUGE pot of boiling, salted water. If there's not enough water and it's not boiling, you'll have problems.

I have Rachel Ray's Oval Spaghetti Pot. I use it for all my pasta. I never have trouble.

My prblem is the water ALWAYS boils over the top and is darn hard to clean off my glass stovetop. If anyone has any suggestions...

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,620
    • Most Online (within 30 mins)
      7,748

    Su p
    Newest Member
    Su p
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Rejoicephd
      Thanks @cristiana I really appreciate hearing all of this... I definitely need to look out better for the shared dishes/pans/ovens thing.  I'm currently not doing a good job of that at all.  But I think I need to make the airfryer a gluten-free only airfryer.  I've been keeping a food diary for these past few days and so far its been interesting.  I think I have 2 issues going on: I get a head/neck/shoulder/jaw ache when I get glutened (as well as feeling fatigued and brain fog).  At least this is what I think are my symptoms from consuming gluten.  I think that the only things I consumed were marked gluten-free, but they were a combination of "certified gluten-free" and "gluten-free", so I think I am definitely worried thinking that the "gluten-free" non-certifieds are not good enough for me.  Also, I feel like the issue of cross-contamination of dishes could be an issue for me too.  But there's also a second issue I'm trying to figure out.  I ate 2 dishes containing chicken this week from gluten-free companies (frozen dish, fully contained and sealed) - one of which had the "certified gluten free" logo on it.  And right after eating, I had bowel movements that I think would be classified as steatorrhea.  I have this type of bowel movement multiple times a week lately, which has become quite miserable. But from my food diary, I can tell that when I don't eat meat or eat fish, I am not experiencing this issue. From my reading, I can see that steatorrhea can result from malabsorption in the gut due to celiac, and I know that I do have issues with malabsorption because I have iron-deficiency anemia (my ferritin was 10 when last tested). I also had low potassium and low Vitamin D when first diagnosed with celiac, but both have come back into the normal range since I started going gluten-free and taking supplements.   Based on what you all are saying, I am now thinking that my iron-deficiency anemia, my steatorrhea, and my head/neck aches may all still be persisting because I'm still consuming this lingering amount of gluten regularly.  I've really got to do a lot to switch over to ONLY eating certified gluten-free products and also creating a clean space within my kitchen that is just for me to use, and probably just skip restaurants completely for a while... Also maybe in the mean time, I might just keep my foods simple.. no dairy or meats (just fish) which my stomach seems happier with. Do you all think this is something I should go into my GI doctor about?  Because when I saw her last, I wasn't having steatorrhea.  My GI symptoms were actually kind of mild, which I thought was sort of strange since I had just got diagnosed with celiac disease.  I was dealing with mostly headaches, etc and so I've been mostly working with a neurologist and physical therapist on these symptoms.. but there's only so much they can do when I trigger a brand new headache/stiff neck every week and I'm starting to think that celiac is at the root of all of this...  Thanks for all your support and insights
    • trents
      Welcome to the forum, @AnneBSunflower! Can you be more specific about the gluten antibodies? Which ones were found? Do you have access to the report and can you post the results? What is a "GI map"? How was this done? Is this a fecal matter test? Are you still consuming oats? Even "Gluten-free" oats? Have you checked all meds and supplements for possible gluten fillers or casings? Oral hygiene products? Are you sharing cooking facilities with wheat eaters?
    • AnneBSunflower
      Hi. I am looking for mystery gluten in my diet due to having a GI map done recently and the results found gluten antibodies. However, let me provide a bit of background. I was diagnosed with Hashimoto's 15 years ago. Ten years ago I consulted with a functional medicine doctor who put me on the AIP diet due to gastrointestinal distress. She did not diagnose me with celiac disease, but my thyroid antibodies skyrocketed when we reintroduced gluten after 6 months on the AIP diet. I have been maintaining a gluten free diet for 10 years. I have on again, off again gut issues, cannot lose weight, chronic vitamin deficiencies despite a diet focused on whole foods, and my thyroid numbers are whacky even with medication (my T3 is good, T4 chronically low, TSH low). My doctor diagnosed me this week as having celiac in addition to the Hashimoto's. Again, I have been eating gluten free for 10 years. My doctor says there is something I am eating that my body is reacting to that has gluten and I have inflammation in my gut. I don't buy anything that is processed without reading the label and it stating it is gluten free. I know things like soy sauce, salad dressing, potato chips (I haven't eaten a potato chip in probably 30 years), roasted nuts, lunch meat, etc. can have gluten. What else? Does Armour Thyroid have gluten? Kirkland Almond non-dairy beverage (doesn't say gluten free, but there are no ingredients that would indicate gluten)? Philadelphia Cream cheese plant-based cream cheese says it is gluten free but it contains maltodextrin, could this still be a source of gluten? If the plant-based cream cheese with maltodextrin could be a source of gluten, could anything labeled gluten free but containing maltodextrin still be a source of gluten?
    • cristiana
      I struggled for a long time.   My TTG levels took an age to come down.  I even gave pure gluten free oats a miss, it took 8 years before I could tolerate them.  Removing dairy temporarily from my diet was hugely helpful.  Check your utensils and the oven you use are scrupulously clean, and don't open roast or bake food uncovered in an oven shared with gluten eaters.  Shared grills must be thoroughly cleaned down, too. Our oven packed up a couple of years after I was diagnosed and after that time the top oven became my family's oven, I use the lower oven.  Also our dishwasher - the old one left a residue, and sharing with gluten eaters I think this was an important factor in my slow recovery.  When the dishwasher packed up I started hand washing the plates and making sure they were really rinsed well.  When we got a new one we bought a Miele does the initial rinse with clean water, not yesterday's old water.   I stopped eating out for a while - that's a biggie.  In recent years, in the UK, thanks to Zoe's Law, caterers are having to really tighten up on catering for people with coeliac disease and allergies so I am now finding eating out much less risky.  But I'd advise being very careful with restaurants where flour is thrown about and is airborne (such as pizzerias) or where harried chefs might cook pasta in glutenous water by mistake, as those are the places I've been glutened in the most.
    • kopiq
      also my hands are always cold, freezing cold in the winter and even cold during hot summer days. its like i have a shield. i feel warm but its not penetrating inside, my teeth chatter as well and my left index finger goes dead white when im super hungry. all dr tests come back fine. im so hopeless.
×
×
  • Create New...